WO2023014908A1 - Lpar1 antagonists and uses thereof - Google Patents

Lpar1 antagonists and uses thereof Download PDF

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Publication number
WO2023014908A1
WO2023014908A1 PCT/US2022/039466 US2022039466W WO2023014908A1 WO 2023014908 A1 WO2023014908 A1 WO 2023014908A1 US 2022039466 W US2022039466 W US 2022039466W WO 2023014908 A1 WO2023014908 A1 WO 2023014908A1
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Prior art keywords
substituted
unsubstituted
membered
heterocycloalkyl
substituent group
Prior art date
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PCT/US2022/039466
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English (en)
French (fr)
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WO2023014908A8 (en
Inventor
Jeffrey Roger Roppe
Austin Chih-Yu Chen
Yifeng Xiong
Thomas Schrader
Lino Valdez
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Contineum Therapeutics Inc
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Pipeline Therapeutics Inc
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Priority to MX2024001608A priority Critical patent/MX2024001608A/es
Application filed by Pipeline Therapeutics Inc filed Critical Pipeline Therapeutics Inc
Priority to EP22853924.3A priority patent/EP4380560A4/en
Priority to KR1020247007354A priority patent/KR20240046204A/ko
Priority to CN202280064596.4A priority patent/CN118043041A/zh
Priority to JP2024507146A priority patent/JP2024530948A/ja
Priority to US18/294,515 priority patent/US20250034110A1/en
Priority to IL310576A priority patent/IL310576A/en
Priority to CA3228299A priority patent/CA3228299A1/en
Priority to AU2022324465A priority patent/AU2022324465A1/en
Publication of WO2023014908A1 publication Critical patent/WO2023014908A1/en
Anticipated expiration legal-status Critical
Publication of WO2023014908A8 publication Critical patent/WO2023014908A8/en
Ceased legal-status Critical Current

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    • A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
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Definitions

  • Lysophosphatidic acid is a family of bioactive phospholipids that are associated with multiple cellular functions. While the family members differ with regards to the length and the degree of saturation of their respective long-chain fatty acid backbone (Fujiwara et al., J. Biol. Chem., 2005, 280, 35038-35050), they are all capped by a glycerolphosphate group through an ester linkage.
  • LPAs are produced biologically from membrane phospholipids through a multi-step cascade mediated by enzymes that include lysophospholipase D (lysoPLD), autotaxin (ATX), phospholipase Al (PLA1), phospholipase A2 (PLA2) and acylglycerol kinase (AGK) (Mutoh et al., British J. Pharmacol., 2012, 165, 829-844).
  • LPAs can regulate numerous cellular signaling pathways by binding to a class of 7-membrane domain G protein-coupled receptors (GPCRs), collectively known as LPA receptors (LPARs), of which six have been characterized: LPAR1, LPAR2, LPAR3, LPAR4, LPAR5, and LPAR6 (Choi, J. W ., Annu. Rev. Pharmacol. Toxicol., 2010, 50, 157-186).
  • GPCRs 7-membrane domain G protein-coupled receptors
  • LPARs LPA receptors
  • the biological responses elicited by the binding of LPAs to LPARs are both wide-ranging and context-dependent (Yung etal., J. Lipid Res. 2014, 55, 1192-1214; Yung et al., Neuron 2015, 85, 669-682).
  • LPA pathway has been implicated in multiple diseases, including cancer, inflammatory diseases, infertility, neuropathic pain, psychotic and neurodegenerative disorders, atherosclerosis, as well as fibrosis of the skin, kidney, lung, and liver (Choi, J. W ., Annu. Rev. Pharmacol. Toxicol., 2010, 50, 157-186;
  • L 1 is a bond or substituted or unsubstituted C1-C5 alkylene.
  • R 1 is unsubstituted C2-C5 alkyl.
  • W 2 is N or C(R 2 ).
  • R 2 is hydrogen, halogen, -CX 2 3 , -CHX 2 2 , -CH 2 X 2 , -OCX 2 3 , -OCH 2 X 2 , -OCHX 2 2 , -CN, -SO I12 R 2D , -SO V2 NR 2A R 2B , -NR 2C NR 2A R 2B , -ONR 2A R 2B , -NHC(O)NR 2C NR 2A R 2B , -NHC(O)NR 2A R 2B , -N(O) m2 , -NR 2A R 2B , -C(O)R 2C , -C(O)OR 2C , -C(O)NR 2A R 2B , -OR 2D , -SR 2D , -NR 2A SO 2 R 2D , -NR 2A C(O)R 2C , -NR 2A C
  • R 3 is hydrogen, halogen, -CX 3 3 , -CHX 3 2 , -CH 2 X 3 , -OCX 3 3 , -OCH 2 X 3 , -OCHX 3 2 , -CN, -SOn 3 R 3B , -SO V3 NR 3A R 3B , -NR 3C NR 3A R 3B , -ONR 3A R 3B , -NHC(O)NR 3C NR 3A R 3B , -NHC(O)NR 3A R 3B , -N(O) m3 , -NR 3A R 3B , -C(O)R 3C , -C(O)OR 3C , -C(O)NR 3A R 3B , -OR 3D , -SR 3D , -NR 3A SO 2 R 3D , -NR 3A C(O)R 3C , -NR 3A C
  • W 4 is N or C(R 4 ).
  • R 4 is hydrogen, halogen, -CX 4 3 , -CHX 4 2 , -CH 2 X 4 , -OCX 4 3 , -OCH 2 X 4 , -OCHX 4 2 , -CN, -SOn 4 R 4D , -SOV 4 NR 4A R 4B , -NR 4C NR 4A R 4B , -ONR 4A R 4B , -NHC(O)NR 4C NR 4A R 4B , -NHC(O)NR 4A R 4B , -N(O)m4, -NR 4A R 4B , -C(O)R 4C , -C(O)OR 4C , -C(O)NR 4A R 4B , -OR 4D , -SR 4D , -NR 4A SO 2 R 4D , -NR 4A C(O)R 4C , -NR 4A C(O)C ,
  • W 5 is N or C(R 5 ).
  • R 5 is hydrogen, halogen, -CX 5 3 , -CHX 5 2 , -CH 2 X 5 , -OCX 5 3 , -OCH 2 X 5 , -OCHX 5 2 , -CN, -SOnsR 5D , -SOV 5 NR 5A R 5B , -NR 5C NR 5A R 5B , -ONR 5A R 5B , -NHC(O)NR 5C NR 5A R 5B , -NHC(O)NR 5A R 5B , -N(O)m5, -NR 5A R 5B , -C(O)R 5C , -C(O)OR 5C , -C(O)NR 5A R 5B , -OR 5D , -SR 5D , -NR 5A SO 2 R 5D , -NR 5A C(O)R 5C , -NR 5A C(O) C(O
  • R 2 and R 3 substituents may optionally be joined to form a substituted or unsubstituted cycloalkyl, substituted or unsubstituted heterocycloalkyl, substituted or unsubstituted aryl, or substituted or unsubstituted heteroaryl.
  • R 3 and R 4 substituents may optionally be joined to form a substituted or unsubstituted cycloalkyl, substituted or unsubstituted heterocycloalkyl, substituted or unsubstituted aryl, or substituted or unsubstituted heteroaryl.
  • R 4 and R 5 substituents may optionally be joined to form a substituted or unsubstituted cycloalkyl, substituted or unsubstituted heterocycloalkyl, substituted or unsubstituted aryl, or substituted or unsubstituted heteroaryl.
  • W 6 is N or C(R 6 ).
  • R 6 is hydrogen, halogen, -CX 6 3 , -CHX 6 2 , -CH 2 X 6 , -OCX 6 3 , -OCH 2 X 6 , -OCHX 6 2 , -CN, -SOn 6 R 6D , -SOV 6 NR 6A R 6B , -NR 6C NR 6A R 6B , -ONR 6A R 6B , -NHC(O)NR 6C NR 6A R 6B , -NHC(O)NR 6A R 6B , -N(O) m6 , -NR 6A R 6B , -C(O)R 6C , -C(O)OR 6C , -C(O)NR 6A R 6B , -OR 6D , -SR 6D , -NR 6A SO 2 R 6D , -NR 6A C(O)R 6C , -NR 6A C
  • W 7 is N, N + -O', or C(R 7 ).
  • R 7 is hydrogen, halogen, -CX 7 3 , -CHX 7 2 , -CH 2 X 7 , -OCX 7 3 , -OCH 2 X 7 , -OCHX 7 2 , -CN, -SOn7R 7D , -SOV7NR 7A R 7B , -NR 7C NR 7A R 7B , -ONR 7A R 7B , -NHC(O)NR 7C NR 7A R 7B , -NHC(O)NR 7A R 7B , -N(O)m7, -NR 7A R 7B , -C(O)R 7C , -C(O)OR 7C , -C(O)NR 7A R 7B , -OR 7D , -SR 7D , -NR 7A SO 2 R 7D ,
  • R 8 is independently halogen, -CX 8 3 , -CHX 8 2 , -CH 2 X 8 , -OCX 8 3 , -OCH 2 X 8 , -OCHX 8 2 , -CN, -SO n8 R 8D , -SO v8 NR 8A R 8B , -NR 8C NR 8A R 8B , -ONR 8A R 8B , -NHC(O)NR 8C NR 8A R 8B , -NHC(O)NR 8A R 8B , -N(O) m8 , -NR 8A R 8B , -C(O)R 8C , -C(O)OR 8C , -C(O)NR 8A R 8B , -OR 8D , -SR 8D , -NR 8A SO 2 R 8D , -NR 8A C(O)R 8C , -NR 8A
  • R 9 is substituted or unsubstituted cycloalkyl or substituted or unsubstituted heterocycloalkyl.
  • R 2A , R 2B , R 2C , R 2D , R 3A , R 3B , R 3C , R 3D , R 4A , R 4B , R 4C , R 4D , R 5A , R 5B , R 5C , R 5D , R 6A , R 6B , R 6C , R 6D , R 7A , R 7B , R 7C , R 7D , R 8A , R 8B , R 8C , and R 8D are independently hydrogen, -CC1 3 , -CBr 3 , -CF 3 , -CI 3 , -CHCl 2 , -CHBr 2 , -CHF 2 , -CHI 2 , -CH 2 C1, -CH 2 Br, -CH 2 F, -CH 2 I, -CN, -OH, -NH 2 , -COOH, -CONH 2 , -
  • X 2 , X 3 , X 4 , X 5 , X 6 , X 7 , and X 8 are independently -F, -Cl, -Br, or -I.
  • n2, n3, n4, n5, n6, n7, and n8 are independently an integer from 0 to 4.
  • the symbols m2, m3, m4, m5, m6, m7, m8, v2, v3, v4, v5, v6, v7, and v8 are independently 1 or 2.
  • the symbol z8 is an integer from 0 to 3.
  • a compound, or a pharmaceutically acceptable salt or solvate thereof, having the formula: are as described herein, including in embodiments. At least one of W 6 or W 7 is N. If W 6 is C(R 6 ) or W 7 is C(R 7 ), then R 10 is not hydrogen. If W 6 and W 7 are both N, then R 3 is not
  • R 10 is hydrogen, halogen, -CX 10 3 , -CHX 10 2 , -CH 2 X 10 , -OCX 10 3 , -OCH 2 X 10 ,
  • R 10 and R 2 substituents may optionally be joined to form a substituted or unsubstituted cycloalkyl, substituted or unsubstituted heterocycloalkyl, substituted or unsubstituted aryl, or substituted or unsubstituted heteroaryl.
  • R 1OA , R 1OB , R 1OC , and R 10D are independently hydrogen, -CCl 3 , -CBrs, -CF3, -Cl 3 , -CHCl 3 , -CHBr 2 , -CHF 2 , -CHI 2 , -CH 2 C1, -CH 2 Br, -CH 2 F, -CH 2 I, -CN, -OH, -NH 2 , -COOH, -CONH 2 , -OCCl 3 , -OCF3, -OCBr 3 , -OCl 3 , -OCHCl 2 , -OCHBr 2 , -OCHI 2 , -OCHF 2 , -OCH 2 C1, -OCH 2 Br, -OCH 2 I, -OCH 2 F, substituted or unsubstituted alkyl, substituted or unsubstituted heteroalkyl, substituted or unsubstituted cycl
  • X 10 is independently -F, -Cl, -Br, or -I.
  • nlO is an integer from 0 to 4.
  • mlO and vlO are independently 1 or 2.
  • a pharmaceutical composition including a compound described herein, or a pharmaceutically acceptable salt or solvate thereof, and a pharmaceutically acceptable excipient.
  • a method of treating a neurodegenerative disorder in a subject in need thereof including administering to the subject in need thereof a therapeutically effective amount of a compound described herein, or a pharmaceutically acceptable salt of solvate thereof.
  • a method of treating an inflammatory disease in a subject in need thereof including administering to the subject in need thereof a therapeutically effective amount of a compound described herein, or a pharmaceutically acceptable salt of solvate thereof.
  • a method of treating a demyelinating disease in a subject in need thereof including administering to the subject in need thereof a therapeutically effective amount of a compound described herein, or a pharmaceutically acceptable salt of solvate thereof.
  • a method of treating fibrotic disease in a subject in need thereof including administering to the subject in need thereof a therapeutically effective amount of a compound described herein, or a pharmaceutically acceptable salt of solvate thereof.
  • a method of treating cancer in a subject in need thereof including administering to the subject in need thereof a therapeutically effective amount of a compound described herein, or a pharmaceutically acceptable salt of solvate thereof.
  • a method of treating an LP ARI -associated disease in a subject in need thereof including administering to the subject in need thereof a therapeutically effective amount of a compound described herein, or a pharmaceutically acceptable salt of solvate thereof.
  • a method of modulating LPAR1 activity in a subject including administering to the subject a compound described herein, or a pharmaceutically acceptable salt or solvate thereof.
  • substituent groups are specified by their conventional chemical formulae, written from left to right, they equally encompass the chemically identical substituents that would result from writing the structure from right to left, e.g., -CH2O- is equivalent to -OCH2-.
  • alkyl by itself or as part of another substituent, means, unless otherwise stated, a straight (i.e., unbranched) or branched carbon chain (or carbon), or combination thereof, which may be fully saturated, mono- or polyunsaturated and can include mono-, di-, and multivalent radicals.
  • the alkyl may include a designated number of carbons (e.g., C1-C 10 means one to ten carbons).
  • the alkyl is fully saturated.
  • the alkyl is monounsaturated.
  • the alkyl is polyunsaturated.
  • Alkyl is an uncyclized chain.
  • saturated hydrocarbon radicals include, but are not limited to, groups such as methyl, ethyl, n-propyl, isopropyl, n-butyl, t-butyl, isobutyl, sec-butyl, methyl, homologs and isomers of, for example, n-pentyl, n-hexyl, n-heptyl, n-octyl, and the like.
  • An unsaturated alkyl group is one having one or more double bonds or triple bonds.
  • Examples of unsaturated alkyl groups include, but are not limited to, vinyl, 2-propenyl, crotyl, 2- isopentenyl, 2-(butadienyl), 2,4-pentadienyl, 3-(l,4-pentadienyl), ethynyl, 1- and 3-propynyl, 3-butynyl, and the higher homologs and isomers.
  • An alkoxy is an alkyl attached to the remainder of the molecule via an oxygen linker (-O-).
  • An alkyl moiety may be an alkenyl moiety.
  • An alkyl moiety may be an alkynyl moiety.
  • An alkenyl includes one or more double bonds.
  • An alkynyl includes one or more triple bonds.
  • alkylene by itself or as part of another substituent, means, unless otherwise stated, a divalent radical derived from an alkyl, as exemplified, but not limited by, -CH2CH2CH2CH2-.
  • an alkyl (or alkylene) group will have from 1 to 24 carbon atoms, with those groups having 10 or fewer carbon atoms being preferred herein.
  • a “lower alkyl” or “lower alkylene” is a shorter chain alkyl or alkylene group, generally having eight or fewer carbon atoms.
  • alkenylene by itself or as part of another substituent, means, unless otherwise stated, a divalent radical derived from an alkene.
  • alkynylene by itself or as part of another substituent, means, unless otherwise stated, a divalent radical derived from an alkyne.
  • the alkylene is fully saturated.
  • the alkylene is monounsaturated.
  • the alkylene is polyunsaturated.
  • An alkenylene includes one or more double bonds.
  • An alkynylene includes one or more triple bonds.
  • heteroalkyl by itself or in combination with another term, means, unless otherwise stated, a stable straight or branched chain, or combinations thereof, including at least one carbon atom and at least one heteroatom (e.g., O, N, P, Si, and S), and wherein the nitrogen and sulfur atoms may optionally be oxidized, and the nitrogen heteroatom may optionally be quaternized.
  • the heteroatom(s) e.g., N, S, Si, or P
  • Heteroalkyl is an uncyclized chain.
  • a heteroalkyl moiety may include one heteroatom (e.g., O, N, S, Si, or P).
  • a heteroalkyl moiety may include two optionally different heteroatoms (e.g., O, N, S, Si, or P).
  • a heteroalkyl moiety may include three optionally different heteroatoms (e.g., O, N, S, Si, or P).
  • a heteroalkyl moiety may include four optionally different heteroatoms (e.g., O, N, S, Si, or P).
  • a heteroalkyl moiety may include five optionally different heteroatoms (e.g., O, N, S, Si, or P).
  • a heteroalkyl moiety may include up to 8 optionally different heteroatoms (e.g., O, N, S, Si, or P).
  • the term “heteroalkenyl,” by itself or in combination with another term, means, unless otherwise stated, a heteroalkyl including at least one double bond.
  • a heteroalkenyl may optionally include more than one double bond and/or one or more triple bonds in additional to the one or more double bonds.
  • heteroalkynyl by itself or in combination with another term, means, unless otherwise stated, a heteroalkyl including at least one triple bond.
  • a heteroalkynyl may optionally include more than one triple bond and/or one or more double bonds in additional to the one or more triple bonds.
  • the heteroalkyl is fully saturated.
  • the heteroalkyl is monounsaturated.
  • the heteroalkyl is polyunsaturated.
  • heteroalkylene by itself or as part of another substituent, means, unless otherwise stated, a divalent radical derived from heteroalkyl, as exemplified, but not limited by, -CH 2 -CH 2 -S-CH 2 -CH 2 - and -CH 2 -S-CH 2 -CH 2 -NH-CH 2 -.
  • heteroatoms can also occupy either or both of the chain termini (e.g., alkyleneoxy, alkylenedioxy, alkyleneamino, alkylenediamino, and the like).
  • heteroalkyl groups include those groups that are attached to the remainder of the molecule through a heteroatom, such as -C(O)R', -C(O)NR', -NR'R", -OR', -SR', and/or -SO 2 R'.
  • heteroalkyl is recited, followed by recitations of specific heteroalkyl groups, such as -NR'R" or the like, it will be understood that the terms heteroalkyl and -NR'R" are not redundant or mutually exclusive. Rather, the specific heteroalkyl groups are recited to add clarity. Thus, the term “heteroalkyl” should not be interpreted herein as excluding specific heteroalkyl groups, such as -NR'R” or the like.
  • heteroalkenylene by itself or as part of another substituent, means, unless otherwise stated, a divalent radical derived from a heteroalkene.
  • heteroalkynylene by itself or as part of another substituent, means, unless otherwise stated, a divalent radical derived from a heteroalkyne.
  • the heteroalkylene is fully saturated.
  • the heteroalkylene is monounsaturated.
  • the heteroalkylene is polyunsaturated.
  • a heteroalkenylene includes one or more double bonds.
  • a heteroalkynylene includes one or more triple bonds.
  • cycloalkyl and heterocycloalkyl mean, unless otherwise stated, cyclic versions of “alkyl” and “heteroalkyl,” respectively. Cycloalkyl and heterocycloalkyl are not aromatic. Additionally, for heterocycloalkyl, a heteroatom can occupy the position at which the heterocycle is attached to the remainder of the molecule. Examples of cycloalkyl include, but are not limited to, cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, 1-cyclohexenyl, 3 -cyclohexenyl, cycloheptyl, and the like.
  • heterocycloalkyl examples include, but are not limited to, 1- (1,2,5,6-tetrahydropyridyl), 1-piperidinyl, 2-piperidinyl, 3-piperidinyl, 4-morpholinyl, 3- morpholinyl, tetrahydrofuran-2-yl, tetrahydrofuran-3-yl, tetrahydrothien-2-yl, tetrahydrothien-3-yl, 1-piperazinyl, 2-piperazinyl, and the like.
  • the cycloalkyl is fully saturated.
  • the cycloalkyl is monounsaturated.
  • the cycloalkyl is polyunsaturated.
  • the heterocycloalkyl is fully saturated.
  • the heterocycloalkyl is monounsaturated.
  • the heterocycloalkyl is polyunsaturated.
  • cycloalkyl means a monocyclic, bicyclic, or a multicyclic cycloalkyl ring system.
  • monocyclic ring systems are cyclic hydrocarbon groups containing from 3 to 8 carbon atoms, where such groups can be saturated or unsaturated, but not aromatic.
  • cycloalkyl groups are fully saturated.
  • a bicyclic or multicyclic cycloalkyl ring system refers to multiple rings fused together wherein at least one of the fused rings is a cycloalkyl ring and wherein the multiple rings are attached to the parent molecular moiety through any carbon atom contained within a cycloalkyl ring of the multiple rings.
  • a cycloalkyl is a cycloalkenyl.
  • the term “cycloalkenyl” is used in accordance with its plain ordinary meaning.
  • a cycloalkenyl is a monocyclic, bicyclic, or a multicyclic cycloalkenyl ring system.
  • a bicyclic or multicyclic cycloalkenyl ring system refers to multiple rings fused together wherein at least one of the fused rings is a cycloalkenyl ring and wherein the multiple rings are attached to the parent molecular moiety through any carbon atom contained within a cycloalkenyl ring of the multiple rings.
  • heterocycloalkyl means a monocyclic, bicyclic, or a multicyclic heterocycloalkyl ring system.
  • heterocycloalkyl groups are fully saturated.
  • a bicyclic or multicyclic heterocycloalkyl ring system refers to multiple rings fused together wherein at least one of the fused rings is a heterocycloalkyl ring and wherein the multiple rings are attached to the parent molecular moiety through any atom contained within a heterocycloalkyl ring of the multiple rings.
  • halo or “halogen,” by themselves or as part of another substituent, mean, unless otherwise stated, a fluorine, chlorine, bromine, or iodine atom. Additionally, terms such as “haloalkyl” are meant to include monohaloalkyl and polyhaloalkyl.
  • halo(Ci-C 4 )alkyl includes, but is not limited to, fluoromethyl, difluoromethyl, trifluoromethyl, 2,2,2-trifluoroethyl, 4-chlorobutyl, 3 -bromopropyl, and the like.
  • acyl means, unless otherwise stated, -C(O)R where R is a substituted or unsubstituted alkyl, substituted or unsubstituted cycloalkyl, substituted or unsubstituted heteroalkyl, substituted or unsubstituted heterocycloalkyl, substituted or unsubstituted aryl, or substituted or unsubstituted heteroaryl.
  • aryl means, unless otherwise stated, a polyunsaturated, aromatic, hydrocarbon substituent, which can be a single ring or multiple rings (preferably from 1 to 3 rings) that are fused together (i.e., a fused ring aryl) or linked covalently.
  • a fused ring aryl refers to multiple rings fused together wherein at least one of the fused rings is an aryl ring and wherein the multiple rings are attached to the parent molecular moiety through any carbon atom contained within an aryl ring of the multiple rings.
  • heteroaryl refers to aryl groups (or rings) that contain at least one heteroatom such as N, O, or S, wherein the nitrogen and sulfur atoms are optionally oxidized, and the nitrogen atom(s) are optionally quatemized.
  • heteroaryl includes fused ring heteroaryl groups (i.e., multiple rings fused together wherein at least one of the fused rings is a heteroaromatic ring and wherein the multiple rings are attached to the parent molecular moiety through any atom contained within a heteroaromatic ring of the multiple rings).
  • a 5,6-fused ring heteroarylene refers to two rings fused together, wherein one ring has 5 members and the other ring has 6 members, and wherein at least one ring is a heteroaryl ring.
  • a 6,6-fused ring heteroarylene refers to two rings fused together, wherein one ring has 6 members and the other ring has 6 members, and wherein at least one ring is a heteroaryl ring.
  • a 6,5-fused ring heteroarylene refers to two rings fused together, wherein one ring has 6 members and the other ring has 5 members, and wherein at least one ring is a heteroaryl ring.
  • a heteroaryl group can be attached to the remainder of the molecule through a carbon or heteroatom.
  • Non-limiting examples of aryl and heteroaryl groups include phenyl, naphthyl, pyrrolyl, pyrazolyl, pyridazinyl, triazinyl, pyrimidinyl, imidazolyl, pyrazinyl, purinyl, oxazolyl, isoxazolyl, thiazolyl, furyl, thienyl, pyridyl, pyrimidyl, benzothiazolyl, benzoxazoyl benzimidazolyl, benzofuran, isobenzofuranyl, indolyl, isoindolyl, benzothiophenyl, isoquinolyl, quinoxalinyl, quinolyl, 1 -naphthyl, 2-naphthyl, 4-biphenyl, 1-pyrrolyl, 2- pyrrolyl, 3 -pyrrol yl, 3 -pyrazolyl, 2-imid
  • arylene and heteroarylene independently or as part of another substituent, mean a divalent radical derived from an aryl and heteroaryl, respectively.
  • a heteroaryl group substituent may be -O- bonded to a ring heteroatom nitrogen.
  • Spirocyclic rings are two or more rings wherein adjacent rings are attached through a single atom.
  • the individual rings within spirocyclic rings may be identical or different.
  • Individual rings in spirocyclic rings may be substituted or unsubstituted and may have different substituents from other individual rings within a set of spirocyclic rings.
  • Possible substituents for individual rings within spirocyclic rings are the possible substituents for the same ring when not part of spirocyclic rings (e.g., substituents for cycloalkyl or heterocycloalkyl rings).
  • Spirocylic rings may be substituted or unsubstituted cycloalkyl, substituted or unsubstituted cycloalkylene, substituted or unsubstituted heterocycloalkyl or substituted or unsubstituted heterocycloalkylene and individual rings within a spirocyclic ring group may be any of the immediately previous list, including having all rings of one type (e.g., all rings being substituted heterocycloalkylene wherein each ring may be the same or different substituted heterocycloalkylene).
  • heterocyclic spirocyclic rings means spirocyclic rings wherein at least one ring is a heterocyclic ring and wherein each ring may be a different ring.
  • substituted spirocyclic rings means that at least one ring is substituted and each substituent may optionally be different.
  • Bridged rings are two ore more rings that share three or more atoms, separating the two bridgehead atoms by a bridge containing at least one atom.
  • Individual rings in bridged rings may be substituted or unsubstituted and may have different substituents from other individual rings within a set of bridged rings.
  • Possible substituents for individual rings within bridged rings are the possible substituents for the same ring when not part of bridged rings (e.g., substituents for cycloalkyl or heterocycloalkyl rings).
  • Bridged rings may be substituted or unsubstituted cycloalkyl, substituted or unsubstituted cycloalkylene, substituted or unsubstituted heterocycloalkyl or substituted or unsubstituted heterocycloalkylene and individual rings within a bridged ring group may be any of the immediately previous list, including having all rings of one type (e.g., all rings being substituted heterocycloalkylene wherein each ring may be the same or different substituted heterocycloalkylene).
  • heterocyclic bridged rings means bridged rings wherein at least one ring is a heterocyclic ring and wherein each ring may be a different ring.
  • substituted bridged rings means that at least one ring is substituted and each substituent may optionally be different.
  • oxo means an oxygen that is double bonded to a carbon atom.
  • alkylarylene as an arylene moiety covalently bonded to an alkylene moiety (also referred to herein as an alkylene linker).
  • alkylarylene group has the formula:
  • An alkylarylene moiety may be substituted (e.g., with a substituent group) on the alkylene moiety or the arylene linker (e.g., at carbons 2, 3, 4, or 6) with halogen, oxo, -N3, -CF 3 , -CCl 3 , -CBr 3 , -Cl 3 , -CN, -CHO, -OH, -NH 2 , -COOH, -CONH 2 , -NO 2 , -SH, -SO2CH 3 , -SO3H, -OSO3H, -SO2NH2, -NHNH 2 , -ONH2, -NHC(O)NHNH 2 , substituted or unsubstituted C1-C5 alkyl or substituted or unsubstituted 2 to 5 membered heteroalkyl).
  • the alkylarylene is un substituted.
  • R, R', R", R'", and R" each preferably independently refer to hydrogen, substituted or unsubstituted heteroalkyl, substituted or unsubstituted cycloalkyl, substituted or unsubstituted heterocycloalkyl, substituted or unsubstituted aryl (e.g., aryl substituted with 1-3 halogens), substituted or unsubstituted heteroaryl, substituted or unsubstituted alkyl, alkoxy, or thioalkoxy groups, or arylalkyl groups.
  • aryl e.g., aryl substituted with 1-3 halogens
  • substituted or unsubstituted heteroaryl substituted or unsubstituted alkyl, alkoxy, or thioalkoxy groups, or arylalkyl groups.
  • each of the R groups is independently selected as are each R', R", R'", and R"" group when more than one of these groups is present.
  • R' and R" are attached to the same nitrogen atom, they can be combined with the nitrogen atom to form a 4-, 5-, 6-, or 7- membered ring.
  • -NR'R includes, but is not limited to, 1-pyrrolidinyl and 4- morpholinyl.
  • alkyl is meant to include groups including carbon atoms bound to groups other than hydrogen groups, such as haloalkyl (e.g., -CF3 and -CH2CF3) and acyl (e.g., -C(O)CH 3 , -C(O)CF 3 , -C(O)CH 2 OCH 3 , and the like).
  • haloalkyl e.g., -CF3 and -CH2CF3
  • acyl e.g., -C(O)CH 3 , -C(O)CF 3 , -C(O)CH 2 OCH 3 , and the like.
  • Substituents for rings may be depicted as substituents on the ring rather than on a specific atom of a ring (commonly referred to as a floating substituent).
  • the substituent may be attached to any of the ring atoms (obeying the rules of chemical valency) and in the case of fused rings or spirocyclic rings, a substituent depicted as associated with one member of the fused rings or spirocyclic rings (a floating substituent on a single ring), may be a substituent on any of the fused rings or spirocyclic rings (a floating substituent on multiple rings).
  • the multiple substituents may be on the same atom, same ring, different atoms, different fused rings, different spirocyclic rings, and each substituent may optionally be different.
  • a point of attachment of a ring to the remainder of a molecule is not limited to a single atom (a floating substituent)
  • the attachment point may be any atom of the ring and in the case of a fused ring or spirocyclic ring, any atom of any of the fused rings or spirocyclic rings while obeying the rules of chemical valency.
  • a ring, fused rings, or spirocyclic rings contain one or more ring heteroatoms and the ring, fused rings, or spirocyclic rings are shown with one more floating substituents (including, but not limited to, points of attachment to the remainder of the molecule), the floating substituents may be bonded to the heteroatoms.
  • the ring heteroatoms are shown bound to one or more hydrogens (e.g., a ring nitrogen with two bonds to ring atoms and a third bond to a hydrogen) in the structure or formula with the floating substituent, when the heteroatom is bonded to the floating substituent, the substituent will be understood to replace the hydrogen, while obeying the rules of chemical valency.
  • Two or more substituents may optionally be joined to form aryl, heteroaryl, cycloalkyl, or heterocycloalkyl groups.
  • Such so-called ring-forming substituents are typically, though not necessarily, found attached to a cyclic base structure.
  • the ring-forming substituents are attached to adjacent members of the base structure.
  • two ring-forming substituents attached to adjacent members of a cyclic base structure create a fused ring structure.
  • the ring-forming substituents are attached to a single member of the base structure.
  • two ringforming substituents attached to a single member of a cyclic base structure create a spirocyclic structure.
  • the ring-forming substituents are attached to non-adjacent members of the base structure.
  • Two of the substituents on adjacent atoms of the aryl or heteroaryl ring may optionally form a ring of the formula -T-C(O)-(CRR') q -U-, wherein T and U are independently -NR-, -O-, -CRR'-, or a single bond, and q is an integer of from 0 to 3.
  • two of the substituents on adjacent atoms of the aryl or heteroaryl ring may optionally be replaced with a substituent of the formula -A-(CH2) r -B-, wherein A and B are independently -CRR'-, -O-, -NR-, -S-, -S(O)-, -S(O)2-, -S(O)2NR'-, or a single bond, and r is an integer of from 1 to 4.
  • One of the single bonds of the new ring so formed may optionally be replaced with a double bond.
  • two of the substituents on adjacent atoms of the aryl or heteroaryl ring may optionally be replaced with a substituent of the formula -(CRR')s-X'- (C"R"R"')d-, where s and d are independently integers of from 0 to 3, and X' is -O-, -NR'-, -S-, -S(O)-, -S(O) 2 -, or -S(O)2NR'-.
  • R, R', R", and R' are preferably independently selected from hydrogen, substituted or unsubstituted alkyl, substituted or unsubstituted heteroalkyl, substituted or unsubstituted cycloalkyl, substituted or unsubstituted heterocycloalkyl, substituted or unsubstituted aryl, and substituted or unsubstituted heteroaryl.
  • heteroatom or “ring heteroatom” are meant to include oxygen (O), nitrogen (N), sulfur (S), phosphorus (P), selenium (Se), and silicon (Si).
  • heteroatom or “ring heteroatom” are meant to include oxygen (O), nitrogen (N), sulfur (S), phosphorus (P), and silicon (Si).
  • a “substituent group,” as used herein, means a group selected from the following moieties:
  • alkyl e.g., C 1 -C 8 alkyl, C 1 -C 6 alkyl, or C1-C 4 alkyl
  • heteroalkyl e.g., 2 to 8 membered heteroalkyl, 2 to 6 membered heteroalkyl, or 2 to 4 membered heteroalkyl
  • cycloalkyl e.g., C 3 -C 8 cycloalkyl, C 3 -C 6 cycloalkyl, or C 5 -C 6 cycloalkyl
  • heterocycloalkyl e.g., 3 to 8 membered heterocycloalkyl, 3 to 6 membered heterocycloalkyl, or 5 to 6 membered heterocycloalkyl
  • aryl e.g., C 6 -C 10 aryl, C 10 aryl, or phenyl
  • heteroaryl e.g., 5 to 10 membered heteroaryl, 5 to 9 membered heteroaryl, or 5
  • alkyl e.g., C 1 -C 8 alkyl, C 1 -C 6 alkyl, or C1-C 4 alkyl
  • heteroalkyl e.g., 2 to 8 membered heteroalkyl, 2 to 6 membered heteroalkyl, or 2 to 4 membered heteroalkyl
  • cycloalkyl e.g., C 3 -C 8 cycloalkyCl, 3 -C 6 cycloalkyl, or C5-C 6 cycloalkyl
  • heterocycloalkyl e.g., 3 to 8 membered heterocycloalkyl, 3 to 6 membered heterocycloalkyl, or 5 to 6 membered heterocycloalkyl
  • aryl e.g., C 6 - C 10 aryl, C 10 aryl, or phenyl
  • heteroaryl e.g., 5 to 10 membered heteroaryl, 5 to 9 membered heteroaryl, or 5 to
  • alkyl e.g., C 1 -C 8 alkyl, C 1 -C 6 alkyl, or C1-C 4 alkyl
  • heteroalkyl e.g., 2 to 8 membered heteroalkyl, 2 to 6 membered heteroalkyl, or 2 to 4 membered heteroalkyl
  • cycloalkyl e.g., C 3 -C 8 cycloalkyl, C 3 -C 6 cycloalkyl, or C5-C 6 cycloalkyl
  • heterocycloalkyl e.g., 3 to 8 membered heterocycloalkyl, 3 to 6 membered heterocycloalkyl, or 5 to 6 membered heterocycloalkyl
  • aryl e.g., C 6 - C 10 aryl, C 10 aryl, or phenyl
  • heteroaryl e.g., 5 to 10 membered heteroaryl, 5 to 9 membered heteroaryl, or 5 to
  • a “size-limited substituent” or “ size-limited substituent group,” as used herein, means a group selected from all of the substituents described above for a “substituent group,” wherein each substituted or unsubstituted alkyl is a substituted or unsubstituted Ci-C 2 o alkyl, each substituted or unsubstituted heteroalkyl is a substituted or unsubstituted 2 to 20 membered heteroalkyl, each substituted or unsubstituted cycloalkyl is a substituted or unsubstituted C 3 -C 8 cycloalkyl, each substituted or unsubstituted heterocycloalkyl is a substituted or unsubstituted 3 to 8 membered heterocycloalkyl, each substituted or unsubstituted aryl is a substituted or unsubstituted C 6 -C 10 aryl, and each substituted or unsubstituted heteroary
  • a “lower substituent” or “ lower substituent group,” as used herein, means a group selected from all of the substituents described above for a “substituent group,” wherein each substituted or unsubstituted alkyl is a substituted or unsubstituted C 1 -C 8 alkyl, each substituted or unsubstituted heteroalkyl is a substituted or unsubstituted 2 to 8 membered heteroalkyl, each substituted or unsubstituted cycloalkyl is a substituted or unsubstitutedC 3 - C7 cycloalkyl, each substituted or unsubstituted heterocycloalkyl is a substituted or unsubstituted 3 to 7 membered heterocycloalkyl, each substituted or unsubstituted aryl is a substituted or unsubstituted phenyl, and each substituted or unsubstituted heteroaryl is a substituted or un
  • each substituted group described in the compounds herein is substituted with at least one substituent group. More specifically, in some embodiments, each substituted alkyl, substituted heteroalkyl, substituted cycloalkyl, substituted heterocycloalkyl, substituted aryl, substituted heteroaryl, substituted alkylene, substituted heteroalkylene, substituted cycloalkylene, substituted heterocycloalkylene, substituted arylene, and/or substituted heteroarylene described in the compounds herein are substituted with at least one substituent group. In other embodiments, at least one or all of these groups are substituted with at least one size-limited substituent group. In other embodiments, at least one or all of these groups are substituted with at least one lower substituent group.
  • each substituted or unsubstituted alkyl may be a substituted or unsubstituted C1-C20 alkyl
  • each substituted or unsubstituted heteroalkyl is a substituted or unsubstituted 2 to 20 membered heteroalkyl
  • each substituted or unsubstituted cycloalkyl is a substituted or unsubstituted C 3 -C 8 cycloalkyl
  • each substituted or unsubstituted heterocycloalkyl is a substituted or unsubstituted 3 to 8 membered heterocycloalkyl
  • each substituted or unsubstituted aryl is a substituted or unsubstituted C 6 - C 10 aryl
  • each substituted or unsubstituted heteroaryl is a substituted or unsubstituted 5 to 10 membered heteroaryl.
  • each substituted or unsubstituted alkylene is a substituted or unsubstituted C1-C20 alkylene
  • each substituted or unsubstituted heteroalkylene is a substituted or unsubstituted 2 to 20 membered heteroalkylene
  • each substituted or unsubstituted cycloalkylene is a substituted or unsubstituted C 3 -C 8 cycloalkylene
  • each substituted or unsubstituted heterocycloalkylene is a substituted or unsubstituted 3 to 8 membered heterocycloalkylene
  • each substituted or unsubstituted arylene is a substituted or unsubstituted C 6 -C 10 arylene
  • each substituted or unsubstituted heteroarylene is a substituted or unsubstituted 5 to 10 membered heteroarylene.
  • each substituted or unsubstituted alkyl is a substituted or unsubstituted C 1 -C 8 alkyl
  • each substituted or unsubstituted heteroalkyl is a substituted or unsubstituted 2 to 8 membered heteroalkyl
  • each substituted or unsubstituted cycloalkyl is a substituted or unsubstituted C 3 -C7 cycloalkyl
  • each substituted or unsubstituted heterocycloalkyl is a substituted or unsubstituted 3 to 7 membered heterocycloalkyl
  • each substituted or unsubstituted aryl is a substituted or unsubstituted C 6 -C 10 aryl
  • each substituted or unsubstituted heteroaryl is a substituted or unsubstituted 5 to 9 membered heteroaryl.
  • each substituted or unsubstituted alkylene is a substituted or unsubstituted C 1 -C 8 alkylene
  • each substituted or unsubstituted heteroalkylene is a substituted or unsubstituted 2 to 8 membered heteroalkylene
  • each substituted or unsubstituted cycloalkylene is a substituted or unsubstitutedC 3 -C7 cycloalkylene
  • each substituted or unsubstituted heterocycloalkylene is a substituted or unsubstituted 3 to 7 membered heterocycloalkylene
  • each substituted or unsubstituted arylene is a substituted or unsubstituted C 6 -C 10 arylene
  • each substituted or unsubstituted heteroarylene is a substituted or unsubstituted 5 to 9 membered heteroarylene.
  • the compound is a chemical species set forth in the Examples section, figures, or tables
  • a substituted or unsubstituted moiety e.g., substituted or unsubstituted alkyl, substituted or unsubstituted heteroalkyl, substituted or unsubstituted cycloalkyl, substituted or unsubstituted heterocycloalkyl, substituted or unsubstituted aryl, substituted or unsubstituted heteroaryl, substituted or unsubstituted alkylene, substituted or unsubstituted heteroalkylene, substituted or unsubstituted cycloalkylene, substituted or unsubstituted heterocycloalkylene, substituted or unsubstituted arylene, and/or substituted or unsubstituted heteroarylene) is unsubstituted (e.g., is an unsubstituted alkyl, unsubstituted heteroalkyl, unsubstituted cycloalkyl, unsubstituted
  • a substituted or unsubstituted moiety e.g., substituted or unsubstituted alkyl, substituted or unsubstituted heteroalkyl, substituted or unsubstituted cycloalkyl, substituted or unsubstituted heterocycloalkyl, substituted or unsubstituted aryl, substituted or unsubstituted heteroaryl, substituted or unsubstituted alkylene, substituted or unsubstituted heteroalkylene, substituted or unsubstituted cycloalkylene, substituted or unsubstituted heterocycloalkylene, substituted or unsubstituted arylene, and/or substituted or unsubstituted heteroarylene) is substituted (e.g., is a substituted alkyl, substituted heteroalkyl, substituted cycloalkyl, substituted heterocycloalkyl, substituted aryl, substituted heteroaryl, substituted alky
  • a substituted moiety e.g., substituted alkyl, substituted heteroalkyl, substituted cycloalkyl, substituted heterocycloalkyl, substituted aryl, substituted heteroaryl, substituted alkylene, substituted heteroalkylene, substituted cycloalkylene, substituted heterocycloalkylene, substituted arylene, and/or substituted heteroarylene
  • is substituted with at least one substituent group wherein if the substituted moiety is substituted with a plurality of substituent groups, each substituent group may optionally be different. In embodiments, if the substituted moiety is substituted with a plurality of substituent groups, each substituent group is different.
  • a substituted moiety e.g., substituted alkyl, substituted heteroalkyl, substituted cycloalkyl, substituted heterocycloalkyl, substituted aryl, substituted heteroaryl, substituted alkylene, substituted heteroalkylene, substituted cycloalkylene, substituted heterocycloalkylene, substituted arylene, and/or substituted heteroarylene
  • is substituted with at least one size-limited substituent group wherein if the substituted moiety is substituted with a plurality of size-limited substituent groups, each size-limited substituent group may optionally be different. In embodiments, if the substituted moiety is substituted with a plurality of size-limited substituent groups, each size-limited substituent group is different.
  • a substituted moiety e.g., substituted alkyl, substituted heteroalkyl, substituted cycloalkyl, substituted heterocycloalkyl, substituted aryl, substituted heteroaryl, substituted alkylene, substituted heteroalkylene, substituted cycloalkylene, substituted heterocycloalkylene, substituted arylene, and/or substituted heteroarylene
  • is substituted with at least one lower substituent group wherein if the substituted moiety is substituted with a plurality of lower substituent groups, each lower substituent group may optionally be different. In embodiments, if the substituted moiety is substituted with a plurality of lower substituent groups, each lower substituent group is different.
  • a substituted moiety e.g., substituted alkyl, substituted heteroalkyl, substituted cycloalkyl, substituted heterocycloalkyl, substituted aryl, substituted heteroaryl, substituted alkylene, substituted heteroalkylene, substituted cycloalkylene, substituted heterocycloalkylene, substituted arylene, and/or substituted heteroarylene
  • the substituted moiety is substituted with a plurality of groups selected from substituent groups, size-limited substituent groups, and lower substituent groups; each substituent group, size-limited substituent group, and/or lower substituent group
  • each R substituent or L linker that is described as being “substituted” without reference as to the identity of any chemical moiety that composes the “substituted” group also referred to herein as an “open substitution” on an R substituent or L linker or an “openly substituted” R substituent or L linker
  • the recited R substituent or L linker may, in embodiments, be substituted with one or more first substituent groups as defined below.
  • the first substituent group is denoted with a corresponding first decimal point numbering system such that, for example, R 1 may be substituted with one or more first substituent groups denoted by R 1.1 , R 2 may be substituted with one or more first substituent groups denoted by R 2.1 , R 3 may be substituted with one or more first substituent groups denoted by R 3.1 , R 4 may be substituted with one or more first substituent groups denoted by R 4.1 , R 5 may be substituted with one or more first substituent groups denoted by R 5.1 , and the like up to or exceeding an R 100 that may be substituted with one or more first substituent groups denoted by R 100 1 .
  • R 1A may be substituted with one or more first substituent groups denoted by R 1A.1
  • R 2A may be substituted with one or more first substituent groups denoted by R 2A1
  • R 3A may be substituted with one or more first substituent groups denoted by R 3A1
  • R 4A may be substituted with one or more first substituent groups denoted by R 4A1
  • R 5A may be substituted with one or more first substituent groups denoted by R 5A 1 and the like up to or exceeding an R 100A may be substituted with one or more first substituent groups denoted by R 100A 1 .
  • L 1 may be substituted with one or more first substituent groups denoted by R LL1
  • L 2 may be substituted with one or more first substituent groups denoted by R L2 1
  • L 3 may be substituted with one or more first substituent groups denoted by R L3 1
  • L 4 may be substituted with one or more first substituent groups denoted by R L4 - 1
  • L 5 may be substituted with one or more first substituent groups denoted by R L5 1 and the like up to or exceeding an L 100 which may be substituted with one or more first substituent groups denoted by R L100 1 .
  • each numbered R group or L group (alternatively referred to herein as R ww or L w wherein “WW” represents the stated superscript number of the subject R group or L group) described herein may be substituted with one or more first substituent groups referred to herein generally as R ⁇ 1 or R LWW ⁇ respectively.
  • each first substituent group e.g., R 1 - 1 , R 21 , R 31 , R 41 , R 5 1 R 100.1.
  • R L1.1 R L2.1 R L3.1 R L4.1 R L5.1 R L 100.1) ma y be further substituted with one or more second substituent groups (e.g., R 1 2 , R 22 , R 32 , R 42 , R 5.2 R 100.2. J ⁇ IA.2 R 2A2 R 3A.2 R 4A.2 R 5A.2 R 100A.2.
  • each first substituent group which may alternatively be represented herein as R ⁇ 1 as described above, may be further substituted with one or more second substituent groups, which may alternatively be represented herein as R WW.2 .
  • each second substituent group (e.g., R 12 , R 22 , R 32 , R 42 , R 52 ... R100.2, R1A.2 R 2A.2 R 3A.2 R 4A.2 R 5A.2 R 100A.2.
  • R L1.2, R L2.2 R L3.2 R L42 R L5.2 R L100.2) may be further substituted with one or more third substituent groups (e.g., R 1 3 , R 23 , R 33 , R 43 , R 5 3 ... R 1003 ;
  • each second substituent group which may alternatively be represented herein as R WW.2 as described above, may be further substituted with one or more third substituent groups, which may alternatively be represented herein as R ⁇ 3 .
  • Each of the first substituent groups may be optionally different.
  • Each of the second substituent groups may be optionally different.
  • Each of the third substituent groups may be optionally different.
  • WW represents a substituent recited in a claim or chemical formula description herein which is openly substituted.
  • WW represents the stated superscript number of the subject R group (1, 2, 3, 1 A, 2A, 3 A, IB, 2B, 3B, etc.).
  • L ww is a linker recited in a claim or chemical formula description herein which is openly substituted.
  • WW represents the stated superscript number of the subject L group (1, 2, 3, 1 A, 2A, 3 A, IB, 2B, 3B, etc.).
  • each R ⁇ may be unsubstituted or independently substituted with one or more first substituent groups, referred to herein as R ww - 1 ; each first substituent group, R ww - 1 , may be unsubstituted or independently substituted with one or more second substituent groups, referred to herein as R WW 2 ; and each second substituent group may be unsubstituted or independently substituted with one or more third substituent groups, referred to herein as R WW 3 .
  • each L ww linker may be unsubstituted or independently substituted with one or more first substituent groups, referred to herein as R LWW 1 ; each first substituent group, R LWW may be unsubstituted or independently substituted with one or more second substituent groups, referred to herein as RLWW.2.
  • su bstituent group may be unsubstituted or independently substituted with one or more third substituent groups, referred to herein as R LWW - 3 .
  • Each first substituent group is optionally different.
  • Each second substituent group is optionally different.
  • Each third substituent group is optionally different.
  • R ww is phenyl
  • the said phenyl group is optionally substituted by one or more R ww 1 groups as defined herein below, e.g., when R ww 1 is R WW 2 -substituted or unsubstituted alkyl, examples of groups so formed include but are not limited to itself optionally substituted by 1 or more R ww 2 , which R WW 2 is optionally substituted by one or more R WW 3 .
  • R ww group is phenyl substituted by R ww - 1 , which is methyl
  • the methyl group may be further substituted to form groups including but not limited to: unsubstituted alkyl (e.g., C 1 -C 8 , C 1 -C 6 , C1-C 4 , or C1-C2), R WW 2 -substituted or unsubstituted heteroalkyl (e.g., 2 to 8 membered, 2 to 6 membered, 4 to 6 membered, 2 to 3 membered, or 4 to 5 membered), R WW 2 -substituted or unsubstituted cycloalkyl (e.g., C-C 3 8, -CC 36 , C 4 -C 6 , or C 5 -C 6 ), R WW 2 -substituted or unsubstituted heterocycloalkyl (e.g., 3 to 8 membered, 3 to 6
  • R ww 1 is independently oxo, halogen, -CX WW 1 3, -CHX WW , -CH 2 X WW 1 , -OCX WW 1 3, -0CH 2 X WW 1 , -0CHX WW 2, -CN, -OH, -NH 2 , -COOH, -C0NH2, -NO2, -SH, -SO3H, -OSO3H, -SO2NH2, -NHNH 2 , -0NH2, -NHC(O)NHNH 2 , -NHC(O)NH 2 , -NHC(NH)NH 2 , -NHSO2H, -NHC(O)H, -NHC(O)0H, -NHOH, -N3, unsubstituted alkyl (e.g., C 1 -C 8 , C 1 -C 6 , C1-C 4 , or C1-C2), unsubstituted heteroal
  • R WW 2 is independently oxo, halogen, -CX ⁇ - 2 3, -CHX WW 2 2 , -CH 2 X WW 2 , -OCX WW 2 3, -OCH 2 X WW 2 , -OCHX WW 2 2, -CN, -OH, -NH 2 , -COOH, -C0NH 2 , -NO 2 , -SH, -SO3H, -OSO3H, -SO2NH2, -NHNH2, -ONH2, -NHC(O)NHNH 2 , -NHC(O)NH 2 , -NHC(NH)NH 2 , -NHSO2H, -NHC(O)H, -NHC(O)0H, -NHOH, -N3, R ww ’-substituted or unsubstituted alkyl (e.g., C 1 -C 8 , C 1 -C 6 , C1-C 4
  • R WW 2 is independently oxo, halogen, -CX WW 2 3, -CHX WW 2 2, -CH 2 X WW 2 , -OCX WW 2 3, -OCH 2 X WW 2 , -OCHX WW 2 2, -CN, -OH, -NH 2 , -COOH, -C0NH 2 , -NO2, -SH, -SO3H, -OSO3H, -SO2NH2, -NHNH2, -ONH2, -NHC(O)NHNH 2 , -NHC(O)NH 2 , -NHC(NH)NH 2 , -NHSO2H, -NHC(O)H, -NHC(O)0H, -NHOH, -N3, unsubstituted alkyl (e.g., C 1 -C 8 , C 1 -C 6 , C1-C 4 , or C1-C2), unsubstituted heteroalkyl (e
  • x WW 2 is independently -F, -Cl, -Br, or -I.
  • R ww - 1 first substituent groups
  • R ww 2 second substituent groups
  • R ww 3 third substituent groups
  • R ww 3 third substituent groups
  • Each first substituent group is optionally different.
  • Each second substituent group is optionally different.
  • Each third substituent group is optionally different.
  • the “WW” symbol in the R ww - 1 , R WW 2 and R WW 3 refers to the designated number of one of the two different R ww substituents.
  • R ww 1 is R 100A - 1 , R WW 2 i s preceding paragraphs.
  • R LWW 1 is independently oxo, halogen, -CX LWW 1 3 , -CHX LWW , -CH 2 X LWW 1 , -OCX LWW 1 3, -OCH 2 X LWW -OCHX LWW 2, -CN, -OH, -NH 2 , -COOH, -CONH 2 , -NO2, -SH, -SO3H, -OSO3H, -SO2NH2, -NHNH 2 , -0NH2, -NHC(O)NHNH 2 , -NHC(O)NH 2 , -NHC(NH)NH 2 , -NHSO2H, -NHC(O)H, -NHC(O)OH, -NHOH, -N3, R LWW ⁇ substituted or unsubstituted alkyl (e.g., C 1 -C 8 , C 1 -C 6 , C 1
  • substituted or unsubstituted cycloalkyl e.g.C, 3 -C8,C 3 -C 6 , C 4 -C 6 , or C 5 -C 6
  • R LWW 2 -substituted or unsubstituted heterocycloalkyl e.g., 3 to 8 membered, 3 to 6 membered, 4 to 6 membered, 4 to 5 membered, or 5 to 6 membered
  • R LWW 2 -substituted or unsubstituted aryl e.g., C 6 -C12, C 6 -C 10 , or phenyl
  • R LWW 2 -substituted or unsubstituted heteroaryl e.g., 5 to 12 membered, 5 to 10 membered, 5 to 9 membered, or 5 to 6 membered).
  • R LWW 1 is independently oxo, halogen, -CX LWW 1 3 , -CHX LWW 1 2 , -CH 2 X LWW 1 , -OCX LWW 1 3 , -OCH 2 X LWW ⁇ -OCHX LWW 1 2 , -CN, -OH, -NH 2 , -COOH, -CONH2, -NO2, -SH, -SO3H, -OSO3H, -SO2NH2, -NHNH2, -ONH2, -NHC(O)NHNH 2 , -NHC(O)NH 2 , -NHC(NH)NH 2 , -NHSO2H, -NHC(O)H, -NHC(O)OH, -NHOH, -N3, unsubstituted alkyl (e.g., C 1 -C 8 , C 1 -C 6 , C1-C 4 , -
  • R LWW 2 is independently oxo, halogen, -CX LWW 2 3 , -CHX LWW 2 2 , -CH 2 X LWW 2 , -OCX LWW 2 3, -OCH 2 X LWW 2 , -OCHX LWW 2 2, -CN, -OH, -NH 2 , -COOH, -CONH2, -NO2, -SH, -SO3H, -OSO3H, -SO2NH2, -NHNH2, -0NH2, -NHC(O)NHNH 2 , -NHC(O)NH 2 , -NHC(NH)NH 2 , -NHSO2H, -NHC(O)H, -NHC(O)0H, -NHOH, -N3, R LWW 3 -substituted or unsubstituted alkyl (e.g., C 1 -C 8 , C 1 -C 8
  • R LWW2 is independently oxo, halogen, -CX LWW 2 3, -CHX LWW 2 2, -CH 2 X LWW 2 , -OCX LWW 2 3 , -OCH 2 X LWW 2 , -OCHX LWW 2 2 , -CN, -OH, -NH 2 , -COOH, -CONH2, -NO2, -SH, -SO3H, -OSO3H, -SO2NH2, -NHNH 2 , -0NH2, -NHC(O)NHNH 2 , -NHC(O)NH 2 , -NHC(NH)NH 2 , -NHSO2H, -NHC(O)H, -NHC(O)0H, -NHOH, -N3, unsubstituted alkyl (e.g., C 1 -C 8 , C 1 -C 6 , C1-C 4 , unsub
  • R LWW 3 is independently oxo, halogen, -CX LWW 3 3 , -CHX LWW 3 2 , -CH 2 X LWW 3 , -OCX LWW 3 3, -OCH 2 X LWW 3 , -OCHX LWW 3 2, -CN, -OH, -NH 2 , -COOH, -CONH2, -NO2, -SH, -SO3H, -OSO3H, -SO2NH2, -NHNH2, -0NH2, -NHC(O)NHNH 2 , -NHC(O)NH 2 , -NHC(NH)NH 2 , -NHSO2H, -NHC(O)H, -NHC(O)0H, -NHOH, -N3, unsubstituted alkyl (e.g., C 1 -C 8 , C 1 -C 6 , C1-C 4 , or
  • R group (R ww group) is hereby defined as independently oxo, halogen, -CX WW 3, -CHX WW 2, -CH 2 X WW , -OCX WW 3, -OCH 2 X WW , -OCHX WW 2 , -CN, -OH, -NH 2 , -COOH, -CONH2, -NO2, -SH, -SO3H, -OSO3H, -SO2NH2, -NHNH2, -0NH2, -NHC(O)NHNH 2 , -NHC(O)NH 2 , -NHC(NH)NH 2 , -NHSO 4 H, -NHC(O)H, -NHC(O)OH, -NHOH, -N 3 , R WW I -substituted
  • X ww is independently -F, -Cl, -Br, or -I.
  • WW represents the stated superscript number of the subject R group (e.g., 1, 2, 3, 1 A, 2A, 3A, IB, 2B, 3B, etc.).
  • R WW 1 , RWW.2, an dR WW 3 are as defined above.
  • L group is herein defined as independently a bond, -O-, -NH-, -C(O)-, -C(O)NH-, -NHC(O)-, -NHC(O)NH-, -NHC(NH)NH-, -C(O)O-, -OC(O)-, -S-, -SO2-, -SO2NH-, R LWW '- substituted or unsubstituted alkylene (e.g., C 1 -C 8 , C 1 -C 6 , C1-C 4 , or C1-C2), R LWW ⁇ -substituted or unsubstituted heteroalkylene (e.g., 2 to 8 membered, 2 to 6 membered
  • WW represents the stated superscript number of the subject L group (1, 2, 3, 1 A, 2A, 3A, IB, 2B, 3B, etc.).
  • R LWW as well as R LWW 2 and RLWW. 3 are as defined above.
  • C 6 rtain compounds of the present disclosure possess asymmetric carbon atoms (optical or chiral centers) or double bonds; the enantiomers, racemates, diastereomers, tautomers, geometric isomers, stereoisometric forms that may be defined, in terms of absolute stereochemistry, as (R)-or (S)- or, as (D)- or (L)- for amino acids, and individual isomers are encompassed within the scope of the present disclosure.
  • the compounds of the present disclosure do not include those that are known in art to be too unstable to synthesize and/or isolate.
  • the present disclosure is meant to include compounds in racemic and optically pure forms.
  • Optically active (R)- and (S)-, or (D)- and (L)-isomers may be prepared using chiral synthons or chiral reagents, or resolved using conventional techniques.
  • the compounds described herein contain olefinic bonds or other centers of geometric asymmetry, and unless specified otherwise, it is intended that the compounds include both E and Z geometric isomers.
  • isomers refers to compounds having the same number and kind of atoms, and hence the same molecular weight, but differing in respect to the structural arrangement or configuration of the atoms.
  • tautomer refers to one of two or more structural isomers which exist in equilibrium and which are readily converted from one isomeric form to another.
  • structures depicted herein are also meant to include all stereochemical forms of the structure; i.e., the R and S configurations for each asymmetric center. Therefore, single stereochemical isomers as well as enantiomeric and diastereomeric mixtures of the present compounds are within the scope of the disclosure.
  • structures depicted herein are also meant to include compounds which differ only in the presence of one or more isotopically enriched atoms.
  • compounds having the present structures except for the replacement of a hydrogen by a deuterium or tritium, or the replacement of a carbon by 13 C- or 14 C-enriched carbon are within the scope of this disclosure.
  • the compounds of the present disclosure may also contain unnatural proportions of atomic isotopes at one or more of the atoms that constitute such compounds.
  • the compounds may be radiolabeled with radioactive isotopes, such as for example tritium ( 3 H), iodine-125 ( 125 I), or carbon-14 ( 14 C). All isotopic variations of the compounds of the present disclosure, whether radioactive or not, are encompassed within the scope of the present disclosure.
  • each amino acid position that contains more than one possible amino acid is specifically contemplated that each member of the Markush group should be considered separately, thereby comprising another embodiment, and the Markush group is not to be read as a single unit.
  • bioconjugate and “bioconjugate linker” refer to the resulting association between atoms or molecules of bioconjugate reactive groups or bioconjugate reactive moieties.
  • the association can be direct or indirect.
  • a conjugate between a first bioconjugate reactive group e.g., -NFb, -COOH, -N- hydroxysuccinimide, or -maleimide
  • a second bioconjugate reactive group e.g., sulfhydryl, sulfur-containing amino acid, amine, amine sidechain containing amino acid, or carboxylate
  • covalent bond or linker e.g., a first linker of second linker
  • indirect e.g., by non-covalent bond (e.g., electrostatic interactions (e.g., ionic bond, hydrogen bond, halogen bond), van der Waals interactions (e.g., dipole-
  • bioconjugates or bioconjugate linkers are formed using bioconjugate chemistry (i.e., the association of two bioconjugate reactive groups) including, but are not limited to nucleophilic substitutions (e.g., reactions of amines and alcohols with acyl halides, active esters), electrophilic substitutions (e.g., enamine reactions) and additions to carbon-carbon and carbon-heteroatom multiple bonds (e.g., Michael reaction, Diels-Alder addition).
  • bioconjugate chemistry i.e., the association of two bioconjugate reactive groups
  • nucleophilic substitutions e.g., reactions of amines and alcohols with acyl halides, active esters
  • electrophilic substitutions e.g., enamine reactions
  • additions to carbon-carbon and carbon-heteroatom multiple bonds e.g., Michael reaction, Diels-Alder addition.
  • the first bioconjugate reactive group e.g., maleimide moiety
  • the second bioconjugate reactive group e.g., a sulfhydryl
  • the first bioconjugate reactive group (e.g., haloacetyl moiety) is covalently attached to the second bioconjugate reactive group (e.g., a sulfhydryl).
  • the first bioconjugate reactive group (e.g., pyridyl moiety) is covalently attached to the second bioconjugate reactive group (e.g., a sulfhydryl).
  • the first bioconjugate reactive group e.g., -N- hydroxysuccinimide moiety
  • is covalently attached to the second bioconjugate reactive group (e.g., an amine).
  • the first bioconjugate reactive group (e.g., maleimide moiety) is covalently attached to the second bioconjugate reactive group (e.g., a sulfhydryl).
  • the first bioconjugate reactive group (e.g., -sulfo-N-hydroxysuccinimide moiety) is covalently attached to the second bioconjugate reactive group (e.g., an amine).
  • bioconjugate reactive moi eties used for bioconjugate chemistries herein include, for example: (a) carboxyl groups and various derivatives thereof including, but not limited to, N-hydroxysuccinimide esters, N-hydroxybenztri azole esters, acid halides, acyl imidazoles, thioesters, p-nitrophenyl esters, alkyl, alkenyl, alkynyl and aromatic esters; (b) hydroxyl groups which can be converted to esters, ethers, aldehydes, etc.; (c) haloalkyl groups wherein the halide can be later displaced with a nucleophilic group such as, for example, an amine, a carboxylate anion, thiol anion, carbanion, or an alkoxide ion, thereby resulting in the covalent attachment of a new group at the site of the halogen atom; (d) dienophile groups which are capable of participating
  • bioconjugate reactive groups can be chosen such that they do not participate in, or interfere with, the chemical stability of the conjugate described herein.
  • a reactive functional group can be protected from participating in the crosslinking reaction by the presence of a protecting group.
  • the bioconjugate comprises a molecular entity derived from the reaction of an unsaturated bond, such as a maleimide, and a sulfhydryl group.
  • an analog is used in accordance with its plain ordinary meaning within Chemistry and Biology and refers to a chemical compound that is structurally similar to another compound (i.e., a so-called “reference” compound) but differs in composition, e.g., in the replacement of one atom by an atom of a different element, or in the presence of a particular functional group, or the replacement of one functional group by another functional group, or the absolute stereochemistry of one or more chiral centers of the reference compound. Accordingly, an analog is a compound that is similar or comparable in function and appearance but not in structure or origin to a reference compound.
  • a or “an”, as used in herein means one or more.
  • substituted with a[n] means the specified group may be substituted with one or more of any or all of the named substituents.
  • a group such as an alkyl or heteroaryl group
  • the group may contain one or more unsubstituted C1-C20 alkyls, and/or one or more unsubstituted 2 to 20 membered heteroalkyls.
  • R-substituted where a moiety is substituted with an R substituent, the group may be referred to as “R-substituted.” Where a moiety is R-substituted, the moiety is substituted with at least one R substituent and each R substituent is optionally different. Where a particular R group is present in the description of a chemical genus (such as Formula (I)), a Roman alphabetic symbol may be used to distinguish each appearance of that particular R group.
  • each R 13 substituent may be distinguished as R 13 A , R 13 B , R 13 c , R 13 D , etc., wherein each of R 13 A , R 13 B , R 13 c , R 13 D , etc. is defined within the scope of the definition of R 13 and optionally differently.
  • protecting group is used in accordance with its ordinary meaning in organic chemistry and refers to a moiety covalently bound to a heteroatom, heterocycloalkyl, or heteroaryl to prevent reactivity of the heteroatom, heterocycloalkyl, or heteroaryl during one or more chemical reactions performed prior to removal of the protecting group.
  • a protecting group is bound to a heteroatom (e.g., O) during a part of a multipart synthesis wherein it is not desired to have the heteroatom react (e.g., a chemical reduction) with the reagent. Following protection the protecting group may be removed (e.g., by modulating the pH).
  • the protecting group is an alcohol protecting group.
  • Non-limiting examples of alcohol protecting groups include acetyl, benzoyl, benzyl, methoxymethyl ether (MOM), tetrahydropyranyl (THP), and silyl ether (e.g., trimethyl silyl (TMS), tert-butyldimethylsilyl (TBS)).
  • the protecting group is an amine protecting group.
  • Non-limiting examples of amine protecting groups include carbobenzyloxy (Cbz), tert-butyl oxy carbonyl (BOC), 9-Fluorenylmethyloxycarbonyl (FMOC), acetyl, benzoyl, benzyl, carbamate, p-methoxybenzyl ether (PMB), and tosyl (Ts).
  • salts are meant to include salts of the active compounds that are prepared with relatively nontoxic acids or bases, depending on the particular substituents found on the compounds described herein.
  • base addition salts can be obtained by contacting the neutral form of such compounds with a sufficient amount of the desired base, either neat or in a suitable inert solvent.
  • pharmaceutically acceptable base addition salts include sodium, potassium, calcium, ammonium, organic amino, or magnesium salt, or a similar salt.
  • acid addition salts can be obtained by contacting the neutral form of such compounds with a sufficient amount of the desired acid, either neat or in a suitable inert solvent.
  • Examples of pharmaceutically acceptable acid addition salts include those derived from inorganic acids like hydrochloric, hydrobromic, nitric, carbonic, monohydrogencarbonic, phosphoric, monohydrogenphosphoric, dihydrogenphosphoric, sulfuric, monohydrogensulfuric, hydriodic, or phosphorous acids and the like, as well as the salts derived from relatively nontoxic organic acids like acetic, propionic, isobutyric, maleic, malonic, benzoic, succinic, suberic, fumaric, lactic, mandelic, phthalic, benzenesulfonic, p- tolylsulfonic, citric, tartaric, oxalic, methanesulfonic, and the like.
  • inorganic acids like hydrochloric, hydrobromic, nitric, carbonic, monohydrogencarbonic, phosphoric, monohydrogenphosphoric, dihydrogenphosphoric, sulfuric, monohydrogensulfuric, hydriodic,
  • C 6 rtain specific compounds of the present disclosure contain both basic and acidic functionalities that allow the compounds to be converted into either base or acid addition salts.
  • the compounds of the present disclosure may exist as salts, such as with pharmaceutically acceptable acids.
  • the present disclosure includes such salts.
  • Non-limiting examples of such salts include hydrochlorides, hydrobromides, phosphates, sulfates, methanesulfonates, nitrates, maleates, acetates, citrates, fumarates, proprionates, tartrates (e.g., (+)-tartrates, (-)-tartrates, or mixtures thereof including racemic mixtures), succinates, benzoates, and salts with amino acids such as glutamic acid, and quaternary ammonium salts (e.g., methyl iodide, ethyl iodide, and the like). These salts may be prepared by methods known to those skilled in the art.
  • the neutral forms of the compounds are preferably regenerated by contacting the salt with a base or acid and isolating the parent compound in the conventional manner.
  • the parent form of the compound may differ from the various salt forms in certain physical properties, such as solubility in polar solvents.
  • the present disclosure provides compounds, which are in a prodrug form.
  • Prodrugs of the compounds described herein are those compounds that readily undergo chemical changes under physiological conditions to provide the compounds of the present disclosure.
  • Prodrugs of the compounds described herein may be converted in vivo after administration.
  • prodrugs can be converted to the compounds of the present disclosure by chemical or biochemical methods in an ex vivo environment, such as, for example, when contacted with a suitable enzyme or chemical reagent.
  • C 6 rtain compounds of the present disclosure can exist in unsolvated forms as well as solvated forms, including hydrated forms. In general, the solvated forms are equivalent to unsolvated forms and are encompassed within the scope of the present disclosure. C 6 rtain compounds of the present disclosure may exist in multiple crystalline or amorphous forms. In general, all physical forms are equivalent for the uses contemplated by the present disclosure and are intended to be within the scope of the present disclosure.
  • a polypeptide, or a cell is “recombinant” when it is artificial or engineered, or derived from or contains an artificial or engineered protein or nucleic acid (e.g., non-natural or not wild type).
  • a polynucleotide that is inserted into a vector or any other heterologous location, e.g., in a genome of a recombinant organism, such that it is not associated with nucleotide sequences that normally flank the polynucleotide as it is found in nature is a recombinant polynucleotide.
  • a protein expressed in vitro or in vivo from a recombinant polynucleotide is an example of a recombinant polypeptide.
  • a polynucleotide sequence that does not appear in nature for example a variant of a naturally occurring gene, is recombinant.
  • a cell can be identified by well-known methods in the art including, for example, presence of an intact membrane, staining by a particular dye, ability to produce progeny or, in the case of a gamete, ability to combine with a second gamete to produce a viable offspring.
  • C 6 lls may include prokaryotic and eukaroytic cells.
  • Prokaryotic cells include but are not limited to bacteria.
  • Eukaryotic cells include but are not limited to yeast cells and cells derived from plants and animals, for example mammalian, insect (e.g., spodoptera) and human cells.
  • C 6 lls may be useful when they are naturally nonadherent or have been treated not to adhere to surfaces, for example by trypsinization.
  • treating refers to any indicia of success in the treatment or amelioration of an injury, disease, pathology or condition, including any objective or subjective parameter such as abatement; remission; diminishing of symptoms or making the injury, pathology or condition more tolerable to the patient; slowing in the rate of degeneration or decline; making the final point of degeneration less debilitating; improving a patient’s physical or mental well-being.
  • the treatment or amelioration of symptoms can be based on objective or subjective parameters; including the results of a physical examination, neuropsychiatric exams, and/or a psychiatric evaluation. For example, the certain methods presented herein successfully treat cancer by decreasing the incidence of cancer and or causing remission of cancer.
  • treating cancer includes slowing the rate of growth or spread of cancer cells, reducing metastasis, or reducing the growth of metastatic tumors.
  • the term “treating” and conjugations thereof, include prevention of an injury, pathology, condition, or disease.
  • treating is preventing.
  • treating does not include preventing.
  • the treating or treatment is not prophylactic treatment.
  • An “effective amount” is an amount sufficient for a compound to accomplish a stated purpose relative to the absence of the compound (e.g., achieve the effect for which it is administered, treat a disease, reduce enzyme activity, increase enzyme activity, reduce signaling pathway, reduce one or more symptoms of a disease or condition.
  • an “effective amount” is an amount sufficient to contribute to the treatment, prevention, or reduction of a symptom or symptoms of a disease, which could also be referred to as a “therapeutically effective amount” when referred to in this context.
  • a “reduction” of a symptom or symptoms means decreasing of the severity or frequency of the symptom(s), or elimination of the symptom(s).
  • a “prophylactically effective amount” of a drug is an amount of a drug that, when administered to a subject, will have the intended prophylactic effect, e.g., preventing or delaying the onset (or reoccurrence) of an injury, disease, pathology or condition, or reducing the likelihood of the onset (or reoccurrence) of an injury, disease, pathology, or condition, or their symptoms.
  • the full prophylactic effect does not necessarily occur by administration of one dose, and may occur only after administration of a series of doses.
  • a prophylactically effective amount may be administered in one or more administrations.
  • An “activity decreasing amount,” as used herein, refers to an amount of antagonist required to decrease the activity of an enzyme relative to the absence of the antagonist.
  • a “function disrupting amount,” as used herein, refers to the amount of antagonist required to disrupt the function of an enzyme or protein relative to the absence of the antagonist.
  • An “activity increasing amount,” as used herein, refers to an amount of agonist required to increase the activity of an enzyme relative to the absence of the agonist.
  • a “function increasing amount,” as used herein, refers to the amount of agonist required to increase the function of an enzyme or protein relative to the absence of the agonist. The exact amounts will depend on the purpose of the treatment, and will be ascertainable by one skilled in the art using known techniques (see, e.g., Lieberman, Pharmaceutical Dosage Forms (vols.
  • Control or “control experiment” is used in accordance with its plain ordinary meaning and refers to an experiment in which the subjects or reagents of the experiment are treated as in a parallel experiment except for omission of a procedure, reagent, or variable of the experiment. In some instances, the control is used as a standard of comparison in evaluating experimental effects. In some embodiments, a control is the measurement of the activity (e.g., signaling pathway) of a protein in the absence of a compound as described herein (including embodiments, examples, figures, or Tables).
  • activity e.g., signaling pathway
  • Contacting is used in accordance with its plain ordinary meaning and refers to the process of allowing at least two distinct species (e.g., chemical compounds including biomolecules, or cells) to become sufficiently proximal to react, interact or physically touch. It should be appreciated; however, the resulting reaction product can be produced directly from a reaction between the added reagents or from an intermediate from one or more of the added reagents which can be produced in the reaction mixture.
  • species e.g., chemical compounds including biomolecules, or cells
  • the term “contacting” may include allowing two species to react, interact, or physically touch, wherein the two species may be a compound as described herein and a cellular component (e.g., protein, ion, lipid, nucleic acid, nucleotide, amino acid, protein, particle, organelle, cellular compartment, microorganism, virus, lipid droplet, vesicle, small molecule, protein complex, protein aggregate, or macromolecule).
  • a cellular component e.g., protein, ion, lipid, nucleic acid, nucleotide, amino acid, protein, particle, organelle, cellular compartment, microorganism, virus, lipid droplet, vesicle, small molecule, protein complex, protein aggregate, or macromolecule.
  • contacting includes allowing a compound described herein to interact with a cellular component (e.g., protein, ion, lipid, nucleic acid, nucleotide, amino acid, protein, particle, virus, lipid droplet, organelle, cellular compartment, microorganism, vesicle, small molecule, protein complex, protein aggregate, or macromolecule) that is involved in a signaling pathway.
  • a cellular component e.g., protein, ion, lipid, nucleic acid, nucleotide, amino acid, protein, particle, virus, lipid droplet, organelle, cellular compartment, microorganism, vesicle, small molecule, protein complex, protein aggregate, or macromolecule
  • activation As defined herein, the term “activation,” “activate,” “activating” and the like in reference to a protein refers to conversion of a protein into a biologically active derivative from an initial inactive or deactivated state.
  • the terms reference activation, or activating, sensitizing, or up-regulating signal transduction or enzymatic activity or the amount of a protein decreased in a disease.
  • agonist refers to a substance capable of detectably increasing the expression or activity of a given gene or protein.
  • the agonist can increase expression or activity by at least 10%, 20%, 30%, 40%, 50%, 60%, 70%, 80%, 90%, 95%, 96%, 97%, 98%, or 99% in comparison to a control in the absence of the agonist.
  • expression or activity is 1.5-fold, 2-fold, 3-fold, 4-fold, 5-fold, 10-fold or higher than the expression or activity in the absence of the agonist.
  • the term “inhibition,” “inhibit,” “inhibiting” and the like in reference to a cellular component-inhibitor interaction means negatively affecting (e.g., decreasing) the activity or function of the cellular component (e.g., decreasing the signaling pathway stimulated by a cellular component (e.g., protein, ion, lipid, virus, lipid droplet, nucleic acid, nucleotide, amino acid, protein, particle, organelle, cellular compartment, microorganism, vesicle, small molecule, protein complex, protein aggregate, or macromolecule)), relative to the activity or function of the cellular component in the absence of the inhibitor.
  • a cellular component e.g., protein, ion, lipid, virus, lipid droplet, nucleic acid, nucleotide, amino acid, protein, particle, organelle, cellular compartment, microorganism, vesicle, small molecule, protein complex, protein aggregate, or macromolecule
  • inhibition means negatively affecting (e.g., decreasing) the concentration or levels of the cellular component relative to the concentration or level of the cellular component in the absence of the inhibitor.
  • inhibition refers to reduction of a disease or symptoms of disease.
  • inhibition refers to a reduction in the activity of a signal transduction pathway or signaling pathway (e.g., reduction of a pathway involving the cellular component).
  • inhibition includes, at least in part, partially or totally blocking stimulation, decreasing, preventing, or delaying activation, or inactivating, desensitizing, or down-regulating the signaling pathway or enzymatic activity or the amount of a cellular component.
  • inhibitor refers to a substance capable of detectably decreasing the expression or activity of a given gene or protein.
  • the antagonist can decrease expression or activity by at least 10%, 20%, 30%, 40%, 50%, 60%, 70%, 80%, 90%, 95%, 96%, 97%, 98%, or 99% in comparison to a control in the absence of the antagonist.
  • expression or activity is 1.5-fold, 2-fold, 3-fold, 4-fold, 5-fold, 10-fold or lower than the expression or activity in the absence of the antagonist.
  • lysophosphatidic acid receptor 1 antagonist or “LPAR1 antagonist” refers to any exogenously administered compound or agent that is capable of partially or completely inhibiting, or reversing, the effect of an agonist (e.g., lysophosphatidic acid) on the LPAR1 receptor.
  • LPAR1 antagonist refers to any exogenously administered compound or agent that is capable of partially or completely inhibiting, or reversing, the effect of an agonist (e.g., lysophosphatidic acid) on the LPAR1 receptor.
  • the term is inclusive of compounds or agents characterized or described as antagonists, partial antagonists, and negative allosteric modulators.
  • modulator refers to a composition that increases or decreases the level of a target molecule or the function of a target molecule or the physical state of the target of the molecule (e.g., a target may be a cellular component (e.g., protein, ion, lipid, virus, lipid droplet, nucleic acid, nucleotide, amino acid, protein, particle, organelle, cellular compartment, microorganism, vesicle, small molecule, protein complex, protein aggregate, or macromolecule)) relative to the absence of the composition.
  • a target may be a cellular component (e.g., protein, ion, lipid, virus, lipid droplet, nucleic acid, nucleotide, amino acid, protein, particle, organelle, cellular compartment, microorganism, vesicle, small molecule, protein complex, protein aggregate, or macromolecule)) relative to the absence of the composition.
  • a target may be a cellular component (e.g., protein, ion
  • expression includes any step involved in the production of the polypeptide including, but not limited to, transcription, post-transcriptional modification, translation, post-translational modification, and secretion. Expression can be detected using conventional techniques for detecting protein (e.g., ELISA, Western blotting, flow cytometry, immunofluorescence, immunohistochemistry, etc.).
  • modulate is used in accordance with its plain ordinary meaning and refers to the act of changing or varying one or more properties. “Modulation” refers to the process of changing or varying one or more properties. For example, as applied to the effects of a modulator on a target protein, to modulate means to change by increasing or decreasing a property or function of the target molecule or the amount of the target molecule.
  • “Patient” or “subject in need thereof’ refers to a living organism suffering from or prone to a disease or condition that can be treated by administration of a pharmaceutical composition as provided herein.
  • Non-limiting examples include humans, other mammals, bovines, rats, mice, dogs, monkeys, goat, sheep, cows, deer, and other non-mammalian animals.
  • a patient is human.
  • Disease or “condition” refer to a state of being or health status of a patient or subject capable of being treated with the compounds or methods provided herein.
  • the disease is a disease related to (e.g., caused by) a cellular component (e.g., protein, ion, lipid, nucleic acid, nucleotide, amino acid, protein, particle, organelle, cellular compartment, microorganism, vesicle, small molecule, protein complex, protein aggregate, or macromolecule).
  • a cellular component e.g., protein, ion, lipid, nucleic acid, nucleotide, amino acid, protein, particle, organelle, cellular compartment, microorganism, vesicle, small molecule, protein complex, protein aggregate, or macromolecule.
  • the disease is a neurodegenerative disease.
  • the disease is an inflammatory disease.
  • the disease is posthemorrhagic encephalitis.
  • the disease is a demyelinating disease. In embodiments, the disease is multiple sclerosis. In embodiments, the disease is a fibrotic disease. In embodiments, the disease is pulmonary fibrosis. In embodiments, the disease is idiopathic pulmonary fibrosis. In embodiments, the disease is a cancer. In embodiments, the disease is glioblastoma.
  • neurodegenerative disease refers to a disease or condition in which the function of a subject’s nervous system becomes impaired.
  • Examples of neurodegenerative diseases that may be treated with a compound, pharmaceutical composition, or method described herein include Alexander’s disease, Alper’s disease, Alzheimer’s disease, Amyotrophic lateral sclerosis, Ataxia telangiectasia, Batten disease (also known as Spielmeyer-Vogt-Sjogren-Batten disease), Bovine spongiform encephalopathy (BSE), Canavan disease, Cockayne syndrome, Corticobasal degeneration, Creutzfeldt- Jakob disease, frontotemporal dementia, Gerstmann-Straussler-Scheinker syndrome, Huntington’s disease, HIV-associated dementia, Kennedy’s disease, Krabbe’s disease, kuru, Lewy body dementia, Machado-Joseph disease (Spinocerebellar ataxia type 3), Multiple sclerosis
  • inflammatory disease refers to a disease or condition characterized by aberrant inflammation (e.g., an increased level of inflammation compared to a control such as a healthy person not suffering from a disease).
  • inflammatory diseases include autoimmune diseases, arthritis, rheumatoid arthritis, psoriatic arthritis, juvenile idiopathic arthritis, multiple sclerosis, systemic lupus erythematosus (SLE), myasthenia gravis, juvenile onset diabetes, diabetes mellitus type 1, Guillain-Barre syndrome, Hashimoto’s encephalitis, Hashimoto’s thyroiditis, ankylosing spondylitis, psoriasis, Sjogren’s syndrome, vasculitis, glomerulonephritis, auto-immune thyroiditis, Behcet’s disease, Crohn’s disease, ulcerative colitis, bullous pemphigoid, sarcoidosis, ichthyosis
  • the term “demyelinating disease” refers to any disease or condition characterized by damage to the protective covering (e.g., myelin sheath) that surrounds nerve fibers (e.g., in the brain, optic nerves, or spinal cord).
  • the demyelinating disease is a demyelinating disease of the central nervous system.
  • the demyelinating disease is multiple sclerosis.
  • the demyelinating disease is a demyelinating disease of the peripheral nervous system.
  • Fibrotic disease refers to any disease or condition characterized by the formation of excess fibrous connective tissue.
  • the formation of excess fibrous connective tissue may be in response to a reparative or reactive process.
  • Fibrotic diseases include but are not limited to pulmonary fibrosis (e.g., idiopathic pulmonary fibrosis (IPF)), liver fibrosis (e.g., nonalcoholic steatohepatitis (NASH)), myelofibrosis, skin fibrosis (e.g., scleroderma), ocular fibrosis, mediastinal fibrosis, cardiac fibrosis, kidney fibrosis, stromal fibrosis, epidural fibrosis, epithelial fibrosis, or idiopathic fibrosis.
  • pulmonary fibrosis e.g., idiopathic pulmonary fibrosis (IPF)
  • liver fibrosis e.g., nonalcoholic steatohe
  • cardiovascular diseases that may be treated with a compound, pharmaceutical composition, or method described herein include, but are not limited to, stroke, heart failure, hypertension, hypertensive heart disease, myocardial infarction, angina pectoris, tachycardia, cardiomyopathy, rheumatic heart disease, cardiomyopathy, heart arrhythmia, congenital heart disease, valvular heart disease, carditis, aortic aneurysms, peripheral artery disease, thromboembolic disease, and venous thrombosis.
  • cancer refers to all types of cancer, neoplasm or malignant tumors found in mammals (e.g., humans), including leukemia, lymphoma, carcinomas and sarcomas.
  • exemplary cancers that may be treated with a compound or method provided herein include cancer of the thyroid, endocrine system, brain, breast, cervix, colon, head and neck, liver, kidney, lung, non-small cell lung, melanoma, mesothelioma, ovary, sarcoma, stomach, uterus, medulloblastoma, colorectal cancer, or pancreatic cancer.
  • Additional examples include, Hodgkin’s Disease, Non-Hodgkin’s Lymphoma, multiple myeloma, neuroblastoma, glioma, glioblastoma multiforme, ovarian cancer, rhabdomyosarcoma, primary thrombocytosis, primary macroglobulinemia, primary brain tumors, cancer, malignant pancreatic insulanoma, malignant carcinoid, urinary bladder cancer, premalignant skin lesions, testicular cancer, lymphomas, thyroid cancer, esophageal cancer, genitourinary tract cancer, malignant hypercalcemia, endometrial cancer, adrenal cortical cancer, neoplasms of the endocrine or exocrine pancreas, medullary thyroid cancer, medullary thyroid carcinoma, melanoma, colorectal cancer, papillary thyroid cancer, hepatocellular carcinoma, or prostate cancer.
  • leukemia refers broadly to progressive, malignant diseases of the blood- forming organs and is generally characterized by a distorted proliferation and development of leukocytes and their precursors in the blood and bone marrow. Leukemia is generally clinically classified on the basis of (1) the duration and character of the disease-acute or chronic; (2) the type of cell involved; myeloid (myelogenous), lymphoid (lymphogenous), or monocytic; and (3) the increase or non-increase in the number abnormal cells in the blood- leukemic or aleukemic (subleukemic).
  • Exemplary leukemias that may be treated with a compound or method provided herein include, for example, acute nonlymphocytic leukemia, chronic lymphocytic leukemia, acute granulocytic leukemia, chronic granulocytic leukemia, acute promyelocytic leukemia, adult T-cell leukemia, aleukemic leukemia, a leukocythemic leukemia, basophylic leukemia, blast cell leukemia, bovine leukemia, chronic myelocytic leukemia, leukemia cutis, embryonal leukemia, eosinophilic leukemia, Gross’ leukemia, hairy-cell leukemia, hemoblastic leukemia, hemocytoblastic leukemia, histiocytic leukemia, stem cell leukemia, acute monocytic leukemia, leukopenic leukemia, lymphatic leukemia, lymphoblastic leukemia, lymphocytic leukemia, lymphogenous leukemia,
  • lymphoma refers to a group of cancers affecting hematopoietic and lymphoid tissues. It begins in lymphocytes, the blood cells that are found primarily in lymph nodes, spleen, thymus, and bone marrow. Two main types of lymphoma are non-Hodgkin lymphoma and Hodgkin’s disease. Hodgkin’s disease represents approximately 15% of all diagnosed lymphomas. This is a cancer associated with Reed- Sternberg malignant B lymphocytes. Non-Hodgkin’ s lymphomas (NHL) can be classified based on the rate at which cancer grows and the type of cells involved.
  • B-cell lymphomas that may be treated with a compound or method provided herein include, but are not limited to, small lymphocytic lymphoma, Mantle cell lymphoma, follicular lymphoma, marginal zone lymphoma, extranodal (MALT) lymphoma, nodal (monocytoid B-cell) lymphoma, splenic lymphoma, diffuse large cell B-lymphoma, Burkitt’s lymphoma, lymphoblastic lymphoma, immunoblastic large cell lymphoma, or precursor B-lymphoblastic lymphoma.
  • Exemplary T- cell lymphomas that may be treated with a compound or method provided herein include, but are not limited to, cutaneous T-cell lymphoma, peripheral T-cell lymphoma, anaplastic large cell lymphoma, mycosis fungoides, and precursor T-lymphoblastic lymphoma.
  • sarcoma generally refers to a tumor which is made up of a substance like the embryonic connective tissue and is generally composed of closely packed cells embedded in a fibrillar or homogeneous substance.
  • Sarcomas that may be treated with a compound or method provided herein include a chondrosarcoma, fibrosarcoma, lymphosarcoma, melanosarcoma, myxosarcoma, osteosarcoma, Abernethy's sarcoma, adipose sarcoma, liposarcoma, alveolar soft part sarcoma, ameloblastic sarcoma, botryoid sarcoma, chloroma sarcoma, chorio carcinoma, embryonal sarcoma, Wilms’ tumor sarcoma, endometrial sarcoma, stromal sarcoma, Ewing’s sarcoma, fascial sarcom
  • melanoma is taken to mean a tumor arising from the melanocytic system of the skin and other organs.
  • Melanomas that may be treated with a compound or method provided herein include, for example, acral-lentiginous melanoma, amelanotic melanoma, benign juvenile melanoma, Cloudman’s melanoma, S91 melanoma, Harding-Passey melanoma, juvenile melanoma, lentigo maligna melanoma, malignant melanoma, nodular melanoma, subungal melanoma, or superficial spreading melanoma.
  • carcinoma refers to a malignant new growth made up of epithelial cells tending to infiltrate the surrounding tissues and give rise to metastases.
  • exemplary carcinomas that may be treated with a compound or method provided herein include, for example, medullary thyroid carcinoma, familial medullary thyroid carcinoma, acinar carcinoma, acinous carcinoma, adenocystic carcinoma, adenoid cystic carcinoma, carcinoma adenomatosum, carcinoma of adrenal cortex, alveolar carcinoma, alveolar cell carcinoma, basal cell carcinoma, carcinoma basocellulare, basaloid carcinoma, basosquamous cell carcinoma, bronchioalveolar carcinoma, bronchiolar carcinoma, bronchogenic carcinoma, cerebriform carcinoma, cholangiocellular carcinoma, chorionic carcinoma, colloid carcinoma, comedo carcinoma, corpus carcinoma, cribriform carcinoma, carcinoma en cuirasse, carcinoma cutaneum, cylindrical carcinoma, cylindrical cell carcinoma, duct carcinoma, carcinoma durum, embryonal carcinoma, encephaloid
  • the terms “metastasis,” “metastatic,” and “metastatic cancer” can be used interchangeably and refer to the spread of a proliferative disease or disorder, e.g., cancer, from one organ or another non-adjacent organ or body part. “Metastatic cancer” is also called “Stage IV cancer.” Cancer occurs at an originating site, e.g., breast, which site is referred to as a primary tumor, e.g., primary breast cancer. Some cancer cells in the primary tumor or originating site acquire the ability to penetrate and infiltrate surrounding normal tissue in the local area and/or the ability to penetrate the walls of the lymphatic system or vascular system circulating through the system to other sites and tissues in the body.
  • a second clinically detectable tumor formed from cancer cells of a primary tumor is referred to as a metastatic or secondary tumor.
  • the metastatic tumor and its cells are presumed to be similar to those of the original tumor.
  • the secondary tumor in the breast is referred to a metastatic lung cancer.
  • metastatic cancer refers to a disease in which a subject has or had a primary tumor and has one or more secondary tumors.
  • non- metastatic cancer or subjects with cancer that is not metastatic refers to diseases in which subjects have a primary tumor but not one or more secondary tumors.
  • metastatic lung cancer refers to a disease in a subject with or with a history of a primary lung tumor and with one or more secondary tumors at a second location or multiple locations, e.g., in the breast.
  • cutaneous metastasis or “skin metastasis” refer to secondary malignant cell growths in the skin, wherein the malignant cells originate from a primary cancer site (e.g., breast).
  • a primary cancer site e.g., breast
  • cancerous cells from a primary cancer site may migrate to the skin where they divide and cause lesions. Cutaneous metastasis may result from the migration of cancer cells from breast cancer tumors to the skin.
  • visceral metastasis refers to secondary malignant cell growths in the interal organs (e.g., heart, lungs, liver, pancreas, intestines) or body cavities (e.g., pleura, peritoneum), wherein the malignant cells originate from a primary cancer site (e.g., head and neck, liver, breast).
  • a primary cancer site e.g., head and neck, liver, breast.
  • a primary cancer site e.g., head and neck, liver, breast
  • Visceral metastasis may result from the migration of cancer cells from liver cancer tumors or head and neck tumors to internal organs.
  • the term “LP ARI -associated disease” refers to any disease or condition caused by aberrant activity or signaling of LPAR1.
  • the LPAR1- associated disease is a neurodegenerative disease.
  • the LP ARI -associated disease is an inflammatory disease.
  • the LP ARI -associated disease is posthemorrhagic encephalitis.
  • the LP ARI -associated disease is a demyelinating disease.
  • the LP ARI -associated disease is multiple sclerosis.
  • the LP ARI -associated disease is a fibrotic disease.
  • the LP ARI -associated disease is pulmonary fibrosis.
  • the LP ARI -associated disease is idiopathic pulmonary fibrosis. In embodiments, the LP ARI -associated disease is a cancer. In embodiments, the LP ARI -associated disease is glioblastoma.
  • drug is used in accordance with its common meaning and refers to a substance which has a physiological effect (e.g., beneficial effect, is useful for treating a subject) when introduced into or to a subject (e.g., in or on the body of a subject or patient).
  • a drug moiety is a radical of a drug.
  • a “detectable agent,” “detectable compound,” “detectable label,” or “detectable moiety” is a substance (e.g., element), molecule, or composition detectable by spectroscopic, photochemical, biochemical, immunochemical, chemical, magnetic resonance imaging, or other physical means.
  • detectable agents include 18 F, 32 P, 33 P, 45 Ti, 47 Sc, 52 Fe, 59 Fe, 62 Cu, 64 Cu, 67 Cu, 67 Ga, 68 Ga, 77 As, 86 Y, 90 Y, 89 Sr, 89 Zr, 94 Tc, 94 Tc, 99m Tc, "Mo, 105 Pd, 105 Rh, m Ag, m In, 123 I, 124 I, 125 I, 131 I, 142 Pr, 143 Pr, 149 Pm, 153 Sm, 154 ' 1581 Gd, 161 Tb, 166 Dy, 166 Ho 169 Er, 175 LU, 177 LU, 186 Re, 188 Re, 189 Re, 194 Ir, 198 Au, 199 Au, 211 At, 211 Pb, 212 Bi, 212 Pb, 213 Bi, 223 Ra, 225 Ac, Cr, V, Mn, Fe, Co, Ni, Cu, La, C 6 , Pr, N
  • Radioactive substances that may be used as imaging and/or labeling agents in accordance with the embodiments of the disclosure include, but are not limited to, 18 F, 32 P, 33 P, 45 Ti, 47 Sc, 52 Fe, 59 Fe, 62 Cu, 64 Cu, 67 Cu, 67 Ga, 68 Ga, 77 As, 86 Y, 90 Y, 89 Sr, 89 Zr, 94 TC, 94 TC, 99m Tc, "Mo, 105 Pd, 105 Rh, m Ag, m In, 123 I, 124 I, 125 I, 131 I, 142 Pr, 143 Pr, 149 Pm, 153 Sm, 154 ' 1581 Gd, 161 Tb, 166 Dy, 166 Ho, 169 Er, 175 Lu, 177 Lu, 186 Re, 188 Re, 189 Re, 194 Ir, 198 Au, 199 Au, 211 At, 211 Pb, 212 Bi
  • Paramagnetic ions that may be used as additional imaging agents in accordance with the embodiments of the disclosure include, but are not limited to, ions of transition and lanthanide metals (e.g., metals having atomic numbers of 21-29, 42, 43, 44, or 57-71). These metals include ions of Cr, V, Mn, Fe, Co, Ni, Cu, La, C 6 , Pr, Nd, Pm, Sm, Eu, Gd, Tb, Dy, Ho, Er, Tm, Yb, and Lu.
  • transition and lanthanide metals e.g., metals having atomic numbers of 21-29, 42, 43, 44, or 57-71.
  • These metals include ions of Cr, V, Mn, Fe, Co, Ni, Cu, La, C 6 , Pr, Nd, Pm, Sm, Eu, Gd, Tb, Dy, Ho, Er, Tm, Yb, and Lu.
  • “Pharmaceutically acceptable excipient” and “pharmaceutically acceptable carrier” refer to a substance that aids the administration of an active agent to and absorption by a subject and can be included in the compositions of the present invention without causing a significant adverse toxicological effect on the patient.
  • Non-limiting examples of pharmaceutically acceptable excipients include water, NaCl, normal saline solutions, lactated Ringer’s, normal sucrose, normal glucose, binders, fillers, disintegrants, lubricants, coatings, sweeteners, flavors, salt solutions (such as Ringer’s solution), alcohols, oils, gelatins, carbohydrates such as lactose, amylose or starch, fatty acid esters, hydroxymethycellulose, polyvinyl pyrrolidine, and colors, and the like.
  • Such preparations can be sterilized and, if desired, mixed with auxiliary agents such as lubricants, preservatives, stabilizers, wetting agents, emulsifiers, salts for influencing osmotic pressure, buffers, coloring, and/or aromatic substances and the like that do not deleteriously react with the compounds of the invention.
  • auxiliary agents such as lubricants, preservatives, stabilizers, wetting agents, emulsifiers, salts for influencing osmotic pressure, buffers, coloring, and/or aromatic substances and the like that do not deleteriously react with the compounds of the invention.
  • auxiliary agents such as lubricants, preservatives, stabilizers, wetting agents, emulsifiers, salts for influencing osmotic pressure, buffers, coloring, and/or aromatic substances and the like that do not deleteriously react with the compounds of the invention.
  • auxiliary agents such as lubricants, preservatives, stabilizers, wetting agents
  • preparation is intended to include the formulation of the active compound with encapsulating material as a carrier providing a capsule in which the active component with or without other carriers, is surrounded by a carrier, which is thus in association with it.
  • cachets and lozenges are included. Tablets, powders, capsules, pills, cachets, and lozenges can be used as solid dosage forms suitable for oral administration.
  • the term “about” means a range of values including the specified value, which a person of ordinary skill in the art would consider reasonably similar to the specified value. In embodiments, about means within a standard deviation using measurements generally acceptable in the art. In embodiments, about means a range extending to +/- 10% of the specified value. In embodiments, about includes the specified value.
  • administering is used in accordance with its plain and ordinary meaning and includes oral administration, administration as a suppository, topical contact, intravenous, intraperitoneal, intramuscular, intralesional, intrathecal, intranasal or subcutaneous administration, or the implantation of a slow-release device, e.g., a mini- osmotic pump, to a subject.
  • Administration is by any route, including parenteral and transmucosal (e.g., buccal, sublingual, palatal, gingival, nasal, vaginal, rectal, or transdermal).
  • Parenteral administration includes, e.g., intravenous, intramuscular, intraarteriole, intradermal, subcutaneous, intraperitoneal, intraventricular, and intracranial.
  • Other modes of delivery include, but are not limited to, the use of liposomal formulations, intravenous infusion, transdermal patches, etc.
  • co -administer it is meant that a composition described herein is administered at the same time, just prior to, or just after the administration of one or more additional therapies, for example cancer therapies such as chemotherapy, hormonal therapy, radiotherapy, or immunotherapy.
  • the compounds of the invention can be administered alone or can be co-administered to the patient. Coadministration is meant to include simultaneous or sequential administration of the compounds individually or in combination (more than one compound).
  • compositions of the present invention can be delivered by transdermally, by a topical route, formulated as applicator sticks, solutions, suspensions, emulsions, gels, creams, ointments, pastes, jellies, paints, powders, and aerosols.
  • the compounds described herein can be used in combination with one another, with other active agents known to be useful in treating a disease associated with cells expressing a disease associated cellular component, or with adjunctive agents that may not be effective alone, but may contribute to the efficacy of the active agent.
  • co-administration includes administering one active agent within 0.5, 1, 2, 4, 6, 8, 10, 12, 16, 20, or 24 hours of a second active agent.
  • Co- administration includes administering two active agents simultaneously, approximately simultaneously (e.g., within about 1, 5, 10, 15, 20, or 30 minutes of each other), or sequentially in any order.
  • co-administration can be accomplished by co-formulation, i.e., preparing a single pharmaceutical composition including both active agents.
  • the active agents can be formulated separately.
  • the active and/or adjunctive agents may be linked or conjugated to one another.
  • compound utilized in the pharmaceutical compositions of the present invention may be administered at the initial dosage of about 0.001 mg/kg to about 1000 mg/kg daily.
  • the dosages may be varied depending upon the requirements of the patient, the severity of the condition being treated, and the compound or drug being employed. For example, dosages can be empirically determined considering the type and stage of disease (e.g., multiple sclerosis, fibrotic disease, encephalitis, or cancer) diagnosed in a particular patient.
  • the dose administered to a patient should be sufficient to affect a beneficial therapeutic response in the patient over time.
  • the size of the dose will also be determined by the existence, nature, and extent of any adverse side effects that accompany the administration of a compound in a particular patient. Determination of the proper dosage for a particular situation is within the skill of the practitioner. Generally, treatment is initiated with smaller dosages which are less than the optimum dose of the compound. Thereafter, the dosage is increased by small increments until the optimum effect under circumstances is reached. For convenience, the total daily dosage may be divided and administered in portions during the day, if desired.
  • a disease e.g., a protein associated disease, disease associated with a cellular component
  • the disease e.g., multiple sclerosis, fibrotic disease, encephalitis, or cancer
  • a symptom of the disease is caused by (in whole or in part) the substance or substance activity or function or the disease or a symptom of the disease may be treated by modulating (e.g., inhibiting or activating) the substance (e.g., cellular component).
  • modulating e.g., inhibiting or activating
  • the substance e.g., cellular component
  • aberrant refers to different from normal. When used to describe enzymatic activity, aberrant refers to activity that is greater or less than a normal control or the average of normal non-diseased control samples. Aberrant activity may refer to an amount of activity that results in a disease, wherein returning the aberrant activity to a normal or non-disease-associated amount (e.g., by administering a compound or using a method as described herein), results in reduction of the disease or one or more disease symptoms.
  • nucleic acid or protein when applied to a nucleic acid or protein, denotes that the nucleic acid or protein is essentially free of other cellular components with which it is associated in the natural state. It can be, for example, in a homogeneous state and may be in either a dry or aqueous solution. Purity and homogeneity are typically determined using analytical chemistry techniques such as polyacrylamide gel electrophoresis or high performance liquid chromatography. A protein that is the predominant species present in a preparation is substantially purified.
  • amino acid refers to naturally occurring and synthetic amino acids, as well as amino acid analogs and amino acid mimetics that function in a manner similar to the naturally occurring amino acids.
  • Naturally occurring amino acids are those encoded by the genetic code, as well as those amino acids that are later modified, e.g., hydroxyproline, - carboxyglutamate, and O-phosphoserine.
  • Amino acid analogs refers to compounds that have the same basic chemical structure as a naturally occurring amino acid, i.e., an a carbon that is bound to a hydrogen, a carboxyl group, an amino group, and an R group, e.g., homoserine, norleucine, methionine sulfoxide, methionine methyl sulfonium. Such analogs have modified R groups (e.g., norleucine) or modified peptide backbones, but retain the same basic chemical structure as a naturally occurring amino acid.
  • Amino acid mimetics refers to chemical compounds that have a structure that is different from the general chemical structure of an amino acid, but that functions in a manner similar to a naturally occurring amino acid.
  • the terms “non-naturally occurring amino acid” and “unnatural amino acid” refer to amino acid analogs, synthetic amino acids, and amino acid mimetics which are not found in nature.
  • Amino acids may be referred to herein by either their commonly known three letter symbols or by the one-letter symbols recommended by the IUPAC-IUB Biochemical Nomenclature Commission. Nucleotides, likewise, may be referred to by their commonly accepted single-letter codes.
  • polypeptide “peptide,” and “protein” are used interchangeably herein to refer to a polymer of amino acid residues, wherein the polymer may in embodiments be conjugated to a moiety that does not consist of amino acids.
  • the terms apply to amino acid polymers in which one or more amino acid residue is an artificial chemical mimetic of a corresponding naturally occurring amino acid, as well as to naturally occurring amino acid polymers and non-naturally occurring amino acid polymers.
  • amino acid or nucleotide base “position” is denoted by a number that sequentially identifies each amino acid (or nucleotide base) in the reference sequence based on its position relative to the N-terminus (or 5'-end). Due to deletions, insertions, truncations, fusions, and the like that must be taken into account when determining an optimal alignment, in general the amino acid residue number in a test sequence determined by simply counting from the N-terminus will not necessarily be the same as the number of its corresponding position in the reference sequence. For example, in a case where a variant has a deletion relative to an aligned reference sequence, there will be no amino acid in the variant that corresponds to a position in the reference sequence at the site of deletion.
  • protein complex is used in accordance with its plain ordinary meaning and refers to a protein which is associated with an additional substance (e.g., another protein, protein subunit, or a compound). Protein complexes typically have defined quaternary structure. The association between the protein and the additional substance may be a covalent bond. In embodiments, the association between the protein and the additional substance (e.g., compound) is via non-covalent interactions. In embodiments, a protein complex refers to a group of two or more polypeptide chains. Proteins in a protein complex are linked by non-covalent protein-protein interactions. A non-limiting example of a protein complex is the proteasome.
  • lysophosphatidic acid receptor refers to one or more of the family of G protein-coupled receptors for lysophosphatidic acid (LPA).
  • LPAR includes LPAR1, LPAR2, LPAR3, LPAR4, LPAR5, and LPAR6.
  • lysophosphatidic acid receptor 1 refers to a G protein- coupled receptor (including homologs, isoforms, and functional fragments thereof) that binds the lipid signaling molecule lysophosphatidic acid (LPA).
  • LPA lipid signaling molecule lysophosphatidic acid
  • the term includes any recombinant or naturally-occurring form of LPAR1 variants thereof that maintain LPAR1 activity (e.g., within at least 30%, 40%, 50%, 60%, 70%, 80%, 90%, 95%, or 100% activity compared to wildtype LPAR1).
  • the LPAR1 protein encoded by the LPAR1 gene has the amino acid sequence set forth in or corresponding to Entrez 1902, UniProt Q92633, RefSeq (protein) NP_001392.2 or RefSeq (protein) NP_476500.1.
  • the LPAR1 gene has the nucleic acid sequence set forth in RefSeq (mRNA) NM_001401.3 or RefSeq (mRNA) NM 057159.2.
  • the amino acid sequence or nucleic acid sequence is the sequence known at the time of filing of the present application.
  • a compound or agent refers to the compound’s or agent’s ability to cause an increase or decrease in activity of a particular molecular target (e.g., protein, enzyme, etc.) preferentially over one or more different molecular targets (e.g., a compound having selectivity toward lysophosphatidic acid receptor 1 (LPAR1) would preferentially inhibit LPAR1 over other lysophosphatidic acid receptors).
  • a particular molecular target e.g., protein, enzyme, etc.
  • LPAR1 lysophosphatidic acid receptor 1
  • an “lysophosphatidic acid receptor 1 selective compound” or “LP ARI -selective compound” refers to a compound (e.g., compound described herein) having selectivity towards lysophosphatidic acid receptor 1 (LPAR1).
  • the compound e.g., compound described herein
  • the compound is about 5-fold, 10-fold, 20-fold, 30-fold, 40- fold, 50-fold, or about 100-fold more selective for lysophosphatidic acid receptor 1 (LPAR1) over one or more of LPAR2, LPAR3, LPAR4, LPAR5, or LPAR6.
  • the compound e.g., compound described herein
  • the compound is at least 5-fold, 10-fold, 20-fold, 30-fold, 40- fold, 50-fold, or at least 100-fold more selective for lysophosphatidic acid receptor 1 (LPAR1) over one or more of LPAR2, LPAR3, LPAR4, LPAR5, or LPAR6.
  • L 1 is a bond or substituted or unsubstituted alkylene (e.g., C 1 -C 8 , C 1 -C 6 , C1-C 4 , or C1-C2).
  • R 1 is substituted or unsubstituted alkyl (e.g., C 1 -C 8 , C 1 -C 6 , C1-C 4 , or C1-C2).
  • W 2 is N or C(R 2 ).
  • R 2 is hydrogen, halogen, -CX 2 3 , -CHX 2 2 , -CH 2 X 2 , -OCX 2 3 , -OCH 2 X 2 , -OCHX 2 2 , -CN, -SO I12 R 2D , -SO V2 NR 2A R 2B , -NR 2C NR 2A R 2B , -ONR 2A R 2B , -NHC(O)NR 2C NR 2A R 2B , -NHC(O)NR 2A R 2B , -N(O) m2 , -NR 2A R 2B , -C(O)R 2C , -C(O)OR 2C , -C(O)NR 2A R 2B , -OR 2D , -SR 2D ,-NR 2A SO 2 R 2D , -NR 2A C(O)R 2C , -NR 2A C(O)R
  • R 3 is hydrogen, halogen, -CX 3 3 , -CHX 3 2 , -CH 2 X 3 , -OCX 3 3 , -OCH 2 X 3 , -OCHX 3 2 , -CN, -SO I13 R 3D , -SO V3 NR 3A R 3B , -NR 3C NR 3A R 3B , -ONR 3A R 3B , -NHC(O)NR 3C NR 3A R 3B , -NHC(O)NR 3A R 3B , -N(O) m3 , -NR 3A R 3B , -C(O)R 3C , -C(O)OR 3C , -C(O)NR 3A R 3B , -OR 3D , -SR 3D ,-NR 3A SO 2 R 3D , -NR 3A C(O)R 3C , -NR 3A C(O)R
  • W 4 is N or C(R 4 ).
  • R 4 is hydrogen, halogen, -CX 4 3 , -CHX 4 2 , -CH 2 X 4 , -OCX 4 3 , -OCH 2 X 4 , -OCHX 4 2 , -CN, -SOn 4 R 4D , -SO v4 NR 4A R 4B , -NR 4C NR 4A R 4B , -ONR 4A R 4B , -NHC(O)NR 4C NR 4A R 4B , -NHC(O)NR 4A R 4B , -N(O)m4, -NR 4A R 4B , -C(O)R 4C , -C(O)OR 4C , -C(O)NR 4A R 4B , -OR 4D , -SR 4D , -NR 4A SO 2 R 4D , -NR 4A C(O)R 4C , -NR 4A C(O)C
  • W 5 is N or C(R 5 ).
  • R 5 is hydrogen, halogen, -CX 5 3 , -CHX 5 2 , -CH 2 X 5 , -OCX 5 3 , -OCH 2 X 5 , -OCHX 5 2 , -CN, -SOnsR 5D , -SO V5 NR 5A R 5B , -NR 5C NR 5A R 5B , -ONR 5A R 5B , -NHC(O)NR 5C NR 5A R 5B , -NHC(O)NR 5A R 5B , -N(O) m5 , -NR 5A R 5B , -C(O)R 5C , -C(O)OR 5C , -C(O)NR 5A R 5B , -OR 5D , -SR 5D , -NR 5A SO 2 R 5D , -NR 5A C(O)R 5C , -NR 5A C
  • R 2 and R 3 substituents may optionally be joined to form a substituted or unsubstituted cycloalkyl (e.g., C 3 -C 8 , C 3 -C 6 , C 4 -C 6 , or C 5 -C 6 ), substituted or unsubstituted heterocycloalkyl (e.g., 3 to 8 membered, 3 to 6 membered, 4 to 6 membered, 4 to 5 membered, or 5 to 6 membered), substituted or unsubstituted aryl (e.g., C 6 -C 10 or phenyl), or substituted or unsubstituted heteroaryl (e.g., 5 to 10 membered, 5 to 9 membered, or 5 to 6 membered).
  • a substituted or unsubstituted cycloalkyl e.g., C 3 -C 8 , C 3 -C 6 , C 4 -C 6 , or C 5 -C
  • R 3 and R 4 substituents may optionally be joined to form a substituted or unsubstituted cycloalkyl (e.g., C 5 -C 8 ,C 3 -C 6 , C 4 -C 6 , or C 5 -C 6 ), substituted or unsubstituted heterocycloalkyl (e.g., 3 to 8 membered, 3 to 6 membered, 4 to 6 membered, 4 to 5 membered, or 5 to 6 membered), substituted or unsubstituted aryl (e.g., C 6 -C 10 or phenyl), or substituted or unsubstituted heteroaryl (e.g., 5 to 10 membered, 5 to 9 membered, or 5 to 6 membered).
  • a substituted or unsubstituted cycloalkyl e.g., C 5 -C 8 ,C 3 -C 6 , C 4 -C 6 , or C 5 -C
  • R 4 and R 5 substituents may optionally be joined to form a substituted or unsubstituted cycloalkyl (e.g.C, 3 -C8,C 3 -C 6 , C 4 -C 6 , or C 5 -C 6 ), substituted or unsubstituted heterocycloalkyl (e.g., 3 to 8 membered, 3 to 6 membered, 4 to 6 membered, 4 to 5 membered, or 5 to 6 membered), substituted or unsubstituted aryl (e.g., C 6 -C 10 or phenyl), or substituted or unsubstituted heteroaryl (e.g., 5 to 10 membered, 5 to 9 membered, or 5 to 6 membered).
  • cycloalkyl e.g.C, 3 -C8,C 3 -C 6 , C 4 -C 6 , or C 5 -C 6
  • W 6 is N or C(R 6 ).
  • R 6 is hydrogen, halogen, -CX 6 3 , -CHX 6 2 , -CH2X 6 , -OCX 6 3 , -OCH2X 6 , -OCHX 6 2 , -CN, -SOn 6 R 6D , -SOV 6 NR 6A R 6B , -NR 6C NR 6A R 6B , -ONR 6A R 6B , -NHC(O)NR 6C NR 6A R 6B , -NHC(O)NR 6A R 6B , -N(O)m6, -NR 6A R 6B , -C(O)R 6C , -C(O)OR 6C , -C(O)NR 6A R 6B , -OR 6D , -SR 6D , -NR 6A SO 2 R 6D , -NR 6A C(O)R 6C , -NR 6A C(O)OR 6D ,
  • W 7 is N, N + -O', or C(R 7 ).
  • R 7 is hydrogen, halogen, -CX 7 3 , -CHX 7 2 , -CH 2 X 7 , -OCX 7 3 , -OCH2X 7 , -OCHX 7 2 , -CN, -SOn7R 7D , -SOV7NR 7A R 7B , -NR 7C NR 7A R 7B , -ONR 7A R 7B , -NHC(O)NR 7C NR 7A R 7B , -NHC(O)NR 7A R 7B , -N(O)m7, -NR 7A R 7B , -C(O)R 7C , -C(O)OR 7C , -C(O)NR 7A R 7B , -OR 7D , -SR 7D , -NR 7A SO 2 R 7D , -NR 7A C(O)R 7C , -NR 7A C(O)OR
  • R 8 is independently halogen, -CX 8 3 , -CHX 8 2 , -CH 2 X 8 , -OCX 8 3 , -OCH 2 X 8 , -OCHX 8 2 , -CN, -SO n8 R 8D , -SO V8 NR 8A R 8B , -NR 8C NR 8A R 8B , -ONR 8A R 8B , -NHC(O)NR 8C NR 8A R 8B , -NHC(O)NR 8A R 8B , -N(O) m8 , -NR 8A R 8B , -C(O)R 8C , -C(O)OR 8C , -C(O)NR 8A R 8B , -OR 8D , -SR 8D ,-NR 8A SO 2 R 8D , -NR 8A C(O)R 8C , -NR 8A C(O)R
  • R 9 is substituted or unsubstituted cycloalkyl (e.g.C, 3 -QC, 3 -C 6 , C 4 -C 6 , or C 5 -C 6 ) or substituted or unsubstituted heterocycloalkyl (e.g., 3 to 8 membered, 3 to 6 membered, 4 to 6 membered, 4 to 5 membered, or 5 to 6 membered).
  • cycloalkyl e.g.C, 3 -QC, 3 -C 6 , C 4 -C 6 , or C 5 -C 6
  • heterocycloalkyl e.g., 3 to 8 membered, 3 to 6 membered, 4 to 6 membered, 4 to 5 membered, or 5 to 6 membered.
  • R 2A , R 2B , R 2C , R 2D , R 3A , R 3B , R 3C , R 3D , R 4A , R 4B , R 4C , R 4D , R 5A , R 5B , R 5C , R 5D , R 6A , R 6B , R 6C , R 6D , R 7A , R 7B , R 7C , R 7D , R 8A , R 8B , R 8C , and R 8D are independently hydrogen, -CCl 3 , -CBr 3 , -CF 3 , -Cl 3 , -CHCl 2 , -CHBr 2 , -CHF 2 , -CHI 2 , -CH 2 C1, -CH 2 Br, -CH 2 F, -CH 2 I, -CN, -OH, -NH 2 , -COOH, -C0NH 2 ,
  • n2, n3, n4, n5, n6, n7, and n8 are independently an integer from 0 to 4.
  • the symbol z8 is an integer from 0 to 3.
  • the compound has the formula: L 1 R 1 , R 6 , R 8 , z8, and R 9 are as described herein, including in embodiments.
  • the compound has the formula: .
  • L 1 , R 1 , R 6 , R 8 , z8, and R 9 are as described herein, including in embodiments.
  • the compound has the formula: L 1 , R 1 , R 6 , R 8 , z8, and R 9 are as described herein, including in embodiments.
  • the compound has the formula: L 1 , R 1 , R 6 , R 8 , z8, and R 9 are as described herein, including in embodiments.
  • the compound has the formula: L 1 , R 1 , R 7 , R 8 , z8, and R 9 are as described herein, including in embodiments.
  • the compound has the formula: L 1 , R 1 , R 7 , R 8 , z8, and R 9 are as described herein, including in embodiments.
  • the compound has the formula: L 1 , R 1 , R 7 , R 8 , z8, and R 9 are as described herein, including in embodiments.
  • the compound has the formula: L 1 , R 1 , R 6 , R 7 , z8, and R 9 are as described herein, including in embodiments.
  • the compound has the formula: L 1 , R 1 , R 8 , z8, and R 9 are as described herein, including in embodiments.
  • the compound has the formula: L 1 , R 1 , R 8 , z8, and R 9 are as described herein, including in embodiments.
  • the compound has the formula: L 1 , R 1 , R 8 , z8, and R 9 are as described herein, including in embodiments.
  • the compound has the formula: L 1 , R 1 , R 8 , z8, and R 9 are as described herein, including in embodiments.
  • the compound has the formula: L 1 , R 1 , R 6 , R 7 , R 8 , z8, and R 9 are as described herein, including in embodiments.
  • the compound has the formula: L 1 , R 1 , R 6 , R 7 , R 8 , z8, and R 9 are as described herein, including in embodiments.
  • the compound has the formula: L 1 , R 1 , R 6 , R 7 , R 8 , z8, and R 9 are as described herein, including in embodiments.
  • the compound has the formula: L 1 , R 1 , R 6 , R 7 , R 8 , z8, and R 9 are as described herein, including in embodiments.
  • a substituted R 1 (e.g., substituted alkyl) is substituted with at least one substituent group, size-limited substituent group, or lower substituent group; wherein if the substituted R 1 is substituted with a plurality of groups selected from substituent groups, size-limited substituent groups, and lower substituent groups; each substituent group, sizelimited substituent group, and/or lower substituent group may optionally be different.
  • R 1 when R 1 is substituted, it is substituted with at least one substituent group.
  • R 1 when R 1 is substituted, it is substituted with at least one size-limited substituent group.
  • R 1 when R 1 is substituted, it is substituted with at least one lower substituent group.
  • R 1 is unsubstituted alkyl. In embodiments, R 1 is unsubstituted C2- C5 alkyl. In embodiments, R 1 is unsubstituted C2 alkyl. In embodiments, R 1 is unsubstituted ethyl. In embodiments, R 1 is unsubstituteCd 3 alkyl. In embodiments, R 1 is unsubstituted propyl. In embodiments, R 1 is unsubstituted n-propyl. In embodiments, R 1 is unsubstituted isopropyl (i.e., isopropyl). In embodiments, R 1 is unsubstituted C 4 alkyl.
  • R 1 is unsubstituted butyl. In embodiments, R 1 is unsubstituted n-butyl. In embodiments, R 1 is unsubstituted isobutyl. In embodiments, R 1 is unsubstituted tert-butyl. In embodiments, R 1 is unsubstituted C5 alkyl. In embodiments, R 1 is unsubstituted pentyl. In embodiments, R 1 is unsubstituted n-pentyl. In embodiments, R 1 is unsubstituted tert-pentyl. In embodiments, R 1 is unsubstituted neopentyl.
  • R 1 is unsubstituted isopentyl. In embodiments, R 1 is unsubstituted sec-pentyl. In embodiments, R 1 is unsubstituted 3- pentyl. In embodiments, R 1 is unsubstituted sec-isopentyl. In embodiments, R 1 is unsubstituted 2-methylbutyl.
  • W 2 is N. In embodiments, W 2 is C(R 2 ). In embodiments, W 2 is CH.
  • W 4 is N. In embodiments, W 4 is C(R 4 ). In embodiments, W 4 is CH. [0208] In embodiments, W 5 is N. In embodiments, W 5 is C(R 5 ). In embodiments, W 5 is CH.
  • a compound, or a pharmaceutically acceptable salt or solvate thereof having the formula: L 1 , R 2 , R 3 , R 4 , R 5 , W 6 , W 7 , R 8 , z8, and R 9 are as described herein, including in embodiments. At least one of W 6 or W 7 is N. If W 6 is C(R 6 ) or W 7 is C(R 7 ), then R 10 is not hydrogen. If W 6 and W 7 are both N, then R 3 is not
  • R 10 is hydrogen, halogen, -CX 10 3 , -CHX 10 2 , -CH 2 X 10 , -OCX 10 3 , -OCH 2 X 10 , -OCHX 10 2 , -CN, -SOnioR 10D , -SOvioNR 10A R 10B , -NR 1OC NR 1OA R 1OB , -ONR 10A R 10B , -NHC(O)NR 10C NR 10A R 10B , -NHC(O)NR 10A R 10B , -N(O)mio, -NR 10A R 10B , -C(O)R 10C , -C(O)OR 10C , -C(O)NR 10A R 10B , -OR 10D , -SR 1OD , -NR 10A SO 2 R 10D , -NR 10A C(O)R 10C , -NR 10A C(O)C
  • R 10 and R 2 substituents may optionally be joined to form a substituted or unsubstituted cycloalkyl (e.g., C 3 -C 8 , C 3 -C 6 , C 4 -C 6 , or C 5 -C 6 ), substituted or unsubstituted heterocycloalkyl (e.g., 3 to 8 membered, 3 to 6 membered, 4 to 6 membered, 4 to 5 membered, or 5 to 6 membered), substituted or unsubstituted aryl (e.g., C 6 -C 10 or phenyl), or substituted or unsubstituted heteroaryl (e.g., 5 to 10 membered, 5 to 9 membered, or 5 to 6 membered).
  • a substituted or unsubstituted cycloalkyl e.g., C 3 -C 8 , C 3 -C 6 , C 4 -C 6 , or C 5 -C
  • R 1OA , R 1OB , R 1OC , and R 10D are independently hydrogen, -CCl 3 , -CBrs, -CF3, -Cl 3 , -CHCl2, -CHBr 2 , -CHF 2 , -CHI 2 , -CH 2 C1, -CH 2 Br, -CH 2 F, -CH 2 I, -CN, -OH, -NH 2 , -COOH, -CONH 2 , -OCCl 3 , -OCF3, -OCBr 3 , -OCl 3 , -OCHCl 2 , -OCHBr 2 , -OCHI 2 , -OCHF 2 , -OCH 2 C1, -OCH 2 Br, -OCH 2 I, -OCH 2 F, substituted or unsubstituted alkyl (e.g., C 1 -C 8 , C 1 -C 6 , C1-C 4 , substituted
  • X 10 is independently -F, -Cl, -Br, or -I.
  • nlO is an integer from 0 to 4.
  • the compound has the formula: L 1 , R 2 , R 3 , R 4 , R 5 , R 6 , R 8 , z8, R 9 , and R 10 are as described herein, including in embodiments.
  • the compound has the formula: L 1 , R 2 , R 3 , R 4 , R 5 , R 7 , R 8 , z8, R 9 , and R 10 are as described herein, including in embodiments.
  • the compound has the formula: L 1 , R 2 , R 3 , R 4 , R 5 , R 8 , z8, R 9 , and R 10 are as described herein, including in embodiments.
  • the compound has the formula: L 1 , R 6 , R 8 , z8, R 9 , and R 10 are as described herein, including in embodiments.
  • the compound has the formula: L 1 , R 7 , R 8 , z8, R 9 , and R 10 are as described herein, including in embodiments.
  • the compound has the formula: L 1 , R 8 , z8, R 9 , and R 10 are as described herein, including in embodiments.
  • a substituted R 10 (e.g., substituted alkyl, substituted heteroalkyl, substituted cycloalkyl, substituted heterocycloalkyl, substituted aryl, and/or substituted heteroaryl) is substituted with at least one substituent group, size-limited substituent group, or lower substituent group; wherein if the substituted R 10 is substituted with a plurality of groups selected from substituent groups, size-limited substituent groups, and lower substituent groups; each substituent group, size-limited substituent group, and/or lower substituent group may optionally be different.
  • R 10 when R 10 is substituted, it is substituted with at least one substituent group.
  • R 10 when R 10 is substituted, it is substituted with at least one size-limited substituent group.
  • R 10 when R 10 is substituted, it is substituted with at least one lower substituent group.
  • a substituted R 10A (e.g., substituted alkyl, substituted heteroalkyl, substituted cycloalkyl, substituted heterocycloalkyl, substituted aryl, and/or substituted heteroaryl) is substituted with at least one substituent group, size-limited substituent group, or lower substituent group; wherein if the substituted R 10A is substituted with a plurality of groups selected from substituent groups, size-limited substituent groups, and lower substituent groups; each substituent group, size-limited substituent group, and/or lower substituent group may optionally be different.
  • R 10A when R 10A is substituted, it is substituted with at least one substituent group.
  • R 10A when R 10A is substituted, it is substituted with at least one size-limited substituent group.
  • R 10A when R 10A is substituted, it is substituted with at least one lower substituent group.
  • a substituted R 10B (e.g., substituted alkyl, substituted heteroalkyl, substituted cycloalkyl, substituted heterocycloalkyl, substituted aryl, and/or substituted heteroaryl) is substituted with at least one substituent group, size-limited substituent group, or lower substituent group; wherein if the substituted R 10B is substituted with a plurality of groups selected from substituent groups, size-limited substituent groups, and lower substituent groups; each substituent group, size-limited substituent group, and/or lower substituent group may optionally be different.
  • R 10B when R 10B is substituted, it is substituted with at least one substituent group.
  • R 10B when R 10B is substituted, it is substituted with at least one size-limited substituent group.
  • R 10B when R 10B is substituted, it is substituted with at least one lower substituent group.
  • a substituted ring formed when R 10A and R 10B substituents bonded to the same nitrogen atom are joined e.g., substituted heterocycloalkyl and/or substituted heteroaryl
  • at least one substituent group, size-limited substituent group, or lower substituent group e.g., substituted heterocycloalkyl and/or substituted heteroaryl
  • the substituted ring formed when R 10A and R 10B substituents bonded to the same nitrogen atom are joined is substituted with a plurality of groups selected from substituent groups, size-limited substituent groups, and lower substituent groups; each substituent group, size-limited substituent group, and/or lower substituent group may optionally be different.
  • when the substituted ring formed when R 10A and R 10B substituents bonded to the same nitrogen atom are joined is substituted, it is substituted with at least one substituent group. In embodiments, when the substituted ring formed when R 10A and R 10B substituents bonded to the same nitrogen atom are joined is substituted, it is substituted with at least one size-limited substituent group. In embodiments, when the substituted ring formed when R 10A and R 10B substituents bonded to the same nitrogen atom are joined is substituted, it is substituted with at least one lower substituent group.
  • a substituted R 10C (e.g., substituted alkyl, substituted heteroalkyl, substituted cycloalkyl, substituted heterocycloalkyl, substituted aryl, and/or substituted heteroaryl) is substituted with at least one substituent group, size-limited substituent group, or lower substituent group; wherein if the substituted R 10C is substituted with a plurality of groups selected from substituent groups, size-limited substituent groups, and lower substituent groups; each substituent group, size-limited substituent group, and/or lower substituent group may optionally be different.
  • R 10C when R 10C is substituted, it is substituted with at least one substituent group.
  • R 10C when R 10C is substituted, it is substituted with at least one size-limited substituent group.
  • R 10C when R 10C is substituted, it is substituted with at least one lower substituent group.
  • a substituted R 10D (e.g., substituted alkyl, substituted heteroalkyl, substituted cycloalkyl, substituted heterocycloalkyl, substituted aryl, and/or substituted heteroaryl) is substituted with at least one substituent group, size-limited substituent group, or lower substituent group; wherein if the substituted R 10D is substituted with a plurality of groups selected from substituent groups, size-limited substituent groups, and lower substituent groups; each substituent group, size-limited substituent group, and/or lower substituent group may optionally be different.
  • R 10D when R 10D is substituted, it is substituted with at least one substituent group.
  • R 10D when R 10D is substituted, it is substituted with at least one size-limited substituent group.
  • R 10D when R 10D is substituted, it is substituted with at least one lower substituent group.
  • R 10 is hydrogen, halogen, -CCl 3 , -CBr 3 , -CF3, -Cl 3 , -CHCI2, -CHBr 2 , -CHF 2 , -CHI 2 , -CH 2 C1, -CH 2 Br, -CH 2 F, -CH 2 I, -OCCl 3 , -OCF3, -OCBr 3 , -OCl 3 , -OCHCl 3 , -OCHBr 2 , -OCHI 2 , -OCHF 2 , -OCH 2 C1, -OCH 2 Br, -OCH 2 I, -OCH 2 F, -CN, -SO3H, -OSO3H, -SO 2 NH 2 , -NHNH 2 , -ONH 2 , -NHC(O)NHNH 2 , -NHC(O)NH 2 , -NO 2 , -NH 2 ,
  • R 10 is hydrogen, -CHF 2 , substituted or unsubstituted C 1 -C 6 alkyl, substituted or unsubstituted 2 to 6 membered heteroalkyl, or substituted or unsubstitutCed 3 - C 8 cycloalkyl.
  • R 10 is hydrogen, -CHF 2 , substituted or unsubstituted C 1 -C 6 alkyl, or substituted or unsubstituted 2 to 6 membered heteroalkyl.
  • R 10 is hydrogen or unsubstituted C 1 -C 6 alkyl.
  • R 10 is hydrogen.
  • R 10 is unsubstituted Ci alkyl. In embodiments, R 10 is unsubstituted methyl. In embodiments,
  • R 10 is unsubstituted C 2 alkyl. In embodiments, R 10 is unsubstituted ethyl. In embodiments,
  • R 10 is unsubstituteCd 3 alkyl. In embodiments, R 10 is unsubstituted propyl. In embodiments,
  • R 10 is unsubstituted n-propyl. In embodiments, R 10 is unsubstituted isopropyl (i.e., isopropyl). In embodiments, R 10 is -CH(CD3) 2 . In embodiments, R 10 is In embodiments, R 10 is unsubstituted C 4 alkyl. In embodiments, R 10 is unsubstituted butyl. In embodiments, R 10 is unsubstituted n-butyl. In embodiments, R 10 is unsubstituted isobutyl. In embodiments, R 10 is unsubstituted tert-butyl. In embodiments, R 10 is unsubstituted C5 alkyl.
  • R 10 is unsubstituted pentyl. In embodiments, R 10 is unsubstituted n-pentyl.
  • R 10 is unsubstituted tert-pentyl. In embodiments, R 10 is unsubstituted neopentyl. In embodiments, R 10 is unsubstituted isopentyl. In embodiments, R 10 is unsubstituted sec-pentyl. In embodiments, R 10 is unsubstituted 3-pentyl. In embodiments, R 10 is unsubstituted sec-isopentyl. In embodiments, R 10 is unsubstituted 2-methylbutyl. In embodiments, R 10 is unsubstituted C 6 alkyl. In embodiments, R 10 is unsubstituted hexyl.
  • R 10 is substituted C 1 -C 6 alkyl. In embodiments, R 10 is substituted 2 to 6 membered heteroalkyl. In embodiments, R 10 is -CH(CH 3 )OCH 3 . In embodiments, R 10 is -CF(CH 3 ) 2 . In embodiments, R 10 is -C(CH 3 )2(OH). In embodiments, R 10 is -CH(CH 3 )(CH2OH). In embodiments, R 10 is -CHF2. In embodiments, R 10 is unsubstituted C 3 -C 8 cycloalkyl. In embodiments, R 10 is unsubstituted cyclopropyl.
  • R 10 is unsubstituted cyclobutyl. In embodiments, R 10 is unsubstituted cyclopentyl. In embodiments, R 10 is unsubstituted cyclohexyl. In embodiments, R 10 is unsubstituted cycloheptyl. In embodiments, R 10 is unsubstituted cyclooctyl.
  • a substituted R 2 (e.g., substituted alkyl, substituted heteroalkyl, substituted cycloalkyl, substituted heterocycloalkyl, substituted aryl, and/or substituted heteroaryl) is substituted with at least one substituent group, size-limited substituent group, or lower substituent group; wherein if the substituted R 2 is substituted with a plurality of groups selected from substituent groups, size-limited substituent groups, and lower substituent groups; each substituent group, size-limited substituent group, and/or lower substituent group may optionally be different.
  • R 2 when R 2 is substituted, it is substituted with at least one substituent group.
  • R 2 when R 2 is substituted, it is substituted with at least one size-limited substituent group.
  • R 2 when R 2 is substituted, it is substituted with at least one lower substituent group.
  • a substituted R 2A (e.g., substituted alkyl, substituted heteroalkyl, substituted cycloalkyl, substituted heterocycloalkyl, substituted aryl, and/or substituted heteroaryl) is substituted with at least one substituent group, size-limited substituent group, or lower substituent group; wherein if the substituted R 2A is substituted with a plurality of groups selected from substituent groups, size-limited substituent groups, and lower substituent groups; each substituent group, size-limited substituent group, and/or lower substituent group may optionally be different.
  • R 2A when R 2A is substituted, it is substituted with at least one substituent group.
  • R 2A when R 2A is substituted, it is substituted with at least one size-limited substituent group.
  • R 2A when R 2A is substituted, it is substituted with at least one lower substituent group.
  • a substituted R 2B (e.g., substituted alkyl, substituted heteroalkyl, substituted cycloalkyl, substituted heterocycloalkyl, substituted aryl, and/or substituted heteroaryl) is substituted with at least one substituent group, size-limited substituent group, or lower substituent group; wherein if the substituted R 2B is substituted with a plurality of groups selected from substituent groups, size-limited substituent groups, and lower substituent groups; each substituent group, size-limited substituent group, and/or lower substituent group may optionally be different.
  • R 2B when R 2B is substituted, it is substituted with at least one substituent group.
  • R 2B when R 2B is substituted, it is substituted with at least one size-limited substituent group.
  • R 2B when R 2B is substituted, it is substituted with at least one lower substituent group.
  • a substituted ring formed when R 2A and R 2B substituents bonded to the same nitrogen atom are joined e.g., substituted heterocycloalkyl and/or substituted heteroaryl
  • at least one substituent group, size-limited substituent group, or lower substituent group e.g., substituted heterocycloalkyl and/or substituted heteroaryl
  • the substituted ring formed when R 2A and R 2B substituents bonded to the same nitrogen atom are joined is substituted with a plurality of groups selected from substituent groups, size-limited substituent groups, and lower substituent groups; each substituent group, size-limited substituent group, and/or lower substituent group may optionally be different.
  • when the substituted ring formed when R 2A and R 2B substituents bonded to the same nitrogen atom are joined is substituted, it is substituted with at least one substituent group. In embodiments, when the substituted ring formed when R 2A and R 2B substituents bonded to the same nitrogen atom are joined is substituted, it is substituted with at least one size-limited substituent group. In embodiments, when the substituted ring formed when R 2A and R 2B substituents bonded to the same nitrogen atom are joined is substituted, it is substituted with at least one lower substituent group.
  • a substituted R 2C (e.g., substituted alkyl, substituted heteroalkyl, substituted cycloalkyl, substituted heterocycloalkyl, substituted aryl, and/or substituted heteroaryl) is substituted with at least one substituent group, size-limited substituent group, or lower substituent group; wherein if the substituted R 2C is substituted with a plurality of groups selected from substituent groups, size-limited substituent groups, and lower substituent groups; each substituent group, size-limited substituent group, and/or lower substituent group may optionally be different. In embodiments, when R 2C is substituted, it is substituted with at least one substituent group.
  • R 2C when R 2C is substituted, it is substituted with at least one size-limited substituent group. In embodiments, when R 2C is substituted, it is substituted with at least one lower substituent group.
  • a substituted R 2D e.g., substituted alkyl, substituted heteroalkyl, substituted cycloalkyl, substituted heterocycloalkyl, substituted aryl, and/or substituted heteroaryl
  • R 2D is substituted with at least one substituent group, size-limited substituent group, or lower substituent group; wherein if the substituted R 2D is substituted with a plurality of groups selected from substituent groups, size-limited substituent groups, and lower substituent groups; each substituent group, size-limited substituent group, and/or lower substituent group may optionally be different.
  • R 2D when R 2D is substituted, it is substituted with at least one substituent group. In embodiments, when R 2D is substituted, it is substituted with at least one size-limited substituent group. In embodiments, when R 2D is substituted, it is substituted with at least one lower substituent group.
  • R 2 is hydrogen, halogen, -CX 2 3, -CHX 2 2, -CH2X 2 , -OCX 2 3, -OCH2X 2 , -OCHX 2 2, -CN, -SOn2R 2D , -SO v2 NR 2A R 2B , -NHC(O)NR 2A R 2B , -NR 2A R 2B , -C(O)R 2C , -C(O)OR 2C , -C(O)NR 2A R 2B , -OR 2D , -SR 2D , -NR 2A SO 2 R 2D , -NR 2A C(O)R 2C , -NR 2A C(O)OR 2C , -SF5, -N3, substituted or unsubstituted alkyl, substituted or unsubstituted heteroalkyl, substituted or unsubstituted cycloalkyl, substitute
  • R 2 is hydrogen, halogen, -CCl 3 , -CBr3, -CF3, -Cl 3 , -CHCI2, -CHBr 2 , -CHF 2 , -CHI2, -CH2CI, -CH 2 Br, -CH 2 F, -CH 2 I, -OCCl 3 , -OCF3, -OCBr 3 , -OCl 3 , -OCHCl 2 , -OCHBr 2 , -OCHb, -OCHF2, -OCH2CI, -OCH 2 Br, -OCH 2 I, -OCH 2 F, -CN, -SO3H, -OSO3H, -SO2NH2, -NHNH 2 , -ONH2, -NHC(O)NHNH 2 , -NHC(O)NH 2 , -NO2, -NH 2 , -C(O)H, -C(O)OH
  • R 2 is hydrogen, halogen, -CCl 3 , -CBr3, -CF3, -Cl 3 , -CHCI2, -CHBr 2 , -CHF 2 , -CHI2, -CH2CI, -CH 2 Br, -CH 2 F, -CH 2 I, -OCCl 3 , -OCF3, -OCBr 3 , -OCl 3 , -OCHCl 2 , -OCHBr 2 , -OCHI 2 , -OCHF 2 , -OCH 2 C1, -OCH 2 Br, -OCH 2 I, -OCH 2 F, -CN, -SO3H, -OSO3H, -SO2NH2, -NHC(O)NH 2 , -NH 2 , -C(O)H, -C(O)OH, -CONH2, -OH, -SH, -NHSO2H, -NHC
  • R 2 is hydrogen or unsubstituted C 1 -C 6 alkyl. In embodiments, R 2 is hydrogen. In embodiments, R 2 is unsubstituted methyl. In embodiments, R 2 is unsubstituted ethyl. In embodiments, R 2 is unsubstituted propyl. In embodiments, R 2 is unsubstituted n-propyl. In embodiments, R 2 is unsubstituted isopropyl. In embodiments, R 2 is unsubstituted butyl. In embodiments, R 2 is unsubstituted n-butyl. In embodiments, R 2 is unsubstituted isobutyl. In embodiments, R 2 is unsubstituted tert-butyl. In embodiments, R 2 is unsubstituted pentyl. In embodiments, R 2 is unsubstituted hexyl.
  • a substituted ring formed when R 10 and R 2 substituents are joined is substituted with at least one substituent group, size-limited substituent group, or lower substituent group; wherein if the substituted ring formed when R 10 and R 2 substituents are joined is substituted with a plurality of groups selected from substituent groups, sizelimited substituent groups, and lower substituent groups; each substituent group, size-limited substituent group, and/or lower substituent group may optionally be different.
  • R 10 and R 2 substituents may optionally be joined to form a substituted or unsubstituted heteroaryl. In embodiments, R 10 and R 2 substituents may optionally be joined to form a substituted or unsubstituted 5 to 6 membered heteroaryl. In embodiments, R 10 and R 2 substituents may optionally be joined to form a methyl-substituted 5 to 6 membered heteroaryl. In embodiments, R 10 and R 2 substituents may optionally be joined to form
  • a substituted R 3 (e.g., substituted alkyl, substituted heteroalkyl, substituted cycloalkyl, substituted heterocycloalkyl, substituted aryl, and/or substituted heteroaryl) is substituted with at least one substituent group, size-limited substituent group, or lower substituent group; wherein if the substituted R 3 is substituted with a plurality of groups selected from substituent groups, size-limited substituent groups, and lower substituent groups; each substituent group, size-limited substituent group, and/or lower substituent group may optionally be different.
  • R 3 when R 3 is substituted, it is substituted with at least one substituent group.
  • R 3 when R 3 is substituted, it is substituted with at least one size-limited substituent group.
  • R 3 when R 3 is substituted, it is substituted with at least one lower substituent group.
  • a substituted R 3A (e.g., substituted alkyl, substituted heteroalkyl, substituted cycloalkyl, substituted heterocycloalkyl, substituted aryl, and/or substituted heteroaryl) is substituted with at least one substituent group, size-limited substituent group, or lower substituent group; wherein if the substituted R 3A is substituted with a plurality of groups selected from substituent groups, size-limited substituent groups, and lower substituent groups; each substituent group, size-limited substituent group, and/or lower substituent group may optionally be different.
  • R 3A when R 3A is substituted, it is substituted with at least one substituent group.
  • R 3A when R 3A is substituted, it is substituted with at least one size-limited substituent group.
  • R 3A when R 3A is substituted, it is substituted with at least one lower substituent group.
  • a substituted R 3B (e.g., substituted alkyl, substituted heteroalkyl, substituted cycloalkyl, substituted heterocycloalkyl, substituted aryl, and/or substituted heteroaryl) is substituted with at least one substituent group, size-limited substituent group, or lower substituent group; wherein if the substituted R 3B is substituted with a plurality of groups selected from substituent groups, size-limited substituent groups, and lower substituent groups; each substituent group, size-limited substituent group, and/or lower substituent group may optionally be different.
  • R 3B when R 3B is substituted, it is substituted with at least one substituent group.
  • R 3B when R 3B is substituted, it is substituted with at least one size-limited substituent group.
  • R 3B when R 3B is substituted, it is substituted with at least one lower substituent group.
  • a substituted ring formed when R 3A and R 3B substituents bonded to the same nitrogen atom are joined e.g., substituted heterocycloalkyl and/or substituted heteroaryl
  • at least one substituent group, size-limited substituent group, or lower substituent group e.g., substituted heterocycloalkyl and/or substituted heteroaryl
  • the substituted ring formed when R 3A and R 3B substituents bonded to the same nitrogen atom are joined is substituted with a plurality of groups selected from substituent groups, size-limited substituent groups, and lower substituent groups; each substituent group, size-limited substituent group, and/or lower substituent group may optionally be different.
  • when the substituted ring formed when R 3A and R 3B substituents bonded to the same nitrogen atom are joined is substituted, it is substituted with at least one substituent group. In embodiments, when the substituted ring formed when R 3A and R 3B substituents bonded to the same nitrogen atom are joined is substituted, it is substituted with at least one size-limited substituent group. In embodiments, when the substituted ring formed when R 3A and R 3B substituents bonded to the same nitrogen atom are joined is substituted, it is substituted with at least one lower substituent group.
  • a substituted R 3C (e.g., substituted alkyl, substituted heteroalkyl, substituted cycloalkyl, substituted heterocycloalkyl, substituted aryl, and/or substituted heteroaryl) is substituted with at least one substituent group, size-limited substituent group, or lower substituent group; wherein if the substituted R 3C is substituted with a plurality of groups selected from substituent groups, size-limited substituent groups, and lower substituent groups; each substituent group, size-limited substituent group, and/or lower substituent group may optionally be different.
  • R 3C when R 3C is substituted, it is substituted with at least one substituent group.
  • R 3C when R 3C is substituted, it is substituted with at least one size-limited substituent group.
  • R 3C when R 3C is substituted, it is substituted with at least one lower substituent group.
  • a substituted R 3D (e.g., substituted alkyl, substituted heteroalkyl, substituted cycloalkyl, substituted heterocycloalkyl, substituted aryl, and/or substituted heteroaryl) is substituted with at least one substituent group, size-limited substituent group, or lower substituent group; wherein if the substituted R 3D is substituted with a plurality of groups selected from substituent groups, size-limited substituent groups, and lower substituent groups; each substituent group, size-limited substituent group, and/or lower substituent group may optionally be different.
  • R 3D when R 3D is substituted, it is substituted with at least one substituent group.
  • R 3D when R 3D is substituted, it is substituted with at least one size-limited substituent group.
  • R 3D when R 3D is substituted, it is substituted with at least one lower substituent group.
  • R 3 is hydrogen, halogen, -CX 3 3, -CHX 3 2, -CH2X 3 , -OCX 3 3, -OCH2X 3 , -OCHX 3 2, -CN, -SOn 3 R 3D , -SOV3NR 3A R 3B , -NHC(O)NR 3A R 3B , -NR 3A R 3B , -C(O)R 3C , -C(O)OR 3C , -C(O)NR 3A R 3B , -OR 3D , -SR 3D , -NR 3A SO 2 R 3D , -NR 3A C(O)R 3C , -NR 3A C(O)OR 3C , -SF5, -N3, substituted or unsubstituted alkyl, substituted or unsubstituted heteroalkyl, substituted or unsubstituted cycloalkyl, substituted or
  • R 3 is hydrogen, halogen, -CCl 3 , -CBrs, -CF3, -Cl 3 , -CHCI2, -CHBr 2 , -CHF 2 , -CHI 2 , -CH 2 C1, -CH 2 Br, -CH 2 F, -CH 2 I, -OCCl 3 , -OCF3, -OCBr 3 , -OCl 3 , -OCHCl 2 , -OCHBr 2 , -OCHI 2 , -OCHF 2 , -OCH 2 C1, -OCH 2 Br, -OCH 2 I, -OCH 2 F, -CN, -SO3H, -OSO3H, -SO 2 NH 2 , -NHNH 2 , -0NH 2 , -NHC(O)NHNH 2 , -NHC(O)NH 2 , -NO 2 , -NH 2 , -
  • R 3 is hydrogen, halogen, -CCl 3 , -CBr3, -CF3, -Cl 3 , -CHCl 2 , -CHBr 2 , -CHF 2 , -CHI 2 , -CH 2 C1, -CH 2 Br, -CH 2 F, -CH 2 I, -OCCl 3 , -OCF3, -OCBr 3 , -OCl 3 , -OCHCl 2 , -OCHBr 2 , -OCHI 2 , -OCHF 2 , -OCH 2 C1, -OCH 2 Br, -OCH 2 I, -OCH 2 F, -CN, -SO3H, -OSO3H, -SO 2 NH 2 , -NHC(O)NH 2 , -NH 2 , -C(O)H, -C(O)OH, -CONH 2 , -OH, -SH,
  • R 3 is hydrogen or unsubstituted C 1 -C 6 alkyl. In embodiments, R 3 is hydrogen. In embodiments, R 3 is unsubstituted methyl. In embodiments, R 3 is unsubstituted ethyl. In embodiments, R 3 is unsubstituted propyl. In embodiments, R 3 is unsubstituted n-propyl. In embodiments, R 3 is unsubstituted isopropyl. In embodiments, R 3 is unsubstituted butyl. In embodiments, R 3 is unsubstituted n-butyl. In embodiments, R 3 is unsubstituted isobutyl. In embodiments, R 3 is unsubstituted tert-butyl. In embodiments, R 3 is unsubstituted pentyl. In embodiments, R 3 is unsubstituted hexyl.
  • a substituted ring formed when R 2 and R 3 substituents are joined is substituted with at least one substituent group, size-limited substituent group, or lower substituent group; wherein if the substituted ring formed when R 2 and R 3 substituents are joined is substituted with a plurality of groups selected from substituent groups, sizelimited substituent groups, and lower substituent groups; each substituent group, size-limited substituent group, and/or lower substituent group may optionally be different.
  • a substituted R 4 (e.g., substituted alkyl, substituted heteroalkyl, substituted cycloalkyl, substituted heterocycloalkyl, substituted aryl, and/or substituted heteroaryl) is substituted with at least one substituent group, size-limited substituent group, or lower substituent group; wherein if the substituted R 4 is substituted with a plurality of groups selected from substituent groups, size-limited substituent groups, and lower substituent groups; each substituent group, size-limited substituent group, and/or lower substituent group may optionally be different.
  • R 4 when R 4 is substituted, it is substituted with at least one substituent group.
  • R 4 when R 4 is substituted, it is substituted with at least one size-limited substituent group.
  • R 4 when R 4 is substituted, it is substituted with at least one lower substituent group.
  • a substituted R 4A (e.g., substituted alkyl, substituted heteroalkyl, substituted cycloalkyl, substituted heterocycloalkyl, substituted aryl, and/or substituted heteroaryl) is substituted with at least one substituent group, size-limited substituent group, or lower substituent group; wherein if the substituted R 4A is substituted with a plurality of groups selected from substituent groups, size-limited substituent groups, and lower substituent groups; each substituent group, size-limited substituent group, and/or lower substituent group may optionally be different.
  • R 4A when R 4A is substituted, it is substituted with at least one substituent group.
  • R 4A when R 4A is substituted, it is substituted with at least one size-limited substituent group.
  • R 4A when R 4A is substituted, it is substituted with at least one lower substituent group.
  • a substituted R 4B (e.g., substituted alkyl, substituted heteroalkyl, substituted cycloalkyl, substituted heterocycloalkyl, substituted aryl, and/or substituted heteroaryl) is substituted with at least one substituent group, size-limited substituent group, or lower substituent group; wherein if the substituted R 4B is substituted with a plurality of groups selected from substituent groups, size-limited substituent groups, and lower substituent groups; each substituent group, size-limited substituent group, and/or lower substituent group may optionally be different.
  • R 4B when R 4B is substituted, it is substituted with at least one substituent group.
  • R 4B when R 4B is substituted, it is substituted with at least one size-limited substituent group.
  • R 4B when R 4B is substituted, it is substituted with at least one lower substituent group.
  • a substituted ring formed when R 4A and R 4B substituents bonded to the same nitrogen atom are joined e.g., substituted heterocycloalkyl and/or substituted heteroaryl
  • at least one substituent group, size-limited substituent group, or lower substituent group e.g., substituted heterocycloalkyl and/or substituted heteroaryl
  • the substituted ring formed when R 4A and R 4B substituents bonded to the same nitrogen atom are joined is substituted with a plurality of groups selected from substituent groups, size-limited substituent groups, and lower substituent groups; each substituent group, size-limited substituent group, and/or lower substituent group may optionally be different.
  • when the substituted ring formed when R 4A and R 4B substituents bonded to the same nitrogen atom are joined is substituted, it is substituted with at least one substituent group. In embodiments, when the substituted ring formed when R 4A and R 4B substituents bonded to the same nitrogen atom are joined is substituted, it is substituted with at least one size-limited substituent group. In embodiments, when the substituted ring formed when R 4A and R 4B substituents bonded to the same nitrogen atom are joined is substituted, it is substituted with at least one lower substituent group.
  • a substituted R 4C (e.g., substituted alkyl, substituted heteroalkyl, substituted cycloalkyl, substituted heterocycloalkyl, substituted aryl, and/or substituted heteroaryl) is substituted with at least one substituent group, size-limited substituent group, or lower substituent group; wherein if the substituted R 4C is substituted with a plurality of groups selected from substituent groups, size-limited substituent groups, and lower substituent groups; each substituent group, size-limited substituent group, and/or lower substituent group may optionally be different.
  • R 4C when R 4C is substituted, it is substituted with at least one substituent group.
  • R 4C when R 4C is substituted, it is substituted with at least one size-limited substituent group.
  • R 4C when R 4C is substituted, it is substituted with at least one lower substituent group.
  • a substituted R 4D (e.g., substituted alkyl, substituted heteroalkyl, substituted cycloalkyl, substituted heterocycloalkyl, substituted aryl, and/or substituted heteroaryl) is substituted with at least one substituent group, size-limited substituent group, or lower substituent group; wherein if the substituted R 4D is substituted with a plurality of groups selected from substituent groups, size-limited substituent groups, and lower substituent groups; each substituent group, size-limited substituent group, and/or lower substituent group may optionally be different.
  • R 4D when R 4D is substituted, it is substituted with at least one substituent group.
  • R 4D when R 4D is substituted, it is substituted with at least one size-limited substituent group.
  • R 4D when R 4D is substituted, it is substituted with at least one lower substituent group.
  • R 4 is hydrogen, halogen, -CX 4 3, -CHX 4 2, -CH2X 4 , -OCX 4 3, -OCH2X 4 , -OCHX 4 2, -CN, -SOn 4 R 4D , -SOV 4 NR 4A R 4B , -NHC(O)NR 4A R 4B , -NR 4A R 4B , -C(O)R 4C , -C(O)OR 4C , -C(O)NR 4A R 4B , -OR 4D , -SR 4D , -NR 4A SO 2 R 4D , -NR 4A C(O)R 4C , -NR 4A C(O)OR 4C , -SF5, -N3, substituted or unsubstituted alkyl, substituted or unsubstituted heteroalkyl, substituted or unsubstituted cycloalkyl, substituted
  • R 4 is hydrogen, halogen, -CCl 3 , -CBr3, -CF3, -Cl 3 , -CHCI2, -CHBr 2 , -CHF 2 , -CHI2, -CH2CI, -CH 2 Br, -CH 2 F, -CH 2 I, -OCCl 3 , -OCF3, -OCBr 3 , -OCl 3 , -OCHCl 2 , -OCHBr 2 , -OCH2, -OCHF2, -OCH2CI, -OCH 2 Br, -OCH 2 I, -OCH 2 F, -CN, -SO3H, -OSO3H, -SO2NH2, -NHNH 2 , -ONH2, -NHC(O)NHNH 2 , -NHC(O)NH 2 , -NO2, -NH 2 , -C(O)H, -C(O)OH,
  • R 4 is hydrogen, halogen, -CCl 3 , -CBr3, -CF3, -Cl 3 , -CHCI2, -CHBr 2 , -CHF 2 , -CHI2, -CH2CI, -CH 2 Br, -CH 2 F, -CH 2 I, -OCCl 3 , -OCF3, -OCBr 3 , -OCl 3 , -OCHCl 2 , -OCHBr 2 , -OCHI 2 , -OCHF 2 , -OCH 2 C1, -OCH 2 Br, -OCH 2 I, -OCH 2 F, -CN, -SO3H, -OSO3H, -SO2NH2, -NHC(O)NH 2 , -NH 2 , -C(O)H, -C(O)OH, -CONH2, -OH, -SH, -NHSO2H, -NHC
  • R 4 is hydrogen or unsubstituted C 1 -C 6 alkyl. In embodiments, R 4 is hydrogen. In embodiments, R 4 is unsubstituted methyl. In embodiments, R 4 is unsubstituted ethyl. In embodiments, R 4 is unsubstituted propyl. In embodiments, R 4 is unsubstituted n-propyl. In embodiments, R 4 is unsubstituted isopropyl. In embodiments, R 4 is unsubstituted butyl. In embodiments, R 4 is unsubstituted n-butyl. In embodiments, R 4 is unsubstituted isobutyl. In embodiments, R 4 is unsubstituted tert-butyl. In embodiments, R 4 is unsubstituted pentyl. In embodiments, R 4 is unsubstituted hexyl.
  • a substituted ring formed when R 3 and R 4 substituents are joined is substituted with at least one substituent group, size-limited substituent group, or lower substituent group; wherein if the substituted ring formed when R 3 and R 4 substituents are joined is substituted with a plurality of groups selected from substituent groups, sizelimited substituent groups, and lower substituent groups; each substituent group, size-limited substituent group, and/or lower substituent group may optionally be different.
  • a substituted R 5 (e.g., substituted alkyl, substituted heteroalkyl, substituted cycloalkyl, substituted heterocycloalkyl, substituted aryl, and/or substituted heteroaryl) is substituted with at least one substituent group, size-limited substituent group, or lower substituent group; wherein if the substituted R 5 is substituted with a plurality of groups selected from substituent groups, size-limited substituent groups, and lower substituent groups; each substituent group, size-limited substituent group, and/or lower substituent group may optionally be different.
  • R 5 when R 5 is substituted, it is substituted with at least one substituent group.
  • R 5 when R 5 is substituted, it is substituted with at least one size-limited substituent group.
  • R 5 when R 5 is substituted, it is substituted with at least one lower substituent group.
  • a substituted R 5A (e.g., substituted alkyl, substituted heteroalkyl, substituted cycloalkyl, substituted heterocycloalkyl, substituted aryl, and/or substituted heteroaryl) is substituted with at least one substituent group, size-limited substituent group, or lower substituent group; wherein if the substituted R 5A is substituted with a plurality of groups selected from substituent groups, size-limited substituent groups, and lower substituent groups; each substituent group, size-limited substituent group, and/or lower substituent group may optionally be different.
  • R 5A when R 5A is substituted, it is substituted with at least one substituent group.
  • R 5A when R 5A is substituted, it is substituted with at least one size-limited substituent group.
  • R 5A when R 5A is substituted, it is substituted with at least one lower substituent group.
  • a substituted R 5B (e.g., substituted alkyl, substituted heteroalkyl, substituted cycloalkyl, substituted heterocycloalkyl, substituted aryl, and/or substituted heteroaryl) is substituted with at least one substituent group, size-limited substituent group, or lower substituent group; wherein if the substituted R 5B is substituted with a plurality of groups selected from substituent groups, size-limited substituent groups, and lower substituent groups; each substituent group, size-limited substituent group, and/or lower substituent group may optionally be different.
  • R 5B when R 5B is substituted, it is substituted with at least one substituent group.
  • R 5B when R 5B is substituted, it is substituted with at least one size-limited substituent group.
  • R 5B when R 5B is substituted, it is substituted with at least one lower substituent group.
  • a substituted ring formed when R 5A and R 5B substituents bonded to the same nitrogen atom are joined e.g., substituted heterocycloalkyl and/or substituted heteroaryl
  • at least one substituent group, size-limited substituent group, or lower substituent group e.g., substituted heterocycloalkyl and/or substituted heteroaryl
  • the substituted ring formed when R 5A and R 5B substituents bonded to the same nitrogen atom are joined is substituted with a plurality of groups selected from substituent groups, size-limited substituent groups, and lower substituent groups; each substituent group, size-limited substituent group, and/or lower substituent group may optionally be different.
  • when the substituted ring formed when R 5A and R 5B substituents bonded to the same nitrogen atom are joined is substituted, it is substituted with at least one substituent group. In embodiments, when the substituted ring formed when R 5A and R 5B substituents bonded to the same nitrogen atom are joined is substituted, it is substituted with at least one size-limited substituent group. In embodiments, when the substituted ring formed when R 5A and R 5B substituents bonded to the same nitrogen atom are joined is substituted, it is substituted with at least one lower substituent group.
  • a substituted R 5C (e.g., substituted alkyl, substituted heteroalkyl, substituted cycloalkyl, substituted heterocycloalkyl, substituted aryl, and/or substituted heteroaryl) is substituted with at least one substituent group, size-limited substituent group, or lower substituent group; wherein if the substituted R 5C is substituted with a plurality of groups selected from substituent groups, size-limited substituent groups, and lower substituent groups; each substituent group, size-limited substituent group, and/or lower substituent group may optionally be different.
  • R 5C when R 5C is substituted, it is substituted with at least one substituent group.
  • R 5C when R 5C is substituted, it is substituted with at least one size-limited substituent group.
  • R 5C when R 5C is substituted, it is substituted with at least one lower substituent group.
  • a substituted R 5D (e.g., substituted alkyl, substituted heteroalkyl, substituted cycloalkyl, substituted heterocycloalkyl, substituted aryl, and/or substituted heteroaryl) is substituted with at least one substituent group, size-limited substituent group, or lower substituent group; wherein if the substituted R 5D is substituted with a plurality of groups selected from substituent groups, size-limited substituent groups, and lower substituent groups; each substituent group, size-limited substituent group, and/or lower substituent group may optionally be different.
  • R 5D when R 5D is substituted, it is substituted with at least one substituent group.
  • R 5D when R 5D is substituted, it is substituted with at least one size-limited substituent group.
  • R 5D when R 5D is substituted, it is substituted with at least one lower substituent group.
  • R 5 is hydrogen, halogen, -CX 5 3, -CHX 5 2, -CH2X 5 , -OCX 5 3, -OCH2X 5 , -OCHX 5 2, -CN, -SOn 5 R 5D , -SOV 5 NR 5A R 5B , -NHC(O)NR 5A R 5B , -NR 5A R 5B , -C(O)R 5C , -C(O)OR 5C , -C(O)NR 5A R 5B , -OR 5D , -SR 5D , -NR 5A SO 2 R 5D , -NR 5A C(O)R 5C , -NR 5A C(O)OR 5C , -SF5, -N3, substituted or unsubstituted alkyl, substituted or unsubstituted heteroalkyl, substituted or unsubstituted cycloalkyl, substituted
  • R 5 is hydrogen, halogen, -CCl 3 , -CBr3, -CF3, -Cl 3 , -CHCI2, -CHBr 2 , -CHF 2 , -CHI2, -CH2CI, -CH 2 Br, -CH 2 F, -CH 2 I, -OCCl 3 , -OCF3, -OCBr 3 , -OCl 3 , -OCHCl 2 , -OCHBr 2 , -OCHb, -OCHF2, -OCH2CI, -OCH 2 Br, -OCH 2 I, -OCH 2 F, -CN, -SO3H, -OSO3H, -SO2NH2, -NHNH 2 , -ONH2, -NHC(O)NHNH 2 , -NHC(O)NH 2 , -NO2, -NH 2 , -C(O)H, -C(O)OH
  • R 5 is hydrogen, halogen, -CCl 3 , -CBr3, -CF3, -Cl 3 , -CHCI2, -CHBr 2 , -CHF 2 , -CHI2, -CH2CI, -CH 2 Br, -CH 2 F, -CH 2 I, -OCCl 3 , -OCF3, -OCBr 3 , -OCl 3 , -OCHCl 2 , -OCHBr 2 , -OCHI 2 , -OCHF 2 , -OCH 2 C1, -OCH 2 Br, -OCH 2 I, -OCH 2 F, -CN, -SO 3 H, -OSO 3 H, -SO 2 NH 2 , -NHC(O)NH 2 , -NH 2 , -C(O)H, -C(O)OH, -CONH 2 , -OH, -SH, -NHSO 2 H
  • R 5 is hydrogen or unsubstituted C 1 -C 6 alkyl. In embodiments, R 5 is hydrogen. In embodiments, R 5 is unsubstituted methyl. In embodiments, R 5 is unsubstituted ethyl. In embodiments, R 5 is unsubstituted propyl. In embodiments, R 5 is unsubstituted n-propyl. In embodiments, R 5 is unsubstituted isopropyl. In embodiments, R 5 is unsubstituted butyl. In embodiments, R 5 is unsubstituted n-butyl. In embodiments, R 5 is unsubstituted isobutyl. In embodiments, R 5 is unsubstituted tert-butyl. In embodiments, R 5 is unsubstituted pentyl. In embodiments, R 5 is unsubstituted hexyl.
  • a substituted ring formed when R 4 and R 5 substituents are joined is substituted with at least one substituent group, size-limited substituent group, or lower substituent group; wherein if the substituted ring formed when R 4 and R 5 substituents are joined is substituted with a plurality of groups selected from substituent groups, sizelimited substituent groups, and lower substituent groups; each substituent group, size-limited substituent group, and/or lower substituent group may optionally be different.
  • W 6 is N. In embodiments, W 6 is C(R 6 ). In embodiments, W 6 is CH.
  • a substituted R 6 (e.g., substituted alkyl, substituted heteroalkyl, substituted cycloalkyl, substituted heterocycloalkyl, substituted aryl, and/or substituted heteroaryl) is substituted with at least one substituent group, size-limited substituent group, or lower substituent group; wherein if the substituted R 6 is substituted with a plurality of groups selected from substituent groups, size-limited substituent groups, and lower substituent groups; each substituent group, size-limited substituent group, and/or lower substituent group may optionally be different.
  • R 6 when R 6 is substituted, it is substituted with at least one substituent group.
  • R 6 when R 6 is substituted, it is substituted with at least one size-limited substituent group.
  • R 6 when R 6 is substituted, it is substituted with at least one lower substituent group.
  • a substituted R 6A (e.g., substituted alkyl, substituted heteroalkyl, substituted cycloalkyl, substituted heterocycloalkyl, substituted aryl, and/or substituted heteroaryl) is substituted with at least one substituent group, size-limited substituent group, or lower substituent group; wherein if the substituted R 6A is substituted with a plurality of groups selected from substituent groups, size-limited substituent groups, and lower substituent groups; each substituent group, size-limited substituent group, and/or lower substituent group may optionally be different.
  • R 6A when R 6A is substituted, it is substituted with at least one substituent group.
  • R 6A when R 6A is substituted, it is substituted with at least one size-limited substituent group.
  • R 6A when R 6A is substituted, it is substituted with at least one lower substituent group.
  • a substituted R 6B (e.g., substituted alkyl, substituted heteroalkyl, substituted cycloalkyl, substituted heterocycloalkyl, substituted aryl, and/or substituted heteroaryl) is substituted with at least one substituent group, size-limited substituent group, or lower substituent group; wherein if the substituted R 6B is substituted with a plurality of groups selected from substituent groups, size-limited substituent groups, and lower substituent groups; each substituent group, size-limited substituent group, and/or lower substituent group may optionally be different.
  • R 6B when R 6B is substituted, it is substituted with at least one substituent group.
  • R 6B when R 6B is substituted, it is substituted with at least one size-limited substituent group.
  • R 6B when R 6B is substituted, it is substituted with at least one lower substituent group.
  • a substituted ring formed when R 6A and R 6B substituents bonded to the same nitrogen atom are joined e.g., substituted heterocycloalkyl and/or substituted heteroaryl
  • at least one substituent group, size-limited substituent group, or lower substituent group e.g., substituted heterocycloalkyl and/or substituted heteroaryl
  • the substituted ring formed when R 6A and R 6B substituents bonded to the same nitrogen atom are joined is substituted with a plurality of groups selected from substituent groups, size-limited substituent groups, and lower substituent groups; each substituent group, size-limited substituent group, and/or lower substituent group may optionally be different.
  • when the substituted ring formed when R 6A and R 6B substituents bonded to the same nitrogen atom are joined is substituted, it is substituted with at least one substituent group. In embodiments, when the substituted ring formed when R 6A and R 6B substituents bonded to the same nitrogen atom are joined is substituted, it is substituted with at least one size-limited substituent group. In embodiments, when the substituted ring formed when R 6A and R 6B substituents bonded to the same nitrogen atom are joined is substituted, it is substituted with at least one lower substituent group.
  • a substituted R 6C (e.g., substituted alkyl, substituted heteroalkyl, substituted cycloalkyl, substituted heterocycloalkyl, substituted aryl, and/or substituted heteroaryl) is substituted with at least one substituent group, size-limited substituent group, or lower substituent group; wherein if the substituted R 6C is substituted with a plurality of groups selected from substituent groups, size-limited substituent groups, and lower substituent groups; each substituent group, size-limited substituent group, and/or lower substituent group may optionally be different.
  • R 6C when R 6C is substituted, it is substituted with at least one substituent group.
  • R 6C when R 6C is substituted, it is substituted with at least one size-limited substituent group.
  • R 6C when R 6C is substituted, it is substituted with at least one lower substituent group.
  • a substituted R 6D (e.g., substituted alkyl, substituted heteroalkyl, substituted cycloalkyl, substituted heterocycloalkyl, substituted aryl, and/or substituted heteroaryl) is substituted with at least one substituent group, size-limited substituent group, or lower substituent group; wherein if the substituted R 6D is substituted with a plurality of groups selected from substituent groups, size-limited substituent groups, and lower substituent groups; each substituent group, size-limited substituent group, and/or lower substituent group may optionally be different.
  • R 6D when R 6D is substituted, it is substituted with at least one substituent group.
  • R 6D when R 6D is substituted, it is substituted with at least one size-limited substituent group.
  • R 6D when R 6D is substituted, it is substituted with at least one lower substituent group.
  • R 6 is hydrogen, halogen, -CX 6 3, -CHX 6 2, -CH2X 6 , -OCX 6 3 , -OCH2X 6 , -OCHX 6 2, -CN, -SOn 6 R 6D , -SO V6 NR 6A R 6B , -NHC(O)NR 6A R 6B , -NR 6A R 6B , -C(O)R 6C , -C(O)OR 6C , -C(O)NR 6A R 6B , -OR 6D , -SR 6D , -NR 6A SO 2 R 6D , -NR 6A C(O)R 6C , -NR 6A C(O)OR 6C , -SF5, -N3, substituted or unsubstituted alkyl, substituted or unsubstituted heteroalkyl, substituted or unsubstituted cycloalkyl,
  • R 6 is hydrogen, halogen, -CCl 3 , -CBrs, -CF3, -Cl 3 , -CHCI2, -CHBr 2 , -CHF 2 , -CHI 2 , -CH 2 C1, -CH 2 Br, -CH 2 F, -CH 2 I, -OCCl 3 , -OCF3, -OCBr 3 , -OCl 3 , -OCHCl 2 , -OCHBr 2 , -OCHI 2 , -OCHF 2 , -OCH 2 C1, -OCH 2 Br, -OCH 2 I, -OCH 2 F, -CN, -SO3H, -OSO3H, -SO 2 NH 2 , -NHNH 2 , -0NH 2 , -NHC(O)NHNH 2 , -NHC(O)NH 2 , -NO 2 , -NH 2 , -
  • R 6 is hydrogen, halogen, -CCl 3 , -CBr3, -CF3, -Cl 3 , -CHCl 2 , -CHBr 2 , -CHF 2 , -CHI 2 , -CH 2 C1, -CH 2 Br, -CH 2 F, -CH 2 I, -OCCl 3 , -OCF3, -OCBr 3 , -OCl 3 , -OCHCl 2 , -OCHBr 2 , -OCHI 2 , -OCHF 2 , -OCH 2 C1, -OCH 2 Br, -OCH 2 I, -OCH 2 F, -CN, -SO3H, -OSO3H, -SO 2 NH 2 , -NHC(O)NH 2 , -NH 2 , -C(O)H, -C(O)OH, -CONH 2 , -OH, -SH,
  • R 6 is hydrogen, -OCHF 2 , unsubstituted C 1 -C 6 alkyl, or unsubstituted 2 to 6 membered heteroalkyl. In embodiments, R 6 is hydrogen. In embodiments, R 6 is -OCHF 2 . In embodiments, R 6 is unsubstituted methyl. In embodiments, R 6 is unsubstituted ethyl. In embodiments, R 6 is unsubstituted propyl. In embodiments, R 6 is unsubstituted n-propyl. In embodiments, R 6 is unsubstituted isopropyl. In embodiments, R 6 is unsubstituted butyl.
  • R 6 is unsubstituted n-butyl. In embodiments, R 6 is unsubstituted isobutyl. In embodiments, R 6 is unsubstituted tert-butyl. In embodiments, R 6 is unsubstituted pentyl. In embodiments, R 6 is unsubstituted hexyl. In embodiments, R 6 is unsubstituted methoxy. In embodiments, R 6 is unsubstituted ethoxy. In embodiments, R 6 is unsubstituted proproxy. In embodiments, R 6 is unsubstituted n-propoxy. In embodiments, R 6 is unsubstituted isopropoxy. In embodiments, R 6 is -OCD3. In embodiments, R 6 is unsubstituted butoxy. In embodiments, R 6 is . In embodiments, R 6 is . In embodiments, R 6 is
  • W 7 is N. In embodiments, W 7 is N + -O". In embodiments, W 7 is C(R 7 ). In embodiments, W 7 is CH.
  • a substituted R 7 (e.g., substituted alkyl, substituted heteroalkyl, substituted cycloalkyl, substituted heterocycloalkyl, substituted aryl, and/or substituted heteroaryl) is substituted with at least one substituent group, size-limited substituent group, or lower substituent group; wherein if the substituted R 7 is substituted with a plurality of groups selected from substituent groups, size-limited substituent groups, and lower substituent groups; each substituent group, size-limited substituent group, and/or lower substituent group may optionally be different.
  • R 7 when R 7 is substituted, it is substituted with at least one substituent group.
  • R 7 when R 7 is substituted, it is substituted with at least one size-limited substituent group.
  • R 7 when R 7 is substituted, it is substituted with at least one lower substituent group.
  • a substituted R 7A (e.g., substituted alkyl, substituted heteroalkyl, substituted cycloalkyl, substituted heterocycloalkyl, substituted aryl, and/or substituted heteroaryl) is substituted with at least one substituent group, size-limited substituent group, or lower substituent group; wherein if the substituted R 7A is substituted with a plurality of groups selected from substituent groups, size-limited substituent groups, and lower substituent groups; each substituent group, size-limited substituent group, and/or lower substituent group may optionally be different.
  • R 7A when R 7A is substituted, it is substituted with at least one substituent group.
  • R 7A when R 7A is substituted, it is substituted with at least one size-limited substituent group.
  • R 7A when R 7A is substituted, it is substituted with at least one lower substituent group.
  • a substituted R 7B (e.g., substituted alkyl, substituted heteroalkyl, substituted cycloalkyl, substituted heterocycloalkyl, substituted aryl, and/or substituted heteroaryl) is substituted with at least one substituent group, size-limited substituent group, or lower substituent group; wherein if the substituted R 7B is substituted with a plurality of groups selected from substituent groups, size-limited substituent groups, and lower substituent groups; each substituent group, size-limited substituent group, and/or lower substituent group may optionally be different.
  • R 7B when R 7B is substituted, it is substituted with at least one substituent group.
  • R 7B when R 7B is substituted, it is substituted with at least one size-limited substituent group.
  • R 7B when R 7B is substituted, it is substituted with at least one lower substituent group.
  • a substituted ring formed when R 7A and R 7B substituents bonded to the same nitrogen atom are joined e.g., substituted heterocycloalkyl and/or substituted heteroaryl
  • at least one substituent group, size-limited substituent group, or lower substituent group e.g., substituted heterocycloalkyl and/or substituted heteroaryl
  • the substituted ring formed when R 7A and R 7B substituents bonded to the same nitrogen atom are joined is substituted with a plurality of groups selected from substituent groups, size-limited substituent groups, and lower substituent groups; each substituent group, size-limited substituent group, and/or lower substituent group may optionally be different.
  • when the substituted ring formed when R 7A and R 7B substituents bonded to the same nitrogen atom are joined is substituted, it is substituted with at least one substituent group. In embodiments, when the substituted ring formed when R 7A and R 7B substituents bonded to the same nitrogen atom are joined is substituted, it is substituted with at least one size-limited substituent group. In embodiments, when the substituted ring formed when R 7A and R 7B substituents bonded to the same nitrogen atom are joined is substituted, it is substituted with at least one lower substituent group.
  • a substituted R 7C (e.g., substituted alkyl, substituted heteroalkyl, substituted cycloalkyl, substituted heterocycloalkyl, substituted aryl, and/or substituted heteroaryl) is substituted with at least one substituent group, size-limited substituent group, or lower substituent group; wherein if the substituted R 7C is substituted with a plurality of groups selected from substituent groups, size-limited substituent groups, and lower substituent groups; each substituent group, size-limited substituent group, and/or lower substituent group may optionally be different.
  • R 7C when R 7C is substituted, it is substituted with at least one substituent group.
  • R 7C when R 7C is substituted, it is substituted with at least one size-limited substituent group.
  • R 7C when R 7C is substituted, it is substituted with at least one lower substituent group.
  • a substituted R 7D (e.g., substituted alkyl, substituted heteroalkyl, substituted cycloalkyl, substituted heterocycloalkyl, substituted aryl, and/or substituted heteroaryl) is substituted with at least one substituent group, size-limited substituent group, or lower substituent group; wherein if the substituted R 7D is substituted with a plurality of groups selected from substituent groups, size-limited substituent groups, and lower substituent groups; each substituent group, size-limited substituent group, and/or lower substituent group may optionally be different.
  • R 7D when R 7D is substituted, it is substituted with at least one substituent group.
  • R 7D when R 7D is substituted, it is substituted with at least one size-limited substituent group.
  • R 7D when R 7D is substituted, it is substituted with at least one lower substituent group.
  • R 7 is hydrogen, halogen, -CX 7 3, -CHX 7 2, -CH2X 7 , -OCX 7 3, -OCH2X 7 , -OCHX 7 2, -CN, -SOn7R 7D , -SOV7NR 7A R 7B , -NHC(O)NR 7A R 7B , -NR 7A R 7B , -C(O)R 7C , -C(O)OR 7C , -C(O)NR 7A R 7B , -OR 7D , -SR 7D , -NR 7A SO 2 R 7D , -NR 7A C(O)R 7C , -NR 7A C(O)OR 7C , -SF5, -N3, substituted or unsubstituted alkyl, substituted or unsubstituted heteroalkyl, substituted or unsubstituted cycloalkyl, substituted or
  • R 7 is hydrogen, halogen, -CCl 3 , -CBr3, -CF3, -Cl 3 , -CHCI2, -CHBr 2 , -CHF 2 , -CHI2, -CH2CI, -CH 2 Br, -CH 2 F, -CH 2 I, -OCCl 3 , -OCF3, -OCBr 3 , -OCl 3 , -OCHCl 2 , -OCHBr 2 , -OCHb, -OCHF2, -OCH2CI, -OCH 2 Br, -OCH 2 I, -OCH 2 F, -CN, -SO3H, -OSO3H, -SO2NH2, -NHNH 2 , -ONH2, -NHC(O)NHNH 2 , -NHC(O)NH 2 , -NO2, -NH 2 , -C(O)H, -C(O)OH
  • R 7 is hydrogen, halogen, -CCl 3 , -CBr3, -CF3, -Cl 3 , -CHCI2, -CHBr 2 , -CHF 2 , -CHI2, -CH2CI, -CH 2 Br, -CH 2 F, -CH 2 I, -OCCl 3 , -OCF3, -OCBr 3 , -OCl 3 , -OCHCl 2 , -OCHBr 2 , -OCHI 2 , -OCHF 2 , -OCH 2 C1, -OCH 2 Br, -OCH 2 I, -OCH 2 F, -CN, -SO3H, -OSO3H, -SO2NH2, -NHC(O)NH 2 , -NH 2 , -C(O)H, -C(O)OH, -CONH2, -OH, -SH, -NHSO2H, -NHC
  • R 7 is hydrogen, halogen, -OCHF2, or unsubstituted C 1 -C 6 alkyl. In embodiments, R 7 is hydrogen. In embodiments, R 7 is halogen. In embodiments, R 7 is -F. In embodiments, R 7 is -Cl. In embodiments, R 7 is -Br. In embodiments, R 7 is -OCHF2. In embodiments, R 7 is unsubstituted methyl. In embodiments, R 7 is unsubstituted ethyl. In embodiments, R 7 is unsubstituted propyl. In embodiments, R 7 is unsubstituted n-propyl.
  • R 7 is unsubstituted isopropyl. In embodiments, R 7 is unsubstituted butyl. In embodiments, R 7 is unsubstituted n-butyl. In embodiments, R 7 is unsubstituted isobutyl. In embodiments, R 7 is unsubstituted tert-butyl. In embodiments, R 7 is unsubstituted pentyl. In embodiments, R 7 is unsubstituted hexyl.
  • a substituted R 8 (e.g., substituted alkyl, substituted heteroalkyl, substituted cycloalkyl, substituted heterocycloalkyl, substituted aryl, and/or substituted heteroaryl) is substituted with at least one substituent group, size-limited substituent group, or lower substituent group; wherein if the substituted R 8 is substituted with a plurality of groups selected from substituent groups, size-limited substituent groups, and lower substituent groups; each substituent group, size-limited substituent group, and/or lower substituent group may optionally be different.
  • R 8 when R 8 is substituted, it is substituted with at least one substituent group.
  • R 8 when R 8 is substituted, it is substituted with at least one size-limited substituent group.
  • R 8 when R 8 is substituted, it is substituted with at least one lower substituent group.
  • a substituted R 8A (e.g., substituted alkyl, substituted heteroalkyl, substituted cycloalkyl, substituted heterocycloalkyl, substituted aryl, and/or substituted heteroaryl) is substituted with at least one substituent group, size-limited substituent group, or lower substituent group; wherein if the substituted R 8A is substituted with a plurality of groups selected from substituent groups, size-limited substituent groups, and lower substituent groups; each substituent group, size-limited substituent group, and/or lower substituent group may optionally be different.
  • R 8A when R 8A is substituted, it is substituted with at least one substituent group.
  • R 8A when R 8A is substituted, it is substituted with at least one size-limited substituent group.
  • R 8A when R 8A is substituted, it is substituted with at least one lower substituent group.
  • a substituted R 8B (e.g., substituted alkyl, substituted heteroalkyl, substituted cycloalkyl, substituted heterocycloalkyl, substituted aryl, and/or substituted heteroaryl) is substituted with at least one substituent group, size-limited substituent group, or lower substituent group; wherein if the substituted R 8B is substituted with a plurality of groups selected from substituent groups, size-limited substituent groups, and lower substituent groups; each substituent group, size-limited substituent group, and/or lower substituent group may optionally be different.
  • R 8B when R 8B is substituted, it is substituted with at least one substituent group.
  • R 8B when R 8B is substituted, it is substituted with at least one size-limited substituent group.
  • R 8B when R 8B is substituted, it is substituted with at least one lower substituent group.
  • a substituted ring formed when R 8A and R 8B substituents bonded to the same nitrogen atom are joined e.g., substituted heterocycloalkyl and/or substituted heteroaryl
  • at least one substituent group, size-limited substituent group, or lower substituent group e.g., substituted heterocycloalkyl and/or substituted heteroaryl
  • the substituted ring formed when R 8A and R 8B substituents bonded to the same nitrogen atom are joined is substituted with a plurality of groups selected from substituent groups, size-limited substituent groups, and lower substituent groups; each substituent group, size-limited substituent group, and/or lower substituent group may optionally be different.
  • when the substituted ring formed when R 8A and R 8B substituents bonded to the same nitrogen atom are joined is substituted, it is substituted with at least one substituent group. In embodiments, when the substituted ring formed when R 8A and R 8B substituents bonded to the same nitrogen atom are joined is substituted, it is substituted with at least one size-limited substituent group. In embodiments, when the substituted ring formed when R 8A and R 8B substituents bonded to the same nitrogen atom are joined is substituted, it is substituted with at least one lower substituent group.
  • a substituted R 8C (e.g., substituted alkyl, substituted heteroalkyl, substituted cycloalkyl, substituted heterocycloalkyl, substituted aryl, and/or substituted heteroaryl) is substituted with at least one substituent group, size-limited substituent group, or lower substituent group; wherein if the substituted R 8C is substituted with a plurality of groups selected from substituent groups, size-limited substituent groups, and lower substituent groups; each substituent group, size-limited substituent group, and/or lower substituent group may optionally be different.
  • R 8C when R 8C is substituted, it is substituted with at least one substituent group.
  • R 8C when R 8C is substituted, it is substituted with at least one size-limited substituent group.
  • R 8C when R 8C is substituted, it is substituted with at least one lower substituent group.
  • a substituted R 8D (e.g., substituted alkyl, substituted heteroalkyl, substituted cycloalkyl, substituted heterocycloalkyl, substituted aryl, and/or substituted heteroaryl) is substituted with at least one substituent group, size-limited substituent group, or lower substituent group; wherein if the substituted R 8D is substituted with a plurality of groups selected from substituent groups, size-limited substituent groups, and lower substituent groups; each substituent group, size-limited substituent group, and/or lower substituent group may optionally be different.
  • R 8D when R 8D is substituted, it is substituted with at least one substituent group.
  • R 8D when R 8D is substituted, it is substituted with at least one size-limited substituent group.
  • R 8D when R 8D is substituted, it is substituted with at least one lower substituent group.
  • R 8 is independently halogen, -CX 8 3, -CHX 8 2, -CH2X 8 , -OCX 8 3, -OCH2X 8 , -OCHX 8 2 , -CN, -SO I1X R XD , -SO V8 NR 8A R 8B , -NHC(O)NR 8A R 8B , -NR 8A R 8B , -C(O)R 8C , -C(O)OR 8C , -C(O)NR 8A R 8B , -OR 8D , -SR 8D ,-NR 8A SO 2 R 8D , -NR 8A C(O)R 8C , -NR 8A C(O)OR 8C , -SF5, -N3, substituted or unsubstituted alkyl, substituted or unsubstituted heteroalkyl, substituted or unsubstituted cycloalkyl,
  • R 8 is independently halogen, -CCl 3 , -CBr3, -CF3, -Cl 3 , -CHCI2, -CHBr 2 , -CHF 2 , -CHI2, -CH2CI, -CH 2 Br, -CH 2 F, -CH 2 I, -OCCl 3 , -OCF3, -OCBr 3 , -OCl 3 , -OCHCl 2 , -OCHBr 2 , -OCHb, -OCHF2, -OCH2CI, -OCH 2 Br, -OCH 2 I, -OCH 2 F, -CN, -SO3H, -OSO3H, -SO2NH2, -NHNH 2 , -ONH2, -NHC(O)NHNH 2 , -NHC(O)NH 2 , -NO2, -NH 2 , -C(O)H, -C(O)OH,
  • R 8 is independently halogen, -CCl 3 , -CBr3, -CF3, -Cl 3 , -CHCI2, -CHBr 2 , -CHF 2 , -CHI2, -CH2CI, -CH 2 Br, -CH 2 F, -CH 2 I, -OCCl 3 , -OCF3, -OCBr 3 , -OCl 3 , -OCHCl 2 , -OCHBr 2 , -OCHI 2 , -OCHF 2 , -OCH 2 C1, -OCH 2 Br, -OCH 2 I, -OCH 2 F, -CN, -SO3H, -OSO3H, -SO2NH2, -NHC(O)NH 2 , -NH 2 , -C(O)H, -C(O)OH, -CONH2, -OH, -SH, -NHSO2H, -NHC(
  • R 8 is independently halogen, -CF3, -CHF2, -CN, -OCHF2, -C(O)R 8C , -C(O)OR 8C , -OR 8D , unsubstituted C 1 -C 6 alkyl, unsubstituted 2 to 8 membered heteroalkyl, unsubstituted C 3 -C 8 cycloalkyl, or un substituted phenyl.
  • R 8C is independently hydrogen or unsubstituted C 1 -C 6 alkyl. In embodiments, R 8C is independently hydrogen. In embodiments, R 8C is independently unsubstituted methyl. In embodiments, R 8C is independently unsubstituted ethyl. In embodiments, R 8C is independently unsubstituted propyl. In embodiments, R 8C is independently unsubstituted n-propyl. In embodiments, R 8C is independently unsubstituted isopropyl. In embodiments, R 8C is independently unsubstituted butyl. In embodiments, R 8C is independently unsubstituted n-butyl.
  • R 8C is independently unsubstituted isobutyl. In embodiments, R 8C is independently unsubstituted tert-butyl. In embodiments, R 8C is independently unsubstituted pentyl. In embodiments, R 8C is independently unsubstituted hexyl.
  • R 8D is independently hydrogen or unsubstituted C 1 -C 6 alkyl. In embodiments, R 8D is independently hydrogen. In embodiments, R 8D is independently unsubstituted methyl. In embodiments, R 8D is independently unsubstituted ethyl. In embodiments, R 8D is independently unsubstituted propyl. In embodiments, R 8D is independently unsubstituted n-propyl. In embodiments, R 8D is independently unsubstituted isopropyl. In embodiments, R 8D is independently unsubstituted butyl. In embodiments, R 8D is independently unsubstituted n-butyl.
  • R 8D is independently unsubstituted isobutyl. In embodiments, R 8D is independently unsubstituted tert-butyl. In embodiments, R 8D is independently unsubstituted pentyl. In embodiments, R 8D is independently unsubstituted hexyl.
  • R 8 is independently -F, -Cl, -Br, -CF3, -CHF2, -CN, -C(O)H, -0CHF2, -0CH 3 , -OCH2CH 3 , -OCH2CF3, -OCH(CH 3 )CH 2 OCH 3 , -OCH2CHF2, unsubstituted methyl, unsubstituted cyclopropyl, or unsubstituted phenyl.
  • R 8 is independently -F, -Cl, -Br, -CF3, -CHF2, -OH, -CN, -C(O)H, -0CHF2, -0CH 3 , -OCH2CH 3 , -OCH2CF3, -OCH(CH 3 )CH 2 OCH 3 , -OCH2CHF2, substituted or unsubstituted methyl, unsubstituted cyclopropyl, or unsubstituted phenyl.
  • R 8 is independently -F. In embodiments, R 8 is independently -Cl. In embodiments, R 8 is independently -Br. In embodiments, R 8 is independently -CF3. In embodiments, R 8 is independently -CHF2. In embodiments, R 8 is independently -OH. In embodiments, R 8 is independently -CN. In embodiments, R 8 is independently -C(O)H. In embodiments, R 8 is independently -C(O)OCH 3 . In embodiments, R 8 is independently -OCHF2. In embodiments, R 8 is independently unsubstituted C 1 -C 6 alkyl. In embodiments, R 8 is independently unsubstituted methyl.
  • R 8 is independently unsubstituted ethyl. In embodiments, R 8 is independently unsubstituted propyl. In embodiments, R 8 is independently unsubstituted n-propyl. In embodiments, R 8 is independently unsubstituted isopropyl. In embodiments, R 8 is independently unsubstituted butyl. In embodiments, R 8 is independently unsubstituted n-butyl. In embodiments, R 8 is independently unsubstituted isobutyl. In embodiments, R 8 is independently unsubstituted tert-butyl. In embodiments, R 8 is independently unsubstituted pentyl.
  • R 8 is independently unsubstituted hexyl. In embodiments, R 8 is independently substituted C 1 -C 6 alkyl. In embodiments, R 8 is independently substituted methyl. In embodiments, R 8 is independently substituted ethyl. In embodiments, R 8 is independently substituted propyl. In embodiments, R 8 is independently substituted n-propyl. In embodiments, R 8 is independently substituted isopropyl. In embodiments, R 8 is independently substituted butyl. In embodiments, R 8 is independently substituted n-butyl. In embodiments, R 8 is independently substituted isobutyl. In embodiments, R 8 is independently substituted tert-butyl.
  • R 8 is independently substituted pentyl. In embodiments, R 8 is independently substituted hexyl. In embodiments, R 8 is independently -CH2-(unsubstituted phenyl). In embodiments, R 8 is independently substituted or unsubstituted 2 to 8 membered heteroalkyl. In embodiments, R 8 is independently unsubstituted methoxy. In embodiments, R 8 is independently -OCD3. In embodiments, R 8 is independently unsubstituted ethoxy. In embodiments, R 8 is independently unsubstituted propoxy. In embodiments, R 8 is independently unsubstituted n-propoxy. In embodiments, R 8 is independently unsubstituted isopropoxy.
  • R 8 is independently unsubstituted butoxy. In embodiments, R 8 is independently -CH2OCH 3 . In embodiments, R 8 is independently -OCH2CF3. In embodiments, R 8 is independently -OCH2CHF2. In embodiments, R 8 is independently -OCH2CH2F. In embodiments, R 8 is independently . In embodiments, R 8 is independently 3 . In embodiments, R 8 is independently VO.
  • R 8 is independently unsubstituted C 5 -C 8 cycloalkyl. In embodiments, R 8 is independently unsubstituted cyclopropyl. In embodiments, R 8 is independently unsubstituted cyclobutyl. In embodiments, R 8 is independently unsubstituted cyclopentyl. In embodiments, R 8 is independently unsubstituted cyclohexyl. In embodiments, R 8 is independently unsubstituted phenyl.
  • two R 8 substituents are joined to form an unsubstituted C 5 -Cx cycloalkyl. In embodiments, two R 8 substituents are joined to form an unsubstituted C 3 cycloalkyl. In embodiments, two R 8 substituents are joined to form an unsubstituted C 4 cycloalkyl. In embodiments, two R 8 substituents are joined to form an unsubstituted C5 cycloalkyl. In embodiments, two R 8 substituents are joined to form an unsubstituted C 6 , cycloalkyl. In embodiments, two R 8 substituents are joined to form an unsubstituted C7 cycloalkyl. In embodiments, two R 8 substituents are joined to form an unsubstituted C 8 cycloalkyl.
  • z8 is 0. In embodiments, z8 is 1. In embodiments, z8 is 2. In embodiments, z8 is 3.
  • R 6 and R 7 are as described herein, including in embodiments.
  • R 8.1 R 8.2 , and R 8.3 are independently hydrogen or any value of R 8 as described herein, including in embodiments.
  • R 8.1 , R 8.2 , and R 8.3 are independently hydrogen or any value of R 8 as desc ribed herein, including in embodiments. and R 7 are as described herein, including in embodiments. R 8.1 R 8.2 , and R 8.3 are independently hydrogen or any value of R 8 as described herein, including in embodiments.
  • a substituted R 8.1 (e.g., substituted alkyl, substituted heteroalkyl, substituted cycloalkyl, substituted heterocycloalkyl, substituted aryl, and/or substituted heteroaryl) is substituted with at least one substituent group, size-limited substituent group, or lower substituent group; wherein if the substituted R 8.1 is substituted with a plurality of groups selected from substituent groups, size-limited substituent groups, and lower substituent groups; each substituent group, size-limited substituent group, and/or lower substituent group may optionally be different.
  • R 8.1 when R 8.1 is substituted, it is substituted with at least one substituent group.
  • R 8.1 when R 8.1 is substituted, it is substituted with at least one size-limited substituent group.
  • R 8.1 when R 8.1 is substituted, it is substituted with at least one lower substituent group.
  • a substituted R 8.2 (e.g., substituted alkyl, substituted heteroalkyl, substituted cycloalkyl, substituted heterocycloalkyl, substituted aryl, and/or substituted heteroaryl) is substituted with at least one substituent group, size-limited substituent group, or lower substituent group; wherein if the substituted R 8.2 is substituted with a plurality of groups selected from substituent groups, size-limited substituent groups, and lower substituent groups; each substituent group, size-limited substituent group, and/or lower substituent group may optionally be different.
  • R 8.2 when R 8.2 is substituted, it is substituted with at least one substituent group.
  • R 8.2 when R 8.2 is substituted, it is substituted with at least one size-limited substituent group.
  • R 8.2 when R 8.2 is substituted, it is substituted with at least one lower substituent group.
  • a substituted R 8.3 (e.g., substituted alkyl, substituted heteroalkyl, substituted cycloalkyl, substituted heterocycloalkyl, substituted aryl, and/or substituted heteroaryl) is substituted with at least one substituent group, size-limited substituent group, or lower substituent group; wherein if the substituted R 8.3 is substituted with a plurality of groups selected from substituent groups, size-limited substituent groups, and lower substituent groups; each substituent group, size-limited substituent group, and/or lower substituent group may optionally be different.
  • R 8.3 when R 8.3 is substituted, it is substituted with at least one substituent group.
  • R 8.3 when R 8.3 is substituted, it is substituted with at least one size-limited substituent group.
  • R 8.3 when R 8.3 is substituted, it is substituted with at least one lower substituent group.
  • a substituted ring formed when R 8.2 and R 8.3 substituents are joined is substituted with at least one substituent group, size-limited substituent group, or lower substituent group; wherein if the substituted ring formed when R 8.2 and R 8.3 substituents are joined is substituted with a plurality of groups selected from substituent groups, size-limited substituent groups, and lower substituent groups; each substituent group, size-limited substituent group, and/or lower substituent group may optionally be different.
  • R 8.1 R 8.2 , and R 8.3 are independently hydrogen, halogen, -CX 8 3, -CHX 8 2, -CH 2 X 8 , -OCX 8 3 , -OCH 2 X 8 , -OCHX 8 2, -CN, -SOnsR 8D , -SO v8 NR 8A R 8B , -NR 8C NR 8A R 8B , -ONR 8A R 8B , -NHC(O)NR 8C NR 8A R 8B , -NHC(O)NR 8A R 8B , -N(O) m8 , -NR 8A R 8B , -C(O)R 8C , -C(O)OR 8C , -C(O)NR 8A R 8B , -OR 8D , -SR 8D , -NR 8A SO 2 R 8D , -NR 8A C(O)R
  • R 8.1 R 8.2 , and R 8.3 are independently hydrogen, halogen, -CX 8 3, -CHX 8 2, -CH 2 X 8 , -OCX 8 3 , -OCH 2 X 8 , -OCHX 8 2, -CN, -SOnsR 8D , -SOV 8 NR 8A R 8B , -NHC(O)NR 8A R 8B , -NR 8A R 8B , -C(O)R 8C , -C(O)OR 8C , -C(O)NR 8A R 8B , -OR 8D , -SR 8D , -NR 8A SO 2 R 8D , -NR 8A C(O)R 8C , -NR 8A C(O)OR 8C , -SF 5 , -N 3 , substituted or unsubstituted alkyl, substituted or unsubstituted heteroalkyl
  • R 8.1 R 8.2 , and R 8.3 are independently hydrogen, halogen, -CCl 3 , -CBr 3 , -CF 3 , -Cl 3 , -CHCI2, -CHBr 2 , -CHF 2 , -CHI 2 , -CH 2 C1, -CH 2 Br, -CH 2 F, -CH 2 I, -OCCl 3 , -OCF3, -OCBr,, -OCl 3 , -OCHCl 2 , -OCHBr 2 , -OCHI 2 , -OCHF 2 , -OCH 2 C1, -OCH 2 Br, -OCH 2 I, -OCH2F, -CN, -SO3H, -OSO3H, -SO2NH2, -NHNH 2 , -ONH2, -NHC(O)NHNH 2 , -NHC(O)NH 2 , -NO2, -
  • R 8.1 R 8.2 , and R 8.3 are independently hydrogen, halogen, -CCl 3 , -CBr 3 , -CF 3 , -Cl 3 , -CHCI2, -CHBr 2 , -CHF 2 , -CHI 2 , -CH 2 C1, -CH 2 Br, -CH 2 F, -CH 2 I, -OCCl 3 , -OCF3, -OCBr 3 , -OCl 3 , -OCHCl 2 , -OCHBr 2 , -OCHI 2 , -OCHF 2 , -OCH 2 C1, -OCH 2 Br, -OCH 2 I, -OCH2F, -CN, -SO3H, -OSO3H, -SO2NH2, -NHC(O)NH 2 , -NH 2 , -C(O)H, -C(O)OH, -CONH2, -CONH2, -CONH
  • R 8.1 is -F. In embodiments, R 8.1 is -Cl. In embodiments, R 8.1 is -Br. In embodiments, R 8.1 is -CF3. In embodiments, R 8.1 is -CHF2. In embodiments, R 8.1 is -CN. In embodiments, R 8.1 is -C(O)H. In embodiments, R 8.1 is -C(O)OCH 3 . In embodiments, R 8.1 is -OCHF2. In embodiments, R 8.1 is unsubstituted C 1 -C 6 alkyl. In embodiments, R 8.1 is unsubstituted methyl. In embodiments, R 8.1 is unsubstituted ethyl.
  • R 8.1 is unsubstituted propyl. In embodiments, R 8.1 is unsubstituted n-propyl. In embodiments, R 8.1 is unsubstituted isopropyl. In embodiments, R 8.1 is unsubstituted butyl. In embodiments, R 8.1 is unsubstituted n-butyl. In embodiments, R 8.1 is unsubstituted isobutyl. In embodiments, R 8.1 is unsubstituted tert-butyl. In embodiments, R 8.1 is unsubstituted pentyl. In embodiments, R 8.1 is unsubstituted hexyl.
  • R 8.1 is substituted Ci- C 6 , alkyl. In embodiments, R 8.1 is substituted methyl. In embodiments, R 8.1 is substituted ethyl. In embodiments, R 8.1 is substituted propyl. In embodiments, R 8.1 is substituted n- propyl. In embodiments, R 8.1 is substituted isopropyl. In embodiments, R 8.1 is substituted butyl. In embodiments, R 8.1 is substituted n-butyl. In embodiments, R 8.1 is substituted isobutyl. In embodiments, R 8.1 is substituted tert-butyl. In embodiments, R 8.1 is substituted pentyl. In embodiments, R 8.1 is substituted hexyl.
  • R 8.1 is -CH2-(unsubstituted phenyl). In embodiments, R 8.1 is substituted or unsubstituted 2 to 8 membered heteroalkyl. In embodiments, R 8.1 is unsubstituted methoxy. In embodiments, R 8.1 is -OCD3. In embodiments, R 8.1 is unsubstituted ethoxy. In embodiments, R 8.1 is unsubstituted propoxy. In embodiments, R 8.1 is unsubstituted n-propoxy. In embodiments, R 8.1 is unsubstituted isopropoxy. In embodiments, R 8.1 is unsubstituted butoxy. In embodiments, R 8.1 is -CH2OCH 3 .
  • R 8.1 is -OCH2CF3. In embodiments, R 8.1 is -OCH2CHF2. In embodiments, R 8.1 is -OCH2CH2F. In embodiments, R 8.1 is In embodiments, R 8.1 is In embodiments, R 8.1 is In embodiments, R 8.1 is unsubstituted C 3 -C 8 cycloalkyl. In embodiments, R 8.1 is unsubstituted cyclopropyl. In embodiments, R 8.1 is unsubstituted cyclobutyl. In embodiments, R 8.1 is unsubstituted cyclopentyl. In embodiments, R 8.1 is unsubstituted cyclohexyl. In embodiments, R 8.1 is unsubstituted phenyl.
  • R 8.2 is -F. In embodiments, R 8.2 is -Cl. In embodiments, R 8.2 is -Br. In embodiments, R 8.2 is -CF3. In embodiments, R 82 is -CHF2. In embodiments, R 82 is -CN. In embodiments, R 8.2 is -C(O)H. In embodiments, R 8.2 is -C(O)OCH 3 . In embodiments, R 8.2 is -OCHF2. In embodiments, R 82 is unsubstituted C 1 -C 6 alkyl. In embodiments, R 8.2 is unsubstituted methyl. In embodiments, R 8.2 is unsubstituted ethyl.
  • R 8.2 is unsubstituted propyl. In embodiments, R 8.2 is unsubstituted n-propyl. In embodiments, R 8.2 is unsubstituted isopropyl. In embodiments, R 8.2 is unsubstituted butyl. In embodiments, R 8.2 is unsubstituted n-butyl. In embodiments, R 82 is unsubstituted isobutyl. In embodiments, R 8.2 is unsubstituted tert-butyl. In embodiments, R 82 is unsubstituted pentyl. In embodiments, R 8.2 is unsubstituted hexyl.
  • R 8.2 is substituted Ci- C 6 , alkyl. In embodiments, R 8.2 is substituted methyl. In embodiments, R 8.2 is substituted ethyl. In embodiments, R 8.2 is substituted propyl. In embodiments, R 8.2 is substituted n- propyl. In embodiments, R 8.2 is substituted isopropyl. In embodiments, R 8.2 is substituted butyl. In embodiments, R 8.2 is substituted n-butyl. In embodiments, R 8.2 is substituted isobutyl. In embodiments, R 8.2 is substituted tert-butyl. In embodiments, R 8.2 is substituted pentyl. In embodiments, R 8.2 is substituted hexyl.
  • R 8.2 is -CH2-(unsubstituted phenyl). In embodiments, R 8.2 is substituted or unsubstituted 2 to 8 membered heteroalkyl. In embodiments, R 8.2 is unsubstituted methoxy. In embodiments, R 8.2 is -OCD3. In embodiments, R 82 is unsubstituted ethoxy. In embodiments, R 82 is unsubstituted propoxy. In embodiments, R 8.2 is unsubstituted n-propoxy. In embodiments, R 8.2 is unsubstituted isopropoxy. In embodiments, R 8.2 is unsubstituted butoxy. In embodiments, R 8.2 is -CH2OCH 3 .
  • R 82 is -OCH2CF3.. In embodiments, R 8.2 is -OCH2CHF2. In embodiments, R 82 is -OCH2CH2F. In embodiments, R 8.2 is in embodiments, R 8.2 is In embodiments, R 8.2 is In embodiments, R 8.2 is unsubstituted C 3 -C 8 cycloalkyl. In embodiments, R 8.2 is unsubstituted cyclopropyl. In embodiments, R 8.2 is unsubstituted cyclobutyl. In embodiments, R 82 is unsubstituted cyclopentyl. In embodiments, R 8.2 is unsubstituted cyclohexyl. In embodiments, R 82 is unsubstituted phenyl.
  • R 8.3 is -F. In embodiments, R 8.3 is -Cl. In embodiments, R 8.3 is -Br. In embodiments, R 8.3 is -CF3. In embodiments, R 8.3 is -CHF2. In embodiments, R 8.3 is -CN. In embodiments, R 8.3 is -C(O)H. In embodiments, R 8.3 is -C(O)OCH 3 . In embodiments, R 8.3 is -OCHF2. In embodiments, R 8.3 is unsubstituted C 1 -C 6 alkyl. In embodiments, R 8.3 is unsubstituted methyl. In embodiments, R 8.3 is unsubstituted ethyl.
  • R 8.3 is unsubstituted propyl. In embodiments, R 8.3 is unsubstituted n-propyl. In embodiments, R 8.3 is unsubstituted isopropyl. In embodiments, R 8.3 is unsubstituted butyl. In embodiments, R 8.3 is unsubstituted n-butyl. In embodiments, R 8.3 is unsubstituted isobutyl. In embodiments, R 8.3 is unsubstituted tert-butyl. In embodiments, R 8.3 is unsubstituted pentyl. In embodiments, R 8.3 is unsubstituted hexyl.
  • R 8.3 is substituted Ci- C 6 , alkyl. In embodiments, R 8.3 is substituted methyl. In embodiments, R 8.3 is substituted ethyl. In embodiments, R 8.3 is substituted propyl. In embodiments, R 8.3 is substituted n- propyl. In embodiments, R 8.3 is substituted isopropyl. In embodiments, R 8.3 is substituted butyl. In embodiments, R 8.3 is substituted n-butyl. In embodiments, R 8.3 is substituted isobutyl. In embodiments, R 8.3 is substituted tert-butyl. In embodiments, R 8.3 is substituted pentyl. In embodiments, R 8.3 is substituted hexyl.
  • R 8.3 is -CH2-(unsubstituted phenyl). In embodiments, R 8.3 is substituted or unsubstituted 2 to 8 membered heteroalkyl. In embodiments, R 8.3 is unsubstituted methoxy. In embodiments, R 8.3 is -OCD3. In embodiments, R 8.3 is unsubstituted ethoxy. In embodiments, R 8.3 is unsubstituted propoxy. In embodiments, R 8.3 is unsubstituted n-propoxy. In embodiments, R 8.3 is unsubstituted isopropoxy. In embodiments, R 8.3 is unsubstituted butoxy. In embodiments, R 8.3 is -CH2OCH 3 .
  • R 8.3 is -OCH2CF3. In embodiments, R 8.3 is -OCH2CHF2. In embodiments, R 8.3 is -OCH2CH2F. In embodiments, R 8.3 is In embodiments, R 8.3 is In embodiments, R 8.3 is In embodiments, R 8.3 is unsubstituted C 3 -C 8 cycloalkyl. In embodiments, R 8.3 is unsubstituted cyclopropyl. In embodiments, R 8.3 is unsubstituted cyclobutyl. In embodiments, R 8.3 is unsubstituted cyclopentyl. In embodiments, R 8.3 is unsubstituted cyclohexyl. In embodiments, R 8.3 is unsubstituted phenyl.
  • R 8.2 and R 8.3 substituents are joined to form an unsubstituted C-C 3 8 cycloalkyl. In embodiments, R 8.2 and R 8.3 substituents are joined to form an unsubstituted C 3 cycloalkyl. In embodiments, R 8.2 and R 8.3 substituents are joined to form an unsubstituted C 4 cycloalkyl. In embodiments, R 8.2 and R 8.3 substituents are joined to form an unsubstituted C5 cycloalkyl. In embodiments, R 8.2 and R 8.3 substituents are joined to form an unsubstituted G> cycloalkyl.
  • R 8.2 and R 8.3 substituents are joined to form an unsubstituted C7 cycloalkyl. In embodiments, R 8.2 and R 8.3 substituents are joined to form an unsubstituted Cx cycloalkyl. [0329] In embodiments, [0330] In embodiments,
  • a substituted L 1 (e.g., substituted alkylene) is substituted with at least one substituent group, size-limited substituent group, or lower substituent group; wherein if the substituted L 1 is substituted with a plurality of groups selected from substituent groups, size-limited substituent groups, and lower substituent groups; each substituent group, size-limited substituent group, and/or lower substituent group may optionally be different.
  • L 1 when L 1 is substituted, it is substituted with at least one substituent group.
  • when L 1 is substituted it is substituted with at least one size-limited substituent group.
  • when L 1 is substituted it is substituted with at least one lower substituent group.
  • L 1 is a bond or substituted or unsubstituted C1-C5 alkylene. In embodiments, L 1 is a bond or unsubstituted C1-C5 alkylene. In embodiments, L 1 is a bond. In embodiments, L 1 is unsubstituted methylene. In embodiments, L 1 is unsubstituted ethylene. In embodiments, L 1 is unsubstituted propylene. In embodiments, L 1 is unsubstituted butylene. In embodiments, L 1 is unsubstituted pentylene.
  • a substituted R 9 (e.g., substituted cycloalkylene and/or substituted heterocycloalkylene) is substituted with at least one substituent group, size-limited substituent group, or lower substituent group; wherein if the substituted R 9 is substituted with a plurality of groups selected from substituent groups, size-limited substituent groups, and lower substituent groups; each substituent group, size-limited substituent group, and/or lower substituent group may optionally be different.
  • R 9 when R 9 is substituted, it is substituted with at least one substituent group.
  • R 9 when R 9 is substituted, it is substituted with at least one size-limited substituent group.
  • R 9 when R 9 is substituted, it is substituted with at least one lower substituent group.
  • R 9 is substituted or unsubstituted C 3 -C 8 cycloalkyl or substituted or unsubstituted 3 to 8 membered heterocycloalkyl.
  • R 9 is an R 11 -substituted or unsubstituted cycloalkyl or R 11 - substituted or unsubstituted heterocycloalkyl.
  • R 11 is independently oxo, halogen, -CX n 3 , -CHX 11 2 , -CH2X 11 , -OCX 11 3 , -OCH2X 11 , -OCHX 11 2, -CN, -SOn11R 11D , -SOv11NR 11A R 11B , -NR 11C NR 11A R 11B , -ONR 11A R 11B , -NHC(O)NR 11C NR 11A R 11B , -NHC(O)NR 11A R 11B , -N(O)m11, -NR 11A R 11B , -C(O)R 11C , -C(O)OR 11c , -C(O)NR 11A R 11B , -OR 11D , -SR 11D , -NR 11A SO 2 R 11D , -NR 11A C(O)R 11C , -NR 11A C(O)C
  • R 11A , R 11B , R 11C , and R 11D are independently hydrogen, -CCl 3 , -CBrs, -CF3, -Cl 3 , -CHCl2, -CHBr 2 , -CHF 2 , -CHI 2 , -CH 2 C1, -CH 2 Br, -CH 2 F, -CH 2 I, -CN, -OH, -NH 2 , -COOH, -CONH 2 , -OCCl 3 , -OCF3, -OCBr 3 , -OCl 3 , -OCHCl 2 , -OCHBr 2 , -OCHI 2 , -OCHF 2 , -OCH 2 C1, -OCH 2 Br, -OCH 2 I, -OCH 2 F, substituted or unsubstituted alkyl (e.g., C 1 -C 8 , C 1 -C 6 , C1-C 4 , substituted
  • X 11 is independently -F, -Cl, -Br, or -I.
  • nl 1 is independently an integer from 0 to 4.
  • mi l and vl 1 are independently 1 or 2.
  • R 9 is an R 11 -substituted or unsubstituted C 3 -C 8 cycloalkyl or R 11 - substituted or unsubstituted 3 to 8 membered heterocycloalkyl. In embodiments, R 9 is an R 11 -substituted or unsubstituted spirocyclic cycloalkyl or R 11 -substituted or unsubstituted spirocyclic heterocycloalkyl.
  • R 9 is an R 11 -substituted or unsubstituted C 6 - C 12 spirocyclic cycloalkyl or R 11 -substituted or unsubstituted 6 to 12 membered spirocyclic heterocycloalkyl. In embodiments, R 9 is an R 11 -substituted or unsubstituted bridged cycloalkyl or R 11 -substituted or unsubstituted bridged heterocycloalkyl.
  • R 9 is an R 11 - substituted or unsubstituted C 5 - C 12 bridged cycloalkyl or R 11 - substituted or unsubstituted 5 to 12 membered spirocyclic heterocycloalkyl. [0343] In embodiments, R 9 is
  • R 12 is hydrogen, halogen, -CX 12 3 , -CHX 12 2 , -CH 2 X 12 , -OCX 12 3 , -OCH 2 X 12 , -OCHX 12 2 , -SOni 2 R 12D , -SOvi 2 NR 12A R 12B , -C(O)R 12C , -C(O)OR 12C , -C(O)NR 12A R 12B , -OR 12D , substituted or unsubstituted alkyl (e.g., C 1 -C 8 , C 1 -C 6 , C1-C 4 , or C1-C2), substituted or unsubstituted heteroalkyl (e.g., 2 to 8 membered, 2 to 6 membered, 4 to 6 membered, 2 to 3 membered, or 4 to 5 membered), substituted or unsubstituted cycloalkyl (e.g.,
  • R 12A , R 12B , R 12C , and R 12D are independently hydrogen, -CC1 3 , -CBr 3 , -CF 3 , -CI 3 , -CHCl 2 , -CHBr 2 , -CHF 2 , -CHI 2 , -CH 2 C1, -CH 2 Br, -CH 2 F, -CH 2 I, -CN, -OH, -NH 2 , -COOH, -CONH 2 , -OCC1 3 , -OCF 3 , -OCBr 3 , -OCI 3 , -OCHCl 2 , -OCHBr 2 , -OCHI 2 , -OCHF 2 , -OCH 2 C1, -OCH 2 Br, -OCH 2 I, -OCH 2 F, substituted or unsubstituted alkyl (e.g., C 1 -C 8 , C 1 -C 6 ,
  • nl2 is independently an integer from 0 to 4.
  • vl2 is independently 1 or 2.
  • the symbol z11 is an integer from 0 to 13.
  • R 9 is
  • R 11 , z11, and R 12 are as described herein, including in embodiments.
  • R 9 is R 11 , z11, and R 12 are as described herein, including in embodiments.
  • a substituted R 11 (e.g., substituted alkyl, substituted heteroalkyl, substituted cycloalkyl, substituted heterocycloalkyl, substituted aryl, and/or substituted heteroaryl) is substituted with at least one substituent group, size-limited substituent group, or lower substituent group; wherein if the substituted R 11 is substituted with a plurality of groups selected from substituent groups, size-limited substituent groups, and lower substituent groups; each substituent group, size-limited substituent group, and/or lower substituent group may optionally be different.
  • R 11 when R 11 is substituted, it is substituted with at least one substituent group.
  • R 11 when R 11 is substituted, it is substituted with at least one size-limited substituent group.
  • R 11 when R 11 is substituted, it is substituted with at least one lower substituent group.
  • a substituted R 11A (e.g., substituted alkyl, substituted heteroalkyl, substituted cycloalkyl, substituted heterocycloalkyl, substituted aryl, and/or substituted heteroaryl) is substituted with at least one substituent group, size-limited substituent group, or lower substituent group; wherein if the substituted R 11A is substituted with a plurality of groups selected from substituent groups, size-limited substituent groups, and lower substituent groups; each substituent group, size-limited substituent group, and/or lower substituent group may optionally be different.
  • R 11A when R 11A is substituted, it is substituted with at least one substituent group.
  • R 11A when R 11A is substituted, it is substituted with at least one size-limited substituent group.
  • R 11A when R 11A is substituted, it is substituted with at least one lower substituent group.
  • a substituted R 11B (e.g., substituted alkyl, substituted heteroalkyl, substituted cycloalkyl, substituted heterocycloalkyl, substituted aryl, and/or substituted heteroaryl) is substituted with at least one substituent group, size-limited substituent group, or lower substituent group; wherein if the substituted R 11B is substituted with a plurality of groups selected from substituent groups, size-limited substituent groups, and lower substituent groups; each substituent group, size-limited substituent group, and/or lower substituent group may optionally be different.
  • R 11B when R 11B is substituted, it is substituted with at least one substituent group.
  • R 11B when R 11B is substituted, it is substituted with at least one size-limited substituent group.
  • R 11B when R 11B is substituted, it is substituted with at least one lower substituent group.
  • a substituted ring formed when R 11A and R 11B substituents bonded to the same nitrogen atom are joined e.g., substituted heterocycloalkyl and/or substituted heteroaryl
  • at least one substituent group, size-limited substituent group, or lower substituent group e.g., substituted heterocycloalkyl and/or substituted heteroaryl
  • the substituted ring formed when R 11A and R 11B substituents bonded to the same nitrogen atom are joined is substituted with a plurality of groups selected from substituent groups, size-limited substituent groups, and lower substituent groups; each substituent group, size-limited substituent group, and/or lower substituent group may optionally be different.
  • when the substituted ring formed when R 11A and R 11B substituents bonded to the same nitrogen atom are joined is substituted, it is substituted with at least one substituent group. In embodiments, when the substituted ring formed when R 11A and R 11B substituents bonded to the same nitrogen atom are joined is substituted, it is substituted with at least one size-limited substituent group. In embodiments, when the substituted ring formed when R 11A and R 11B substituents bonded to the same nitrogen atom are joined is substituted, it is substituted with at least one lower substituent group.
  • a substituted R 11C (e.g., substituted alkyl, substituted heteroalkyl, substituted cycloalkyl, substituted heterocycloalkyl, substituted aryl, and/or substituted heteroaryl) is substituted with at least one substituent group, size-limited substituent group, or lower substituent group; wherein if the substituted R 11C is substituted with a plurality of groups selected from substituent groups, size-limited substituent groups, and lower substituent groups; each substituent group, size-limited substituent group, and/or lower substituent group may optionally be different.
  • R 11C when R 11C is substituted, it is substituted with at least one substituent group.
  • R 11C when R 11C is substituted, it is substituted with at least one size-limited substituent group.
  • R 11C when R 11C is substituted, it is substituted with at least one lower substituent group.
  • a substituted R 11D (e.g., substituted alkyl, substituted heteroalkyl, substituted cycloalkyl, substituted heterocycloalkyl, substituted aryl, and/or substituted heteroaryl) is substituted with at least one substituent group, size-limited substituent group, or lower substituent group; wherein if the substituted R 11D is substituted with a plurality of groups selected from substituent groups, size-limited substituent groups, and lower substituent groups; each substituent group, size-limited substituent group, and/or lower substituent group may optionally be different.
  • R 11D when R 11D is substituted, it is substituted with at least one substituent group.
  • R 11D when R 11D is substituted, it is substituted with at least one size-limited substituent group.
  • R 11D when R 11D is substituted, it is substituted with at least one lower substituent group.
  • R 11 is independently oxo, halogen, -CX 11 3, -CHX 11 2, -CH2X 11 , -OCX 11 3 , -OCH2X 11 , -OCHX 11 2 , -CN, -SOn11R 11D , -SOv11NR 11A R 11B , -NHC(O)NR 11A R 11B , -NR 11A R 11B , -C(O)R 11C , -C(O)OR 11C , -C(O)NR 11A R 11B , -OR 11D , -SR 11D , -NR 11A SO2R 11D , -NR 11A C(O)R 11C , -NR 11A C(O)OR 11C , -SF5, -N3, substituted or unsubstituted alkyl, substituted or unsubstituted heteroalkyl, substituted or unsubstituted cycl
  • R 11 is independently oxo, halogen, -CCl 3 , -CBr3, -CF3, -Cl 3 , -CHCl 2 , -CHBr 2 , -CHF 2 , -CHI2, -CH2CI, -CH 2 Br, -CH 2 F, -CH 2 I, -OCCl 3 , -OCF3, -OCBr 3 , -OCl 3 , -OCHCl 2 , -OCHBr 2 , -OCHb, -OCHF2, -OCH2CI, -OCH 2 Br, -OCH 2 I, -OCH 2 F, -CN, -SO 3 H, -OSO 3 H, -SO2NH2, -NHNH 2 , -0NH2, -NHC(O)NHNH 2 , -NHC(O)NH 2 , -NO 2 , -NH 2 , -C(O)
  • R 11 is independently oxo, halogen, -CCl 3 , -CBrs, -CF3, -Cl 3 , -CHCl 2 , -CHBr 2 , -CHF 2 , -CHI2, -CH2CI, -CH 2 Br, -CH 2 F, -CH 2 I, -OCCl 3 , -OCF3, -OCBr 3 , -OCl 3 , -OCHCl 2 , -OCHBr 2 , -OCHl 2 , -OCHF2, -OCH2CI, -OCH 2 Br, -OCH 2 I, -OCH 2 F, -CN, -SO3H, -OSO3H, -SO2NH2, -NHC(O)NH 2 , -NH 2 , -C(O)H, -C(O)OH, -CONH2, -OH, -SH, -NHSO2NH2, -NHC
  • R 11 is independently oxo, halogen, -CX 11 3, -CN, -C(O)OR 11c , -C(O)NR 11A R 11B , -C(O)R 11c , -OR 11D , substituted or unsubstituted C 1 -C 6 alkyl, or substituted or unsubstituted 2 to 5 membered heteroalkyl.
  • R 11 is independently oxo, halogen, -CX 11 3, -CHX 11 2, -CN, -SOn11R 11D , -C(O)R 11c , -C(O)OR 11c , -C(O)NR 11A R 11B , -C(O)R 11c , -OR 11D , -NR 11A SO 2 R 11D , -NR 11A C(O)R 11C , -NR 11A C(O)OR 11C , substituted or unsubstituted C 1 -C 6 alkyl, substituted or unsubstituted 2 to 5 membered heteroalkyl, or substituted or unsubstituted 5 to 10 membered heteroaryl.
  • R 11A is independently hydrogen or unsubstituted C 1 -C 6 alkyl; and R 11B is independently hydrogen. In embodiments, R 11A is independently hydrogen. In embodiments, R 11A is independently unsubstituted C 1 -C 6 alkyl. In embodiments, R 11A is independently unsubstituted methyl. In embodiments, R 11A is independently unsubstituted ethyl. In embodiments, R 11A is independently unsubstituted propyl. In embodiments, R 11A is independently unsubstituted n-propyl. In embodiments, R 11A is independently unsubstituted isopropyl.
  • R 11A is independently unsubstituted butyl. In embodiments, R 11A is independently unsubstituted n-butyl. In embodiments, R 11A is independently unsubstituted isobutyl. In embodiments, R 11A is independently unsubstituted tert-butyl. In embodiments, R 11A is independently unsubstituted pentyl. In embodiments, R 11A is independently unsubstituted hexyl. In embodiments, R 11A is independently -OH. In embodiments, R 11A is independently -C(O)CH 3 . In embodiments, R 11B is independently hydrogen.
  • R 11C is independently hydrogen or unsubstituted C 1 -C 6 alkyl. In embodiments, R 11C is independently hydrogen. In embodiments, R 11C is independently unsubstituted C 1 -C 6 alkyl. In embodiments, R 11C is independently unsubstituted methyl. In embodiments, R 11C is independently unsubstituted ethyl. In embodiments, R 11C is independently unsubstituted propyl. In embodiments, R 11C is independently unsubstituted n- propyl. In embodiments, R 11C is independently unsubstituted isopropyl. In embodiments, R 11C is independently unsubstituted butyl.
  • R 11C is independently unsubstituted n-butyl. In embodiments, R 11C is independently unsubstituted isobutyl. In embodiments, R 11C is independently unsubstituted tert-butyl. In embodiments, R 11C is independently unsubstituted pentyl. In embodiments, R 11C is independently unsubstituted hexyl. In embodiments, R 11C is independently substituted or unsubstituted 5 to 10 membered heteroaryl. In embodiments, R 11C is independently unsubstituted thiazolyl. In embodiments,
  • R 11C is independently
  • R 11D is independently hydrogen or unsubstituted C 1 -C 6 alkyl. In embodiments, R 11D is independently hydrogen. In embodiments, R 11D is independently unsubstituted C 1 -C 6 alkyl. In embodiments, R 11D is independently unsubstituted methyl. In embodiments, R 11D is independently unsubstituted ethyl. In embodiments, R 11D is independently unsubstituted propyl. In embodiments, R 11D is independently unsubstituted n- propyl. In embodiments, R 11D is independently unsubstituted isopropyl. In embodiments, R 11D is independently unsubstituted butyl.
  • R 11D is independently unsubstituted n-butyl. In embodiments, R 11D is independently unsubstituted isobutyl. In embodiments, R 11D is independently unsubstituted tert-butyl. In embodiments, R 11D is independently unsubstituted pentyl. In embodiments, R 11D is independently unsubstituted hexyl.
  • two R 11 substituents are joined to form a substituted or unsubstituted cycloalkyl. In embodiments, two R 11 substituents are joined to form a substituted or unsubstituted C 5 -C 8 cycloalkyl. In embodiments, two R 11 substituents are joined to form an unsubstituted cyclopropyl. In embodiments, two R 11 substituents are joined to form an unsubstituted cyclobutyl. In embodiments, two R 11 substituents are joined to form an unsubstituted cyclopentyl. In embodiments, two R 11 substituents are joined to form an unsubstituted cyclohexyl. In embodiments, two R 11 substituents are joined to form an unsubstituted cycloheptyl. In embodiments, two R 11 substituents are joined to form an unsubstituted cyclooctyl.
  • R 11 is independently oxo. In embodiments, R 11 is independently halogen. In embodiments, R 11 is -F. In embodiments, R 11 is independently -CF3. In embodiments, R 11 is independently -CHF2. In embodiments, R 11 is independently -CN. In embodiments, R 11 is independently -OH. In embodiments, R 11 is independently -C(O)OH. In embodiments, R 11 is independently -C(O)OCH 3 . In embodiments, R 11 is independently -C(O)OCH2CH 3 . In embodiments, R 11 is independently -C(O)CH 3 . In embodiments, R 11 is independently -C(O)NH2.
  • R 11 is independently -C(O)NHOH. In embodiments, R 11 is independently -S(O)2CH 3 . In embodiments, R 11 is independently -NHC(O)CH 3 . In embodiments, R 11 is independently -C(O)H. In embodiments, R 11 is independently -NHS(O)2CH 3 . In embodiments, R 11 is independently -C(O)NHS(O)2CH 3 . In embodiments, R 11 is independently unsubstituted Ci-C 6 , alkyl. In embodiments, R 11 is independently unsubstituted methyl. In embodiments, R 11 is independently unsubstituted ethyl.
  • R 11 is independently unsubstituted propyl. In embodiments, R 11 is independently unsubstituted n-propyl. In embodiments, R 11 is independently unsubstituted isopropyl. In embodiments, R 11 is independently unsubstituted butyl. In embodiments, R 11 is independently unsubstituted n-butyl. In embodiments, R 11 is independently unsubstituted isobutyl. In embodiments, R 11 is independently unsubstituted tert-butyl. In embodiments, R 11 is independently unsubstituted pentyl. In embodiments, R 11 is independently unsubstituted hexyl.
  • R 11 is independently substituted C 1 -C 6 alkyl. In embodiments, R 11 is independently substituted methyl. In embodiments, R 11 is independently substituted ethyl. In embodiments, R 11 is independently substituted propyl. In embodiments, R 11 is independently substituted n-propyl. In embodiments, R 11 is independently substituted isopropyl. In embodiments, R 11 is independently substituted butyl. In embodiments, R 11 is independently substituted n-butyl. In embodiments, R 11 is independently substituted isobutyl. In embodiments, R 11 is independently substituted tert-butyl. In embodiments, R 11 is independently substituted pentyl. In embodiments, R 11 is independently substituted hexyl.
  • R 11 is independently substituted or unsubstituted 2 to 6 membered heteroalkyl. In embodiments, R 11 is independently unsubstituted methoxy. In embodiments, R 11 is independently unsubstituted ethoxy. In embodiments, R 11 is independently unsubstituted propoxy. In embodiments, R 11 is independently unsubstituted n-propoxy. In embodiments, R 11 is independently unsubstituted isopropoxy. In embodiments, R 11 is independently unsubstituted butoxy. In embodiments, R 11 is independently In embodiments, R 11 is independently In embodiments, R 11 is independently In embodiments, R 11 is independently . In embodiments, R 11 is independently . In embodiments, R 11 is independently .
  • R 11 is independently . In embodiments, R 11 is independently . In embodiments, R 11 is independently . In embodiments, R 11 is independently . In embodiments, R 11 is independently In embodiments, R 11 is independently embodiments, R 11 is independently . In embodiments, R 11 is independently
  • R 11 is independently In embodiments, R 11 is independently . In embodiments, R 11 is independently . In embodiments, R 11 is independently . In embodiments, R 11 is independently substituted or unsubstituted 5 to 10 membered heteroaryl. In embodiments, R 11 is independently unsubstituted pyridyl. In embodiments, R 11 is independently unsubstituted 2-pyridyl. In embodiments, R 11 is independently unsubstituted 3-pyridyl. In embodiments, R 11 is independently unsubstituted 4-pyridyl. In embodiments, R 11 is independently unsubstituted oxazolyl. In embodiments, R 11 is independently unsubstituted isoxazolyl. In embodiments, R 11 is independently substituted isoxazolyl. In embodiments, R 11 is independently . In embodiments, R 11 is independently unsubstituted tetrazolyl.
  • embodimenzts1,1 is 0. In embodimenzts1,1 is 1. In embodimenzts1,1 is 2. In embodiments, z11 is 3. In embodiments, z11 is 4. In embodiments, z11 is 5. In embodiments, z11 is 6. In embodiments, z11 is 7. In embodiments, z11 is 8. In embodiments, z11 is 9. In embodimenzts1,1 is 10. In embodiments, z11 is 11. In embodiments, z11 is 12. In embodimenzts1,1 is 13.
  • a substituted R 12 (e.g., substituted alkyl, substituted heteroalkyl, substituted cycloalkyl, substituted heterocycloalkyl, substituted aryl, and/or substituted heteroaryl) is substituted with at least one substituent group, size-limited substituent group, or lower substituent group; wherein if the substituted R 12 is substituted with a plurality of groups selected from substituent groups, size-limited substituent groups, and lower substituent groups; each substituent group, size-limited substituent group, and/or lower substituent group may optionally be different.
  • R 12 when R 12 is substituted, it is substituted with at least one substituent group.
  • R 12 when R 12 is substituted, it is substituted with at least one size-limited substituent group.
  • R 12 when R 12 is substituted, it is substituted with at least one lower substituent group.
  • a substituted R 12A (e.g., substituted alkyl, substituted heteroalkyl, substituted cycloalkyl, substituted heterocycloalkyl, substituted aryl, and/or substituted heteroaryl) is substituted with at least one substituent group, size-limited substituent group, or lower substituent group; wherein if the substituted R 12A is substituted with a plurality of groups selected from substituent groups, size-limited substituent groups, and lower substituent groups; each substituent group, size-limited substituent group, and/or lower substituent group may optionally be different. In embodiments, when R 12A is substituted, it is substituted with at least one substituent group.
  • R 12A when R 12A is substituted, it is substituted with at least one size-limited substituent group. In embodiments, when R 12A is substituted, it is substituted with at least one lower substituent group.
  • a substituted R 12B e.g., substituted alkyl, substituted heteroalkyl, substituted cycloalkyl, substituted heterocycloalkyl, substituted aryl, and/or substituted heteroaryl
  • R 12B is substituted with at least one substituent group, size-limited substituent group, or lower substituent group; wherein if the substituted R 12B is substituted with a plurality of groups selected from substituent groups, size-limited substituent groups, and lower substituent groups; each substituent group, size-limited substituent group, and/or lower substituent group may optionally be different.
  • R 12B when R 12B is substituted, it is substituted with at least one substituent group. In embodiments, when R 12B is substituted, it is substituted with at least one size-limited substituent group. In embodiments, when R 12B is substituted, it is substituted with at least one lower substituent group.
  • a substituted ring formed when R 12A and R 12B substituents bonded to the same nitrogen atom are joined e.g., substituted heterocycloalkyl and/or substituted heteroaryl
  • at least one substituent group, size-limited substituent group, or lower substituent group e.g., substituted heterocycloalkyl and/or substituted heteroaryl
  • the substituted ring formed when R 12A and R 12B substituents bonded to the same nitrogen atom are joined is substituted with a plurality of groups selected from substituent groups, size-limited substituent groups, and lower substituent groups; each substituent group, size-limited substituent group, and/or lower substituent group may optionally be different.
  • when the substituted ring formed when R 12A and R 12B substituents bonded to the same nitrogen atom are joined is substituted, it is substituted with at least one substituent group. In embodiments, when the substituted ring formed when R 12A and R 12B substituents bonded to the same nitrogen atom are joined is substituted, it is substituted with at least one size-limited substituent group. In embodiments, when the substituted ring formed when R 12A and R 12B substituents bonded to the same nitrogen atom are joined is substituted, it is substituted with at least one lower substituent group.
  • a substituted R 12C (e.g., substituted alkyl, substituted heteroalkyl, substituted cycloalkyl, substituted heterocycloalkyl, substituted aryl, and/or substituted heteroaryl) is substituted with at least one substituent group, size-limited substituent group, or lower substituent group; wherein if the substituted R 12C is substituted with a plurality of groups selected from substituent groups, size-limited substituent groups, and lower substituent groups; each substituent group, size-limited substituent group, and/or lower substituent group may optionally be different.
  • R 12C when R 12C is substituted, it is substituted with at least one substituent group.
  • R 12C when R 12C is substituted, it is substituted with at least one size-limited substituent group.
  • R 12C when R 12C is substituted, it is substituted with at least one lower substituent group.
  • a substituted R 12D (e.g., substituted alkyl, substituted heteroalkyl, substituted cycloalkyl, substituted heterocycloalkyl, substituted aryl, and/or substituted heteroaryl) is substituted with at least one substituent group, size-limited substituent group, or lower substituent group; wherein if the substituted R 12D is substituted with a plurality of groups selected from substituent groups, size-limited substituent groups, and lower substituent groups; each substituent group, size-limited substituent group, and/or lower substituent group may optionally be different.
  • R 12D when R 12D is substituted, it is substituted with at least one substituent group.
  • R 12D when R 12D is substituted, it is substituted with at least one size-limited substituent group.
  • R 12D when R 12D is substituted, it is substituted with at least one lower substituent group.
  • R 12 is hydrogen, halogen, -CX 12 3, -CHX 12 2, -CH2X 12 , -OCX 12 3, -OCH2X 12 , -OCHX 12 2, -CN, -SOn 12 R 12D , -SOvi 2 NR 12A R 12B , -NHC(O)NR 12A R 12B , -NR 12A R 12B , -C(O)R 12C , -C(O)OR 12C , -C(O)NR 12A R 12B , -OR 12D , -SR 12D , -NR 12A SO 2 R 12D , -NR 12A C(O)R 12C , -NR 12A C(O)OR 12C , -SF5, -N3, substituted or unsubstituted alkyl, substituted or unsubstituted heteroalkyl, substituted or unsubstituted cycloalkyl, substituted
  • R 12 is hydrogen, halogen, -CCl 3 , -CBr 3 , -CF3, -Cl 3 , -CHCI2, -CHBr 2 , -CHF 2 , -CHI2, -CH2CI, -CH 2 Br, -CH 2 F, -CH 2 I, -OCCl 3 , -OCF3, -OCBr 3 , -OCl 3 , -OCHCl 2 , -OCHBr 2 , -OCHCl, 2 -OCHF2, -OCH2CI, -OCH 2 Br, -OCH 2 I, -OCH 2 F, -CN, -SO3H, -OSO3H, -SO2NH2, -C(O)H, -C(O)OH, -CONH2, -OH, substituted or unsubstituted alkyl, substituted or unsubstituted heteroalkyl, substituted or unsub
  • R 12 is hydrogen, halogen, -CCl 3 , -CBr 3 , -CF3, -Cl 3 , -CHCI2, -CHBr 2 , -CHF 2 , -CHI2, -CH2CI, -CH 2 Br, -CH 2 F, -CH 2 I, -OCCl 3 , -OCF3, -OCBr 3 , -OCl 3 , -OCHCl 2 , -OCHBr 2 , -OCHI 2 , -OCHF 2 , -OCH 2 C1, -OCH 2 Br, -OCH 2 I, -OCH 2 F, -CN, -SO3H, -OSO3H, -SO2NH2, -NHC(O)NH 2 , -NH 2 , -C(O)H, -C(O)OH, -CONH2, -OH, -SH, -NHSO2H, -
  • R 12 is hydrogen, -C(O)R 12C , -SOn 12 R 12D , -SO v i2NR 12A R 12B , -C(O)OR 12C , -C(O)NR 12A R 12B , unsubstituted C 1 -C 6 alkyl, unsubstituted C 5 -C 8 cycloalkyl, or unsubstituted 3 to 8 membered heterocycloalkyl.
  • R 12A is hydrogen, unsubstituted C 1 -C 6 alkyl, or unsubstituted C- 3 C 8 cycloalkyl; and R 12B is hydrogen.
  • R 12A is hydrogen.
  • R 12A is unsubstituted C 1 -C 6 alkyl.
  • R 12A is unsubstituted methyl.
  • R 12A is unsubstituted ethyl.
  • R 12A is unsubstituted propyl.
  • R 12A is unsubstituted n-propyl.
  • R 12A is unsubstituted isopropyl.
  • R 12A is unsubstituted butyl. In embodiments, R 12A is unsubstituted n-butyl. In embodiments, R 12A is unsubstituted isobutyl. In embodiments, R 12A is unsubstituted tert-butyl. In embodiments, R 12A is unsubstituted pentyl. In embodiments, R 12A is unsubstituted hexyl. In embodiments, R 12A is unsubstituted C 3 -C 8 cycloalkyl. In embodiments, R 12A is unsubstituted cyclopropyl. In embodiments, R 12A is unsubstituted cyclobutyl. In embodiments, R 12A is unsubstituted cyclopentyl. In embodiments, R 12A is unsubstituted cyclohexyl. In embodiments, R 12B is hydrogen.
  • R 12C is substituted or unsubstituted C 1 -C 6 alkyl, substituted or unsubstituted 2 to 6 membered heteroalkyl, or substituted or unsubstituted C 3 -C 8 cycloalkyl.
  • R 12C is hydrogen.
  • R 12C is unsubstituted C 1 -C 6 alkyl.
  • R 12C is unsubstituted methyl.
  • R 12C is unsubstituted ethyl.
  • R 12C is unsubstituted propyl.
  • R 12C is unsubstituted n-propyl.
  • R 12C is unsubstituted isopropyl. In embodiments, R 12C is unsubstituted butyl. In embodiments, R 12C is unsubstituted n-butyl. In embodiments, R 12C is unsubstituted isobutyl. In embodiments, R 12C is unsubstituted tert-butyl. In embodiments, R 12C is unsubstituted pentyl. In embodiments, R 12C is unsubstituted hexyl. In embodiments, R 12C is unsubstituted C 3 -C 8 cycloalkyl. In embodiments, R 12C is unsubstituted cyclopropyl.
  • R 12C is unsubstituted cyclobutyl. In embodiments, R 12C is unsubstituted cyclopentyl. In embodiments, R 12C is unsubstituted cyclohexyl.
  • R 12D is unsubstituted C 1 -C 6 alkyl. In embodiments, R 12D is hydrogen. In embodiments, R 12D is unsubstituted C 1 -C 6 alkyl. In embodiments, R 12D is unsubstituted methyl. In embodiments, R 12D is unsubstituted ethyl. In embodiments, R 12D is unsubstituted propyl. In embodiments, R 12D is unsubstituted n-propyl. In embodiments, R 12D is unsubstituted isopropyl. In embodiments, R 12D is unsubstituted butyl.
  • R 12D is unsubstituted n-butyl. In embodiments, R 12D is unsubstituted isobutyl. In embodiments, R 12D is unsubstituted tert-butyl. In embodiments, R 12D is unsubstituted pentyl. In embodiments, R 12D is unsubstituted hexyl.
  • R 9 is In embodiments, R 9
  • R 9 is In embodiments, R 9 is In embodiments, R 9 is In embodiments, R 9 is . In embodiments, R 9 is . In embodiments, R 9 is . In embodiments, R 9 is
  • R 9 is i n embodiments, R 9 is In 0 embodiments, R 9 is In embodiments, R 9 is In embodiments, R 9 is in embodiments, R 9 is In embodiments, R 9 is embodiments, R 9 is . In embodiments, R 9 is In embodiments, R 9 is In embodiments, R 9 is In embodiments, R 9 is embodiments, R 9 is . In embodiments, R 9 is In embodiments, R 9 is In embodiments, embodiments, embodiments, embodiments, embodiments, embodiments, embodiments, R 9 is In embodiments, R 9 is In embodiments, , , embodiments, embodiments, R 9 is embodiments, embodiments, R 9 is . , in embodiments, R 9 embodiments, R 9 is . In embodiments, R 9 is . In embodiments, R 9 is . In embodiments, R 9 is . In embodiments, R 9 is . In embodiments, embodiments, R 9 is . In embodiments, embodiments, embodiments, , , , , , ,
  • R 9 is in embodiments, R 9 is In embodiments, embodiments, R 9 is embodiments, embodiments, R 9 is embodiments, R 9 is In embodiments, R 9 is embodiments, embodiments, embodiments, embodiments, embodiments, embodiments, R 9 is . In embodiments, R 9 is . In embodiments,
  • R 9 is . In embodiments, R 9 is . In embodiments, R 9 is , In embodiments, R 9 is . , . In embodiments, R 9 is , embodiments, , embodiments, R 9 is . In embodiments, R 9 is . In embodiments, R 9 is H
  • R 9 is . In embodiments, R 9 is . In embodiments, R 9 is . In embodiments, R 9 is
  • R 1 when R 1 is substituted, R 1 is substituted with one or more first substituent groups denoted by R 1 1 as explained in the definitions section above in the description of “first substituent group(s)”. In embodiments, when an R 1 1 substituent group is substituted, the R 1 1 substituent group is substituted with one or more second substituent groups denoted by R 1 2 as explained in the definitions section above in the description of “first substituent group(s)”. In embodiments, when an R 1 2 substituent group is substituted, the R 1 2 substituent group is substituted with one or more third substituent groups denoted by R 1 3 as explained in the definitions section above in the description of “first substituent group(s)”.
  • R 1 , R 1 A , R 1 2 , and R 1 3 have values corresponding to the values of R ww , R ww A , R WW 2 , and R WW 3 , respectively, as explained in the definitions section above in the description of “first substituent group(s)”, wherein R ww ', RR WW.1 , R WW 2 , and R ww 3 correspond to R 1 , R 1 A , R 1 2 , and R 1 3 , respectively.
  • R 2 when R 2 is substituted, R 2 is substituted with one or more first substituent groups denoted by R 2 1 as explained in the definitions section above in the description of “first substituent group(s)”. In embodiments, when an R 2 1 substituent group is substituted, the R 2 1 substituent group is substituted with one or more second substituent groups denoted by R 2 2 as explained in the definitions section above in the description of “first substituent group(s)”. In embodiments, when an R 2 2 substituent group is substituted, the R 2 2 substituent group is substituted with one or more third substituent groups denoted by R 2 3 as explained in the definitions section above in the description of “first substituent group(s)”.
  • R 2 , R 2 R 22 , and R 2 3 have values corresponding to the values of R ww , R ww R ww - 2 , anc
  • R 2A when R 2A is substituted, R 2A is substituted with one or more first substituent groups denoted by R 2A 1 as explained in the definitions section above in the description of “first substituent group(s)”.
  • R 2A 1 substituent group when an R 2A 1 substituent group is substituted, the R 2A 1 substituent group is substituted with one or more second substituent by g
  • R 2B when R 2B is substituted, R 2B is substituted with one or more first substituent groups denoted by R 2B 1 as explained in the definitions section above in the description of “first substituent group(s)”. In embodiments, when an R 2B 1 substituent group is substituted, the R 2B 1 substituent group is substituted with one or more second substituent groups denoted by R 2B 2 as explained in the definitions section above in the description of “first substituent group(s)”. In embodiments, when an R 2B 2 substituent group is substituted, y
  • R 2A and R 2B substituents bonded to the same nitrogen atom are optionally joined to form a moiety that is substituted (e.g., a substituted heterocycloalkyl or substituted heteroaryl), the moiety is substituted with one or more first substituent groups denoted by R 2A 1 as explained in the definitions section above in the description of “first substituent group(s)”.
  • R 2A 1 substituent group when an R 2A 1 substituent group is substituted, the R 2A 1 substituent group is substituted with one or more second substituent groups denoted by R 2A 2 as explained in the definitions section above in the description of “first substituent group(s)”.
  • R 2A 2 substituent group when an R 2A 2 substituent group is substituted, the R 2A 2
  • R 2A and R 2B substituents bonded to the same nitrogen atom are optionally joined to form a moiety that is substituted (e.g., a substituted heterocycloalkyl or substituted heteroaryl), the moiety is substituted with one or more first substituent groups denoted by R 2B 1 as explained in the definitions section above in the description of “first substituent group(s)”.
  • R 2B 1 substituent group when an R 2B 1 substituent group is substituted, the R 2B 1 substituent group is substituted with one or more second substituent groups denoted by R 2B 2 as explained in the definitions section above in the description of “first substituent
  • R 2C when R 2C is substituted, R 2C is substituted with one or more first substituent groups denoted by R 2C 1 as explained in the definitions section above in the description of “first substituent group(s)”.
  • R 2C 1 substituent group when an R 2C 1 substituent group is substituted, the R 2C 1 substituent group is substituted with one or more second substituent groups denoted by R 2C 2 as explained in the definitions section above in the description of “first substituent group(s)”.
  • R 2C 2 substituent group when an R 2C 2 substituent group is substituted, the R 2C 2 substituent group is substituted with one or more third substituent groups denoted by R 2C 3 as explained in the definitions section above in the description of “first substituent
  • R 2D when R 2D is substituted, R 2D is substituted with one or more first substituent groups denoted by R 2D 1 as explained in the definitions section above in the description of “first substituent group(s)”.
  • R 2D 1 substituent group when an R 2D 1 substituent group is substituted, the R 2D 1 substituent group is substituted with one or more second substituent groups denoted by R 2D 2 as explained in the definitions section above in the description of “first substituent group(s)”.
  • R 2D 2 substituent group when an R 2D 2 substituent group is substituted,
  • R 3 when R 3 is substituted, R 3 is substituted with one or more first substituent groups denoted by R 3 1 as explained in the definitions section above in the description of “first substituent group(s)”. In embodiments, when an R 3 1 substituent group is substituted, the R 3 1 substituent group is substituted with one or more second substituent groups denoted by R 3 2 as explained in the definitions section above in the description of “first substituent group(s)”. In embodiments, when an R 3 2 substituent group is substituted,
  • R 3A when R 3A is substituted, R 3A is substituted with one or more first substituent groups denoted by R 3A 1 as explained in the definitions section above in the description of “first substituent group(s)”.
  • R 3A 1 substituent group when an R 3A 1 substituent group is substituted, the R 3A 1 substituent group is substituted with one or more second substituent groups denoted by R 3A 2 as explained in the definitions section above in the description of “first substituent group(s)”.
  • R 3A 2 substituent group when an R 3A 2 substituent group is substituted, the R 3A 2 substituent group is substituted with one or more third substituent groups denoted by R 3A 3 as explained in the definitions section above in the description of “first substituent
  • R 3B when R 3B is substituted, R 3B is substituted with one or more first substituent groups denoted by R 3B 1 as explained in the definitions section above in the description of “first substituent group(s)”.
  • R 3B 1 substituent group when an R 3B 1 substituent group is substituted, the R 3B 1 substituent group is substituted with one or more second substituent groups denoted by R 3B 2 as explained in the definitions section above in the description of “first substituent group(s)”.
  • R 3B 2 substituent group when an R 3B 2 substituent group is substituted, the R 3B 2 substituent group is substituted with one or more third substituent groups denoted by R 3B 3 as explained in the definitions section above in the description of “first substituent
  • R 3A and R 3B substituents bonded to the same nitrogen atom are optionally joined to form a moiety that is substituted (e.g., a substituted heterocycloalkyl or substituted heteroaryl), the moiety is substituted with one or more first substituent groups denoted by R 3A 1 as explained in the definitions section above in the description of “first substituent group(s)”.
  • R 3A 1 substituent group when an R 3A 1 substituent group is substituted, the R 3A 1 substituent group is substituted with one or more second substituent groups denoted by R 3A 2 as explained in the definitions section above in the description of “first substituent group(s)”.
  • R 3A 2 substituent group when an R 3A 2 substituent group is substituted, the R 3A 2 substituent group is substituted with one or more third substituent groups denoted by R 3A 3 as explained in the definitions section above in the description of “first substituent group(s)”.
  • R 3A 1 , R 3A 2 , and R 3A 3 have values corresponding to the values of
  • R 3A and R 3B substituents bonded to the same nitrogen atom are optionally joined to form a moiety that is substituted (e.g., a substituted heterocycloalkyl or substituted heteroaryl), the moiety is substituted with one or more first substituent groups denoted by R 3B 1 as explained in the definitions section above in the description of “first substituent group(s)”.
  • R 3B 1 substituent group when an R 3B 1 substituent group is substituted, the R 3B 1 substituent group is substituted with one or more second substituent groups denoted by R 3B 2 as explained in the definitions section above in the description of “first substituent group(s)”.
  • R 3B 2 substituent group when an R 3B 2 substituent group is substituted, the R 3B 2 substituent group is substituted with one or more third substituent groups denoted by R 3B 3 as explained in the definitions section above in the description of “first substituent group(s)”.
  • R 3C when R 3C is substituted, R 3C is substituted with one or more first substituent groups denoted by R 3C 1 as explained in the definitions section above in the description of “first substituent group(s)”.
  • R 3C 1 substituent group when an R 3C 1 substituent group is substituted, the R 3C 1 substituent group is substituted with one or more second substituent groups denoted by R 3C 2 as explained in the definitions section above in the description of “first substituent group(s)”.
  • R 3C 2 substituent group when an R 3C 2 substituent group is substituted, the R 3C 2 substituent group is substituted with one or more third substituent groups denoted by R 3C 3 as explained in the definitions section above in the description of “first substituent
  • R 3D when R 3D is substituted, R 3D is substituted with one or more first substituent groups denoted by R 3D 1 as explained in the definitions section above in the description of “first substituent group(s)”.
  • R 3D 1 substituent group when an R 3D 1 substituent group is substituted, the R 3D 1 substituent group is substituted with one or more second substituent groups denoted by R 3D 2 as explained in the definitions section above in the description of “first substituent group(s)”.
  • R 3D 2 substituent group when an R 3D 2 substituent group is substituted, the R 3D 2 substituent group is substituted with one or more third substituent groups denoted by R 3D 3 as explained in the definitions section above in the description of “first substituent
  • R 4 when R 4 is substituted, R 4 is substituted with one or more first substituent groups denoted by R 4 1 as explained in the definitions section above in the description of “first substituent group(s)”.
  • R 4 1 substituent group when an R 4 1 substituent group is substituted, the R 4 1 substituent group is substituted with one or more second substituent groups denoted by R 4 2 as explained in the definitions section above in the description of “first substituent group(s)”.
  • R 4 2 substituent group when an R 4 2 substituent group is substituted, the R 4 2 substituent group is substituted with one or more third substituent groups denoted by
  • R 4A when R 4A is substituted, R 4A is substituted with one or more first substituent groups denoted by R 4A 1 as explained in the definitions section above in the description of “first substituent group(s)”.
  • R 4A 1 substituent group when an R 4A 1 substituent group is substituted, the R 4A 1 substituent group is substituted with one or more second substituent groups denoted by R 4A 2 as explained in the definitions section above in the description of “first substituent group(s)”.
  • R 4A 2 substituent group when an R 4A 2 substituent group is substituted, the R 4A 2 substituent group is substituted with one or more third substituent groups denoted by R 4A 3 as explained in the definitions section above in the description of “first substituent
  • R 4B when R 4B is substituted, R 4B is substituted with one or more first substituent groups denoted by R 4B 1 as explained in the definitions section above in the description of “first substituent group(s)”.
  • R 4B 1 substituent group when an R 4B 1 substituent group is substituted, the R 4B 1 substituent group is substituted with one or more second substituent groups denoted by R 4B 2 as explained in the definitions section above in the description of “first substituent group(s)”.
  • R 4B 2 substituent group when an R 4B 2 substituent group is substituted, the R 4B 2 substituent group is substituted with one or more third substituent groups denoted by R 4B 3 as explained in the definitions section above in the description of “first substituent
  • R 4A and R 4B substituents bonded to the same nitrogen atom are optionally joined to form a moiety that is substituted (e.g., a substituted heterocycloalkyl or substituted heteroaryl), the moiety is substituted with one or more first substituent groups denoted by R 4A 1 as explained in the definitions section above in the description of “first substituent group(s)”.
  • R 4A 1 substituent group when an R 4A 1 substituent group is substituted, the R 4A 1 substituent group is substituted with one or more second substituent groups denoted by R 4A 2 as explained in the definitions section above in the description of “first substituent group(s)”.
  • R 4A 2 substituent group when an R 4A 2 substituent group is substituted, the R 4A 2 substituent group is substituted with one or more third substituent groups denoted by R 4A 3 as explained in the definitions section above in the description of “first substituent group(s)”.
  • R 4A and R 4B substituents bonded to the same nitrogen atom are optionally joined to form a moiety that is substituted (e.g., a substituted heterocycloalkyl or substituted heteroaryl), the moiety is substituted with one or more first substituent groups denoted by R 4B 1 as explained in the definitions section above in the description of “first substituent group(s)”.
  • R 4B 1 substituent group when an R 4B 1 substituent group is substituted, the R 4B 1 substituent group is substituted with one or more second substituent groups denoted by R 4B 2 as explained in the definitions section above in the description of “first substituent group(s)”.
  • R 4B 2 substituent group when an R 4B 2 substituent group is substituted, the R 4B 2 substituent group is substituted with one or more third substituent groups denoted by R 4B 3 as explained in the definitions section above in the description of “first substituent group(s)”.
  • R 4C when R 4C is substituted, R 4C is substituted with one or more first substituent groups denoted by R 4C 1 as explained in the definitions section above in the description of “first substituent group(s)”.
  • R 4C 1 substituent group when an R 4C 1 substituent group is substituted, the R 4C 1 substituent group is substituted with one or more second substituent groups denoted by R 4C 2 as explained in the definitions section above in the description of “first substituent group(s)”.
  • R 4C 2 substituent group when an R 4C 2 substituent group is substituted, the R 4C 2 substituent group is substituted with one or more third substituent groups denoted by
  • R 4D when R 4D is substituted, R 4D is substituted with one or more first substituent groups denoted by R 4D 1 as explained in the definitions section above in the description of “first substituent group(s)”.
  • R 4D 1 substituent group when an R 4D 1 substituent group is substituted, the R 4D 1 substituent group is substituted with one or more second substituent groups denoted by R 4D 2 as explained in the definitions section above in the description of “first substituent group(s)”.
  • R 4D 2 substituent group when an R 4D 2 substituent group is substituted, the R 4D 2 substituent group is substituted with one or more third substituent groups denoted by section above in the description of “first substituent group(s)”, wherein R ww , R ww - 1 , R WW 2 , and R ww 3 correspond to R 4D , R 4D 1 , R 4D 2 , and R 4D 3 , respectively.
  • R 5 when R 5 is substituted, R 5 is substituted with one or more first substituent groups denoted by R 5 1 as explained in the definitions section above in the description of “first substituent group(s)”.
  • R 5 1 substituent group when an R 5 1 substituent group is substituted, the R 5 1 substituent group is substituted with one or more second substituent groups denoted by R 5 2 as explained in the definitions section above in the description of “first substituent group(s)”.
  • R 5 2 substituent group when an R 5 2 substituent group is substituted, the R 5 2 substituent group is substituted with one or more third substituent groups denoted by R 5 3 as explained in the definitions section above in the description of “first substituent
  • R 5A when R 5A is substituted, R 5A is substituted with one or more first substituent groups denoted by R 5A 1 as explained in the definitions section above in the description of “first substituent group(s)”.
  • R 5A 1 substituent group when an R 5A 1 substituent group is substituted, the R 5A 1 substituent group is substituted with one or more second substituent groups denoted by R 5A 2 as explained in the definitions section above in the description of “first substituent group(s)”.
  • R 5A 2 substituent group when an R 5A 2 substituent group is substituted, the R 5A 2 substituent group is substituted with one or more third substituent groups denoted by R 5A 3 as explained in the definitions section above in the description of “first substituent
  • R 5B when R 5B is substituted, R 5B is substituted with one or more first substituent groups denoted by R 5B 1 as explained in the definitions section above in the description of “first substituent group(s)”. In embodiments, when an R 5B 1 substituent group is substituted, the R 5B 1 substituent group is substituted with one or more second substituent groups denoted by R 5B 2 as explained in the definitions section above in the description of “first substituent group(s)”. In embodiments, when an R 5B 2 substituent group is substituted, the R 5B 2 substituent group is substituted with one or more third substituent groups denoted by R 5B 3 as explained in the definitions section above in the description of “first substituent group(s)”.
  • R 5B , R 5B 1 , R 5B 2 , and R 5B 3 have values corresponding to the values of R ww , R ww - 1 , R WW 2 , and R WW 3 , respectively, as explained in the definitions section above in the description of “first substituent group(s)”, wherein R ww , R ww - 1 , R WW 2 , and R ww 3 correspond to R 5B , R 5B 1 , R 5B 2 , and R 5B 3 , respectively.
  • R 5A and R 5B substituents bonded to the same nitrogen atom are optionally joined to form a moiety that is substituted (e.g., a substituted heterocycloalkyl or substituted heteroaryl), the moiety is substituted with one or more first substituent groups denoted by R 5A 1 as explained in the definitions section above in the description of “first substituent group(s)”.
  • R 5A 1 substituent group when an R 5A 1 substituent group is substituted, the R 5A 1 substituent group is substituted with one or more second substituent groups denoted by R 5A 2 as explained in the definitions section above in the description of “first substituent group(s)”.
  • R 5A 2 substituent group when an R 5A 2 substituent group is substituted, the R 5A 2 substituent group is substituted with one or more third substituent groups denoted by R 5A 3 as explained in the definitions section above in the description of “first substituent group(s)”.
  • R 5A and R 5B substituents bonded to the same nitrogen atom are optionally joined to form a moiety that is substituted (e.g., a substituted heterocycloalkyl or substituted heteroaryl), the moiety is substituted with one or more first substituent groups denoted by R 5B 1 as explained in the definitions section above in the description of “first substituent group(s)”.
  • R 5B 1 substituent group when an R 5B 1 substituent group is substituted, the R 5B 1 substituent group is substituted with one or more second substituent groups denoted by R 5B 2 as explained in the definitions section above in the description of “first substituent group(s)”.
  • R 5B 2 substituent group when an R 5B 2 substituent group is substituted, the R 5B 2 substituent group is substituted with one or more third substituent groups denoted by R 5B 3 as explained in the definitions section above in the description of “first substituent group(s)”.
  • first substituent group(s) wherein R ww - 1 , R WW 2 , and R WW 3 correspond to R 5B 1 , R 5B 2 , and R 5B 3 , respectively.
  • R 5C when R 5C is substituted, R 5C is substituted with one or more first substituent groups denoted by R 5C 1 as explained in the definitions section above in the description of “first substituent group(s)”.
  • R 5C 1 substituent group when an R 5C 1 substituent group is substituted, the R 5C 1 substituent group is substituted with one or more second substituent groups denoted by R 5C 2 as explained in the definitions section above in the description of “first substituent group(s)”.
  • R 5C 2 substituent group when an R 5C 2 substituent group is substituted, the R 5C 2 substituent group is substituted with one or more third substituent groups denoted by
  • R 5D when R 5D is substituted, R 5D is substituted with one or more first substituent groups denoted by R 5D 1 as explained in the definitions section above in the description of “first substituent group(s)”.
  • R 5D 1 substituent group when an R 5D 1 substituent group is substituted, the R 5D 1 substituent group is substituted with one or more second substituent groups denoted by R 5D 2 as explained in the definitions section above in the description of “first substituent group(s)”.
  • R 5D 2 substituent group when an R 5D 2 substituent group is substituted, the R 5D 2 substituent group is substituted with one or more third substituent groups denoted by R 5D 3 as explained in the definitions section above in the description of “first substituent group(s)”.
  • R 5D , R 5D 1 , R 5D 2 , and R 5D 3 have values corresponding
  • R 6 when R 6 is substituted, R 6 is substituted with one or more first substituent groups denoted by R 6 1 as explained in the definitions section above in the description of “first substituent group(s)”. In embodiments, when an R 6 1 substituent group is substituted, the R 6 1 substituent group is substituted with one or more second substituent groups denoted by R 6 2 as explained in the definitions section above in the description of “first substituent group(s)”. In embodiments, when an R 6 2 substituent group is substituted, the R 6 2 substituent group is substituted with one or more third substituent groups denoted by R 6 3 as explained in the definitions section above in the description of “first substituent group(s)”. In the above embodiments, R 6 , R 6 1 , R 62 , and R 6 3 have values corresponding to
  • R 6A when R 6A is substituted, R 6A is substituted with one or more first substituent groups denoted by R 6A 1 as explained in the definitions section above in the description of “first substituent group(s)”.
  • R 6A 1 substituent group when an R 6A 1 substituent group is substituted, the R 6A 1 substituent group is substituted with one or more second substituent groups denoted by R 6A 2 as explained in the definitions section above in the description of “first substituent group(s)”.
  • R 6A 2 substituent group when an R 6A 2 substituent group is substituted, the R 6A 2 substituent group is substituted with one or more third substituent groups denoted by R 6A 3 as explained in the definitions section above in the description of “first substituent
  • R 6B when R 6B is substituted, R 6B is substituted with one or more first substituent groups denoted by R 6B 1 as explained in the definitions section above in the description of “first substituent group(s)”.
  • R 6B 1 substituent group when an R 6B 1 substituent group is substituted, the R 6B 1 substituent group is substituted with one or more second substituent groups denoted by R 6B 2 as explained in the definitions section above in the description of “first substituent group(s)”.
  • R 6B 2 substituent group when an R 6B 2 substituent group is substituted, the R 6B 2 substituent group is substituted with one or more third substituent groups denoted by R 6B 3 as explained in the definitions section above in the description of “first substituent
  • R 6A and R 6B substituents bonded to the same nitrogen atom are optionally joined to form a moiety that is substituted (e.g., a substituted heterocycloalkyl or substituted heteroaryl), the moiety is substituted with one or more first substituent groups denoted by R 6A 1 as explained in the definitions section above in the description of “first substituent group(s)”.
  • R 6A 1 substituent group when an R 6A 1 substituent group is substituted, the R 6A 1 substituent group is substituted with one or more second substituent groups denoted by R 6A 2 as explained in the definitions section above in the description of “first substituent group(s)”.
  • R 6A 2 substituent group when an R 6A 2 substituent group is substituted, the R 6A 2 substituent group is substituted with one or more third substituent groups denoted by R 6A 3 as explained in the definitions section above in the description of “first substituent group(s)”.
  • R 6A 1 , R 6A 2 , and R 6A 3 have values corresponding to the values of
  • R 6A and R 6B substituents bonded to the same nitrogen atom are optionally joined to form a moiety that is substituted (e.g., a substituted heterocycloalkyl or substituted heteroaryl), the moiety is substituted with one or more first substituent groups denoted by R 6B 1 as explained in the definitions section above in the description of “first substituent group(s)”.
  • R 6B 1 substituent group when an R 6B 1 substituent group is substituted, the R 6B 1 substituent group is substituted with one or more second substituent groups denoted by R 6B 2 as explained in the definitions section above in the description of “first substituent group(s)”.
  • R 6B 2 substituent group when an R 6B 2 substituent group is substituted, the R 6B 2 substituent group is substituted with one or more third substituent groups denoted by R 6B 3 as explained in the definitions section above in the description of “first substituent group(s)”.
  • R 6B 1 , R 6B 2 , and R 6B 3 have values corresponding to the values of
  • R 6C when R 6C is substituted, R 6C is substituted with one or more first substituent groups denoted by R 6C 1 as explained in the definitions section above in the description of “first substituent group(s)”. In embodiments, when an R 6C 1 substituent group is substituted, the R 6C 1 substituent group is substituted with one or more second substituent groups denoted by R 6C 2 as explained in the definitions section above in the description of “first substituent group(s)”. In embodiments, when an R 6C 2 substituent group is substituted, the R 6C 2 substituent group is substituted with one or more third substituent groups denoted by R 6C 3 as explained in the definitions section above in the description of “first substituent group(s)”.
  • R 6C , R 6C 1 , R 6C 2 , and R 6C 3 have values corresponding to the values of R ww , R ww - 1 , R WW 2 , and R WW 3 , respectively, as explained in the definitions section above in the description of “first substituent group(s)”, wherein R ww , R ww - 1 , R WW 2 , and R ww 3 correspond to R 6C , R 6C 1 , R 6C 2 , and R 6C 3 , respectively.
  • R 6D when R 6D is substituted, R 6D is substituted with one or more first substituent groups denoted by R 6D 1 as explained in the definitions section above in the description of “first substituent group(s)”.
  • R 6D 1 substituent group when an R 6D 1 substituent group is substituted, the R 6D 1 substituent group is substituted with one or more second substituent groups denoted by R 6D 2 as explained in the definitions section above in the description of “first substituent group(s)”.
  • R 6D 2 substituent group when an R 6D 2 substituent group is substituted, the R 6D 2 substituent group is substituted with one or more third substituent groups denoted by R 6D 3 as explained in the definitions section above in the description of “first substituent group(s)”.
  • R 6D , R 6D 1 , R 6D 2 , and R 6D 3 have values corresponding
  • R 7 when R 7 is substituted, R 7 is substituted with one or more first substituent groups denoted by R 7 1 as explained in the definitions section above in the description of “first substituent group(s)”.
  • R 7 1 substituent group when an R 7 1 substituent group is substituted, the R 7 1 substituent group is substituted with one or more second substituent groups denoted by R 7 2 as explained in the definitions section above in the description of “first substituent group(s)”.
  • R 7 2 substituent group when an R 7 2 substituent group is substituted, the R 7 2 substituent group is substituted with one or more third substituent groups denoted by R 7 3 as explained in the definitions section above in the description of “first substituent
  • R 7A when R 7A is substituted, R 7A is substituted with one or more first substituent groups denoted by R 7A 1 as explained in the definitions section above in the description of “first substituent group(s)”.
  • R 7A 1 substituent group when an R 7A 1 substituent group is substituted, the R 7A 1 substituent group is substituted with one or more second substituent groups denoted by R 7A 2 as explained in the definitions section above in the description of “first substituent group(s)”.
  • R 7A 2 substituent group when an R 7A 2 substituent group is substituted, the R 7A 2 substituent group is substituted with one or more third substituent groups denoted by R 7A 3 as explained in the definitions section above in the description of “first substituent
  • R 7B when R 7B is substituted, R 7B is substituted with one or more first substituent groups denoted by R 7B 1 as explained in the definitions section above in the description of “first substituent group(s)”.
  • R 7B 1 substituent group when an R 7B 1 substituent group is substituted, the R 7B 1 substituent group is substituted with one or more second substituent groups denoted by R 7B 2 as explained in the definitions section above in the description of “first substituent group(s)”.
  • R 7B 2 substituent group when an R 7B 2 substituent group is substituted, the R 7B 2 substituent group is substituted with one or more third substituent groups denoted by R 7B 3 as explained in the definitions section above in the description of “first substituent group(s)”.
  • R 7B , R 7B 1 , R 7B 2 , and R 7B 3 have values corresponding
  • R 7A and R 7B substituents bonded to the same nitrogen atom are optionally joined to form a moiety that is substituted (e.g., a substituted heterocycloalkyl or substituted heteroaryl), the moiety is substituted with one or more first substituent groups denoted by R 7A 1 as explained in the definitions section above in the description of “first substituent group(s)”.
  • R 7A 1 substituent group when an R 7A 1 substituent group is substituted, the R 7A 1 substituent group is substituted with one or more second substituent groups denoted by R 7A 2 as explained in the definitions section above in the description of “first substituent group(s)”.
  • R 7A 2 substituent group when an R 7A 2 substituent group is substituted, the R 7A 2 substituent group is substituted with one or more third substituent groups denoted by R 7A 3 as explained in the definitions section above in the description of “first substituent group(s)”.
  • R 7A and R 7B substituents bonded to the same nitrogen atom are optionally joined to form a moiety that is substituted (e.g., a substituted heterocycloalkyl or substituted heteroaryl), the moiety is substituted with one or more first substituent groups denoted by R 7B 1 as explained in the definitions section above in the description of “first substituent group(s)”.
  • R 7B 1 substituent group when an R 7B 1 substituent group is substituted, the R 7B 1 substituent group is substituted with one or more second substituent groups denoted by R 7B 2 as explained in the definitions section above in the description of “first substituent group(s)”.
  • R 7B 2 substituent group when an R 7B 2 substituent group is substituted, the R 7B 2 substituent group is substituted with one or more third substituent groups denoted by R 7B 3 as explained in the definitions section above in the description of “first substituent group(s)”.
  • R 7B 1 , R 7B 2 , and R 7B 3 have values corresponding to the values of
  • R 7C when R 7C is substituted, R 7C is substituted with one or more first substituent groups denoted by R 7C 1 as explained in the definitions section above in the description of “first substituent group(s)”.
  • R 7C 1 substituent group when an R 7C 1 substituent group is substituted, the R 7C 1 substituent group is substituted with one or more second substituent groups denoted by R 7C 2 as explained in the definitions section above in the description of “first substituent group(s)”.
  • R 7C 2 substituent group when an R 7C 2 substituent group is substituted, the R 7C 2 substituent group is substituted with one or more third substituent groups denoted by R 7C 3 as explained in the definitions section above in the description of “first substituent
  • R 7D when R 7D is substituted, R 7D is substituted with one or more first substituent groups denoted by R 7D 1 as explained in the definitions section above in the description of “first substituent group(s)”.
  • R 7D 1 substituent group when an R 7D 1 substituent group is substituted, the R 7D 1 substituent group is substituted with one or more second substituent groups denoted by R 7D 2 as explained in the definitions section above in the description of “first substituent group(s)”.
  • R 7D 2 substituent group when an R 7D 2 substituent group is substituted, the R 7D 2 substituent group is substituted with one or more third substituent groups denoted by R 7D 3 as explained in the definitions section above in the description of “first substituent group(s)”.
  • R 7D , R 7D 1 , R 7D 2 , and R 7D 3 have values corresponding
  • R 8 when R 8 is substituted, R 8 is substituted with one or more first substituent groups denoted by R 8 1 as explained in the definitions section above in the description of “first substituent group(s)”. In embodiments, when an R 8 1 substituent group is substituted, the R 8 1 substituent group is substituted with one or more second substituent groups denoted by R 8 2 as explained in the definitions section above in the description of “first substituent group(s)”. In embodiments, when an R 8 2 substituent group is substituted, the R 8 2 substituent group is substituted with one or more third substituent groups denoted by R 8 3 as explained in the definitions section above in the description of “first substituent
  • R 8A when R 8A is substituted, R 8A is substituted with one or more first substituent groups denoted by R 8A 1 as explained in the definitions section above in the description of “first substituent group(s)”.
  • R 8A 1 substituent group when an R 8A 1 substituent group is substituted, the R 8A 1 substituent group is substituted with one or more second substituent groups denoted by R 8A 2 as explained in the definitions section above in the description of “first substituent group(s)”.
  • R 8A 2 substituent group when an R 8A 2 substituent group is substituted, the R 8A 2 substituent group is substituted with one or more third substituent groups denoted by R 8A 3 as explained in the definitions section above in the description of “first substituent
  • R 8B when R 8B is substituted, R 8B is substituted with one or more first substituent groups denoted by R 8B 1 as explained in the definitions section above in the description of “first substituent group(s)”.
  • R 8B 1 substituent group when an R 8B 1 substituent group is substituted, the R 8B 1 substituent group is substituted with one or more second substituent groups denoted by R 8B 2 as explained in the definitions section above in the description of “first substituent group(s)”.
  • R 8B 2 substituent group when an R 8B 2 substituent group is substituted, the R 8B 2 substituent group is substituted with one or more third substituent groups denoted by R 8B 3 as explained in the definitions section above in the description of “first substituent
  • R 8A and R 8B substituents bonded to the same nitrogen atom are optionally joined to form a moiety that is substituted (e.g., a substituted heterocycloalkyl or substituted heteroaryl), the moiety is substituted with one or more first substituent groups denoted by R 8A 1 as explained in the definitions section above in the description of “first substituent group(s)”.
  • R 8A 1 substituent group when an R 8A 1 substituent group is substituted, the R 8A 1 substituent group is substituted with one or more second substituent groups denoted by R 8A 2 as explained in the definitions section above in the description of “first substituent group(s)”.
  • R 8A 2 substituent group when an R 8A 2 substituent group is substituted, the R 8A 2 substituent group is substituted with one or more third substituent groups denoted by R 8A 3 as explained in the definitions section above in the description of “first substituent group(s)”.
  • R 8A and R 8B substituents bonded to the same nitrogen atom are optionally joined to form a moiety that is substituted (e.g., a substituted heterocycloalkyl or substituted heteroaryl), the moiety is substituted with one or more first substituent groups denoted by R 8B 1 as explained in the definitions section above in the description of “first substituent group(s)”.
  • R 8B 1 substituent group when an R 8B 1 substituent group is substituted, the R 8B 1 substituent group is substituted with one or more second substituent groups denoted by R 8B 2 as explained in the definitions section above in the description of “first substituent group(s)”.
  • R 8B 2 substituent group when an R 8B 2 substituent group is substituted, the R 8B 2 substituent group is substituted with one or more third substituent groups denoted by R 8B 3 as explained in the definitions section above in the description of “first substituent group(s)”.
  • R 8C when R 8C is substituted, R 8C is substituted with one or more first substituent groups denoted by R 8C 1 as explained in the definitions section above in the description of “first substituent group(s)”.
  • R 8C 1 substituent group when an R 8C 1 substituent group is substituted, the R 8C 1 substituent group is substituted with one or more second substituent groups denoted by R 8C 2 as explained in the definitions section above in the description of “first substituent group(s)”.
  • R 8C 2 substituent group when an R 8C 2 substituent group is substituted, the R 8C 2 substituent group is substituted with one or more third substituent groups denoted by R 8C 3 as explained in the definitions section above in the description of “first substituent
  • R 8D when R 8D is substituted, R 8D is substituted with one or more first substituent groups denoted by R 8D 1 as explained in the definitions section above in the description of “first substituent group(s)”. In embodiments, when an R 8D 1 substituent group is substituted, the R 8D 1 substituent group is substituted with one or more second substituent groups denoted by R 8D 2 as explained in the definitions section above in the description of “first substituent group(s)”.
  • R 8D 2 substituent group when an R 8D 2 substituent group is substituted, the R 8D 2 substituent group is substituted with one or more third substituent groups denoted by R 8D 3 as explained in the definitions section above in the description of “first substituent section above in the description of “first substituent group(s)”, wherein R ww , R ww - 1 , R WW 2 , and R ww 3 correspond to R 8D , R 8D 1 , R 8D 2 , and R 8D 3 , respectively.
  • R 8.1 when R 8.1 is substituted, R 8.1 is substituted with one or more first substituent groups denoted by R 8.1 1 as explained in the definitions section above in the description of “first substituent group(s)”.
  • R 8.1 1 substituent group when an R 8.1 1 substituent group is substituted, the R 8.1 1 substituent group is substituted with one or more second substituent groups denoted by R 8.12 as explained in the definitions section above in the description of “first substituent group(s)”.
  • R 8.12 substituent group when an R 8.12 substituent group is substituted, the R 8.12 substituent group is substituted with one or more third substituent groups denoted by R 8.13 as explained in the definitions section above in the description of “first substituent group(s)”.
  • R 8.1 , R 8.1 1 , R 8.12 , and R 8.13 have values corresponding to the values of R ww , R WW 1 , reS p ec i V ely, as explained in the definitions section above in the description of “first substituent group(s)”, wherein R ww , R ww - 1 , R WW 2 , and R ww 3 correspond to R 8.1 R 8.11 , R 8.12 , and R 8.13 , respectively.
  • R 8.2 when R 8.2 is substituted, R 82 is substituted with one or more first substituent groups denoted by R 8.2 1 as explained in the definitions section above in the description of “first substituent group(s)”.
  • R 8.2 1 substituent group when an R 8.2 1 substituent group is substituted, the R 8.21 substituent group is substituted with one or more second substituent groups denoted by R 8.22 as explained in the definitions section above in the description of “first substituent group(s)”.
  • R 8.22 substituent group when an R 8.22 substituent group is substituted, the R 8.22 substituent group is substituted with one or more third substituent groups denoted by R 8.23 as explained in the definitions section above in the description of “first substituent group(s)”.
  • R 82 , R 82 1 , R 82 2 , and R 8.23 have values corresponding to the values of R ww , R WW 1 , reS p ec i V ely, as explained in the definitions section above in the description of “first substituent group(s)”, wherein R ww , R ww - 1 , R WW 2 , and R ww 3 correspond to R 8.2 , R 82 1 , R 82 2 , and R 8.23 , respectively.
  • R 8.3 when R 8.3 is substituted, R 8.3 is substituted with one or more first substituent groups denoted by R 8.3 1 as explained in the definitions section above in the description of “first substituent group(s)”.
  • R 8.3 1 substituent group when an R 8.3 1 substituent group is substituted, the R 8.3 1 substituent group is substituted with one or more second substituent groups denoted by R 8.32 as explained in the definitions section above in the description of “first substituent group(s)”.
  • R 8.32 substituent group when an R 8.32 substituent group is substituted, the R 8.32 substituent group is substituted with one or more third substituent groups denoted by R 8.33 as explained in the definitions section above in the description of “first substituent group(s)”.
  • R 8.3 , R 8.3 1 , R 8.32 , and R 8.33 have values corresponding to the values of R ww , R ww - 1 , R WW 2 , and R WW 3 , respectively, as explained in the definitions section above in the description of “first substituent group(s)”, wherein R ww , R ww - 1 , R WW 2 , and R ww 3 correspond to R 8.3 , R 8.3 1 , R 8.32 , and R 8.33 , respectively.
  • R 8.2 and R 8.3 substituents are optionally joined to form a moiety that is substituted (e.g., a substituted cycloalkyl, substituted heterocycloalkyl, substituted aryl, or substituted heteroaryl), the moiety is substituted with one or more first substituent groups denoted by R 8.2 1 as explained in the definitions section above in the description of “first substituent group(s)”.
  • R 8.2 1 substituent group when an R 8.2 1 substituent group is substituted, the R 8.2 1 substituent group is substituted with one or more second substituent groups denoted by R 8.22 as explained in the definitions section above in the description of “first substituent group(s)”.
  • R 8.22 substituent group when an R 8.22 substituent group is substituted, the R 8.22 substituent group is substituted with one or more third substituent groups denoted by R 8.23 as explained in the definitions section above in the description of “first substituent group(s)”.
  • R 82 1 , R 8.22 , and R 8.23 have values corresponding to the values of R ww - 1 , R ww - 2 , respectively, as explained in the definitions section above in the description of “first substituent group(s)”, wherein R ww - 1 , R WW 2 , and R WW 3 correspond to R 82 1 , R 8.22 , and R 8.23 , respectively.
  • R 8.2 and R 8.3 substituents are optionally joined to form a moiety that is substituted (e.g., a substituted cycloalkyl, substituted heterocycloalkyl, substituted aryl, or substituted heteroaryl), the moiety is substituted with one or more first substituent groups denoted by R 8.3 1 as explained in the definitions section above in the description of “first substituent group(s)”.
  • R 8.3 1 substituent group when an R 8.3 1 substituent group is substituted, the R 8.3 1 substituent group is substituted with one or more second substituent groups denoted by R 8.32 as explained in the definitions section above in the description of “first substituent group(s)”.
  • R 8.32 substituent group when an R 8.32 substituent group is substituted, the R 8.32 substituent group is substituted with one or more third substituent groups denoted by R 8.33 as explained in the definitions section above in the description of “first substituent group(s)”.
  • R 83 1 , R 8.32 , and R 8.3 3 have values corresponding to the values of R ww - 1 , R ww - 2 , anc
  • R 9 when R 9 is substituted, R 9 is substituted with one or more first substituent groups denoted by R 9 1 as explained in the definitions section above in the description of “first substituent group(s)”. In embodiments, when an R 9 1 substituent group is substituted, the R 9 1 substituent group is substituted with one or more second substituent groups denoted by R 9 2 as explained in the definitions section above in the description of “first substituent group(s)”. In embodiments, when an R 9 2 substituent group is substituted, the R 9 2 substituent group is substituted with one or more third substituent groups denoted by R 9 3 as explained in the definitions section above in the description of “first substituent group(s)”.
  • R 9 , R 9 1 , R 92 , and R 9 3 have values corresponding to the values of R ww , R WW 1 , R ww - 2 , respectively, as explained in the definitions section above in the description of “first substituent group(s)”, wherein R ww , R ww - 1 , R WW 2 , and R ww 3 correspond to R 9 , R 9 1 , R 9 2 , and R 9 3 , respectively.
  • R 10 when R 10 is substituted, R 10 is substituted with one or more first substituent groups denoted by R 10 1 as explained in the definitions section above in the description of “first substituent group(s)”. In embodiments, when an R 10 1 substituent group is substituted, the R 10 1 substituent group is substituted with one or more second substituent groups denoted by R 10 2 as explained in the definitions section above in the description of “first substituent group(s)”. In embodiments, when an R 10 2 substituent group is substituted, the R 10 2 substituent group is substituted with one or more third substituent groups denoted by R 10 3 as explained in the definitions section above in the description of “first substituent group(s)”.
  • R 10 , R 10 1 , R 102 , and R 10 3 have values corresponding to the values of R ww , R WW 1 , reS p ec i V ely, as explained in the definitions section above in the description of “first substituent group(s)”, wherein R ww , R ww - 1 , R WW 2 , and R ww 3 correspond to R 10 , R 10 1 , R 102 , and R 10 3 , respectively.
  • R 10A when R 10A is substituted, R 10A is substituted with one or more first substituent groups denoted by R 10A 1 as explained in the definitions section above in the description of “first substituent group(s)”. In embodiments, when an R 10A 1 substituent group is substituted, the R 10A 1 substituent group is substituted with one or more second substituent groups denoted by R 10A 2 as explained in the definitions section above in the description of “first substituent group(s)”. In embodiments, when an R 10A 2 substituent group is substituted, the R 10A 2 substituent group is substituted with one or more third substituent groups denoted by R 10A 3 as explained in the definitions section above in the description of “first substituent group(s)”.
  • R 10A , R 10A 1 , R 10A 2 , and R 10A 3 have values corresponding to the values of R ww , R ww - 1 , R WW 2 , and R WW 3 , respectively, as explained in the definitions section above in the description of “first substituent group(s)”, wherein R ww , R WW 1 , RWW.2, an j j ⁇ ww.3 correS p Onc
  • R 10B when R 10B is substituted, R 10B is substituted with one or more first substituent groups denoted by R 10B 1 as explained in the definitions section above in the description of “first substituent group(s)”.
  • R 10B 1 substituent group when an R 10B 1 substituent group is substituted, the R 10B 1 substituent group is substituted with one or more second substituent groups denoted by R 10B 2 as explained in the definitions section above in the description of “first substituent group(s)”.
  • R 10B 2 substituent group when an R 10B 2 substituent group is substituted, the R 10B 2 substituent group is substituted with one or more third substituent groups denoted by R 10B 3 as explained in the definitions section above in the description of “first substituent group(s)”.
  • R 10B , R 10B 1 , R 10B 2 , and R 10B 3 have values corresponding to the values of R ww , R WW 1 , R W2 and R WW 3 , respectively, as explained in the definitions section above in the description of “first substituent group(s)”, wherein R ww , R WW 1 , RWW.2, an j j ⁇ ww.3 correS p Onc
  • R 10A and R 10B substituents bonded to the same nitrogen atom are optionally joined to form a moiety that is substituted (e.g., a substituted heterocycloalkyl or substituted heteroaryl), the moiety is substituted with one or more first substituent groups denoted by R 10A 1 as explained in the definitions section above in the description of “first substituent group(s)”.
  • R 10A 1 substituent group when an R 10A 1 substituent group is substituted, the R 10A 1 substituent group is substituted with one or more second substituent groups denoted by R 10A 2 as explained in the definitions section above in the description of “first substituent group(s)”.
  • R 10A 1 , R 10A 2 , and R 10A 3 have values corresponding to the values of R WW 1 , reS p e ctively, as explained in the definitions section above in the description of “first substituent group(s)”, wherein R WW 1 , R ww - 2 , anc j pww.3 correspond to R 10A 1 , R 10A 2 , and R 10A 3 , respectively.
  • R 10A and R 10B substituents bonded to the same nitrogen atom are optionally joined to form a moiety that is substituted (e.g., a substituted heterocycloalkyl or substituted heteroaryl), the moiety is substituted with one or more first substituent groups denoted by R 10B 1 as explained in the definitions section above in the description of “first substituent group(s)”.
  • R 10B 1 substituent group when an R 10B 1 substituent group is substituted, the RIOE.I su b s ptuent group is substituted with one or more second substituent groups denoted by R 10B 2 as explained in the definitions section above in the description of “first substituent group(s)”.
  • R 10B 2 substituent group when an R 10B 2 substituent group is substituted, the R 10B 2 substituent group is substituted with one or more third substituent groups denoted by R 10B 3 as explained in the definitions section above in the description of “first substituent group(s)”.
  • R 10B 1 , R 10B 2 , and R 10B 3 have values corresponding to the values of R ww R WW.2, an j R ww.3, reS p ec ively, as explained in the definitions section above in the description of “first substituent group(s)”, wherein R WW 1 , R ww - 2 , an j R ww.3 correS p O nd to RIOB.I, R I° B 2 , ANC
  • R 10C when R 10C is substituted, R 10C is substituted with one or more first substituent groups denoted by R 10C 1 as explained in the definitions section above in the description of “first substituent group(s)”.
  • R 10C 1 substituent group when an R 10C 1 substituent group is substituted, the R 10C 1 substituent group is substituted with one or more second substituent groups denoted by R 10C 2 as explained in the definitions section above in the description of “first substituent group(s)”.
  • R 10C 2 substituent group when an R 10C 2 substituent group is substituted, the R 10C 2 substituent group is substituted with one or more third substituent groups denoted by R 10C 3 as explained in the definitions section above in the description of “first substituent group(s)”.
  • R 10C , R 10C 1 , R 10C 2 , and R 10C 3 have values corresponding to the values of R ww , R WW 1 , R W2 and R WW 3 , respectively, as explained in the definitions section above in the description of “first substituent group(s)”, wherein R ww , R ww i ; R WW.2, an j R WW.3 correS p Onc
  • R 10D when R 10D is substituted, R 10D is substituted with one or more first substituent groups denoted by R 10D 1 as explained in the definitions section above in the description of “first substituent group(s)”.
  • R 10D 1 substituent group when an R 10D 1 substituent group is substituted, the R 10D 1 substituent group is substituted with one or more second substituent groups denoted by R 10D 2 as explained in the definitions section above in the description of “first substituent group(s)”.
  • R 10D 2 substituent group when an R 10D 2 substituent group is substituted, the R 10D 2 substituent group is substituted with one or more third substituent groups denoted by R 10D 3 as explained in the definitions section above in the description of “first substituent group(s)”.
  • R 10D , R 10D 1 , R 10D 2 , and R 10D 3 have values corresponding to the values of R ww , R ww - 1 , R WW 2 , and R WW 3 , respectively, as explained in the definitions section above in the description of “first substituent group(s)”, wherein R ww , R WW 1 , RWW.2, an j j ⁇ ww.3 correS p Onc
  • R 11 when R 11 is substituted, R 11 is substituted with one or more first substituent groups denoted by R 1U as explained in the definitions section above in the description of “first substituent group(s)”. In embodiments, when an R 11 1 substituent group is substituted, the R 11 1 substituent group is substituted with one or more second substituent groups denoted by R 11 2 as explained in the definitions section above in the description of “first substituent group(s)”. In embodiments, when an R 11 2 substituent group is substituted, the R 11 2 substituent group is substituted with one or more third substituent groups denoted by R 11 3 as explained in the definitions section above in the description of “first substituent group(s)”.
  • R 11 , R 11 1 , R 11 2 , and R 11 3 have values corresponding to the values of R ww , R WW 1 , respectively, as explained in the definitions section above in the description of “first substituent group(s)”, wherein R ww , R ww - 1 , R WW 2 , and R ww 3 correspond to R 11 , R 11 1 , R 11 2 , and R 11 3 , respectively.
  • R 11A when R 11A is substituted, R 11A is substituted with one or more first substituent groups denoted by R 11A 1 as explained in the definitions section above in the description of “first substituent group(s)”. In embodiments, when an R 11A 1 substituent group is substituted, the R 11A 1 substituent group is substituted with one or more second substituent groups denoted by R 11A 2 as explained in the definitions section above in the description of “first substituent group(s)”. In embodiments, when an R 11A 2 substituent group is substituted, the R 11A 2 substituent group is substituted with one or more third substituent groups denoted by R 11A 3 as explained in the definitions section above in the description of “first substituent group(s)”.
  • R 11A , R 11A 1 , R 11A 2 , and R 11A 3 have values corresponding to the values of R ww , R WW 1 , R W2 and R WW 3 , respectively, as explained in the definitions section above in the description of “first substituent group(s)”, wherein R ww , R WW 1 , RWW.2, an j j ⁇ ww.3 correS p Onc
  • R 11B when R 11B is substituted, R 11B is substituted with one or more first substituent groups denoted by R 11B 1 as explained in the definitions section above in the description of “first substituent group(s)”. In embodiments, when an R 11B 1 substituent group is substituted, the R 11B 1 substituent group is substituted with one or more second substituent groups denoted by R 11B 2 as explained in the definitions section above in the description of “first substituent group(s)”. In embodiments, when an R 11B 2 substituent group is substituted, the R 11B 2 substituent group is substituted with one or more third substituent groups denoted by R 11B 3 as explained in the definitions section above in the description of “first substituent group(s)”.
  • R 11B , R 11B 1 , R 11B 2 , and R 11B 3 have values corresponding to the values of R ww , R WW 1 , R W2 and R WW 3 , respectively, as explained in the definitions section above in the description of “first substituent group(s)”, wherein R ww , R WW 1 , J ⁇ WW.2, an j j ⁇ ww.3 correS p Onc
  • R 11A and R 11B substituents bonded to the same nitrogen atom are optionally joined to form a moiety that is substituted (e.g., a substituted heterocycloalkyl or substituted heteroaryl), the moiety is substituted with one or more first substituent groups denoted by R 11A 1 as explained in the definitions section above in the description of “first substituent group(s)”.
  • R 11A 1 substituent group when an R 11A 1 substituent group is substituted, the R 11A 1 substituent group is substituted with one or more second substituent groups denoted by R 11A 2 as explained in the definitions section above in the description of “first substituent group(s)”.
  • R 11A 1 , R 11A 2 , and R 11A 3 have values corresponding to the values of R WW 1 , reS p ec ively, as explained in the definitions section above in the description of “first substituent group(s)”, wherein R WW 1 , R ww - 2 , an j pww.3 correspond to R 11A 1 , R 11A 2 , and R 11A 3 , respectively.
  • R 11A and R 11B substituents bonded to the same nitrogen atom are optionally joined to form a moiety that is substituted (e.g., a substituted heterocycloalkyl or substituted heteroaryl), the moiety is substituted with one or more first substituent groups denoted by R 11B 1 as explained in the definitions section above in the description of “first substituent group(s)”.
  • R 11B 1 substituent group when an R 11B 1 substituent group is substituted, the R 11B 1 substituent group is substituted with one or more second substituent groups denoted by R 11B 2 as explained in the definitions section above in the description of “first substituent group(s)”.
  • R 11B 2 substituent group when an R 11B 2 substituent group is substituted, the R 11B 2 substituent group is substituted with one or more third substituent groups denoted by R 11B 3 as explained in the definitions section above in the description of “first substituent group(s)”.
  • R 11B 1 , R 11B 2 , and R 11B 3 have values corresponding to the values of R ww RWW.2, an j pww.3, reS p ec ively, as explained in the definitions section above in the description of “first substituent group(s)”, wherein R WW 1 , R ww - 2 , an j pww.3 correS p O nd to R 11 E.I, R11B.2, an j R11B.3, respectively.
  • R 11C when R 11C is substituted, R 11C is substituted with one or more first substituent groups denoted by R 11C 1 as explained in the definitions section above in the description of “first substituent group(s)”. In embodiments, when an R 11C 1 substituent group is substituted, the R 11C 1 substituent group is substituted with one or more second substituent groups denoted by R 11C 2 as explained in the definitions section above in the description of “first substituent group(s)”. In embodiments, when an R 11C 2 substituent group is substituted, the R 11C 2 substituent group is substituted with one or more third substituent groups denoted by R 11C 3 as explained in the definitions section above in the description of “first substituent group(s)”.
  • R 11C , R 11C 1 , R 11C 2 , and R 11C 3 have values corresponding to the values of R ww , R WW 1 , R W2 and R WW 3 , respectively, as explained in the definitions section above in the description of “first substituent group(s)”, wherein R ww , R WW 1 , pww.2, an j j ⁇ ww.3 correS p Onc
  • R 11D when R 11D is substituted, R 11D is substituted with one or more first substituent groups denoted by R 11D 1 as explained in the definitions section above in the description of “first substituent group(s)”. In embodiments, when an R 11D 1 substituent group is substituted, the R 11D 1 substituent group is substituted with one or more second substituent groups denoted by R 11D 2 as explained in the definitions section above in the description of “first substituent group(s)”. In embodiments, when an R 11D 2 substituent group is substituted, the R 11D 2 substituent group is substituted with one or more third substituent groups denoted by R 11D 3 as explained in the definitions section above in the description of “first substituent group(s)”.
  • R 11D , R 11D 1 , R 11D 2 , and R 11D 3 have values corresponding to the values of R ww , R WW 1 , R W2 and R WW 3 , respectively, as explained in the definitions section above in the description of “first substituent group(s)”, wherein R ww , R WW 1 , pww.2, an j j ⁇ ww.3 correspond to R 11D , R 11D 1 , R 11D 2 , and R 11D 3 , respectively.
  • R 12 when R 12 is substituted, R 12 is substituted with one or more first substituent groups denoted by R 12 1 as explained in the definitions section above in the description of “first substituent group(s)”. In embodiments, when an R 12 1 substituent group is substituted, the R 12 1 substituent group is substituted with one or more second substituent groups denoted by R 12 2 as explained in the definitions section above in the description of “first substituent group(s)”. In embodiments, when an R 12 2 substituent group is substituted, the R 12 2 substituent group is substituted with one or more third substituent groups denoted by R 12 3 as explained in the definitions section above in the description of “first substituent group(s)”.
  • R 12 , R 12 1 , R 122 , and R 12 3 have values corresponding to the values of R ww , R WW 1 , respectively, as explained in the definitions section above in the description of “first substituent group(s)”, wherein R ww , R ww - 1 , R WW 2 , and R ww 3 correspond to R 12 , R 12 1 , R 122 , and R 12 3 , respectively.
  • R 12A when R 12A is substituted, R 12A is substituted with one or more first substituent groups denoted by R 12A 1 as explained in the definitions section above in the description of “first substituent group(s)”. In embodiments, when an R 12A 1 substituent group is substituted, the R 12A 1 substituent group is substituted with one or more second substituent groups denoted by R 12A 2 as explained in the definitions section above in the description of “first substituent group(s)”. In embodiments, when an R 12A 2 substituent group is substituted, the R 12A 2 substituent group is substituted with one or more third substituent groups denoted by R 12A 3 as explained in the definitions section above in the description of “first substituent group(s)”.
  • R 12A , R 12A 1 , R 12A 2 , and R 12A 3 have values corresponding to the values of R ww , R WW 1 , R W2 and R WW 3 , respectively, as explained in the definitions section above in the description of “first substituent group(s)”, wherein R ww , R WW 1 , pww.2, an j j ⁇ ww.3 correS p Onc
  • R 12B when R 12B is substituted, R 12B is substituted with one or more first substituent groups denoted by R 12B 1 as explained in the definitions section above in the description of “first substituent group(s)”. In embodiments, when an R 12B 1 substituent group is substituted, the R 12B 1 substituent group is substituted with one or more second substituent groups denoted by R 12B 2 as explained in the definitions section above in the description of “first substituent group(s)”. In embodiments, when an R 12B 2 substituent group is substituted, the R 12B 2 substituent group is substituted with one or more third substituent groups denoted by R 12B 3 as explained in the definitions section above in the description of “first substituent group(s)”.
  • R 12B , R 12B 1 , R 12B 2 , and R 12B 3 have values corresponding to the values of R ww , R WW 1 , R W2 and R WW 3 , respectively, as explained in the definitions section above in the description of “first substituent group(s)”, wherein R ww , R WW 1 , R WW - 2 , an j j ⁇ ww.3 correS p Onc
  • R 12A and R 12B substituents bonded to the same nitrogen atom are optionally joined to form a moiety that is substituted (e.g., a substituted heterocycloalkyl or substituted heteroaryl), the moiety is substituted with one or more first substituent groups denoted by R 12A 1 as explained in the definitions section above in the description of “first substituent group(s)”.
  • R 12A 1 substituent group when an R 12A 1 substituent group is substituted, the R 12A 1 substituent group is substituted with one or more second substituent groups denoted by R 12A 2 as explained in the definitions section above in the description of “first substituent group(s)”.
  • R 12A 1 , R 12A 2 , and R 12A 3 have values corresponding to the values of R ww reS p ec ively, as explained in the definitions section above in the description of “first substituent group(s)”, wherein R WW 1 , R ww - 2 , an j pww.3 correspond to R1 2A .I, R 12A 2 , and R 12A 3 , respectively.
  • R 12A and R 12B substituents bonded to the same nitrogen atom are optionally joined to form a moiety that is substituted (e.g., a substituted heterocycloalkyl or substituted heteroaryl), the moiety is substituted with one or more first substituent groups denoted by R 12B 1 as explained in the definitions section above in the description of “first substituent group(s)”.
  • R 12B 1 substituent group when an R 12B 1 substituent group is substituted, the R 12B 1 substituent group is substituted with one or more second substituent groups denoted by R 12B 2 as explained in the definitions section above in the description of “first substituent group(s)”.
  • R 12B 2 substituent group when an R 12B 2 substituent group is substituted, the R 12B 2 substituent group is substituted with one or more third substituent groups denoted by R 12B 3 as explained in the definitions section above in the description of “first substituent group(s)”.
  • R 12B 1 , R 12B 2 , and R 12B 3 have values corresponding to the values of R WW 1 , reS p e ctively, as explained in the definitions section above in the description of “first substituent group(s)”, wherein R WW 1 , R ww - 2 , anc j pww.3 correspond to R12B.I, R 12B 2 , and R 12B 3 , respectively.
  • R 12C when R 12C is substituted, R 12C is substituted with one or more first substituent groups denoted by R 12C 1 as explained in the definitions section above in the description of “first substituent group(s)”. In embodiments, when an R 12C 1 substituent group is substituted, the R 12C 1 substituent group is substituted with one or more second substituent groups denoted by R 12C 2 as explained in the definitions section above in the description of “first substituent group(s)”. In embodiments, when an R 12C 2 substituent group is substituted, the R 12C 2 substituent group is substituted with one or more third substituent groups denoted by R 12C 3 as explained in the definitions section above in the description of “first substituent group(s)”.
  • R 12C , R 12C 1 , R 12C 2 , and R 12C 3 have values corresponding to the values of R ww , R WW 1 , R W2 and R WW 3 , respectively, as explained in the definitions section above in the description of “first substituent group(s)”, wherein R ww , R WW 1 , J ⁇ WW.2, an j j ⁇ ww.3 correS p Onc
  • R 12D when R 12D is substituted, R 12D is substituted with one or more first substituent groups denoted by R 12D 1 as explained in the definitions section above in the description of “first substituent group(s)”.
  • R 12D 1 substituent group when an R 12D 1 substituent group is substituted, the R 12D 1 substituent group is substituted with one or more second substituent groups denoted by R 12D 2 as explained in the definitions section above in the description of “first substituent group(s)”.
  • R 12D 2 substituent group when an R 12D 2 substituent group is substituted, the R 12D 2 substituent group is substituted with one or more third substituent groups denoted by R 12D 3 as explained in the definitions section above in the description of “first substituent group(s)”.
  • R 12D , R 12D 1 , R 12D 2 , and R 12D 3 have values corresponding to the values of R ww , R WW 1 , R W2 and R WW 3 , respectively, as explained in the definitions section above in the description of “first substituent group(s)”, wherein R ww , R WW 1 , pww.2, an j j ⁇ ww.3 correS p Onc
  • R 2 and R 3 substituents are optionally joined to form a moiety that is substituted (e.g., a substituted cycloalkyl, substituted heterocycloalkyl, substituted aryl, or substituted heteroaryl), the moiety is substituted with one or more first substituent groups denoted by R 2 1 as explained in the definitions section above in the description of “first substituent group(s)”.
  • R 2 1 substituent group when an R 2 1 substituent group is substituted, the R 2 1 substituent group is substituted with one or more second substituent groups denoted by R 2 2 as explained in the definitions section above in the description of “first substituent group(s)”.
  • R 2 2 substituent group when an R 2 2 substituent group is substituted, the R 2 2 substituent group is substituted with one or more third substituent groups denoted by R 2 3 as explained in the definitions section above in the description of “first substituent group(s)”.
  • R 2 and R 3 substituents are optionally joined to form a moiety that is substituted (e.g., a substituted cycloalkyl, substituted heterocycloalkyl, substituted aryl, or substituted heteroaryl), the moiety is substituted with one or more first substituent groups denoted by R 3 1 as explained in the definitions section above in the description of “first substituent group(s)”.
  • R 3 1 substituent group when an R 3 1 substituent group is substituted, the R 3 1 substituent group is substituted with one or more second substituent groups denoted by R 3 2 as explained in the definitions section above in the description of “first substituent group(s)”.
  • R 3 2 substituent group when an R 3 2 substituent group is substituted, the R 3 2 substituent group is substituted with one or more third substituent groups denoted by R 3 3 as explained in the definitions section above in the description of “first substituent group(s)”.
  • R 3 R 3 2 , and R 3 3 have values corresponding to the values of R WW 1 , R WW 2 , and R ww - 3 , respectively, as explained in the definitions section above in the description of “first substituent group(s)”, wherein R WW I , R WW 2 , and R WW 3 correspond to R 3 R 3 2 , and R 3 3 , respectively.
  • R 3 and R 4 substituents are optionally joined to form a moiety that is substituted (e.g., a substituted cycloalkyl, substituted heterocycloalkyl, substituted aryl, or substituted heteroaryl), the moiety is substituted with one or more first substituent groups denoted by R 3 1 as explained in the definitions section above in the description of “first substituent group(s)”.
  • R 3 1 substituent group when an R 3 1 substituent group is substituted, the R 3 1 substituent group is substituted with one or more second substituent groups denoted by R 3 2 as explained in the definitions section above in the description of “first substituent group(s)”.
  • R 3 R 3 2 , and R 3 3 have values corresponding to the values of R WW 1 , R WW 2 , and R ww - 3 , respectively, as explained in the definitions section above in the description of “first substituent group(s)”, wherein R WW 1 , R ww - 2 , anc
  • R 3 and R 4 substituents are optionally joined to form a moiety that is substituted (e.g., a substituted cycloalkyl, substituted heterocycloalkyl, substituted aryl, or substituted heteroaryl), the moiety is substituted with one or more first substituent groups denoted by R 4 1 as explained in the definitions section above in the description of “first substituent group(s)”.
  • R 4 1 when an R 4 1 substituent group is substituted, the R 4 1 substituent group is substituted with one or more second substituent groups denoted by R 4 2 as explained in the definitions section above in the description of “first substituent group(s)”.
  • R 4 2 substituent group when an R 4 2 substituent group is substituted, the R 4 2 substituent group is substituted with one or more third substituent groups denoted by R 4 3 as explained in the definitions section above in the description of “first substituent group(s)”.
  • R 4 1 , R 4 2 , and R 4 3 have values corresponding to the values of R WW 1 , R WW 2 , and R ww - 3 , respectively, as explained in the definitions section above in the description of “first substituent group(s)”, wherein R ww - 1 , R WW 2 , and R WW 3 correspond to R 4 1 , R 42 , and R 4 3 , respectively.
  • R 4 and R 5 substituents are optionally joined to form a moiety that is substituted (e.g., a substituted cycloalkyl, substituted heterocycloalkyl, substituted aryl, or substituted heteroaryl), the moiety is substituted with one or more first substituent groups denoted by R 4 1 as explained in the definitions section above in the description of “first substituent group(s)”.
  • R 4 1 substituent group when an R 4 1 substituent group is substituted, the R 4 1 substituent group is substituted with one or more second substituent groups denoted by R 4 2 as explained in the definitions section above in the description of “first substituent group(s)”.
  • R 4 2 substituent group when an R 4 2 substituent group is substituted, the R 4 2 substituent group is substituted with one or more third substituent groups denoted by R 4 3 as explained in the definitions section above in the description of “first substituent group(s)”.
  • R 4 1 , R 4 2 , and R 4 3 have values corresponding to the values of R WW 1 , R WW 2 , and R ww - 3 , respectively, as explained in the definitions section above in the description of “first substituent group(s)”, wherein R WW I , R WW 2 , and R WW 3 correspond to R 4 1 , R 42 , and R 4 3 , respectively.
  • R 4 and R 5 substituents are optionally joined to form a moiety that is substituted (e.g., a substituted cycloalkyl, substituted heterocycloalkyl, substituted aryl, or substituted heteroaryl), the moiety is substituted with one or more first substituent groups denoted by R 5 1 as explained in the definitions section above in the description of “first substituent group(s)”.
  • R 5 1 when an R 5 1 substituent group is substituted, the R 5 1 substituent group is substituted with one or more second substituent groups denoted by R 5 2 as explained in the definitions section above in the description of “first substituent group(s)”.
  • R 5 2 substituent group when an R 5 2 substituent group is substituted, the R 5 2 substituent group is substituted with one or more third substituent groups denoted by R 5 3 as explained in the definitions section above in the description of “first substituent group(s)”.
  • R 5 R 5 2 , and R 5 3 have values corresponding to the values of R WW 1 , R WW 2 , and R ww - 3 , respectively, as explained in the definitions section above in the description of
  • R 10 and R 2 substituents are optionally joined to form a moiety that is substituted (e.g., a substituted cycloalkyl, substituted heterocycloalkyl, substituted aryl, or substituted heteroaryl), the moiety is substituted with one or more first substituent groups denoted by R 10 1 as explained in the definitions section above in the description of “first substituent group(s)”.
  • R 10 1 substituent group when an R 10 1 substituent group is substituted, the R 10 1 substituent group is substituted with one or more second substituent groups denoted by R 10 2 as explained in the definitions section above in the description of “first substituent group(s)”.
  • R 10 2 substituent group when an R 10 2 substituent group is substituted, the R 10 2 substituent group is substituted with one or more third substituent groups denoted by R 10 3 as explained in the definitions section above in the description of “first substituent group(s)”.
  • R 10 1 , R 10 2 , and R 10 3 have values corresponding to the
  • R 10 and R 2 substituents are optionally joined to form a moiety that is substituted (e.g., a substituted cycloalkyl, substituted heterocycloalkyl, substituted aryl, or substituted heteroaryl), the moiety is substituted with one or more first substituent groups denoted by R 2 1 as explained in the definitions section above in the description of “first substituent group(s)”.
  • R 2 1 substituent group when an R 2 1 substituent group is substituted, the R 2 1 substituent group is substituted with one or more second substituent groups denoted by R 2 2 as explained in the definitions section above in the description of “first substituent group(s)”.
  • R 2 2 substituent group when an R 2 2 substituent group is substituted, the R 2 2 substituent group is substituted with one or more third substituent groups denoted by R 2 3 as explained in the definitions section above in the description of “first substituent group(s)”.
  • R 2 1 , R 2 2 , and R 2 3 have values corresponding to the values of R ww - 1 , RTM a nd R WW 3 , respectively, as explained in the definitions section above in the description of “first substituent group(s)”, wherein R WW 1 , R ww - 2 , a nd R WW 3 correspond to R 2 R 2 2 , and R 2 3 , respectively.
  • L 1 when L 1 is substituted, L 1 is substituted with one or more first substituent groups denoted by R L1 1 as explained in the definitions section above in the description of “first substituent group(s)”.
  • R L1 1 substituent group when an R L1 1 substituent group is substituted, the R L1 1 substituent group is substituted with one or more second substituent groups denoted by R L1 2 as explained in the definitions section above in the description of “first substituent group(s)”.
  • R L1 2 substituent group when an R L1 2 substituent group is substituted, the R L1 2 substituent group is substituted with one or more third substituent groups denoted by R L1 3 as explained in the definitions section above in the description of “first substituent
  • the compound embodiments, the , embodiments, the compound i embodiments, the compound is In embodiments, the compound embodiments, the compound i embodiments, the compound is In embodiments, the compound embodiments, the compound is In embodiments, the compound is In embodiments, the compound is in embodiments, the compound is
  • the compound is embodiments, the compound is In embodiments, the compound is In embodiments, the compound is embodiments, the compound is In embodiments, the compound is embodiments, the compound is In embodiments, the compound is embodiments, the compound is In embodiments, the compound is embodiments, the compound is In embodiments, the compound is embodiments, the compound is . In embodiments,
  • the compound is . in embodiments, the compound is i n embodiments, the compound is
  • the compound is . in embodiments, the compound is . In embodiments, the compound is In embodiments, the compound is
  • the compound is embodiments, the compound is In embodiments, the compound is In embodiments, the compound is In embodiments, the compound is
  • the compound is embodiments, the compound embodiments, the compound is In embodiments, the compound i
  • the compound is In embodiments, the In embodiments, the compound is In embodiments, the compound is
  • the compound i embodiments, the In embodiments, the compound is In embodiments the compound is
  • the compound is In embodiments, the In embodiments, the compound is
  • the compound is N-(2-aminoethyl)-2-aminoethyl-N-(2-aminoethyl)-2-aminoethyl-N-(2-aminoethyl)-2-aminoethyl-N-(2-aminoethyl)-2-aminoethyl-N-(2-aminoethyl)-2-aminoethyl
  • the compound is In embodiments, the In embodiments, the compound is In embodiments, the compound is
  • the compound is In embodiments, the In embodiments, the compound is
  • the compound is N-(2-aminoethyl)-2-aminoethyl-N-(2-aminoethyl)-2-aminoethyl-N-(2-aminoethyl)-2-aminoethyl-N-(2-aminoethyl)-2-aminoethyl-N-(2-aminoethyl)-2-aminoethyl
  • the compound In embodiments, the compound in embodiments, the
  • the compound embodiments, the embodiments, the compound is N-(2-aminoethyl)-2-aminoethyl-N-(2-aminoethyl)-2-aminoethyl-N-(2-aminoethyl)-2-aminoethyl-N-(2-aminoethyl)-2-aminoethyl-N-(2-aminoethyl)
  • the compound i embodiments, the compound embodiments, the compound
  • the compound embodiments, the compound embodiments, the compound is embodiments, the compound i embodiments, the compound is In embodiments, the compound embodiments, the compound embodiments, the compound is In embodiments, the compound i embodiments, the compound is In embodiments, the compound i embodiments, the compound i embodiments, the compound is In embodiments, the compound embodiments, the compound i embodiments, the compound is embodiments, the compound is In embodiments, the compound embodiments, the compound i embodiments, the compound, the compound is embodiments, the compound is In embodiments, the compound embodiments, the compound i embodiments, the compound, the compound is embodiments, the compound is embodiments, the compound is embodiments, the compound is embodiments, the compound i embodiments, the compound is In embodiments, the compound embodiments, the compound i embodiments, the compound
  • the compound i embodiments, the compound is In embodiments, the compound i embodiments, the compound is In embodiments, the compound i embodiments, the compound i embodiments, the
  • the compound embodiments, the embodiments, the compound is In embodiments, the compound i embodiments, the compound embodiments, the compound is In embodiments, the compound i
  • the compound embodiments, the embodiments, the compound is embodiments, the compound embodiments, the compound embodiments, the compound. the compound
  • the compound embodiments, the compound i embodiments, the compound is In embodiments, the compound i embodiments, the compound is In embodiments, the compound embodiments, the compound embodiments, the compound is In embodiments, the compound i embodiments, the compound is embodiments, the compound i embodiments, the compound is , embodiments, the compound i embodiments, the compound is In embodiments, the compound i embodiments, the compound i embodiments, the compound is In embodiments, the compound i embodiments, the compound i embodiments, the compound is In embodiments, the compound, the compound i embodiments, the compound is In embodiments, the compound
  • the compound embodiments, the embodiments, the compound is N-(2-aminoethyl)-2-aminoethyl-N-(2-aminoethyl)-2-aminoethyl-N-(2-aminoethyl)-2-aminoethyl-N-(2-aminoethyl)-2-aminoethyl-N-(2-aminoethyl)
  • the compound embodiments, the , In embodiments, the compound embodiments, the compound i embodiments, the compound is embodiments, the compound embodiments, the compound is In embodiments, the compound i embodiments, the compound embodiments, the compound is In embodiments, the compound embodiments, the compound i embodiments, the compound is embodiments, the compound i embodiments, the compound is embodiments, the compound i embodiments, the compound is In embodiments, the compound embodiments, the compound i embodiments, the compound is In embodiments, the compound i embodiments, the compound is embodiments, the compound i embodiments, the compound is embodiments, the compound i embodiments, the compound is embodiments, the compound i embodiments, the compound is embodiments, the compound i embodiments, the compound is embodiments, the compound i embodiments, the compound is embodiments, the compound i embodiments, the compound is embodiments, the compound i embodiments, the compound is embodiments, the compound i embodiments, the compound is embodiments, the compound i embodiments, the compound is where
  • the compound embodiments, the compound embodiments, the compound i embodiments, the compound i embodiments, the compound is In embodiments, the compound i In embodiments, the compound is In embodiments, the , embodiments, the compound i embodiments, the compound embodiments, the compound i
  • the compound i embodiments, the compound embodiments, the compound is embodiments, the compound is In embodiments, the compound i embodiments, the compound i embodiments, the compound is In embodiments, the compound is In embodiments, the compound i embodiments, the compound is
  • the compound is C0 2 H . In embodiments, the compound i embodiments, the compound embodiments, the compound i In embodiments, the compound i embodiments, the compound i embodiments, the compound is In embodiments, the compound embodiments, the compound is In embodiments, the compound i embodiments, the compound embodiments, the compound , In embodiments, the compound i embodiments, the compound
  • the compound i embodiments, the compound embodiments, the compound embodiments, the compound i embodiments, the compound is In embodiments, the compound i embodiments, the compound i embodiments, the compound is
  • the compound in embodiments, is CN . In embodiments, the compound i embodiments, the compound is embodiments, the compound i embodiments, the compound is
  • the compound is SO 2 Me j n embodiments, the compound i embodiments, the compound is embodiments, the compound is In embodiments, the compound i embodiments, the compound embodiments, the compound
  • the compound i embodiments, the embodiments, the compound is embodiments, the compound i embodiments, the compound is In embodiments, the compound i embodiments, the compound embodiments, the compound is , embodiments, the compound i embodiments, the compound is In embodiments, the compound embodiments, the compound embodiments, the compound is, the compound i embodiments, the compound is in embodiments, the compound embodiments, the compound embodiments, the compound is
  • the compound is CO 2 Me
  • the compound i embodiments, the compound In embodiments, the compound
  • the compound embodiments, the compound i embodiments, the compound is In embodiments, the compound In embodiments, the compound embodiments, the embodiments, the compound is , In embodiments, the compound i embodiments, the compound i embodiments, the compound is
  • the compound is CO 2 H
  • the compound is CO 2 H
  • the compound i embodiments, the embodiments, the compound is
  • the compound is CO 2 H In embodiments, the compound is CO 2 H In embodiments, the compound i embodiments, the compound embodiments, the compound i embodiments, the compound is embodiments, the compound i embodiments, the compound embodiments, the compound is , p
  • the compound is C0 2 H
  • the compound i embodiments, the compound embodiments, the compound is embodiments, the compound
  • the compound is C0 2 H
  • the compound i embodiments, the compound
  • the compound is CO 2 H
  • the compound is CO 2 H
  • the compound i embodiments, the compound i embodiments, the compound is In embodiments, the compound i embodiments, the compound embodiments, the compound embodiments, the compound i embodiments, the compound is embodiments, the compound i embodiments, the compound is In embodiments, the compound embodiments, the compound i embodiments, the compound is ,
  • the compound embodiments, the compound embodiments, the compound i embodiments, the compound is embodiments, the compound embodiments, the compound is embodiments, the compound embodiments, the compound i
  • the compound i embodiments, the compound embodiments, the compound embodiments, the compound embodiments, the compound is nd ,
  • the compound i embodiments, the compound i embodiments, the compound is In embodiments, the compound embodiments, the compound i embodiments, the compound embodiments, the compound embodiments, the compound embodiments, the compound embodiments, the compound is embodiments, the compound embodiments, the compound is embodiments, the compound is In embodiments, the compound i embodiments, the compound i embodiments, the compound In embodiments, the compound embodiments, the compound embodiments, the compound embodiments, the compound i embodiments, the compound is In embodiments, the compound i embodiments, the compound i embodiments, the compound , embodiments, the compound , the compound i embodiments, the compound is In embodiments, the compound i embodiments, the compound i embodiments, the compound , embodiments, the compound , embodiments, the compound is In embodiments, the compound i embodiments, the compound i embodiments, the compound , embodiments, the compound , the compound , the compound i embodiments, the compound is In embodiments, the compound i embodiments, the compound i
  • the compound embodiments, the compound i embodiments, the compound is
  • the compound i embodiments, the compound embodiments, the compound In embodiments, the compound is
  • the compound embodiments, the compound i embodiments, the compound is In embodiments, the compound
  • the compound is useful as a comparator compound.
  • the comparator compound can be used to assess the activity of a test compound as set forth in an assay described herein (e.g., in the examples section, figures, or tables).
  • the compound is a compound as described herein, including in embodiments.
  • the compound is a compound described herein (e.g., in the examples section, figures, tables, or claims).
  • R 10 is not hydrogen, halogen, unsubstituted methyl, or unsubstituted alkoxy.
  • R 10 is not hydrogen.
  • R 10 is not halogen.
  • R 10 is not -F.
  • R 10 is not -Cl. In embodiments, R 10 is not -CH 3 . In embodiments, R 10 is not substituted or unsubstituted heteroalkyl. In embodiments, R 10 is not substituted or unsubstituted 2 to 6 membered heteroalkyl. In embodiments, R 10 is not unsubstituted alkoxy. In embodiments, R 10 is not unsubstituted methoxy. In embodiments, R 10 is not unsubstituted ethoxy. In embodiments, R 10 is not unsubstituted propoxy. In embodiments, R 10 is not unsubstituted butoxy.
  • R 10 and R 2 substituents are not joined to form a substituted or unsubstituted cycloalkyl, substituted or unsubstituted heterocycloalkyl, substituted or unsubstituted aryl, or substituted or unsubstituted heteroaryl. In embodiments, R 10 and R 2 substituents are not joined to form a substituted or unsubstituted heteroaryl. In embodiments, R 10 and R 2 substituents are not joined to form a substituted or unsubstituted 5 to 6 membered heteroaryl. In embodiments, R 10 and R 2 substituents are not joined to form a methylsubstituted 5 to 6 membered heteroaryl. In embodiments, R 10 and R 2 substituents are not joined to form
  • R 3 is not halogen. In embodiments, R 3 is not -F. In embodiments, R 3 is not -Cl. In embodiments, R 3 is not -OH. In embodiments, R 3 is not -S(O)2CH 3 . In embodiments, R 3 is not -CH 3 .
  • R 9 is not unsubstituted C 3 -C 8 cycloalkyl. In embodiments, R 9 is not unsubstituted cyclopropyl. In embodiments, R 9 is not unsubstituted cyclobutyl. In embodiments, R 9 is not unsubstituted cyclopentyl. In embodiments, R 9 is not unsubstituted cyclobutyl. In embodiments, R 9 is not unsubstituted cyclopentyl. In embodiments, R 9 is not unsubstituted cyclohexyl. In embodiments, R 9 is not unsubstituted cycloheptyl.
  • R 9 is not unsubstituted cyclooctyl.
  • -lAR 9 is not wherein R 11 and z11 are as described herein, including in embodiments.
  • -I ⁇ -R 9 is not embodiments, -I ⁇ -R 9 is not In embodiments, -lAR 9 is not embodiments, -I ⁇ -R 9 is not wherein R 11 and z11 are as described herein, including in embodiments.
  • -I ⁇ -R 9 is not embodiments, -I ⁇ -R 9 is not In embodiments, -I ⁇ -R 9 is not embodiments, -I ⁇ -R 9 is not In embodiments, -I ⁇ -R 9 is not wherein R 12 is as described herein, including in embodiments. In embodiments, -I ⁇ -R 9 is not In embodiments, -lAR 9 is not r12 , wherein R 12 is as described herein, including in embodiments. In embodiments, -I ⁇ -R 9 is not R 12 , wherein R 12 is as described herein, d including in embodiments. In embodiments, -I ⁇ -R 9 is not H . In embodiments, -I ⁇ -R 9 is not j n embodiments, - -R 9 is not
  • a pharmaceutical composition including a compound described herein, or a pharmaceutically acceptable salt or solvate thereof, and a pharmaceutically acceptable excipient.
  • the compound is a compound of formula (I), (I- 1 a), (I- lb), (1-1 c), (I- Id), (I-2a), (I-2b), (I-2c), (I-2d), (1-3 a), (I-3b), (1-3 c), (1-3 d), (I-4a), (I-4b), (I-4c), (I-4d), (II), (Il-la), (II- lb), (II-2a), (II-2b), (II-3a), or (II-3b).
  • the compound is a compound of formula (I).
  • the compound is a compound of formula (I- la).
  • the compound is a compound of formula (I-lb). In embodiments, the compound is a compound of formula (I-lc). In embodiments, the compound is a compound of formula (I- Id). In embodiments, the compound is a compound of formula (I-2a). In embodiments, the compound is a compound of formula (I-2b). In embodiments, the compound is a compound of formula (I-2c). In embodiments, the compound is a compound of formula (I-2d). In embodiments, the compound is a compound of formula (I-3a). In embodiments, the compound is a compound of formula (I-3b). In embodiments, the compound is a compound of formula (I-3c). In embodiments, the compound is a compound of formula (1-3 d).
  • the compound is a compound of formula (I-4a). In embodiments, the compound is a compound of formula (I-4b). In embodiments, the compound is a compound of formula (I-4c). In embodiments, the compound is a compound of formula (I-4d). In embodiments, the compound is a compound of formula (II). In embodiments, the compound is a compound of formula (Il-la). In embodiments, the compound is a compound of formula (Il-lb). In embodiments, the compound is a compound of formula (II-2a). In embodiments, the compound is a compound of formula (II-2b). In embodiments, the compound is a compound of formula (II-3a). In embodiments, the compound is a compound of formula (II-3b).
  • the pharmaceutical composition includes an effective amount of the compound. In embodiments, the pharmaceutical composition includes a therapeutically effective amount of the compound.
  • a method of treating a neurodegenerative disorder in a subject in need thereof including administering to the subject in need thereof a therapeutically effective amount of a compound described herein, or a pharmaceutically acceptable salt of solvate thereof.
  • a method of treating an inflammatory disease in a subject in need thereof including administering to the subject in need thereof a therapeutically effective amount of a compound described herein, or a pharmaceutically acceptable salt of solvate thereof.
  • the inflammatory disease is encephalitis. In embodiments, the inflammatory disease is post-hemorrhagic encephalitis. In embodiments, the inflammatory disease is ocular inflammation. In embodiments, the inflammatory disease is conjunctivitis. In embodiments, the inflammatory disease is allergic conjunctivitis. In embodiments, the inflammatory disease is vernal keratoconjunctivitis. In embodiments, the inflammatory disease is papillary conjunctivitis. In embodiments, the inflammatory disease is Sjogren’s syndrome. In embodiments, the inflammatory disease is inflammatory disease with dry eyes.
  • a method of treating a demyelinating disease in a subject in need thereof including administering to the subject in need thereof a therapeutically effective amount of a compound described herein, or a pharmaceutically acceptable salt of solvate thereof.
  • the demyelinating disease is a demyelinating disease of the central nervous system. In embodiments, the demyelinating disease is multiple sclerosis. In embodiments, the demyelinating disease is a demyelinating disease of the peripheral nervous system. [0487] In an aspect is provided a method of treating fibrotic disease in a subject in need thereof, the method including administering to the subject in need thereof a therapeutically effective amount of a compound described herein, or a pharmaceutically acceptable salt of solvate thereof.
  • the fibrotic disease is pulmonary fibrosis.
  • the fibrotic disease is skin fibrosis.
  • the fibrotic disease is liver fibrosis.
  • the fibrotic disease is ocular fibrosis.
  • the fibrotic disease is idiopathic pulmonary fibrosis.
  • the fibrotic disease is scleroderma.
  • the fibrotic disease is nonalcoholic steatohepatitis.
  • the fibrotic disease is ocular fibrosis.
  • the fibrotic disease is hypertrophic scarring or keloids (e.g., burn induced or surgical, sarcoidosis, scleroderma, spinal cord injury/fibrosis, myelofibrosis, vascular restenosis, atherosclerosis, arteriosclerosis, Wegener’s granulomatosis, mixed connective tissue disease, or Peyronie’s disease).
  • the fibrotic disease is iatrogenic pulmonary fibrosis.
  • the fibrotic disease is radiation-induced fibrosis.
  • the fibrotic disease is silicosis-induced pulmonary fibrosis.
  • the fibrotic disease is asbestos-induced pulmonary fibrosis.
  • the fibrotic disease is pleural fibrosis. In embodiments, the fibrotic disease is pulmonary fibrosis associated with SARS-CoV-2 infection and/or COVID-19. In embodiments, the fibrotic disease is pulmonary fibrosis secondary to systemic inflammatory disease. In embodiments, the fibrotic disease is pulmonary fibrosis secondary to sarcoidosis. In embodiments, the fibrotic disease is gut fibrosis. In embodiments, the fibrotic disease is head and neck fibrosis. In embodiments, the fibrotic disease is cirrhosis. In embodiments, the fibrotic disease is alcohol-induced liver fibrosis. In embodiments, the fibrotic disease is endometriosis.
  • the fibrotic disease is spinal cord fibrosis. In embodiments, the fibrotic disease is myelofibrosis. In embodiments, the fibrotic disease is cardiac fibrosis. In embodiments, the fibrotic disease is perivascular fibrosis. In embodiments, the fibrotic disease is Peyronie’s disease. In embodiments, the fibrotic disease is abdominal or bowel adhesions. In embodiments, the fibrotic disease is bladder fibrosis. In embodiments, the fibrotic disease is fibrosis of the nasal passages. In embodiments, the fibrotic disease is fibrosis mediated by fibroblasts. In embodiments, the fibrotic disease is renal fibrosis associated with chronic kidney disease (CKD).
  • CKD chronic kidney disease
  • the cancer is brain cancer.
  • the cancer is glioblastoma.
  • the cancer is a solid tumor (e.g., of the bladder, bowel, brain, breast, endometrium, heart, kidney, lung, lymphatic tissue (e.g., lymphoma), ovary, pancreas or other endocrine organ (e.g., thyroid), prostate, skin (e.g., melanoma or basal cell cancer)) or hematological tumors (e.g., leukemia) at any stage of the disease with or without metastases.
  • lymphatic tissue e.g., lymphoma
  • pancreas or other endocrine organ e.g., thyroid
  • prostate e.g., melanoma or basal cell cancer
  • hematological tumors e.g., leukemia
  • the cancer is acute lymphoblastic leukemia, acute myeloid leukemia, adrenocortical carcinoma, anal cancer, appendix cancer, astrocytomas, atypical teratoid/rhabdoid tumor, basal cell carcinoma, bile duct cancer, bladder cancer, bone cancer (e.g., osteosarcoma or malignant fibrous histiocytoma), brain stem glioma, brain tumors, brain and spinal cord tumors, breast cancer, bronchial tumors, Burkitt lymphoma, cervical cancer, chronic lymphocytic leukemia, chronic myelogenous leukemia, colon cancer, colorectal cancer, craniopharyngioma, cutaneous T-cell lymphoma, embryonal tumors, endometrial cancer, ependymoblastoma, ependymoma, esophageal cancer, Ewing sarcoma family of tumors, eye cancer, retino
  • a method of treating an LP ARI -associated disease in a subject in need thereof including administering to the subject in need thereof a therapeutically effective amount of a compound described herein, or a pharmaceutically acceptable salt of solvate thereof.
  • the LP ARI -associated disease is a neurodegenerative disease. In embodiments, the LP ARI -associated disease is an inflammatory disease. In embodiments, the LP ARI -associated disease is post-hemorrhagic encephalitis. In embodiments, the LP ARI -associated disease is a demyelinating disease. In embodiments, the LPAR1- associated disease is multiple sclerosis. In embodiments, the LP ARI -associated disease is a fibrotic disease. In embodiments, the LP ARI -associated disease is pulmonary fibrosis. In embodiments, the LP ARI -associated disease is idiopathic pulmonary fibrosis.
  • the LP ARI -associated disease is cancer (e.g., brain cancer, ovarian cancer, colon cancer, prostate cancer, breast cancer, melanoma, head and neck cancer, bowel cancer, colorectal cancer, or thyroid cancer).
  • the LP ARI -associated disease is pain (e.g., neuropathic pain, acute pain, or chronic pain).
  • the LP ARI -associated disease is a respiratory or allergic disorder.
  • the respiratory or allergic disorder is asthma, peribronchiolar fibrosis, obliterative bronchiolitis, or chronic obstructive pulmonary disease (COPD).
  • COPD chronic obstructive pulmonary disease
  • the COPD is chronic bronchitis or emphysema, pulmonary hypertension, interstitial lung fibrosis and/or airway inflammation, or cystic fibrosis.
  • the respiratory disease is adult respiratory distress syndrome or allergic (extrinsic) asthma, non- allergic (intrinsic) asthma, acute severe asthma, chronic asthma, clinical asthma, nocturnal asthma, allergen-induced asthma, aspirin-sensitive asthma, exercise-induced asthma, isocapnic hyperventilation, child-onset asthma, adult-onset asthma, cough-variant asthma, occupational asthma, steroid-resistant asthma, seasonal asthma, seasonal allergic rhinitis, perennial allergic rhinitis, and hypoxia.
  • the LP ARI -associated disease is a nervous system disorder.
  • the nervous system disorder is Alzheimer’s Disease, cerebral edema, cerebral ischemia, stroke, multiple sclerosis, neuropathies, Parkinson’s Disease, a nervous condition found after blunt or surgical trauma (including post-surgical cognitive dysfunction and spinal cord or bram stem injury), degenerative disk disease, or sciatica.
  • the LP ARI -associated disease is a cardiovascular disorder.
  • the cardiovascular disorder is arrhythmia (e.g., atrial or ventricular); atherosclerosis and its sequelae; angina; cardiac rhythm disturbances; myocardial ischemia; myocardial infarction; cardiac or vascular aneurysm; vasculitis; stroke; peripheral obstructive arteriopathy of a limb, an organ, or a tissue; reperfusion injury following ischemia of the brain, heart or other organ or tissue; endotoxic, surgical, or traumatic shock; hypertension; valvular heart disease; heart failure; abnormal blood pressure; shock; vasoconstriction (including that associated with migraines); vascular abnormality, or a cardiovascular insufficiency limited to a single organ or tissue.
  • arrhythmia e.g., atrial or ventricular
  • atherosclerosis and its sequelae angina
  • cardiac rhythm disturbances myocardial ischemia
  • myocardial infarction cardiac or vascular
  • the LP ARI -associated disease is lung fibrosis, kidney fibrosis, liver fibrosis, scarring, asthma, rhinitis, chronic obstructive pulmonary disease (COPD), pulmonary hypertension, interstitial lung fibrosis, arthritis, allergy, psoriasis, inflammatory bowel disease, adult respiratory distress syndrome, myocardial infarction, aneurysm, stroke, cancer, pain, proliferative disorders, or inflammatory conditions.
  • COPD chronic obstructive pulmonary disease
  • the LP ARI -associated disease is a liver disease.
  • the liver disease is hepatitis C, liver cancer, familial combined hyperlipidemia, non-alcoholic fatty liver disease (NAFLD), progressive familial intrahepatic cholestasis, primary biliary cirrhosis (PBC), or primary sclerosing cholangitis (PSC).
  • the liver disease is primary sclerosing cholangitis (PSC).
  • the liver disease includes portal hypertension.
  • liver cancer includes hepatocellular carcinoma (HCC), cholangiocarcinoma, angiosarcoma, or hemangiosarcoma.
  • NAFLD includes steatosis. In embodiments, NAFLD includes NASH. In embodiments, NAFLD or NASH includes liver fibrosis. In embodiments, NAFLD or NASH includes liver cirrhosis. In embodiments, NAFLD or NASH includes compensated liver cirrhosis. In embodiments, NAFLD or NASH includes decompensated liver fibrosis. In embodiments, NAFLD includes hepatocellular carcinoma (HCC). In embodiments, the liver disease is NASH.
  • HCC hepatocellular carcinoma
  • a method of modulating LPAR1 activity in a subject including administering to the subject a compound described herein, or a pharmaceutically acceptable salt or solvate thereof.
  • Embodiment Pl A compound, or a pharmaceutically acceptable salt or solvate thereof, having the formula: wherein
  • L 1 is a bond or substituted or unsubstituted C1-C5 alkylene
  • R 1 is unsubstituted C2-C5 alkyl
  • W 2 is N or C(R 2 );
  • R 2 is hydrogen, halogen, -CX 2 3 , -CHX 2 2 , -CH 2 X 2 , -OCX 2 3 , -OCH 2 X 2 , -OCHX 2 2 ,
  • R 3 is hydrogen, halogen, -CX 3 3 , -CHX 3 2 , -CH 2 X 3 , -OCX 3 3 , -OCH 2 X 3 , -OCHX 3 2 ,
  • W 4 is N or C(R 4 );
  • R 4 is hydrogen, halogen, -CX 4 3 , -CHX 4 2 , -CH 2 X 4 , -OCX 4 3 , -OCH 2 X 4 , -OCHX 4 2 , -CN, -SOn 4 R 4D , -SOV 4 NR 4A R 4B , -NR 4C NR 4A R 4B , -ONR 4A R 4B , -NHC(O)NR 4C NR 4A R 4B , -NHC(O)NR 4A R 4B , -N(O)m4, -NR 4A R 4B , -C(O)R 4C , -C(O)OR 4C , -C(O)NR 4A R 4B , -OR 4D , -SR 4D , -NR 4A SO 2 R 4D , -NR 4A C(O)R 4C , -NR 4A C(O)OR 4C
  • W 5 is N or C(R 5 );
  • R 5 is hydrogen, halogen, -CX 5 3 , -CHX 5 2 , -CH 2 X 5 , -OCX 5 3 , -OCH 2 X 5 , -OCHX 5 2 ,
  • R 2 and R 3 substituents may optionally be joined to form a substituted or unsubstituted cycloalkyl, substituted or unsubstituted heterocycloalkyl, substituted or unsubstituted aryl, or substituted or unsubstituted heteroaryl;
  • R 3 and R 4 substituents may optionally be joined to form a substituted or unsubstituted cycloalkyl, substituted or unsubstituted heterocycloalkyl, substituted or unsubstituted aryl, or substituted or unsubstituted heteroaryl;
  • R 4 and R 5 substituents may optionally be joined to form a substituted or unsubstituted cycloalkyl, substituted or unsubstituted heterocycloalkyl, substituted or unsubstituted aryl, or substituted or unsubstituted heteroaryl;
  • W 6 is N or C(R 6 );
  • R 6 is hydrogen, halogen, -CX 6 3 , -CHX 6 2 , -CH 2 X 6 , -OCX 6 3 , -OCH 2 X 6 , -OCHX 6 2 ,
  • R 7 is hydrogen, halogen, -CX 7 3 , -CHX 7 2 , -CH 2 X 7 , -OCX 7 3 , -OCH 2 X 7 , -OCHX 7 2 ,
  • R 8 is independently halogen, -CX 8 3 , -CHX 8 2 , -CH 2 X 8 , -OCX 8 3 , -OCH 2 X 8 , -OCHX 8 2 , -CN, -SO n8 R 8D , -SO V8 NR 8A R 8B , -NR 8C NR 8A R 8B , -ONR 8A R 8B , -NHC(O)NR 8C NR 8A R 8B , -NHC(O)NR 8A R 8B , -N(O) m8 , -NR 8A R 8B , -C(O)R 8C , -C(O)OR 8C , -C(O)NR 8A R 8B , -OR 8D , -SR 8D , -NR 8A SO 2 R 8D , -NR 8A C(O)R 8C , -NR 8A C(O)
  • R 9 is substituted or unsubstituted cycloalkyl or substituted or unsubstituted heterocycloalkyl
  • R2A R2B R2C R2D R3A R3B R3C R3D R4A R4B R4C R4D R5A R5B R5C R5D R6A R6B R6C R 6D , R 7A , R 7B , R 7C , R 7D , R 8A , R 8B , R 8C , and R 8D are independently hydrogen, -CC1 3 , -CBr 3 , -CF 3 , -CI 3 , -CHCl 2 , -CHBr 2 , -CHF 2 , -CHI 2 , -CH 2 C1, -CH 2 Br, -CH 2 F, -CH 2 I, -CN, -OH, -NH 2 , -COOH, -CONH 2 , -OCC1 3 , -OCF 3 , -OCBr 3 , -OCI 3 , -OCHCl 2 , -OCHBr
  • X 2 , X 3 , X 4 , X 5 , X 6 , X 7 , and X 8 are independently -F, -Cl, -Br, or -I; n2, n3, n4, n5, n6, n7, and n8 are independently an integer from 0 to 4; m2, m3, m4, m5, m6, m7, m8, v2, v3, v4, v5, v6, v7, and v8 are independently 1 or 2; and z8 is an integer from 0 to 3.
  • Embodiment P2 The compound of embodiment Pl, having the formula:
  • Embodiment P3 The compound of embodiment Pl, having the formula:
  • Embodiment P4 The compound of embodiment Pl, having the formula:
  • Embodiment P5. The compound of embodiment Pl, having the formula:
  • Embodiment P6 The compound of one of embodiments Pl to P5, wherein R 1 is unsubstitutedC 3 alkyl.
  • Embodiment P7 The compound of one of embodiments Pl to P5, wherein R 1 is isopropyl.
  • Embodiment P8 A compound, or a pharmaceutically acceptable salt or solvate thereof, having the formula: wherein
  • L 1 is a bond or substituted or unsubstituted C1-C5 alkylene
  • R 2 is hydrogen, halogen, -CX 2 3 , -CHX 2 2 , -CH 2 X 2 , -OCX 2 3 , -OCH 2 X 2 , -OCHX 2 2 ,
  • R 3 is hydrogen, halogen, -CX 3 3 , -CHX 3 2 , -CH 2 X 3 , -OCX 3 3 , -OCH 2 X 3 , -OCHX 3 2 ,
  • R 4 is hydrogen, halogen, -CX 4 3 , -CHX 4 2 , -CH 2 X 4 , -OCX 4 3 , -OCH 2 X 4 , -OCHX 4 2 ,
  • R 5 is hydrogen, halogen, -CX 5 3 , -CHX 5 2 , -CH 2 X 5 , -OCX 5 3 , -OCH 2 X 5 , -OCHX 5 2 ,
  • R 2 and R 3 substituents may optionally be joined to form a substituted or unsubstituted cycloalkyl, substituted or unsubstituted heterocycloalkyl, substituted or unsubstituted aryl, or substituted or unsubstituted heteroaryl;
  • R 3 and R 4 substituents may optionally be joined to form a substituted or unsubstituted cycloalkyl, substituted or unsubstituted heterocycloalkyl, substituted or unsubstituted aryl, or substituted or unsubstituted heteroaryl;
  • R 4 and R 5 substituents may optionally be joined to form a substituted or unsubstituted cycloalkyl, substituted or unsubstituted heterocycloalkyl, substituted or unsubstituted aryl, or substituted or unsubstituted heteroaryl;
  • W 6 is N or C(R 6 );
  • R 6 is hydrogen, halogen, -CX 6 3 , -CHX 6 2 , -CH 2 X 6 , -OCX 6 3 , -OCH 2 X 6 , -OCHX 6 2 ,
  • W 7 is N, N + -O', or C(R 7 );
  • R 7 is hydrogen, halogen, -CX 7 3 , -CHX 7 2 , -CH 2 X 7 , -OCX 7 3 , -OCH 2 X 7 , -OCHX 7 2 ,
  • R 8 is independently halogen, -CX 8 3 , -CHX 8 2 , -CH 2 X 8 , -OCX 8 3 , -OCH 2 X 8 , -OCHX 8 2 , -CN, -SO n8 R 8D , -SO V8 NR 8A R 8B , -NR 8C NR 8A R 8B , -ONR 8A R 8B , -NHC(O)NR 8C NR 8A R 8B , -NHC(O)NR 8A R 8B , -N(O) m8 , -NR 8A R 8B , -C(O)R 8C , -C(O)OR 8C , -C(O)NR 8A R 8B , -OR 8D , -SR 8D , -NR 8A SO 2 R 8D , -NR 8A C(O)R 8C , -NR 8A C(O)
  • R 9 is substituted or unsubstituted cycloalkyl or substituted or unsubstituted heterocycloalkyl
  • R 10 is hydrogen, halogen, -CX 10 3 , -CHX 10 2 , -CH 2 X 10 , -OCX 10 3 , -OCH 2 X 10 , -OCHX 10 2 , -CN, -SOnioR 10D , -SOvioNR 10A R 10B , -NR 1OC NR 1OA R 1OB , -ONR 10A R 10B , -NHC(O)NR 10C NR 10A R 10B , -NHC(O)NR 10A R 10B , -N(O)mio, -NR 10A R 10B , -C(O)R 10C , -C(O)OR 10C , -C(O)NR 10A R 10B , -OR 10D , -SR 1OD , -NR 10A SO 2 R 10D , -NR 10A C(O)R 10C , -NR 10A C(O)OR
  • R 10 and R 2 substituents may optionally be joined to form a substituted or unsubstituted cycloalkyl, substituted or unsubstituted heterocycloalkyl, substituted or unsubstituted aryl, or substituted or unsubstituted heteroaryl;
  • R2A R2B R2C R2D R3A R3B R3C R3D R4A R4B R4C R4D R5A R5B R5C R5D R6A R6B R6C R 6D , R 7A , R 7B , R 7C , R 7D , R 8A , R 8B , R 8C , R 8D , R 1OA , R 1OB , R 1OC , and R 10D are independently hydrogen, -CC1 3 , -CBr 3 , -CF 3 , -CI 3 , -CHCl 2 , -CHBr 2 , -CHF 2 , -CHI 2 , -CH 2 C1, -CH 2 Br, -CH 2 F, -CH 2 I, -CN, -OH, -NH 2 , -COOH, -CONH 2 , -OCC1 3 , -OCF 3 , -OCBr 3 ,
  • X 2 , X 3 , X 4 , X 5 , X 6 , X 7 , X 8 , and X 10 are independently -F, -Cl, -Br, or -I; n2, n3, n4, n5, n6, n7, n8, and nlO are independently an integer from 0 to 4; m2, m3, m4, m5, m6, m7, m8, mlO, v2, v3, v4, v5, v6, v7, v8, and vlO are independently 1 or 2; and z8 is an integer from 0 to 3; wherein at least one of W 6 or W 7 is N; wherein if W 6 is C(R 6 ) or W 7 is C(R 7 ), then R 10 is not hydrogen; wherein if W 6 and W 7 are both N, then R 3 is not -S(O)2CH 3 ; and wherein if W 6 is CH and W
  • Embodiment P9 The compound of embodiment P8, having the formula:
  • Embodiment P10 The compound of embodiment P8, having the formula:
  • Embodiment Pl The compound of one of embodiments P8 to PIO, wherein R 10 is hydrogen or unsubstituted C 1 -C 6 alkyl.
  • Embodiment P12 The compound of one of embodiments P8 to P10, wherein R 10 is isopropyl.
  • Embodiment P13 The compound of one of embodiments Pl to P12, wherein R 6 is hydrogen, -OCHF2, unsubstituted C 1 -C 6 alkyl, or unsubstituted 2 to 6 membered heteroalkyl.
  • Embodiment P14 The compound of one of embodiments Pl to P12, wherein R 6 is hydrogen, -OCHF2, unsubstituted methoxy, or unsubstituted isopropoxy.
  • Embodiment Pl 5 The compound of one of embodiments Pl to P14, wherein R 7 is hydrogen, -F, -Cl, -Br, or -OCHF2.
  • Embodiment Pl 6. The compound of one of embodiments Pl to Pl 5, wherein R 8 is independently halogen, -CC1 3 , -CBr 3 , -CF 3 , -CI 3 , -CHCl 2 , -CHBr 2 , -CHF 2 , -CHI 2 , -CH 2 C1, -CH 2 Br, -CH 2 F, -CH 2 I, -OCC1 3 , -OCF 3 , -OCBr 3 , -OCI 3 , -OCHCl 2 , -OCHBr 2 , -OCHI 2 , -OCHF 2 , -OCH 2 C1, -OCH 2 Br, -OCH 2 I, -OCH 2 F, -CN, -SO
  • Embodiment Pl 7 The compound of one of embodiments Pl to Pl 5, wherein R 8 is independently halogen, -CF 3 , -CHF 2 , -CN, -OCHF 2 , -C(O)R 8C , -C(O)OR 8C , -OR 8D , unsubstituted C 1 -C 6 alkyl, unsubstituted 2 to 8 membered heteroalkyl, unsubstituted C 3 -C 8 cycloalkyl, or unsubstituted phenyl.
  • R 8 is independently halogen, -CF 3 , -CHF 2 , -CN, -OCHF 2 , -C(O)R 8C , -C(O)OR 8C , -OR 8D , unsubstituted C 1 -C 6 alkyl, unsubstituted 2 to 8 membered heteroalkyl, unsubstituted C 3 -C 8 cycl
  • Embodiment Pl 8 The compound of embodiment Pl 7, wherein R 8C is independently hydrogen or unsubstituted C 1 -C 6 alkyl.
  • Embodiment Pl 9 The compound of embodiment Pl 7, wherein R 8D is independently unsubstituted C 1 -C 6 alkyl.
  • Embodiment P20 The compound of one of embodiments Pl to Pl 5, wherein R 8 is independently -F, -Cl, -Br, -CF 3 , -CHF 2 , -CN, -C(O)H, -C(O)OCH 3 , -OCHF 2 , -OCH 3 , -OCH 2 CH 3 , -OCH 2 CF 3 , -OCH(CH 3 )CH 2 OCH 3 , -OCH 2 CHF 2 , unsubstituted methyl, unsubstituted cyclopropyl, or unsubstituted phenyl.
  • R 8 is independently -F, -Cl, -Br, -CF 3 , -CHF 2 , -CN, -C(O)H, -C(O)OCH 3 , -OCHF 2 , -OCH 3 , -OCH 2 CH 3 , -OCH 2 CF 3
  • Embodiment P21 The compound of one of embodiments Pl to Pl 5, wherein two R 8 substituents are joined to form an unsubstituted C5 cycloalkyl.
  • Embodiment P22 The compound of one of embodiments Pl to P21, wherein L 1 is a bond or unsubstituted C1-C5 alkylene.
  • Embodiment P23 The compound of one of embodiments Pl to P21, wherein L 1 is a bond.
  • Embodiment P24 The compound of one of embodiments Pl to P21, wherein L 1 is unsubstituted methylene.
  • Embodiment P25 The compound of one of embodiments Pl to P24, wherein R 9 is an R 11 - substituted or unsubstituted cycloalkyl or R 11 -substituted or unsubstituted heterocycloalkyl;
  • R 11 is independently oxo, halogen, -CX 11 3, -CHX 11 2, -CH2X 11 , -OCX 11 3,
  • X 11 is independently -F, -Cl, -Br, or -I; nl 1 is independently an integer from 0 to 4; and mi l and vl 1 are independently 1 or 2.
  • Embodiment P26 The compound of embodiment P25, wherein R 9 is an R 11 - substituted or unsubstituted C 3 -C 8 cycloalkyl or R 11 -substituted or unsubstituted 3 to 8 membered heterocycloalkyl.
  • Embodiment P27 The compound of embodiment P25, wherein R 9 is an R 11 - substituted or unsubstituted spirocyclic cycloalkyl or R 11 -substituted or unsubstituted spirocyclic heterocycloalkyl.
  • Embodiment P28 The compound of embodiment P25, wherein R 9 is
  • R 12 is hydrogen, halogen, -CX 12 3 , -CHX 12 2 , -CH 2 X 12 , -OCX 12 3 , -OCH 2 X 12 ,
  • R12A, R 12B R 12C, an j R 12D are i nc ] e p enc ] en ly hydrogen, -CC1 3 , -CBr 3 , -CF 3 , -CI 3 , -CHCl 2 , -CHBr 2 , -CHF 2 , -CHI 2 , -CH 2 C1, -CH 2 Br, -CH 2 F, -CH 2 I, -CN, -OH, -NH 2 , -COOH, -CONH 2 , -OCC1 3 , -OCF 3 , -OCBr 3 , -OCI 3 , -OCHCh, -OCHBr 2 , -OCHI 2 , -OCHF 2 , -OCH 2 C1, -OCH 2 Br, -OCH 2 I, -OCH 2 F, substituted or unsubstituted alkyl, substituted or unsubstituted
  • X 12 is independently -F, -Cl, -Br, or -I; nl2 is independently an integer from 0 to 4; vl2 is independently 1 or 2; and z11 is an integer from 0 to 13.
  • Embodiment P29 The compound of embodiment P28, wherein R 9 is
  • Embodiment P30 The compound of one of embodiments P25 to P29, wherein R 11 is independently oxo, halogen, -CX 11 3 , -CN, -C(O)OR 11c , -C(O)NR 11A R 11B , -C(O)R 11c , -OR 11D , substituted or unsubstituted C 1 -C 6 alkyl, or substituted or unsubstituted 2 to 5 membered heteroalkyl.
  • Embodiment P31 The compound of embodiment P30, wherein R 11A is independently hydrogen or unsubstituted C 1 -C 6 alkyl; and R 11B is independently hydrogen.
  • Embodiment P32 The compound of embodiment P30, wherein R 11C is independently hydrogen or unsubstituted C 1 -C 6 alkyl.
  • Embodiment P33 The compound of embodiment P30, wherein R 11D is independently hydrogen or unsubstituted C 1 -C 6 alkyl.
  • Embodiment P34 The compound of one of embodiments P25 to P29, wherein two R 11 substituents are joined to form a substituted or unsubstituted cycloalkyl.
  • Embodiment P35 The compound of one of embodiments P28 to P29, wherein R 12 is hydrogen, -C(O)R 12C , -SO ni2 R 12D , -SO V I 2 NR 12A R 12B , -C(O)OR 12C , -C(O)NR 12A R 12B , unsubstituted C 1 -C 6 alkyl, unsubstituted Cx-Cx cycloalkyl, or unsubstituted 3 to 8 membered heterocycloalkyl.
  • Embodiment P36 The compound of embodiment P35, wherein R 12A is hydrogen, unsubstituted C 1 -C 6 alkyl, or unsubstituted C 5 -C 8 cycloalkyl; and R 12B is hydrogen.
  • Embodiment P37 The compound of embodiment P35, wherein R 12C is substituted or unsubstituted C 1 -C 6 alkyl, substituted or unsubstituted 2 to 6 membered heteroalkyl, or substituted or unsubstituted C 5 -Cx cycloalkyl.
  • Embodiment P38 The compound of embodiment P35, wherein R 12D is unsubstituted C 1 -C 6 alkyl.
  • Embodiment P39 The compound of one of embodiments Pl to P24, wherein R 9 is
  • Embodiment P40 A compound, or a pharmaceutically acceptable salt or solvate thereof, having the formula:
  • Embodiment P41 A pharmaceutical composition comprising the compound of one of embodiments Pl to P40, or a pharmaceutically acceptable salt or solvate thereof, and a pharmaceutically acceptable excipient.
  • Embodiment P42 A method of treating a neurodegenerative disorder in a subject in need thereof, said method comprising administering to the subject in need thereof a therapeutically effective amount of a compound of one of embodiments Pl to P40, or a pharmaceutically acceptable salt or solvate thereof.
  • Embodiment P43 A method of treating an inflammatory disease in a subject in need thereof, said method comprising administering to the subject in need thereof a therapeutically effective amount of a compound of one of embodiments Pl to P40, or a pharmaceutically acceptable salt or solvate thereof.
  • Embodiment P44 The method of embodiment P43, wherein the inflammatory disease is encephalitis.
  • Embodiment P45 The method of embodiment P44, wherein the encephalitis is post-hemorrhagic encephalitis.
  • Embodiment P46 A method of treating a demyelinating disease in a subject in need thereof, said method comprising administering to the subject in need thereof a therapeutically effective amount of a compound of one of embodiments Pl to P40, or a pharmaceutically acceptable salt or solvate thereof.
  • Embodiment P47 The method of embodiment P46, wherein the demyelinating disease is a demyelinating disease of the central nervous system.
  • Embodiment P48 The method of embodiment P47, wherein the demyelinating disease is multiple sclerosis.
  • Embodiment P49 The method of embodiment P46, wherein the demyelinating disease is a demyelinating disease of the peripheral nervous system.
  • Embodiment P50 A method of treating a fibrotic disease in a subject in need thereof, said method comprising administering to the subject in need thereof a therapeutically effective amount of a compound of one of embodiments Pl to P40, or a pharmaceutically acceptable salt or solvate thereof.
  • Embodiment P51 The method of embodiment P50, wherein the fibrotic disease is pulmonary fibrosis, skin fibrosis, liver fibrosis, or ocular fibrosis.
  • Embodiment P52 The method of embodiment P50, wherein the fibrotic disease is idiopathic pulmonary fibrosis, scleroderma, nonalcoholic steatohepatitis, or ocular fibrosis.
  • Embodiment P53 A method of treating cancer in a subject in need thereof, said method comprising administering to the subject in need thereof a therapeutically effective amount of a compound of one of embodiments Pl to P40, or a pharmaceutically acceptable salt or solvate thereof.
  • Embodiment P54 The method of embodiment P53, wherein the cancer is brain cancer.
  • Embodiment P55 The method of embodiment P54, wherein the cancer is glioblastoma.
  • Embodiment P56 A method of modulating LPAR1 activity in a subject, said method comprising administering to the subject a compound of one of embodiments Pl to P40, or a pharmaceutically acceptable salt or solvate thereof.
  • Embodiment 1 A compound, or a pharmaceutically acceptable salt or solvate thereof, having the formula: wherein
  • L 1 is a bond or substituted or unsubstituted C1-C5 alkylene
  • R 1 is unsubstituted C2-C5 alkyl
  • W 2 is N or C(R 2 );
  • R 2 is hydrogen, halogen, -CX 2 3 , -CHX 2 2 , -CH 2 X 2 , -OCX 2 3 , -OCH 2 X 2 ,
  • R 3 is hydrogen, halogen, -CX 3 3 , -CHX 3 2 , -CH 2 X 3 , -OCX 3 3 , -OCH 2 X 3 ,
  • W 4 is N or C(R 4 );
  • R 4 is hydrogen, halogen, -CX 4 3 , -CHX 4 2 , -CH 2 X 4 , -OCX 4 3 , -OCH 2 X 4 ,
  • W 5 is N or C(R 5 );
  • R 5 is hydrogen, halogen, -CX 5 3 , -CHX 5 2 , -CH 2 X 5 , -OCX 5 3 , -OCH 2 X 5 ,
  • R 2 and R 3 substituents may optionally be joined to form a substituted or unsubstituted cycloalkyl, substituted or unsubstituted heterocycloalkyl, substituted or unsubstituted aryl, or substituted or unsubstituted heteroaryl;
  • R 3 and R 4 substituents may optionally be joined to form a substituted or unsubstituted cycloalkyl, substituted or unsubstituted heterocycloalkyl, substituted or unsubstituted aryl, or substituted or unsubstituted heteroaryl;
  • R 4 and R 5 substituents may optionally be joined to form a substituted or unsubstituted cycloalkyl, substituted or unsubstituted heterocycloalkyl, substituted or unsubstituted aryl, or substituted or unsubstituted heteroaryl;
  • W 6 is N or C(R 6 );
  • R 6 is hydrogen, halogen, -CX 6 3 , -CHX 6 2 , -CH2X 6 , -OCX 6 3 , -OCH2X 6 , -OCHX 6 2, -CN, -SOn 6 R 6D , -SO V6 NR 6A R 6B , -NR 6C NR 6A R 6B , -ONR 6A R 6B , -NHC(O)NR 6C NR 6A R 6B , -NHC(O)NR 6A R 6B , -N(O)m6, -NR 6A R 6B , -C(O)R 6C , -C(O)OR 6C , -C(O)NR 6A R 6B , -OR 6D , -SR 6D , -NR 6A SO 2 R 6D , -NR 6A C(O)R 6C , -NR 6A C(O)OR 6C , -
  • W 7 is N, N + -O', or C(R 7 );
  • R 7 is hydrogen, halogen, -CX 7 3 , -CHX 7 2 , -CH 2 X 7 , -OCX 7 3 , -OCH2X 7 , -OCHX 7 2, -CN, -SOn7R 7D , -SOV7NR 7A R 7B , -NR 7C NR 7A R 7B , -ONR 7A R 7B , -NHC(O)NR 7C NR 7A R 7B , -NHC(O)NR 7A R 7B , -N(O)m7, -NR 7A R 7B , -C(O)R 7C , -C(O)OR 7C , -C(O)NR 7A R 7B , -OR 7D , -SR 7D , -NR 7A SO 2 R 7D , -NR 7A C(O)R 7C , -NR 7A C(O)OR 7C ,
  • R 8 is independently halogen, -CX 8 3 , -CHX 8 2 , -CH 2 X 8 , -OCX 8 3 , -OCH2X 8 , -OCHX 8 2 , -CN, -SO n8 R 8D , -SO V8 NR 8A R 8B , -NR 8C NR 8A R 8B , -ONR 8A R 8B , -NHC(O)NR 8C NR 8A R 8B , -NHC(O)NR 8A R 8B , -N(O) m8 , -NR 8A R 8B , -C(O)R 8C , -C(O)OR 8C , -C(O)NR 8A R 8B , -OR 8D , -SR 8D , -NR 8A SO 2 R 8D , -NR 8A C(O)R 8C , -NR 8A C(O)OR
  • X 2 , X 3 , X 4 , X 5 , X 6 , X 7 , and X 8 are independently -F, -Cl, -Br, or -I; n2, n3, n4, n5, n6, n7, and n8 are independently an integer from 0 to 4; m2, m3, m4, m5, m6, m7, m8, v2, v3, v4, v5, v6, v7, and v8 are independently 1 or 2; and z8 is an integer from 0 to 3.
  • Embodiment 2 The compound of embodiment 1, having the formula:
  • Embodiment 3 The compound of embodiment 1, having the formula:
  • Embodiment 4 The compound of embodiment 1, having the formula:
  • Embodiment 5 The compound of embodiment 1, having the formula:
  • Embodiment 6 The compound of one of embodiments 1 to 5, wherein R 1 is unsubstitutedC 3 alkyl.
  • Embodiment 7 The compound of one of embodiments 1 to 5, wherein R 1 is isopropyl.
  • Embodiment 8 A compound, or a pharmaceutically acceptable salt or solvate thereof, having the formula: wherein
  • L 1 is a bond or substituted or unsubstituted C1-C5 alkylene
  • R 2 is hydrogen, halogen, -CX 2 3 , -CHX 2 2 , -CH 2 X 2 , -OCX 2 3 , -OCH 2 X 2 ,
  • R 4 is hydrogen, halogen, -CX 4 3 , -CHX 4 2 , -CH 2 X 4 , -OCX 4 3 , -OCH 2 X 4 ,
  • R 5 is hydrogen, halogen, -CX 5 3 , -CHX 5 2 , -CH 2 X 5 , -OCX 5 3 , -OCH 2 X 5 ,
  • R 2 and R 3 substituents may optionally be joined to form a substituted or unsubstituted cycloalkyl, substituted or unsubstituted heterocycloalkyl, substituted or unsubstituted aryl, or substituted or unsubstituted heteroaryl;
  • R 3 and R 4 substituents may optionally be joined to form a substituted or unsubstituted cycloalkyl, substituted or unsubstituted heterocycloalkyl, substituted or unsubstituted aryl, or substituted or unsubstituted heteroaryl;
  • R 4 and R 5 substituents may optionally be joined to form a substituted or unsubstituted cycloalkyl, substituted or unsubstituted heterocycloalkyl, substituted or unsubstituted aryl, or substituted or unsubstituted heteroaryl;
  • W 6 is N or C(R 6 );
  • R 6 is hydrogen, halogen, -CX 6 3 , -CHX 6 2 , -CH2X 6 , -OCX 6 3 , -OCH2X 6 , -OCHX 6 2, -CN, -SOn 6 R 6D , -SO V6 NR 6A R 6B , -NR 6C NR 6A R 6B , -ONR 6A R 6B , -NHC(O)NR 6C NR 6A R 6B , -NHC(O)NR 6A R 6B , -N(O)m6, -NR 6A R 6B , -C(O)R 6C , -C(O)OR 6C , -C(O)NR 6A R 6B , -OR 6D , -SR 6D , -NR 6A SO 2 R 6D , -NR 6A C(O)R 6C , -NR
  • W 7 is N, N + -O', or C(R 7 );
  • R 7 is hydrogen, halogen, -CX 7 3 , -CHX 7 2 , -CH 2 X 7 , -OCX 7 3 , -OCH2X 7 , -OCHX 7 2, -CN, -SOn7R 7D , -SOV7NR 7A R 7B , -NR 7C NR 7A R 7B , -ONR 7A R 7B , -NHC(O)NR 7C NR 7A R 7B , -NHC(O)NR 7A R 7B , -N(O)m7, -NR 7A R 7B , -C(O)R 7C , -C(O)OR 7C , -C(O)NR 7A R 7B , -OR 7D , -SR 7D , -NR 7A SO 2 R 7D , -NR 7A C(O)R 7C , -NR 7A C(O)OR 7C ,
  • R 8 is independently halogen, -CX 8 3 , -CHX 8 2 , -CH 2 X 8 , -OCX 8 3 , -OCH2X 8 , -OCHX 8 2 , -CN, -SO n8 R 8D , -SO V8 NR 8A R 8B , -NR 8C NR 8A R 8B , -ONR 8A R 8B , -NHC(O)NR 8C NR 8A R 8B , -NHC(O)NR 8A R 8B , -N(O) m8 , -NR 8A R 8B , -C(O)R 8C , -C(O)OR 8C , -C(O)NR 8A R 8B , -OR 8D , -SR 8D , -NR 8A SO 2 R 8D , -NR 8A C(O)R 8C , -NR 8A C(O)OR
  • R 9 is substituted or unsubstituted cycloalkyl or substituted or unsubstituted heterocycloalkyl
  • R 10 is hydrogen, halogen, -CX 10 3 , -CHX 10 2 , -CH 2 X 10 , -OCX 10 3 , -OCH2X 10 , -OCHX 10 2, -CN, -SOnioR 10D , -SOvioNR 10A R 10B , -NR 1OC NR 1OA R 1OB , -ONR 10A R 10B , -NHC(O)NR 10C NR 10A R 10B , -NHC(O)NR 10A R 10B , -N(O)mio, -NR 10A R 10B , -C(O)R 10C , -C(O)OR 10C , -C(O)NR 10A R 10B , -OR 10D , -SR 1OD , -NR 10A SO2R 10D , -NR 10A C(O)R 10C , -NR 10A C(O)OR 10C
  • R 10 and R 2 substituents may optionally be joined to form a substituted or unsubstituted cycloalkyl, substituted or unsubstituted heterocycloalkyl, substituted or unsubstituted aryl, or substituted or unsubstituted heteroaryl; 2A R2B R2C 2D 3A R3B R3C 3D 4A R4B R4C R4D 5A 5B 5C R5D R6A R6B R6C R 6D , R 7A , R 7B , R 7C , R 7D , R 8A , R 8B , R 8C , R 8D , R 1OA , R 1OB , R 1OC , and R 10D are independently hydrogen, -CC1 3 , -CBr 3 , -CF 3 , -CI 3 , -CHCl 2 , -CHBr 2 , -CHF 2 , -CHI 2 , -CH 2 C
  • X 2 , X 3 , X 4 , X 5 , X 6 , X 7 , X 8 , and X 10 are independently -F, -Cl, -Br, or -I; n2, n3, n4, n5, n6, n7, n8, and nlO are independently an integer from 0 to 4; m2, m3, m4, m5, m6, m7, m8, mlO, v2, v3, v4, v5, v6, v7, v8, and vlO are independently 1 or 2; and z8 is an integer from 0 to 3; wherein at least one of W 6 or W 7 is N; wherein if W 6 is C(R 6 ) or W 7 is C(R 7 ), then R 10 is not hydrogen; wherein if W 6 and W 7 are both N, then R 3 is not -S(O)2CH 3 ; and wherein if W 6 is CH and W
  • Embodiment 9 The compound of embodiment 8, having the formula:
  • Embodiment 10 The compound of embodiment 8, having the formula: [0565] Embodiment 11. The compound of one of embodiments 8 to 10, wherein R 10 is hydrogen or unsubstituted C 1 -C 6 alkyl.
  • Embodiment 12 The compound of one of embodiments 8 to 10, wherein R 10 is isopropyl.
  • Embodiment 13 The compound of one of embodiments 1 to 12, wherein R 6 is hydrogen, -OCHF2, unsubstituted C 1 -C 6 alkyl, or unsubstituted 2 to 6 membered heteroalkyl.
  • Embodiment 14 The compound of one of embodiments 1 to 12, wherein R 6 is hydrogen, -OCHF2, unsubstituted methoxy, or unsubstituted isopropoxy.
  • Embodiment 15 The compound of one of embodiments 1 to 14, wherein R 7 is hydrogen, -F, -Cl, -Br, or -OCHF2.
  • Embodiment 16 The compound of one of embodiments 1 to 15, wherein R 8 is independently halogen, -CCl 3 , -CBr 3 , -CF 3 , -CI 3 , -CHCI2, -CHBr 2 , -CHF 2 , -CHI 2 , -CH 2 C1, -CH 2 Br, -CH 2 F, -CH2I, -OCC1 3 , -OCF 3 , -OCBr 3 , -OCI 3 , -OCHCl 2 , -OCHBr 2 , -OCHI 2 , -OCHF2, -OCH2CI, -OCH 2 Br, -OCH2I, -OCH2F, -CN, -SO 3 H, -OSO 3 H, -SO2NH2, -NHNH 2 , -ONH2, -NHC(O)NHNH 2 , -NHC(O)NH 2 , -NO2,
  • Embodiment 17 The compound of one of embodiments 1 to 15, wherein R 8 is independently halogen, -CF 3 , -CHF 2 , -CN, -OCHF 2 , -C(O)R 8C , -C(O)OR 8C , -OR 8D , unsubstituted C 1 -C 6 alkyl, unsubstituted 2 to 8 membered heteroalkyl, unsubstituted C 3 -C 8 cycloalkyl, or unsubstituted phenyl.
  • R 8 is independently halogen, -CF 3 , -CHF 2 , -CN, -OCHF 2 , -C(O)R 8C , -C(O)OR 8C , -OR 8D , unsubstituted C 1 -C 6 alkyl, unsubstituted 2 to 8 membered heteroalkyl, unsubstituted C 3 -C 8 cycloal
  • Embodiment 18 The compound of embodiment 17, wherein R 8C is independently hydrogen or unsubstituted C 1 -C 6 alkyl.
  • Embodiment 19 The compound of embodiment 17, wherein R 8D is independently unsubstituted C 1 -C 6 alkyl.
  • Embodiment 20 The compound of one of embodiments 1 to 15, wherein R 8 is independently -F, -Cl, -Br, -CF 3 , -CHF 2 , -CN, -C(O)H, -C(O)OCH 3 , -OCHF 2 , -OCH 3 , -OCH2CH 3 , -OCH2CF3, -OCH(CH 3 )CH 2 OCH 3 , -OCH2CHF2, unsubstituted methyl, unsubstituted cyclopropyl, or unsubstituted phenyl.
  • R 8 is independently -F, -Cl, -Br, -CF 3 , -CHF 2 , -CN, -C(O)H, -C(O)OCH 3 , -OCHF 2 , -OCH 3 , -OCH2CH 3 , -OCH2CF3, -OCH(CH 3 )
  • Embodiment 21 The compound of one of embodiments 1 to 15, wherein two R 8 substituents are joined to form an unsubstituted C 8 cycloalkyl.
  • Embodiment 22 The compound of one of embodiments 1 to 21, wherein L 1 is a bond or unsubstituted C1-C5 alkylene.
  • Embodiment 23 The compound of one of embodiments 1 to 21, wherein L 1 is a bond.
  • Embodiment 24 The compound of one of embodiments 1 to 21, wherein L 1 is unsubstituted methylene.
  • Embodiment 25 The compound of one of embodiments 1 to 24, wherein R 9 is an R 11 - substituted or unsubstituted cycloalkyl or R 11 -substituted or unsubstituted heterocycloalkyl;
  • R 11 is independently oxo, halogen, -CX 11 3, -CHX 11 2, -CH2X 11 , -OCX 11 3, -OCH2X 11 , -OCHX 11 2, -CN, -SOn11R 11D , -SOv11NR 11A R 11B , -NR 11C NR 11A R 11B , -ONR 11A R 11B , -NHC(O)NR 11C NR 11A R 11B , -NHC(O)NR 11A R 11B , -N(O)m11, -NR 11A R 11B , -C(O)R 11C , -C(O)OR 11C , -C(O)NR 11A R 11B , -OR 11D , -SR 11D , -NR 11A SO 2 R 11D , -NR 11A C(O)R 11C , -NR 11A C(O)OR 11C , -NR 11
  • X 11 is independently -F, -Cl, -Br, or -I; nl 1 is independently an integer from 0 to 4; and mi l and vl 1 are independently 1 or 2.
  • Embodiment 26 The compound of embodiment 25, wherein R 9 is an R 11 - substituted or unsubstituted C 5 -Cx cycloalkyl or R 11 -substituted or unsubstituted 3 to 8 membered heterocycloalkyl.
  • Embodiment 27 The compound of embodiment 25, wherein R 9 is an R 11 - substituted or unsubstituted spirocyclic cycloalkyl or R 11 -substituted or unsubstituted spirocyclic heterocycloalkyl.
  • Embodiment 28 The compound of embodiment 25, wherein R 9 is R 12 is hydrogen, halogen, -CX 12 3 , -CHX 12 2 , -CH 2 X 12 , -OCX 12 3 , -OCH 2 X 12 , -OCHX 12 2 , -SOni 2 R 12D , -SOvi 2 NR 12A R 12B , -C(O)R 12C , -C(O)OR 12C , -C(O)NR 12A R 12B , -OR 12D , substituted or unsubstituted alkyl, substituted or unsubstituted heteroalkyl, substituted or unsubstituted cycloalkyl, substituted or unsubstituted heterocycloalkyl, substituted or unsubstituted aryl, or substituted or unsubstituted heteroaryl;
  • R12A, R 12B R 12C, an j R 12D are i n d e p en d en ly hydrogen, -CC1 3 , -CBr 3 , -CF 3 , -CI 3 , -CHCl 2 , -CHBr 2 , -CHF 2 , -CHI 2 , -CH 2 C1, -CH 2 Br, -CH 2 F, -CH 2 I, -CN, -OH, -NH 2 , -COOH, -CONH 2 , -OCC1 3 , -OCF 3 , -OCBr 3 , -OCI 3 , -OCHCl 2 , -OCHBr 2 , -OCHI 2 , -OCHF 2 , -OCH 2 C1, -OCH 2 Br, -OCH 2 I, -OCH 2 F, substituted or unsubstituted alkyl, substituted or unsubstituted
  • X 12 is independently -F, -Cl, -Br, or -I; nl2 is independently an integer from 0 to 4; vl2 is independently 1 or 2; and z11 is an integer from 0 to 13.
  • Embodiment 29 The compound of embodiment 28, wherein R 9 is
  • Embodiment 30 The compound of one of embodiments 25 to 29, wherein R 11 is independently oxo, halogen, -CX 11 3 , -CHX n 2 , -CN, -SO n 11R 11D , -C(O)R 11c , -C(O)OR 11c , -C(O)NR 11A R 11B , -C(O)R 11c , -OR 11D , -NR 11A SO 2 R 11D , -NR 11A C(O)R 11C , -NR 11A C(O)OR 11C , substituted or unsubstituted C 1 -C 6 alkyl, substituted or unsubstituted 2 to 5 membered heteroalkyl, or substituted or unsubstituted 5 to 10 membered heteroaryl.
  • Embodiment 31 The compound of embodiment 30, wherein R 11A is independently hydrogen or unsubstituted C 1 -C 6 alkyl; and R 11B is independently hydrogen.
  • Embodiment 32 The compound of embodiment 30, wherein R 11C is independently hydrogen or unsubstituted C 1 -C 6 alkyl.
  • Embodiment 33 The compound of embodiment 30, wherein R 11D is independently hydrogen or unsubstituted C 1 -C 6 alkyl.
  • Embodiment 34 The compound of one of embodiments 25 to 29, wherein two R 11 substituents are joined to form a substituted or unsubstituted cycloalkyl.
  • Embodiment 35 The compound of one of embodiments 28 to 29, wherein R 12 is hydrogen, -C(O)R 12C , -SO ni2 R 12D , -SO V I 2 NR 12A R 12B , -C(O)OR 12C , -C(O)NR 12A R 12B , unsubstituted C 1 -C 6 alkyl, unsubstituted Cx-Cx cycloalkyl, or unsubstituted 3 to 8 membered heterocycloalkyl.
  • Embodiment 36 The compound of embodiment 35, wherein R 12A is hydrogen, unsubstituted C 1 -C 6 alkyl, or unsubstituted Cx-Cx cycloalkyl; and R 12B is hydrogen.
  • Embodiment 37 The compound of embodiment 35, wherein R 12C is substituted or unsubstituted C 1 -C 6 alkyl, substituted or unsubstituted 2 to 6 membered heteroalkyl, or substituted or unsubstituted Cx-Cx cycloalkyl.
  • Embodiment 38 The compound of embodiment 35, wherein R 12D is unsubstituted C 1 -C 6 alkyl.
  • Embodiment 39 The compound of one of embodiments 1 to 24, wherein R 9 is
  • Embodiment 40 A compound, or a pharmaceutically acceptable salt or solvate thereof, having the formula: ⁇
  • Embodiment 41 A pharmaceutical composition comprising the compound of one of embodiments 1 to 40, or a pharmaceutically acceptable salt or solvate thereof, and a pharmaceutically acceptable excipient.
  • Embodiment 42 A method of treating a neurodegenerative disorder in a subject in need thereof, said method comprising administering to the subject in need thereof a therapeutically effective amount of a compound of one of embodiments 1 to 40, or a pharmaceutically acceptable salt or solvate thereof.
  • Embodiment 43 A method of treating an inflammatory disease in a subject in need thereof, said method comprising administering to the subject in need thereof a therapeutically effective amount of a compound of one of embodiments 1 to 40, or a pharmaceutically acceptable salt or solvate thereof.
  • Embodiment 44 The method of embodiment 43, wherein the inflammatory disease is encephalitis.
  • Embodiment 45 The method of embodiment 44, wherein the encephalitis is post-hemorrhagic encephalitis.
  • Embodiment 46 A method of treating a demyelinating disease in a subject in need thereof, said method comprising administering to the subject in need thereof a therapeutically effective amount of a compound of one of embodiments 1 to 40, or a pharmaceutically acceptable salt or solvate thereof.
  • Embodiment 47 The method of embodiment 46, wherein the demyelinating disease is a demyelinating disease of the central nervous system.
  • Embodiment 48 The method of embodiment 47, wherein the demyelinating disease is multiple sclerosis.
  • Embodiment 49 The method of embodiment 46, wherein the demyelinating disease is a demyelinating disease of the peripheral nervous system.
  • Embodiment 50 A method of treating a fibrotic disease in a subject in need thereof, said method comprising administering to the subject in need thereof a therapeutically effective amount of a compound of one of embodiments 1 to 40, or a pharmaceutically acceptable salt or solvate thereof.
  • Embodiment 5E The method of embodiment 50, wherein the fibrotic disease is pulmonary fibrosis, skin fibrosis, liver fibrosis, or ocular fibrosis.
  • Embodiment 52 The method of embodiment 50, wherein the fibrotic disease is idiopathic pulmonary fibrosis, scleroderma, nonalcoholic steatohepatitis, or ocular fibrosis.
  • Embodiment 53 A method of treating cancer in a subject in need thereof, said method comprising administering to the subject in need thereof a therapeutically effective amount of a compound of one of embodiments 1 to 40, or a pharmaceutically acceptable salt or solvate thereof.
  • Embodiment 54 The method of embodiment 53, wherein the cancer is brain cancer.
  • Embodiment 55 The method of embodiment 54, wherein the cancer is glioblastoma.
  • Embodiment 56 A method of modulating LPAR1 activity in a subject, said method comprising administering to the subject a compound of one of embodiments 1 to 40, or a pharmaceutically acceptable salt or solvate thereof.
  • MS Multiple sclerosis
  • a chronic progressive disorder is an inflammatory autoimmune disease whereby the dysregulated immune system attacks the patient’s own protective myelin sheath. If left unchecked, the signal transduction along denuded axons can become increasingly deteriorated, eventually leading to the permanent damage of the affected nerve fibers.
  • MS patients have increased levels of LPAs in the serum (Balood et al., Hum. Immunol., 2014, 75, 411-413).
  • LPA can induce a pro-inflammatory response through the activation of LPAR1 found in MS patient monocyte-derived macrophages by stimulating the production of pro-inflammatory cytokines such as interleukin- ip (IL-1 P) and tumor necrosis factor alpha (TNFa), as well as suppressing the production of anti-inflammatory cytokines such as interleukin-2 (IL-2).
  • pro-inflammatory cytokines such as interleukin- ip (IL-1 P) and tumor necrosis factor alpha (TNFa
  • IL-2 interleukin-2
  • EAE mouse experimental autoimmune encephalomyelitis
  • While dampening the inflammatory immune attack on the myelin sheath can constitute an effective approach to the treatment of MS, promoting the remyelination of damaged, denuded axons would represent another attractive approach (Deshmukh et al., Nature, 2013, 502, 327- 332).
  • neuronal remyelination can be achieved by driving the differentiation of oligodendrocyte precursor cells (OPC 8 ), an endogenous stem cell, to myelin-producing oligodendrocytes (Najm et al., Nature, 2015, 522, 216-220). It has been demonstrated that LPAR1 is highly expressed in OPC 8 .
  • LPAR1 myelin-protein positive
  • LPA-LPAR1 signaling axis has been shown to play an important role in both demyelination (i.e., promotion of an inflammatory environment) and remyelination (i.e., prevention of OPC differentiation into oligodendrocyte) of axons, the identification of a potent and selective LPAR1 antagonists would thus be of significant relevance in the treatment of MS and other inflammatory demyelination disorders.
  • Suitable reference books and treatises that detail the synthesis of reactants useful in the preparation of compounds described herein, or provide references to articles that describe the preparation include for example, “Synthetic Organic Chemistry,” New York: John Wiley & Sons, Inc., 1982; Sandler S. R. etal. , “Organic Functional Group Preparations,” 2 nd ed., New York: Academic Press, 1983; House, H. O., “Modern Synthetic Reactions,” 2 nd ed., Menlo Park: W. A.

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WO2024159176A1 (en) * 2023-01-27 2024-08-02 Contineum Therapeutics, Inc. Crystalline compound of an lpar1 antagonist
WO2025193711A1 (en) * 2024-03-12 2025-09-18 Contineum Therapeutics, Inc. Peripherally restricted lpar1 antagonists and uses thereof

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