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  • A61K31/5375—1,4-Oxazines, e.g. morpholine
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  • C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
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  • C12Y301/03048—Protein-tyrosine-phosphatase (3.1.3.48)

Definitions

• PTPN2 encodes a protein tyrosine phosphatase that has been implicated in a number of intracellular signaling pathways of immune cells.
• PTPN2 can negatively regulate ab TCR T cell receptor (TCR) signaling by dephosphorylating and inactivating, e.g., the Src family kinase including LCK.
• TCR ab TCR T cell receptor
• PTPN2 can antagonize growth factor or cytokine -mediated signaling required for T cell function, homeostasis, and/or differentiation by dephosphorylating and inactivating JAK family kinases, e.g., JAK-1 and JAK-3, and/or target substrates of the JAK family kinases, e.g., STAT-1, STAT-3, and STAT-5.
• JAK family kinases e.g., JAK-1 and JAK-3
• target substrates of the JAK family kinases e.g., STAT-1, STAT-3, and STAT-5.
• PTPN2 single nucleotide polymorphisms have been linked with the development of several human autoimmune diseases including, but are not limited to, type 1 diabetes, rheumatoid arthritis, Crohn's disease, and celiac disease.
• SNPs single nucleotide polymorphisms
• a PTPN2 variant, rsl893217(C) has been associated with about 40% decrease in PTPN2 mRNA expression in CD4+ T cells, as well as the development of type 1 diabetes.
• PTPN2 mRNA expression levels in lung cancer tissues have been shown to be higher than those in normal lung tissues or adjacent normal tissues, such overexpression of PTPN2 promoting proliferation of lung cancer cells.
• two PTPN2 SNPs, rs2847297 and rs2847282 have been associated with a decrease in both PTPN2 mRNA expression and lung cancer risk, especially squamous cell lung carcinoma risk.
• Cancer is the second leading cause of human death. There were close to 10 million deaths from cancer worldwide in 2018 and 17 million new cases were diagnosed. In the United States alone, cancer causes the death of over a half-million people annually, with some 1.7 million new cases diagnosed per year (excluding basal cell and squamous cell skin cancers). Lung, liver, stomach, and bowel are the most common causes of cancer death worldwide, accounting for more than four in ten of all cancer deaths.
• compositions and methods of the present disclosure address these needs and provide additional advantages.
• W 1 is N, N(R 1 ), C(R 1 ), C(R 1 )(R 1a ), C(O), S(O), S(O) 2 , S(O)(NR 1 ), S(O)(R 1 ), or P(O)(R 1 );
• W 2 is N, N(R 2 ), C(R 2 ), C(R 2 )(R 2a ), C(O), S(O), S(O) 2 , S(O)(NR 2 ), S(O)(R 2 ), or P(O)(R 2 );
• W 3 is N, N(R 3 ), C(R 3 ), C(R 3 )(R 3a ), C(O), S(O), S(O) 2 , S(O)(NR 3 ), S(O)(R 3 ), or P(O)(R 3 );
• W 4 is N, N(R 1 ), C(R 1 ), C(R 1 )(R 1a ), C(O
• X is C(R 5 ).
• Y is C(R 6 ).
• Z is C(R 7 ).
• J 1 is N and J 2 is C(R 9 )(R 9a ).
• J 1 is C(R 8 ) and J 2 is C(R 9 )(R 9a ).
• J 2 is CH 2 .
• J 1 is C and J 2 is C(R 9 ).
• J 3 is N(H).
• the subject compound, or a pharmaceutically acceptable salt or solvate thereof has the structure of Formula (Ia-3), (Ib-3), or (Ic-3): ( )
• the subject compound, or a pharmaceutically acceptable salt or solvate thereof has the structure of Formula (Ia-3): Formula (Ia-3).
• W 1 is N
• W 2 is C(R 2 )
• W 3 is C(R 3 )
• W 4 is C(R 4 ).
• R 2 is hydrogen
• R 3 is hydrogen
• R 4 is hydrogen.
• the subject compound, or a pharmaceutically acceptable salt or solvate thereof has the structure of Formula (Ig-3), (Ih-3), or (Ii-3): [0021] In some embodiments, the subject compound, or a pharmaceutically acceptable salt or solvate thereof, has the structure of Formula (Ig-3): Formula (Ig-3). [0022] In some embodiments, W 1 is C(R 1 ) and W 2 is C(R 2 ). [0023] In some embodiments, R 1 is hydrogen and R 2 is hydrogen. [0024] In some embodiments, W 3 is C(O) and W 4 is N(R 4 ). [0025] In some embodiments, R 4 is methyl.
• a compound of Formula (II-3), or a pharmaceutically acceptable salt or solvate thereof Formula (II-3); wherein: V 1 is a bond or S; V 4 is a bond or S, wherein when V 1 is a bond then V 4 is S and when V 1 is S, then V 4 is a bond; V 2 is N or C(R 2 ); V 3 is N or C(R 3 ); X is N or C(R 5 ); Y is N or C(R 6 ); Z is N or C(R 7 ); J 1 is N, C, or C(R 8 ); J 2 is N, N(R 9 ), C(R 9 ), C(R 9 )(R 9a ), or C(O); J 3 is N(R 10 ) or C(R 10 )(R 10a ); R 2 and R 2a are independently selected from hydrogen, halogen, -CN, C 1-6 alkyl, C 2-6 alkenyl, C 2-6 alkynyl
• R 5 is selected from hydrogen and halogen.
• R 6 is -OH.
• R 7 is hydrogen.
• R 9 is hydrogen, R 9a is hydrogen, and R 10 is hydrogen.
• R 2 is -OR 12 ; and R 12 is independently selected from C 1-6 alkyl, C 3-6 cycloalkyl, -CH 2 - C 3-6 cycloalkyl, C 2-9 heterocycloalkyl, and -CH 2 -C 2-9 heterocycloalkyl, wherein C 1-6 alkyl, C 3-6 cycloalkyl, -CH 2 -C 3- 6 cycloalkyl, C 2-9 heterocycloalkyl, and -CH 2 -C 2-9 heterocycloalkyl, are optionally substituted with one, two, or three R 20k .
• R 20k is independently selected from oxo, -CN, halogen, -CN, C 1-6 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 3-6 cycloalkyl, -CH 2 -C 3-6 cycloalkyl, C 1-6 heteroalkyl, C 2-9 heterocycloalkyl, -CH 2 -C 2-9 heterocycloalkyl, C 6-10 aryl, -CH 2 -C 6-10 aryl, C 1-9 heteroaryl, -CH 2 -C 1-9 heteroaryl, -OR 21 , -SR 21 , -N(R 22 )(R 23 ), -C(O)OR 22 , - C(O)N(R 22 )(R 23 ), -C(O)C(O)N(R 22 )(R 23 ), -OC(O)N(R 22 )(R 23 ), -N(R 24 )
• R 2 is selected from , and .
• R 2 is -N(R 12 )(R 13 );
• R 13 is independently hydrogen;
• R 12 is independently selected from C 1-6 alkyl, C 3-6 cycloalkyl, -CH 2 -C 3-6 cycloalkyl, C 2-9 heterocycloalkyl, -CH 2 -C 2-9 heterocycloalkyl, C 6-10 aryl, - CH 2 -C 6-10 aryl, C 1-9 heteroaryl, and -CH 2 -C 1-9 heteroaryl, wherein C 1-6 alkyl, C 3-6 cycloalkyl, -CH 2 -C 3-6 cycloalkyl, C 2- 9 heterocycloalkyl, -CH 2 -C 2-9 heterocycloalkyl, C 6-10 aryl, -CH 2 -C 6-10 aryl, C 1-9 heteroaryl, and -CH 2 -C 1-9
• R 20k is independently selected from oxo, -CN, halogen, -CN, C 1-6 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 3-6 cycloalkyl, -CH 2 -C 3-6 cycloalkyl, C 1-6 heteroalkyl, C 2-9 heterocycloalkyl, -CH 2 -C 2-9 heterocycloalkyl, C 6-10 aryl, -CH 2 -C 6-10 aryl, C 1-9 heteroaryl, -CH 2 -C 1-9 heteroaryl, -OR 21 , -SR 21 , -N(R 22 )(R 23 ), -C(O)OR 22 , - C(O)N(R 22 )(R 23 ), -C(O)C(O)N(R 22 )(R 23 ), -OC(O)N(R 22 )(R 23 ), -N(R 24 )
• R 2 is selected from C 1-6 alkyl, C 2-6 alkynyl, C 3-6 cycloalkyl, C 2-9 heterocycloalkyl, C 6 - 10aryl, and C 1-9 heteroaryl, wherein C 1-6 alkyl, C 2-6 alkynyl, C 3-6 cycloalkyl, C 2-9 heterocycloalkyl, C 6-10 aryl, and C 1 - 9heteroaryl are optionally substituted with one, two, or three R 20b .
• R 20b is independently selected from oxo, -CN, halogen, C 1-6 alkyl, C 3-6 cycloalkyl, - N(R 22 )(R 23 ), -C(O)R 25 , -S(O) 2 R 25 , and -P(O)(R 25 ) 2 , wherein C 1-6 alkyl and C 3-6 cycloalkyl are optionally substituted with one, two, or three groups independently selected from halogen, oxo, -CN, C 1-6 alkyl, C 1-6 haloalkyl, C 1-6 alkoxy, C 1-6 haloalkoxy, -OR 21 , -SR 21 , -N(R 22 )(R 23 ), -C(O)OR 22 , -C(O)N(R 22 )(R 23 ), -C(O)C(O)N(R 22 )(R 23 ), -OC(O
• R 2 is selected from C 1-6 alkyl, C 2-9 heterocycloalkyl, C 1-9 heteroaryl, -OR 12 , - N(R 12 )(R 13 ), -C(O)R 15 , -C(O)N(R 12 )(R 13 ), wherein C 1-6 alkyl, C 2-9 heterocycloalkyl, and C 1-9 heteroaryl are optionally substituted with one, two, or three R 20b .
• R 2 is selected from -OR 12 , -N(R 12 )(R 13 ), -C(O)R 15 , -C(O)N(R 12 )(R 13 );
• R 13 is hydrogen;
• R 26 is independently selected from halogen, oxo, -CN, C 1-6 alkyl, C 1-6 haloalkyl, C 1-6 alkoxy, C 1-6 haloalkoxy, - OR 21 , -SR 21 , -N(R 22 )(R 23 ), -C(O)OR 22 , -C(O)N(R 22 )(R 23 ), -C(O)C(O)N(R 22 )(R 23 ), -OC(O)N(R 22 )(R 23 ), - N(R 24 )C(O)N(R 22 )(R 23 ), -N(R 24 )C(O)OR 25 , -N(R 24 )
• R 2 is selected from -OR 12 , -N(R 12 )(R 13 ), -C(O)R 15 , -C(O)N(R 12 )(R 13 );
• R 13 is hydrogen;
• R 26 is independently selected from halogen, oxo, -CN, C 1-6 alkyl, C 1-6 haloalkyl, C 1-6 alkoxy, C 1-6 haloalkoxy, - OR 21 , -SR 21 , -N(R 22 )(R 23 ), -C(O)OR 22 , -C(O)N(R 22 )(R 23 ), -C(O)C(O)N(R 22 )(R 23 ), -OC(O)N(R 22 )(R 23 ), - N(R 24 )C(O)N(R 22 )(R 23 ), -N(R 24 )C(O)OR 25 , -N(R 24 )
• R 2 is selected from R 26 is independently selected from halogen, oxo, -CN, C 1-6 alkyl, C 1-6 haloalkyl, C 1-6 alkoxy, C 1-6 haloalkoxy, - OR 21 , -SR 21 , -N(R 22 )(R 23 ), -C(O)OR 22 , -C(O)N(R 22 )(R 23 ), -C(O)C(O)N(R 22 )(R 23 ), -OC(O)N(R 22 )(R 23 ), - N(R 24 )C(O)N(R 22 )(R 23 ), -N(R 24 )C(O)OR 25 , -N(R 24 )C(O)R 25 , -N(R 24 )S(O) 2 R 25 , -C(O)R 25 , -S(O) 2 R 25 , -S(O) 2 R 25 , -
• R 26 is independently selected from halogen, oxo, -CN, C 1-6 alkyl, C 1-6 haloalkyl, C 1-6 alkoxy, C 1-6 haloalkoxy, - OR 21 , -SR 21 , -N(R 22 )(R 23 ), -C(O)OR 22 , -C(O)N(R 22 )(R 23 ), -C(O)C(O)N(R 22 )(R 23 ), -OC(O)N(R 22 )(R 23 ), - N(R 24 )C(O)N(R 22 )(R 23 ), -N(R 24 )C(O)OR 25 , -N(R 24 )C(O)R 25 , -N(R 24 )S(O) 2 R 25 , -C(O)R 25 , -S(O) 2 R 25 , - S(O) 2 N(R 22 )(R 23 ),
• R 3 is selected from hydrogen, halogen, -CN, C 1-6 alkyl, C 3-6 cycloalkyl, C 2 - 9heterocycloalkyl, -OR 12 , -SR 12 , and -N(R 12 )(R 13 ), wherein C 1-6 alkyl, C 3-6 cycloalkyl, and C 2-9 heterocycloalkyl are optionally substituted with one, two, or three R 20c .
• R 3 is selected from hydrogen, halogen, -CN, C 1-6 alkyl, C 3-6 cycloalkyl, and -OR 12 , wherein C 1-6 alkyl and C 3-6 cycloalkyl are optionally substituted with one, two, or three R 20c .
• a compound, or a pharmaceutically acceptable salt or solvate thereof selected from:
• a pharmaceutical composition comprising a compound described herein, or a pharmaceutically acceptable salt or solvate thereof, and a pharmaceutically acceptable excipient.
• a method of treating cancer in a subject in need thereof comprising administering to the subject a therapeutically effective amount of a compound described herein, or a pharmaceutically acceptable salt or solvate thereof.
• a method of potentiating immunity of a cell comprising: contacting the cell with a compound described herein, thereby potentiating immunity of the cell, wherein the cell comprises (i) a chimeric T-cell receptor sequence encoding a T-cell receptor fusion protein (TFP) and/or (ii) a chimeric antigen receptor (CAR) sequence encoding a CAR, wherein each of TFP and CAR exhibits specific binding to an antigen.
• TFP T-cell receptor fusion protein
• CAR chimeric antigen receptor
• a method of potentiating immunity of a cell comprising: (a) contacting the cell with a compound described herein; and (b) introducing to the cell (i) a chimeric T-cell receptor sequence encoding a T-cell receptor fusion protein (TFP) and/or (ii) a chimeric antigen receptor (CAR) sequence encoding a CAR, wherein each of TFP and CAR exhibits specific binding to an antigen, thereby potentiating immunity of the cell.
• the cell is a lymphoid cell.
• the method further comprises administering the cell to a subject in need thereof.
• the method further comprises administering the compound described herein to the subject prior to, concurrent with, or subsequent to the administering the cell.
• a cell of the subject prior to the administering the compound described herein, a cell of the subject exhibits expression or activity of PTPN2.
• a method of potentiating immunity of a subject in need thereof comprising: (a) selecting the subject that exhibits expression or activity of PTPN2; and (b) downregulating expression or activity of PTPN2 by introducing a compound described herein to a cell of the subject, thereby potentiating immunity of the subject.
• a method of potentiating immunity of a subject in need thereof comprising: administering a lymphoid cell to the subject; and administering a compound described herein to the subject, thereby potentiating immunity of the subject.
• a method of potentiating anti-tumor or anti-cancer immunity of a subject in need thereof comprising: (a) contacting a lymphoid cell of the subject with a compound described herein, thereby potentiating the anti-tumor or anti-cancer immunity of the subject.
• a method of treating tumor or cancer of a subject in need thereof comprising: (a) contacting a lymphoid cell of the subject with a compound described herein, thereby treating the tumor or cancer of the subject.
• a method of treating tumor or cancer of a subject in need thereof comprising administering to said subject an effective amount of a compound described herein and an additional agent selected from the group consisting of a chemotherapeutic agent and an immune modulator.
• a method of treating tumor or cancer of a subject in need thereof comprising administering to said subject an effective amount of a compound described herein in conjunction with a cell therapy.
• a compound of Formula (I), or a pharmaceutically acceptable salt or solvate thereof Formula (I); wherein: W 1 is N, N(R 1 ), O, C(R 1 ), C(R 1 )(R 1a ), C(O), S(O), S(O) 2 , S(O)(NR 1 ), S(O)(R 1 ), or P(O)(R 1 ); W 2 is N, N(R 2 ), O, C(R 2 ), C(R 2 )(R 2a ), C(O), S(O), S(O) 2 , S(O)(NR 2 ), S(O)(R 2 ), or P(O)(R 2 ); W 3 is N, N(R 3 ), O, C(R 3 ), C(R 3 )(R 3a ), C(O), S(O), S(O) 2 , S(O)(NR 3 ), S(O)(R 3 ), or P(O)(R 1 );
• X is C(R 5 ).
• Y is C(R 6 ).
• Z is C(R 7 ).
• J 1 is N and J 2 is C(R 9 )(R 9a ).
• J 1 is C(R 8 ) and J 2 is C(R 9 )(R 9a ).
• J 2 is CH 2 .
• J 1 is C and J 2 is C(R 9 ).
• J 2 is C(H).
• J 3 is N(R 10 ).
• J 3 is N(H).
• the compound has the structure of Formula (Ia): Formula (Ia); wherein at least one of W 1 , W 2 , W 3 , and W 4 is N.
• the compound has the structure of Formula (Ib): Formula (Ib); wherein at least one of W 1 , W 2 , W 3 , and W 4 is N.
• the compound has the structure of Formula (Ic): Formula (Ic); wherein at least one of W 1 , W 2 , W 3 , and W 4 is N.
• W 1 is N
• W 2 is C(R 2 )
• W 3 is C(R 3 )
• W 4 is C(R 4 ).
• W 1 is C(R 1 )
• W 2 is N
• W 3 is C(R 3 )
• W 4 is C(R 4 ).
• W 1 is C(R 1 ), W 2 is C(R 2 ), W 3 is N, and W 4 is C(R 4 ).
• W 1 is C(R 1 ), W 2 is C(R 2 ), W 3 is C(R 3 ), and W 4 is N.
• the compound has the structure of Formula (Ig): Formula (Ig); wherein at least one of W 1 , W 2 , W 3 , and W 4 is N, N(R 3 ), N(R 4 ), or O.
• the compound has the structure of Formula (Ih): Formula (Ih); wherein at least one of W 1 , W 2 , W 3 , and W 4 is N, N(R 3 ), N(R 4 ), or O.
• the compound has the structure of Formula (Ii): Formula (Ii); wherein at least one of W 1 , W 2 , W 3 , and W 4 is N, N(R 3 ), N(R 4 ), or O.
• W 1 is C(R 1 ) and W 2 is C(R 2 ).
• W 3 is N(R 3 ) and W 4 is C(O).
• W 3 is C(O) and W 4 is N(R 4 ).
• W 3 is O and W 4 is C(R 4 )(R 4a ).
• the compound has the structure of Formula (Ij): Formula (Ij); wherein at least one of W 1 , W 2 , W 3 , and W 4 is N(R 1 ), N(R 2 ), N, or O.
• the compound has the structure of Formula (Ik): Formula (Ik); wherein at least one of W 1 , W 2 , W 3 , and W 4 is N(R 1 ), N(R 2 ), N, or O.
• the compound has the structure of Formula (Im): Formula (Im); wherein at least one of W 1 , W 2 , W 3 , and W 4 is N, N(R 3 ), N(R 4 ), or O.
• W 1 is C(R 1 )(R 1a )
• W 2 is O
• W 3 is C(R 3 )
• W 4 is C(R 4 ).
• W 1 is CO, N(R1) or C(R 1 )(R 1a );
• W 2 is CO , N(R2), or C(R 2 )(R 2a );
• W 3 is N, or C(R 3 ); and
• W 4 is N, or C(R 4 ).
• the compound has the structure of Formula (Iv): Formula (Iv); wherein at least one of W 1 , W 2 , W 3 , and W 4 is N(R 1 ), N(R 4 ), N, or O.
• the compound has the structure of Formula (Iw): Formula (Iw); wherein at least one of W 1 , W 2 , W 3 , and W 4 is N(R 1 ), N(R 4 ), N, or O.
• the compound has the structure of Formula (Ix): Formula (Ix); wherein at least one of W 1 , W 2 , W 3 , and W 4 is N(R 1 ), N(R 4 ), N, or O.
• the compound has the structure of Formula (Io): Formula (Io); wherein W 1 is C(R 1 ); W 2 is C(R 2 ); and W 4 is C(R 4 )(R 4a ), C(O), S(O), S(O) 2 , S(O)(NR 4 ), S(O)(R 4 ), or P(O)(R 4 ).
• W 1 is C(R 1 ); W 2 is C(R 2 ); and W 4 is C(R 4 )(R 4a ), C(O), S(O), S(O) 2 , S(O)(NR 4 ), S(O)(R 4 ), or P(O)(R 4 ).
• the compound has the structure of Formula (Ioa): Formula (Ioa).
• the compound has the structure of Formula (Iob): Formula (Iob).
• the compound has the structure of Formula (Ioc): Formula (Ioc).
• the compound has the structure of Formula (Ip): Formula (Ip); wherein: W 1 is C(R 1 )(R 1a ), C(O), S(O), S(O) 2 , S(O)(NR 1 ), S(O)(R 1 ), or P(O)(R 1 ); W 3 is C(R 3 ); and W 4 is C(R 4 ).
• W 1 is C(R 1 )(R 1a ), C(O), S(O), S(O) 2 , S(O)(NR 1 ), S(O)(R 1 ), or P(O)(R 1 );
• W 3 is C(R 3 ); and W 4 is C(R 4 ).
• the compound has the structure of Formula (Ipa): Formula (Ipa).
• the compound has the structure of Formula (Ipb): Formula (Ipb).
• the compound has the structure of Formula (Ipc): Formula (Ipc).
• the compound has the structure of Formula (Ipd): Formula (Iq); wherein W 1 is N or C(R 1 ); W 2 is N or C(R 2 ); W 3 is N or C(R 3 ); and W 4 is N(R 4 ), C(R 4 )(R 4a ), C(O), S(O), S(O) 2 , S(O)(NR 4 ), S(O)(R 4 ), or P(O)(R 4 ).
• the compound has the structure of Formula (Iq): Formula (Ir); wherein W 1 is N or C(R 1 ); W 2 is N or C(R 2 ); W 3 is N or C(R 3 ); and W 4 is N(R 4 ), C(R 4 )(R 4a ), C(O), S(O), S(O) 2 , S(O)(NR 4 ), S(O)(R 4 ), or P(O)(R 4 ).
• the compound has the structure of Formula (Ir): Formula (Is); wherein W 1 is N or C(R 1 ); W 2 is N or C(R 2 ); W 3 is N or C(R 3 ); and W 4 is N(R 4 ), C(R 4 )(R 4a ), C(O), S(O), S(O) 2 , S(O)(NR 4 ), S(O)(R 4 ), or P(O)(R 4 ).
• W 4 is C(O).
• X is C(R 5 ).
• Y is C(R 6 ).
• Z is C(R 7 ).
• J 1 is N and J 2 is C(R 9 )(R 9a ).
• J 1 is C(R 8 ) and J 2 is C(R 9 )(R 9a ).
• J 2 is CH 2 .
• J 1 is C and J 2 is C(R 9 ).
• J 2 is C(H).
• J 3 is N(R 10 ).
• J 3 is N(H).
• the compound has the structure of Formula (IIIb): Formula (IIIb).
• the compound has the structure of Formula (IIIc): Formula (IIIc).
• W 1 is C(O).
• W 2 is N(R 2 ).
• W 3 and W 4 are connected by a double bond.
• W 2 is C(O).
• W 1 is N(R 1 ) and W 3 and W 4 are connected by a double bond.
• W 3 is C(O).
• W 2 is N(R 2 ) and W 1 is C(R 1 )(R 1a ).
• W 4 is N(R 4 ).
• W 4 is C(R 4 )(R 4a ). In some embodiments of the compound, or a pharmaceutically acceptable salt or solvate thereof, W 4 is N(R 4 ) and W 1 and W 2 are connected by a double bond. In some embodiments of the compound, or a pharmaceutically acceptable salt or solvate thereof, W 4 is C(O). In some embodiments of the compound, or a pharmaceutically acceptable salt or solvate thereof, W 1 is O. In some embodiments of the compound, or a pharmaceutically acceptable salt or solvate thereof, W 2 is C(R 2 )(R 2a ) and W 3 is C(R 3 )(R 3a ).
• W 2 is C(R 2 ) and W 3 is C(R 3 ).
• the compound has the structure of Formula (IIId): Formula (IIId).
• the compound has the structure of Formula (IIIe):
• the compound has the structure of Formula (IIIf).
• the compound has the structure of Formula (IIIg): Formula (IIIg). [00101] In some embodiments of the compound, or a pharmaceutically acceptable salt or solvate thereof, the compound has the structure of Formula (IIIh): Formula (IIIh). [00102] In some embodiments of the compound, or a pharmaceutically acceptable salt or solvate thereof, the compound has the structure of Formula (IIIi): Formula (IIIi). [00103] In some embodiments of the compound, or a pharmaceutically acceptable salt or solvate thereof, the compound has the structure of Formula (IIIj): Formula (IIIj).
• the compound has the structure of Formula (IIIk): Formula (IIIk). [00105] In some embodiments of the compound, or a pharmaceutically acceptable salt or solvate thereof, the compound has the structure of Formula (IIIl): Formula (IIIl). [00106] In some embodiments of the compound, or a pharmaceutically acceptable salt or solvate thereof, the compound has the structure of Formula (IIIm): Formula (IIIm). [00107] In some embodiments of the compound, or a pharmaceutically acceptable salt or solvate thereof, the compound has the structure of Formula (IIIn): Formula (IIIn).
• the compound has the structure of Formula (IIIo): Formula (IIIo).
• the compound has the structure of Formula (IIIp): Formula (IIIp).
• the compound has the structure of Formula (IIIq): Formula (IIIq).
• the compound has the structure of Formula (IIIr): Formula (IIIr).
• the compound has the structure of Formula (IIIs): Formula (IIIs). [00113] In some embodiments of the compound, or a pharmaceutically acceptable salt or solvate thereof, the compound has the structure of Formula (IIIt): Formula (IIIt). [00114] In some embodiments of the compound, or a pharmaceutically acceptable salt or solvate thereof, the compound has the structure of Formula (IIIu): Formula (IIIu).
• a compound of Formula (II), or a pharmaceutically acceptable salt or solvate thereof Formula (II); wherein: V 1 is a bond or S; V 4 is a bond or S, wherein when V 1 is a bond then V 4 is S and when V 1 is S, then V 4 is a bond; V 2 is N or C(R 2 ); V 3 is N or C(R 3 ); X is N or C(R 5 ); Y is N or C(R 6 ); Z is N or C(R 7 ); J 1 is N, C, or C(R 8 ); J 2 is N, N(R 9 ), C(R 9 ), C(R 9 )(R 9a ), or C(O); J 3 is N(R 10 ) or C(R 10 )(R 10a ); R 2 and R 2a are independently selected from hydrogen, halogen, -CN, C 1-6 alkyl, C 2-6 alkenyl, C 2-6 alkynyl,
• X is C(R 5 ).
• Y is C(R 6 ).
• Z is C(R 7 ).
• J 1 is N and J 2 is C(R 9 )(R 9a ).
• J 1 is C(R 8 ) and J 2 is C(R 9 )(R 9a ).
• J 2 is CH 2 .
• J 1 is C and J 2 is C(R 9 ).
• J 2 is C(H).
• J 3 is N(R 10 ).
• J 3 is N(H).
• V 1 is a bond and V 4 is S.
• V 1 is S and V 4 is a bond.
• the compound has the structure of Formula (IIa): Formula (IIa).
• the compound has the structure of Formula (IIb): Formula (IIb).
• the compound has the structure of Formula (IIc): Formula (IIc).
• the compound has the structure of Formula (IId): Formula (IId). [00121] In some embodiments of the compound, or a pharmaceutically acceptable salt or solvate thereof, the compound has the structure of Formula (IIe): Formula (IIe). [00122] In some embodiments of the compound, or a pharmaceutically acceptable salt or solvate thereof, the compound has the structure of Formula (IIf): Formula (IIf). [00123] In some embodiments of the compound, or a pharmaceutically acceptable salt or solvate thereof, R 5 is selected from hydrogen, halogen, and C 1-6 alkyl optionally substituted with one, two, or three R 20e .
• R 5 is selected from hydrogen and halogen.
• R 6 is selected from hydrogen, halogen, -OR 12a , and C 1-6 alkyl optionally substituted with one, two, or three R 20f .
• R 6 is -OH.
• R 7 is selected from hydrogen, halogen, and C 1-6 alkyl optionally substituted with one, two, or three R 20g .
• R 7 is hydrogen.
• R 9 is hydrogen.
• R 9a is hydrogen.
• R 10 is hydrogen.
• R 2 is selected from hydrogen, halogen, C 1-6 alkyl, C 2-9 heterocycloalkyl, C 1-9 heteroaryl, -OR 12 , -SR 12 , -N(R 12 )(R 13 ), - C(O)R 15 , -C(O)N(R 12 )(R 13 ), -S(O) 2 R 15 , and -S(O) 2 N(R 12 )(R 13 )-, wherein C 1-6 alkyl, C 2-9 heterocycloalkyl, and C 1- 9 heteroaryl are optionally substituted with one, two, or three R 20b .
• R 2 is selected from C 1-6 alkyl, C 2-9 heterocycloalkyl, C 1-9 heteroaryl, -OR 12 , -N(R 12 )(R 13 ), -C(O)R 15 , -C(O)N(R 12 )(R 13 ), wherein C 1-6 alkyl, C 2-9 heterocycloalkyl, and C 1-9 heteroaryl are optionally substituted with one, two, or three R 20b .
• R 2 is selected from -OR 12 , -N(R 12 )(R 13 ), -C(O)R 15 , -C(O)N(R 12 )(R 13 ); R 13 is hydrogen;
• R 26 is independently selected from halogen, oxo, -CN, C 1-6 alkyl, C 1-6 haloalkyl, C 1-6 alkoxy, C 1-6 haloalkoxy, - OR 21 , -SR 21 , -N(R 22 )(R 23 ), -C(O)OR 22 , -C(O)N(R 22 )(R 23 ), -C(O)C(O)N(R 22 )(R 23 ), -OC(O)N(R 22 )(R 23 ), - N(R 24 )C(O)N(R 22 )(R 23 ), -N(R 24 )C(O)OR 25 , -N(R 24 )C(O)R 25 , -N(R 24 )S(O) 2 R 25 , -C(O)R 25 , -S(O) 2 R 25 , - S(O) 2 N(R 22 )(R 23 ),
• R 2 is selected from -OR 12 , -N(R 12 )(R 13 ), -C(O)R 15 , -C(O)N(R 12 )(R 13 );
• R 13 is hydrogen;
• R 26 is independently selected from halogen, oxo, -CN, C 1-6 alkyl, C 1-6 haloalkyl, C 1-6 alkoxy, C 1-6 haloalkoxy, - OR 21 , -SR 21 , -N(R 22 )(R 23 ), -C(O)OR 22 , -C(O)N(R 22 )(R 23 ), -C(O)C(O)N(R 22 )(R 23 ), -OC(O)N(R 22 )(R 23 ), - N(R 24 )C(O)N(R 22 )(R 23 ), -N(R 24 )C(O)N(R 22 )(R 23 ), -N(R
• R 26 is independently selected from halogen, oxo, -CN, C 1-6 alkyl, C 1-6 haloalkyl, C 1-6 alkoxy, C 1-6 haloalkoxy, - OR 21 , -SR 21 , -N(R 22 )(R 23 ), -C(O)OR 22 , -C(O)N(R 22 )(R 23 ), -C(O)C(O)N(R 22 )(R 23 ), -OC(O)N(R 22 )(R 23 ), - N(R 24 )C(O)N(R 22 )(R 23 ), -N(R 24 )C(O)OR 25 , -N(R 24 )C(O)R 25 , -N(R 24 )S(O) 2 R 25 , -C(O)R 25 , -S(O) 2 R 25 , -C(O)R 25 , -S(O) 2 R
• R 26 is independently selected from halogen, oxo, -CN, C 1-6 alkyl, C 1-6 haloalkyl, C 1-6 alkoxy, C 1-6 haloalkoxy, - OR 21 , -SR 21 , -N(R 22 )(R 23 ), -C(O)OR 22 , -C(O)N(R 22 )(R 23 ), -C(O)C(O)N(R 22 )(R 23 ), -OC(O)N(R 22 )(R 23 ), - N(R 24 )C(O)N(R 22 )(R 23 ), -N(R 24 )C(O)OR 25 , -N(R 24 )C(O)R 25 , -N(R 24 )S(O) 2 R 25 , -C(O)R 25 , -S
• R 3 is selected from hydrogen, halogen, -CN, C 1-6 alkyl, C 3-6 cycloalkyl, C 2-9 heterocycloalkyl, -OR 12 , -SR 12 , and - N(R 12 )(R 13 ), wherein C 1-6 alkyl, C 3-6 cycloalkyl, and C 2-9 heterocycloalkyl are optionally substituted with one, two, or three R 20c .
• R 3 is selected from hydrogen, halogen, -CN, C 1-6 alkyl, C 3-6 cycloalkyl, and -OR 12 , wherein C 1-6 alkyl and C 3-6 cycloalkyl are optionally substituted with one, two, or three R 20c .
• a compound, or a pharmaceutically acceptable salt or solvate thereof selected from: [00140]
• a pharmaceutical composition comprising a compound described herein, or a pharmaceutically acceptable salt or solvate thereof, and a pharmaceutically acceptable excipient.
• a method of treating cancer in a subject in need thereof comprising administering to the subject a therapeutically effective amount of a compound described herein, including in embodiments thereof, or a pharmaceutically acceptable salt or solvate thereof.
• a method of potentiating immunity of a cell comprising: (a) contacting the cell with a compound described herein, including in embodiments thereof, thereby potentiating immunity of the cell, wherein the cell comprises (i) a chimeric T-cell receptor sequence encoding a T-cell receptor fusion protein (TFP) and/or (ii) a chimeric antigen receptor (CAR) sequence encoding a CAR, wherein each of TFP and CAR exhibits specific binding to an antigen.
• TFP T-cell receptor fusion protein
• CAR chimeric antigen receptor
• a method of potentiating immunity of a cell comprising: (a) contacting the cell with a compound described herein, including in embodiments; and (b) introducing to the cell (i) a chimeric T-cell receptor sequence encoding a T-cell receptor fusion protein (TFP) and/or (ii) a chimeric antigen receptor (CAR) sequence encoding a CAR, wherein each of TFP and CAR exhibits specific binding to an antigen, thereby potentiating immunity of the cell.
• TFP T-cell receptor fusion protein
• CAR chimeric antigen receptor
• the cell e.g., lymphoid cell
• the cell retains expression or activity of PTPN2 prior to (a).
• a subject method further comprises administering the cell to a subject in need thereof.
• a subject method further comprises administering a compound described herein, including in embodiments thereof, to the subject prior to, concurrent with, or subsequent to the administering the cell.
• a cell of the subject exhibits expression or activity of PTPN2.
• a method of potentiating immunity of a subject in need thereof comprising: administering a lymphoid cell to the subject, thereby potentiating immunity of the subject, wherein expression or activity of PTPN2 in the lymphoid cell is transiently downregulated.
• the method further comprises transiently downregulating the expression or activity of PTPN2 in the lymphoid cell.
• the transiently downregulating is performed once, or performed intermittently for a desired number of times, such as two or more times.
• the transiently downregulating comprises introducing a compound described herein, including in embodiments thereof, to a cell of interest.
• a first intermittent dosing regimen of a compound described herein and a second intermittent dosing regimen of the compound is the same or different.
• a lymphoid cell being contacted by a subject compound prior to the transiently downregulating, a lymphoid cell being contacted by a subject compound exhibits expression or activity of PTPN2.
• the lymphoid cell comprises (i) a chimeric T-cell receptor sequence encoding a T-cell receptor fusion protein (TFP) and/or (ii) a chimeric antigen receptor (CAR) sequence encoding a CAR, wherein each of TFP and CAR exhibits specific binding to an antigen.
• TFP T-cell receptor fusion protein
• CAR chimeric antigen receptor
• the method further comprises administering a compound described herein to the subject prior to, concurrent with, or subsequent to the administering the lymphoid cell.
• the subject exhibits expression or activity of PTPN2.
• a method of potentiating immunity of a subject in need thereof comprising: (a) selecting the subject that exhibits expression or activity of PTPN2; and (b) downregulating expression or activity of PTPN2 in a cell of the subject, thereby potentiating immunity of the subject.
• the step (b) is performed in vivo or ex vivo.
• the downregulating comprises introducing a compound described herein, to the cell.
• the downregulating comprises transiently downregulating the expression or activity of PTPN2.
• the transiently downregulating is performed once or multiple times such as two, three or more times.
• a first intermittent dosing regimen of a compound described herein is the same as a second intermittent dosing regimen utilizing a the compound disclosed herein.
• the first intermittent dosing regimen of a compound described herein is different from that of a second intermittent dosing regimen.
• a cell of the subject being treated can be a lymphoid cell comprising (i) a chimeric T-cell receptor sequence encoding a T-cell receptor fusion protein (TFP) and/or (ii) a chimeric antigen receptor (CAR) sequence encoding a CAR, wherein each of TFP and CAR exhibits specific binding to an antigen.
• the cell of the subject does not exhibit a mutation of (i) a first gene encoding PTPN2 or (ii) a second gene operatively linked to PTPN2, wherein the mutation inhibits the expression and/or activity of PTPN2.
• a method described herein further comprises selecting a subject that exhibits expression or activity of PTPN2.
• the step of selecting comprises performing a nucleic acid assay using at least a portion of a genome or transcriptome of the cell of the subject to detect the mutation.
• the selecting comprises performing a protein assay to detect a functionally active PTPN2 or a functionally inactive PTPN2.
• the administering the compound described herein can be performed prior to, concurrent with, or subsequent to the administering the lymphoid cell.
• the administering a compound described herein is performed separately from the administering the lymphoid cell.
• a cell of the subject typically exhibits expression or activity of PTPN2 [00148]
• a method of potentiating anti-tumor or anti-cancer immunity of a subject in need thereof comprising: (a) contacting a lymphoid cell of the subject with a compound described herein, thereby potentiating the anti-tumor or anti-cancer immunity of the subject.
• contemplated immunity comprises anti-tumor, anti-cancer activity, anti-viral infection activity, and/or anti-bacterial infection activity.
• a method of treating tumor or cancer of a subject in need thereof comprising: (a) contacting a lymphoid cell of the subject with a compound described herein, thereby treating the tumor or cancer of the subject.
• the step of contacting a lymphoid cell is performed in vivo.
• the step of contacting is performed ex vivo, and subsequently followed by introducing the lymphoid cell to the subject.
• the lymphoid cell being contacted by a compound disclosed herein comprises (i) a chimeric T-cell receptor sequence encoding a T-cell receptor fusion protein (TFP) and/or (ii) a chimeric antigen receptor (CAR) sequence encoding a CAR, wherein each of TFP and CAR exhibits specific binding to an antigen.
• TFP T-cell receptor fusion protein
• CAR chimeric antigen receptor
• the method further comprises (b) introducing to the lymphoid cell (i) a chimeric T-cell receptor sequence encoding a T-cell receptor fusion protein (TFP) and/or (ii) a chimeric antigen receptor (CAR) sequence encoding a CAR, wherein each of TFP and CAR exhibits specific binding to an antigen.
• a chimeric T-cell receptor sequence encoding a T-cell receptor fusion protein (TFP) and/or
• a chimeric antigen receptor (CAR) sequence encoding a CAR, wherein each of TFP and CAR exhibits specific binding to an antigen.
• (a) is performed prior to, concurrent with, or subsequent to (b).
• a method of potentiating anti-tumor or anti-cancer immunity of a subject in need thereof comprising: (a) downregulating expression or activity of PTPN2 in a lymphoid cell of the subject, thereby potentiating the anti-tumor or anti-cancer immunity of the subject.
• a method of treating tumor or cancer of a subject in need thereof comprising: (a) downregulating expression or activity of PTPN2 in a lymphoid cell of the subject, thereby treating the tumor or cancer of the subject.
• the downregulating is performed in vivo. In some embodiments, the downregulating is performed ex vivo, and subsequently followed by introducing the lymphoid cell to the subject. In some embodiments, the method further comprises administering the lymphoid cell to the subject prior to, concurrent with, or subsequent to the downregulating. In some embodiments, the downregulating comprises introducing a compound described herein, to the lymphoid cell. In some embodiments, the downregulating comprises transiently downregulating the expression or activity of PTPN2. Where desired, the transiently downregulating is performed once or multiple times such as two, three or more times.
• a first intermittent dosing regimen of a compound described herein is the same as that of a second intermittent dosing regimen of the compound. In some embodiments, the first intermittent dosing regimen of a compound described herein is different from that of the second intermittent dosing regimen of the compound. In some embodiments, the method further comprises (b) introducing to the lymphoid cell (i) a chimeric T-cell receptor sequence encoding a T-cell receptor fusion protein (TFP) and/or (ii) a chimeric antigen receptor (CAR) sequence encoding a CAR, wherein each of TFP and CAR exhibits specific binding to an antigen.
• TFP T-cell receptor fusion protein
• CAR chimeric antigen receptor
• a method of increasing efficacy or reducing side effect of a cell therapy for a subject in need thereof comprising: (a) administering to the subject a cell comprising a chimeric antigen receptor (CAR) sequence encoding a CAR, wherein the CAR comprises an antigen-binding domain and an intracellular signaling domain, wherein the intracellular signaling domain is minimally required for activation of the CAR upon binding to an antigen; and (b) administering a compound described herein to the subject prior to, concurrent with, or subsequent to (a).
• CAR chimeric antigen receptor
• the cell including but not limited to lymphoid cell retains expression or activity of PTPN2 prior to (b).
• a cell of the subject typically exhibits expression or activity of PTPN2.
• a method of increasing efficacy or reducing side effect of a cell therapy for a subject in need thereof comprising: (a) administering to the subject a sub-therapeutic amount of a cell comprising a chimeric antigen receptor (CAR) sequence encoding a CAR, (b) administering a compound described herein, to the subject prior to, concurrent with, or subsequent to (a).
• CAR chimeric antigen receptor
• the cell including but not limited to lymphoid cell retains expression or activity of PTPN2 prior to (b).
• the compounds disclosed herein or utilized in the method disclosed reduces PTPN2 signaling in a cell.
• the compounds disclosed herein do not regulate site-specific recombination of a gene encoding PTPN2.
• the compounds disclosed herein are configured to bind PTPN2, or are exhibiting binding specificity to PTPN2 in comparison to other tyrosine phosphatases.
• a compound described herein exhibits IC50 of less than or equal to 5 ⁇ M for PTPN2.
• the practice of any of the subject methods further comprises monitoring, concurrent with or subsequent to the administration of the compound described herein, and/or the lymphoid cell, one or more health parameters of the subject selected from the group consisting of: temperature, wheezing, sweating, fatigue, weight, insomnia, diarrhea, infections, and mental disorders.
• the method further comprises detecting, concurrent with or subsequent to the administration of the compound described herein, the lymphoid cell, one or more inflammatory biomarkers selected from the group consisting of: antibodies, cytokines, radicals, and coagulation factors, disclosed herein.
• practicing a subject method may involve (1) contacting a cell with a compound described herein (2) administering a lymphoid cell to the subject, (3) downregulating the expression or activity of PTPN2 in a cell of a subject, (4) administering a compound described herein, to a subject, (5) contacting a lymphoid cell of a subject with a compound described herein, and/or (6) downregulating the expression or activity of PTPN2 in the lymphoid cell of the subject is performed prior to, concurrent with, or subsequent to an administration of another agent (second agent) or therapy to the subject.
• another agent second agent
• the second agent is selected from the group consisting of a chemotherapeutic agent, a radioactive agent, a small molecule agent targeting a tumor marker, an antigen-binding agent specifically binding to a tumor marker, and an immune modulator.
• the second agent is a checkpoint inhibitor.
• the second agent includes without limitation an inhibitor of PD1, PD-L1, LAG3, CTLA4, CD160, BTLA, LAIR1, TIM3, 2B4, CD 9 3, OX40, Siglec-15, and TIGIT.
• the second agent is an inhibitor of IDO or mTOR.
• a second therapy to be combined is a cell therapy comprising stem cells or lymphoid cells.
• the TFP comprises a TCR subunit that comprises (1) a TCR extracellular domain capable of specific binding to an antigen, and (2) an intracellular signaling domain, wherein the TFP forms a TCR complex.
• the TCR extracellular domain comprises element (1) an antigen binding domain capable of specific binding to the antigen, and element (2) an extracellular domain or portion thereof of a protein selected from the group consisting of a TCR alpha chain, a TCR beta chain, a CD3 epsilon TCR subunit, a CD3 gamma TCR subunit, a CD3 delta TCR, wherein elements (1) and (2) are operatively linked together.
• the TCR intracellular domain comprises a stimulatory domain from an intracellular signaling domain of epsilon chain, delta chain, and/or a gamma chain of cluster of differentiation 3 (CD3). In some embodiments, the TCR intracellular domain comprises a stimulatory domain from an intracellular signaling domain of TCR alpha, or from an intracellular signaling domain of TCR beta.
• the TFP comprises a transmembrane domain including a transmembrane domain of a protein selected from the group consisting of a TCR alpha chain, a TCR beta chain, a TCR zeta chain, a CD3 epsilon TCR subunit, a CD3 gamma TCR subunit, a CD3 delta TCR subunit, CD45, CD4, CD5, CD8, CD9, CD16, CD22, CD33, CD28, CD37, CD64, CD80, CD86, CD134, CD137, and CD154.
• the TFP comprises a costimulatory domain.
• the costimulatory domain of the TFP is selected from the group consisting of: a functional signaling domain of a protein selected from the group consisting of CD27, CD28, 4-1BB (CD137), OX40, CD30, CD40, PD-1, ICOS, lymphocyte function-associated antigen-1 (LFA-1), CD2, CD7, LIGHT, NKG2C, B7-H3, a ligand that specifically binds with CD83, CDS, ICAM-1, GITR, BAFFR, HVEM (LIGHTR), SLAMF7, NKp80 (KLRF1), CD160, CD19, CD4, CD8alpha, CD8beta, IL2R beta, IL2R gamma, IL7R alpha, ITGA4, VLA1, CD49a, ITGA4, IA4, CD49D, ITGA6, VLA-6, CD49f, ITGAD, CD11d, ITGAE, CD103, ITGAL, CD11a, LFA-1, I
• the CAR comprises an antigen-binding domain and an intracellular signaling domain.
• the intracellular signaling domain of the CAR comprises a primary signaling domain and/or a costimulatory signaling domain, wherein the primary signaling domain comprises a functional signaling domain of a protein chosen from CD3 zeta, CD3 gamma, CD3 delta, CD3 epsilon, common FcR gamma (FCERIG), FcR beta (Fc Epsilon Rib), CD79a, CD79b, Fcgamma Rlla, DAP10, or DAP12.
• the intracellular signaling domain of the CAR comprises a costimulatory signaling domain that comprises a functional signaling domain of a protein selected from the group consisting of CD27, CD28, 4-lBB (CD137), OX40, CD30, CD40, PD-1, ICOS, lymphocyte function-associated antigen- 1 (LFA-1), CD2, CD7, LIGHT, NKG2C, B7-H3, a ligand that specifically binds with CD83, CDS, ICAM-1, GITR, BAFFR, HVEM (LIGHTR), SLAMF7, NKp80 (KLRF1), CD160, CD19, CD4, CD8alpha, CD8beta, IL2R beta, IL2R gamma, IL7R alpha, ITGA4, VLA1, CD49a, ITGA4, IA4, CD49D, ITGA6, VLA-6, CD49f, ITGAD, CDlld, ITGAE, CD103, ITGAL, CDlla, L
• the intracellular signaling domain of the CAR comprises a primary signaling domain and/or a costimulatory signaling domain, wherein the primary signaling domain and/or the costimulatory signaling domain is minimally required for activation of the CAR upon binding to an antigen.
• the CAR is a first generation CAR in which the primary signaling domain is a member selected from the group consisting of CD3zeta, CD28, 4-1BB, OX40, DAP10, ICOS, and a variant thereof.
• the CAR is a second generation CAR in which (i) the primary signaling domain is a member selected from the group consisting of CD3zeta, CD28, 4-1BB, OX40, DAP10, ICOS, and a variant thereof, and (ii) the co- stimulatory signaling domain is a different member selected from the group consisting of CD3zeta, CD28, 4-1BB, OX40, DAP10, ICOS, and a variant thereof.
• the antigen is a tumor antigen or cancer antigen a tumor antigen selected from a group consisting of: TSHR, CD19, CD123, CD22, CD30, CD171, CS-1, CLL-1, CD33, EGFRvIII , GD2, GD3, BCMA, Tn Ag, PSMA, RORl, FLT3, FAP, TAG72, CD38, CD44v6, CEA, EPCAM, B7H3, KIT, IL-13Ra2, Mesothelin, IL-llRa, PSCA, PRSS21, VEGFR2, LewisY, CD24, PDGFR-beta, SSEA-4, CD20, Folate receptor alpha, ERBB2 (Her2/neu), MUC1, EGFR, NCAM, Prostase, PAP, ELF2M, Ephrin B2, IGF-I receptor, CAIX, LMP2, gplOO, bcr-abl, tyrosinase
• the antigen comprises a neoantigen encoded by a tumor-specific mutated gene.
• the side effect comprises cytokine release syndrome (CRS), inflammatory disorder, or autoimmune disorder.
• CRS cytokine release syndrome
• a modified cell comprising (i) a chimeric T-cell receptor sequence encoding a T- cell receptor fusion protein (TFP) and/or (ii) a chimeric antigen receptor (CAR) sequence encoding a CAR, wherein each of TFP and CAR exhibits specific binding to an antigen, wherein expression or activity of PTPN2 in the cell is downregulated, to potentiate immunity of the modified cell.
• TFP T- cell receptor fusion protein
• CAR chimeric antigen receptor
• the modified cell exhibits a mutation of (i) a first gene encoding PTPN2 or (ii) a second gene operatively linked to PTPN2, wherein the mutation inhibits the expression and/or activity of PTPN2.
• the expression or activity of PTPN2 is transiently downregulated in the modified cell.
• the expression or activity of PTPN2 is downregulated by a compound described herein.
• a subject compound modifying the cell (i) does not regulate site-specific recombination of a gene encoding PTPN2.
• a subject compound modifying a cell is a the small molecule exhibiting IC 50 of less than or equal to 5 ⁇ M for PTPN2.
• the TFP (contained in a modified cell) comprises a TCR subunit that comprises (1) a TCR extracellular domain capable of specific binding to the antigen, and (2) an intracellular signaling domain, wherein the TFP forms a TCR complex.
• the TCR extracellular domain comprises element (1) an antigen binding domain capable of specific binding to the antigen, and element (2) an extracellular domain or portion thereof of a protein selected from the group consisting of a TCR alpha chain, a TCR beta chain, a CD3 epsilon TCR subunit, a CD3 gamma TCR subunit, a CD3 delta TCR, wherein elements (1) and (2) are operatively linked together.
• the TCR intracellular domain comprises a stimulatory domain from an intracellular signaling domain of epsilon chain, delta chain, and/or a gamma chain of cluster of differentiation 3 (CD3).
• the TCR intracellular domain comprises a stimulatory domain from an intracellular signaling domain of TCR alpha, or from an intracellular signaling domain of TCR beta.
• the TFP comprises a transmembrane domain including a transmembrane domain of a protein selected from the group consisting of a TCR alpha chain, a TCR beta chain, a TCR zeta chain, a CD3 epsilon TCR subunit, a CD3 gamma TCR subunit, a CD3 delta TCR subunit, CD45, CD4, CD5, CD8, CD9, CD16, CD22, CD33, CD28, CD37, CD64, CD80, CD86, CD134, CD137, and CD154.
• the TFP comprises a costimulatory domain, including without limitation: a functional signaling domain of a protein selected from the group consisting of CD27, CD28, 4-1BB (CD137), OX40, CD30, CD40, PD-1, ICOS, lymphocyte function- associated antigen-1 (LFA-1), CD2, CD7, LIGHT, NKG2C, B7-H3, a ligand that specifically binds with CD83, CDS, ICAM-1, GITR, BAFFR, HVEM (LIGHTR), SLAMF7, NKp80 (KLRF1), CD160, CD19, CD4, CD8alpha, CD8beta, IL2R beta, IL2R gamma, IL7R alpha, ITGA4, VLA1, CD49a, ITGA4, IA4, CD49D, ITGA6, VLA-6, CD49f, ITGAD, CD11d, ITGAE, CD103, ITGAL, CD11a, LFA-1, ITGAM,
• the modified cell is a modified lymphoid cell.
• the modified lymphoid cell is a member or variant thereof selected from the group consisting of: a T cell, B cell, NK cell, KHYG cell, T helper cell, regulatory T cell, memory T cell, tumor infiltration T cell (TIL), antigen presenting cell, and dendritic cell.
• the modified lymphoid cell is a variant of a member selected from the group consisting of: a CD4+ T cell, a CD8+ T cell, and a CD4+ and CD8+ T cell.
• any of the subject compounds, modified cells, and any other agent described herein may be applied (e.g., utilized) in any of the subject methods described herein.
• any compounds, modified cell and any other agent described in the context of a subject method is embodied and contemplated as a subject composition.
• Clusters of points represent, from left to right in form of a group of 3 vertical dots representative of replicate experiments: 1 ng/ml IFN ⁇ DMSO, a first reference compound at 100 ⁇ M, the first reference compound at 50 ⁇ M, a subject compound in Table 6, a second reference compound, a third reference compound, another subject compound in Table 6, and yet another subject compound in Table 6, a fourth reference compound; FIG.1B.
• Clusters of points represent, from left to right: No IFN ⁇ , IFN ⁇ , the fourth reference compound at 10 ⁇ M, a subject compound in Table 6 at 10 ⁇ M; Y-axis %MHCI Increase (Normalized) 0-200; FIG.1C.
• FIG.2 depicts tumor infiltrating lymphocyte exhaustion as shown by high TIM3 and PD1 expression and low Slamf6 expression in tumor associated CD8+ cells but not spleen associated cells.
• FIG.3 depicts tumor growth inhibition using B16F10 mouse model treated with a subject PTPN2 inhibitor disclosed herein.
• FIG.4A depicts day 7 tumor infiltrating CD8 T cell phenotype in B16F10 Model
• FIG.4B depicts day 7 tumor infiltrating macrophage phenotype in B16F10 Model. INCORPORATION BY REFERENCE [00161] All publications, patents, and patent applications mentioned in this specification are herein incorporated by reference to the same extent as if each individual publication, patent, or patent application was specifically and individually indicated to be incorporated by reference.
• Standard techniques can be used for chemical syntheses, chemical analyses, pharmaceutical preparation, formulation, and delivery, and treatment of patients.
• Standard techniques can be used for recombinant DNA, oligonucleotide synthesis, and tissue culture and transformation (e.g., electroporation, lipofection). Reactions and purification techniques can be performed e.g., using kits of manufacturer's specifications or as commonly accomplished in the art or as described herein.
• expression refers to the process by which a polynucleotide is transcribed into mRNA and/or the process by which the transcribed mRNA (also referred to as a “transcript”) is subsequently translated into peptides, polypeptides, or proteins.
• the transcripts and the encoded polypeptides are collectedly referred to as “gene product.” If the polynucleotide is derived from genomic DNA, expression may include splicing of the mRNA in a eukaryotic cell.
• the level of expression (or alternatively, the “expression level”) of a PTPN2 gene can be determined, for example, by determining the level of PTPN2polynucleotides, polypeptides or gene products.
• “Aberrantly expressed” or “aberrant expression” as applied to a nucleotide sequence (e.g., a gene) or polypeptide sequence in a subject refers to the aberrant production of the mRNA transcribed and/or translated from the nucleotide sequence or the protein product encoded by the nucleotide sequence.
• a differentially expressed sequence may be overexpressed (or aberrantly high expression) or underexpressed (or aberrantly low expression) as compared to the expression level of a reference sample (i.e., a reference level).
• overexpression is an increase in expression can be at least 1.25 fold, or alternatively, at least 1 fold, or alternatively, at least 2 fold, or alternatively, at least 3 fold, or alternatively, at least 4 fold, or alternatively, at least 10 fold expression over that detected in a reference sample.
• underexpression is a reduction in expression can be at least 1.25 fold, or alternatively, at least 1 fold, or alternatively, at least 2 fold, or alternatively, at least 3 fold, or alternatively, at least 4 fold, or alternatively, at least 10 fold expression under that detected in a reference sample. Underexpression also encompasses absence of expression of a particular sequence as evidenced by the absence of detectable expression in a test subject when compared to a reference sample.
• “Signal transduction” is a process during which stimulatory or inhibitory signals are transmitted into and within a cell to elicit an intracellular response. A molecule can mediate its signaling effect via direct or indirect interaction with downstream molecules of the same pathway or related pathway(s).
• PTPN2 signaling can involve a host of downstream molecules including but not limited to one or more of the following proteins: STAT1 and STAT5.
• a “control” or “control sample” is an alternative sample or subject used in an experiment for comparison purpose.
• the term “reference level” refers to a control level used to evaluate a test level.
• a reference level may be a control.
• a biomarker may be considered to be underexpressed when the expression level of that biomarker is lower than a reference level.
• the reference level can be determined by a plurality of methods, provided that the resulting reference level accurately provides a level of a biomarker above which exists a first group of subjects having a different probability of exhibiting a clinically beneficial response to treatment with a PTPN2 inhibitor than that of a second group of patients having levels of the biomarker below the reference level.
• the reference level may be determined, for example, by measuring the level of expression of a biomarker in tumorous or non-tumorous cancer cells from the same tissue as the tissue of the cancer cells to be tested.
• the reference level may be a level of a biomarker determined in vitro.
• a reference level may be determined by comparison of the level of a biomarker in populations of subjects having the same cancer.
• Two or more separate groups of subjects may be determined by identification of subsets of populations of the cohort that have the same or similar levels of a biomarker. Determination of a reference level can then be made based on a level that distinguishes these separate groups.
• a reference level may be a single number, equally applicable to every subject, or a reference level can vary according to specific subpopulations of subjects. For example, older men may have a different reference level than younger men for the same cancer, and women may have a different reference level than men for the same cancer.
• the reference level may be some level determined for each subject individually.
• the reference level may be a ratio of a biomarker level in a cancer cell of a subject relative to the biomarker level in a normal cell within the same subject.
• a reference level is a numerical range of gene expression that is obtained from a statistical sampling from a population of individuals having cancer. The sensitivity of the individuals having cancer to treatment with a PTPN2 inhibitor may be known.
• the reference level is derived by comparing gene expression to a control gene that is expressed in the same cellular environment at relatively stable levels (e.g. a housekeeping gene such as an actin). Comparison to a reference level may be a qualitative assessment or a quantitative determination.
• determining means determining if an analyte is present or not (e.g., detection). These terms can include both quantitative and/or qualitative determinations. Assessing may be relative or absolute. A relative amount could be, for example, high, medium or low. An absolute amount could reflect the measured strength of a signal or the translation of this signal strength into another quantitative format, such as micrograms/mL. “Detecting the presence of” can include determining the amount of something present, as well as determining whether it is present or absent.
• antagonists are used interchangeably, and they refer to a compound, or a biological molecule having the ability to effect inhibition of a biological function of a target protein (e.g., PTPN2), whether by inhibiting the activity or expression of the target protein. Accordingly, the terms “antagonist” and “inhibitors” are defined in the context of the biological role of the target protein. While preferred antagonists herein specifically interact with (e.g., bind to) the target, compounds that inhibit a biological activity of the target protein by interacting with other members of the signal transduction pathway of which the target protein is a member are also specifically included within this definition.
• an activity of a target protein may involve interaction (e.g., binding) between the target protein and a substrate of the target protein
• the terms “antagonist” and “inhibitors” can refer to a compound having the ability to interact with (e.g., bind to) the subject of the target protein, to indirectly inhibit the biological activity of the target protein. In some cases, such compound may bind both the target protein and one or more kinds of the substrate.
• a preferred biological activity inhibited by an antagonist is associated with the development, growth, maintenance, or spread of a cancer or a tumor.
• the term “cell proliferation” refers to a phenomenon by which the cell number has changed as a result of division.
• administer refers to the methods that may be used to enable delivery of agents or compositions to the desired site of biological action. These methods include, but are not limited to parenteral administration (e.g., intravenous, subcutaneous, intraperitoneal, intramuscular, intravascular, intrathecal, intranasal, intravitreal, infusion and local injection), transmucosal injection, oral administration, administration as a suppository, and topical administration. Administration is by any route, including parenteral.
• Parenteral administration includes, e.g., intravenous, intramuscular, intra-arteriole, intradermal, subcutaneous, intraperitoneal, intraventricular, and intracranial.
• Other modes of delivery include, but are not limited to, the use of liposomal formulations, intravenous infusion, transplantation, etc.
• One skilled in the art will know of additional methods for administering a therapeutically effective amount of a composition of the present disclosure for preventing or relieving one or more symptoms associated with a disease.
• systemic administration refers to administration of agents or compositions such that the agents or compositions become distributed in a subject’s body. The distribution of the agents or compositions throughout the subject’s body may be an even distribution.
• the distribution may be preferential, resulting in a higher localization of the agents or compositions in one or more desired sites.
• a desired site may be the blood or another site that is reachable by the vascular system.
• systemic routes of administration include administration by (1) introducing the agent directly into the vascular system or (2) oral, pulmonary, or intramuscular administration wherein the agent is adsorbed, enters the vascular system, and is carried to one or more desired site(s) of action via the blood.
• non-systemic administration refers to administration of agents or compositions such that the agents or compositions are administered locally to the target site of interest of a subject’s body to effect primarily a local effect.
• co-administration encompass administration of two or more agents to a subject so that both agents and/or their metabolites can assert their respective functions.
• Co-administration includes simultaneous administration in separate compositions, administration at different times in separate compositions, or administration in a composition in which both agents are present.
• subject includes, but is not limited to, humans of any age group, e.g., a pediatric subject (e.g., infant, child or adolescent) or adult subject (e.g., young adult, middle-aged adult or senior adult)) and/or other primates (e.g., cynomolgus monkeys or rhesus monkeys); mammals, including commercially relevant mammals such as cattle, pigs, horses, sheep, goats, cats, and/or dogs; and/or birds, including commercially relevant birds such as chickens, ducks, geese, quail, and/or turkeys.
• the methods described herein can be useful in both human therapeutics and veterinary applications.
• the subject is a mammal, and in some embodiments, the subject is human.
• the term “downregulating PTPN2 activity”, as used herein, refers to slowing, reducing, altering, inhibiting, as well as completely eliminating and/or preventing PTPN2 activity.
• effector function refers to a specialized function of a cell. Effector function of a T-cell, for example, may be cytolytic activity or helper activity including the secretion of cytokines.
• intracellular signaling domain refers to the portion of a protein which transduces the effector function signal and directs the cell to perform a specialized function.
• immune effector cell and “effector cell” are used interchangeably here. They refer to a cell that is involved in an immune response, e.g., in the promotion of an immune effector response.
• immune effector cells include T cells, e.g., alpha/beta T cells and gamma/delta T cells, B cells, natural killer (NK) cells, natural killer T (NKT) cells, mast cells, and myeloic-derived phagocytes.
• lymphoid cell or “lymphoid cells” refers to any of the cells responsible for the production of immunity mediated by cells or antibodies and including lymphocytes, lymphoblasts, and plasma cells.
• Lymphoid cells include granulocytes such as asophils, eosinophils, and neutrophils; mast cells; monocytes which can develop into macrophages; antigen-presenting cells such as dendritic cells; and lymphocytes such as natural killer cells (NK cells), B cells, and T cells (including activated T cells).
• T cells include both naive and memory cells (e.g. central memory or TCM, effector memory or TEM and effector memory RA or TEMRA), effector cells (e.g. cytotoxic T cells or CTLs or Tc cells), helper cells (e.g. Thl, Th2, Th3, Th9, Th7, TFH), regulatory cells (e.g.
• transiently downregulated generally means that a downregulation of expression or activity of a target molecule (e.g., PTPN2) is not permanent.
• a transient downregulation may not be a permanent downregulation.
• a transient downregulation may involve downregulating (e.g., reducing) expression or activity of a target molecule for a period of time, followed by regaining at least a portion of expression or activity level of the target molecule that was previously downregulated.
• a transient downregulation can involve an intermittent downregulation of a target molecule (e.g., PTPN2).
• a target molecule e.g., PTPN2
• the term “intermittent” is used herein to describe a process that is not continuous. An intermittent process may be followed by a break or stop. A plurality of intermittent processes may involve alternatively starting and stopping a same process or different processes.
• the term “intermittent dosing regimen” as used here refers to a dosing regimen that comprises administering a pharmaceutical composition, followed by a rest period.
• side effect as used herein refers to any complication, unwanted, or pathological outcome of a therapy that occurs in addition to or in place of a desired treatment outcome of the therapy.
• Examples of a side effect may include, but are not limited to, (i) off-target cell toxicity, (ii) on-target off-tumor toxicity, and/or (iii) autoimmunity (e.g., chronic autoimmunity).
• the term "efficacy" of a treatment or method, as used herein, can be measured based on changes in the course of disease or condition in response to such treatment or method.
• the efficacy of a treatment or method of the present disclosure may be measured by its impact on signs or symptoms of a disease or condition of a subject, e.g., a tumor or cancer of the subject.
• a response may be achieved when a subject having the disease or condition experiences partial or total alleviation of the disease or condition, or reduction of one or more symptoms of the disease or condition.
• a response is achieved when a subject suffering from a tumor exhibits a reduction in the tumor size after the treatment or method, as provided in the present disclosure.
• the efficacy may be measured by assessing cancer cell death, reduction of tumor (e.g., as evidenced by tumor size reduction), and/or inhibition of tumor growth, progression, and dissemination.
• Optional or “optionally” means that a subsequently described event or circumstance may or may not occur and that the description includes instances when the event or circumstance occurs and instances in which it does not.
• the term “optionally substituted” or “substituted” means that the referenced group may be substituted with one or more additional group(s) individually and independently selected from alkyl, alkenyl, cycloalkyl, aryl, heteroaryl, heterocycloalkyl, -OH, alkoxy, aryloxy, alkylthio, arylthio, alkylsulfoxide, arylsulfoxide, alkylsulfone, arylsulfone, -CN, alkyne, C 1 -C 6 alkylalkyne, halo, acyl, acyloxy, -CO 2 H, -CO 2 -alkyl, nitro, haloalkyl, fluoroalkyl, and amino, including mono-
• C 1 -C x includes C 1 -C 2 , C 1 -C3... C 1 -C x .
• C 1 -C x refers to the number of carbon atoms that make up the moiety to which it designates (excluding optional substituents).
• Alkyl refers to a straight or branched hydrocarbon chain radical consisting solely of carbon and hydrogen atoms, containing no unsaturation, having from one to fifteen carbon atoms (e.g., C 1 -C 15 alkyl).
• an alkyl comprises one to thirteen carbon atoms (e.g., C 1 -C 1 3 alkyl). In certain embodiments, an alkyl comprises one to eight carbon atoms (e.g., C 1 -C8 alkyl). In other embodiments, an alkyl comprises one to five carbon atoms (e.g., C 1 -C 5 alkyl). In other embodiments, an alkyl comprises one to four carbon atoms (e.g., C 1 -C 4 alkyl). In other embodiments, an alkyl comprises one to three carbon atoms (e.g., C 1 -C 3 alkyl).
• an alkyl comprises one to two carbon atoms (e.g., C 1 -C 2 alkyl). In other embodiments, an alkyl comprises one carbon atom (e.g., C 1 alkyl). In other embodiments, an alkyl comprises five to fifteen carbon atoms (e.g., C 5 -C 15 alkyl). In other embodiments, an alkyl comprises five to eight carbon atoms (e.g., C 5 -C 8 alkyl). In other embodiments, an alkyl comprises two to five carbon atoms (e.g., C 2 -C 5 alkyl). In other embodiments, an alkyl comprises three to five carbon atoms (e.g., C3-C 5 alkyl).
• the alkyl group is selected from methyl, ethyl, 1-propyl (n-propyl), 1-methylethyl (iso-propyl), 1-butyl (n-butyl), 1-methylpropyl (sec-butyl), 2- methylpropyl (iso-butyl), 1,1-dimethylethyl (tert-butyl), 1-pentyl (n-pentyl).
• the alkyl is attached to the rest of the molecule by a single bond.
• an alkyl group is optionally substituted by one or more of the following substituents: halo, cyano, nitro, oxo, thioxo, imino, oximo, trimethylsilanyl, -OR a , -SR a , -OC(O)-R a , -N(R a ) 2 , -C(O)R a , -C(O)OR a , -C(O)N(R a ) 2 , -N(R a )C(O)OR a , -OC(O)- N(R a ) 2 , -N(R a )C(O)R a , -N(R a )S(O) t R a (where t is 1 or 2), -S(O) t OR a (where t is 1 or 2), -S(O) t R a
• Alkoxy or “alkoxyl” refers to a radical bonded through an oxygen atom of the formula –O-alkyl, where alkyl is an alkyl chain as defined above.
• Alkenyl refers to a straight or branched hydrocarbon chain radical group consisting solely of carbon and hydrogen atoms, containing at least one carbon-carbon double bond, and having from two to twelve carbon atoms. In some embodiments, an alkenyl comprises two to eight carbon atoms. In other embodiments, an alkenyl comprises two to four carbon atoms.
• alkenyl is attached to the rest of the molecule by a single bond, for example, ethenyl (i.e., vinyl), prop-1-enyl (i.e., allyl), but-1-enyl, pent-1-enyl, penta-1,4-dienyl, and the like.
• ethenyl i.e., vinyl
• prop-1-enyl i.e., allyl
• but-1-enyl i.e., pent-1-enyl, penta-1,4-dienyl, and the like.
• an alkenyl group is optionally substituted by one or more of the following substituents: halo, cyano, nitro, oxo, thioxo, imino, oximo, trimethylsilanyl, -OR a , -SR a , -OC(O)-R a , - N(R a ) 2 , -C(O)R a , -C(O)OR a , -C(O)N(R a ) 2 , -N(R a )C(O)OR a , -OC(O)-N(R a ) 2 , -N(R a )C(O)R a , -N(R a )S(O) t R a (where t is 1 or 2), -S(O)tOR a (where t is 1 or 2), -S(O)tOR a (where t is 1 or 2),
• Alkynyl refers to a straight or branched hydrocarbon chain radical group consisting solely of carbon and hydrogen atoms, containing at least one carbon-carbon triple bond, having from two to twelve carbon atoms.
• an alkynyl comprises two to eight carbon atoms.
• an alkynyl comprises two to six carbon atoms.
• an alkynyl comprises two to four carbon atoms.
• the alkynyl is attached to the rest of the molecule by a single bond, for example, ethynyl, propynyl, butynyl, pentynyl, hexynyl, and the like.
• an alkynyl group is optionally substituted by one or more of the following substituents: halo, cyano, nitro, oxo, thioxo, imino, oximo, trimethylsilanyl, -OR a , - SR a , -OC(O)-R a , -N(R a ) 2 , -C(O)R a , -C(O)OR a , -C(O)N(R a ) 2 , -N(R a )C(O)OR a , -OC(O)-N(R a ) 2 , -N(R a )C(O)R a , - N(R a )S(O)tR a (where t is 1 or 2), -S(O)tOR a (where t is 1 or 2), -S(O)tOR a (where t is 1 or 2)
• Alkylene or "alkylene chain” refers to a straight or branched divalent hydrocarbon chain linking the rest of the molecule to a radical group, consisting solely of carbon and hydrogen, containing no unsaturation and having from one to twelve carbon atoms, for example, methylene, ethylene, propylene, n-butylene, and the like.
• the alkylene chain is attached to the rest of the molecule through a single bond and to the radical group through a single bond.
• the points of attachment of the alkylene chain to the rest of the molecule and to the radical group are through one carbon in the alkylene chain or through any two carbons within the chain.
• an alkylene comprises one to eight carbon atoms (e.g., C 1 -C 8 alkylene). In other embodiments, an alkylene comprises one to five carbon atoms (e.g., C 1 -C 5 alkylene). In other embodiments, an alkylene comprises one to four carbon atoms (e.g., C 1 -C 4 alkylene). In other embodiments, an alkylene comprises one to three carbon atoms (e.g., C 1 -C 3 alkylene). In other embodiments, an alkylene comprises one to two carbon atoms (e.g., C 1 -C 2 alkylene). In other embodiments, an alkylene comprises one carbon atom (e.g., C 1 alkylene).
• an alkylene comprises five to eight carbon atoms (e.g., C 5 -C 8 alkylene). In other embodiments, an alkylene comprises two to five carbon atoms (e.g., C 2 -C 5 alkylene). In other embodiments, an alkylene comprises three to five carbon atoms (e.g., C 3 -C 5 alkylene).
• an alkylene chain is optionally substituted by one or more of the following substituents: halo, cyano, nitro, oxo, thioxo, imino, oximo, trimethylsilanyl, -OR a , -SR a , -OC(O)-R a , -N(R a ) 2 , -C(O)R a , -C(O)OR a , -C(O)N(R a ) 2 , -N(R a )C(O)OR a , -OC(O)- N(R a ) 2 , -N(R a )C(O)R a , -N(R a )S(O) t R a (where t is 1 or 2), -S(O) t OR a (where t is 1 or 2), -S(O) t R a
• alkenylene or "alkenylene chain” refers to a straight or branched divalent hydrocarbon chain linking the rest of the molecule to a radical group, consisting solely of carbon and hydrogen, containing at least one carbon- carbon double bond, and having from two to twelve carbon atoms.
• the alkenylene chain is attached to the rest of the molecule through a single bond and to the radical group through a single bond.
• an alkenylene comprises two to eight carbon atoms (e.g., C 2 -C 8 alkenylene).
• an alkenylene comprises two to five carbon atoms (e.g., C 2 -C 5 alkenylene).
• an alkenylene comprises two to four carbon atoms (e.g., C 2 -C 4 alkenylene). In other embodiments, an alkenylene comprises two to three carbon atoms (e.g., C 2 -C 3 alkenylene). In other embodiments, an alkenylene comprises five to eight carbon atoms (e.g., C 5 - C 8 alkenylene). In other embodiments, an alkenylene comprises two to five carbon atoms (e.g., C 2 -C 5 alkenylene). In other embodiments, an alkenylene comprises three to five carbon atoms (e.g., C 3 -C 5 alkenylene).
• an alkenylene chain is optionally substituted by one or more of the following substituents: halo, cyano, nitro, oxo, thioxo, imino, oximo, trimethylsilanyl, -OR a , -SR a , -OC(O)-R a , - N(R a ) 2 , -C(O)R a , -C(O)OR a , -C(O)N(R a ) 2 , -N(R a )C(O)OR a , -OC(O)-N(R a ) 2 , -N(R a )C(O)R a , -N(R a )S(O) t R a (where t is 1 or 2), -S(O) t OR a (where t is 1 or 2), -S(O) t R a (where t is 1 or
• Alkynylene or “alkynylene chain” refers to a straight or branched divalent hydrocarbon chain linking the rest of the molecule to a radical group, consisting solely of carbon and hydrogen, containing at least one carbon- carbon triple bond, and having from two to twelve carbon atoms.
• the alkynylene chain is attached to the rest of the molecule through a single bond and to the radical group through a single bond.
• an alkynylene comprises two to eight carbon atoms (e.g., C 2 -C 8 alkynylene).
• an alkynylene comprises two to five carbon atoms (e.g., C 2 -C 5 alkynylene).
• an alkynylene comprises two to four carbon atoms (e.g., C 2 -C 4 alkynylene). In other embodiments, an alkynylene comprises two to three carbon atoms (e.g., C 2 -C 3 alkynylene). In other embodiments, an alkynylene comprises two carbon atom (e.g., C 2 alkylene). In other embodiments, an alkynylene comprises five to eight carbon atoms (e.g., C 5 -C 8 alkynylene). In other embodiments, an alkynylene comprises three to five carbon atoms (e.g., C3-C 5 alkynylene).
• an alkynylene chain is optionally substituted by one or more of the following substituents: halo, cyano, nitro, oxo, thioxo, imino, oximo, trimethylsilanyl, -OR a , -SR a , -OC(O)-R a , -N(R a ) 2 , - C(O)R a , -C(O)OR a , -C(O)N(R a ) 2 , -N(R a )C(O)OR a , -OC(O)-N(R a ) 2 , -N(R a )C(O)R a , -N(R a )S(O) t R a (where t is 1 or 2), -S(O)tOR a (where t is 1 or 2), -S(O)tOR a (where t is 1 or 2)
• aromatic refers to a planar ring having a delocalized ⁇ -electron system containing 4n+2 ⁇ electrons, where n is an integer. Aromatic rings can be formed from five, six, seven, eight, nine, or more than nine atoms. Aromatics can be optionally substituted.
• aromatic includes both aryl groups (e.g., phenyl, naphthalenyl) and heteroaryl groups (e.g., pyridinyl, quinolinyl).
• Aryl refers to a radical derived from an aromatic monocyclic or multicyclic hydrocarbon ring system by removing a hydrogen atom from a ring carbon atom.
• the aromatic monocyclic or multicyclic hydrocarbon ring system contains only hydrogen and carbon from five to eighteen carbon atoms, where at least one of the rings in the ring system is fully unsaturated, i.e., it contains a cyclic, delocalized (4n+2) ⁇ –electron system in accordance with the Hückel theory.
• the ring system from which aryl groups are derived include, but are not limited to, groups such as benzene, fluorene, indane, indene, tetralin and naphthalene.
• aryl or the prefix “ar-” (such as in “aralkyl”) is meant to include aryl radicals optionally substituted by one or more substituents independently selected from alkyl, alkenyl, alkynyl, halo, fluoroalkyl, cyano, nitro, optionally substituted aryl, optionally substituted aralkyl, optionally substituted aralkenyl, optionally substituted aralkynyl, optionally substituted cycloalkyl, optionally substituted cycloalkylalkyl, optionally substituted heterocycloalkyl, optionally substituted heterocycloalkylalkyl, optionally substituted heteroaryl, optionally substituted heteroarylalkyl, -R b -OR a , -R b -OC(O)-R a , -R b -OC(O)-OR a , -R b -OC(O)-OR a , -R
• Aralkyl refers to a radical of the formula -R c -aryl where R c is an alkylene chain as defined above, for example, methylene, ethylene, and the like.
• the alkylene chain part of the aralkyl radical is optionally substituted as described above for an alkylene chain.
• the aryl part of the aralkyl radical is optionally substituted as described above for an aryl group.
• “Aralkenyl” refers to a radical of the formula –R d -aryl where R d is an alkenylene chain as defined above.
• the aryl part of the aralkenyl radical is optionally substituted as described above for an aryl group.
• alkenylene chain part of the aralkenyl radical is optionally substituted as defined above for an alkenylene group.
• "Aralkynyl” refers to a radical of the formula -R e -aryl, where R e is an alkynylene chain as defined above.
• the aryl part of the aralkynyl radical is optionally substituted as described above for an aryl group.
• the alkynylene chain part of the aralkynyl radical is optionally substituted as defined above for an alkynylene chain.
• Alkoxy refers to a radical bonded through an oxygen atom of the formula -O-R c -aryl where R c is an alkylene chain as defined above, for example, methylene, ethylene, and the like.
• the alkylene chain part of the aralkyl radical is optionally substituted as described above for an alkylene chain.
• the aryl part of the aralkyl radical is optionally substituted as described above for an aryl group.
• cycloalkyl refers to a monocyclic or polycyclic non-aromatic radical, wherein each of the atoms forming the ring (i.e. skeletal atoms) is a carbon atom.
• Cycloalkyls may be saturated or partially unsaturated.
• a cycloalkyl ring is fused with an aryl, heteroaryl, heterocycloalkyl, or a second cycloalkyl ring.
• a cycloalkyl ring is a spirocyclic cycloalkyl ring.
• cycloalkyl groups include groups having from 3 to 10 ring atoms. Depending on the structure, a cycloalkyl group can be a monoradical or a diradical (i.e., a cycloalkylene group).
• cycloalkyl refers to a stable non-aromatic monocyclic or polycyclic hydrocarbon radical consisting solely of carbon and hydrogen atoms, which includes fused or bridged ring systems, having from three to fifteen carbon atoms.
• a cycloalkyl comprises three to ten carbon atoms.
• a cycloalkyl comprises five to seven carbon atoms.
• the cycloalkyl is attached to the rest of the molecule by a single bond. Cycloalkyl is saturated (i.e., containing single C-C bonds only) or unsaturated (i.e., containing one or more double bonds or triple bonds).
• Examples of monocyclic cycloalkyls include, e.g., cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl, and cyclooctyl.
• An unsaturated cycloalkyl is also referred to as "cycloalkenyl.”
• Examples of monocyclic cycloalkenyls include, e.g., cyclopentenyl, cyclohexenyl, cycloheptenyl, and cyclooctenyl.
• Polycyclic cycloalkyl radicals include, for example, adamantyl, norbornyl (i.e., bicyclo[2.2.1]heptanyl), norbornenyl, decalinyl, 7,7-dimethyl-bicyclo[2.2.1]heptanyl, and the like.
• Cycloalkylalkyl refers to a radical of the formula –R c -cycloalkyl where R c is an alkylene chain as defined above. The alkylene chain and the cycloalkyl radical may be optionally substituted.
• Cycloalkylalkynyl refers to a radical of the formula –R c -cycloalkyl where R c is an alkynylene chain as defined above. The alkynylene chain and the cycloalkyl radical may be optionally substituted as defined above.
• Cycloalkylalkoxy refers to a radical bonded through an oxygen atom of the formula –O-R c -cycloalkyl where R c is an alkylene chain as defined above.
• carboxylic acid bioisostere refers to a functional group or moiety that exhibits similar physical, biological and/or chemical properties as a carboxylic acid moiety.
• carboxylic acid bioisosteres include, but are not limited to, [00222] "Halo” or “halogen” refers to bromo, chloro, fluoro or iodo substituents.
• haloalkyl refers to an alkyl group that is substituted with one or more halogens. The halogens may be the same or they may be different.
• haloalkyls include -CH 2 Cl, -CF 3 , -CHF 2 , - CH 2 CF 3 , -CF 2 CF 3 , and the like.
• fluoroalkyl refers to an alkyl radical, as defined above, that is substituted by one or more fluoro radicals, as defined above, for example, trifluoromethyl, difluoromethyl, fluoromethyl, 2,2,2-trifluoroethyl, 1-fluoromethyl-2-fluoroethyl, and the like.
• the alkyl part of the fluoroalkyl radical is optionally substituted as defined above for an alkyl group.
• fluoroalkyl and “fluoroalkoxy” include alkyl and alkoxy groups, respectively, that are substituted with one or more fluorine atoms.
• fluoroalkyls include -CF 3 , -CHF 2 , -CH 2 F, - CH 2 CF 3 , -CF 2 CF 3 , -CF 2 -CFC 2 F 3 , -CF(CH 3 ) 3 , and the like.
• Non-limiting examples of fluoroalkoxy groups include - OCF 3 , -OCHF 2 , -OCH 2 F, -OCH 2 CF 3 , -OCF 2 CF 3 , -OCF 2 CF 2 CF 3 , -OCF(CH 3 ) 2 , and the like.
• the term “heteroalkyl” refers to an alkyl radical where one or more skeletal chain atoms is selected from an atom other than carbon, e.g., oxygen, nitrogen, sulfur, phosphorus, silicon, or combinations thereof. The heteroatom(s) may be placed at any interior position of the heteroalkyl group.
• heteroalkyl may have from 1 to 6 carbon atoms.
• bond or “single bond” refers to a chemical bond between two atoms, or two moieties when the atoms joined by the bond are considered to be part of larger substructure.
• substituent “R” appearing by itself and without a number designation refers to a substituent selected from among from alkyl, haloalkyl, heteroalkyl, alkenyl, alkynyl, cycloalkyl, aryl, heteroaryl (bonded through a ring carbon), and heterocycloalkyl.
• a “heterocycloalkyl” group or “heteroalicyclic” group refers to a cycloalkyl group, wherein at least one skeletal ring atom is a heteroatom selected from nitrogen, oxygen and sulfur. Heterocycloalkyls may be saturated or partially unsaturated.
• a heterocycloalkyl ring is fused with an aryl, heteroaryl, cycloalkyl, or a second heterocycloalkyl ring.
• the term heterocycloalkyl also includes all ring forms of the carbohydrates, including but not limited to the monosaccharides, the disaccharides and the oligosaccharides.
• a heterocycloalkyl ring is a spirocyclic heterocycloalkyl ring.
• a heterocycloalkyl ring is a bridged heterocycloalkyl ring. Unless otherwise noted, heterocycloalkyls may have from 2 to 10 carbons in the ring.
• a heterocycloalkyl group can be a monoradical or a diradical (i.e., a heterocycloalkylene group).
• heterocycloalkyl refers to a stable 3- to 18-membered non-aromatic ring radical that comprises two to twelve carbon atoms and from one to six heteroatoms selected from nitrogen, oxygen and sulfur.
• the heterocycloalkyl radical is a monocyclic, bicyclic, tricyclic or tetracyclic ring system, which optionally includes fused or bridged ring systems.
• the heteroatoms in the heterocycloalkyl radical are optionally oxidized.
• One or more nitrogen atoms, if present, are optionally quaternized.
• the heterocycloalkyl radical is partially or fully saturated.
• heterocycloalkyl is attached to the rest of the molecule through any atom of the ring(s).
• heterocycloalkyl radicals include, but are not limited to, dioxolanyl, thienyl[1,3]dithianyl, decahydroisoquinolyl, imidazolinyl, imidazolidinyl, isothiazolidinyl, isoxazolidinyl, morpholinyl, octahydroindolyl, octahydroisoindolyl, 2-oxopiperazinyl, 2-oxopiperidinyl, 2-oxopyrrolidinyl, oxazolidinyl, piperidinyl, piperazinyl, 4-piperidonyl, pyrrolidinyl, pyrazolidinyl, quinuclidinyl, thiazolidinyl, tetrahydrofuryl, trithianyl, tetra
• N-heterocycloalkyl or “N-attached heterocycloalkyl” refers to a heterocycloalkyl radical as defined above containing at least one nitrogen and where the point of attachment of the heterocycloalkyl radical to the rest of the molecule is through a nitrogen atom in the heterocycloalkyl radical.
• N-heterocycloalkyl radicals include, but are not limited to, 1-morpholinyl, 1-piperidinyl, 1-piperazinyl, 1-pyrrolidinyl, pyrazolidinyl, imidazolinyl, and imidazolidinyl.
• C-heterocycloalkyl or “C-attached heterocycloalkyl” refers to a heterocycloalkyl radical as defined above containing at least one heteroatom and where the point of attachment of the heterocycloalkyl radical to the rest of the molecule is through a carbon atom in the heterocycloalkyl radical.
• C-heterocycloalkyl radicals include, but are not limited to, 2-morpholinyl, 2- or 3- or 4-piperidinyl, 2-piperazinyl, 2- or 3-pyrrolidinyl, and the like.
• Heterocycloalkylalkyl refers to a radical of the formula –R c -heterocycloalkyl where R c is an alkylene chain as defined above. If the heterocycloalkyl is a nitrogen-containing heterocycloalkyl, the heterocycloalkyl is optionally attached to the alkyl radical at the nitrogen atom. The alkylene chain of the heterocycloalkylalkyl radical may be optionally substituted. The heterocycloalkyl part of the heterocycloalkylalkyl radical may be optionally substituted.
• Heterocycloalkylalkoxy refers to a radical bonded through an oxygen atom of the formula –O- R c -heterocycloalkyl where R c is an alkylene chain as defined above. If the heterocycloalkyl is a nitrogen-containing heterocycloalkyl, the heterocycloalkyl is optionally attached to the alkyl radical at the nitrogen atom. The alkylene chain of the heterocycloalkylalkoxy radical may be optionally substituted. The heterocycloalkyl part of the heterocycloalkylalkoxy radical may be optionally substituted.
• Heteroaryl refers to a radical derived from a 3- to 18-membered aromatic ring radical that comprises two to seventeen carbon atoms and from one to six heteroatoms selected from nitrogen, oxygen and sulfur.
• the heteroaryl radical is a monocyclic, bicyclic, tricyclic or tetracyclic ring system, wherein at least one of the rings in the ring system is fully unsaturated, i.e., it contains a cyclic, delocalized (4n+2) ⁇ –electron system in accordance with the Hückel theory.
• Heteroaryl includes fused or bridged ring systems.
• the heteroatom(s) in the heteroaryl radical is optionally oxidized.
• heteroaryl is attached to the rest of the molecule through any atom of the ring(s).
• heteroaryls include, but are not limited to, azepinyl, acridinyl, benzimidazolyl, benzindolyl, 1,3-benzodioxolyl, benzofuranyl, benzooxazolyl, benzo[d]thiazolyl, benzothiadiazolyl, benzo[b][1,4]dioxepinyl, benzo[b][1,4]oxazinyl, 1,4-benzodioxanyl, benzonaphthofuranyl, benzoxazolyl, benzodioxolyl, benzodioxinyl, benzopyranyl, benzopyranonyl, benzofuranyl, benzofuranonyl, benzothienyl (benzothienyl (benzothion
• heteroaryl is meant to include heteroaryl radicals as defined above which are optionally substituted by one or more substituents selected from alkyl, alkenyl, alkynyl, halo, fluoroalkyl, haloalkenyl, haloalkynyl, oxo, thioxo, cyano, nitro, optionally substituted aryl, optionally substituted aralkyl, optionally substituted aralkenyl, optionally substituted aralkynyl, optionally substituted cycloalkyl, optionally substituted cycloalkylalkyl, optionally substituted heterocycloalkyl, optionally substituted heterocycloalkylalkyl, optionally substituted heteroaryl, optionally substituted heteroarylalkyl, -R b -OR a , -R b -OC(O)-R a
• N-heteroaryl refers to a heteroaryl radical as defined above containing at least one nitrogen and where the point of attachment of the heteroaryl radical to the rest of the molecule is through a nitrogen atom in the heteroaryl radical.
• An N-heteroaryl radical is optionally substituted as described above for heteroaryl radicals.
• C-heteroaryl refers to a heteroaryl radical as defined above and where the point of attachment of the heteroaryl radical to the rest of the molecule is through a carbon atom in the heteroaryl radical.
• a C-heteroaryl radical is optionally substituted as described above for heteroaryl radicals.
• Heteroarylalkyl refers to a radical of the formula –R c -heteroaryl, where R c is an alkylene chain as defined above. If the heteroaryl is a nitrogen-containing heteroaryl, the heteroaryl is optionally attached to the alkyl radical at the nitrogen atom.
• the alkylene chain of the heteroarylalkyl radical is optionally substituted as defined above for an alkylene chain.
• the heteroaryl part of the heteroarylalkyl radical is optionally substituted as defined above for a heteroaryl group.
• Heteroarylalkoxy refers to a radical bonded through an oxygen atom of the formula –O-R c -heteroaryl, where R c is an alkylene chain as defined above. If the heteroaryl is a nitrogen-containing heteroaryl, the heteroaryl is optionally attached to the alkyl radical at the nitrogen atom.
• the alkylene chain of the heteroarylalkoxy radical is optionally substituted as defined above for an alkylene chain.
• the heteroaryl part of the heteroarylalkoxy radical is optionally substituted as defined above for a heteroaryl group.
• the compounds disclosed herein in some embodiments, contain one or more asymmetric centers and thus give rise to enantiomers, diastereomers, and other stereoisomeric forms that are defined, in terms of absolute stereochemistry, as (R)- or (S)-. Unless stated otherwise, it is intended that all stereoisomeric forms of the compounds disclosed herein are contemplated by this disclosure. When the compounds described herein contain alkene double bonds, and unless specified otherwise, it is intended that this disclosure includes both E and Z geometric isomers (e.g., cis or trans.) Likewise, all possible isomers, as well as their racemic and optically pure forms, and all tautomeric forms are also intended to be included.
• geometric isomer refers to E or Z geometric isomers (e.g., cis or trans) of an alkene double bond.
• positional isomer refers to structural isomers around a central ring, such as ortho-, meta-, and para- isomers around a benzene ring.
• a "tautomer” refers to a molecule wherein a proton shift from one atom of a molecule to another atom of the same molecule is possible.
• tautomeric equilibrium includes: [00242]
• the compounds disclosed herein exist in tautomeric forms. The structures of said compounds are illustrated in the one tautomeric form for clarity. The alternative tautomeric forms are expressly included in this disclosure, such as, for example, the structures illustrated below.
• the compounds disclosed herein, in some embodiments are used in different enriched isotopic forms, e.g., enriched in the content of 2 H, 3 H, 11 C, 13 C and/or 14 C.
• the compound is deuterated in at least one position. Such deuterated forms can be made by the procedure described in U.S.
• structures depicted herein are intended 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 the present disclosure.
• the compounds of the present disclosure optionally contain unnatural proportions of atomic isotopes at one or more atoms that constitute such compounds.
• the compounds may be labeled with isotopes, such as for example, deuterium ( 2 H), tritium ( 3 H), iodine-125 ( 125 I) or carbon-14 ( 14 C).
• isotopes such as for example, deuterium ( 2 H), tritium ( 3 H), iodine-125 ( 125 I) or carbon-14 ( 14 C).
• Isotopic substitution with 2 H, 11 C, 13 C, 14 C, 15 C, 12 N, 13 N, 15 N, 16 N, 16 O, 17 O, 14 F, 15 F, 16 F, 17 F, 18 F, 33 S, 34 S, 35 S, 36 S, 35 Cl, 37 Cl, 79 Br, 81 Br, 125 I are all contemplated.
• the compounds disclosed herein have some or all of the 1 H atoms replaced with 2 H atoms.
• the methods of synthesis for deuterium-containing compounds are known in the art and include, by way of non-limiting example only, the following synthetic methods.
• Deuterium substituted compounds are synthesized using various methods such as described in: Dean, Dennis C.; Editor. Recent Advances in the Synthesis and Applications of Radiolabeled Compounds for Drug Discovery and Development. [In: Curr., Pharm. Des., 2000; 6 (10)] 2000, 110 pp; George W.; Varma, Rajender S.
• Deuterium-transfer reagents suitable for use in nucleophilic substitution reactions are readily available and may be employed to transfer a deuterium-substituted carbon atom under nucleophilic substitution reaction conditions to the reaction substrate.
• CD3I is illustrated, by way of example only, in the reaction schemes below.
• Deuterium-transfer reagents such as lithium aluminum deuteride (LiAlD 4 ), are employed to transfer deuterium under reducing conditions to the reaction substrate.
• LiAlD 4 is illustrated, by way of example only, in the reaction schemes below.
• “Pharmaceutically acceptable salt” includes both acid and base addition salts.
• a pharmaceutically acceptable salt of any of the compounds described herein is intended to encompass any and all pharmaceutically suitable salt forms.
• Preferred pharmaceutically acceptable salts of the compounds described herein are pharmaceutically acceptable acid addition salts and pharmaceutically acceptable base addition salts.
• “Pharmaceutically acceptable acid addition salt” refers to those salts which retain the biological effectiveness and properties of the free bases, which are not biologically or otherwise undesirable, and which are formed with inorganic acids such as hydrochloric acid, hydrobromic acid, sulfuric acid, nitric acid, phosphoric acid, hydroiodic acid, hydrofluoric acid, phosphorous acid, and the like. Also included are salts that are formed with organic acids such as aliphatic mono- and dicarboxylic acids, phenyl-substituted alkanoic acids, hydroxy alkanoic acids, alkanedioic acids, aromatic acids, aliphatic and. aromatic sulfonic acids, etc.
• acetic acid trifluoroacetic acid, propionic acid, glycolic acid, pyruvic acid, oxalic acid, maleic acid, malonic acid, succinic acid, fumaric acid, tartaric acid, citric acid, benzoic acid, cinnamic acid, mandelic acid, methanesulfonic acid, ethanesulfonic acid, p-toluenesulfonic acid, salicylic acid, and the like.
• Exemplary salts thus include sulfates, pyrosulfates, bisulfates, sulfites, bisulfites, nitrates, phosphates, monohydrogenphosphates, dihydrogenphosphates, metaphosphates, pyrophosphates, chlorides, bromides, iodides, acetates, trifluoroacetates, propionates, caprylates, isobutyrates, oxalates, malonates, succinate suberates, sebacates, fumarates, maleates, mandelates, benzoates, chlorobenzoates, methylbenzoates, dinitrobenzoates, phthalates, benzenesulfonates, toluenesulfonates, phenylacetates, citrates, lactates, malates, tartrates, methanesulfonates, and the like.
• Acid addition salts of basic compounds are, in some embodiments, prepared by contacting the free base forms with a sufficient amount of the desired acid to produce the salt according to methods and techniques with which a skilled artisan is familiar.
• “Pharmaceutically acceptable base addition salt” refers to those salts that retain the biological effectiveness and properties of the free acids, which are not biologically or otherwise undesirable. These salts are prepared from addition of an inorganic base or an organic base to the free acid.
• Pharmaceutically acceptable base addition salts are, in some embodiments, formed with metals or amines, such as alkali and alkaline earth metals or organic amines.
• Salts derived from inorganic bases include, but are not limited to, sodium, potassium, lithium, ammonium, calcium, magnesium, iron, zinc, copper, manganese, aluminum salts and the like.
• Salts derived from organic bases include, but are not limited to, salts of primary, secondary, and tertiary amines, substituted amines including naturally occurring substituted amines, cyclic amines and basic ion exchange resins, for example, isopropylamine, trimethylamine, diethylamine, triethylamine, tripropylamine, ethanolamine, diethanolamine, 2-dimethylaminoethanol, 2-diethylaminoethanol, dicyclohexylamine, lysine, arginine, histidine, caffeine, procaine, N,N-dibenzylethylenediamine, chloroprocaine, hydrabamine, choline, betaine, ethylenediamine, ethylenedianiline, N-methylglucamine, glucosamine, methylglucamine, theobromine, purines, piperazine, piperidine, N-ethylpiperidine, polyamine resins and the like.
• polypeptide “peptide” and “protein” are used interchangeably herein to refer to polymers of amino acids of any length.
• the polymer may be linear or branched, it may comprise modified amino acids, and it may be interrupted by non-amino acids.
• the terms also encompass an amino acid polymer that has been modified; for example, disulfide bond formation, glycosylation, lipidation, acetylation, phosphorylation, or any other manipulation, such as conjugation with a labeling component.
• amino acid refers to either natural and/or unnatural or synthetic amino acids, including glycine and both the D or L optical isomers, and amino acid analogs and peptidomimetics.
• polynucleotide refers to a polymeric form of nucleotides of any length, either deoxyribonucleotides or ribonucleotides, or analogs thereof. Polynucleotides may have any three dimensional structure, and may perform any function, known or unknown.
• polynucleotides coding or non-coding regions of a gene or gene fragment, loci (locus) defined from linkage analysis, exons, introns, messenger RNA (mRNA), transfer RNA, ribosomal RNA, short interfering RNA (siRNA), short-hairpin RNA (shRNA), micro-RNA (miRNA), ribozymes, cDNA, recombinant polynucleotides, branched polynucleotides, plasmids, vectors, isolated DNA of any sequence, isolated RNA of any sequence, nucleic acid probes, and primers.
• loci locus defined from linkage analysis, exons, introns, messenger RNA (mRNA), transfer RNA, ribosomal RNA, short interfering RNA (siRNA), short-hairpin RNA (shRNA), micro-RNA (miRNA), ribozymes, cDNA, recombinant polynucleotides, branched poly
• a polynucleotide may comprise one or more modified nucleotides, such as methylated nucleotides and nucleotide analogs, such as peptide nucleic acid (PNA), Morpholino and locked nucleic acid (LNA), glycol nucleic acid (GNA), threose nucleic acid (TNA), 2’-fluoro, 2’-OMe, and phosphorothiolated DNA. If present, modifications to the nucleotide structure may be imparted before or after assembly of the polymer. The sequence of nucleotides may be interrupted by non-nucleotide components.
• modified nucleotides such as methylated nucleotides and nucleotide analogs, such as peptide nucleic acid (PNA), Morpholino and locked nucleic acid (LNA), glycol nucleic acid (GNA), threose nucleic acid (TNA), 2’-fluoro, 2’-OMe, and
• a polynucleotide may be further modified after polymerization, such as by conjugation with a labeling component or other conjugation target.
• expression refers to the process by which a polynucleotide is transcribed from a DNA template (such as into mRNA or other RNA transcript) and/or the process by which a transcribed mRNA is subsequently translated into peptides, polypeptides, or proteins. Transcripts and encoded polypeptides may be collectively referred to as “gene product.” If the polynucleotide is derived from genomic DNA, expression may include splicing of the mRNA in a eukaryotic cell.
• therapeutic agent refers to a molecule or compound that confers some beneficial effect upon administration to a subject.
• the beneficial effect includes enablement of diagnostic determinations; amelioration of a disease, symptom, disorder, or pathological condition; reducing or preventing the onset of a disease, symptom, disorder or condition; and generally counteracting a disease, symptom, disorder or pathological condition.
• treatment or “treating,” or “palliating” or “ameliorating” are used interchangeably. These terms refer to an approach for obtaining beneficial or desired results including but not limited to a therapeutic benefit and/or a prophylactic benefit.
• compositions may be administered to a subject at risk of developing a particular disease, condition, or symptom, or to a subject reporting one or more of the physiological symptoms of a disease, even though the disease, condition, or symptom may not have yet been manifested.
• prophylactic benefit includes reducing the incidence and/or worsening of one or more diseases, conditions, or symptoms under treatment (e.g. as between treated and untreated populations, or between treated and untreated states of a subject).
• “treatment”, “treating”, palliating”, or “ameliorating” does not include a prophylactic benefit.
• the term “effective amount” or “therapeutically effective amount” refers to the amount of an agent that is sufficient to effect beneficial or desired results.
• the therapeutically effective amount may vary depending upon one or more of: the subject and disease condition being treated, the weight and age of the subject, the severity of the disease condition, the manner of administration and the like, which can readily be determined by one of ordinary skill in the art.
• An effective amount of an active agent may be administered in a single dose or in multiple doses.
• a component may be described herein as having at least an effective amount, or at least an amount effective, such as that associated with a particular goal or purpose, such as any described herein.
• the term “effective amount” also applies to a dose that will provide an image for detection by an appropriate imaging method.
• the specific dose may vary depending on one or more of: the particular agent chosen, the dosing regimen to be followed, whether it is administered in combination with other compounds, timing of administration, the tissue to be imaged, and the physical delivery system in which it is carried.
• the term “in vivo” refers to an event that takes place in a subject's body.
• the term “ex vivo” refers to an event that first takes place outside of the subject’s body for a subsequent in vivo application into a subject’s body.
• an ex vivo preparation may involve preparation of cells outside of a subject’s body for the purpose of introduction of the prepared cells into the same or a different subject’s body.
• in vitro refers to an event that takes place outside of a subject’s body.
• an in vitro assay encompasses any assay run outside of a subject’s body.
• In vitro assays encompass cell-based assays in which cells alive or dead are employed.
• In vitro assays also encompass a cell-free assay in which no intact cells are employed.
• Compounds [00264] The compounds, or a pharmaceutically acceptable salts or solvates thereof, disclosed herein are PTPN2 inhibitors and have a wide range of applications in therapeutics, diagnostics, and other biomedical research.
• a compound of Formula (I), or a pharmaceutically acceptable salt or solvate thereof Formula (I); wherein: W 1 is N, N(R 1 ), O, C(R 1 ), C(R 1 )(R 1a ), C(O), S(O), S(O) 2 , S(O)(NR 1 ), S(O)(R 1 ), or P(O)(R 1 ); W 2 is N, N(R 2 ), O, C(R 2 ), C(R 2 )(R 2a ), C(O), S(O), S(O) 2 , S(O)(NR 2 ), S(O)(R 2 ), or P(O)(R 2 ); W 3 is N, N(R 3 ), O, C(R 3 ), C(R 3 )(R 3a ), C(O), S(O), S(O) 2 , S(O)(NR 3 ), S(O)(R 3 ), or P(O)(R 1 );
• R 6 is selected from hydrogen, halogen, -CN, C 1-6 alkyl, C 2 - 6 alkenyl, C 2-6 alkynyl, C 3-6 cycloalkyl, C 2-9 heterocycloalkyl, C 6-10 aryl, C 1-9 heteroaryl, -OR 16 , -N(R 12 )(R 16 ), -OR 12a , - SR 12 , -N(R 12 )(R 13 ), -C(O)OR 12 , -OC(O)N(R 12 )(R 13 ), -N(R 14 )C(O)N(R 12 )(R 13 ), -N(R 14 )C(O)OR 12 ,
• W 1 is N, N(R 1 ), O, C(R 1 ), C(R 1 )(R 1a ), C(O), S(O), S(O) 2 , S(O)(NR 1 ), S(O)(R 1 ), or P(O)(R 1 );
• W 2 is N, N(R 2 ), O, C(R 2 ), C(R 2 )(R 2a ), C(O), S(O), S(O) 2 , S(O)(NR 2 ), S(O)(R 2 ), or P(O)(R 2 );
• W 3 is N, N(R 3 ), O, C(R 3 ), C(R 3 )(R 3a ), C(O), S(O), S(O) 2 , S(O)(NR 3 ), S(O)(R 3 ), or P(O)(R 3 );
• W 4 is N, N(R 4 ), C(R 4 ), C(R 4 ), C(R
• W 1 is N, N(R 1 ), O, C(R 1 ), C(R 1 )(R 1a ), C(O), S(O), S(O) 2 , S(O)(NR 1 ), S(O)(R 1 ), or P(O)(R 1 );
• W 2 is N, N(R 2 ), O, C(R 2 ), C(R 2 )(R 2a ), C(O), S(O), S(O) 2 , S(O)(NR 2 ), S(O)(R 2 ), or P(O)(R 2 );
• W 3 is N, N(R 3 ), O, C(R 3 ), C(R 3 )(R 3a ), S(O), S(O) 2 , S(O)(NR 3 ), S(O)(R 3 ), or P(O)(R 3 );
• W 4 is N, N(R 4 ), C(R 4 ), C(R 4 ), C(R 4 )(
• the compound is a compound of Formula (Ia): Formula (Ia); wherein at least one of W 1 , W 2 , W 3 , and W 4 is N. R 5 , R 6 , R 7 , R 9 , R 9a , and R 10 are as described herein.
• the compound is a compound of Formula (Ib): Formula (Ib); wherein at least one of W 1 , W 2 , W 3 , and W 4 is N. R 5 , R 6 , R 7 , R 9 , and R 10 are as described herein.
• the compound is a compound of Formula (Ic): Formula (Ic); wherein at least one of W 1 , W 2 , W 3 , and W 4 is N.
• R 5 , R 6 , R 7 , R 9 , R 9a , and R 10 are as described herein.
• the compound is a compound of Formula (Ig): Formula (Ig); wherein at least one of W 1 , W 2 , W 3 , and W 4 is N, N(R 3 ), N(R 4 ), or O.
• R 5 , R 6 , R 7 , R 9 , R 9a , and R 10 are as described herein.
• the compound is a compound of Formula (Ih): Formula (Ih); wherein at least one of W 1 , W 2 , W 3 , and W 4 is N, N(R 3 ), N(R 4 ), or O. R 5 , R 6 , R 7 , R 9 , and R 10 are as described herein.
• the compound is a compound of Formula (Ii): Formula (Ii); wherein at least one of W 1 , W 2 , W 3 , and W 4 is N, N(R 3 ), N(R 4 ), or O.
• R 5 , R 6 , R 7 , R 9 , R 9a , and R 10 are as described herein.
• the compound is a compound of Formula (Ij): Formula (Ij); wherein at least one of W 1 , W 2 , W 3 , and W 4 is N(R 1 ), N(R 2 ), N, or O. R 5 , R 6 , R 7 , R 9 , R 9a , and R 10 are as described herein.
• the compound is a compound of Formula (Ik): Formula (Ik); wherein at least one of W 1 , W 2 , W 3 , and W 4 is N(R 1 ), N(R 2 ), N, or O.
• R 5 , R 6 , R 7 , R 9 , and R 10 are as described herein.
• the compound is a compound of Formula (Im): Formula (Im); wherein at least one of W 1 , W 2 , W 3 , and W 4 is N, N(R 3 ), N(R 4 ), or O.
• R 5 , R 6 , R 7 , R 9 , R 9a , and R 10 are as described herein.
• the compound is a compound of Formula (Iv): Formula (Iv); wherein at least one of W 1 , W 2 , W 3 , and W 4 is N(R 1 ), N(R 4 ), N, or O.
• the compound is a compound of Formula (Iw): Formula (Iw); wherein at least one of W 1 , W 2 , W 3 , and W 4 is N(R 1 ), N(R 4 ), N, or O.
• R 5 , R 6 , R 7 , R 9 , and R 10 are as described herein.
• the compound is a compound of Formula (Ix): Formula (Ix); wherein at least one of W 1 , W 2 , W 3 , and W 4 is N(R 1 ), N(R 4 ), N, or O.
• the compound is a compound of Formula (Io): Formula (Io).
• W 1 , W 2 , W 4 , X, Y, Z, J 1 , J 2 , and J 3 are as described herein.
• W 1 is C(R 1 );
• W 2 is C(R 2 );
• W 4 is C(R 4 )(R 4a ), C(O), S(O), S(O) 2 , S(O)(NR 4 ), S(O)(R 4 ), or P(O)(R 4 ).
• the compound is a compound of Formula (Ioa): Formula (Ioa); W 1 , W 2 , W 4 , R 5 , R 6 , R 7 , R 9 , R 9a , and R 10 are as described herein.
• W 1 is C(R 1 );
• W 2 is C(R 2 );
• W 4 is C(R 4 )(R 4a ), C(O), S(O), S(O) 2 , S(O)(NR 4 ), S(O)(R 4 ), or P(O)(R 4 ).
• the compound is a compound of Formula (Iob): Formula (Iob); W 1 , W 2 , W 4 , R 5 , R 6 , R 7 , R 9 , and R 10 are as described herein.
• W 1 is C(R 1 );
• W 2 is C(R 2 );
• W 4 is C(R 4 )(R 4a ), C(O), S(O), S(O) 2 , S(O)(NR 4 ), S(O)(R 4 ), or P(O)(R 4 ).
• the compound is a compound of Formula (Ioc): Formula (Ioc); W 1 , W 2 , W 4 , R 5 , R 6 , R 7 , R 9 , R 9a , and R 10 are as described herein.
• W 1 is C(R 1 );
• W 2 is C(R 2 );
• W 4 is C(R 4 )(R 4a ), C(O), S(O), S(O) 2 , S(O)(NR 4 ), S(O)(R 4 ), or P(O)(R 4 ).
• the compound is a compound of Formula (Ip): Formula (Ip); W 1 , W 3 , W 4 , X, Y, Z, J 1 , J 2 , and J 3 are as described herein.
• W 1 is C(R 1 )(R 1a ), C(O), S(O), S(O) 2 , S(O)(NR 1 ), S(O)(R 1 ), or P(O)(R 1 );
• W 3 is C(R 3 ); and W 4 is C(R 4 ).
• the compound is a compound of Formula (Ipa): Formula (Ipa); W 1 , W 3 , W 4 , R 5 , R 6 , R 7 , R 9 , R 9a , and R 10 are as described herein.
• W 1 is C(R 1 )(R 1a ), C(O), S(O), S(O) 2 , S(O)(NR 1 ), S(O)(R 1 ), or P(O)(R 1 );
• W 3 is C(R 3 ); and W 4 is C(R 4 ).
• the compound is a compound of Formula (Ipb): Formula (Ipb); W 1 , W 3 , W 4 , R 5 , R 6 , R 7 , R 9 , and R 10 are as described herein.
• W 1 is C(R 1 )(R 1a ), C(O), S(O), S(O) 2 , S(O)(NR 1 ), S(O)(R 1 ), or P(O)(R 1 );
• W 3 is C(R 3 ); and W 4 is C(R 4 ).
• the compound is a compound of Formula (Ipc): Formula (Ipc); W 1 , W 3 , W 4 , R 5 , R 6 , R 7 , R 9 , R 9a , and R 10 are as described herein.
• W 1 is C(R 1 )(R 1a ), C(O), S(O), S(O) 2 , S(O)(NR 1 ), S(O)(R 1 ), or P(O)(R 1 );
• W 3 is C(R 3 ); and W 4 is C(R 4 ).
• the compound is a compound of Formula (Ipd): Formula (Iq); wherein W 1 is N or C(R 1 ); W 2 is N or C(R 2 ); W 3 is N or C(R 3 ); and W 4 is N(R 4 ), C(R 4 )(R 4a ), C(O), S(O), S(O) 2 , S(O)(NR 4 ), S(O)(R 4 ), or P(O)(R 4 ).
• R 5 , R 6 , R 7 , R 9 , R 9a , and R 10 are as described herein.
• the compound is a compound of Formula (Ir): Formula (Ir); wherein W 1 is N or C(R 1 ); W 2 is N or C(R 2 ); W 3 is N or C(R 3 ); and W 4 is N(R 4 ), C(R 4 )(R 4a ), C(O), S(O), S(O) 2 , S(O)(NR 4 ), S(O)(R 4 ), or P(O)(R 4 ).
• R 5 , R 6 , R 7 , R 9 , and R 10 are as described herein.
• the compound is a compound of Formula (Is): Formula (Is); wherein W 1 is N or C(R 1 ); W 2 is N or C(R 2 ); W 3 is N or C(R 3 ); and W 4 is N(R 4 ), C(R 4 )(R 4a ), C(O), S(O), S(O) 2 , S(O)(NR 4 ), S(O)(R 4 ), or P(O)(R 4 ).
• R 5 , R 6 , R 7 , R 9 , R 9a , and R 10 are as described herein.
• the compound is a compound of Formula (Ipd): Formula (Iy); wherein W 1 is N(R 1 ), C(R 1 )(R 1a ), C(O), S(O), S(O) 2 , S(O)(NR 1 ), S(O)(R 1 ), or P(O)(R 1 ); W 2 is N or C(R 2 ); W 3 is N or C(R 3 ); and W 4 is N or C(R 4 ).
• R 5 , R 6 , R 7 , R 9 , R 9a , and R 10 are as described herein.
• the compound is a compound of Formula (Ir): Formula (Iz); wherein W 1 is N(R 1 ), C(R 1 )(R 1a ), C(O), S(O), S(O) 2 , S(O)(NR 1 ), S(O)(R 1 ), or P(O)(R 1 ); W 2 is N or C(R 2 ); W 3 is N or C(R 3 ); and W 4 is N or C(R 4 ).
• R 5 , R 6 , R 7 , R 9 , and R 10 are as described herein.
• the compound is a compound of Formula (Is): Formula (Iaa); wherein W 1 is N(R 1 ), C(R 1 )(R 1a ), C(O), S(O), S(O) 2 , S(O)(NR 1 ), S(O)(R 1 ), or P(O)(R 1 ); W 2 is N or C(R 2 ); W 3 is N or C(R 3 ); and W 4 is N or C(R 4 ).
• R 5 , R 6 , R 7 , R 9 , R 9a , and R 10 are as described herein.
• W 1 is N, N(R 1 ), O, C(R 1 ), C(R 1 )(R 1a ), C(O), S(O), S(O) 2 , S(O)(NR 1 ), S(O)(R 1 ), or P(O)(R 1 );
• W 2 is N, N(R 2 ), O, C(R 2 ), C(R 2 )(R 2a ), C(O), S(O), S(O) 2 , S(O)(NR 2 ), S(O)(R 2 ), or P(O)(R 2 );
• W 3 is N, N(R 3 ), O, C(R 3 ), C(R 3 )(R 3a ), C(O), S(O), S(O) 2 , S(O)(NR 3 ), S(O)(R 3 ), or P(O)(R 3 );
• W 4 is N, N(R 4 ), C(R 4 ), C(R 4 ), C(R
• W 1 is N, N(R 1 ), O, C(R 1 ), C(R 1 )(R 1a ), C(O), S(O), S(O) 2 , S(O)(NR 1 ), S(O)(R 1 ), or P(O)(R 1 );
• W 2 is N, N(R 2 ), O, C(R 2 ), C(R 2 )(R 2a ), C(O), S(O), S(O) 2 , S(O)(NR 2 ), S(O)(R 2 ), or P(O)(R 2 );
• W 3 is N, N(R 3 ), O, C(R 3 ), C(R 3 )(R 3a ), S(O), S(O) 2 , S(O)(NR 3 ), S(O)(R 3 ), or P(O)(R 3 );
• W 4 is N, N(R 4 ), C(R 4 ), C(R 4 ), C(R 4 )(
• the compound, or a pharmaceutically acceptable salt or solvate thereof has the structure of Formula (IIIa): Formula (IIIa); wherein at least one of W 1 , W 2 , W 3 , and W 4 is N, N(R 1 ), N(R 2 ), N(R 3 ), N(R 4 ), or O and at least one of W 1 , W 2 , W 3 , and W 4 is C(O), S(O), S(O) 2 , S(O)(NR 1 ), S(O)(R 1 ), P(O)(R 1 ), S(O)(NR 2 ), S(O)(R 2 ), P(O)(R 2 ), S(O)(NR 3 ), S(O)(R 3 ), P(O)(R 3 ), S(O)(NR 4 ), S(O)(R 4 ), or P(O)(R 4 ).
• W 1 , W 2 , W 3 , and W 4 is N, N(R 1 ), N(R
• the compound, or a pharmaceutically acceptable salt or solvate thereof has the structure of Formula (IIIb): Formula (IIIb); wherein at least one of W 1 , W 2 , W 3 , and W 4 is N, N(R 1 ), N(R 2 ), N(R 3 ), N(R 4 ), or O and at least one of W 1 , W 2 , W 3 , and W 4 is C(O), S(O), S(O) 2 , S(O)(NR 1 ), S(O)(R 1 ), P(O)(R 1 ), S(O)(NR 2 ), S(O)(R 2 ), P(O)(R 2 ), S(O)(NR 3 ), S(O)(R 3 ), P(O)(R 3 ), S(O)(NR 4 ), S(O)(R 4 ), or
• the compound, or a pharmaceutically acceptable salt or solvate thereof has the structure of Formula (IIIc): Formula (IIIc); wherein at least one of W 1 , W 2 , W 3 , and W 4 is N, N(R 1 ), N(R 2 ), N(R 3 ), N(R 4 ), or O and at least one of W 1 , W 2 , W 3 , and W 4 is C(O), S(O), S(O) 2 , S(O)(NR 1 ), S(O)(R 1 ), P(O)(R 1 ), S(O)(NR 2 ), S(O)(R 2 ), P(O)(R 2 ), S(O)(NR 3 ), S(O)(R 3 ), P(O)(R 3 ), S(O)(R 3 ), S(O)(NR 4 ), S(O)(R 4 ), or P(O)(
• the compound, or a pharmaceutically acceptable salt or solvate thereof has the structure of Formula (IIId): Formula (IIId); wherein W 1 is N(R 1 ), C(R 1 )(R 1a ), C(O), S(O), S(O) 2 , S(O)(NR 1 ), S(O)(R 1 ), or P(O)(R 1 ); W 2 is N(R 2 ), C(R 2 )(R 2a ), C(O), S(O), S(O) 2 , S(O)(NR 2 ), S(O)(R 2 ), or P(O)(R 2 ); W 3 is N(R 3 ), C(R 3 )(R 3a ), C(O), S(O), S(O), S(O) 2 , S(O)(NR 3 ), S(O)(R 3 ), or
• the compound, or a pharmaceutically acceptable salt or solvate thereof has the structure of Formula (IIIe): Formula (IIIe); wherein W 1 is N(R 1 ), C(R 1 )(R 1a ), C(O), S(O), S(O) 2 , S(O)(NR 1 ), S(O)(R 1 ), or P(O)(R 1 ); W 2 is N(R 2 ), C(R 2 )(R 2a ), C(O), S(O), S(O) 2 , S(O)(NR 2 ), S(O)(R 2 ), or P(O)(R 2 ); W 3 is N(R 3 ), C(R 3 )(R 3a ), C(O), S(O), S(O) 2 , S(O)(NR 3 ), S(O)(R 3 ), or P(O)(R 1 ); W 3 is N(R 3 ), C(R 3 )(R 3a ), C(O), S(O), S
• the compound, or a pharmaceutically acceptable salt or solvate thereof has the structure of Formula (IIIf): Formula (IIIf); wherein W 1 is N(R 1 ), C(R 1 )(R 1a ), C(O), S(O), S(O) 2 , S(O)(NR 1 ), S(O)(R 1 ), or P(O)(R 1 ); W 2 is N(R 2 ), C(R 2 )(R 2a ), C(O), S(O), S(O) 2 , S(O)(NR 2 ), S(O)(R 2 ), or P(O)(R 2 ); W 3 is N(R 3 ), C(R 3 )(R 3a ), C(O), S(O), S(O) 2 , S(O)(NR 3 ), S(O)(R 3 ), or P(O)(R
• the compound, or a pharmaceutically acceptable salt or solvate thereof has the structure of Formula (IIIg): Formula (IIIg); wherein W 1 is N or C(R 1 ); W 2 is N or C(R 2 ); W 3 is N(R 3 ), C(R 3 )(R 3a ), C(O), S(O), S(O) 2 , S(O)(NR 3 ), S(O)(R 3 ), or P(O)(R 3 ); W 4 is N(R 4 ), C(R 4 )(R 4a ), C(O), S(O), S(O) 2 , S(O)(NR 4 ), S(O)(R 4 ), or P(O)(R 4 ); and wherein at least one of W 1 , W 2 , W 3 , and W 4 is N, N(R 1 ), N(R
• the compound, or a pharmaceutically acceptable salt or solvate thereof has the structure of Formula (IIIh): Formula (IIIh); wherein W 1 is N or C(R 1 ); W 2 is N or C(R 2 ); W 3 is N(R 3 ), C(R 3 )(R 3a ), C(O), S(O), S(O) 2 , S(O)(NR 3 ), S(O)(R 3 ), or P(O)(R 3 ); W 4 is N(R 4 ), C(R 4 )(R 4a ), C(O), S(O), S(O) 2 , S(O)(NR 4 ), S(O)(R 4 ), or P(O)(R 4 ); and wherein at least one of W 1 , W 2 , W 3 , and W 4 is N, N(R 1 ), N(
• the compound, or a pharmaceutically acceptable salt or solvate thereof has the structure of Formula (IIIi): Formula (IIIi); wherein W 1 is N or C(R 1 ); W 2 is N or C(R 2 ); W 3 is N(R 3 ), C(R 3 )(R 3a ), C(O), S(O), S(O) 2 , S(O)(NR 3 ), S(O)(R 3 ), or P(O)(R 3 ); W 4 is N(R 4 ), C(R 4 )(R 4a ), C(O), S(O), S(O) 2 , S(O)(NR 4 ), S(O)(R 4 ), or P(O)(R 4 ); and wherein at least one of W 1 , W 2 , W 3 , and W 4 is N, N(R 1 ), N(
• the compound, or a pharmaceutically acceptable salt or solvate thereof has the structure of Formula (IIIj): Formula (IIIj); wherein W 1 is N(R 1 ), C(R 1 )(R 1a ), C(O), S(O), S(O) 2 , S(O)(NR 1 ), S(O)(R 1 ), or P(O)(R 1 ); W 2 is N(R 2 ), C(R 2 )(R 2a ), C(O), S(O), S(O) 2 , S(O)(NR 2 ), S(O)(R 2 ), or P(O)(R 2 ); W 3 is N or C(R 3 ); W 4 is N or C(R 4 ); and wherein at least one of W 1 , W 2 , W 3 , and W 4 is N, N(R 1 ), N(
• the compound, or a pharmaceutically acceptable salt or solvate thereof has the structure of Formula (IIIk): Formula (IIIk); wherein W 1 is N(R 1 ), C(R 1 )(R 1a ), C(O), S(O), S(O) 2 , S(O)(NR 1 ), S(O)(R 1 ), or P(O)(R 1 ); W 2 is N(R 2 ), C(R 2 )(R 2a ), C(O), S(O), S(O) 2 , S(O)(NR 2 ), S(O)(R 2 ), or P(O)(R 2 ); W 3 is N or C(R 3 ); W 4 is N or C(R 4 ); and wherein at least one of W 1 , W 2 , W 3 , and W 4 is N, N(R 1 ), N(
• the compound, or a pharmaceutically acceptable salt or solvate thereof has the structure of Formula (IIIl): Formula (IIIl); wherein W 1 is N(R 1 ), C(R 1 )(R 1a ), C(O), S(O), S(O) 2 , S(O)(NR 1 ), S(O)(R 1 ), or P(O)(R 1 ); W 2 is N(R 2 ), C(R 2 )(R 2a ), C(O), S(O), S(O) 2 , S(O)(NR 2 ), S(O)(R 2 ), or P(O)(R 2 ); W 3 is N or C(R 3 ); W 4 is N or C(R 4 ); and wherein at least one of W 1 , W 2 , W 3 , and W 4 is N, N(R 1 ), N(R
• the compound, or a pharmaceutically acceptable salt or solvate thereof has the structure of Formula (IIIm): Formula (IIIm); wherein W 1 is N or C(R 1 ); W 2 is N(R 2 ), C(R 2 )(R 2a ), C(O), S(O), S(O) 2 , S(O)(NR 2 ), S(O)(R 2 ), or P(O)(R 2 ); W 3 is N(R 3 ), C(R 3 )(R 3a ), C(O), S(O), S(O) 2 , S(O)(NR 3 ), S(O)(R 3 ), or P(O)(R 3 ); W 4 is N or C(R 4 ); and wherein at least one of W 1 , W 2 , W 3 , and W 4 is N, N(R 1 ), N(
• the compound, or a pharmaceutically acceptable salt or solvate thereof has the structure of Formula (IIIn): Formula (IIIn); wherein W 1 is N or C(R 1 ); W 2 is N(R 2 ), C(R 2 )(R 2a ), C(O), S(O), S(O) 2 , S(O)(NR 2 ), S(O)(R 2 ), or P(O)(R 2 ); W 3 is N(R 3 ), C(R 3 )(R 3a ), C(O), S(O), S(O) 2 , S(O)(NR 3 ), S(O)(R 3 ), or P(O)(R 3 ); W 4 is N or C(R 4 ); and wherein at least one of W 1 , W 2 , W 3 , and W 4 is N, N(R 1 ), N(
• the compound, or a pharmaceutically acceptable salt or solvate thereof has the structure of Formula (IIIo): Formula (IIIo); wherein W 1 is N or C(R 1 ); W 2 is N(R 2 ), C(R 2 )(R 2a ), C(O), S(O), S(O) 2 , S(O)(NR 2 ), S(O)(R 2 ), or P(O)(R 2 ); W 3 is N(R 3 ), C(R 3 )(R 3a ), C(O), S(O), S(O) 2 , S(O)(NR 3 ), S(O)(R 3 ), or P(O)(R 3 ); W 4 is N or C(R 4 ); and wherein at least one of W 1 , W 2 , W 3 , and W 4 is N, N(R 1 ), N(
• the compound, or a pharmaceutically acceptable salt or solvate thereof has the structure of Formula (IIIp): Formula (IIIp); wherein W 1 is N(R 1 ), C(R 1 )(R 1a ), C(O), S(O), S(O) 2 , S(O)(NR 1 ), S(O)(R 1 ), or P(O)(R 1 ); W 2 is N(R 2 ), C(R 2 )(R 2a ), C(O), S(O), S(O) 2 , S(O)(NR 2 ), S(O)(R 2 ), or P(O)(R 2 ); W 3 is N or C(R 3 ); W 4 is N or C(R 4 ); and wherein at least one of W 1 , W 2 , W 3 , and W 4 is N, N(R 1 ), N(
• the compound, or a pharmaceutically acceptable salt or solvate thereof has the structure of Formula (IIIq): Formula (IIIq); wherein W 1 is N(R 1 ), C(R 1 )(R 1a ), C(O), S(O), S(O) 2 , S(O)(NR 1 ), S(O)(R 1 ), or P(O)(R 1 ); W 2 is N(R 2 ), C(R 2 )(R 2a ), C(O), S(O), S(O) 2 , S(O)(NR 2 ), S(O)(R 2 ), or P(O)(R 2 ); W 3 is N or C(R 3 ); W 4 is N or C(R 4 ); and wherein at least one of W 1 , W 2 , W 3 , and W 4 is N, N(R 1 ), N(
• the compound, or a pharmaceutically acceptable salt or solvate thereof has the structure of Formula (IIIr): Formula (IIIr); wherein W 1 is N(R 1 ), C(R 1 )(R 1a ), C(O), S(O), S(O) 2 , S(O)(NR 1 ), S(O)(R 1 ), or P(O)(R 1 ); W 2 is N(R 2 ), C(R 2 )(R 2a ), C(O), S(O), S(O) 2 , S(O)(NR 2 ), S(O)(R 2 ), or P(O)(R 2 ); W 3 is N or C(R 3 ); W 4 is N or C(R 4 ); and wherein at least one of W 1 , W 2 , W 3 , and W 4 is N, N(R 1 ), N(R
• the compound, or a pharmaceutically acceptable salt or solvate thereof has the structure of Formula (IIIs): Formula (IIIs); wherein W 1 is N or C(R 1 ); W 2 is N or C(R 2 ); W 3 is N(R 3 ), C(R 3 )(R 3a ), C(O), S(O), S(O) 2 , S(O)(NR 3 ), S(O)(R 3 ), or P(O)(R 3 ); W 4 is N(R 4 ), C(R 4 )(R 4a ), C(O), S(O), S(O) 2 , S(O)(NR 4 ), S(O)(R 4 ), or P(O)(R 4 ); and wherein at least one of W 1 , W 2 , W 3 , and W 4 is N, N(R 1 ), N(
• the compound, or a pharmaceutically acceptable salt or solvate thereof has the structure of Formula (IIIt): Formula (IIIt); wherein W 1 is N or C(R 1 ); W 2 is N or C(R 2 ); W 3 is N(R 3 ), C(R 3 )(R 3a ), C(O), S(O), S(O) 2 , S(O)(NR 3 ), S(O)(R 3 ), or P(O)(R 3 ); W 4 is N(R 4 ), C(R 4 )(R 4a ), C(O), S(O), S(O) 2 , S(O)(NR 4 ), S(O)(R 4 ), or P(O)(R 4 ); and wherein at least one of W 1 , W 2 , W 3 , and W 4 is N, N(R 1 ), N(
• the compound, or a pharmaceutically acceptable salt or solvate thereof has the structure of Formula (IIIu): wherein W 1 is N or C(R 1 ); W 2 is N or C(R 2 ); W 3 is N(R 3 ), C(R 3 )(R 3a ), C(O), S(O), S(O) 2 , S(O)(NR 3 ), S(O)(R 3 ), or P(O)(R 3 ); W 4 is N(R 4 ), C(R 4 )(R 4a ), C(O), S(O), S(O) 2 , S(O)(NR 4 ), S(O)(R 4 ), or P(O)(R 4 ); and wherein at least one of W 1 , W 2 , W 3 , and W 4 is N, N(R 1 ), N(R 2 ), N
• R 5 , R 6 , R 7 , R 9 , R 9a , and R 10 are as described herein.
• W 1 is N, N(R 1 ), O, C(R 1 ), C(R 1 )(R 1a ), S(O), S(O) 2 , S(O)(NR 1 ), S(O)(R 1 ), or P(O)(R 1 );
• W 2 is N, N(R 2 ), O, C(R 2 ), C(R 2 )(R 2a ), S(O), S(O) 2 , S(O)(NR 2 ), S(O)(R 2 ), or P(O)(R 2 );
• W 3 is N, N(R 3 ), O, C(R 3 ), C(R 3 )(R 3a ), S(O), S(O) 2 , S(O)(NR 3 ), S(O)(R 3 ), or P(O)(R 3 );
• W 4 is N, N(R 4 ), C(R 4 ), C(R 4 )(R 4a ), S(O), S(O), S
• the compound, or a pharmaceutically acceptable salt or solvate thereof has the structure of Formula (IVa): Formula (IVa); wherein at least one of W 1 , W 2 , W 3 , and W 4 is S(O), S(O) 2 , S(O)(NR 1 ), S(O)(R 1 ), P(O)(R 1 ), S(O)(NR 2 ), S(O)(R 2 ), P(O)(R 2 ), S(O)(NR 3 ), S(O)(R 3 ), P(O)(R 3 ), S(O)(NR 4 ), S(O)(R 4 ), or P(O)(R 4 ).
• W 1 , W 2 , W 3 , and W 4 is S(O), S(O) 2 , S(O)(NR 1 ), S(O)(R 1 ), P(O)(R 1 ), S(O)(NR 2 ), S(O)(R 2 ), P(O)(R 2
• the compound, or a pharmaceutically acceptable salt or solvate thereof has the structure of Formula (IVb): Formula (IVb); wherein at least one of W 1 , W 2 , W 3 , and W 4 is S(O), S(O) 2 , S(O)(NR 1 ), S(O)(R 1 ), P(O)(R 1 ), S(O)(NR 2 ), S(O)(R 2 ), P(O)(R 2 ), S(O)(NR 3 ), S(O)(R 3 ), P(O)(R 3 ), S(O)(NR 4 ), S(O)(R 4 ), or P(O)(R 4 ).
• R 5 , R 6 , R 7 , R 9 , and R 10 are as described herein.
• the compound, or a pharmaceutically acceptable salt or solvate thereof has the structure of Formula (IVb): Formula (IVb); wherein at least one of W 1 , W 2 , W 3 , and W 4 is S
• W 1 , W 2 , W 3 , and W 4 is S(O), S(O) 2 , S(O)(NR 1 ), S(O)(R 1 ), P(O)(R 1 ), S(O)(NR 2 ), S(O)(R 2 ), P(O)(R 2 ), S(O)(NR 3 ), S(O)(R 3 ), P(O)(R 3 ), S(O)(NR 4 ), S(O)(R 4 ), or P(O)(R 4 ).
• R 5 , R 6 , R 7 , R 9 , R 9a , and R 10 are as described herein.
• the compound, or a pharmaceutically acceptable salt or solvate thereof has the structure of Formula (IVd): Formula (IVd); wherein W 1 is N(R 1 ), C(R 1 )(R 1a ), S(O), S(O) 2 , S(O)(NR 1 ), S(O)(R 1 ), or P(O)(R 1 ); W 2 is N(R 2 ), C(R 2 )(R 2a ), S(O), S(O) 2 , S(O)(NR 2 ), S(O)(R 2 ), or P(O)(R 2 ); W 3 is N(R 3 ), C(R 3 )(R 3a ), S(O), S(O) 2 , S(O)(NR 3 ), S(O)(R 3 ), or P(O)(R 3 ); W 4 is N(R 4 ), C(R 4 )(R 4a ), S(O), S(O) 2 , S(O)(NR 1 ), S
• the compound, or a pharmaceutically acceptable salt or solvate thereof has the structure of Formula (IVe): Formula (IVe); wherein W 1 is N(R 1 ), C(R 1 )(R 1a ), S(O), S(O) 2 , S(O)(NR 1 ), S(O)(R 1 ), or P(O)(R 1 ); W 2 is N(R 2 ), C(R 2 )(R 2a ), S(O), S(O) 2 , S(O)(NR 2 ), S(O)(R 2 ), or P(O)(R 2 ); W 3 is N(R 3 ), C(R 3 )(R 3a ), S(O), S(O) 2 , S(O)(NR 3 ), S(O)(R 3 ), or P(O)(R 3 ); W 4 is N(R 3 ), C(R 3 )(R 3a ), S(O), S(O) 2 , S(O)(NR 3 ), S
• R 5 , R 6 , R 7 , R 9 , and R 10 are as described herein.
• the compound, or a pharmaceutically acceptable salt or solvate thereof has the structure of Formula (IVf): Formula (IVf); wherein W 1 is N(R 1 ), C(R 1 )(R 1a ), S(O), S(O) 2 , S(O)(NR 1 ), S(O)(R 1 ), or P(O)(R 1 ); W 2 is N(R 2 ), C(R 2 )(R 2a ), S(O), S(O) 2 , S(O)(NR 2 ), S(O)(R 2 ), or P(O)(R 2 ); W 3 is N(R 3 ), C(R 3 )(R 3a ), S(O), S(O) 2 , S(O)(NR 3 ), S(O)(R 3 ), or P(O)(R 3 ); W 4 is N(R 4 ), N(R 4 ),
• the compound, or a pharmaceutically acceptable salt or solvate thereof has the structure of Formula (IVg): Formula (IVg); wherein W 1 is N or C(R 1 ); W 2 is N or C(R 2 ); W 3 is N(R 3 ), C(R 3 )(R 3a ), S(O), S(O) 2 , S(O)(NR 3 ), S(O)(R 3 ), or P(O)(R 3 ); W 4 is N(R 4 ), C(R 4 )(R 4a ), S(O), S(O) 2 , S(O)(NR 4 ), S(O)(R 4 ), or P(O)(R 4 ); and wherein at least one of W 3 , and W 4 is S(O), S(O) 2 , S(O)(NR 3 ), S(O)(R 3
• the compound, or a pharmaceutically acceptable salt or solvate thereof has the structure of Formula (IVh): Formula (IVh); wherein W 1 is N or C(R 1 ); W 2 is N or C(R 2 ); W 3 is N(R 3 ), C(R 3 )(R 3a ), S(O), S(O) 2 , S(O)(NR 3 ), S(O)(R 3 ), or P(O)(R 3 ); W 4 is N(R 4 ), C(R 4 )(R 4a ), S(O), S(O) 2 , S(O)(NR 4 ), S(O)(R 4 ), or P(O)(R 4 ); and wherein at least one of W 3 , and W 4 is S(O), S(O) 2 , S(O)(NR 3 ), S(O)(R
• the compound, or a pharmaceutically acceptable salt or solvate thereof has the structure of Formula (IVi): Formula (IVi); wherein W 1 is N or C(R 1 ); W 2 is N or C(R 2 ); W 3 is N(R 3 ), C(R 3 )(R 3a ), S(O), S(O) 2 , S(O)(NR 3 ), S(O)(R 3 ), or P(O)(R 3 ); W 4 is N(R 4 ), C(R 4 )(R 4a ), S(O), S(O) 2 , S(O)(NR 4 ), S(O)(R 4 ), or P(O)(R 4 ); and wherein at least one of W 3 , and W 4 is S(O), S(O) 2 , S(O)(NR 3 ), S(O)(R 3
• the compound, or a pharmaceutically acceptable salt or solvate thereof has the structure of Formula (IVj): Formula (IVj); wherein W 1 is N(R 1 ), C(R 1 )(R 1a ), S(O), S(O) 2 , S(O)(NR 1 ), S(O)(R 1 ), or P(O)(R 1 ); W 2 is N(R 2 ), C(R 2 )(R 2a ), S(O), S(O) 2 , S(O)(NR 2 ), S(O)(R 2 ), or P(O)(R 2 ); W 3 is N or C(R 3 ); W 4 is N or C(R 4 ); and wherein at least one of W 1 and W 2 is S(O), S(O) 2 , S(O)(NR 1 ), S(O)(R 1 );
• the compound, or a pharmaceutically acceptable salt or solvate thereof has the structure of Formula (IVk): Formula (IVk); wherein W 1 is N(R 1 ), C(R 1 )(R 1a ), S(O), S(O) 2 , S(O)(NR 1 ), S(O)(R 1 ), or P(O)(R 1 ); W 2 is N(R 2 ), C(R 2 )(R 2a ), S(O), S(O) 2 , S(O)(NR 2 ), S(O)(R 2 ), or P(O)(R 2 ); W 3 is N or C(R 3 ); W 4 is N or C(R 4 ); and wherein at least one of W 1 and W 2 is S(O), S(O) 2 , S(O)(NR 1 ), S(O)(R 1 );
• the compound, or a pharmaceutically acceptable salt or solvate thereof has the structure of Formula (IVl): Formula (IVl); wherein W 1 is N(R 1 ), C(R 1 )(R 1a ), S(O), S(O) 2 , S(O)(NR 1 ), S(O)(R 1 ), or P(O)(R 1 ); W 2 is N(R 2 ), C(R 2 )(R 2a ), S(O), S(O) 2 , S(O)(NR 2 ), S(O)(R 2 ), or P(O)(R 2 ); W 3 is N or C(R 3 ); W 4 is N or C(R 4 ); and wherein at least one of W 1 and W 2 is S(O), S(O) 2 , S(O)(NR 1 ), S(O)(R 1 ),
• the compound, or a pharmaceutically acceptable salt or solvate thereof has the structure of Formula (IVm): Formula (IVm); wherein W 1 is N or C(R 1 ); W 2 is N(R 2 ), C(R 2 )(R 2a ), S(O), S(O) 2 , S(O)(NR 2 ), S(O)(R 2 ), or P(O)(R 2 ); W 3 is N(R 3 ), C(R 3 )(R 3a ), S(O), S(O) 2 , S(O)(NR 3 ), S(O)(R 3 ), or P(O)(R 3 ); W 4 is N or C(R 4 ); and wherein at least one of W 2 and W 3 is S(O), S(O) 2 , S(O)(NR 2 ), S(O)(R 2 );
• the compound, or a pharmaceutically acceptable salt or solvate thereof has the structure of Formula (IVn): Formula (IVn); wherein W 1 is N or C(R 1 ); W 2 is N(R 2 ), C(R 2 )(R 2a ), S(O), S(O) 2 , S(O)(NR 2 ), S(O)(R 2 ), or P(O)(R 2 ); W 3 is N(R 3 ), C(R 3 )(R 3a ), S(O), S(O) 2 , S(O)(NR 3 ), S(O)(R 3 ), or P(O)(R 3 ); W 4 is N or C(R 4 ); and wherein at least one of W 2 and W 3 is S(O), S(O) 2 , S(O)(NR 2 ), S(O)(R 2 );
• the compound, or a pharmaceutically acceptable salt or solvate thereof has the structure of Formula (IVo): Formula (IVo); wherein W 1 is N or C(R 1 ); W 2 is N(R 2 ), C(R 2 )(R 2a ), S(O), S(O) 2 , S(O)(NR 2 ), S(O)(R 2 ), or P(O)(R 2 ); W 3 is N(R 3 ), C(R 3 )(R 3a ), S(O), S(O) 2 , S(O)(NR 3 ), S(O)(R 3 ), or P(O)(R 3 ); W 4 is N or C(R 4 ); and wherein at least one of W 2 and W 3 is S(O), S(O) 2 , S(O)(NR 2 ), S(O)(R 2 );
• the compound, or a pharmaceutically acceptable salt or solvate thereof has the structure of Formula (IVp): Formula (IVp); wherein W 1 is N(R 1 ), C(R 1 )(R 1a ), S(O), S(O) 2 , S(O)(NR 1 ), S(O)(R 1 ), or P(O)(R 1 ); W 2 is N(R 2 ), C(R 2 )(R 2a ), S(O), S(O) 2 , S(O)(NR 2 ), S(O)(R 2 ), or P(O)(R 2 ); W 3 is N or C(R 3 ); W 4 is N or C(R 4 ); and wherein at least one of W 1 and W 2 is S(O), S(O) 2 , S(O)(NR 1 ), S(O)(R 1 ); and wherein at least one of W 1 and W 2 is S(O), S(O) 2 , S(O)(NR 1 ), S(O)(
• the compound, or a pharmaceutically acceptable salt or solvate thereof has the structure of Formula (IVq): Formula (IVq); wherein W 1 is N(R 1 ), C(R 1 )(R 1a ), S(O), S(O) 2 , S(O)(NR 1 ), S(O)(R 1 ), or P(O)(R 1 ); W 2 is N(R 2 ), C(R 2 )(R 2a ), S(O), S(O) 2 , S(O)(NR 2 ), S(O)(R 2 ), or P(O)(R 2 ); W 3 is N or C(R 3 ); W 4 is N or C(R 4 ); and wherein at least one of W 1 and W 2 is S(O), S(O) 2 , S(O)(NR 1 ), S(O)(R 1 ); and wherein at least one of W 1 and W 2 is S(O), S(O) 2 , S(O)(NR 1 ), S(O)(
• the compound, or a pharmaceutically acceptable salt or solvate thereof has the structure of Formula (IVr): Formula (IVr); wherein W 1 is N(R 1 ), C(R 1 )(R 1a ), S(O), S(O) 2 , S(O)(NR 1 ), S(O)(R 1 ), or P(O)(R 1 ); W 2 is N(R 2 ), C(R 2 )(R 2a ), S(O), S(O) 2 , S(O)(NR 2 ), S(O)(R 2 ), or P(O)(R 2 ); W 3 is N or C(R 3 ); W 4 is N or C(R 4 ); and wherein at least one of W 1 and W 2 is S(O), S(O) 2 , S(O)(NR 1 ), S(O)(R 1 ); and wherein at least one of W 1 and W 2 is S(O), S(O) 2 , S(O)(NR 1 ), S(O)(
• the compound, or a pharmaceutically acceptable salt or solvate thereof has the structure of Formula (IIIs): Formula (IVs); wherein W 1 is N or C(R 1 ); W 2 is N or C(R 2 ); W 3 is N(R 3 ), C(R 3 )(R 3a ), S(O), S(O) 2 , S(O)(NR 3 ), S(O)(R 3 ), or P(O)(R 3 ); W 4 is N(R 4 ), C(R 4 )(R 4a ), S(O), S(O) 2 , S(O)(NR 4 ), S(O)(R 4 ), or P(O)(R 4 ); and wherein at least one of W 3 , and W 4 is S(O), S(O) 2 , S(O)(NR 3 ), S(O)(R 3
• the compound, or a pharmaceutically acceptable salt or solvate thereof has the structure of Formula (IVt): Formula (IVt); wherein W 1 is N or C(R 1 ); W 2 is N or C(R 2 ); W 3 is N(R 3 ), C(R 3 )(R 3a ), S(O), S(O) 2 , S(O)(NR 3 ), S(O)(R 3 ), or P(O)(R 3 ); W 4 is N(R 4 ), C(R 4 )(R 4a ), S(O), S(O) 2 , S(O)(NR 4 ), S(O)(R 4 ), or P(O)(R 4 ); and wherein at least one of W 3 , and W 4 is S(O), S(O) 2 , S(O)(NR 3 ), S(O)(R
• the compound, or a pharmaceutically acceptable salt or solvate thereof has the structure of Formula (IVu): Formula (IVu); wherein W 1 is N or C(R 1 ); W 2 is N or C(R 2 ); W 3 is N(R 3 ), C(R 3 )(R 3a ), S(O), S(O) 2 , S(O)(NR 3 ), S(O)(R 3 ), or P(O)(R 3 ); W 4 is N(R 4 ), C(R 4 )(R 4a ), S(O), S(O) 2 , S(O)(NR 4 ), S(O)(R 4 ), or P(O)(R 4 ); and wherein at least one of W 3 , and W 4 is S(O), S(O) 2 , S(O)(NR 3 ), S(O)(R
• R 5 , R 6 , R 7 , R 9 , R 9a , and R 10 are as described herein.
• the compound, or a pharmaceutically acceptable salt or solvate thereof has the structure of Formula (IIa): Formula (IIa).
• R 2 , R 3 , R 5 , R 6 , R 7 , R 9 , R 9a , and R 10 are as described herein.
• the compound, or a pharmaceutically acceptable salt or solvate thereof has the structure of Formula (IIb): Formula (IIb).
• R 2 , R 3 , R 5 , R 6 , R 7 , R 9 , and R 10 are as described herein.
• the compound, or a pharmaceutically acceptable salt or solvate thereof has the structure of Formula (IIc): Formula (IIc).
• R 2 , R 3 , R 5 , R 6 , R 7 , R 9 , R 9a , and R 10 are as described herein.
• the compound, or a pharmaceutically acceptable salt or solvate thereof has the structure of Formula (IId): Formula (IId).
• R 2 , R 3 , R 5 , R 6 , R 7 , R 9 , R 9a , and R 10 are as described herein.
• the compound, or a pharmaceutically acceptable salt or solvate thereof has the structure of Formula (IIe): Formula (IIe).
• R 2 , R 3 , R 5 , R 6 , R 7 , R 9 , and R 10 are as described herein.
• the compound, or a pharmaceutically acceptable salt or solvate thereof has the structure of Formula (IIf): Formula (IIf).
• R 2 , R 3 , R 5 , R 6 , R 7 , R 9 , R 9a , and R 10 are as described herein.
• the compound, or a pharmaceutically acceptable salt or solvate thereof has the structure of Formula (IIg): Formula (IIg).
• R 3 , R 5 , R 6 , R 7 , R 9 , R 9a , and R 10 are as described herein.
• the compound, or a pharmaceutically acceptable salt or solvate thereof has the structure of Formula (IIh): Formula (IIh).
• R 3 , R 5 , R 6 , R 7 , R 9 , and R 10 are as described herein.
• the compound, or a pharmaceutically acceptable salt or solvate thereof has the structure of Formula (IIi): Formula (IIi).
• R 3 , R 5 , R 6 , R 7 , R 9 , R 9a , and R 10 are as described herein.
• the compound, or a pharmaceutically acceptable salt or solvate thereof has the structure of Formula (IIj): Formula (IIj).
• R 2 , R 5 , R 6 , R 7 , R 9 , R 9a , and R 10 are as described herein.
• the compound, or a pharmaceutically acceptable salt or solvate thereof has the structure of Formula (IIk): Formula (IIk).
• R 2 , R 5 , R 6 , R 7 , R 9 , and R 10 are as described herein.
• the compound, or a pharmaceutically acceptable salt or solvate thereof has the structure of Formula (IIl): Formula (IIl).
• R 2 , R 5 , R 6 , R 7 , R 9 , R 9a , and R 10 are as described herein.
• Sub-formulae of Formula I, II, III, and/or IV are those formula having the same number as the parent formula (e.g., I, II, III, and/or IV) followed by one or more letters.
• sub-formulae of Formula I examples include Ia, Ib, Ic, Id, Ie, If, Ig, Ih, Ii, Ij, Ik, Il, Im, In, Io, Ioa, Iob, Ioc, Ip, Ipa, Ipb, Ipc, Iq, Ir, Is, It, Iu, Iv, Iw, Ix, Iy, Iz, Iaa, Iab, and Iac.
• sub-formulae of Formula II examples include IIa, IIb, IIc, IId, IIe, IIf, IIg, IIh, IIi, IIj, and IIk.
• sub-formulae of Formula III include IIIa, IIIb, IIIc, IIId, IIIe, IIIf, IIIg, IIIh, IIIi, IIIj, IIIk, IIIl, IIIm, IIIn, IIIo, IIIoa, IIIob, IIIoc, IIIp, IIIpa, IIIpb, IIIpc, IIIq, IIIr, IIIs, IIIt, IIIu, IIIv, IIIw, IIIx, IIIy, and IIIz.
• sub-formulae of Formula IV include IVa, IVb, IVc, IVd, IVe, IVf, IVg, IVh, IVi, IVj, IVk, IVl, IVm, IVn, and IVo.
• Formulae (I), (II), (III), (IV); or sub-formulae thereof is understood to include a formula selected from Formulae I, Ia, Ib, Ic, Id, Ie, If, Ig, Ih, Ii, Ij, Ik, Il, Im, In, Io, Ioa, Iob, Ioc, Ip, Ipa, Ipb, Ipc, Iq, Ir, Is, It, Iu, Iv, Iw, Ix, Iy, Iz, Iz, Iaa, Iab, Iac, II, IIa, IIb, IIc, IId, IIe, IIf, IIg, IIh, IIi, IIj, IIk, III, IIIa, IIIb, IIIc, IIId, IIIe, IIIf, IIIg, IIIh, IIIi, IIIj, IIIk, IIIl, IIIm, IIIn, IIIo, IIIoa, IIIob, IIIoc, IIIp, IIIpa,
• V 1 is a bond. In some embodiments of Formula (II), or sub-formulae thereof, V 1 is S. In some embodiments of Formula (II), or sub-formulae thereof, V 4 is a bond. In some embodiments of Formula (II), or sub-formulae thereof, V 4 is S. [00358] In some embodiments of Formula (II), or sub-formulae thereof, V 1 is a bond and V 4 is S. In some embodiments of Formula (II), or sub-formulae thereof, V 4 is a bond and V 1 is S.
• V 2 is N. In some embodiments of Formula (II), or sub-formulae thereof, V 2 is C(R 2 ). [00360] In some embodiments of Formula (II), or sub-formulae thereof, V 3 is N. In some embodiments of Formula (II), or sub-formulae thereof, V 3 is C(R 3 ). [003 6 1] In some embodiments, the compound has Formula: (IIIv) and J 1 , J 2 , J 3 , R 2 , and R 6 are as described herein.
• W 1 is C(O), S(O), S(O) 2 , S(O)(NR 1 ), S(O)(R 1 ), or P(O)(R 1 ). In some embodiments, W 1 is C(O). In some embodiments, R 6 is -OH. [003 6 2] In some embodiments, the compound has Formula: (Iab) and J 1 , J 2 , J 3 , R 2 , and R 6 are as described herein. In some embodiments, R 6 is -OH. [003 6 3] In some embodiments, the compound has Formula: (Iac) and J 1 , J 2 , J 3 , R 2 , and R 6 are as described herein.
• R 6 is -OH.
• the compound has Formula: (IIIw) and J 1 , J 2 , J 3 , R 2 , and R 6 are as described herein.
• W 3 is C(O), S(O), S(O) 2 , S(O)(NR 3 ), S(O)(R 3 ), or P(O)(R 3 ).
• W 3 is C(O).
• R 6 is -OH.
• R 4 is - CH 3 .
• the compound has Formula: (IIIx) and J 1 , J 2 , J 3 , R 2 , and R 6 are as described herein.
• W 3 is C(O), S(O), S(O) 2 , S(O)(NR 3 ), S(O)(R 3 ), or P(O)(R 3 ). In some embodiments, W 3 is C(O). In some embodiments, R 6 is -OH. [003 6 6] In some embodiments, the compound has Formula: (IIIy) and J 1 , J 2 , J 3 , R 2 , and R 6 are as described herein. In some embodiments, W 3 is C(O), S(O), S(O) 2 , S(O)(NR 3 ), S(O)(R 3 ), or P(O)(R 3 ). In some embodiments, W 3 is C(O).
• R 6 is -OH. In some embodiments, R 4 is -CH 3 . [003 6 7] In some embodiments, the compound has Formula: (IIIz) and J 1 , J 2 , J 3 , R 2 , and R 6 are as described herein. In some embodiments, W 4 is C(O), S(O), S(O) 2 , S(O)(NR 4 ), S(O)(R 4 ), or P(O)(R 4 ). In some embodiments, W 4 is C(O). In some embodiments, R 6 is -OH.
• a compound of Formula (XI), or a pharmaceutically acceptable salt or solvate thereof Formula (XI); wherein: W 1 is N, N(R 1 ), O, C(R 1 ), C(R 1 )(R 1a ), C(O), S(O), S(O) 2 , S(O)(NR 1 ), S(O)(R 1 ), or P(O)(R 1 ); W 2 is N, N(R 2 ), O, C(R 2 ), C(R 2 )(R 2a ), C(O), S(O), S(O) 2 , S(O)(NR 2 ), S(O)(R 2 ), or P(O)(R 2 ); W 3 is N, N(R 3 ), O, C(R 3 ), C(R 3 )(R 3a ), C(O), S(O), S(O) 2 , S(O)(NR 3 ), S(O)(R 3 ), or P(O)(R 1 ); W 3 is
• a compound of Formula (XII), or a pharmaceutically acceptable salt or solvate thereof Formula (XII); wherein: V 1 is a bond or S; V 4 is a bond or S, wherein when V 1 is a bond then V 4 is S and when V 1 is S, then V 4 is a bond; V 2 is N or C(R 2 ); V 3 is N or C(R 3 ); X is N or C(R 5 ); Y is N or C(R 6 ); Z is N or C(R 7 ); J 1 is N, C, or C(R 8 ); J 2 is N, N(R 9 ), C(R 9 ), C(R 9 )(R 9a ), or C(O); J 3 is N(R 10 ) or C(R 10 )(R 10a ); R 2 is selected from hydrogen, halogen, -CN, C 1-6 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 3-10
• the compound is a compound of Formula (I’), or a pharmaceutically acceptable salt or solvate thereof: Formula (I’); wherein: X is N or C(R 5 ); Y is N or C(R 6 ); Z is N or C(R 7 ); J 1 is N, C, or C(R 8 ); J 2 is N, N(R 9 ), C(R 9 ), C(R 9 )(R 9a ), or C(O); J 3 is N(R 10 ) or C(R 10 )(R 10a ); R 2 is selected from hydrogen, halogen, -CN, C 1-6 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 3-6 cycloalkyl, C 2 - 9heterocycloalkyl, C 6-10 aryl, C 1-9 heteroaryl, -OR 12 , -SR 12 , -N(R 12 )
• R 5 is -F and R 6 is -OH.
• the compound is a compound of Formula (Ia’): Formula (Ia’); R 2 , R 3 , R 4 , R 5 , R 6 , R 7 , R 9 , R 9a , and R 10 are as described herein.
• R 5 is -F and R 6 is -OH.
• the compound is a compound of Formula (Ib’): R 2 , R 3 , R 4 , R 5 , R 6 , R 7 , R 9 , R 9a , and R 10 are as described herein.
• R 5 is -F and R 6 is - OH.
• the compound is a compound of Formula (Ic’): Formula (Ic’); R 2 , R 3 , R 4 , R 5 , R 6 , R 7 , R 9 , R 9a , and R 10 are as described herein.
• R 5 is -F and R 6 is - OH.
• the compound is a compound of Formula (Ia’-1): Formula (Ia’-1); R 2 , R 3 , R 4 , R 5 , R 6 , R 7 , R 9 , R 9a , and R 10 are as described herein.
• R 5 is -F and R 6 is -OH.
• the compound is a compound of Formula (Ib’-1): Formula (Ib’-1); R 2 , R 5 , R 6 , R 9 , R 9a , and R 10 are as described herein.
• R 5 is -F and R 6 is -OH.
• the compound is a compound of Formula (Ic’-1): Formula (Ic’-1); R 2 , R 5 , R 6 , R 9 , R 9a , and R 10 are as described herein. In embodiments of Formula Ic’-1, R 5 is -F and R 6 is -OH. [00380] In some embodiments, the compound is a compound of Formula (Ia’-2): Formula (Ia’-2); R 2 , R 5 , and R 6 are as described herein. In embodiments of Formula Ia’-2, R 5 is -F and R 6 is -OH.
• the compound is a compound of Formula (Ib’-2): Formula (Ib’-2); R 2 , R 5 , and R 6 are as described herein. In embodiments of Formula Ib’-2, R 5 is -F and R 6 is -OH. [00382] In some embodiments, the compound is a compound of Formula (Ic’-2): Formula (Ic’-2); R 2 , R 5 , and R 6 are as described herein. In embodiments of Formula Ic’-2, R 5 is -F and R 6 is -OH.
• the compound is a compound of Formula (I’’), or a pharmaceutically acceptable salt or solvate thereof: Formula (I’’); wherein: X is N or C(R 5 ); Y is N or C(R 6 ); Z is N or C(R 7 ); J 1 is N, C, or C(R 8 ); J 2 is N, N(R 9 ), C(R 9 ), C(R 9 )(R 9a ), or C(O); J 3 is N(R 10 ) or C(R 10 )(R 10a ); R 1 is selected from hydrogen, halogen, -CN, C 1-6 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 3-6 cycloalkyl, C 2-9 heterocycloalkyl, C 6-10 aryl, C 1-9 heteroaryl, -OR 12 , -SR 12 , -N(R 12 )(R
• R 5 is -F and R 6 is -OH.
• the compound is a compound of Formula (Ia’‘): Formula (Ia’‘); R 1 , R 2 , R 4 , R 5 , R 6 , R 7 , R 9 , R 9a , and R 10 are as described herein.
• R 5 is -F and R 6 is -OH.
• the compound is a compound of Formula (Ib’‘): R 1 , R 2 , R 4 , R 5 , R 6 , R 7 , R 9 , R 9a , and R 10 are as described herein.
• R 5 is -F and R 6 is -OH.
• the compound is a compound of Formula (Ic’‘): Formula (Ic’‘); R 1 , R 2 , R 4 , R 5 , R 6 , R 7 , R 9 , R 9a , and R 10 are as described herein.
• R 5 is -F and R 6 is -OH.
• the compound is a compound of Formula (Ia’‘-1): Formula (Ia’‘-1); R 2 , R 4 , R 5 , R 6 , R 9 , R 9a , and R 10 are as described herein. In embodiments of Formula Ia’’-1, R 5 is -F and R 6 is -OH.
• the compound is a compound of Formula (Ib’‘-1): Formula (Ib’‘-1); R 2 , R 4 , R 5 , R 6 , R 9 , R 9a , and R 10 are as described herein. In embodiments of Formula Ib’’-1, R 5 is -F and R 6 is -OH.
• the compound is a compound of Formula (Ic’‘-1): R 2 , R 4 , R 5 , R 6 , R 9 , R 9a , and R 10 are as described herein.
• R 5 is -F and R 6 is -OH.
• the compound is a compound of Formula (Ia’‘-2): Formula (Ia’‘-2); R 2 , R 4 , R 5 , and R 6 are as described herein.
• R 5 is -F and R 6 is -OH.
• the compound is a compound of Formula (Ib’‘-2): Formula (Ib’‘-2); R 2 , R 4 , R 5 , and R 6 are as described herein. In embodiments of Formula Ib’’-2, R 5 is -F and R 6 is -OH. [003 9 3] In some embodiments, the compound is a compound of Formula (Ic’‘-2): R 2 , R 4 , R 5 , and R 6 are as described herein. In embodiments of Formula Ic’’-2, R 5 is -F and R 6 is -OH.
• the compound is a compound of Formula (I’’’), or a pharmaceutically acceptable salt or solvate thereof: Formula (I’’’); wherein: X is N or C(R 5 ); Y is N or C(R 6 ); Z is N or C(R 7 ); J 1 is N, C, or C(R 8 ); J 2 is N, N(R 9 ), C(R 9 ), C(R 9 )(R 9a ), or C(O); J 3 is N(R 10 ) or C(R 10 )(R 10a ); R 1 is selected from hydrogen, halogen, -CN, C 1-6 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 3-6 cycloalkyl, C 2- 9 heterocycloalkyl, C 6-10 aryl, C 1-9 heteroaryl, -OR 12 , -SR 12 , -N(R 12 ,
• R 5 is -F and R 6 is -OH.
• the compound is a compound of Formula (Ia’‘’): Formula (Ia’‘‘); R 1 , R 2 , R 3 , R 5 , R 6 , R 7 , R 9 , R 9a , and R 10 are as described herein.
• R 5 is -F and R 6 is -OH.
• the compound is a compound of Formula (Ib’‘‘): R 1 , R 2 , R 3 , R 5 , R 6 , R 7 , R 9 , R 9a , and R 10 are as described herein.
• R 5 is -F and R 6 is -OH.
• the compound is a compound of Formula (Ic’‘’): Formula (Ic’‘‘); R 1 , R 2 , R 3 , R 5 , R 6 , R 7 , R 9 , R 9a , and R 10 are as described herein.
• R 5 is -F and R 6 is -OH.
• the compound is a compound of Formula (Ia’‘‘-1): Formula (Ia’‘‘-1); R 2 , R 3 , R 5 , R 6 , R 7 , R 9 , R 9a , and R 10 are as described herein.
• R 5 is -F and R 6 is - OH.
• the compound is a compound of Formula (Ib’‘‘-1): Formula (Ib’‘-1); R 2 , R 5 , R 6 , R 9 , R 9a , and R 10 are as described herein.
• R 5 is -F and R 6 is -OH.
• the compound is a compound of Formula (Ic’‘‘-1): R 2 , R 5 , R 6 , R 9 , R 9a , and R 10 are as described herein.
• R 5 is -F and R 6 is -OH.
• the compound is a compound of Formula (Ia’‘‘-2): Formula (Ia’‘‘-2); R 2 , R 5 , and R 6 are as described herein.
• R 5 is -F and R 6 is -OH.
• the compound is a compound of Formula (Ib’‘‘-2): Formula (Ib’‘‘-2); R 2 , R 5 , and R 6 are as described herein. In embodiments of Formula Ib’’’-2, R 5 is -F and R 6 is -OH. [00404] In some embodiments, the compound is a compound of Formula (Ic’‘‘-2): Formula (Ic’‘‘-2); R 2 , R 5 , and R 6 are as described herein. In embodiments of Formula Ic’’’-2, R 5 is -F and R 6 is -OH.
• the compound is a compound of Formula (III’), or a pharmaceutically acceptable salt or solvate thereof: Formula (III’); wherein: X is N or C(R 5 ); Y is N or C(R 6 ); Z is N or C(R 7 ); J 1 is N, C, or C(R 8 ); J 2 is N, N(R 9 ), C(R 9 ), C(R 9 )(R 9a ), or C(O); J 3 is N(R 10 ) or C(R 10 )(R 10a ); R 2 is selected from hydrogen, halogen, -CN, C 1-6 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 3-6 cycloalkyl, C 2-9 heterocycloalkyl, C 6-10 aryl, C 1-9 heteroaryl, -OR 12 , -SR 12 , -N(R 12 )(R 13
• R 5 is -F and R 6 is -OH.
• the compound is a compound of Formula (IIIa’): Formula (IIIa’); R 2 , R 3 , R 3a , R 4 , R 4a , R 5 , R 6 , R 7 , R 9 , R 9a , and R 10 are as described herein.
• R 5 is -F and R 6 is -OH.
• the compound is a compound of Formula (IIIb’): R 2 , R 3 , R 3a , R 4 , R 4a , R 5 , R 6 , R 7 , R 9 , R 9a , and R 10 are as described herein.
• R 5 is -F and R 6 is -OH.
• the compound is a compound of Formula (IIIc’): Formula (IIIc’); R 2 , R 3 , R 3a , R 4 , R 4a , R 5 , R 6 , R 7 , R 9 , R 9a , and R 10 are as described herein.
• R 5 is -F and R 6 is -OH.
• the compound is a compound of Formula (IIIa’-1): Formula (IIIa’-1); R 2 , R 5 , R 6 , R 9 , R 9a , and R 10 are as described herein.
• R 5 is -F and R 6 is -OH.
• the compound is a compound of Formula (IIIb’-1): Formula (IIIb’-1); R 2 , R 5 , R 6 , R 9 , R 9a , and R 10 are as described herein.
• R 5 is -F and R 6 is -OH.
• the compound is a compound of Formula (IIIc’-1): Formula (IIIc’-1); R 2 , R 5 , R 6 , R 9 , R 9a , and R 10 are as described herein.
• R 5 is -F and R 6 is -OH.
• the compound is a compound of Formula (IIIa’-2): Formula (IIIa’-2); R 2 , R 5 , and R 6 are as described herein.
• R 5 is -F and R 6 is -OH.
• the compound is a compound of Formula (IIIb’-2): Formula (IIIb’-2); R 2 , R 5 , and R 6 are as described herein. In embodiments of Formula IIIb’-2, R 5 is -F and R 6 is -OH. [00415] In some embodiments, the compound is a compound of Formula (IIIc’-2): Formula (IIIc’-2); R 2 , R 5 , and R 6 are as described herein. In embodiments of Formula IIIc’-2, R 5 is -F and R 6 is -OH.
• the compound is a compound of Formula (III’’), or a pharmaceutically acceptable salt or solvate thereof: Formula (III’’); wherein: X is N or C(R 5 ); Y is N or C(R 6 ); Z is N or C(R 7 ); J 1 is N, C, or C(R 8 ); J 2 is N, N(R 9 ), C(R 9 ), C(R 9 )(R 9a ), or C(O); J 3 is N(R 10 ) or C(R 10 )(R 10a ); R 2 is selected from hydrogen, halogen, -CN, C 1-6 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 3-6 cycloalkyl, C 2-9 heterocycloalkyl, C 6-10 aryl, C 1-9 heteroaryl, -OR 12 , -SR 12 , -N(R 12 )(R
• R 5 is -F and R 6 is -OH.
• the compound is a compound of Formula (IIIa’‘): Formula (IIIa’‘); R 2 , R 4 , R 4a , R 5 , R 6 , R 7 , R 9 , R 9a , and R 10 are as described herein.
• R 5 is -F and R 6 is -OH.
• the compound is a compound of Formula (IIIb’‘): R 2 , R 4 , R 4a , R 5 , R 6 , R 7 , R 9 , R 9a , and R 10 are as described herein.
• R 5 is -F and R 6 is -OH.
• the compound is a compound of Formula (IIIc’‘): Formula (IIIc’‘); R 2 , R 4 , R 4a , R 5 , R 6 , R 7 , R 9 , R 9a , and R 10 are as described herein.
• R 5 is -F and R 6 is -OH.
• the compound is a compound of Formula (IIIa’‘-1): Formula (IIIa’‘-1); R 2 , R 5 , R 6 , R 9 , R 9a , and R 10 are as described herein. In embodiments of Formula IIIa’’-1, R 5 is -F and R 6 is -OH. [00422] In some embodiments, the compound is a compound of Formula (IIIb’‘-1): Formula (IIIb’‘-1); R 2 , R 5 , R 6 , R 9 , R 9a , and R 10 are as described herein. In embodiments of Formula IIIb’’-1, R 5 is -F and R 6 is -OH.
• the compound is a compound of Formula (IIIc’‘-1): Formula (IIIc’‘-1); R 2 , R 5 , R 6 , R 9 , R 9a , and R 10 are as described herein. In embodiments of Formula IIIc’’-1, R 5 is -F and R 6 is -OH. [00424] In some embodiments, the compound is a compound of Formula (IIIa’‘-2): Formula (IIIa’‘-2); R 2 , R 5 , and R 6 are as described herein. In embodiments of Formula IIIa’’-2, R 5 is -F and R 6 is -OH.
• the compound is a compound of Formula (IIIb’‘-2): Formula (IIIb’‘-2); R 2 , R 5 , and R 6 are as described herein. In embodiments of Formula IIIb’’-2, R 5 is -F and R 6 is -OH. [00426] In some embodiments, the compound is a compound of Formula (IIIc’‘-2): Formula (IIIc’‘-2); R 2 , R 5 , and R 6 are as described herein. In embodiments of Formula IIIc’’-2, R 5 is -F and R 6 is -OH.
• the compound is a compound of Formula (III’’’), or a pharmaceutically acceptable salt or solvate thereof: Formula (III’’’); wherein: X is N or C(R 5 ); Y is N or C(R 6 ); Z is N or C(R 7 ); J 1 is N, C, or C(R 8 ); J 2 is N, N(R 9 ), C(R 9 ), C(R 9 )(R 9a ), or C(O); J 3 is N(R 10 ) or C(R 10 )(R 10a ); R 2 is selected from hydrogen, halogen, -CN, C 1-6 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 3-6 cycloalkyl, C 2-9 heterocycloalkyl, C 6-10 aryl, C 1-9 heteroaryl, -OR 12 , -SR 12 , -N(R 12 )
• R 5 is -F and R 6 is -OH.
• the compound is a compound of Formula (IIIa’‘’): Formula (IIIa’‘‘); R 2 , R 4 , R 5 , R 6 , R 7 , R 9 , R 9a , and R 10 are as described herein.
• R 5 is -F and R 6 is - OH.
• the compound is a compound of Formula (IIIb’‘’): Formula (IIIb’‘‘); R 2 , R 4 , R 5 , R 6 , R 7 , R 9 , R 9a , and R 10 are as described herein.
• R 5 is -F and R 6 is - OH.
• the compound is a compound of Formula (IIIc’‘‘): Formula (IIIc’‘); R 2 , R 4 , R 5 , R 6 , R 7 , R 9 , R 9a , and R 10 are as described herein.
• R 5 is -F and R 6 is -OH.
• the compound is a compound of Formula (IIIa’‘‘-2): Formula (IIIa’‘‘-2); R 2 , R 4 , R 5 , and R 6 are as described herein.
• R 5 is -F and R 6 is -OH.
• the compound is a compound of Formula (IIIb’‘‘-2): Formula (IIIb’‘‘-2); R 2 , R 4 , R 5 , and R 6 are as described herein.
• R 5 is -F and R 6 is -OH.
• the compound is a compound of Formula (IIIc’‘‘-2): Formula (IIIc’‘‘-2); R 2 , R 4 , R 5 , and R 6 are as described herein.
• R 5 is -F and R 6 is -OH.
• the compound is a compound of Formula (III 4 ), or a pharmaceutically acceptable salt or solvate thereof: Formula (III 4 ); wherein: X is N or C(R 5 ); Y is N or C(R 6 ); Z is N or C(R 7 ); J 1 is N, C, or C(R 8 ); J 2 is N, N(R 9 ), C(R 9 ), C(R 9 )(R 9a ), or C(O); J 3 is N(R 10 ) or C(R 10 )(R 10a ); R 2 is selected from hydrogen, halogen, -CN, C 1-6 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 3-6 cycloalkyl, C 2-9 heterocycloalkyl, C 6-10 aryl, C 1-9 heteroaryl, -OR 12 , -SR 12 , -N(R 12 )(R
• R 5 is -F and R 6 is -OH.
• the compound is a compound of Formula (IIIa 4 ): Formula (IIIa 4 ); R 2 , R 3 , R 4 , R 5 , R 6 , R 7 , R 9 , R 9a , and R 10 are as described herein.
• R 5 is -F and R 6 is -OH.
• the compound is a compound of Formula (IIIb 4 ): Formula (IIIb 4 ); R 2 , R 3 , R 4 , R 5 , R 6 , R 7 , R 9 , R 9a , and R 10 are as described herein.
• R 5 is -F and R 6 is -OH.
• the compound is a compound of Formula (IIIc 4 ): Formula (IIIc 4 ); R 2 , R 3 , R 4 , R 5 , R 6 , R 7 , R 9 , R 9a , and R 10 are as described herein.
• the compound is a compound of Formula (IIIa 4 -1): Formula (IIIa 4 -1); R 2 , R 5 , R 6 , R 9 , R 9a , and R 10 are as described herein. In embodiments of Formula IIIa 4 -1, R 5 is -F and R 6 is -OH. [00441] In some embodiments, the compound is a compound of Formula (IIIb 4 -1): Formula (IIIb 4 -1); R 2 , R 5 , R 6 , R 9 , R 9a , and R 10 are as described herein.
• the compound is a compound of Formula (IIIc 4 -1): Formula (IIIc 4 -1); R 2 , R 5 , R 6 , R 9 , R 9a , and R 10 are as described herein. In embodiments of Formula IIIc 4 -1, R 5 is -F and R 6 is -OH. [00443] In some embodiments, the compound is a compound of Formula (IIIa 4 -2): Formula (IIIa 4 -2); R 2 , R 5 , and R 6 are as described herein. In embodiments of Formula IIIa 4 -2, R 5 is -F and R 6 is -OH.
• the compound is a compound of Formula (IIIb 4 -2): Formula (IIIb 4 -2); R 2 , R 5 , and R 6 are as described herein. In embodiments of Formula IIIb 4 -2, R 5 is -F and R 6 is -OH. [00445] In some embodiments, the compound is a compound of Formula (IIIc 4 -2): Formula (IIIc 4 -2); R 2 , R 5 , and R 6 are as described herein. In embodiments of Formula IIIc 4 -2, R 5 is -F and R 6 is -OH.
• the compound is a compound of Formula (III 5 ), or a pharmaceutically acceptable salt or solvate thereof: Formula (III 5 ); wherein: X is N or C(R 5 ); Y is N or C(R 6 ); Z is N or C(R 7 ); J 1 is N, C, or C(R 8 ); J 2 is N, N(R 9 ), C(R 9 ), C(R 9 )(R 9a ), or C(O); J 3 is N(R 10 ) or C(R 10 )(R 10a ); R 2 is selected from hydrogen, halogen, -CN, C 1-6 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 3-6 cycloalkyl, C 2-9 heterocycloalkyl, C 6-10 aryl, C 1-9 heteroaryl, -OR 12 , -SR 12 , -N(R 12 )(R
• R 5 is -F and R 6 is -OH.
• the compound is a compound of Formula (IIIa 5 ): Formula (IIIa 5 ); R 2 , R 3 , R 5 , R 6 , R 7 , R 9 , R 9a , and R 10 are as described herein.
• R 5 is -F and R 6 is - OH.
• the compound is a compound of Formula (IIIb 5 ): Formula (IIIb 5 ); R 2 , R 3 , R 5 , R 6 , R 7 , R 9 , R 9a , and R 10 are as described herein. In embodiments of Formula IIIb 5 , R 5 is -F and R 6 is - OH.
• the compound is a compound of Formula (IIIc 5 ): Formula (IIIc 5 ); R 2 , R 3 , R 5 , R 6 , R 7 , R 9 , R 9a , and R 10 are as described herein. In embodiments of Formula IIIc 5 , R 5 is -F and R 6 is - OH.
• the compound is a compound of Formula (IIIa 5 -1): Formula (IIIa 5 -1); R 2 , R 5 , R 6 , R 9 , R 9a , and R 10 are as described herein. In embodiments of Formula IIIa 5 -1, R 5 is -F and R 6 is -OH. [00452] In some embodiments, the compound is a compound of Formula (IIIb 5 -1): Formula (IIIb 5 -1); R 2 , R 5 , R 6 , R 9 , R 9a , and R 10 are as described herein. In embodiments of Formula IIIb 5 -1, R 5 is -F and R 6 is -OH.
• the compound is a compound of Formula (IIIc 5 -1): Formula (IIIc 5 -1); R 2 , R 5 , R 6 , R 9 , R 9a , and R 10 are as described herein. In embodiments of Formula IIIc 5 -1, R 5 is -F and R 6 is -OH. [00454] In some embodiments, the compound is a compound of Formula (IIIa 5 -2): Formula (IIIa 5 -2); R 2 , R 5 , and R 6 are as described herein. In embodiments of Formula IIIa 5 -2, R 5 is -F and R 6 is -OH.
• the compound is a compound of Formula (IIIb 5 -2): Formula (IIIb 5 -2); R 2 , R 5 , and R 6 are as described herein. In embodiments of Formula IIIb 5 -2, R 5 is -F and R 6 is -OH. [00456] In some embodiments, the compound is a compound of Formula (IIIc 5 -2): Formula (IIIc 5 -2); R 2 , R 5 , and R 6 are as described herein. In embodiments of Formula IIIc 5 -2, R 5 is -F and R 6 is -OH.
• W 1 is N, N(R 1 ), C(R 1 ), C(R 1 )(R 1a ), C(O), S(O), S(O) 2 , S(O)(NR 1 ), S(O)(R 1 ), or P(O)(R 1 ).
• W 2 is N, N(R 2 ), C(R 2 ), C(R 2 )(R 2a ), C(O), S(O), S(O) 2 , S(O)(NR 2 ), S(O)(R 2 ), or P(O)(R 2 ).
• W 3 is N, N(R 3 ), C(R 3 ), C(R 3 )(R 3a ), C(O), S(O), S(O) 2 , S(O)(NR 3 ), S(O)(R 3 ), or P(O)(R 3 ).
• W 4 is N, N(R 4 ), C(R 4 ), C(R 4 )(R 4a ), C(O), S(O), S(O) 2 , S(O)(NR 4 ), S(O)(R 4 ), or P(O)(R 4 ).
• W 1 is N, N(R 1 ), C(R 1 ), C(R 1 )(R 1a ), or C(O).
• W 2 is N, N(R 2 ), C(R 2 ), C(R 2 )(R 2a ), or C(O).
• W 3 is N, N(R 3 ), C(R 3 ), C(R 3 )(R 3a ), or C(O).
• W 4 is N, N(R 4 ), C(R 4 ), C(R 4 )(R 4a ), or C(O).
• R 2 is C 1-6 alkyl, optionally substituted with one, two, or three R 20b .
• R 2 is C 1 -5alkyl, optionally substituted with one, two, or three R 20b . In some embodiments, R 2 is C 1 - 4alkyl, optionally substituted with one, two, or three R 20b . In some embodiments, R 2 is C 1 -3alkyl, optionally substituted with one, two, or three R 20b . In some embodiments, R 2 is C 1-2 alkyl, optionally substituted with one, two, or three R 20b . In some embodiments, R 2 is C 1 alkyl, optionally substituted with one, two, or three R 20b . In some embodiments, R 2 is C 2 alkyl, optionally substituted with one, two, or three R 20b . In some embodiments, R 2 is C 2 alkyl, optionally substituted with one, two, or three R 20b .
• R 2 is C 3 alkyl, optionally substituted with one, two, or three R 20b . In some embodiments, R 2 is C 4 alkyl, optionally substituted with one, two, or three R 20b . In some embodiments, R 2 is C 5 alkyl, optionally substituted with one, two, or three R 20b . In some embodiments, R 2 is C 6 alkyl, optionally substituted with one, two, or three R 20b . In some embodiments, R 2 is C 1-6 alkyl. In some embodiments, R 2 is C 1 -5alkyl. In some embodiments, R 2 is C 1 -4alkyl. In some embodiments, R 2 is C 1 -3alkyl.
• R 2 is C 1 -2alkyl. In some embodiments, R 2 is C 1 alkyl. In some embodiments, R 2 is C 2 alkyl. In some embodiments, R 2 is C 3 alkyl. In some embodiments, R 2 is C 4 alkyl. In some embodiments, R 2 is C 5 alkyl. In some embodiments, R 2 is C 6 alkyl.
• each R 20b is independently selected from -N(R 22 )(R 23 ), R 22 is C 1-6 alkyl, and R 23 is C 1-6 alkyl. In some embodiments, R 2 is C 2 - 6alkynyl, optionally substituted with one, two, or three R 20b .
• R 2 is C 2 -5alkynyl, optionally substituted with one, two, or three R 20b . In some embodiments, R 2 is C 2-4 alkynyl, optionally substituted with one, two, or three R 20b . In some embodiments, R 2 is C 2-3 alkynyl, optionally substituted with one, two, or three R 20b . In some embodiments, R 2 is C 2 alkynyl, optionally substituted with one, two, or three R 20b . In some embodiments, R 2 is C3alkynyl, optionally substituted with one, two, or three R 20b .
• R 2 is C4alkynyl, optionally substituted with one, two, or three R 20b . In some embodiments, R 2 is C 5 alkynyl, optionally substituted with one, two, or three R 20b . In some embodiments, R 2 is C 6 alkynyl, optionally substituted with one, two, or three R 20b . In some embodiments, R 2 is C 2-6 alkynyl. In some embodiments, R 2 is C 2 -5alkynyl. In some embodiments, R 2 is C 2 - 4alkynyl. In some embodiments, R 2 is C 2 -3alkynyl. In some embodiments, R 2 is C 2 alkynyl.
• R 2 is C 3 alkynyl. In some embodiments, R 2 is C 4 alkynyl. In some embodiments, R 2 is C 5 alkynyl. In some embodiments, R 2 is C 6 alkynyl. In some embodiments, R 2 is selected from In some embodiments, R 2 is In some embodiments, R 2 is In some embodiments, R 2 is In some embodiments, R 2 is In some embo 2 diments, R is [00459] In some embodiments, R 2 is . In some embodiments, R 2 is . [00460] In some embodiments, R 2 is -OR 12 .
• R 2 is -OR 12 and R 12 is independently selected from C 1-6 alkyl, C 3-6 cycloalkyl, -CH 2 -C 3-6 cycloalkyl, C 2-9 heterocycloalkyl, and -CH 2 -C 2-9 heterocycloalkyl, wherein C 1-6 alkyl, C 3-6 cycloalkyl, -CH 2 -C 3-6 cycloalkyl, C 2-9 heterocycloalkyl, and -CH 2 -C 2-9 heterocycloalkyl, are optionally substituted with one, two, or three R 20k .
• R 2 is -OR 12 and R 12 is independently selected from C 1-6 alkyl, C 3-6 cycloalkyl, -CH 2 -C 3-6 cycloalkyl, C 2-9 heterocycloalkyl, and -CH 2 -C 2-9 heterocycloalkyl, wherein C 1- 6 alkyl, C 3-6 cycloalkyl, -CH 2 -C 3-6 cycloalkyl, C 2-9 heterocycloalkyl, and -CH 2 -C 2-9 heterocycloalkyl, are optionally substituted with one, two, or three R 20k ; and each R 20k is independently selected from oxo, -CN, halogen, -CN, C 1- 6 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 3-6 cycloalkyl, -CH 2 -C 3-6 cycloalkyl, C 1-6 heteroalkyl, C 2-9 heterocycloalkyl, -CH
• R 2 is -OR 12 and R 12 is independently selected from C 1-6 alkyl, C 3-6 cycloalkyl, -CH 2 -C 3-6 cycloalkyl, C 2-9 heterocycloalkyl, and -CH 2 -C 2-9 heterocycloalkyl, wherein C 1-6 alkyl, C 3-6 cycloalkyl, -CH 2 -C 3-6 cycloalkyl, C 2-9 heterocycloalkyl, and -CH 2 -C 2-9 heterocycloalkyl, are optionally substituted with one, two, or three R 20k ; and each R 20k is independently selected from oxo, -CN, halogen, -CN, C 1- 6 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 3-6 cycloalkyl, -CH 2 -C 3-6 cycloalkyl, C 2-9 heterocycloalkyl, -CH 2 -C 2 - 9
• R 2 is -OR 12 and R 12 is independently selected from C 1 - 6 alkyl, C 3-6 cycloalkyl, -CH 2 -C 3-6 cycloalkyl, C 2-9 heterocycloalkyl, and -CH 2 -C 2-9 heterocycloalkyl, wherein C 1-6 alkyl, C 3-6 cycloalkyl, -CH 2 -C 3-6 cycloalkyl, C 2-9 heterocycloalkyl, and -CH 2 -C 2-9 heterocycloalkyl, are optionally substituted with one, two, or three R 20k ; and each R 20k is independently selected from oxo, -CN, halogen, -CN, C 1-6 alkyl, C3- 6 cycloalkyl, C 2-9 heterocycloalkyl, C 6-10 aryl, C 1-9 heteroaryl, -OR 21 , and -N(R 22 )(R 23 ), , wherein C 1-6
• R 2 is -OR 12 and R 12 is independently selected from C 1-6 alkyl, C3-4cycloalkyl, C3- 5heterocycloalkyl, and -CH 2 -C 4 -5heterocycloalkyl, wherein C 1-6 alkyl, C3-4cycloalkyl, C3-5heterocycloalkyl, and -CH 2 - C 4-5 heterocycloalkyl, are optionally substituted with one, two, or three R 20k ; and each R 20k is independently selected from oxo, halogen, -CN, C 1-6 alkyl, C 3-6 cycloalkyl, C 2-9 heterocycloalkyl, C 6-10 aryl, C 1-9 heteroaryl, -OR 21 , and - N(R 22 )(R 23 ), wherein C 1-6 alkyl, C 3-6 cycloalkyl, C 2-9 heterocycloalkyl, C 6-10 aryl, and C 1-9 hetero
• R 2 is 2 In some embodiments, R is In some embodiments, R is In some embodiments, R 2 is 2 , In some embodiments, R is In some embodiments, R 2 is . In some embodiments, R 2 is In some embodiments, R 2 is In some embodiments, R 2 is In some embodiments, R 2 is . In some embodiments, R 2 is In some embodiments, R 2 is In some embodiments, R 2 is In some embodiments, R 2 is In some embodiments, R 2 is In some embodiments, R 2 is In some embodiments, R 2 is In some embodiments, R 2 is In some embodiments, R 2 is In some embodiments, R 2 is In some embodiments, R 2 is 2 In some embodiments, R 2 is 2 In some embodiments, R 2 is 2 In some embodiments, R 2 is 2 In some embodiments, R 2 is 2 In some embodiments, R 2 is 2 In some embodiments, R 2 is C.
• R 2 is In some embodiments, R 2 is In some embodiments, R 2 is In some embodiments, R 2 is In some embodiments, R 2 is In some embodiments, R 2 is [004 6 1] In some embodiments, R 2 is -N(R 12 )(R 13 ).
• R 2 is -N(R 12 )(R 13 ), R 13 is hydrogen;
• R 12 is independently selected from C 1-6 alkyl, C 3-6 cycloalkyl, -CH 2 -C 3-6 cycloalkyl, C 2-9 heterocycloalkyl, -CH 2 -C 2 - 9heterocycloalkyl, C 6-10 aryl, -CH 2 -C 6-10 aryl, and C 1-9 heteroaryl, wherein C 1-6 alkyl, C 3-6 cycloalkyl, -CH 2 -C 3- 6 cycloalkyl, C 2-9 heterocycloalkyl, -CH 2 -C 2-9 heterocycloalkyl, C 6-10 aryl, -CH 2 -C 6-10 aryl, and C 1-9 heteroaryl are optionally substituted with one, two, or three R 20k .
• R 2 is -N(R 12 )(R 13 ), R 13 is hydrogen;
• R 12 is independently selected from C 1-6 alkyl, C 3-6 cycloalkyl, -CH 2 -C 3-6 cycloalkyl, C 2-9 heterocycloalkyl, -CH 2 -C 2 - 9 heterocycloalkyl, C 6-10 aryl, -CH 2 -C 6-10 aryl, and C 1-9 heteroaryl, wherein C 1-6 alkyl, C 3-6 cycloalkyl, -CH 2 -C3- 6 cycloalkyl, C 2-9 heterocycloalkyl, -CH 2 -C 2-9 heterocycloalkyl, C 6-10 aryl, -CH 2 -C 6-10 aryl, and C 1-9 heteroaryl are optionally substituted with one, two, or three R 20k ; each R 20k is independently selected from oxo, -CN, halogen, -CN, C 1-6
• R 2 is . In some embodiments, R 2 is . In some embodiments, R 2 is . In some embodiments, R 2 is . In some embodiments, R 2 is . In some embodiments, R 2 is . In some embodiments, R 2 is . In some embodiments, R 2 is . In some embodiments, R 2 is . In some embodiments, R 2 is . In some embodiments, R 2 is . In some embodiments, R 2 is . In some embodiments, R 2 is . In some embodiments, R 2 is . In some embodiments, R 2 is . In some embodiments, R 2 is . In some embodiments, R 2 is . In some embodiments, R 2 is . In some embodiments, R 2 is . In some embodiments, R 2 is . In some embodiments, R 2 is . In some embodiments, R 2 is . In some embodiments, R 2 is . In some embodiments, R 2 is . In some embodiments, R 2 is . In some embodiments, R 2 is
• R 2 is . In some embodiments, R 2 is . In some embodiments, R 2 is . In some embodiments, R 2 is . In some embodiments, R 2 is . In some embodiments, R 2 is . In some embodiments, R 2 is . In some embodiments, R 2 is . In some embodiments, R 2 is . In some embodiments, R 2 is . In some embodiments, R 2 is .
• R 2 is , [004 6 2] In some embodiments, R 2 is selected from C 3-6 cycloalkyl, C 2-9 heterocycloalkyl, C 6-10 aryl, and C 1- 9 heteroaryl, wherein C 3-6 cycloalkyl, C 2-9 heterocycloalkyl, C 6-10 aryl, and C 1-9 heteroaryl are optionally substituted with one, two, or three R 20b .
• R 2 is selected from C 3-6 cycloalkyl, C 2-9 heterocycloalkyl, C 6 - 10aryl, and C 1-9 heteroaryl, wherein C 3-6 cycloalkyl, C 2-9 heterocycloalkyl, C 6-10 aryl, and C 1-9 heteroaryl are optionally substituted with one, two, or three R 20b ; each R 20b is independently selected from oxo, -CN, halogen, C 1-6 alkyl, C 3- 6 cycloalkyl, -N(R 22 )(R 23 ), -C(O)R 25 , -S(O) 2 R 25 , and -P(O)(R 25 ) 2 , wherein C 1-6 alkyl and C 3-6 cycloalkyl are optionally substituted with one, two, or three groups independently selected from halogen, oxo, -CN, C 1-6 alkyl, C 1-6 haloalkyl, C 1-6 alk
• R 2 is selected from C 3-6 cycloalkyl, C 2- 9 heterocycloalkyl, C 6-10 aryl, and C 1-9 heteroaryl, wherein C 3-6 cycloalkyl, C 2-9 heterocycloalkyl, C 6-10 aryl, and C 1 - 9 heteroaryl are optionally substituted with one, two, or three R 20b ; each R 20b is independently selected from oxo, - CN, halogen, C 1-6 alkyl, C 3-6 cycloalkyl, -N(R 22 )(R 23 ), -C(O)R 25 , -S(O) 2 R 25 , and -P(O)(R 25 ) 2 ; each R 22 is independently C 1-6 alkyl; each R 23 is C 1-6 alkyl; and each R 25 is selected from C 1-6 alkyl, C 3-6 cycloalkyl, and -CH 2 -C 3- 6 cycloalkyl.
• R 2 is . In some embodiments, R 2 is . In some embodiments, R 2 is . In some embodiments, R 2 is . In some embodiments, R 2 is . In some embodiments, R 2 is . In some embodiments, R 2 is . In some embodiments, R 2 is . In some embodiments, R 2 is . In some embodiments, R 2 is . In some embodiments, R 2 is . In some embodiments, R 2 is . In some embodiments, R 2 is . In some embodiments, R 2 is . In some embodiments, R 2 is . In some embodiments, R 2 is . In some embodiments, R 2 is . In some embodiments, R 2 is . In some embodiments, R 2 is . In some embodiments, R 2 is . In some embodiments, R 2 is . In some embodiments, R 2 is . In some embodiments, R 2 is . In some embodiments, R 2 is . In some embodiments, R 2 is . In some embodiments, R 2 is
• R 2 is independently selected from -C(O)OR 12 and -C(O)N(R 12 )(R 13 ). In some embodiments, R 2 is independently selected from -C(O)OR 12 and -C(O)N(R 12 )(R 13 ); R 13 is hydrogen; R 12 is C 1-6 alkyl optionally substituted with one, two, or three R 20k ; R 20k is independently selected from oxo, C 3-6 cycloalkyl, -CH 2 -C3- 6 cycloalkyl, C 2-9 heterocycloalkyl, -CH 2 -C 2-9 heterocycloalkyl, C 6-10 aryl, -CH 2 -C 6-10 aryl, C 1-9 heteroaryl, wherein C3- 6 cycloalkyl, -CH 2 -C 3-6 cycloalkyl, C 2-9 heterocycloalkyl, -CH 2 -C 2-9 heterocycloalkyl, -CH 2 -C 2
• R 2 is independently selected from -C(O)OR 12 and -C(O)N(R 12 )(R 13 );
• R 13 is hydrogen;
• R 12 is C 1-6 alkyl optionally substituted with one C 6-10 aryl.
• R 3 is independently selected from -C(O)OR 12 and - C(O)N(R 12 )(R 13 ).
• R 3 is independently selected from -C(O)OR 12 and -C(O)N(R 12 )(R 13 );
• R 13 is hydrogen;
• R 12 is C 1-6 alkyl optionally substituted with one, two, or three R 20k ;
• R 20k is independently selected from oxo, C 3-6 cycloalkyl, -CH 2 -C 3-6 cycloalkyl, C 2-9 heterocycloalkyl, -CH 2 -C 2-9 heterocycloalkyl, C 6-10 aryl, -CH 2 -C 6-10 aryl, C 1-9 heteroaryl, wherein C 3-6 cycloalkyl, -CH 2 -C 3-6 cycloalkyl, C 2-9 heterocycloalkyl, -CH 2 -C 2-9 heterocycloalkyl, C 6 - 10aryl, -CH 2 -C 6-10 aryl, and C 1-9 heteroaryl are optionally substituted with one, two, or three groups
• R 3 is independently selected from -C(O)OR 12 and -C(O)N(R 12 )(R 13 ); R 13 is hydrogen; R 12 is C 1 - 6 alkyl optionally substituted with one C 6-10 aryl.
• R 2 is . In some embodiments, R 2 is . In some embodiments, R 2 is . In some embodiments, R 3 is . In some embodiments, R 3 is . In some embodiments, R 3 is . [004 6 4] In some embodiments, R 2 is selected from and , each of which is optionally substituted with one, two, or three R 20b . In some embodiments, R 2 is optionally substituted with one, two, or three R 20b .
• R 2 is optionally substituted with one, two, or three R 20b . In some embodiments, R 2 is optionally substituted with one, two, or three R 20b . In some embodiments, R 2 is optionally substituted with one, two, or three R 20b . In some embodiments, R 2 is optionally substituted with one, two, or three R 20b . [00465] In some embodiments, R 2 is optionally substituted with one, two, or three R 20k . In some embodiments, R 2 is optionally substituted with one, two, or three R 20k . In some embodiments, R 2 is, optionally substituted with one, two, or three R 20k . In some embodiments, R 2 is .
• R 2 is optionally substituted with one, two, or three R 20k . In some embodiments, R 2 is optionally substituted with one, two, or three R 20k . In some embodiments, R 2 is optionally substituted with one, two, or three R 20k . In some embodiments, R 2 is optionally substituted with one, two, or three R 20k . In some embodiments, R 2 is optionally substituted with one R 20k . In some embodiments, R 2 is optionally substituted with one, two, or three R 20k . In some embodiments, R 2 is optionally substituted with one, two, or three R 20k . In some embodiments, R 2 is optionally substituted with one, two, or three R 20k . In some embodiments, R 2 is optionally substituted with one, two, or three R 20k . In some embodiments, R 2 is optionally substituted with one, two, or three R 20k .
• R 2 is optionally substituted with one, two, or three R 20k . In some embodiments, R 2 is optionally substituted with one, two, or three R 20k . In some embodiments, R 2 is optionally substituted with one, two, or three R 20k and optionally substituted with one, two, or three groups independently selected from halogen, oxo, -CN, C 1-6 alkyl, C 1-6 haloalkyl, C 1-6 alkoxy, C 1-6 haloalkoxy, - OR 21 , -SR 21 , -N(R 22 )(R 23 ), -C(O)OR 22 , -C(O)N(R 22 )(R 23 ), -C(O)C(O)N(R 22 )(R 23 ), -OC(O)N(R 22 )(R 23 ), - N(R 24 )C(O)N(R 22 )(R 23 ), -N(R 24 )C(O)N
• R 2 is optionally substituted with one, two, or three R 20k and optionally substituted with one, two, or three groups independently selected from halogen, oxo, -CN, C 1-6 alkyl, C 1-6 haloalkyl, C 1-6 alkoxy, C 1-6 haloalkoxy, -OR 21 , -SR 21 , -N(R 22 )(R 23 ), -C(O)OR 22 , - C(O)N(R 22 )(R 23 ), -C(O)C(O)N(R 22 )(R 23 ), -OC(O)N(R 22 )(R 23 ), -N(R 24 )C(O)N(R 22 )(R 23 ), -N(R 24 )C(O)OR 25 , - N(R 24 )C(O)R 25 , -N(R 24 )S(O) 2 R 25 , -C(O)R 25
• R 2 is optionally substituted with one, two, or three R 20k . In some embodiments, R 2 is optionally substituted with one, two, or three R 20k . In some embodiments, R 2 is optionally substituted with one, two, or three R 20k . In some embodiments, R 2 is optionally substituted with one, two, or three R 20k .
• R 2 is optionally substituted with one, two, or three R 20k and optionally substituted with one, two, or three groups independently selected from halogen, oxo, -CN, C 1-6 alkyl, C 1-6 haloalkyl, C 1-6 alkoxy, C 1-6 haloalkoxy, -OR 21 , -SR 21 , -N(R 22 )(R 23 ), -C(O)OR 22 , - C(O)N(R 22 )(R 23 ), -C(O)C(O)N(R 22 )(R 23 ), -OC(O)N(R 22 )(R 23 ), -N(R 24 )C(O)N(R 22 )(R 23 ), -N(R 24 )C(O)OR 25 , - N(R 24 )C(O)R 25 , -N(R 24 )S(O) 2 R 25 , -C(O)R 25
• R 2 is optionally substituted with one, two, or three R 20k and optionally substituted with one, two, or three groups independently selected from halogen, oxo, -CN, C 1-6 alkyl, C 1-6 haloalkyl, C 1-6 alkoxy, C 1-6 haloalkoxy, -OR 21 , -SR 21 , -N(R 22 )(R 23 ), -C(O)OR 22 , -C(O)N(R 22 )(R 23 ), -C(O)C(O)N(R 22 )(R 23 ), -OC(O)N(R 22 )(R 23 ), - N(R 24 )C(O)N(R 22 )(R 23 ), -N(R 24 )C(O)OR 25 , -N(R 24 )C(O)R 25 , -N(R 24 )S(O) 2 R 25 , -C(O)R 25
• R 2 is optionally substituted with one, two, or three R 20k .
• R 2 is optionally substituted with one, two, or three R 20k and optionally substituted with one, two, or three groups independently selected from halogen, oxo, -CN, C 1-6 alkyl, C 1-6 haloalkyl, C 1-6 alkoxy, C 1-6 haloalkoxy, -OR 21 , -SR 21 , -N(R 22 )(R 23 ), -C(O)OR 22 , -C(O)N(R 22 )(R 23 ), - C(O)C(O)N(R 22 )(R 23 ), -OC(O)N(R 22 )(R 23 ), -N(R 24 )C(O)N(R 22 )(R 23 ), -N(R 24 )C(O)OR 25 , -N(R 24 )C(O)R 25 , -N(R 24 )
• R 2 is optionally substituted with one, two, or three R 20k and optionally substituted with one, two, or three groups independently selected from halogen, oxo, -CN, C 1-6 alkyl, C 1-6 haloalkyl, C 1-6 alkoxy, C 1-6 haloalkoxy, - OR 21 , -SR 21 , -N(R 22 )(R 23 ), -C(O)OR 22 , -C(O)N(R 22 )(R 23 ), -C(O)C(O)N(R 22 )(R 23 ), -OC(O)N(R 22 )(R 23 ), - N(R 24 )C(O)N(R 22 )(R 23 ), -N(R 24 )C(O)OR 25 , -N(R 24 )C(O)R 25 , -N(R 24 )S(O) 2 R 25 , -C(O)R 25
• R 2 is optionally substituted with one, two, or three R 20k and optionally substituted with one, two, or three groups independently selected from halogen, oxo, -CN, C 1-6 alkyl, C 1-6 haloalkyl, C 1-6 alkoxy, C 1-6 haloalkoxy, -OR 21 , -SR 21 , -N(R 22 )(R 23 ), -C(O)OR 22 , - C(O)N(R 22 )(R 23 ), -C(O)C(O)N(R 22 )(R 23 ), -OC(O)N(R 22 )(R 23 ), -N(R 24 )C(O)N(R 22 )(R 23 ), -N(R 24 )C(O)OR 25 , - N(R 24 )C(O)R 25 , -N(R 24 )S(O) 2 R 25 , -C(O)R 25
• R 2 is optionally substituted with one, two, or three R 20k and optionally substituted with one, two, or three groups independently selected from halogen, oxo, -CN, C 1-6 alkyl, C 1-6 haloalkyl, C 1-6 alkoxy, C 1- 6 haloalkoxy, -OR 21 , -SR 21 , -N(R 22 )(R 23 ), -C(O)OR 22 , -C(O)N(R 22 )(R 23 ), -C(O)C(O)N(R 22 )(R 23 ), -OC(O)N(R 22 )(R 23 ), -N(R 24 )C(O)N(R 22 )(R 23 ), -N(R 24 )C(O)OR 25 , -N(R 24 )C(O)R 25 , -N(R 24 )S(O) 2 R 25 , -C(O)R 25
• R 2 is optionally substituted with one, two, or three R 20 . In some embodiments, R 2 is optionally substituted with one, two, or three R 20k . In some embodiments, R 2 is optionally substituted with one, two, or three R 20 . In some embodiments, R 2 is optionally substituted with one, two, or three R 20k . In some embodiments, R 2 is optionally substituted with one, two, or three R 20k . In some embodiments, R 2 is optionally substituted with one, two, or three R 20k . In some embodiments, R 2 is optionally substituted with one, two, or three R 20k . In some embodiments, R 2 is optionally substituted with one, two, or three R 20k .
• R 2 is optionally substituted with one, two, or three R 20 . In some embodiments, R 2 is optionally substituted with one, two, or three R 20k . In some embodiments, R 2 is optionally substituted with one, two, or three R 20k . In some embodiments, R 2 is optionally substituted with one, two, or three R 20k . In some embodiments, R 2 is optionally substituted with one, two, or three R 20k . In some embodiments, R 2 is optionally substituted with one, two, or three R 20k . In some embodiments, R 2 is optionally substituted with one, two, or three R 20k . In some embodiments, R 2 is optionally substituted with one, two, or three R 20k . In some embodiments, R 2 is optionally substituted with one, two, or three R 20k . In some embodiments, R 2 is optionally substituted with one, two, or three R 20k . In some embodiments, R 2 is optionally substituted with one, two, or three R
• R 2 is optionally substituted with one, two, or three R 20k and optionally substituted with one, two, or three groups independently selected from halogen, oxo, -CN, C 1-6 alkyl, C 1-6 haloalkyl, C 1-6 alkoxy, C 1-6 haloalkoxy, -OR 21 , -SR 21 , -N(R 22 )(R 23 ), -C(O)OR 22 , -C(O)N(R 22 )(R 23 ), -C(O)C(O)N(R 22 )(R 23 ), - OC(O)N(R 22 )(R 23 ), -N(R 24 )C(O)N(R 22 )(R 23 ), -N(R 24 )C(O)OR 25 , -N(R 24 )C(O)R 25 , -N(R 24 )S(O) 2 R 25 , -C(O)R
• R 2 is optionally substituted with one, two, or three R 20k and optionally substituted with one, two, or three groups independently selected from halogen, oxo, -CN, C 1-6 alkyl, C 1-6 haloalkyl, C 1-6 alkoxy, C 1-6 haloalkoxy, -OR 21 , -SR 21 , -N(R 22 )(R 23 ), - C(O)OR 22 , -C(O)N(R 22 )(R 23 ), -C(O)C(O)N(R 22 )(R 23 ), -OC(O)N(R 22 )(R 23 ), -N(R 24 )C(O)N(R 22 )(R 23 ), - N(R 24 )C(O)OR 25 , -N(R 24 )C(O)R 25 , -N(R 24 )S(O) 2 R 25 , -C(O)R 25
• R 2 is optionally substituted with one, two, or three R 20k and optionally substituted with one, two, or three groups independently selected from halogen, oxo, -CN, C 1-6 alkyl, C 1-6 haloalkyl, C 1-6 alkoxy, C 1-6 haloalkoxy, -OR 21 , -SR 21 , -N(R 22 )(R 23 ), -C(O)OR 22 , -C(O)N(R 22 )(R 23 ), -C(O)C(O)N(R 22 )(R 23 ), - OC(O)N(R 22 )(R 23 ), -N(R 24 )C(O)N(R 22 )(R 23 ), -N(R 24 )C(O)OR 25 , -N(R 24 )C(O)R 25 , -N(R 24 )S(O) 2 R 25 , -C(O)R
• R 2 is optionally substituted with one, two, or three R 20k . In some embodiments, R 2 is optionally substituted with one, two, or three R 20k . In some embodiments, R 2 is optionally substituted with one, two, or three R 20k . In some embodiments, R 2 is optionally substituted with one, two, or three R 20k and optionally substituted with one, two, or three groups independently selected from halogen, oxo, - CN, C 1-6 alkyl, C 1-6 haloalkyl, C 1-6 alkoxy, C 1-6 haloalkoxy, -OR 21 , -SR 21 , -N(R 22 )(R 23 ), -C(O)OR 22 , -C(O)N(R 22 )(R 23 ), -C(O)C(O)N(R 22 )(R 23 ), -OC(O)N(R 22 )(R 23 ), -N(R 24 )C(O
• R 2 is optionally substituted with one, two, or three R 20k and optionally substituted with one, two, or three groups independently selected from halogen, oxo, -CN, C 1-6 alkyl, C 1-6 haloalkyl, C 1-6 alkoxy, C 1-6 haloalkoxy, -OR 21 , -SR 21 , -N(R 22 )(R 23 ), -C(O)OR 22 , -C(O)N(R 22 )(R 23 ), -C(O)C(O)N(R 22 )(R 23 ), -OC(O)N(R 22 )(R 23 ), - N(R 24 )C(O)N(R 22 )(R 23 ), -N(R 24 )C(O)OR 25 , -N(R 24 )C(O)R 25 , -N(R 24 )S(O) 2 R 25 , -C(O)R 25
• R 2 is optionally substituted with one, two, or three R 20k and optionally substituted with one, two, or three groups independently selected from halogen, oxo, -CN, C 1-6 alkyl, C 1-6 haloalkyl, C 1-6 alkoxy, C 1-6 haloalkoxy, -OR 21 , -SR 21 , -N(R 22 )(R 23 ), -C(O)OR 22 , - C(O)N(R 22 )(R 23 ), -C(O)C(O)N(R 22 )(R 23 ), -OC(O)N(R 22 )(R 23 ), -N(R 24 )C(O)N(R 22 )(R 23 ), -N(R 24 )C(O)OR 25 , - N(R 24 )C(O)R 25 , -N(R 24 )S(O) 2 R 25 , -C(O)R 25
• R 2 is optionally substituted with one, two, or three R 20k and optionally substituted with one, two, or three groups independently selected from halogen, oxo, -CN, C 1-6 alkyl, C 1-6 haloalkyl, C 1-6 alkoxy, C 1- 6 haloalkoxy, -OR 21 , -SR 21 , -N(R 22 )(R 23 ), -C(O)OR 22 , -C(O)N(R 22 )(R 23 ), -C(O)C(O)N(R 22 )(R 23 ), -OC(O)N(R 22 )(R 23 ), -N(R 24 )C(O)N(R 22 )(R 23 ), -N(R 24 )C(O)OR 25 , -N(R 24 )C(O)R 25 , -N(R 24 )S(O) 2 R 25 , -C(O)R 25
• R 2 is .
• R 2 is optionally substituted with one, two, or three R 20k and optionally substituted with one, two, or three groups independently selected from halogen, oxo, -CN, C 1-6 alkyl, C 1-6 haloalkyl, C 1-6 alkoxy, C 1-6 haloalkoxy, - OR 21 , -SR 21 , -N(R 22 )(R 23 ), -C(O)OR 22 , -C(O)N(R 22 )(R 23 ), -C(O)C(O)N(R 22 )(R 23 ), -OC(O)N(R 22 )(R 23 ), - N(R 24 )C(O)N(R 22 )(R 23 ), -N(R 24 )C(O)OR 25 , -N(R 24 )C(O)R 25 , -N(R 24 )S(O) 2 R 25 , -N(R
• R 2 is optionally substituted with one, two, or three R 20k and optionally substituted with one, two, or three groups independently selected from halogen, oxo, -CN, C 1-6 alkyl, C 1-6 haloalkyl, C 1-6 alkoxy, C 1-6 haloalkoxy, -OR 21 , -SR 21 , -N(R 22 )(R 23 ), -C(O)OR 22 , - C(O)N(R 22 )(R 23 ), -C(O)C(O)N(R 22 )(R 23 ), -OC(O)N(R 22 )(R 23 ), -N(R 24 )C(O)N(R 22 )(R 23 ), -N(R 24 )C(O)OR 25 , - N(R 24 )C(O)R 25 , -N(R 24 )S(O) 2 R 25 , -C(O)R 25
• R 2 is optionally substituted with one, two, or three R 20k and optionally substituted with one, two, or three groups independently selected from halogen, oxo, -CN, C 1-6 alkyl, C 1-6 haloalkyl, C 1-6 alkoxy, C 1-6 haloalkoxy, -OR 21 , -SR 21 , -N(R 22 )(R 23 ), -C(O)OR 22 , -C(O)N(R 22 )(R 23 ), -C(O)C(O)N(R 22 )(R 23 ), -OC(O)N(R 22 )(R 23 ), - N(R 24 )C(O)N(R 22 )(R 23 ), -N(R 24 )C(O)OR 25 , -N(R 24 )C(O)R 25 , -N(R 24 )S(O) 2 R 25 , -C(O)R 25
• R 2 is optionally substituted with one, two, or three R 20k and optionally substituted with one, two, or three groups independently selected from halogen, oxo, -CN, C 1-6 alkyl, C 1-6 haloalkyl, C 1-6 alkoxy, C 1-6 haloalkoxy, -OR 21 , -SR 21 , -N(R 22 )(R 23 ), -C(O)OR 22 , - C(O)N(R 22 )(R 23 ), -C(O)C(O)N(R 22 )(R 23 ), -OC(O)N(R 22 )(R 23 ), -N(R 24 )C(O)N(R 22 )(R 23 ), -N(R 24 )C(O)OR 25 , - N(R 24 )C(O)R 25 , -N(R 24 )S(O) 2 R 25 , -C(O)R 25
• R 2 is optionally substituted with one, two, or three R 20b . In some embodiments, R 2 is optionally substituted with one, two, or three R 20b . In some embodiments, R 2 is optionally substituted with one, two, or three R 20b .
• R 2 is optionally substituted with one, two, or three R 20b and optionally substituted with one, two, or three groups independently selected from halogen, oxo, -CN, C 1-6 alkyl, C 1-6 haloalkyl, C 1-6 alkoxy, C 1-6 haloalkoxy, -OR 21 , -SR 21 , -N(R 22 )(R 23 ), - C(O)OR 22 , -C(O)N(R 22 )(R 23 ), -C(O)C(O)N(R 22 )(R 23 ), -OC(O)N(R 22 )(R 23 ), -N(R 24 )C(O)N(R 22 )(R 23 ), - N(R 24 )C(O)OR 25 , -N(R 24 )C(O)R 25 , -N(R 24 )S(O) 2 R 25 , -C(O)R 25
• R 2 is optionally substituted with one, two, or three R 20b . In some embodiments, R 2 is optionally substituted with one, two, or three R 20b . In some embodiments, R 2 is optionally substituted with one, two, or three R 20b .
• R 2 is optionally substituted with one, two, or three R 20b and optionally substituted with one, two, or three groups independently selected from halogen, oxo, -CN, C 1-6 alkyl, C 1-6 haloalkyl, C 1-6 alkoxy, C 1-6 haloalkoxy, -OR 21 , -SR 21 , -N(R 22 )(R 23 ), - C(O)OR 22 , -C(O)N(R 22 )(R 23 ), -C(O)C(O)N(R 22 )(R 23 ), -OC(O)N(R 22 )(R 23 ), -N(R 24 )C(O)N(R 22 )(R 23 ), - N(R 24 )C(O)OR 25 , -N(R 24 )C(O)R 25 , -N(R 24 )S(O) 2 R 25 , -C(O)R 25
• R 2 is optionally substituted with one, two, or three R 20b and optionally substituted with one, two, or three groups independently selected from halogen, oxo, -CN, C 1-6 alkyl, C 1-6 haloalkyl, C 1-6 alkoxy, C 1-6 haloalkoxy, -OR 21 , -SR 21 , -N(R 22 )(R 23 ), -C(O)OR 22 , -C(O)N(R 22 )(R 23 ), -C(O)C(O)N(R 22 )(R 23 ), - OC(O)N(R 22 )(R 23 ), -N(R 24 )C(O)N(R 22 )(R 23 ), -N(R 24 )C(O)OR 25 , -N(R 24 )C(O)R 25 , -N(R 24 )S(O) 2 R 25 , -C(O)R
• R 2 is optionally substituted with one, two, or three R 20b . In some embodiments, R 2 is optionally substituted with one, two, or three R 20b . In some embodiments, R 2 is optionally substituted with one, two, or three R 20b . In some embodiments, R 2 is optionally substituted with one, two, or three R 20b . In some embodiments, R 2 is optionally substituted with one, two, or three R 20b . In some embodiments, R 2 is optionally substituted with one, two, or three R 20b . In some embodiments, R 2 is optionally substituted with one, two, or three R 20b . In some embodiments, R 2 is optionally substituted with one, two, or three R 20b . In some embodiments, R 2 is optionally substituted with one, two, or three R 20b . In some embodiments, R 2 is optionally substituted with one, two, or three R 20b . In some embodiments, R 2 is optionally substituted with one, two, or three
• R 2 is optionally substituted with one, two, or three R 20b and optionally substituted with one, two, or three groups independently selected from halogen, oxo, -CN, C 1-6 alkyl, C 1-6 haloalkyl, C 1-6 alkoxy, C 1-6 haloalkoxy, -OR 21 , -SR 21 , -N(R 22 )(R 23 ), - C(O)OR 22 , -C(O)N(R 22 )(R 23 ), -C(O)C(O)N(R 22 )(R 23 ), -OC(O)N(R 22 )(R 23 ), -N(R 24 )C(O)N(R 22 )(R 23 ), - N(R 24 )C(O)OR 25 , -N(R 24 )C(O)R 25 , -N(R 24 )S(O) 2 R 25 , -C(O)R 25
• R 2 is optionally substituted with one, two, or three R 20k . In some embodiments, R 2 is optionally substituted with one, two, or three R 20k . In some embodiments, R 2 is optionally substituted with one, two, or three R 20k . In some embodiments, R 3 is optionally substituted with one, two, or three R 20k . In some embodiments, R 3 is optionally substituted with one, two, or three R 20k . In some embodiments, R 3 is optionally substituted with one, two, or three R 20k . [004 6 9] Table 1 selected compound formula
• the subject compound is a compound having a formula comprising a combination of a cell of Table 1 and a cell of Table 2.
• a compound may have the formula of cell A1 of Table 1 and the R 2 of cell B1 of Table 2 and would be described by the formula “A1B1”.
• a compound may have the formula of cell A11 of Table 1 and the R 3 of cell B1 of Table 2 and would be described by the formula “A11B1”.
• a compound may have the formula of cell A9 of Table 1 and the R 2 of cell B1 of Table 2 and R 4 of cell C4 of Table 3 and would be described by the formula “A9B1C4”.
• the subject compound has a formula selected from A1B1, A1B2, A1B3, A1B4, A1B5, A1B6, A1B7, A1B8, A1B9, A1B10, A1B11, A1B12, A1B13, A1B14, A1B15, A1B16, A1B17, A1B18, A1B19, A1B20, A1B21, A1B22, A1B23, A1B24, A1B25, A1B26, A1B27, A1B28, A1B29, A1B30, A1B31, A1B32, A1B33, A1B34, A1B35, A1B36, A1B37, A1B38, A1B39, A1B40, A1B41, A1B42, A1B43, A1B44, A1B45, A1B46, A1B47, A1B48, A1B49, A1B50
• the compound is selected from ,
• X is N. In some embodiments (e.g., including Formulae (I), (II), (III), (IV); or sub-formulae thereof), X is C(R 5 ). In some embodiments (e.g., including Formulae (I), (II), (III), (IV); or sub-formulae thereof), X is CH. In some embodiments (e.g., including Formulae (I), (II), (III), (IV); or sub-formulae thereof), X is C(halogen).
• X is C(F).
• R 5 is hydrogen.
• R 5 is halogen.
• R 5 is -F.
• R 5 is -Cl. In some embodiments (e.g., including Formulae (I), (II), (III), (IV); or sub-formulae thereof), R 5 is -Br. In some embodiments (e.g., including Formulae (I), (II), (III), (IV); or sub-formulae thereof), R 5 is -I. In some embodiments (e.g., including Formulae (I), (II), (III), (IV); or sub-formulae thereof), R 5 is -CN.
• R 5 is C 1-6 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 3- 6 cycloalkyl, C 2-9 heterocycloalkyl, C 6-10 aryl, C 1-9 heteroaryl, -OR 12 , -SR 12 , -N(R 12 )(R 13 ), -C(O)OR 12 , - OC(O)N(R 12 )(R 13 ), -N(R 14 )C(O)N(R 12 )(R 13 ), -N(R 14 )C(O)OR 12 , -N(R 14 )S(O) 2 R 15 , -C(O)R 15 , -S(O)R 15 , -OC(O)R 15 , - C(O)N(R 12 )(R 13 ), -C(O) 2 R 15 , -C(O)R 15 , -S(O)R 15 , -OC(O)
• R 5 is C 1-6 alkyl. In some embodiments (e.g., including Formulae (I), (II), (III), (IV); or sub-formulae thereof), R 5 is C 1 -4alkyl. In some embodiments (e.g., including Formulae (I), (II), (III), (IV); or sub-formulae thereof), R 5 is C 1-3 alkyl. In some embodiments (e.g., including Formulae (I), (II), (III), (IV); or sub-formulae thereof), R 5 is C 1-2 alkyl.
• R 5 is methyl.
• R 5 is hydrogen.
• R 5 is halogen.
• R 5 is -CN.
• R 5 is C 1-6 alkyl, C 2 - 6 alkenyl, C 2-6 alkynyl, C 3-6 cycloalkyl, C 2-9 heterocycloalkyl, C 6-10 aryl, C 1-9 heteroaryl.
• R 5 is -OR 12 , -SR 12 , -N(R 12 )(R 13 ), -C(O)OR 12 , - OC(O)N(R 12 )(R 13 ), -N(R 14 )C(O)N(R 12 )(R 13 ), -N(R 14 )C(O)OR 12 , -N(R 14 )S(O) 2 R 15 , -C(O)R 15 , -S(O)R 15 , -OC(O)R 15 , - C(O)N(R 12 )(R 13 ), -C(O)C(O)N(R 12 )(R 13 ), -N(R 14 )C(O)R 15 , -S(O) 2 R 15 , -S(O) 2 N(R 12 )
• R 5 is C 1-6 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 3- 6 cycloalkyl, C 2-9 heterocycloalkyl, C 6-10 aryl, or C 1-9 heteroaryl substituted with one, two, or three R 20e .
• R 5 is selected from hydrogen, halogen, and C 1-6 alkyl optionally substituted with one, two, or three R 20e .
• R 5 is selected from hydrogen and halogen.
• Y is N.
• Y is C(R 6 ).
• Y is CH.
• Y is C(R 6 ). In some embodiments (e.g., including Formulae (I), (II), (III), (IV); or sub-formulae thereof), Y is C(OH). [00478] In some embodiments (e.g., including Formulae (I), (II), (III), (IV); or sub-formulae thereof), R 6 is -OR 16 . In some embodiments (e.g., including Formulae (I), (II), (III), (IV); or sub-formulae thereof), R 6 is -N(R 12 )(R 16 ).
• R 6 is -OR 12 . In some embodiments (e.g., including Formulae (I), (II), (III), (IV); or sub-formulae thereof), R 6 is -OR 12a . In some embodiments (e.g., including Formulae (I), (II), (III), (IV); or sub-formulae thereof), R 6 is -SR 12 . In some embodiments (e.g., including Formulae (I), (II), (III), (IV); or sub-formulae thereof), R 6 is -N(R 12 )(R 13 ).
• R 6 is C 1-6 alkyl, C 2-6 alkenyl, C 2- 6 alkynyl, C 3-6 cycloalkyl, C 2-9 heterocycloalkyl, C 6-10 aryl, and C 1-9 heteroaryl optionally substituted with one, two, or three R 20f .
• R 6 is -OH.
• R 6 is C 1-6 alkyl. In some embodiments (e.g., including Formulae (I), (II), (III), (IV); or sub-formulae thereof), R 6 is C 1-4 alkyl. In some embodiments (e.g., including Formulae (I), (II), (III), (IV); or sub-formulae thereof), R 6 is C 1-3 alkyl. In some embodiments (e.g., including Formulae (I), (II), (III), (IV); or sub-formulae thereof), R 6 is C 1 -2alkyl.
• R 6 is methyl.
• R 6 is hydrogen.
• R 6 is halogen.
• R 6 is -CN.
• R 6 is C 1-6 alkyl, C 2 - 6 alkenyl, C 2-6 alkynyl, C 3-6 cycloalkyl, C 2-9 heterocycloalkyl, C 6-10 aryl, C 1-9 heteroaryl. In some embodiments (e.g., including Formulae (I), (II), (III), (IV); or sub-formulae thereof), R 6 is -OR 16 .
• R 6 is -N(R 12 )(R 16 ). In some embodiments (e.g., including Formulae (I), (II), (III), (IV); or sub-formulae thereof), R 6 is -OR 12 . In some embodiments (e.g., including Formulae (I), (II), (III), (IV); or sub-formulae thereof), R 6 is -OR 12a . In some embodiments (e.g., including Formulae (I), (II), (III), (IV); or sub-formulae thereof), R 6 is -SR 12 .
• R 6 is -N(R 12 )(R 13 ) . In some embodiments (e.g., including Formulae (I), (II), (III), (IV); or sub-formulae thereof), R 6 is -C(O)OR 12 . In some embodiments (e.g., including Formulae (I), (II), (III), (IV); or sub-formulae thereof), R 6 is -OC(O)N(R 12 )(R 13 ) .
• R 6 is -N(R 14 )C(O)N(R 12 )(R 13 ) . In some embodiments (e.g., including Formulae (I), (II), (III), (IV); or sub-formulae thereof), R 6 is -N(R 14 )C(O)OR 12 . In some embodiments (e.g., including Formulae (I), (II), (III), (IV); or sub-formulae thereof), R 6 is -N(R 14 )S(O) 2 R 15 .
• R 6 is -C(O)R 15 . In some embodiments (e.g., including Formulae (I), (II), (III), (IV); or sub-formulae thereof), R 6 is -S(O)R 15 . In some embodiments (e.g., including Formulae (I), (II), (III), (IV); or sub-formulae thereof), R 6 is -OC(O)R 15 .
• R 6 is -C(O)N(R 12 )(R 13 ) . In some embodiments (e.g., including Formulae (I), (II), (III), (IV); or sub-formulae thereof), R 6 is -C(O)C(O)N(R 12 )(R 13 ) . In some embodiments (e.g., including Formulae (I), (II), (III), (IV); or sub-formulae thereof), R 6 is -N(R 14 )C(O)R 15 .
• R 6 is -CH 2 C(O)N(R 12 )(R 13 ) . In some embodiments (e.g., including Formulae (I), (II), (III), (IV); or sub- formulae thereof), R 6 is -CH 2 N(R 14 )C(O)R 15 . In some embodiments (e.g., including Formulae (I), (II), (III), (IV); or sub-formulae thereof), R 6 is -CH 2 S(O) 2 R 15 .
• R 6 is -CH 2 S(O) 2 N(R 12 )(R 13 ) .
• R 6 is C 1-6 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 3-6 cycloalkyl, C 2-9 heterocycloalkyl, C 6- 10aryl, or C 1-9 heteroaryl substituted with one, two, or three R 20f .
• R 6 is -OH.
• R 6 is selected from hydrogen, halogen, -OR 12a , and C 1 - 6 alkyl optionally substituted with one, two, or three R 20f .
• J 3 is CH 2 and R 6 is selected from hydrogen, halogen, -CN, C 1-6 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 3-6 cycloalkyl, C 2-9 heterocycloalkyl, C 6-10 aryl, C 1-9 heteroaryl, - OR 16 , -N(R 12 )(R 16 ), -OR 12a , -SR 12 , -N(R 12 )(R 13 ), -C(O)OR 12 , -OC(O)N(R 12 )(R 13 ), -N(R 14 )C(O)N(R 12 )(R 13 ), - N(R 14 )C(O)OR 12 , -N(R 14 )S(O) 2 R 15 , -C(O)R 15 , -S(O)R 15 , -OC(
• J 3 is CH 2 and R 6 is selected from hydrogen, halogen, -CN, C 1-6 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 3-6 cycloalkyl, C 2-9 heterocycloalkyl, C 6-10 aryl, C 1-9 heteroaryl, - OR 16 , -N(R 12 )(R 16 ), -SR 12 , -N(R 12 )(R 13 ), -C(O)OR 12 , -OC(O)N(R 12 )(R 13 ), -N(R 14 )C(O)N(R 12 )(R 13 ), - N(R 14 )C(O)OR 12 , -N(R 14 )S(O) 2 R 15 , -C(O)R 15 , -S(O)R 15 , -OC(O)R 15 , -C(O)OR 12 , -C(O) 2 R 15 , -C
• J 3 is CH 2 and R 6 is -OR 16 . In some embodiments of Formulae (I), or sub-formulae thereof, J 3 is CH 2 and R 6 is -N(R 12 )(R 16 ). [00482] In some embodiments (e.g., including Formulae (I), (II), (III), (IV); or sub-formulae thereof), Z is N. In some embodiments (e.g., including Formulae (I), (II), (III), (IV); or sub-formulae thereof), Z is C(R 7 ).
• Z is CH. In some embodiments (e.g., including Formulae (I), (II), (III), (IV); or sub-formulae thereof), Z is C(R 7 ). [00483] In some embodiments (e.g., including Formulae (I), (II), (III), (IV); or sub-formulae thereof), R 7 is hydrogen. In some embodiments (e.g., including Formulae (I), (II), (III), (IV); or sub-formulae thereof), R 7 is halogen.
• R 7 is -CN. In some embodiments (e.g., including Formulae (I), (II), (III), (IV); or sub-formulae thereof), R 7 is C 1-6 alkyl, C 2- 6 alkenyl, C 2-6 alkynyl, C 3-6 cycloalkyl, C 2-9 heterocycloalkyl, C 6-10 aryl, C 1-9 heteroaryl, -OR 12 , -SR 12 , -N(R 12 )(R 13 ), - C(O)OR 12 , -OC(O)N(R 12 )(R 13 ), -N(R 14 )C(O)N(R 12 )(R 13 ), -N(R 14 )C(O)OR 12 , -N(R 14 )S(O) 2 R 15 , -C(O)R 15
• R 7 is C 1-6 alkyl. In some embodiments (e.g., including Formulae (I), (II), (III), (IV); or sub-formulae thereof), R 7 is C 1-4 alkyl. In some embodiments (e.g., including Formulae (I), (II), (III), (IV); or sub- formulae thereof), R 7 is C 1-2 alkyl. In some embodiments (e.g., including Formulae (I), (II), (III), (IV); or sub- formulae thereof), R 7 is methyl.
• R 7 is hydrogen. In some embodiments (e.g., including Formulae (I), (II), (III), (IV); or sub-formulae thereof), R 7 is halogen. In some embodiments (e.g., including Formulae (I), (II), (III), (IV); or sub-formulae thereof), R 7 is -CN.
• R 7 is C 1-6 alkyl, C 2 - 6 alkenyl, C 2-6 alkynyl, C 3-6 cycloalkyl, C 2-9 heterocycloalkyl, C 6-10 aryl, C 1-9 heteroaryl, -OR 12 , -SR 12 , -N(R 12 )(R 13 ), - C(O)OR 12 , -OC(O)N(R 12 )(R 13 ), -N(R 14 )C(O)N(R 12 )(R 13 ), -N(R 14 )C(O)OR 12 , -N(R 14 )S(O) 2 R 15 , -C(O)R 15 , -S(O)R 15 , - OC(O)R 15 , -C(O)N(R 12 )(R 13 ),
• R 7 is C 1-6 alkyl, C 2 - 6 alkenyl, C 2-6 alkynyl, C 3-6 cycloalkyl, C 2-9 heterocycloalkyl, C 6-10 aryl, or C 1-9 heteroaryl substituted with one, two, or three R 20g .
• R 7 is selected from hydrogen, halogen, and C 1-6 alkyl optionally substituted with one, two, or three R 20g .
• R 8 is hydrogen. In some embodiments (e.g., including Formulae (I), (II), (III), (IV); or sub-formulae thereof), R 8 is halogen. In some embodiments (e.g., including Formulae (I), (II), (III), (IV); or sub-formulae thereof), R 8 is -CN.
• R 8 is C 1-6 alkyl, C 2 - 6 alkenyl, C 2-6 alkynyl, C 3-6 cycloalkyl, C 2-9 heterocycloalkyl, C 6-10 aryl, C 1-9 heteroaryl, -OR 12 , -SR 12 , -N(R 12 )(R 13 ), - C(O)OR 12 , -OC(O)N(R 12 )(R 13 ), -N(R 14 )C(O)N(R 12 )(R 13 ), -N(R 14 )C(O)OR 12 , -N(R 14 )S(O) 2 R 15 , -C(O)R 15 , -S(O)R 15 , - OC(O)R 15 , -C(O)N(R 12 )(R 13 ),
• R 8 is C 1-6 alkyl, C 2 - 6 alkenyl, C 2-6 alkynyl, C 3-6 cycloalkyl, C 2-9 heterocycloalkyl, C 6-10 aryl, or C 1-9 heteroaryl substituted with one, two, or three R 20h .
• R 9 is hydrogen.
• R 9 is halogen. In some embodiments (e.g., including Formulae (I), (II), (III), (IV); or sub-formulae thereof), R 9 is -CN. In some embodiments (e.g., including Formulae (I), (II), (III), (IV); or sub-formulae thereof), R 9 is C 1-6 alkyl, C 2- 6 alkenyl, C 2-6 alkynyl, C 3-6 cycloalkyl, C 2-9 heterocycloalkyl, C 6-10 aryl, C 1-9 heteroaryl.
• R 9 is -OR 12 , -SR 12 , -N(R 12 )(R 13 ), -C(O)OR 12 , - OC(O)N(R 12 )(R 13 ), -N(R 14 )C(O)N(R 12 )(R 13 ), -N(R 14 )C(O)OR 12 , -N(R 14 )S(O) 2 R 15 , -C(O)R 15 , -S(O)R 15 , -OC(O)R 15 , - C(O)N(R 12 )(R 13 ), -C(O)C(O)N(R 12 )(R 13 ), -N(R 14 )C(O)R 15 , -S(O) 2 R 15 , -S(O) 2 N(R 12 )
• R 9 is C 1-6 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C3- 6 cycloalkyl, C 2-9 heterocycloalkyl, C 6-10 aryl, or C 1-9 heteroaryl substituted with one, two, or three R 20i .
• R 9a is hydrogen.
• R 9a is halogen. In some embodiments (e.g., including Formulae (I), (II), (III), (IV); or sub-formulae thereof), R 9a is -CN. In some embodiments (e.g., including Formulae (I), (II), (III), (IV); or sub-formulae thereof), R 9a is C 1-6 alkyl, C 2 - 6 alkenyl, C 2-6 alkynyl, C 3-6 cycloalkyl, C 2-9 heterocycloalkyl, C 6-10 aryl, C 1-9 heteroaryl.
• R 9a is -OR 12 , -SR 12 , -N(R 12 )(R 13 ), -C(O)OR 12 , - OC(O)N(R 12 )(R 13 ), -N(R 14 )C(O)N(R 12 )(R 13 ), -N(R 14 )C(O)OR 12 , -N(R 14 )S(O) 2 R 15 , -C(O)R 15 , -S(O)R 15 , -OC(O)R 15 , - C(O)N(R 12 )(R 13 ), -C(O)C(O)N(R 12 )(R 13 ), -N(R 14 )C(O)R 15 , -S(O) 2 R 15 , -S(O) 2 N(R 12 , -SR 12 , -N(R 12 )(R 13 ), -C(O)OR 12 , - OC
• R 9a is C 1-6 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 3- 6 cycloalkyl, C 2-9 heterocycloalkyl, C 6-10 aryl, or C 1-9 heteroaryl substituted with one, two, or three R 20i .
• R 9 and R 9a are combined to form a C 3-6 cycloalkyl.
• R 9 and R 9a are combined to form a C 2-9 heterocycloalkyl. In some embodiments (e.g., including Formulae (I), (II), (III), (IV); or sub-formulae thereof), R 9 and R 9a are combined to form a C 3-6 cycloalkyl substituted with one, two, or three R 20i .
• R 9 and R 9a are combined to form a C 2-9 heterocycloalkyl substituted with one, two, or three R 20i .
• R 9 and R 9a are hydrogen.
• R 10 is hydrogen.
• R 10 is halogen. In some embodiments (e.g., including Formulae (I), (II), (III), (IV); or sub-formulae thereof), R 10 is -CN. In some embodiments (e.g., including Formulae (I), (II), (III), (IV); or sub-formulae thereof), R 10 is C 1-6 alkyl, C 2 - 6 alkenyl, C 2-6 alkynyl, C 3-6 cycloalkyl, C 2-9 heterocycloalkyl, C 6-10 aryl, C 1-9 heteroaryl.
• R 10 is -R 16 . In some embodiments (e.g., including Formulae (I), (II), (III), (IV); or sub-formulae thereof), R 10 is -OR 16 . In some embodiments (e.g., including Formulae (I), (II), (III), (IV); or sub-formulae thereof), R 10 is -N(R 12 )(R 16 ).
• R 10 is -OR 12 , -SR 12 , -N(R 12 )(R 13 ), -C(O)OR 12 , - OC(O)N(R 12 )(R 13 ), -N(R 14 )C(O)N(R 12 )(R 13 ), -N(R 14 )C(O)OR 12 , -N(R 14 )S(O) 2 R 15 , -C(O)R 15 , -S(O)R 15 , -OC(O)R 15 , - C(O)N(R 12 )(R 13 ), -C(O)C(O)N(R 12 )(R 13 ), -N(R 14 )C(O)R 15 , -S(O) 2 R 15 , -S(O) 2 N(R 12 )
• R 10 is C 1-6 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C3- 6 cycloalkyl, C 2-9 heterocycloalkyl, C 6-10 aryl, and C 1-9 heteroaryl substituted with one, two, or three R 20j .
• R 10a is hydrogen.
• R 10a is halogen. In some embodiments (e.g., including Formulae (I), (II), (III), (IV); or sub-formulae thereof), R 10a is -CN. In some embodiments (e.g., including Formulae (I), (II), (III), (IV); or sub-formulae thereof), R 10a is C 1-6 alkyl, C 2- 6 alkenyl, C 2-6 alkynyl, C 3-6 cycloalkyl, C 2-9 heterocycloalkyl, C 6-10 aryl, C 1-9 heteroaryl.
• R 10a is -R 16 . In some embodiments (e.g., including Formulae (I), (II), (III), (IV); or sub-formulae thereof), R 10a is -OR 16 . In some embodiments (e.g., including Formulae (I), (II), (III), (IV); or sub-formulae thereof), R 10a is -N(R 12 )(R 16 ).
• R 10a is -OR 12 , -SR 12 , -N(R 12 )(R 13 ), -C(O)OR 12 , - OC(O)N(R 12 )(R 13 ), -N(R 14 )C(O)N(R 12 )(R 13 ), -N(R 14 )C(O)OR 12 , -N(R 14 )S(O) 2 R 15 , -C(O)R 15 , -S(O)R 15 , -OC(O)R 15 , - C(O)N(R 12 )(R 13 ), -C(O)C(O)N(R 12 )(R 13 ), -N(R 14 )C(O)R 15 , -S(O) 2 R 15 , -S(O) 2 N(R 12 , -SR 12 , -N(R 12 )(R 13 ), -C(O)OR 12 , - OC
• R 10a is C 1-6 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 3- 6 cycloalkyl, C 2-9 heterocycloalkyl, C 6-10 aryl, and C 1-9 heteroaryl substituted with one, two, or three R 20j .
• R 10 and R 10a are combined to form a C 3-6 cycloalkyl.
• R 10 and R 10a are combined to form a C 2-9 heterocycloalkyl. In some embodiments (e.g., including Formulae (I), (II), (III), (IV); or sub-formulae thereof), R 10 and R 10a are combined to form a C 3-6 cycloalkyl substituted with one, two, or three R 20j .
• R 10 and R 10a are combined to form a C 2-9 heterocycloalkyl substituted with one, two, or three R 20j .
• R 10 and R 10a are combined to form a C 2-9 heterocycloalkyl substituted with one, two, or three R 20j .
• J 1 is N.
• J 1 is C.
• J 1 is C(R 8 ).
• J 2 is N.
• J 2 is N(R 9 ).
• J 2 is C(R 9 ).
• J 2 is C(H). In some embodiments (e.g., including Formulae (I), (II), (III), (IV); or sub-formulae thereof), J 2 is C(R 9 )(R 9a ). In some embodiments (e.g., including Formulae (I), (II), (III), (IV); or sub-formulae thereof), J 2 is CH 2 . In some embodiments (e.g., including Formulae (I), (II), (III), (IV); or sub-formulae thereof), J 2 is C(O).
• J 3 is N(R 10 ). In some embodiments (e.g., including Formulae (I), (II), (III), (IV); or sub-formulae thereof), J 3 is C(R 10 )(R 10a ). In some embodiments (e.g., including Formulae (I), (II), (III), (IV); or sub-formulae thereof), J 3 is NH.
• J 3 is CH 2 and R 6 is selected from hydrogen, halogen, -CN, C 1-6 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 3-6 cycloalkyl, C 2-9 heterocycloalkyl, C 6-10 aryl, C 1 - 9 heteroaryl, -OR 16 , -N(R 12 )(R 16 ), -OR 12a , -SR 12 , -N(R 12 )(R 13 ), -C(O)OR 12 , -OC(O)N(R 12 )(R 13 ), - N(R 14 )C(O)N(R 12 )(R 13 ), -N(R 14 )C(O)OR 12 , -N(R 14 )S(O) 2 R 15 , -C(O)R 15 , -S(
• J 3 is CH 2 and R 6 is selected from hydrogen, halogen, -CN, C 1-6 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 3-6 cycloalkyl, C 2-9 heterocycloalkyl, C 6-10 aryl, C 1-9 heteroaryl, -OR 16 , -N(R 12 )(R 16 ), -SR 12 , -N(R 12 )(R 13 ), -C(O)OR 12 , -OC(O)N(R 12 )(R 13 ), - N(R 14 )C(O)N(R 12 )(R 13 ), -N(R 14 )C(O)OR 12 , -N(R 14 )S(O) 2 R 15 , -C(O)R 15 , -S(O)R 15 , -OC(O)R 15 ,
• J 3 is CH 2 and R 6 is -OR 16 . In some embodiments of (e.g., of Formulae (I)), or sub-formulae thereof, J 3 is CH 2 and R 6 is - N(R 12 )(R 16 ). [004 9 7] In some embodiments (e.g., including Formulae (I), (II), (III), (IV); or sub-formulae thereof), J 1 is N and J 2 is C(R 9 )(R 9a ).
• J 1 is C(R 8 ) and J 2 is C(R 9 )(R 9a ).
• J 1 is C and J 2 is C(R 9 ).
• J 1 is N and J 2 is C(R 9 )(R 9a ).
• J 1 is C(R 8 ) and J 2 is C(R 9 )(R 9a ). In some embodiments (e.g., including Formulae (I), (II), (III), (IV); or sub-formulae thereof), J 1 is C and J 2 is C(R 9 ).
• R 9 is hydrogen, -CN, C 1-6 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 3-6 cycloalkyl, C 2- 9 heterocycloalkyl, C 6-10 aryl, C 1-9 heteroaryl, -OR 12 , -C(O)OR 12 , -OC(O)N(R 12 )(R 13 ), -C(O)R 15 , -OC(O)R 15 , - C(O)N(R 12 )(R 13 ), -C(O)C(O)N(R 12 )(R 13 ), -CH 2 C(O)N(R 12 )(R 13 ), -CH 2 N(R 14 )C(O)R 15 , -CH 2 S(O) 2 R 15 , and - CH 2 S(O) 2 N(R 12 )(R 13 ), wherein C 1-6 alkyl, C 2-6 alkenyl, C 2-6 alkynyl
• R 9 is hydrogen, - CN, C 1-6 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 3-6 cycloalkyl, C 2-9 heterocycloalkyl, C 6-10 aryl, C 1-9 heteroaryl, -C(O)OR 12 , - C(O)R 15 , -C(O)N(R 12 )(R 13 ), -C(O)C(O)N(R 12 )(R 13 ), -CH 2 C(O)N(R 12 )(R 13 ), -CH 2 N(R 14 )C(O)R 15 , -CH 2 S(O) 2 R 15 , and -CH 2 S(O) 2 N(R 12 )(R 13 ), wherein C 1-6 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 3-6 cycloalkyl, C 2-9 heterocycloalkyl, C 6-10 aryl, wherein C
• R 9 is hydrogen, -CN, C 1-6 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 3-6 cycloalkyl, C 2-9 heterocycloalkyl, C 6-10 aryl, C 1 - 9 heteroaryl, -OR 12 , -C(O)OR 12 , -OC(O)N(R 12 )(R 13 ), -C(O)R 15 , -OC(O)R 15 , -C(O)N(R 12 )(R 13 ), - C(O)C(O)N(R 12 )(R 13 ), -CH 2 C(O)N(R 12 )(R 13 ), -CH 2 N(R 14 )C(O)R 15 , -CH 2 S(O) 2 R 15 , and -CH 2 S(O) 2 N(R 12 )(R 13 ), wherein C 1-6 alkyl,
• R 9 is hydrogen, -CN, C 1-6 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 3-6 cycloalkyl, C 2-9 heterocycloalkyl, C 6-10 aryl, C 1-9 heteroaryl, -C(O)OR 12 , - C(O)R 15 , -C(O)N(R 12 )(R 13 ), -C(O)C(O)N(R 12 )(R 13 ), -CH 2 C(O)N(R 12 )(R 13 ), -CH 2 N(R 14 )C(O)R 15 , -CH 2 S(O) 2 R 15 , and -CH 2 S(O) 2 N(R 12 )(R 13 ), wherein C 1-6 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 3-6 cycloalkyl, C 2-9 heterocycloalkyl, C 6-10 aryl, C 1-9 heteroary
• R 10 is hydrogen, -CN, C 1-6 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 3-6 cycloalkyl, C 2 - 9 heterocycloalkyl, C 6-10 aryl, C 1-9 heteroaryl, -OR 12 , -C(O)OR 12 , -OC(O)N(R 12 )(R 13 ), -C(O)R 15 , -OC(O)R 15 , - C(O)N(R 12 )(R 13 ), -C(O)C(O)N(R 12 )(R 13 ), -CH 2 C(O)N(R 12 )(R 13 ), -CH 2 N(R 14 )C(O)R 15 , -CH 2 S(O) 2 R 15 , and - CH 2 S(O) 2 N(R 12 )(R 13 ), wherein C 1-6 alkyl, C 2-6 alkenyl, C 2-6 alkyn
• R 10 is hydrogen, - CN, C 1-6 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 3-6 cycloalkyl, C 2-9 heterocycloalkyl, C 6-10 aryl, C 1-9 heteroaryl, -C(O)OR 12 , - C(O)R 15 , -C(O)N(R 12 )(R 13 ), -C(O)C(O)N(R 12 )(R 13 ), -CH 2 C(O)N(R 12 )(R 13 ), -CH 2 N(R 14 )C(O)R 15 , -CH 2 S(O) 2 R 15 , and -CH 2 S(O) 2 N(R 12 )(R 13 ), wherein C 1-6 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 3-6 cycloalkyl, C 2-9 heterocycloalkyl, C 6-10 aryl, wherein C
• R 10 is hydrogen, -CN, C 1-6 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 3-6 cycloalkyl, C 2-9 heterocycloalkyl, C 6-10 aryl, C 1- 9 heteroaryl, -OR 12 , -C(O)OR 12 , -OC(O)N(R 12 )(R 13 ), -C(O)R 15 , -OC(O)R 15 , -C(O)N(R 12 )(R 13 ), - C(O)C(O)N(R 12 )(R 13 ), -CH 2 C(O)N(R 12 )(R 13 ), -CH 2 N(R 14 )C(O)R 15 , -CH 2 S(O) 2 R 15 , and -CH 2 S(O) 2 N(R 12 )(R 13 ), wherein C 1-6 alkyl, C 2-6 alkenyl, C 2-6 alkynyl
• R 10 is hydrogen, -CN, C 1-6 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 3-6 cycloalkyl, C 2-9 heterocycloalkyl, C 6-10 aryl, C 1-9 heteroaryl, -C(O)OR 12 , - C(O)R 15 , -C(O)N(R 12 )(R 13 ), -C(O)C(O)N(R 12 )(R 13 ), -CH 2 C(O)N(R 12 )(R 13 ), -CH 2 N(R 14 )C(O)R 15 , -CH 2 S(O) 2 R 15 , and -CH 2 S(O) 2 N(R 12 )(R 13 ), wherein C 1-6 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 3-6 cycloalkyl, C 2-9 heterocycloalkyl, C 6-10 aryl, C 1-9 heteroary
• W 1 is N. In some embodiments (e.g., including Formulae (I), (II), (III), (IV); or sub-formulae thereof), W 1 is N(R 1 ). In some embodiments (e.g., including Formulae (I), (II), (III), (IV); or sub-formulae thereof), W 1 is O. In some embodiments (e.g., including Formulae (I), (II), (III), (IV); or sub-formulae thereof), W 1 is C(R 1 ).
• W 1 is C(R 1 )(R 1a ). In some embodiments (e.g., including Formulae (I), (II), (III), (IV); or sub-formulae thereof), W 1 is C(O). In some embodiments (e.g., including Formulae (I), (II), (III), (IV); or sub-formulae thereof), W 1 is S(O). In some embodiments (e.g., including Formulae (I), (II), (III), (IV); or sub-formulae thereof), W 1 is S(O) 2 .
• W 1 is S(O)(NR 1 ). In some embodiments (e.g., including Formulae (I), (II), (III), (IV); or sub-formulae thereof), W 1 is S(O)(R 1 ). In some embodiments (e.g., including Formulae (I), (II), (III), (IV); or sub-formulae thereof), W 1 is P(O)(R 1 ). [00501] In some embodiments (e.g., including Formulae (I), (II), (III), (IV); or sub-formulae thereof), R 1 is hydrogen.
• R 1 is halogen. In some embodiments (e.g., including Formulae (I), (II), (III), (IV); or sub-formulae thereof), R 1 is -CN. In some embodiments (e.g., including Formulae (I), (II), (III), (IV); or sub-formulae thereof), R 1 is C 1-6 alkyl, C 2 - 6 alkenyl, C 2-6 alkynyl, C 3-6 cycloalkyl, C 2-9 heterocycloalkyl, C 6-10 aryl, C 1-9 heteroaryl.
• R 1 is -OR 12 , -SR 12 , -N(R 12 )(R 13 ), -C(O)OR 12 , - OC(O)N(R 12 )(R 13 ), -N(R 14 )C(O)N(R 12 )(R 13 ), -N(R 14 )C(O)OR 12 , -N(R 14 )S(O) 2 R 15 , -C(O)R 15 , -S(O)R 15 , -OC(O)R 15 , - C(O)N(R 12 )(R 13 ), -C(O)C(O)N(R 12 )(R 13 ), -N(R 14 )C(O)R 15 , -S(O) 2 R 15 , -S(O) 2 N(R 12 )
• R 1 is C 1-6 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C3- 6 cycloalkyl, C 2-9 heterocycloalkyl, C 6-10 aryl, and C 1-9 heteroaryl substituted with one, two, or three R 20a .
• R 1 is hydrogen, -CN, C 1-6 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 3-6 cycloalkyl, C 2- 9 heterocycloalkyl, C 6-10 aryl, C 1-9 heteroaryl, -OR 12 , -C(O)OR 12 , -OC(O)N(R 12 )(R 13 ), -C(O)R 15 , -OC(O)R 15 , - C(O)N(R 12 )(R 13 ), -C(O)C(O)N(R 12 )(R 13 ), -CH 2 C(O)N(R 12 )(R 13 ), -CH 2 N(R 14 )C(O)R 15 , -CH 2 S(O) 2 R 15 , and - CH 2 S(O) 2 N(R 12 )(R 13 ), wherein C 1-6 alkyl, C 2-6 alkenyl, C 2-6 alkynyl
• R 1 is hydrogen, - CN, C 1-6 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 3-6 cycloalkyl, C 2-9 heterocycloalkyl, C 6-10 aryl, C 1-9 heteroaryl, -C(O)OR 12 , - C(O)R 15 , -C(O)N(R 12 )(R 13 ), -C(O)C(O)N(R 12 )(R 13 ), -CH 2 C(O)N(R 12 )(R 13 ), -CH 2 N(R 14 )C(O)R 15 , -CH 2 S(O) 2 R 15 , and -CH 2 S(O) 2 N(R 12 )(R 13 ), wherein C 1-6 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 3-6 cycloalkyl, C 2-9 heterocycloalkyl, C 6-10 aryl, wherein C
• R 1 is hydrogen, -CN, C 1-6 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 3-6 cycloalkyl, C 2 - 9 heterocycloalkyl, C 6-10 aryl, C 1-9 heteroaryl, -OR 12 , -C(O)OR 12 , -OC(O)N(R 12 )(R 13 ), -C(O)R 15 , -OC(O)R 15 , - C(O)N(R 12 )(R 13 ), -C(O)C(O)N(R 12 )(R 13 ), -CH 2 C(O)N(R 12 )(R 13 ), -CH 2 N(R 14 )C(O)R 15 , -CH 2 S(O) 2 R 15 , and
• R 1 is hydrogen, -CN, C 1-6 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 3-6 cycloalkyl, C 2 - 9 heterocycloalkyl, C 6-10 aryl, C 1-9 heteroaryl, -C(O)OR 12 , -C(O)R 15 , -C(O)N(R 12 )(R 13 ), -C(O)C(O)N(R 12 )(R 13 ), - CH 2 C(O)N(R 12 )(R 13 ), -CH 2 N(R 14 )C(O)R 15 , -CH 2 S(O) 2 R 15 , and -CH 2 S(O) 2 N(R 12 )(R 13 ), wherein C 1-6 alkyl, C 2- 6 alkenyl, C 2-6 alkynyl, C 3-6 cycloalkyl, C 2 - 9 heterocycloalkyl, C 6-10 aryl, C
• R 1 is -CN. In some embodiments, R 1 is -F. In some embodiments, R 1 is -CF 3 . In some embodiments, R 1 is -OCH 3 . In some embodiments, R 1 is cyclopropyl. In some embodiments, R 1 is -OCH 2 CF 3 . In some embodiments, R 1 is -CH 3 . [00503] In some embodiments (e.g., including Formulae (I), (II), (III), (IV); or sub-formulae thereof), R 1a is hydrogen. In some embodiments (e.g., including Formulae (I), (II), (III), (IV); or sub-formulae thereof), R 1a is halogen.
• R 1a is -CN. In some embodiments (e.g., including Formulae (I), (II), (III), (IV); or sub-formulae thereof), R 1a is C 1-6 alkyl, C 2- 6 alkenyl, C 2-6 alkynyl, C 3-6 cycloalkyl, C 2-9 heterocycloalkyl, C 6-10 aryl, C 1-9 heteroaryl.
• R 1a is -OR 12 , -SR 12 , -N(R 12 )(R 13 ), -C(O)OR 12 , - OC(O)N(R 12 )(R 13 ), -N(R 14 )C(O)N(R 12 )(R 13 ), -N(R 14 )C(O)OR 12 , -N(R 14 )S(O) 2 R 15 , -C(O)R 15 , -S(O)R 15 , -OC(O)R 15 , - C(O)N(R 12 )(R 13 ), -C(O)C(O)N(R 12 )(R 13 ), -N(R 14 )C(O)R 15 , -S(O) 2 R 15 , -S(O) 2 N(R 12 , -SR 12 , -N(R 12 )(R 13 ), -C(O)OR 12 , - OC
• R 1a is C 1-6 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C3- 6 cycloalkyl, C 2-9 heterocycloalkyl, C 6-10 aryl, and C 1-9 heteroaryl substituted with one, two, or three R 20a .
• R 1 and R 1a are combined to form a C 3-6 cycloalkyl.
• R 1 and R 1a are combined to form a C 2-9 heterocycloalkyl. In some embodiments (e.g., including Formulae (I), (II), (III), (IV); or sub-formulae thereof), R 1 and R 1a are combined to form a C 3-6 cycloalkyl substituted with one, two, or three R 20a .
• R 1 and R 1a are combined to form a C 2-9 heterocycloalkyl substituted with one, two, or three R 20a .
• W 2 is N.
• W 2 is N(R 2 ).
• W 2 is O. In some embodiments (e.g., including Formulae (I), (II), (III), (IV); or sub-formulae thereof), W 2 is C(R 2 ). In some embodiments (e.g., including Formulae (I), (II), (III), (IV); or sub-formulae thereof), W 2 is C(R 2 )(R 2a ). In some embodiments (e.g., including Formulae (I), (II), (III), (IV); or sub-formulae thereof), W 2 is C(O).
• W 2 is S(O). In some embodiments (e.g., including Formulae (I), (II), (III), (IV); or sub-formulae thereof), W 2 is S(O) 2 . In some embodiments (e.g., including Formulae (I), (II), (III), (IV); or sub-formulae thereof), W 2 is S(O)(NR 2 ). In some embodiments (e.g., including Formulae (I), (II), (III), (IV); or sub-formulae thereof), W 2 is S(O)(R 2 ).
• W 2 is P(O)(R 2 ).
• R 2 is independently hydrogen.
• R 2 is independently halogen.
• R 2 is independently -CN.
• R 2 is independently C 1-6 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 3-6 cycloalkyl, C 2-9 heterocycloalkyl, C 6-10 aryl, or C 1-9 heteroaryl.
• R 2 is independently -OR 12 .
• R 2 is independently -SR 12 .
• R 2 is independently -N(R 12 )(R 13 ). In some embodiments, R 2 is independently -C(O)OR 12 . In some embodiments, R 2 is independently - OC(O)N(R 12 )(R 13 ). In some embodiments, R 2 is independently -N(R 14 )C(O)N(R 12 )(R 13 ). In some embodiments, R 2 is independently -N(R 14 )C(O)OR 12 . In some embodiments, R 2 is independently -N(R 14 )S(O) 2 R 15 . In some embodiments, R 2 is independently -C(O)R 15 . In some embodiments, R 2 is independently -S(O)R 15 .
• R 2 is independently -CH 2 C(O)N(R 12 )(R 13 ). In some embodiments, R 2 is independently -CH 2 N(R 14 )C(O)R 15 . In some embodiments, R 2 is independently -CH 2 S(O) 2 R 15 . In some embodiments, R 2 is independently - CH 2 S(O) 2 N(R 12 )(R 13 ). In some embodiments, R 2 is independently C 1-6 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C3- 6 cycloalkyl, C 2-9 heterocycloalkyl, C 6-10 aryl, and C 1-9 heteroaryl substituted with one, two, or three R 20b .
• R 2 is independently C 1-6 alkyl substituted with one, two, or three R 20b . In some embodiments, R 2 is independently C 2-6 alkenyl substituted with one, two, or three R 20b . In some embodiments, R 2 is independently C 2 - 6 alkynyl substituted with one, two, or three R 20b . In some embodiments, R 2 is independently C 3-6 cycloalkyl substituted with one, two, or three R 20b . In some embodiments, R 2 is independently C 2-9 heterocycloalkyl substituted with one, two, or three R 20b . In some embodiments, R 2 is independently C 6-10 aryl substituted with one, two, or three R 20b .
• R 2 is independently C 1-9 heteroaryl substituted with one, two, or three R 20b .
• R 2 is independently C 1-6 alkyl.
• R 2 is independently C 2-6 alkenyl.
• R 2 is independently C 2-6 alkynyl.
• R 2 is independently C 3-6 cycloalkyl.
• R 2 is independently C 2-9 heterocycloalkyl.
• R 2 is independently C 6-10 aryl.
• R 2 is independently C 1-9 heteroaryl.
• R 2 is independently C 1 alkyl. In some embodiments, R 2 is independently C 2 alkyl.
• R 2 is independently C3alkyl. In some embodiments, R 2 is independently C 4 alkyl. In some embodiments, R 2 is independently C 5 alkyl. In some embodiments, R 2 is independently C 6 alkyl. [00507] In some embodiments, R 2 is independently -OH. In some embodiments, R 2 is independently -SH. In some embodiments, R 2 is independently -NH 2 . In some embodiments, R 2 is independently -C(O)OH. In some embodiments, R 2 is independently -OC(O)NH 2 . In some embodiments, R 2 is independently -NHC(O)NH 2 . In some embodiments, R 2 is independently -NHC(O)OH.
• R 2 is independently -NHS(O) 2 R 15 . In some embodiments, R 2 is independently -C(O)R 15 . In some embodiments, R 2 is independently -S(O)R 15 . In some embodiments, R 2 is independently -OC(O)R 15 . In some embodiments, R 2 is independently -OC(O)CH 3 . In some embodiments, R 2 is independently -C(O)NH 2 . In some embodiments, R 2 is independently -C(O)C(O)NH 2 . In some embodiments, R 2 is independently -NHC(O)R 15 . In some embodiments, R 2 is independently -S(O) 2 R 15 .
• R 2 is independently -CH 2 S(O) 2 NH(R 12 ).
• R 2 is hydrogen, -CN, C 1-6 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 3-6 cycloalkyl, C 2- 9 heterocycloalkyl, C 6-10 aryl, C 1-9 heteroaryl, -OR 12 , -C(O)OR 12 , -OC(O)N(R 12 )(R 13 ), -C(O)R 15 , -OC(O)R 15 , - C(O)N(R 12 )(R 13 ), -C(O)C(O)N(R 12 )(R 13 ), -CH 2 C(O)N(R 12 )(R 13 ), -CH 2 N(R 14 )C(O)R 15 , -CH 2 S(O) 2 R 15 , and - CH 2 S(O) 2 N(
• R 2 is hydrogen, - CN, C 1-6 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 3-6 cycloalkyl, C 2-9 heterocycloalkyl, C 6-10 aryl, C 1-9 heteroaryl, -C(O)OR 12 , - C(O)R 15 , -C(O)N(R 12 )(R 13 ), -C(O)C(O)N(R 12 )(R 13 ), -CH 2 C(O)N(R 12 )(R 13 ), -CH 2 N(R 14 )C(O)R 15 , -CH 2 S(O) 2 R 15 , and -CH 2 S(O) 2 N(R 12 )(R 13 ), wherein C 1-6 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 3-6 cycloalkyl, C 2-9 heterocycloalkyl, C 6-10 aryl, wherein C
• R 2 is hydrogen, -CN, C 1-6 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 3-6 cycloalkyl, C 2- 9 heterocycloalkyl, C 6-10 aryl, C 1-9 heteroaryl, -OR 12 , -C(O)OR 12 , -OC(O)N(R 12 )(R 13 ), -C(O)R 15 , -OC(O)R 15 , - C(O)N(R 12 )(R 13 ), -C(O)C(O)N(R 12 )(R 13 ), -CH 2 C(O)N(R 12 )(R 13 ), -CH 2 N(R 14 )C(O)R 15 , -CH 2 S(O) 2 R 15 , and - CH
• R 2 is hydrogen, -CN, C 1-6 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 3-6 cycloalkyl, C 2 - 9 heterocycloalkyl, C 6-10 aryl, C 1-9 heteroaryl, -C(O)OR 12 , -C(O)R 15 , -C(O)N(R 12 )(R 13 ), -C(O)C(O)N(R 12 )(R 13 ), - CH 2 C(O)N(R 12 )(R 13 ), -CH 2 N(R 14 )C(O)R 15 , -CH 2 S(O) 2 R 15 , and -CH 2 S(O) 2 N(R 12 )(R 13 ), wherein C 1-6 alkyl, C 2- 6 alkenyl, C 2-6 alkynyl, C 3-6 cycloalkyl, C 2 - 9 heterocycloalkyl, C 6-10 aryl, C
• R 2a is independently hydrogen. In some embodiments, R 2a is independently halogen. In some embodiments, R 2a is independently -CN. In some embodiments, R 2a is independently C 1-6 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 3-6 cycloalkyl, C 2-9 heterocycloalkyl, C 6-10 aryl, or C 1-9 heteroaryl. In some embodiments, R 2a is independently -OR 12 . In some embodiments, R 2a is independently -SR 12 . In some embodiments, R 2a is independently -N(R 12 )(R 13 ). In some embodiments, R 2a is independently -C(O)OR 12 .
• R 2a is independently -OC(O)N(R 12 )(R 13 ). In some embodiments, R 2a is independently -N(R 14 )C(O)N(R 12 )(R 13 ). In some embodiments, R 2a is independently -N(R 14 )C(O)OR 12 . In some embodiments, R 2a is independently -N(R 14 )S(O) 2 R 15 . In some embodiments, R 2a is independently -C(O)R 15 . In some embodiments, R 2a is independently -S(O)R 15 . In some embodiments, R 2a is independently -OC(O)R 15 .
• R 2a is independently -CH 2 C(O)N(R 12 )(R 13 ). In some embodiments, R 2a is independently -CH 2 N(R 14 )C(O)R 15 . In some embodiments, R 2a is independently -CH 2 S(O) 2 R 15 . In some embodiments, R 2a is independently - CH 2 S(O) 2 N(R 12 )(R 13 ). In some embodiments, R 2a is independently C 1-6 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 3- 6 cycloalkyl, C 2-9 heterocycloalkyl, C 6-10 aryl, and C 1-9 heteroaryl substituted with one, two, or three R 20b .
• R 2a is independently C 1-6 alkyl substituted with one, two, or three R 20b . In some embodiments, R 2a is independently C 2-6 alkenyl substituted with one, two, or three R 20b . In some embodiments, R 2a is independently C 2- 6 alkynyl substituted with one, two, or three R 20b . In some embodiments, R 2a is independently C 3-6 cycloalkyl substituted with one, two, or three R 20b . In some embodiments, R 2a is independently C 2-9 heterocycloalkyl substituted with one, two, or three R 20b . In some embodiments, R 2a is independently C 6-10 aryl substituted with one, two, or three R 20b .
• R 2a is independently C 1-9 heteroaryl substituted with one, two, or three R 20b .
• R 2a is independently C 1-6 alkyl.
• R 2a is independently C 2-6 alkenyl.
• R 2a is independently C 2-6 alkynyl.
• R 2a is independently C 3-6 cycloalkyl.
• R 2a is independently C 2-9 heterocycloalkyl.
• R 2a is independently C 6 - 10aryl.
• R 2a is independently C 1-9 heteroaryl.
• R 2a is independently -OH.
• R 2a is independently -SH.
• R 2a is independently -NH 2 . In some embodiments, R 2a is independently -C(O)OH. In some embodiments, R 2a is independently -OC(O)NH 2 . In some embodiments, R 2a is independently -NHC(O)NH 2 . In some embodiments, R 2a is independently -NHC(O)OH. In some embodiments, R 2a is independently -NHS(O) 2 R 15 . In some embodiments, R 2a is independently -C(O)R 15 . In some embodiments, R 2a is independently -S(O)R 15 . In some embodiments, R 2a is independently -OC(O)R 15 .
• R 2a is independently -CH 2 S(O) 2 R 15 . In some embodiments, R 2a is independently -CH 2 S(O) 2 NH 2 . [00512] In some embodiments, R 2a is independently -NH(R 12 ). In some embodiments, R 2a is independently - OC(O)N(R 12 )(R 13 ). In some embodiments, R 2a is independently -NHC(O)N(R 12 ). In some embodiments, R 2a is independently -NHC(O)OR 12 . In some embodiments, R 2a is independently -C(O)N(R 12 )(R 13 ) .
• R 2 and R 2a are combined to form a C3- 6 cycloalkyl substituted with one, two, or three R 20b . In some embodiments, R 2 and R 2a are combined to form a C 2 - 9 heterocycloalkyl substituted with one, two, or three R 20b . In some embodiments, R 2 and R 2a are combined to form a C 3 cycloalkyl. In some embodiments, R 2 and R 2a are combined to form a C 4 cycloalkyl. In some embodiments, R 2 and R 2a are combined to form a C 5 cycloalkyl. In some embodiments, R 2 and R 2a are combined to form a C 6 cycloalkyl.
• R 2 and R 2a are combined to form a C 2 heterocycloalkyl. In some embodiments, R 2 and R 2a are combined to form a C3 heterocycloalkyl. In some embodiments, R 2 and R 2a are combined to form a C 4 heterocycloalkyl. In some embodiments, R 2 and R 2a are combined to form a C 5 heterocycloalkyl. In some embodiments, R 2 and R 2a are combined to form a C 6 heterocycloalkyl. In some embodiments, R 2 and R 2a are combined to form a C7 heterocycloalkyl. In some embodiments, R 2 and R 2a are combined to form a C8 heterocycloalkyl.
• R 2 and R 2a are combined to form a C9 heterocycloalkyl.
• R 2 and R 2a are combined to form a C 3 heterocycloalkyl substituted with one, two, or three R 20b .
• R 2 and R 2a are combined to form a C 4 heterocycloalkyl substituted with one, two, or three R 20b .
• R 2 and R 2a are combined to form a C5 heterocycloalkyl substituted with one, two, or three R 20b .
• R 2 and R 2a are combined to form a C 6 heterocycloalkyl substituted with one, two, or three R 20b .
• R 2 and R 2a are combined to form a C 7 heterocycloalkyl substituted with one, two, or three R 20b . In some embodiments, R 2 and R 2a are combined to form a C 8 heterocycloalkyl substituted with one, two, or three R 20b . In some embodiments, R 2 and R 2a are combined to form a C9 heterocycloalkyl substituted with one, two, or three R 20b .
• R 2 is selected from hydrogen, halogen, C 1-6 alkyl, C 2-9 heterocycloalkyl, C 1- 9 heteroaryl, -OR 12 , -SR 12 , -N(R 12 )(R 13 ), -C(O)R 15 , -C(O)N(R 12 )(R 13 ), -S(O) 2 R 15 , and -S(O) 2 N(R 12 )(R 13 )-, wherein C 1- 6 alkyl, C 2-9 heterocycloalkyl, and C 1-9 heteroaryl are optionally substituted with one, two, or three R 20b .
• R 2 is selected from C 1-6 alkyl, C 2-9 heterocycloalkyl, C 1-9 heteroaryl, -OR 12 , - N(R 12 )(R 13 ), -C(O)R 15 , -C(O)N(R 12 )(R 13 ), wherein C 1-6 alkyl, C 2-9 heterocycloalkyl, and C 1-9 heteroaryl are optionally substituted with one, two, or three R 20b .
• R 2 is -OR 12 .
• R 2 is -N(R 12 )(R 13 ).
• R 2 is -C(O)R 15 .
• R 2 is -C(O)N(R 12 )(R 13 ). In some embodiments, R 2 is -OR 12 . In some embodiments, R 2 is -NH(R 12 ). In some embodiments, R 2 is -C(O)R 15 . In some embodiments, R 2 is -C(O)NH(R 12 ). In some embodiments, R 12 is C 1 -C 6 alkyl. In some embodiments, R 12 is C 1 -C 6 alkyl substituted with one R 20k . In some embodiments, R 12 is C 1 alkyl substituted with one R 20k . In some embodiments, R 12 is C 2 alkyl substituted with one R 20k .
• R 12 is C3alkyl substituted with one R 20k . In some embodiments, R 12 is C4alkyl substituted with one R 20k . In some embodiments, R 12 is C 5 alkyl substituted with one R 20k . In some embodiments, R 12 is C 6 alkyl substituted with one R 20k . In some embodiments, R 12 is C 2-9 heterocycloalkyl substituted with one R 20k . In some embodiments, R 12 is C4heterocycloalkyl substituted with one R 20k . In some embodiments, R 12 is C3heterocycloalkyl substituted with one R 20k . In some embodiments, R 12 is C3heterocycloalkyl. In some embodiments, R 12 is C3heterocycloalkyl.
• R 12 is C 1 -C 6 alkyl substituted with two R 20k .
• R 15 is C 1 -C 6 alkyl.
• R 15 is C 1 -C 6 alkyl substituted with one R 20k .
• R 15 is C 1 alkyl substituted with one R 20k .
• R 15 is C 2 alkyl substituted with one R 20k .
• R 15 is C3alkyl substituted with one R 20k .
• R 15 is C4alkyl substituted with one R 20k .
• R 15 is C 5 alkyl substituted with one R 20k .
• R 15 is C 6 alkyl substituted with one R 20k . In some embodiments, R 15 is C 2-9 heterocycloalkyl substituted with one R 20k . In some embodiments, R 15 is C4heterocycloalkyl substituted with one R 20k . In some embodiments, R 15 is C3heterocycloalkyl substituted with one R 20k . In some embodiments, R 15 is C3heterocycloalkyl. In some embodiments, R 15 is C 1 -C 6 alkyl substituted with two R 20k . In some embodiments, R 20k is independently -NHS(O) 2 R 25 and R 25 is C 3-6 cycloalkyl.
• R 20k is independently -S(O) 2 R 25 and R 25 is C 1-6 alkyl. In some embodiments, R 20k is -OR 21 and R 21 is C 3-6 cycloalkyl. In some embodiments, R 20k is -CF 3 . In some embodiments, R 20k is -C(halogen) 3 . In some embodiments, R 20k is independently halogen. In some embodiments, R 20k is independently -F. In some embodiments, R 20k is independently C 3-6 cycloalkyl. In some embodiments, R 20k is -OR 21 and R 21 is C 1-6 alkyl. In some embodiments, R 20k is -CN. In some embodiments, R 20k is C 6-10 aryl.
• R 20k is phenyl. In some embodiments, R 20k is C 2-9 heterocycloalkyl. In some embodiments, R 20k is C 5 heterocycloalkyl. In some embodiments, R 20k is C5heterocycloalkyl substituted with C 1-6 alkyl. [00518] In some embodiments, R 2 is C 1-9 heteroaryl substituted with one R 20k . In some embodiments, R 2 is C 3 heteroaryl substituted with one R 20b . In some embodiments, R 2 is C 2-9 heterocycloalkyl. In some embodiments, R 2 is C 4 heterocycloalkyl. In some embodiments, R 2 is C 2-9 heterocycloalkyl substituted with one R 20b .
• R 2 is -N(R 14 )C(O)R 15 . In some embodiments, R 2 is C 2-6 alkynyl. In some embodiments, R 20b is independently -NHS(O) 2 R 25 and R 25 is C 3-6 cycloalkyl. In some embodiments, R 20b is independently -S(O) 2 R 25 and R 25 is C 1-6 alkyl. In some embodiments, R 20b is -OR 21 and R 21 is C 3-6 cycloalkyl. In some embodiments, R 20b is -CF 3 . In some embodiments, R 20b is -C(halogen) 3 . In some embodiments, R 20b is independently halogen.
• R 20b is independently -F. In some embodiments, R 20b is independently C 3-6 cycloalkyl. In some embodiments, R 20b is -OR 21 and R 21 is C 1-6 alkyl. In some embodiments, R 20b is -CN. In some embodiments, R 20b is C 6-10 aryl. In some embodiments, R 20b is phenyl. In some embodiments, R 20b is C 2-9 heterocycloalkyl. In some embodiments, R 20b is C 5 heterocycloalkyl. In some embodiments, R 20b is C 5 heterocycloalkyl substituted with C 1- 6 alkyl. In some embodiments, R 2 is C 1-6 alkyl substituted with one R 20b .
• R 20b is C 1 -C 6 alkyl. In some embodiments, R 20b is C 1 -C 6 alkyl substituted with C 1 -C 6 alkyl substituted with -NHS(O) 2 R 25 and R 25 is C3- 6 cycloalkyl. In some embodiments, R 20b is C 1 -C 6 alkyl substituted with C 2-9 heterocycloalkyl substituted with - S(O) 2 R 25 and R 25 is C 1-6 alkyl. In some embodiments, R 20b is C 1 -C 6 alkyl substituted with C 4 heterocycloalkyl substituted with -S(O) 2 R 25 and R 25 is C 1-6 alkyl.
• R 20b is C 1 -C 6 alkyl substituted with C3heterocycloalkyl substituted with -S(O) 2 R 25 and R 25 is C 1-6 alkyl. In some embodiments, R 20b is C 1 -C 6 alkyl substituted with C 3 heterocycloalkyl. In some embodiments, R 20b is C 1 -C 6 alkyl substituted with C 1 -C 6 alkyl substituted with two halogen. In some embodiments, R 20b is C 1 -C 6 alkyl substituted with C 1 -C 6 alkyl substituted with -OR 21 and R 21 is C 3-6 cycloalkyl.
• R 20b is C 1 -C 6 alkyl substituted with C 1 -C 6 alkyl substituted with -CF3. In some embodiments, R 20b is C 1 -C 6 alkyl substituted with C 1 -C 6 alkyl substituted with -C(halogen) 3 . In some embodiments, R 20b is C 1 -C 6 alkyl substituted with C 1 -C 6 alkyl substituted with halogen. In some embodiments, R 20b is C 1 -C 6 alkyl substituted with C 1 -C 6 alkyl substituted with -F.
• R 20b is C 1 -C 6 alkyl substituted with C 1 -C 6 alkyl substituted with C 3-6 cycloalkyl. In some embodiments, R 20b is C 1 -C 6 alkyl substituted with C 1 -C 6 alkyl substituted with -OR 21 and R 21 is C 1-6 alkyl. In some embodiments, R 20b is C 1 -C 6 alkyl substituted with C 1 -C 6 alkyl substituted with -CN. In some embodiments, R 20b is C 1 -C 6 alkyl substituted with C 1 -C 6 alkyl substituted with C 6-10 aryl.
• R 20b is C 1 -C 6 alkyl substituted with C 1 -C 6 alkyl substituted with phenyl. In some embodiments, R 20b is C 1 -C 6 alkyl substituted with C 1 -C 6 alkyl substituted with C 2-9 heterocycloalkyl. In some embodiments, R 20b is C 1 -C 6 alkyl substituted with C 1 -C 6 alkyl substituted with C5heterocycloalkyl. In some embodiments, R 20b is C 1 -C 6 alkyl substituted with C 1 -C 6 alkyl substituted with C 5 heterocycloalkyl substituted with C 1- 6 alkyl.
• R 2 is selected from -OR 12 , -N(R 12 )(R 13 ), -C(O)R 15 , and -C(O)N(R 12 )(R 13 );
• R 13 is hydrogen;
• R 26 is independently selected from halogen, oxo, -CN, C 1-6 alkyl, C 1-6 haloalkyl, C 1-6 alkoxy, C 1-6 haloalkoxy, -OR 21 , - SR 21 , -N(R 22 )(R 23 ), -C(O)OR 22 , -C(O)N(R 22 )(R 23 ), -C(O)C(O)N(R 22 )(R 23 ), -OC(O)N(R 22 )(R 23 ), - N(R 24 )C(O)N(R 22 )(R 23 ), -N(R 24 )C(O)OR 25 , -N(R
• R 26 is independently selected from -CN, C 1-6 alkyl, C 1- 6 haloalkyl, C 1-6 alkoxy, C 1-6 haloalkoxy, -C(O)OR 22 , -C(O)N(R 22 )(R 23 ), -C(O)C(O)N(R 22 )(R 23 ), and -C(O)R 25 .
• R 2 is selected from -OR 12 , -N(R 12 )(R 13 ), -C(O)R 15 , and -C(O)N(R 12 )(R 13 );
• R 13 is hydrogen;
• R 26 is independently selected from halogen, oxo, -CN, C 1-6 alkyl, C 1-6 haloalkyl, C 1-6 alkoxy, C 1-6 haloalkoxy, -OR 21 , - SR 21 , -N(R 22 )(R 23 ), -C(O)OR 22 , -C(O)N(R 22 )(R 23 ), -C(O)C(O)N(R 22 )(R 23 ), -OC(O)N(R 22 )(R 23 ), - N(R 24 )C(O)N(R 22 )(R 23 ), -N(R 24 )C(O)OR 25 , -N(R 24 )C(
• R 26 is independently selected from -CN, C 1-6 alkyl, C 1- 6 haloalkyl, C 1-6 alkoxy, C 1-6 haloalkoxy, -C(O)OR 22 , -C(O)N(R 22 )(R 23 ), -C(O)C(O)N(R 22 )(R 23 ), and -C(O)R 25 .
• R 2 is selected from , and R 26 is independently selected from halogen, oxo, -CN, C 1-6 alkyl, C 1-6 haloalkyl, C 1-6 alkoxy, C 1-6 haloalkoxy, -OR 21 , -SR 21 , -N(R 22 )(R 23 ), -C(O)OR 22 , -C(O)N(R 22 )(R 23 ), -C(O)C(O)N(R 22 )(R 23 ), -OC(O)N(R 22 )(R 23 ), -N(R 24 )C(O)N(R 22 )(R 23 ), - N(R 24 )C(O)OR 25 , -N(R 24 )C(O)R 25 , -N(R 24 )S(O) 2 R 25 , -C(O)R 25 , -S(O) 2 R 25 , -S(O) 2 R 25
• R 26 is independently selected from -CN, C 1-6 alkyl, C 1-6 haloalkyl, C 1-6 alkoxy, C 1-6 haloalkoxy, - C(O)OR 22 , -C(O)N(R 22 )(R 23 ), -C(O)C(O)N(R 22 )(R 23 ), and -C(O)R 25 .
• R 2 is selected from -OR 12 , -N(R 12 )(R 13 ), -C(O)R 15 , and -C(O)N(R 12 )(R 13 ); R 13 is hydrogen;
• R 26 is independently selected from halogen, oxo, -CN, C 1- alkyl, C 6 1- 6 haloalkyl, C 1-6 alkoxy, C 1-6 haloalkoxy, -OR 21 , -SR 21 , -N(R 22 )(R 23 ), -C(O)OR 22 , -C(O)N(R 22 )(R 23 ), - C(O)C(O)N(R 22 )(R 23 ), -OC(O)N(R 22 )(R 23 ), -N(R 24 )C(O)N(R 22 )(R 23 ), -N(R 24 )C(O)OR 25 , -N(R 24 )C(O)R 25 , - N(R 24 )S(O) 2 R 25 , -C(O)R 25 , -S(O) 2 R 25 , -S(O) 2 N(R 22 )(R 23 ,
• R 2 is independently ; and R 26 is independently selected from halogen, oxo, -CN, C 1-6 alkyl, C 1-6 haloalkyl, C 1-6 alkoxy, C 1-6 haloalkoxy, -OR 21 , -SR 21 , -N(R 22 )(R 23 ), - C(O)OR 22 , -C(O)N(R 22 )(R 23 ), -C(O)C(O)N(R 22 )(R 23 ), -OC(O)N(R 22 )(R 23 ), -N(R 24 )C(O)N(R 22 )(R 23 ), - N(R 24 )C(O)OR 25 , -N(R 24 )C(O)R 25 , -N(R 24 )S(O) 2 R 25 , -C(O)R 25 , -S(O) 2 R 25 , -S(O) 2 R 25 ,
• R 2 is . In some embodiments, R 2 is . In some embodiments, R2 is . In some embodiments, R 2 is . In some embodiments, R 2 is . In some embodiments, R 2 is . In some embodiments, R 2 is -CN. In some embodiments, R 2 is -F. In some embodiments, R 2 is -CF3. In some embodiments, R 2 is -OCH 3 . In some embodiments, R 2 is cyclopropyl. In some embodiments, R 2 is -OCH 2 CF 3 . In some embodiments, R 2 is -CH 3 .
• W 3 is N. In some embodiments (e.g., including Formulae (I), (II), (III), (IV); or sub-formulae thereof), W 3 is N(R 3 ). In some embodiments (e.g., including Formulae (I), (II), (III), (IV); or sub-formulae thereof), W 3 is O. In some embodiments (e.g., including Formulae (I), (II), (III), (IV); or sub-formulae thereof), W 3 is C(R 3 ).
• W 3 is C(R 3 )(R 3a ). In some embodiments (e.g., including Formulae (I), (II), (III), (IV); or sub-formulae thereof), W 3 is C(O). In some embodiments (e.g., including Formulae (I), (II), (III), (IV); or sub-formulae thereof), W 3 is S(O). In some embodiments (e.g., including Formulae (I), (II), (III), (IV); or sub-formulae thereof), W 3 is S(O) 2 .
• W 3 is S(O)(NR 3 ). In some embodiments (e.g., including Formulae (I), (II), (III), (IV); or sub-formulae thereof), W 3 is S(O)(R 3 ). In some embodiments (e.g., including Formulae (I), (II), (III), (IV); or sub-formulae thereof), W 3 is P(O)(R 3 ). [00526] In some embodiments (e.g., including Formulae (I), (II), (III), (IV); or sub-formulae thereof), R 3 is independently hydrogen.
• R 3 is independently halogen. In some embodiments (e.g., including Formulae (I), (II), (III), (IV); or sub- formulae thereof), R 3 is independently -CN. In some embodiments (e.g., including Formulae (I), (II), (III), (IV); or sub-formulae thereof), R 3 is independently C 1-6 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 3-6 cycloalkyl, C 2-9 heterocycloalkyl, C 6-10 aryl, or C 1-9 heteroaryl.
• R 3 is independently -OR 12 , -SR 12 , -N(R 12 )(R 13 ), -C(O)OR 12 , -OC(O)N(R 12 )(R 13 ), -N(R 14 )C(O)N(R 12 )(R 13 ), - N(R 14 )C(O)OR 12 , -N(R 14 )S(O) 2 R 15 , -C(O)R 15 , -S(O)R 15 , -OC(O)R 15 , -C(O)N(R 12 )(R 13 ), -C(O)C(O)N(R 12 )(R 13 ), - N(R 14 )C(O)R 15 , -S(O) 2 R 15 , -S(O) 2 N(R 12 )
• R 3 is independently C 1-6 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 3-6 cycloalkyl, C 2- 9 heterocycloalkyl, C 6-10 aryl, or C 1-9 heteroaryl substituted with one, two, or three R 20c .
• R 3 is hydrogen, -CN, C 1-6 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 3-6 cycloalkyl, C 2- 9 heterocycloalkyl, C 6-10 aryl, C 1-9 heteroaryl, -OR 12 , -C(O)OR 12 , -C(O)N(R 12 )(R 13 ), -C(O)C(O)N(R 12 )(R 13 ), - CH 2 C(O)N(R 12 )(R 13 ), -CH 2 N(R 14 )C(O)R 15 , -CH 2 S(O) 2 R 15 , and -CH 2 S(O) 2 N(R 12 )(R 13 ), wherein C 1-6 alkyl, C 2- 6 alkenyl, C 2-6 alkynyl, C 3-6 cycloalkyl, C 2-9 heterocycloalkyl, C 6-10 aryl, wherein C 1-6 alkyl,
• R 3 is hydrogen, -CN, C 1-6 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 3-6 cycloalkyl, C 2-9 heterocycloalkyl, C 6-10 aryl, C 1-9 heteroaryl, - OR 12 , -C(O)OR 12 , -C(O)N(R 12 )(R 13 ), -C(O)C(O)N(R 12 )(R 13 ), -CH 2 C(O)N(R 12 )(R 13 ), -CH 2 N(R 14 )C(O)R 15 , - CH 2 S(O) 2 R 15 , and -CH 2 S(O) 2 N(R 12 )(R 13 ), wherein C 1-6 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 3-6 cycloalkyl, C 2-9 heterocycloalkyl, C 6-10 aryl, C 1-9 heteroaryl, -
• R 3 is hydrogen, -CN, C 1-6 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 3-6 cycloalkyl, C 2-9 heterocycloalkyl, C 6- 10 aryl, C 1-9 heteroaryl, -C(O)OR 12 , -C(O)N(R 12 )(R 13 ), -C(O)C(O)N(R 12 )(R 13 ), -CH 2 C(O)N(R 12 )(R 13 ), - CH 2 N(R 14 )C(O)R 15 , -CH 2 S(O) 2 R 15 , and -CH 2 S(O) 2 N(R 12 )(R 13 ), wherein C 1-6 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C3- 6 cycloalkyl, C 2-9 heterocycloalkyl, C 6-10 aryl, and C 1-9 heteroaryl are optionally
• R 3 is hydrogen, -CN, C 1-6 alkyl, C 2- 6 alkenyl, C 2-6 alkynyl, C 3-6 cycloalkyl, C 2-9 heterocycloalkyl, C 6-10 aryl, C 1-9 heteroaryl, -C(O)OR 12 , -C(O)N(R 12 )(R 13 ), - C(O)C(O)N(R 12 )(R 13 ), -CH 2 C(O)N(R 12 )(R 13 ), -CH 2 N(R 14 )C(O)R 15 , -CH 2 S(O) 2 R 15 , and -CH 2 S(O) 2 N(R 12 )(R 13 ), wherein C 1-6 alkyl, C 2-6 alkenyl, C 2-6 alkynyl,
• R 3 is hydrogen, -CN, C 1-6 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 3-6 cycloalkyl, C 2- 9 heterocycloalkyl, C 6-10 aryl, C 1-9 heteroaryl, -OR 12 , -C(O)OR 12 , -OC(O)N(R 12 )(R 13 ), -C(O)R 15 , -OC(O)R 15 , - C(O)N(R 12 )(R 13 ), -C(O)C(O)N(R 12 )(R 13 ), -CH 2 C(O)N(R 12 )(R 13 ), -CH 2 N(R 14 )C(O)R 15 , -CH 2 S(O) 2 R 15 , and - CH 2 S(O) 2 N(R 12 )(R 13 ), wherein C 1-6 alkyl, C 2-6 alkenyl, C 2-6 alkynyl
• R 3 is hydrogen, - CN, C 1-6 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 3-6 cycloalkyl, C 2-9 heterocycloalkyl, C 6-10 aryl, C 1-9 heteroaryl, -C(O)OR 12 , - C(O)R 15 , -C(O)N(R 12 )(R 13 ), -C(O)C(O)N(R 12 )(R 13 ), -CH 2 C(O)N(R 12 )(R 13 ), -CH 2 N(R 14 )C(O)R 15 , -CH 2 S(O) 2 R 15 , and -CH 2 S(O) 2 N(R 12 )(R 13 ), wherein C 1-6 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 3-6 cycloalkyl, C 2-9 heterocycloalkyl, C 6-10 aryl, wherein C
• R 3 is hydrogen, -CN, C 1-6 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 3-6 cycloalkyl, C 2 - 9 heterocycloalkyl, C 6-10 aryl, C 1-9 heteroaryl, -OR 12 , -C(O)OR 12 , -OC(O)N(R 12 )(R 13 ), -C(O)R 15 , -OC(O)R 15 , - C(O)N(R 12 )(R 13 ), -C(O)C(O)N(R 12 )(R 13 ), -CH 2 C(O)N(R 12 )(R 13 ), -CH 2 N(R 14 )C(O)R 15 , -CH 2 S(O) 2 R 15 , and
• R 3 is hydrogen, -CN, C 1-6 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 3-6 cycloalkyl, C 2 - 9 heterocycloalkyl, C 6-10 aryl, C 1-9 heteroaryl, -C(O)OR 12 , -C(O)R 15 , -C(O)N(R 12 )(R 13 ), -C(O)C(O)N(R 12 )(R 13 ), - CH 2 C(O)N(R 12 )(R 13 ), -CH 2 N(R 14 )C(O)R 15 , -CH 2 S(O) 2 R 15 , and -CH 2 S(O) 2 N(R 12 )(R 13 ), wherein C 1-6 alkyl, C 2- 6 alkenyl, C 2-6 alkynyl, C 3-6 cycloalkyl, C 2 - 9 heterocycloalkyl, C 6-10 aryl, C
• R 3a is independently hydrogen. In some embodiments (e.g., including Formulae (I), (II), (III), (IV); or sub-formulae thereof), R 3a is independently halogen. In some embodiments (e.g., including Formulae (I), (II), (III), (IV); or sub- formulae thereof), R 3a is independently -CN.
• R 3a is independently C 1-6 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 3-6 cycloalkyl, C 2-9 heterocycloalkyl, C 6-10 aryl, or C 1-9 heteroaryl.
• R 3a is independently -OR 12 , -SR 12 , -N(R 12 )(R 13 ), -C(O)OR 12 , -OC(O)N(R 12 )(R 13 ), -N(R 14 )C(O)N(R 12 )(R 13 ), -N(R 14 )C(O)OR 12 , -N(R 14 )S(O) 2 R 15 , -C(O)R 15 , -S(O)R 15 , -OC(O)R 15 , -C(O)N(R 12 )(R 13 ), -C(O)C(O)N(R 12 )(R 13 ), - N(R 14 )C(O)R 15 , -S(O) 2 R 15 , -S(O) 2 N(R 12 )
• R 3a is independently C 1-6 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 3-6 cycloalkyl, C 2- 9 heterocycloalkyl, C 6-10 aryl, or C 1-9 heteroaryl substituted with one, two, or three R 20c .
• R 3 and R 3a are combined to form a C 3-6 cycloalkyl.
• R 3 and R 3a are combined to form a C 2-9 heterocycloalkyl. In some embodiments (e.g., including Formulae (I), (II), (III), (IV); or sub-formulae thereof), R 3 and R 3a are combined to form a C 3-6 cycloalkyl substituted with one, two, or three R 20c .
• R 3 and R 3a are combined to form a C 2-9 heterocycloalkyl substituted with one, two, or three R 20c .
• R 3 is selected from hydrogen, halogen, -CN, C 1-6 alkyl, C 3-6 cycloalkyl, C 2-9 heterocycloalkyl, -OR 12 , -SR 12 , and -N(R 12 )(R 13 ), wherein C 1-6 alkyl, C 3-6 cycloalkyl, and C 2-9 heterocycloalkyl are optionally substituted with one, two, or three R 20c .
• R 3 is selected from hydrogen, halogen, -CN, C 1-6 alkyl, C 3-6 cycloalkyl, and -OR 12 , wherein C 1-6 alkyl and C 3-6 cycloalkyl are optionally substituted with one, two, or three R 20c .
• R 3 is -CN.
• R 3 is - F.
• R 3 is -CF3.
• R 3 is -OCH 3 .
• R 3 is cyclopropyl.
• R 3 is -OCH 2 CF 3 . In some embodiments, R 3 is -CH 3 . [00533] In some embodiments (e.g., including Formulae (I), (II), (III), (IV); or sub-formulae thereof), W 4 is N. In some embodiments (e.g., including Formulae (I), (II), (III), (IV); or sub-formulae thereof), W 4 is N(R 4 ). In some embodiments (e.g., including Formulae (I), (II), (III), (IV); or sub-formulae thereof), W 4 is O.
• W 4 is C(R 4 ). In some embodiments (e.g., including Formulae (I), (II), (III), (IV); or sub-formulae thereof), W 4 is C(R 4 )(R 4a ). In some embodiments (e.g., including Formulae (I), (II), (III), (IV); or sub-formulae thereof), W 4 is C(O). In some embodiments (e.g., including Formulae (I), (II), (III), (IV); or sub-formulae thereof), W 4 is S(O).
• W 4 is S(O) 2 . In some embodiments (e.g., including Formulae (I), (II), (III), (IV); or sub-formulae thereof), W 4 is S(O)(NR 4 ). In some embodiments (e.g., including Formulae (I), (II), (III), (IV); or sub-formulae thereof), W 4 is S(O)(R 4 ). In some embodiments (e.g., including Formulae (I), (II), (III), (IV); or sub-formulae thereof), W 4 is P(O)(R 4 ).
• R 4 is independently hydrogen. In some embodiments (e.g., including Formulae (I), (II), (III), (IV); or sub-formulae thereof), R 4 is independently halogen. In some embodiments (e.g., including Formulae (I), (II), (III), (IV); or sub- formulae thereof), R 4 is independently -CN.
• R 4 is independently C 1-6 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 3-6 cycloalkyl, C 2-9 heterocycloalkyl, C 6-10 aryl, C 1-9 heteroaryl.
• R 4 is independently -OR 12 , -SR 12 , -N(R 12 )(R 13 ), -C(O)OR 12 , -OC(O)N(R 12 )(R 13 ), -N(R 14 )C(O)N(R 12 )(R 13 ), - N(R 14 )C(O)OR 12 , -N(R 14 )S(O) 2 R 15 , -C(O)R 15 , -S(O)R 15 , -OC(O)R 15 , -C(O)N(R 12 )(R 13 ), -C(O)C(O)N(R 12 )(R 13 ), - N(R 14 )C(O)R 15 , -S(O) 2 R 15 , -S(O) 2 N(R 12 )
• R 4 is independently C 1-6 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 3-6 cycloalkyl, C 2 - 9 heterocycloalkyl, C 6-10 aryl, or C 1-9 heteroaryl substituted with one, two, or three R 20d . In some embodiments (e.g., including Formulae (I), (II), (III), (IV); or sub-formulae thereof), R 4 is independently C 1-6 alkyl.
• R 4 is independently C 1-4 alkyl. In some embodiments (e.g., including Formulae (I), (II), (III), (IV); or sub-formulae thereof), R 4 is independently C 1 -3alkyl. In some embodiments (e.g., including Formulae (I), (II), (III), (IV); or sub-formulae thereof), R 4 is independently C 1 -2alkyl. In some embodiments (e.g., including Formulae (I), (II), (III), (IV); or sub-formulae thereof), R 4 is independently methyl.
• R 4 is -CN. In some embodiments, R 4 is -F. In some embodiments, R 4 is -CF 3 . In some embodiments, R 4 is -OCH 3 . In some embodiments, R 4 is cyclopropyl. In some embodiments, R 4 is -OCH 2 CF3. In some embodiments, R 4 is -CH 3 .
• R 4 is hydrogen, -CN, C 1-6 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 3-6 cycloalkyl, C 2 - 9 heterocycloalkyl, C 6-10 aryl, C 1-9 heteroaryl, -OR 12 , -C(O)OR 12 , -OC(O)N(R 12 )(R 13 ), -C(O)R 15 , -OC(O)R 15 , - C(O)N(R 12 )(R 13 ), -C(O)C(O)N(R 12 )(R 13 ), -CH 2 C(O)N(R 12 )(R 13 ), -CH 2 N(R 14 )C(O)R 15 , -CH 2 S(O) 2 R 15 , and - CH 2 S(O) 2 N(R 12 )(R 13 ), wherein C 1-6 alkyl, C 2-6 alkenyl, C 2-6 alkyn
• R 4 is hydrogen, - CN, C 1-6 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 3-6 cycloalkyl, C 2-9 heterocycloalkyl, C 6-10 aryl, C 1-9 heteroaryl, -C(O)OR 12 , - C(O)R 15 , -C(O)N(R 12 )(R 13 ), -C(O)C(O)N(R 12 )(R 13 ), -CH 2 C(O)N(R 12 )(R 13 ), -CH 2 N(R 14 )C(O)R 15 , -CH 2 S(O) 2 R 15 , and -CH 2 S(O) 2 N(R 12 )(R 13 ), wherein C 1-6 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 3-6 cycloalkyl, C 2-9 heterocycloalkyl, C 6-10 aryl, wherein C
• R 4 is hydrogen, -CN, C 1-6 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 3-6 cycloalkyl, C 2- 9 heterocycloalkyl, C 6-10 aryl, C 1-9 heteroaryl, -OR 12 , -C(O)OR 12 , -OC(O)N(R 12 )(R 13 ), -C(O)R 15 , -OC(O)R 15 , - C(O)N(R 12 )(R 13 ), -C(O)C(O)N(R 12 )(R 13 ), -CH 2 C(O)N(R 12 )(R 13 ), -CH 2 N(R 14 )C(O)R 15 , -CH 2 S(O) 2 R 15 , and - CH
• R 4 is hydrogen, -CN, C 1-6 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 3-6 cycloalkyl, C 2- 9 heterocycloalkyl, C 6-10 aryl, C 1-9 heteroaryl, -C(O)OR 12 , -C(O)R 15 , -C(O)N(R 12 )(R 13 ), -C(O)C(O)N(R 12 )(R 13 ), - CH 2 C(O)N(R 12 )(R 13 ), -CH 2 N(R 14 )C(O)R 15 , -CH 2 S(O) 2 R 15 , and -CH 2 S(O) 2 N(R 12 )(R 13 ), wherein C 1-6 alkyl, C 2 - 6 alkenyl, C 2-6 alkynyl, C 3-6 cycloalkyl, C 2- 9 heterocycloalkyl, C 6-10 aryl, C 1-9
• R 4a is independently hydrogen. In some embodiments (e.g., including Formulae (I), (II), (III), (IV); or sub-formulae thereof), R 4a is independently halogen. In some embodiments (e.g., including Formulae (I), (II), (III), (IV); or sub- formulae thereof), R 4a is independently -CN.
• R 4a is independently C 1-6 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 3-6 cycloalkyl, C 2-9 heterocycloalkyl, C 6-10 aryl, C 1-9 heteroaryl.
• R 4a is independently -OR 12 , -SR 12 , -N(R 12 )(R 13 ), -C(O)OR 12 , -OC(O)N(R 12 )(R 13 ), -N(R 14 )C(O)N(R 12 )(R 13 ), -N(R 14 )C(O)OR 12 , -N(R 14 )S(O) 2 R 15 , -C(O)R 15 , -S(O)R 15 , -OC(O)R 15 , -C(O)N(R 12 )(R 13 ), -C(O)C(O)N(R 12 )(R 13 ), - N(R 14 )C(O)R 15 , -S(O) 2 R 15 , -S(O) 2 N(R 12 )
• R 4a is independently C 1-6 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 3-6 cycloalkyl, C 2- 9 heterocycloalkyl, C 6-10 aryl, or C 1-9 heteroaryl substituted with one, two, or three R 20d .
• R 4a is independently C 1-6 alkyl.
• R 4a is independently C 1 -4alkyl. In some embodiments (e.g., including Formulae (I), (II), (III), (IV); or sub-formulae thereof), R 4a is independently C 1-3 alkyl. In some embodiments (e.g., including Formulae (I), (II), (III), (IV); or sub-formulae thereof), R 4a is independently C 1-2 alkyl. In some embodiments (e.g., including Formulae (I), (II), (III), (IV); or sub-formulae thereof), R 4a is independently methyl.
• R 4 and R 4a are combined to form a C 3-6 cycloalkyl. In some embodiments (e.g., including Formulae (I), (II), (III), (IV); or sub- formulae thereof), R 4 and R 4a are combined to form a C 2-9 heterocycloalkyl. In some embodiments (e.g., including Formulae (I), (II), (III), (IV); or sub-formulae thereof), R 4 and R 4a are combined to form a C 3-6 cycloalkyl substituted with one, two, or three R 20d .
• R 4 and R 4a are combined to form a C 2-9 heterocycloalkyl substituted with one, two, or three R 20d .
• W 5 is N.
• W 5 is C.
• W 6 is N. In some embodiments (e.g., including Formulae (I), (II), (III), (IV); or sub-formulae thereof), W 6 is C. [00540] In some embodiments (e.g., including Formulae (I), (II), (III), (IV); or sub-formulae thereof), at least one of W 1 , W 2 , W 3 , W 4 , W 5 , and W 6 is N, N(R 1 ), N(R 2 ), N(R 3 ), or N(R 4 ).
• At least one of W 1 , W 2 , W 3 , and W 4 is N, N(R 1 ), N(R 2 ), N(R 3 ), or N(R 4 ).
• two Ring A are double bonds.
• three Ring A are double bonds.
• no Ring A are double bonds.
• one Ring A is a double bond. In some embodiments of Formulae (III), or sub-formulae thereof, two Ring A are double bonds. [00542]
• W 3 is C(O), S(O), S(O) 2 , S(O)(NR 3 ), S(O)(R 3 ), or P(O)(R 3 );
• W 4 is N(R 4 );
• W 1 is C(R 1 ); and
• W 2 is C(R 2 ).
• W 1 is C(O), S(O), S(O) 2 , S(O)(NR 1 ), S(O)(R 1 ), or P(O)(R 1 );
• W 2 is N(R 2 );
• W 3 is C(R 3 )(R 3a ); and
• W 4 is C(R 4 )(R 4a ).
• W 3 is C(O), S(O), S(O) 2 , S(O)(NR 3 ), S(O)(R 3 ), or P(O)(R 3 );
• W 4 is N(R 4 );
• W 2 is N(R 2 ); and
• W 1 is C(R 1 )(R 1a ).
• W 3 is C(O), S(O), S(O) 2 , S(O)(NR 3 ), S(O)(R 3 ), or P(O)(R 3 );
• W 2 is N(R 2 );
• W 1 is C(R 1 )(R 1a );
• W 4 is C(R 4 )(R 4a ).
• W 3 is C(O), S(O), S(O) 2 , S(O)(NR 3 ), S(O)(R 3 ), or P(O)(R 3 );
• W 2 is N(R 2 );
• W 1 is C(R 1 ); and W 4 is N.
• W 3 is C(O), S(O), S(O) 2 , S(O)(NR 3 ), S(O)(R 3 ), or P(O)(R 3 );
• W 2 is N(R 2 );
• W 1 is C(R 1 );
• W 4 is C(R 4 ).
• W 4 is C(O), S(O), S(O) 2 , S(O)(NR 4 ), S(O)(R 4 ), or P(O)(R 4 );
• W 3 is N(R 3 ); W 1 is N; and W 2 is C(R 2 ).
• W 4 is C(O), S(O), S(O) 2 , S(O)(NR 4 ), S(O)(R 4 ), or P(O)(R 4 ); W 3 is N(R 3 ); W 1 is C(R 1 ); and W 2 is C(R 2 ). In some embodiments of Formula (III), or sub-formulae thereof, W 3 is C(O), S(O), S(O) 2 , S(O)(NR 3 ), S(O)(R 3 ), or P(O)(R 3 ); W 4 is N(R 4 ); W 2 is C(R 2 ); and W 1 is C(R 1 ).
• W 1 is C(O), S(O), S(O) 2 , S(O)(NR 1 ), S(O)(R 1 ), or P(O)(R 1 );
• W 2 is N(R 2 );
• W 3 is C(R 3 ); and
• W 4 is C(R 4 ).
• W 1 is C(O), S(O), S(O) 2 , S(O)(NR 1 ), S(O)(R 1 ), or P(O)(R 1 );
• W 2 is N(R 2 );
• W 3 is C(R 3 ); and W 4 is N.
• W 4 is C(O), S(O), S(O) 2 , S(O)(NR 4 ), S(O)(R 4 ), or P(O)(R 4 );
• W 3 is C(R 3 )(R 3a ); W 1 is O; and W 2 is C(R 2 )(R 2a ).
• W 4 is C(O), S(O), S(O) 2 , S(O)(NR 4 ), S(O)(R 4 ), or P(O)(R 4 );
• W 3 is C(R 3 ); W 1 is O; and W 2 is C(R 2 ).
• W 1 is C(O), S(O), S(O) 2 , S(O)(NR 1 ), S(O)(R 1 ), or P(O)(R 1 );
• W 3 is C(R 3 )(R 3a );
• W 4 is O; and
• W 2 is C(R 2 )(R 2a ).
• W 1 is C(O), S(O), S(O) 2 , S(O)(NR 1 ), S(O)(R 1 ), or P(O)(R 1 );
• W 3 is C(R 3 ); W 4 is O; and W 2 is C(R 2 ).
• W 1 is C(R 1 ); W 2 is C(R 2 ); W 3 is N; and W 4 is N.
• W 1 is C(R 1 ); W 2 is C(R 2 ); W 3 is C(R 3 ); and W 4 is N.
• W 1 is C(R 1 ); W 2 is C(R 2 ); W 3 is N; and W 4 is C(R 4 ). In some embodiments (e.g., including Formulae (I), (II), (III), (IV); or sub-formulae thereof), W 1 is N; W 2 is C(R 2 ); W 3 is C(R 3 ); and W 4 is C(R 4 ).
• W 1 is N
• W 2 is C(R 2 )
• W 3 is C(R 3 )
• W 4 is C(R 4 ).
• W 1 is C(R 1 )
• W 2 is N
• W 3 is C(R 3 )
• W 4 is C(R 4 ).
• W 1 is C(R 1 ), W 2 is C(R 2 ), W 3 is N, and W 4 is C(R 4 ). In some embodiments (e.g., including Formulae (I), (II), (III), (IV); or sub-formulae thereof), W 1 is C(R 1 ), W 2 is C(R 2 ), W 3 is C(R 3 ), and W 4 is N. In some embodiments (e.g., including Formulae (I), (II), (III), (IV); or sub-formulae thereof), W 1 is C(R 1 ) and W 2 is C(R 2 ).
• W 3 is N(R 3 ) and W 4 is C(O). In some embodiments (e.g., including Formulae (I), (II), (III), (IV); or sub- formulae thereof), W 3 is C(O) and W 4 is N(R 4 ). In some embodiments (e.g., including Formulae (I), (II), (III), (IV); or sub-formulae thereof), W 3 is O and W 4 is C(R 4 )(R 4a ).
• W 1 is C(R 1 )(R 1a ), W 2 is O, W 3 is C(R 3 ), and W 4 is C(R 4 ).
• W 1 is CO, N(R1) or C(R 1 )(R 1a ); W 2 is CO , N(R2), or C(R 2 )(R 2a ); W 3 is N, or C(R 3 ); and W 4 is N, or C(R 4 ).
• W 3 and W 4 are connected by a double bond.
• W 1 is is N(R 1 ) and W 3 and W 4 are connected by a double bond.
• W 2 is N(R 2 ) and W 1 is C(R 1 )(R 1a ).
• W 4 is N(R 4 ) and W 1 and W 2 are connected by a double bond.
• W 2 is C(R 2 )(R 2a ) and W 3 is C(R 3 )(R 3a ).
• W 2 is C(R 2 ) and W 3 is C(R 3 ).
• W 4 is C(O), S(O), S(O) 2 , S(O)(NR 4 ), S(O)(R 4 ), or P(O)(R 4 ); W 3 is N; and W 2 is C(R 2 ). In some embodiments of Formula (III), or sub-formulae thereof, W 4 is C(O), S(O), S(O) 2 , S(O)(NR 4 ), S(O)(R 4 ), or P(O)(R 4 ); W 2 is N; and W 3 is C(R 3 ).
• W 4 is C(O), S(O), S(O) 2 , S(O)(NR 4 ), S(O)(R 4 ), or P(O)(R 4 );
• W 3 is C(R 3 ); and W 2 is C(R 2 ).
• W 4 is C(O), S(O), S(O) 2 , S(O)(NR 4 ), S(O)(R 4 ), or P(O)(R 4 );
• W 3 is N; and W 2 is N.
• W 1 is C(O), S(O), S(O) 2 , S(O)(NR 1 ), S(O)(R 1 ), or P(O)(R 1 ); W 3 is N; and W 2 is C(R 2 ). In some embodiments of Formula (III), or sub-formulae thereof, W 1 is C(O), S(O), S(O) 2 , S(O)(NR 1 ), S(O)(R 1 ), or P(O)(R 1 ); W 2 is N; and W 3 is C(R 3 ).
• W 1 is C(O), S(O), S(O) 2 , S(O)(NR 1 ), S(O)(R 1 ), or P(O)(R 1 );
• W 3 is C(R 3 ); and
• W 2 is C(R 2 ).
• W 1 is C(O), S(O), S(O) 2 , S(O)(NR 1 ), S(O)(R 1 ), or P(O)(R 1 );
• W 3 is N; and W 2 is N.
• R 12 is independently hydrogen. In some embodiments (e.g., including Formulae (I), (II), (III), (IV); or sub-formulae thereof), R 12 is independently C 1-6 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 3-6 cycloalkyl, -CH 2 -C 3-6 cycloalkyl, C 2 - 9 heterocycloalkyl, -CH 2 -C 2-9 heterocycloalkyl, C 6-10 aryl, -CH 2 -C 6-10 aryl, or C 1-9 heteroaryl, wherein C 1-6 alkyl, C 2- 6 alkenyl, C 2-6 alkynyl, C 3-6 cycloalkyl, -CH 2 -C 3-6 cycloalkyl, C 2-9 heterocycloalkyl, -
• R 12 is independently C 1-6 alkyl optionally substituted with one, two, or three R 20k . In some embodiments (e.g., including Formulae (I), (II), (III), (IV); or sub-formulae thereof), R 12 is independently C 1-6 alkyl. In some embodiments (e.g., including Formulae (I), (II), (III), (IV); or sub-formulae thereof), R 12 is independently C 1 -4alkyl.
• R 12 is independently C 1-3 alkyl. In some embodiments (e.g., including Formulae (I), (II), (III), (IV); or sub-formulae thereof), R 12 is independently C 1-2 alkyl. In some embodiments (e.g., including Formulae (I), (II), (III), (IV); or sub-formulae thereof), R 12 is methyl. [00546] In some embodiments (e.g., including Formulae (I), (II), (III), (IV); or sub-formulae thereof), R 12a is independently hydrogen.
• R 12a is independently C 1-6 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 3-6 cycloalkyl, -CH 2 -C 3-6 cycloalkyl, -CH 2 -C 2- 9 heterocycloalkyl, C 6-10 aryl, -CH 2 -C 6-10 aryl, and C 1-9 heteroaryl, wherein C 1-6 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 3- 6 cycloalkyl, -CH 2 -C 3-6 cycloalkyl, -CH 2 -C 2-9 heterocycloalkyl, C 6-10 aryl, -CH 2 -C 6-10 aryl, and C 1-9 heteroaryl are optionally substituted with one, two, or three R 20k .
• R 12a is independently C 1-6 alkyl optionally substituted with one, two, or three R 20k . In some embodiments (e.g., including Formulae (I), (II), (III), (IV); or sub-formulae thereof), R 12a is independently C 1- 6 alkyl. In some embodiments (e.g., including Formulae (I), (II), (III), (IV); or sub-formulae thereof), R 12a is independently C 1 -4alkyl.
• R 12 is independently C 1-3 alkyl. In some embodiments (e.g., including Formulae (I), (II), (III), (IV); or sub- formulae thereof), R 12a is independently C 1-2 alkyl. In some embodiments (e.g., including Formulae (I), (II), (III), (IV); or sub-formulae thereof), R 12a is methyl. [00547] In some embodiments (e.g., including Formulae (I), (II), (III), (IV); or sub-formulae thereof), R 12 is independently hydrogen.
• R 12 is independently C 1-6 alkyl. In some embodiments (e.g., including Formulae (I), (II), (III), (IV); or sub- formulae thereof), R 12 is independently C 2-6 alkenyl. In some embodiments (e.g., including Formulae (I), (II), (III), (IV); or sub-formulae thereof), R 12 is independently C 2-6 alkynyl. In some embodiments (e.g., including Formulae (I), (II), (III), (IV); or sub-formulae thereof), R 12 is independently C 3-6 cycloalkyl.
• R 12 is independently -CH 2 -C 3-6 cycloalkyl. In some embodiments (e.g., including Formulae (I), (II), (III), (IV); or sub-formulae thereof), R 12 is independently C 2 - 9 heterocycloalkyl. In some embodiments (e.g., including Formulae (I), (II), (III), (IV); or sub-formulae thereof), R 12 is independently -CH 2 -C 2-9 heterocycloalkyl.
• R 12 is independently C 6-10 aryl. In some embodiments (e.g., including Formulae (I), (II), (III), (IV); or sub-formulae thereof), R 12 is independently -CH 2 -C 6-10 aryl. In some embodiments (e.g., including Formulae (I), (II), (III), (IV); or sub-formulae thereof), R 12 is independently C 1-9 heteroaryl.
• R 12 is independently C 1-6 alkyl substituted with one, two, or three R 20k . In some embodiments (e.g., including Formulae (I), (II), (III), (IV); or sub-formulae thereof), R 12 is independently C 2-6 alkenyl substituted with one, two, or three R 20k . In some embodiments (e.g., including Formulae (I), (II), (III), (IV); or sub-formulae thereof), R 12 is independently C 2-6 alkynyl substituted with one, two, or three R 20k .
• R 12 is independently C 3-6 cycloalkyl substituted with one, two, or three R 20k . In some embodiments (e.g., including Formulae (I), (II), (III), (IV); or sub-formulae thereof), R 12 is independently -CH 2 -C3- 6 cycloalkyl substituted with one, two, or three R 20k .
• R 12 is independently C 2-9 heterocycloalkyl substituted with one, two, or three R 20k . In some embodiments (e.g., including Formulae (I), (II), (III), (IV); or sub-formulae thereof), R 12 is independently - CH 2 -C 2-9 heterocycloalkyl substituted with one, two, or three R 20k . In some embodiments (e.g., including Formulae (I), (II), (III), (IV); or sub-formulae thereof), R 12 is independently C 6-10 aryl substituted with one, two, or three R 20k .
• R 12 is independently - CH 2 -C 6-10 aryl substituted with one, two, or three R 20k . In some embodiments (e.g., including Formulae (I), (II), (III), (IV); or sub-formulae thereof), R 12 is independently C 1-9 heteroaryl substituted with one, two, or three R 20k . [00549] In some embodiments (e.g., including Formulae (I), (II), (III), (IV); or sub-formulae thereof), R 12a is independently hydrogen.
• R 12a is independently C 1-6 alkyl. In some embodiments (e.g., including Formulae (I), (II), (III), (IV); or sub- formulae thereof), R 12a is independently C 2-6 alkenyl. In some embodiments (e.g., including Formulae (I), (II), (III), (IV); or sub-formulae thereof), R 12a is independently C 2-6 alkynyl. In some embodiments (e.g., including Formulae (I), (II), (III), (IV); or sub-formulae thereof), R 12a is independently C 3-6 cycloalkyl.
• R 12a is independently -CH 2 -C 3-6 cycloalkyl. In some embodiments (e.g., including Formulae (I), (II), (III), (IV); or sub-formulae thereof), R 12a is independently - CH 2 -C 2-9 heterocycloalkyl. In some embodiments (e.g., including Formulae (I), (II), (III), (IV); or sub-formulae thereof), R 12a is independently C 6-10 aryl.
• R 12a is independently -CH 2 -C 6-10 aryl. In some embodiments (e.g., including Formulae (I), (II), (III), (IV); or sub-formulae thereof), R 12a is independently C 1-9 heteroaryl. In some embodiments (e.g., including Formulae (I), (II), (III), (IV); or sub-formulae thereof), R 12a is independently C 1-6 alkyl substituted with one, two, or three R 20k .
• R 12a is independently C 2-6 alkenyl substituted with one, two, or three R 20k . In some embodiments (e.g., including Formulae (I), (II), (III), (IV); or sub-formulae thereof), R 12a is independently C 2-6 alkynyl substituted with one, two, or three R 20k . In some embodiments (e.g., including Formulae (I), (II), (III), (IV); or sub-formulae thereof), R 12a is independently C 3-6 cycloalkyl substituted with one, two, or three R 20k .
• R 12a is independently -CH 2 -C 3-6 cycloalkyl substituted with one, two, or three R 20k . In some embodiments (e.g., including Formulae (I), (II), (III), (IV); or sub-formulae thereof), R 12a is independently -CH 2 -C 2-9 heterocycloalkyl substituted with one, two, or three R 20k .
• R 12a is independently C 6-10 aryl substituted with one, two, or three R 20k . In some embodiments (e.g., including Formulae (I), (II), (III), (IV); or sub- formulae thereof), R 12a is independently -CH 2 -C 6-10 aryl substituted with one, two, or three R 20k . In some embodiments (e.g., including Formulae (I), (II), (III), (IV); or sub-formulae thereof), R 12a is independently C 1 - 9 heteroaryl substituted with one, two, or three R 20k .
• R 13 is independently hydrogen. In some embodiments (e.g., including Formulae (I), (II), (III), (IV); or sub-formulae thereof), R 13 is independently C 1-6 alkyl. In some embodiments (e.g., including Formulae (I), (II), (III), (IV); or sub- formulae thereof), R 13 is independently C 1-6 haloalkyl.
• R 12 and R 13 together with the nitrogen to which they are attached, form a C 2-9 heterocycloalkyl ring.
• R 12 and R 13 together with the nitrogen to which they are attached, form a C 2-9 heterocycloalkyl ring substituted with one, two, or three R 20k .
• R 14 is independently hydrogen. In some embodiments (e.g., including Formulae (I), (II), (III), (IV); or sub-formulae thereof), R 14 is independently C 1-6 alkyl. In some embodiments (e.g., including Formulae (I), (II), (III), (IV); or sub- formulae thereof), R 14 is independently C 1-6 haloalkyl. [00553] In some embodiments (e.g., including Formulae (I), (II), (III), (IV); or sub-formulae thereof), R 15 is independently C 1-6 alkyl.
• R 15 is independently C 2-6 alkenyl. In some embodiments (e.g., including Formulae (I), (II), (III), (IV); or sub-formulae thereof), R 15 is independently C 2-6 alkynyl. In some embodiments (e.g., including Formulae (I), (II), (III), (IV); or sub-formulae thereof), R 15 is independently C 3-6 cycloalkyl. In some embodiments (e.g., including Formulae (I), (II), (III), (IV); or sub-formulae thereof), R 15 is independently C 1-6 heteroalkyl.
• R 15 is independently C 2-9 heterocycloalkyl. In some embodiments (e.g., including Formulae (I), (II), (III), (IV); or sub-formulae thereof), R 15 is independently C 6 - 10 aryl. In some embodiments (e.g., including Formulae (I), (II), (III), (IV); or sub-formulae thereof), R 15 is independently C 1-9 heteroaryl.
• R 15 is independently C 1-6 alkyl substituted with one, two, or three R 20k . In some embodiments (e.g., including Formulae (I), (II), (III), (IV); or sub-formulae thereof), R 15 is independently C 2-6 alkenyl substituted with one, two, or three R 20k . In some embodiments (e.g., including Formulae (I), (II), (III), (IV); or sub-formulae thereof), R 15 is independently C 2-6 alkynyl substituted with one, two, or three R 20k .
• R 15 is independently C 3-6 cycloalkyl substituted with one, two, or three R 20k . In some embodiments (e.g., including Formulae (I), (II), (III), (IV); or sub-formulae thereof), R 15 is independently C 1-6 heteroalkyl substituted with one, two, or three R 20k . In some embodiments (e.g., including Formulae (I), (II), (III), (IV); or sub-formulae thereof), R 15 is independently C 2-9 heterocycloalkyl substituted with one, two, or three R 20k .
• R 15 is independently C 6-10 aryl substituted with one, two, or three R 20k . In some embodiments (e.g., including Formulae (I), (II), (III), (IV); or sub-formulae thereof), R 15 is independently C 1-9 heteroaryl substituted with one, two, or three R 20k .
• R 15 is independently selected C 1-6 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 3-6 cycloalkyl, C 2 - 9 heterocycloalkyl, C 6-10 aryl, and C 1-9 heteroaryl, wherein C 1-6 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 3-6 cycloalkyl, C 2 - 9 heterocycloalkyl, C 6-10 aryl, and C 1-9 heteroaryl are optionally substituted with one, two, or three R 20k .
• R 15 is independently selected C 1-6 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 3-6 cycloalkyl, C 2-9 heterocycloalkyl, C 6-10 aryl, and C 1-9 heteroaryl.
• R 15 is independently selected from C 1-6 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 3-6 cycloalkyl, C 2-9 heterocycloalkyl, C 6-10 aryl, and C 1-9 heteroaryl substituted with one, two, or three R 20k .
• R 16 is independently -C 1-6 alkylene-OP(O)(OR 16a )(OR 16b ).
• R 16 is independently -C 1-6 alkylene-OP(O)(OR 16a )(OR 16b ), wherein the C 1-6 alkylene is substituted with one, two, or three R 20l .
• R 16 is independently -P(O)(OR 16a )(OR 16b ).
• R 16 is independently -C 1 alkylene-OP(O)(OR 16a )(OR 16b ). In some embodiments (e.g., including Formulae (I), (II), (III), (IV); or sub-formulae thereof), R 16 is independently -C 1 alkylene-OP(O)(OR 16a )(OR 16b ), wherein the C 1 alkylene is substituted with one or two R 20l .
• R 16 is independently -C 2 alkylene-OP(O)(OR 16a )(OR 16b ). In some embodiments (e.g., including Formulae (I), (II), (III), (IV); or sub-formulae thereof), R 16 is independently -C 2 alkylene-OP(O)(OR 16a )(OR 16b ), wherein the C 2 alkylene is substituted with one, two, or three R 20l .
• R 16 is independently -C 3 alkylene-OP(O)(OR 16a )(OR 16b ). In some embodiments (e.g., including Formulae (I), (II), (III), (IV); or sub-formulae thereof), R 16 is independently - C3alkylene-OP(O)(OR 16a )(OR 16b ), wherein the C3alkylene is substituted with one, two, or three R 20l .
• R 16 is independently - C 4 alkylene-OP(O)(OR 16a )(OR 16b ). In some embodiments (e.g., including Formulae (I), (II), (III), (IV); or sub- formulae thereof), R 16 is independently -C 4 alkylene-OP(O)(OR 16a )(OR 16b ), wherein the C4alkylene is substituted with one, two, or three R 20l .
• R 16 is independently -C 5 alkylene-OP(O)(OR 16a )(OR 16b ). In some embodiments (e.g., including Formulae (I), (II), (III), (IV); or sub-formulae thereof), R 16 is independently -C 5 alkylene-OP(O)(OR 16a )(OR 16b ), wherein the C5alkylene is substituted with one, two, or three R 20l .
• R 16 is independently -C 6 alkylene-OP(O)(OR 16a )(OR 16b ). In some embodiments (e.g., including Formulae (I), (II), (III), (IV); or sub-formulae thereof), R 16 is independently -C 6 alkylene- OP(O)(OR 16a )(OR 16b ), wherein the C 6 alkylene is substituted with one, two, or three R 20l .
• R 16a is independently hydrogen. In some embodiments (e.g., including Formulae (I), (II), (III), (IV); or sub-formulae thereof), R 16a is independently C 1-6 alkyl. In some embodiments (e.g., including Formulae (I), (II), (III), (IV); or sub- formulae thereof), R 16a is independently C 2-6 alkenyl. In some embodiments (e.g., including Formulae (I), (II), (III), (IV); or sub-formulae thereof), R 16a is independently C 2-6 alkynyl.
• R 16a is independently C 3-6 cycloalkyl. In some embodiments (e.g., including Formulae (I), (II), (III), (IV); or sub-formulae thereof), R 16a is independently -CH 2 -C 3-6 cycloalkyl. In some embodiments (e.g., including Formulae (I), (II), (III), (IV); or sub-formulae thereof), R 16a is independently - CH 2 -C 2-9 heterocycloalkyl.
• R 16a is independently C 6-10 aryl. In some embodiments (e.g., including Formulae (I), (II), (III), (IV); or sub- formulae thereof), R 16a is independently -CH 2 -C 6-10 aryl. In some embodiments (e.g., including Formulae (I), (II), (III), (IV); or sub-formulae thereof), R 16a is independently C 1-9 heteroaryl.
• R 16a is independently C 1-6 alkyl substituted with one, two, or three R 20m . In some embodiments (e.g., including Formulae (I), (II), (III), (IV); or sub-formulae thereof), R 16a is independently C 2-6 alkenyl substituted with one, two, or three R 20m . In some embodiments (e.g., including Formulae (I), (II), (III), (IV); or sub-formulae thereof), R 16a is independently C 2-6 alkynyl substituted with one, two, or three R 20m .
• R 16a is independently C 3-6 cycloalkyl substituted with one, two, or three R 20m . In some embodiments (e.g., including Formulae (I), (II), (III), (IV); or sub-formulae thereof), R 16a is independently -CH 2 -C 3-6 cycloalkyl substituted with one, two, or three R 20m .
• R 16a is independently -CH 2 -C 2-9 heterocycloalkyl substituted with one, two, or three R 20m . In some embodiments (e.g., including Formulae (I), (II), (III), (IV); or sub-formulae thereof), R 16a is independently C 6-10 aryl substituted with one, two, or three R 20m .
• R 16a is independently -CH 2 -C 6-10 aryl substituted with one, two, or three R 20m .
• R 16a is independently C 1- 9 heteroaryl substituted with one, two, or three R 20m .
• R 16b is independently hydrogen.
• R 16b is independently C 1-6 alkyl. In some embodiments (e.g., including Formulae (I), (II), (III), (IV); or sub- formulae thereof), R 16b is independently C 2-6 alkenyl. In some embodiments (e.g., including Formulae (I), (II), (III), (IV); or sub-formulae thereof), R 16b is independently C 2-6 alkynyl. In some embodiments (e.g., including Formulae (I), (II), (III), (IV); or sub-formulae thereof), R 16b is independently C 3-6 cycloalkyl.
• R 16b is independently -CH 2 -C 3-6 cycloalkyl. In some embodiments (e.g., including Formulae (I), (II), (III), (IV); or sub-formulae thereof), R 16b is independently - CH 2 -C 2-9 heterocycloalkyl. In some embodiments (e.g., including Formulae (I), (II), (III), (IV); or sub-formulae thereof), R 16b is independently C 6-10 aryl.
• R 16b is independently -CH 2 -C 6-10 aryl. In some embodiments (e.g., including Formulae (I), (II), (III), (IV); or sub-formulae thereof), R 16b is independently C 1-9 heteroaryl. In some embodiments (e.g., including Formulae (I), (II), (III), (IV); or sub-formulae thereof), R 16b is independently C 1-6 alkyl substituted with one, two, or three R 20m .
• R 16b is independently C 2-6 alkenyl substituted with one, two, or three R 20m . In some embodiments (e.g., including Formulae (I), (II), (III), (IV); or sub-formulae thereof), R 16b is independently C 2-6 alkynyl substituted with one, two, or three R 20m . In some embodiments (e.g., including Formulae (I), (II), (III), (IV); or sub-formulae thereof), R 16b is independently C 3-6 cycloalkyl substituted with one, two, or three R 20m .
• R 16b is independently -CH 2 -C 3-6 cycloalkyl substituted with one, two, or three R 20m . In some embodiments (e.g., including Formulae (I), (II), (III), (IV); or sub-formulae thereof), R 16b is independently -CH 2 -C 2-9 heterocycloalkyl substituted with one, two, or three R 20m .
• R 16b is independently C 6-10 aryl substituted with one, two, or three R 20m . In some embodiments (e.g., including Formulae (I), (II), (III), (IV); or sub- formulae thereof), R 16b is independently -CH 2 -C 6-10 aryl substituted with one, two, or three R 20m . In some embodiments (e.g., including Formulae (I), (II), (III), (IV); or sub-formulae thereof), R 16b is independently C 1 - 9 heteroaryl substituted with one, two, or three R 20m .
• X is N. In some embodiments (e.g., including Formulae (XI), (XII), (XIII), and/or (XIV); or sub-formulae thereof), X is C(R 5 ). In some embodiments (e.g., including Formulae (XI), (XII), (XIII), and/or (XIV); or sub-formulae thereof), X is CH.
• X is C(halogen). In some embodiments (e.g., including Formulae (XI), (XII), (XIII), and/or (XIV); or sub-formulae thereof), X is C(F). [00559] In some embodiments (e.g., including Formulae (XI), (XII), (XIII), and/or (XIV); or sub-formulae thereof), R 5 is hydrogen.
• R 5 is halogen. In some embodiments (e.g., including Formulae (XI), (XII), (XIII), and/or (XIV); or sub- formulae thereof), R 5 is -F. In some embodiments (e.g., including Formulae (XI), (XII), (XIII), and/or (XIV); or sub-formulae thereof), R 5 is -Cl.
• R 5 is -Br. In some embodiments (e.g., including Formulae (XI), (XII), (XIII), and/or (XIV); or sub-formulae thereof), R 5 is -I. In some embodiments (e.g., including Formulae (XI), (XII), (XIII), and/or (XIV); or sub-formulae thereof), R 5 is -CN.
• R 5 is C 1-6 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 3-6 cycloalkyl, C 2 - 9 heterocycloalkyl, C 6-10 aryl, C 1-9 heteroaryl, -OR 12 , -SR 12 , -N(R 12 )(R 13 ), -C(O)OR 12 , -OC(O)N(R 12 )(R 13 ), - N(R 14 )C(O)N(R 12 )(R 13 ), -N(R 14 )C(O)OR 12 , -N(R 14 )S(O) 2 R 15 , -C(O)R 15 , -S(O)R 15 , -OC(O)R 15 , -C(O)N(R 12 )N(R 12 )
• R 5 is C 1-6 alkyl. In some embodiments (e.g., including Formulae (XI), (XII), (XIII), and/or (XIV); or sub-formulae thereof), R 5 is C 1 -4alkyl. In some embodiments (e.g., including Formulae (XI), (XII), (XIII), and/or (XIV); or sub-formulae thereof), R 5 is C 1 -3alkyl.
• R 5 is C 1-2 alkyl. In some embodiments (e.g., including Formulae (XI), (XII), (XIII), and/or (XIV); or sub-formulae thereof), R 5 is methyl. [00560] In some embodiments (e.g., including Formulae (XI), (XII), (XIII), and/or (XIV); or sub-formulae thereof), R 5 is hydrogen.
• R 5 is halogen. In some embodiments (e.g., including Formulae (XI), (XII), (XIII), and/or (XIV); or sub- formulae thereof), R 5 is -CN.
• R 5 is C 1-6 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 3-6 cycloalkyl, C 2-9 heterocycloalkyl, C 6-10 aryl, C 1 - 9 heteroaryl.
• R 5 is -OR 12 , -SR 12 , -N(R 12 )(R 13 ), -C(O)OR 12 , -OC(O)N(R 12 )(R 13 ), -N(R 14 )C(O)N(R 12 )(R 13 ), - N(R 14 )C(O)OR 12 , -N(R 14 )S(O) 2 R 15 , -C(O)R 15 , -S(O)R 15 , -OC(O)R 15 , -C(O)N(R 12 )(R 13 ), -C(O)C(O)N(R 12 )(R 13 ), - N(R 14 )C(O)R 15 , -S(O) 2 R 15 , -S(O) 2 R 15 , -S(O) 2 R 15 , -S(O) 2 R 15 , -S(O) 2 R 15 , -S(
• R 5 is C 1-6 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 3-6 cycloalkyl, C 2-9 heterocycloalkyl, C 6-10 aryl, or C 1-9 heteroaryl substituted with one, two, or three R 20e .
• R 5 is selected from hydrogen, halogen, and C 1-6 alkyl optionally substituted with one, two, or three R 20e .
• R 5 is selected from hydrogen and halogen.
• Y is N.
• Y is C(R 6 ). In some embodiments (e.g., including Formulae (XI), (XII), (XIII), and/or (XIV); or sub-formulae thereof), Y is CH. In some embodiments (e.g., including Formulae (XI), (XII), (XIII), and/or (XIV); or sub- formulae thereof), Y is C(R 6 ).
• Y is C(OH).
• R 6 is -OR 16 .
• R 6 is -N(R 12 )(R 16 ).
• R 6 is -OR 12 . In some embodiments (e.g., including Formulae (XI), (XII), (XIII), and/or (XIV); or sub-formulae thereof), R 6 is -OR 12a . In some embodiments (e.g., including Formulae (XI), (XII), (XIII), and/or (XIV); or sub-formulae thereof), R 6 is -SR 12 .
• R 6 is -N(R 12 )(R 13 ). In some embodiments (e.g., including Formulae (XI), (XII), (XIII), and/or (XIV); or sub-formulae thereof), R 6 is C 1-6 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 3-6 cycloalkyl, C 2-9 heterocycloalkyl, C 6-10 aryl, and C 1-9 heteroaryl optionally substituted with one, two, or three R 20f .
• R 6 is -OH. In some embodiments (e.g., including Formulae (XI), (XII), (XIII), and/or (XIV); or sub-formulae thereof), R 6 is C 1 - 6 alkyl. In some embodiments (e.g., including Formulae (XI), (XII), (XIII), and/or (XIV); or sub-formulae thereof), R 6 is C 1-4 alkyl.
• R 6 is C 1-3 alkyl. In some embodiments (e.g., including Formulae (XI), (XII), (XIII), and/or (XIV); or sub-formulae thereof), R 6 is C 1 -2alkyl. In some embodiments (e.g., including Formulae (XI), (XII), (XIII), and/or (XIV); or sub-formulae thereof), R 6 is methyl.
• R 6 is hydrogen. In some embodiments (e.g., including Formulae (XI), (XII), (XIII), and/or (XIV); or sub-formulae thereof), R 6 is halogen. In some embodiments (e.g., including Formulae (XI), (XII), (XIII), and/or (XIV); or sub- formulae thereof), R 6 is -CN.
• R 6 is C 1-6 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 3-6 cycloalkyl, C 2-9 heterocycloalkyl, C 6-10 aryl, C 1- 9 heteroaryl. In some embodiments (e.g., including Formulae (XI), (XII), (XIII), and/or (XIV); or sub-formulae thereof), R 6 is -OR 16 .
• R 6 is -N(R 12 )(R 16 ). In some embodiments (e.g., including Formulae (XI), (XII), (XIII), and/or (XIV); or sub-formulae thereof), R 6 is -OR 12 . In some embodiments (e.g., including Formulae (XI), (XII), (XIII), and/or (XIV); or sub-formulae thereof), R 6 is -OR 12a .
• R 6 is -SR 12 . In some embodiments (e.g., including Formulae (XI), (XII), (XIII), and/or (XIV); or sub-formulae thereof), R 6 is -N(R 12 )(R 13 ) . In some embodiments (e.g., including Formulae (XI), (XII), (XIII), and/or (XIV); or sub-formulae thereof), R 6 is -C(O)OR 12 .
• R 6 is -OC(O)N(R 12 )(R 13 ) . In some embodiments (e.g., including Formulae (XI), (XII), (XIII), and/or (XIV); or sub-formulae thereof), R 6 is - N(R 14 )C(O)N(R 12 )(R 13 ) .
• R 6 is -N(R 14 )C(O)OR 12 . In some embodiments (e.g., including Formulae (XI), (XII), (XIII), and/or (XIV); or sub-formulae thereof), R 6 is -N(R 14 )S(O) 2 R 15 . In some embodiments (e.g., including Formulae (XI), (XII), (XIII), and/or (XIV); or sub-formulae thereof), R 6 is -C(O)R 15 .
• R 6 is -S(O)R 15 . In some embodiments (e.g., including Formulae (XI), (XII), (XIII), and/or (XIV); or sub-formulae thereof), R 6 is -OC(O)R 15 . In some embodiments (e.g., including Formulae (XI), (XII), (XIII), and/or (XIV); or sub-formulae thereof), R 6 is - C(O)N(R 12 )(R 13 ) .
• R 6 is -C(O)C(O)N(R 12 )(R 13 ) . In some embodiments (e.g., including Formulae (XI), (XII), (XIII), and/or (XIV); or sub-formulae thereof), R 6 is -N(R 14 )C(O)R 15 . In some embodiments (e.g., including Formulae (XI), (XII), (XIII), and/or (XIV); or sub-formulae thereof), R 6 is -S(O) 2 R 15 .
• R 6 is -CH 2 C(O)N(R 12 )(R 13 ) . In some embodiments (e.g., including Formulae (XI), (XII), (XIII), and/or (XIV); or sub-formulae thereof), R 6 is -CH 2 N(R 14 )C(O)R 15 . In some embodiments (e.g., including Formulae (XI), (XII), (XIII), and/or (XIV); or sub-formulae thereof), R 6 is -CH 2 S(O) 2 R 15 .
• R 6 is -CH 2 S(O) 2 N(R 12 )(R 13 ) .
• R 6 is C 1- 6 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 3-6 cycloalkyl, C 2-9 heterocycloalkyl, C 6-10 aryl, or C 1-9 heteroaryl substituted with one, two, or three R 20f .
• R 6 is selected from hydrogen, halogen, -OR 12a , and C 1 - 6 alkyl optionally substituted with one, two, or three R 20f .
• J 3 is CH 2 and R 6 is selected from hydrogen, halogen, -CN, C 1-6 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 3-6 cycloalkyl, C 2-9 heterocycloalkyl, C 6-10 aryl, C 1-9 heteroaryl, - OR 16 , -N(R 12 )(R 16 ), -OR 12a , -SR 12 , -N(R 12 )(R 13 ), -C(O)OR 12 , -OC(O)N(R 12 )(R 13 ), -N(R 14 )C(O)N(R 12 )(R 13 ), - N(R 14 )C(O)OR 12 , -N(R 14 )S(O) 2 R 15 , -C(O)R 15 , -S(O)R 15 , -OC
• J 3 is CH 2 and R 6 is selected from hydrogen, halogen, -CN, C 1-6 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 3-6 cycloalkyl, C 2-9 heterocycloalkyl, C 6-10 aryl, C 1-9 heteroaryl, - OR 16 , -N(R 12 )(R 16 ), -SR 12 , -N(R 12 )(R 13 ), -C(O)OR 12 , -OC(O)N(R 12 )(R 13 ), -N(R 14 )C(O)N(R 12 )(R 13 ), - N(R 14 )C(O)OR 12 , -N(R 14 )S(O) 2 R 15 , -C(O)R 15 , -S(O)R 15 , -OC(O)R 15 , -C(O)OR 12 , -C(O) 2 R 15 , -C
• J 3 is CH 2 and R 6 is -OR 16 . In some embodiments of Formulae (I), or sub-formulae thereof, J 3 is CH 2 and R 6 is -N(R 12 )(R 16 ). [005 6 7] In some embodiments (e.g., including Formulae (XI), (XII), (XIII), and/or (XIV); or sub-formulae thereof), Z is N. In some embodiments (e.g., including Formulae (XI), (XII), (XIII), and/or (XIV); or sub-formulae thereof), Z is C(R 7 ).
• Z is CH. In some embodiments (e.g., including Formulae (XI), (XII), (XIII), and/or (XIV); or sub-formulae thereof), Z is CH. In some embodiments (e.g., including Formulae (XI), (XII), (XIII), and/or (XIV); or sub- formulae thereof), Z is C(R 7 ). [005 6 8] In some embodiments (e.g., including Formulae (XI), (XII), (XIII), and/or (XIV); or sub-formulae thereof), R 7 is hydrogen.
• R 7 is halogen. In some embodiments (e.g., including Formulae (XI), (XII), (XIII), and/or (XIV); or sub- formulae thereof), R 7 is -CN.
• R 7 is C 1-6 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 3-6 cycloalkyl, C 2-9 heterocycloalkyl, C 6-10 aryl, C 1 - 9 heteroaryl, -OR 12 , -SR 12 , -N(R 12 )(R 13 ), -C(O)OR 12 , -OC(O)N(R 12 )(R 13 ), -N(R 14 )C(O)N(R 12 )(R 13 ), - N(R 14 )C(O)OR 12 , -N(R 14 )S(O) 2 R 15 , -C(O)R 15 , -S(O)R 15 , -OC(O)R 15 , -C(O)N(R 12 )
• R 7 is C 1- 6 alkyl. In some embodiments (e.g., including Formulae (XI), (XII), (XIII), and/or (XIV); or sub-formulae thereof), R 7 is C 1 -4alkyl. In some embodiments (e.g., including Formulae (XI), (XII), (XIII), and/or (XIV); or sub-formulae thereof), R 7 is C 1-2 alkyl.
• R 7 is methyl.
• R 7 is hydrogen.
• R 7 is halogen.
• R 7 is -CN. In some embodiments (e.g., including Formulae (XI), (XII), (XIII), and/or (XIV); or sub- formulae thereof), R 7 is C 1-6 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 3-6 cycloalkyl, C 2-9 heterocycloalkyl, C 6-10 aryl, C 1- 9 heteroaryl, -OR 12 , -SR 12 , -N(R 12 )(R 13 ), -C(O)OR 12 , -OC(O)N(R 12 )(R 13 ), -N(R 14 )C(O)N(R 12 )(R 13 ), - N(R 14 )C(O)OR 12 , -N(R 14 )S(O) 2 R
• R 7 is C 1-6 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 3-6 cycloalkyl, C 2-9 heterocycloalkyl, C 6-10 aryl, or C 1-9 heteroaryl substituted with one, two, or three R 20g .
• R 7 is selected from hydrogen, halogen, and C 1-6 alkyl optionally substituted with one, two, or three R 20g .
• R 8 is hydrogen.
• R 8 is halogen.
• R 8 is -CN. In some embodiments (e.g., including Formulae (XI), (XII), (XIII), and/or (XIV); or sub-formulae thereof), R 8 is C 1-6 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 3-6 cycloalkyl, C 2-9 heterocycloalkyl, C 6-10 aryl, C 1 - 9 heteroaryl, -OR 12 , -SR 12 , -N(R 12 )(R 13 ), -C(O)OR 12 , -OC(O)N(R 12 )(R 13 ), -N(R 14 )C(O)N(R 12 )(R 13 ), - N(R 14 )C(O)OR 12 , -N(R 14 )S(O)
• R 8 is C 1-6 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 3-6 cycloalkyl, C 2 - 9 heterocycloalkyl, C 6-10 aryl, or C 1-9 heteroaryl substituted with one, two, or three R 20h .
• R 9 is hydrogen.
• R 9 is halogen. In some embodiments (e.g., including Formulae (XI), (XII), (XIII), and/or (XIV); or sub- formulae thereof), R 9 is -CN.
• R 9 is C 1-6 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 3-6 cycloalkyl, C 2-9 heterocycloalkyl, C 6-10 aryl, C 1- 9 heteroaryl.
• R 9 is -OR 12 , -SR 12 , -N(R 12 )(R 13 ), -C(O)OR 12 , -OC(O)N(R 12 )(R 13 ), -N(R 14 )C(O)N(R 12 )(R 13 ), - N(R 14 )C(O)OR 12 , -N(R 14 )S(O) 2 R 15 , -C(O)R 15 , -S(O)R 15 , -OC(O)R 15 , -C(O)N(R 12 )(R 13 ), -C(O)C(O)N(R 12 )(R 13 ), - N(R 14 )C(O)R 15 , -S(O) 2 R 15 , -S(O) 2 R 15 , -S(O) 2 R 15 , -S(O) 2 R 15 , -S(O) 2 R 15 , -S(
• R 9 is C 1-6 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 3-6 cycloalkyl, C 2-9 heterocycloalkyl, C 6-10 aryl, or C 1-9 heteroaryl substituted with one, two, or three R 20i .
• R 9a is hydrogen.
• R 9a is halogen. In some embodiments (e.g., including Formulae (XI), (XII), (XIII), and/or (XIV); or sub- formulae thereof), R 9a is -CN.
• R 9a is C 1-6 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 3-6 cycloalkyl, C 2-9 heterocycloalkyl, C 6-10 aryl, C 1- 9 heteroaryl.
• R 9a is -OR 12 , -SR 12 , -N(R 12 )(R 13 ), -C(O)OR 12 , -OC(O)N(R 12 )(R 13 ), -N(R 14 )C(O)N(R 12 )(R 13 ), - N(R 14 )C(O)OR 12 , -N(R 14 )S(O) 2 R 15 , -C(O)R 15 , -S(O)R 15 , -OC(O)R 15 , -C(O)N(R 12 )(R 13 ), -C(O)C(O)N(R 12 )(R 13 ), - N(R 14 )C(O)R 15 , -S(O) 2 R 15 , -S(O)
• R 9a is C 1-6 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 3-6 cycloalkyl, C 2-9 heterocycloalkyl, C 6-10 aryl, or C 1-9 heteroaryl substituted with one, two, or three R 20i .
• R 9 and R 9a are combined to form a C 3-6 cycloalkyl.
• R 9 and R 9a are combined to form a C 2-9 heterocycloalkyl. In some embodiments (e.g., including Formulae (XI), (XII), (XIII), and/or (XIV); or sub-formulae thereof), R 9 and R 9a are combined to form a C 3-6 cycloalkyl substituted with one, two, or three R 20i .
• R 9 and R 9a are combined to form a C 2-9 heterocycloalkyl substituted with one, two, or three R 20i .
• R 9 and R 9a are hydrogen.
• R 10 is hydrogen.
• R 10 is halogen. In some embodiments (e.g., including Formulae (XI), (XII), (XIII), and/or (XIV); or sub- formulae thereof), R 10 is -CN.
• R 10 is C 1-6 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 3-6 cycloalkyl, C 2-9 heterocycloalkyl, C 6-10 aryl, C 1- 9 heteroaryl. In some embodiments (e.g., including Formulae (XI), (XII), (XIII), and/or (XIV); or sub-formulae thereof), R 10 is -R 16 .
• R 10 is -OR 16 . In some embodiments (e.g., including Formulae (XI), (XII), (XIII), and/or (XIV); or sub-formulae thereof), R 10 is -N(R 12 )(R 16 ).
• R 10 is -OR 12 , -SR 12 , -N(R 12 )(R 13 ), -C(O)OR 12 , -OC(O)N(R 12 )(R 13 ), - N(R 14 )C(O)N(R 12 )(R 13 ), -N(R 14 )C(O)OR 12 , -N(R 14 )S(O) 2 R 15 , -C(O)R 15 , -S(O)R 15 , -OC(O)R 15 , -C(O)N(R 12 )(R 13 ), - C(O)C(O)N(R 12 )(R 13 ), -N(R 14 )C(O)R 15 , -S(O) 2 R 15 , -S(O) 2 R 15 , -S(O) 2 R 15 , -S(O) 2 R 15 , -S(O) 2 R 15 , -S(
• R 10 is C 1-6 alkyl, C 2-6 alkenyl, C 2- 6 alkynyl, C 3-6 cycloalkyl, C 2-9 heterocycloalkyl, C 6-10 aryl, and C 1-9 heteroaryl substituted with one, two, or three R 20j .
• R 10a is hydrogen.
• R 10a is halogen. In some embodiments (e.g., including Formulae (XI), (XII), (XIII), and/or (XIV); or sub- formulae thereof), R 10a is -CN.
• R 10a is C 1-6 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 3-6 cycloalkyl, C 2-9 heterocycloalkyl, C 6-10 aryl, C 1 - 9 heteroaryl. In some embodiments (e.g., including Formulae (XI), (XII), (XIII), and/or (XIV); or sub-formulae thereof), R 10a is -R 16 .
• R 10a is -OR 16 . In some embodiments (e.g., including Formulae (XI), (XII), (XIII), and/or (XIV); or sub-formulae thereof), R 10a is -N(R 12 )(R 16 ).
• R 10a is -OR 12 , -SR 12 , -N(R 12 )(R 13 ), -C(O)OR 12 , -OC(O)N(R 12 )(R 13 ), - N(R 14 )C(O)N(R 12 )(R 13 ), -N(R 14 )C(O)OR 12 , -N(R 14 )S(O) 2 R 15 , -C(O)R 15 , -S(O)R 15 , -OC(O)R 15 , -C(O)N(R 12 )(R 13 ), - C(O)C(O)N(R 12 )(R 13 ), -N(R 14 )C(O)R 15 , -S(O) 2 R 15 , -S(O)
• R 10a is C 1-6 alkyl, C 2-6 alkenyl, C 2- 6 alkynyl, C 3-6 cycloalkyl, C 2-9 heterocycloalkyl, C 6-10 aryl, and C 1-9 heteroaryl substituted with one, two, or three R 20j .
• R 10 and R 10a are combined to form a C 3-6 cycloalkyl.
• R 10 and R 10a are combined to form a C 2-9 heterocycloalkyl. In some embodiments (e.g., including Formulae (XI), (XII), (XIII), and/or (XIV); or sub-formulae thereof), R 10 and R 10a are combined to form a C 3-6 cycloalkyl substituted with one, two, or three R 20j .
• R 10 and R 10a are combined to form a C 2 - 9 heterocycloalkyl substituted with one, two, or three R 20j .
• J 1 is N.
• J 1 is C.
• J 1 is C(R 8 ).
• J 2 is N.
• J 2 is N(R 9 ).
• J 2 is C(R 9 ). In some embodiments (e.g., including Formulae (XI), (XII), (XIII), and/or (XIV); or sub-formulae thereof), J 2 is C(H). In some embodiments (e.g., including Formulae (XI), (XII), (XIII), and/or (XIV); or sub-formulae thereof), J 2 is C(R 9 )(R 9a ).
• J 2 is CH 2 . In some embodiments (e.g., including Formulae (XI), (XII), (XIII), and/or (XIV); or sub-formulae thereof), J 2 is C(O). [00580] In some embodiments (e.g., including Formulae (XI), (XII), (XIII), and/or (XIV); or sub-formulae thereof), J 3 is N(R 10 ).
• J 3 is C(R 10 )(R 10a ). In some embodiments (e.g., including Formulae (XI), (XII), (XIII), and/or (XIV); or sub-formulae thereof), J 3 is NH.
• J 3 is CH 2 and R 6 is selected from hydrogen, halogen, -CN, C 1-6 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 3-6 cycloalkyl, C 2-9 heterocycloalkyl, C 6-10 aryl, C 1- 9 heteroaryl, -OR 16 , -N(R 12 )(R 16 ), -OR 12a , -SR 12 , -N(R 12 )(R 13 ), -C(O)OR 12 , -OC(O)N(R 12 )(R 13 ), - N(R 14 )C(O)N(R 12 )(R 13 ), -N(R 14 )C(O)OR 12 , -N(R 14 )S(O) 2 R 15 , -C(O)R 15 , -S(O)R
• J 3 is CH 2 and R 6 is selected from hydrogen, halogen, -CN, C 1-6 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 3-6 cycloalkyl, C 2-9 heterocycloalkyl, C 6-10 aryl, C 1-9 heteroaryl, -OR 16 , -N(R 12 )(R 16 ), -SR 12 , -N(R 12 )(R 13 ), -C(O)OR 12 , -OC(O)N(R 12 )(R 13 ), - N(R 14 )C(O)N(R 12 )(R 13 ), -N(R 14 )C(O)OR 12 , -N(R 14 )S(O) 2 R 15 , -C(O)R 15 , -S(O)R 15 , -OC(O)R 15 ,
• J 3 is CH 2 and R 6 is -OR 16 . In some embodiments of (e.g., of Formulae (I)), or sub-formulae thereof, J 3 is CH 2 and R 6 is - N(R 12 )(R 16 ). [00582] In some embodiments (e.g., including Formulae (XI), (XII), (XIII), and/or (XIV); or sub-formulae thereof), J 1 is N and J 2 is C(R 9 )(R 9a ).
• J 1 is C(R 8 ) and J 2 is C(R 9 )(R 9a ).
• J 1 is C and J 2 is C(R 9 ).
• J 1 is N and J 2 is C(R 9 )(R 9a ).
• J 1 is C(R 8 ) and J 2 is C(R 9 )(R 9a ).
• J 1 is C and J 2 is C(R 9 ).
• R 9 is hydrogen, -CN, C 1-6 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 3-6 cycloalkyl, C 2- 9 heterocycloalkyl, C 6-10 aryl, C 1-9 heteroaryl, -OR 12 , -C(O)OR 12 , -OC(O)N(R 12 )(R 13 ), -C(O)R 15 , -OC(O)R 15 , - C(O)N(R 12 )(R 13 ), -C(O)C(O)N(R 12 )(R 13 ), -CH 2 C(O)N(R 12 )(R 13 ), -CH 2 N(R 14 )C(O)R 15 , -CH 2 S(O) 2 R 15 , and - CH 2 S(O) 2 N(R 12 )(R 13 ), wherein C 1-6 alkyl, C 2-6 alkenyl, C 2-6 alkynyl
• R 9 is hydrogen, - CN, C 1-6 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 3-6 cycloalkyl, C 2-9 heterocycloalkyl, C 6-10 aryl, C 1-9 heteroaryl, -C(O)OR 12 , - C(O)R 15 , -C(O)N(R 12 )(R 13 ), -C(O)C(O)N(R 12 )(R 13 ), -CH 2 C(O)N(R 12 )(R 13 ), -CH 2 N(R 14 )C(O)R 15 , -CH 2 S(O) 2 R 15 , and -CH 2 S(O) 2 N(R 12 )(R 13 ), wherein C 1-6 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 3-6 cycloalkyl, C 2-9 heterocycloalkyl, C 6-10 aryl, wherein C
• R 9 is hydrogen, -CN, C 1-6 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 3-6 cycloalkyl, C 2-9 heterocycloalkyl, C 6-10 aryl, C 1 - 9 heteroaryl, -OR 12 , -C(O)OR 12 , -OC(O)N(R 12 )(R 13 ), -C(O)R 15 , -OC(O)R 15 , -C(O)N(R 12 )(R 13 ), - C(O)C(O)N(R 12 )(R 13 ), -CH 2 C(O)N(R 12 )(R 13 ), -CH 2 N(R 14 )C(O)R 15 , -CH 2 S(O) 2 R 15 , and -CH 2 S(O) 2 N(R 12 )(R 13 ), wherein C 1-6 alkyl,
• R 9 is hydrogen, -CN, C 1-6 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 3-6 cycloalkyl, C 2-9 heterocycloalkyl, C 6-10 aryl, C 1-9 heteroaryl, -C(O)OR 12 , - C(O)R 15 , -C(O)N(R 12 )(R 13 ), -C(O)C(O)N(R 12 )(R 13 ), -CH 2 C(O)N(R 12 )(R 13 ), -CH 2 N(R 14 )C(O)R 15 , -CH 2 S(O) 2 R 15 , and -CH 2 S(O) 2 N(R 12 )(R 13 ), wherein C 1-6 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 3-6 cycloalkyl, C 2-9 heterocycloalkyl, C 6-10 aryl, C 1-9 heteroary
• R 10 is hydrogen, -CN, C 1-6 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 3-6 cycloalkyl, C 2 - 9 heterocycloalkyl, C 6-10 aryl, C 1-9 heteroaryl, -OR 12 , -C(O)OR 12 , -OC(O)N(R 12 )(R 13 ), -C(O)R 15 , -OC(O)R 15 , - C(O)N(R 12 )(R 13 ), -C(O)C(O)N(R 12 )(R 13 ), -CH 2 C(O)N(R 12 )(R 13 ), -CH 2 N(R 14 )C(O)R 15 , -CH 2 S(O) 2 R 15 , and - CH 2 S(O) 2 N(R 12 )(R 13 ), wherein C 1-6 alkyl, C 2-6 alkenyl, C 2-6 alkyn
• R 10 is hydrogen, - CN, C 1-6 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 3-6 cycloalkyl, C 2-9 heterocycloalkyl, C 6-10 aryl, C 1-9 heteroaryl, -C(O)OR 12 , - C(O)R 15 , -C(O)N(R 12 )(R 13 ), -C(O)C(O)N(R 12 )(R 13 ), -CH 2 C(O)N(R 12 )(R 13 ), -CH 2 N(R 14 )C(O)R 15 , -CH 2 S(O) 2 R 15 , and -CH 2 S(O) 2 N(R 12 )(R 13 ), wherein C 1-6 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 3-6 cycloalkyl, C 2-9 heterocycloalkyl, C 6-10 aryl, wherein C
• R 10 is hydrogen, -CN, C 1-6 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 3-6 cycloalkyl, C 2-9 heterocycloalkyl, C 6-10 aryl, C 1- 9 heteroaryl, -OR 12 , -C(O)OR 12 , -OC(O)N(R 12 )(R 13 ), -C(O)R 15 , -OC(O)R 15 , -C(O)N(R 12 )(R 13 ), - C(O)C(O)N(R 12 )(R 13 ), -CH 2 C(O)N(R 12 )(R 13 ), -CH 2 N(R 14 )C(O)R 15 , -CH 2 S(O) 2 R 15 , and -CH 2 S(O) 2 N(R 12 )(R 13 ), wherein C 1-6 alkyl, C 2-6 alkenyl, C 2-6 alkynyl
• R 10 is hydrogen, -CN, C 1-6 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 3-6 cycloalkyl, C 2-9 heterocycloalkyl, C 6-10 aryl, C 1-9 heteroaryl, -C(O)OR 12 , - C(O)R 15 , -C(O)N(R 12 )(R 13 ), -C(O)C(O)N(R 12 )(R 13 ), -CH 2 C(O)N(R 12 )(R 13 ), -CH 2 N(R 14 )C(O)R 15 , -CH 2 S(O) 2 R 15 , and -CH 2 S(O) 2 N(R 12 )(R 13 ), wherein C 1-6 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 3-6 cycloalkyl, C 2-9 heterocycloalkyl, C 6-10 aryl, C 1-9 heteroary
• W 1 is N. In some embodiments (e.g., including Formulae (XI), (XII), (XIII), and/or (XIV); or sub-formulae thereof), W 1 is N(R 1 ). In some embodiments (e.g., including Formulae (XI), (XII), (XIII), and/or (XIV); or sub-formulae thereof), W 1 is O.
• W 1 is C(R 1 ). In some embodiments (e.g., including Formulae (XI), (XII), (XIII), and/or (XIV); or sub-formulae thereof), W 1 is C(R 1 ). In some embodiments (e.g., including Formulae (XI), (XII), (XIII), and/or (XIV); or sub-formulae thereof), W 1 is C(R 1 )(R 1a ). In some embodiments (e.g., including Formulae (XI), (XII), (XIII), and/or (XIV); or sub-formulae thereof), W 1 is C(O).
• W 1 is S(O). In some embodiments (e.g., including Formulae (XI), (XII), (XIII), and/or (XIV); or sub-formulae thereof), W 1 is S(O) 2 . In some embodiments (e.g., including Formulae (XI), (XII), (XIII), and/or (XIV); or sub-formulae thereof), W 1 is S(O)(NR 1 ).
• W 1 is S(O)(R 1 ). In some embodiments (e.g., including Formulae (XI), (XII), (XIII), and/or (XIV); or sub-formulae thereof), W 1 is P(O)(R 1 ). [00586] In some embodiments (e.g., including Formulae (XI), (XII), (XIII), and/or (XIV); or sub-formulae thereof), R 1 is hydrogen.
• R 1 is halogen. In some embodiments (e.g., including Formulae (XI), (XII), (XIII), and/or (XIV); or sub- formulae thereof), R 1 is -CN.
• R 1 is C 1-6 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 3-6 cycloalkyl, C 2-9 heterocycloalkyl, C 6-10 aryl, C 1- 9 heteroaryl.
• R 1 is -OR 12 , -SR 12 , -N(R 12 )(R 13 ), -C(O)OR 12 , -OC(O)N(R 12 )(R 13 ), -N(R 14 )C(O)N(R 12 )(R 13 ), - N(R 14 )C(O)OR 12 , -N(R 14 )S(O) 2 R 15 , -C(O)R 15 , -S(O)R 15 , -OC(O)R 15 , -C(O)N(R 12 )(R 13 ), -C(O)C(O)N(R 12 )(R 13 ), - N(R 14 )C(O)R 15 , -S(O) 2 R 15 , -S(O) 2 R 15 , -S(O) 2 R 15 , -S(O) 2 R 15 , -S(O) 2 R 15 , -S(
• R 1 is C 1-6 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 3-6 cycloalkyl, C 2- 9 heterocycloalkyl, C 6-10 aryl, and C 1-9 heteroaryl substituted with one, two, or three R 20a .
• R 1 is hydrogen, -CN, C 1-6 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 3-6 cycloalkyl, C 2 - 9 heterocycloalkyl, C 6-10 aryl, C 1-9 heteroaryl, -OR 12 , -C(O)OR 12 , -OC(O)N(R 12 )(R 13 ), -C(O)R 15 , -OC(O)R 15 , - C(O)N(R 12 )(R 13 ), -C(O)C(O)N(R 12 )(R 13 ), -CH 2 C(O)N(R 12 )(R 13 ), -CH 2 N(R 14 )C(O)R 15 , -CH 2 S(O) 2 R 15 , and - CH 2 S(O) 2 N(R 12 )(R 13 ), wherein C 1-6 alkyl, C 2-6 alkenyl, C 2-6 alkyn
• R 1 is hydrogen, - CN, C 1-6 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 3-6 cycloalkyl, C 2-9 heterocycloalkyl, C 6-10 aryl, C 1-9 heteroaryl, -C(O)OR 12 , - C(O)R 15 , -C(O)N(R 12 )(R 13 ), -C(O)C(O)N(R 12 )(R 13 ), -CH 2 C(O)N(R 12 )(R 13 ), -CH 2 N(R 14 )C(O)R 15 , -CH 2 S(O) 2 R 15 , and -CH 2 S(O) 2 N(R 12 )(R 13 ), wherein C 1-6 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 3-6 cycloalkyl, C 2-9 heterocycloalkyl, C 6-10 aryl, wherein C
• R 1 is hydrogen, -CN, C 1-6 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 3-6 cycloalkyl, C 2- 9 heterocycloalkyl, C 6-10 aryl, C 1-9 heteroaryl, -OR 12 , -C(O)OR 12 , -OC(O)N(R 12 )(R 13 ), -C(O)R 15 , -OC(O)R 15 , - C(O)N(R 12 )(R 13 ), -C(O)C(O)N(R 12 )(R 13 ), -CH 2 C(O)N(R 12 )(R 13 ), -CH 2 N(R 14 )C(O)R 15 , -CH 2 S(O) 2 R 15 , and - CH
• R 1 is hydrogen, -CN, C 1-6 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 3-6 cycloalkyl, C 2- 9 heterocycloalkyl, C 6-10 aryl, C 1-9 heteroaryl, -C(O)OR 12 , -C(O)R 15 , -C(O)N(R 12 )(R 13 ), -C(O)C(O)N(R 12 )(R 13 ), - CH 2 C(O)N(R 12 )(R 13 ), -CH 2 N(R 14 )C(O)R 15 , -CH 2 S(O) 2 R 15 , and -CH 2 S(O) 2 N(R 12 )(R 13 ), wherein C 1-6 alkyl, C 2 - 6 alkenyl, C 2-6 alkynyl, C 3-6 cycloalkyl, C 2- 9 heterocycloalkyl, C 6-10 aryl, C 1-9
• R 1 is -CN. In some embodiments, R 1 is -F. In some embodiments, R 1 is -CF3. In some embodiments, R 1 is -OCH 3 . In some embodiments, R 1 is cyclopropyl. In some embodiments, R 1 is -OCH 2 CF3. In some embodiments, R 1 is -CH 3 . [00588] In some embodiments (e.g., including Formulae (XI), (XII), (XIII), and/or (XIV); or sub-formulae thereof), R 1a is hydrogen.
• R 1a is halogen. In some embodiments (e.g., including Formulae (XI), (XII), (XIII), and/or (XIV); or sub- formulae thereof), R 1a is -CN.
• R 1a is C 1-6 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 3-6 cycloalkyl, C 2-9 heterocycloalkyl, C 6-10 aryl, C 1- 9 heteroaryl.
• R 1a is -OR 12 , -SR 12 , -N(R 12 )(R 13 ), -C(O)OR 12 , -OC(O)N(R 12 )(R 13 ), -N(R 14 )C(O)N(R 12 )(R 13 ), - N(R 14 )C(O)OR 12 , -N(R 14 )S(O) 2 R 15 , -C(O)R 15 , -S(O)R 15 , -OC(O)R 15 , -C(O)N(R 12 )(R 13 ), -C(O)C(O)N(R 12 )(R 13 ), - N(R 14 )C(O)R 15 , -S(O) 2 R 15 , -S(O)
• R 1a is C 1-6 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 3-6 cycloalkyl, C 2 - 9 heterocycloalkyl, C 6-10 aryl, and C 1-9 heteroaryl substituted with one, two, or three R 20a .
• R 1 and R 1a are combined to form a C 3-6 cycloalkyl.
• R 1 and R 1a are combined to form a C 2-9 heterocycloalkyl. In some embodiments (e.g., including Formulae (XI), (XII), (XIII), and/or (XIV); or sub-formulae thereof), R 1 and R 1a are combined to form a C 3-6 cycloalkyl substituted with one, two, or three R 20a .
• R 1 and R 1a are combined to form a C 2- 9 heterocycloalkyl substituted with one, two, or three R 20a .
• W 2 is N.
• W 2 is N(R 2 ).
• W 2 is O. In some embodiments (e.g., including Formulae (XI), (XII), (XIII), and/or (XIV); or sub-formulae thereof), W 2 is C(R 2 ). In some embodiments (e.g., including Formulae (XI), (XII), (XIII), and/or (XIV); or sub-formulae thereof), W 2 is C(R 2 )(R 2a ).
• W 2 is C(O). In some embodiments (e.g., including Formulae (XI), (XII), (XIII), and/or (XIV); or sub-formulae thereof), W 2 is S(O). In some embodiments (e.g., including Formulae (XI), (XII), (XIII), and/or (XIV); or sub-formulae thereof), W 2 is S(O) 2 .
• W 2 is S(O)(NR 2 ). In some embodiments (e.g., including Formulae (XI), (XII), (XIII), and/or (XIV); or sub-formulae thereof), W 2 is S(O)(R 2 ). In some embodiments (e.g., including Formulae (XI), (XII), (XIII), and/or (XIV); or sub-formulae thereof), W 2 is P(O)(R 2 ).
• R 3a is independently hydrogen. In some embodiments (e.g., including Formulae (XI), (XII), (XIII), and/or (XIV); or sub-formulae thereof), R 3a is independently halogen. In some embodiments (e.g., including Formulae (XI), (XII), (XIII), and/or (XIV); or sub-formulae thereof), R 3a is independently -CN.
• R 3a is independently C 1-6 alkyl, C 2-6 alkenyl, C 2 - 6 alkynyl, C 3-6 cycloalkyl, C 2-9 heterocycloalkyl, C 6-10 aryl, or C 1-9 heteroaryl.
• R 3a is independently -OR 12 , -SR 12 , - N(R 12 )(R 13 ), -C(O)OR 12 , -OC(O)N(R 12 )(R 13 ), -N(R 14 )C(O)N(R 12 )(R 13 ), -N(R 14 )C(O)OR 12 , -N(R 14 )S(O) 2 R 15 , - C(O)R 15 , -S(O)R 15 , -OC(O)R 15 , -C(O)N(R 12 )(R 13 ), -C(O)C(O)N(R 12 )(R 13 ), -N(R 14 )C(O)R 15 , -S(O) 2 R 15 , - S(O)
• R 3a is independently C 1-6 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 3-6 cycloalkyl, C 2-9 heterocycloalkyl, C 6- 10aryl, or C 1-9 heteroaryl substituted with one, two, or three R 20c .
• R 3 and R 3a are combined to form a C 3-6 cycloalkyl.
• R 3 and R 3a are combined to form a C 2-9 heterocycloalkyl. In some embodiments (e.g., including Formulae (XI), (XII), (XIII), and/or (XIV); or sub-formulae thereof), R 3 and R 3a are combined to form a C 3-6 cycloalkyl substituted with one, two, or three R 20c .
• R 3 and R 3a are combined to form a C 2- 9 heterocycloalkyl substituted with one, two, or three R 20c .
• R 3 is selected from hydrogen, halogen, -CN, C 1-6 alkyl, C 3-6 cycloalkyl, C 2-9 heterocycloalkyl, -OR 12 , -SR 12 , and - N(R 12 )(R 13 ), wherein C 1-6 alkyl, C 3-6 cycloalkyl, and C 2-9 heterocycloalkyl are optionally substituted with one, two, or three R 20c .
• R 3 is selected from hydrogen, halogen, -CN, C 1-6 alkyl, C 3-6 cycloalkyl, and -OR 12 , wherein C 1-6 alkyl and C3- 6 cycloalkyl are optionally substituted with one, two, or three R 20c .
• R 3 is -CN.
• R 3 is -F.
• R 3 is -CF 3 .
• R 3 is -OCH 3 .
• R 3 is cyclopropyl.
• R 3 is -OCH 2 CF3. In some embodiments, R 3 is -CH 3 .
• W 4 is N. In some embodiments (e.g., including Formulae (XI), (XII), (XIII), and/or (XIV); or sub-formulae thereof), W 4 is N(R 4 ). In some embodiments (e.g., including Formulae (XI), (XII), (XIII), and/or (XIV); or sub- formulae thereof), W 4 is O.
• W 4 is C(R 4 ). In some embodiments (e.g., including Formulae (XI), (XII), (XIII), and/or (XIV); or sub-formulae thereof), W 4 is C(R 4 ). In some embodiments (e.g., including Formulae (XI), (XII), (XIII), and/or (XIV); or sub-formulae thereof), W 4 is C(R 4 )(R 4a ). In some embodiments (e.g., including Formulae (XI), (XII), (XIII), and/or (XIV); or sub-formulae thereof), W 4 is C(O).
• W 4 is S(O). In some embodiments (e.g., including Formulae (XI), (XII), (XIII), and/or (XIV); or sub-formulae thereof), W 4 is S(O). In some embodiments (e.g., including Formulae (XI), (XII), (XIII), and/or (XIV); or sub-formulae thereof), W 4 is S(O) 2 . In some embodiments (e.g., including Formulae (XI), (XII), (XIII), and/or (XIV); or sub-formulae thereof), W 4 is S(O)(NR 4 ).
• W 4 is S(O)(R 4 ). In some embodiments (e.g., including Formulae (XI), (XII), (XIII), and/or (XIV); or sub-formulae thereof), W 4 is P(O)(R 4 ). [00596] In some embodiments (e.g., including Formulae (XI), (XII), (XIII), and/or (XIV); or sub-formulae thereof), R 4 is independently hydrogen.
• R 4 is independently halogen. In some embodiments (e.g., including Formulae (XI), (XII), (XIII), and/or (XIV); or sub-formulae thereof), R 4 is independently -CN.
• R 4 is independently C 1-6 alkyl, C 2-6 alkenyl, C 2 - 6 alkynyl, C 3-6 cycloalkyl, C 2-9 heterocycloalkyl, C 6-10 aryl, C 1-9 heteroaryl.
• R 4 is independently -OR 12 , -SR 12 , -N(R 12 )(R 13 ), -C(O)OR 12 , -OC(O)N(R 12 )(R 13 ), -N(R 14 )C(O)N(R 12 )(R 13 ), -N(R 14 )C(O)OR 12 , -N(R 14 )S(O) 2 R 15 , -C(O)R 15 , -S(O)R 15 , -OC(O)R 15 , -C(O)N(R 12 )(R 13 ), -C(O)C(O)N(R 12 )(R 13 ), -N(R 14 )C(O)R 15 , -S(O) 2 R 15 , -S(O)
• R 4 is independently C 1-6 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 3-6 cycloalkyl, C 2-9 heterocycloalkyl, C 6-10 aryl, or C 1-9 heteroaryl substituted with one, two, or three R 20d .
• R 4 is independently C 1-6 alkyl.
• R 4 is independently C 1-4 alkyl. In some embodiments (e.g., including Formulae (XI), (XII), (XIII), and/or (XIV); or sub-formulae thereof), R 4 is independently C 1 -3alkyl. In some embodiments (e.g., including Formulae (XI), (XII), (XIII), and/or (XIV); or sub-formulae thereof), R 4 is independently C 1-2 alkyl.
• R 4 is independently methyl.
• R 4 is -CN.
• R 4 is -F.
• R 4 is -CF3.
• R 4 is -OCH 3 .
• R 4 is cyclopropyl.
• R 4 is -OCH 2 CF3.
• R 4 is -CH 3 .
• R 4 is hydrogen, -CN, C 1-6 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 3-6 cycloalkyl, C 2- 9 heterocycloalkyl, C 6-10 aryl, C 1-9 heteroaryl, -OR 12 , -C(O)OR 12 , -OC(O)N(R 12 )(R 13 ), -C(O)R 15 , -OC(O)R 15 , - C(O)N(R 12 )(R 13 ), -C(O)C(O)N(R 12 )(R 13 ), -CH 2 C(O)N(R 12 )(R 13 ), -CH 2 N(R 14 )C(O)R 15 , -CH 2 S(O) 2 R 15 , and - CH 2 S(O) 2 N(R 12 )(R 13 ), wherein C 1-6 alkyl, C 2-6 alkenyl, C 2-6 alkynyl
• R 4 is hydrogen, - CN, C 1-6 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 3-6 cycloalkyl, C 2-9 heterocycloalkyl, C 6-10 aryl, C 1-9 heteroaryl, -C(O)OR 12 , - C(O)R 15 , -C(O)N(R 12 )(R 13 ), -C(O)C(O)N(R 12 )(R 13 ), -CH 2 C(O)N(R 12 )(R 13 ), -CH 2 N(R 14 )C(O)R 15 , -CH 2 S(O) 2 R 15 , and -CH 2 S(O) 2 N(R 12 )(R 13 ), wherein C 1-6 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 3-6 cycloalkyl, C 2-9 heterocycloalkyl, C 6-10 aryl, wherein C
• R 4 is hydrogen, -CN, C 1-6 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 3-6 cycloalkyl, C 2- 9 heterocycloalkyl, C 6-10 aryl, C 1-9 heteroaryl, -OR 12 , -C(O)OR 12 , -OC(O)N(R 12 )(R 13 ), -C(O)R 15 , -OC(O)R 15 , - C(O)N(R 12 )(R 13 ), -C(O)C(O)N(R 12 )(R 13 ), -CH 2 C(O)N(R 12 )(R 13 ), -CH 2 N(R 14 )C(O)R 15 , -CH 2 S(O) 2 R 15 , and - CH
• R 4 is hydrogen, -CN, C 1-6 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 3-6 cycloalkyl, C 2- 9 heterocycloalkyl, C 6-10 aryl, C 1-9 heteroaryl, -C(O)OR 12 , -C(O)R 15 , -C(O)N(R 12 )(R 13 ), -C(O)C(O)N(R 12 )(R 13 ), - CH 2 C(O)N(R 12 )(R 13 ), -CH 2 N(R 14 )C(O)R 15 , -CH 2 S(O) 2 R 15 , and -CH 2 S(O) 2 N(R 12 )(R 13 ), wherein C 1-6 alkyl, C 2- 6 alkenyl, C 2-6 alkynyl, C 3-6 cycloalkyl, C 2- 9 heterocycloalkyl, C 6-10 aryl, C 1-9 heteroary
• R 4a is independently hydrogen. In some embodiments (e.g., including Formulae (XI), (XII), (XIII), and/or (XIV); or sub-formulae thereof), R 4a is independently halogen. In some embodiments (e.g., including Formulae (XI), (XII), (XIII), and/or (XIV); or sub-formulae thereof), R 4a is independently -CN.
• R 4a is independently C 1-6 alkyl, C 2-6 alkenyl, C 2 - 6 alkynyl, C 3-6 cycloalkyl, C 2-9 heterocycloalkyl, C 6-10 aryl, C 1-9 heteroaryl.
• R 4a is independently -OR 12 , -SR 12 , - N(R 12 )(R 13 ), -C(O)OR 12 , -OC(O)N(R 12 )(R 13 ), -N(R 14 )C(O)N(R 12 )(R 13 ), -N(R 14 )C(O)OR 12 , -N(R 14 )S(O) 2 R 15 , - C(O)R 15 , -S(O)R 15 , -OC(O)R 15 , -C(O)N(R 12 )(R 13 ), -C(O)C(O)N(R 12 )(R 13 ), -N(R 14 )C(O)R 15 , -S(O) 2 R 15 , - S(O)
• R 4a is independently C 1-6 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 3-6 cycloalkyl, C 2-9 heterocycloalkyl, C 6- 10aryl, or C 1-9 heteroaryl substituted with one, two, or three R 20d .
• R 4a is independently C 1-6 alkyl.
• R 4a is independently C 1-4 alkyl. In some embodiments (e.g., including Formulae (XI), (XII), (XIII), and/or (XIV); or sub-formulae thereof), R 4a is independently C 1 -3alkyl. In some embodiments (e.g., including Formulae (XI), (XII), (XIII), and/or (XIV); or sub- formulae thereof), R 4a is independently C 1 -2alkyl.
• R 4a is independently methyl. [00599] In some embodiments (e.g., including Formulae (XI), (XII), (XIII), and/or (XIV); or sub-formulae thereof), R 4 and R 4a are combined to form a C 3-6 cycloalkyl. In some embodiments (e.g., including Formulae (XI), (XII), (XIII), and/or (XIV); or sub-formulae thereof), R 4 and R 4a are combined to form a C 2-9 heterocycloalkyl.
• R 4 and R 4a are combined to form a C 3-6 cycloalkyl substituted with one, two, or three R 20d .
• R 4 and R 4a are combined to form a C 2 - 9 heterocycloalkyl substituted with one, two, or three R 20d .
• W 5 is N. In some embodiments (e.g., including Formulae (XI), (XII), (XIII), and/or (XIV); or sub-formulae thereof), W 5 is C. In some embodiments (e.g., including Formulae (XI), (XII), (XIII), and/or (XIV); or sub-formulae thereof), W 5 is CH.
• W 6 is N. In some embodiments (e.g., including Formulae (XI), (XII), (XIII), and/or (XIV); or sub-formulae thereof), W 6 is C. In some embodiments (e.g., including Formulae (XI), (XII), (XIII), and/or (XIV); or sub-formulae thereof), W 6 is CH.
• At least one of W 1 , W 2 , W 3 , W 4 , W 5 , and W 6 is N, N(R 1 ), N(R 2 ), N(R 3 ), or N(R 4 ).
• at least one of W 1 , W 2 , W 3 , and W 4 is N, N(R 1 ), N(R 2 ), N(R 3 ), or N(R 4 ).
• two Ring A are double bonds.
• three Ring A are double bonds.
• no Ring A are double bonds.
• one Ring A is a double bond.
• two Ring A are double bonds.
• W 3 is C(O), S(O), S(O) 2 , S(O)(NR 3 ), S(O)(R 3 ), or P(O)(R 3 );
• W 4 is N(R 4 );
• W 1 is C(R 1 ); and
• W 2 is C(R 2 ).
• W 1 is C(O), S(O), S(O) 2 , S(O)(NR 1 ), S(O)(R 1 ), or P(O)(R 1 );
• W 2 is N(R 2 );
• W 3 is C(R 3 )(R 3a ); and
• W 4 is C(R 4 )(R 4a ).
• W 3 is C(O), S(O), S(O) 2 , S(O)(NR 3 ), S(O)(R 3 ), or P(O)(R 3 );
• W 4 is N(R 4 );
• W 2 is N(R 2 ); and
• W 1 is C(R 1 )(R 1a ).
• W 3 is C(O), S(O), S(O) 2 , S(O)(NR 3 ), S(O)(R 3 ), or P(O)(R 3 );
• W 2 is N(R 2 );
• W 1 is C(R 1 )(R 1a ); and
• W 4 is C(R 4 )(R 4a ).
• W 3 is C(O), S(O), S(O) 2 , S(O)(NR 3 ), S(O)(R 3 ), or P(O)(R 3 ); W 2 is N(R 2 ); W 1 is C(R 1 ); and W 4 is N.
• W 3 is C(O), S(O), S(O) 2 , S(O)(NR 3 ), S(O)(R 3 ), or P(O)(R 3 ); W 2 is N(R 2 ); W 1 is C(R 1 ); and W 4 is C(R 4 ).
• W 4 is C(O), S(O), S(O) 2 , S(O)(NR 4 ), S(O)(R 4 ), or P(O)(R 4 ); W 3 is N(R 3 ); W 1 is N; and W 2 is C(R 2 ). In some embodiments of Formula (XIII), or sub-formulae thereof, W 4 is C(O), S(O), S(O) 2 , S(O)(NR 4 ), S(O)(R 4 ), or P(O)(R 4 ); W 3 is N(R 3 ); W 1 is C(R 1 ); and W 2 is C(R 2 ).
• W 3 is C(O), S(O), S(O) 2 , S(O)(NR 3 ), S(O)(R 3 ), or P(O)(R 3 );
• W 4 is N(R 4 );
• W 2 is C(R 2 ); and
• W 1 is C(R 1 ).
• W 1 is C(O), S(O), S(O) 2 , S(O)(NR 1 ), S(O)(R 1 ), or P(O)(R 1 );
• W 2 is N(R 2 );
• W 3 is C(R 3 ); and W 4 is C(R 4 ).
• W 1 is C(O), S(O), S(O) 2 , S(O)(NR 1 ), S(O)(R 1 ), or P(O)(R 1 );
• W 2 is N(R 2 );
• W 3 is C(R 3 ); and W 4 is N.
• W 4 is C(O), S(O), S(O) 2 , S(O)(NR 4 ), S(O)(R 4 ), or P(O)(R 4 );
• W 3 is C(R 3 )(R 3a ); W 1 is O; and W 2 is C(R 2 )(R 2a ).
• W 4 is C(O), S(O), S(O) 2 , S(O)(NR 4 ), S(O)(R 4 ), or P(O)(R 4 );
• W 3 is C(R 3 );
• W 1 is O;
• W 2 is C(R 2 ).
• W 1 is C(O), S(O), S(O) 2 , S(O)(NR 1 ), S(O)(R 1 ), or P(O)(R 1 );
• W 3 is C(R 3 )(R 3a );
• W 4 is O; and W 2 is C(R 2 )(R 2a ).
• W 1 is C(O), S(O), S(O) 2 , S(O)(NR 1 ), S(O)(R 1 ), or P(O)(R 1 ); W 3 is C(R 3 ); W 4 is O; and W 2 is C(R 2 ). [00605] In some embodiments (e.g., including Formulae (XI), (XII), (XIII), and/or (XIV); or sub-formulae thereof), W 1 is C(R 1 ); W 2 is C(R 2 ); W 3 is N; and W 4 is N.
• W 1 is C(R 1 ); W 2 is C(R 2 ); W 3 is C(R 3 ); and W 4 is N. In some embodiments (e.g., including Formulae (XI), (XII), (XIII), and/or (XIV); or sub-formulae thereof), W 1 is C(R 1 ); W 2 is C(R 2 ); W 3 is N; and W 4 is C(R 4 ).
• W 1 is N; W 2 is C(R 2 ); W 3 is C(R 3 ); and W 4 is C(R 4 ).
• W 1 is N, W 2 is C(R 2 ), W 3 is C(R 3 ), and W 4 is C(R 4 ).
• W 1 is C(R 1 ), W 2 is N, W 3 is C(R 3 ), and W 4 is C(R 4 ). In some embodiments (e.g., including Formulae (XI), (XII), (XIII), and/or (XIV); or sub-formulae thereof), W 1 is C(R 1 ), W 2 is C(R 2 ), W 3 is N, and W 4 is C(R 4 ).
• W 1 is C(R 1 )
• W 2 is C(R 2 )
• W 3 is C(R 3 )
• W 4 is N.
• W 1 is C(R 1 )
• W 2 is C(R 2 ).
• W 3 is N(R 3 ) and W 4 is C(O). In some embodiments (e.g., including Formulae (XI), (XII), (XIII), and/or (XIV); or sub- formulae thereof), W 3 is C(O) and W 4 is N(R 4 ). In some embodiments (e.g., including Formulae (XI), (XII), (XIII), and/or (XIV); or sub-formulae thereof), W 3 is O and W 4 is C(R 4 )(R 4a ).
• W 1 is C(R 1 )(R 1a )
• W 2 is O
• W 3 is C(R 3 )
• W 4 is C(R 4 ).
• W 1 is CO, N(R1) or C(R 1 )(R 1a ); W 2 is CO , N(R2), or C(R 2 )(R 2a ); W 3 is N, or C(R 3 ); and W 4 is N, or C(R 4 ).
• W 3 and W 4 are connected by a double bond.
• W 1 is is N(R 1 ) and W 3 and W 4 are connected by a double bond.
• W 2 is N(R 2 ) and W 1 is C(R 1 )(R 1a ).
• W 4 is N(R 4 ) and W 1 and W 2 are connected by a double bond.
• W 2 is C(R 2 )(R 2a ) and W 3 is C(R 3 )(R 3a ).
• W 2 is C(R 2 ) and W 3 is C(R 3 ).
• W 4 is C(O), S(O), S(O) 2 , S(O)(NR 4 ), S(O)(R 4 ), or P(O)(R 4 ); W 3 is N; and W 2 is C(R 2 ).
• W 4 is C(O), S(O), S(O) 2 , S(O)(NR 4 ), S(O)(R 4 ), or P(O)(R 4 ); W 2 is N; and W 3 is C(R 3 ).
• W 4 is C(O), S(O), S(O) 2 , S(O)(NR 4 ), S(O)(R 4 ), or P(O)(R 4 ); W 3 is C(R 3 ); and W 2 is C(R 2 ).
• W 4 is C(O), S(O), S(O) 2 , S(O)(NR 4 ), S(O)(R 4 ), or P(O)(R 4 ); W 3 is N; and W 2 is N.
• W 1 is C(O), S(O), S(O) 2 , S(O)(NR 1 ), S(O)(R 1 ), or P(O)(R 1 ); W 3 is N; and W 2 is C(R 2 ).
• W 1 is C(O), S(O), S(O) 2 , S(O)(NR 1 ), S(O)(R 1 ), or P(O)(R 1 ); W 2 is N; and W 3 is C(R 3 ).
• W 1 is C(O), S(O), S(O) 2 , S(O)(NR 1 ), S(O)(R 1 ), or P(O)(R 1 ); W 3 is C(R 3 ); and W 2 is C(R 2 ).
• W 1 is C(O), S(O), S(O) 2 , S(O)(NR 1 ), S(O)(R 1 ), or P(O)(R 1 ); W 3 is N; and W 2 is N.
• R 12 is independently hydrogen.
• R 12 is independently C 1-6 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 3-6 cycloalkyl, -CH 2 -C 3-6 cycloalkyl, C 2-9 heterocycloalkyl, -CH 2 -C 2-9 heterocycloalkyl, C 6-10 aryl, -CH 2 -C 6-10 aryl, or C 1-9 heteroaryl, wherein C 1-6 alkyl, C 2 - 10 aryl, -CH 2 -C 6-10 aryl, and C 1-9 heteroaryl are optionally substituted with one, two, or three R 20k .
• R 12 is independently C 1-6 alkyl optionally substituted with one, two, or three R 20k . In some embodiments (e.g., including Formulae (XI), (XII), (XIII), and/or (XIV); or sub-formulae thereof), R 12 is independently C 1-6 alkyl. In some embodiments (e.g., including Formulae (XI), (XII), (XIII), and/or (XIV); or sub-formulae thereof), R 12 is independently C 1 -4alkyl.
• R 12 is independently C 1-3 alkyl. In some embodiments (e.g., including Formulae (XI), (XII), (XIII), and/or (XIV); or sub-formulae thereof), R 12 is independently C 1-2 alkyl. In some embodiments (e.g., including Formulae (XI), (XII), (XIII), and/or (XIV); or sub-formulae thereof), R 12 is methyl.
• R 12a is independently hydrogen.
• R 12a is independently C 1-6 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 3-6 cycloalkyl, -CH 2 -C 3- 6 cycloalkyl, -CH 2 -C 2-9 heterocycloalkyl, C 6-10 aryl, -CH 2 -C 6-10 aryl, and C 1-9 heteroaryl, wherein C 1-6 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 3-6 cycloalkyl, -CH 2 -C 3-6 cycloalkyl, -CH 2 -C 2 -C 2
• R 12a is independently C 1-6 alkyl optionally substituted with one, two, or three R 20k . In some embodiments (e.g., including Formulae (XI), (XII), (XIII), and/or (XIV); or sub-formulae thereof), R 12a is independently C 1-6 alkyl. In some embodiments (e.g., including Formulae (XI), (XII), (XIII), and/or (XIV); or sub-formulae thereof), R 12a is independently C 1 -4alkyl.
• R 12 is independently C 1-3 alkyl. In some embodiments (e.g., including Formulae (XI), (XII), (XIII), and/or (XIV); or sub-formulae thereof), R 12a is independently C 1 -2alkyl. In some embodiments (e.g., including Formulae (XI), (XII), (XIII), and/or (XIV); or sub- formulae thereof), R 12a is methyl.
• R 12 is independently hydrogen. In some embodiments (e.g., including Formulae (XI), (XII), (XIII), and/or (XIV); or sub-formulae thereof), R 12 is independently C 1-6 alkyl. In some embodiments (e.g., including Formulae (XI), (XII), (XIII), and/or (XIV); or sub-formulae thereof), R 12 is independently C 2-6 alkenyl.
• R 12 is independently C 2-6 alkynyl. In some embodiments (e.g., including Formulae (XI), (XII), (XIII), and/or (XIV); or sub-formulae thereof), R 12 is independently C 3-6 cycloalkyl. In some embodiments (e.g., including Formulae (XI), (XII), (XIII), and/or (XIV); or sub-formulae thereof), R 12 is independently -CH 2 -C 3-6 cycloalkyl.
• R 12 is independently C 2-9 heterocycloalkyl. In some embodiments (e.g., including Formulae (XI), (XII), (XIII), and/or (XIV); or sub-formulae thereof), R 12 is independently -CH 2 -C 2-9 heterocycloalkyl. In some embodiments (e.g., including Formulae (XI), (XII), (XIII), and/or (XIV); or sub-formulae thereof), R 12 is independently C 6-10 aryl.
• R 12 is independently -CH 2 -C 6-10 aryl. In some embodiments (e.g., including Formulae (XI), (XII), (XIII), and/or (XIV); or sub-formulae thereof), R 12 is independently C 1-9 heteroaryl. [00610] In some embodiments (e.g., including Formulae (XI), (XII), (XIII), and/or (XIV); or sub-formulae thereof), R 12 is independently C 1-6 alkyl substituted with one, two, or three R 20k .
• R 12 is independently C 2-6 alkenyl substituted with one, two, or three R 20k . In some embodiments (e.g., including Formulae (XI), (XII), (XIII), and/or (XIV); or sub-formulae thereof), R 12 is independently C 2-6 alkynyl substituted with one, two, or three R 20k .
• R 12 is independently C 3-6 cycloalkyl substituted with one, two, or three R 20k . In some embodiments (e.g., including Formulae (XI), (XII), (XIII), and/or (XIV); or sub-formulae thereof), R 12 is independently -CH 2 -C 3-6 cycloalkyl substituted with one, two, or three R 20k .
• R 12 is independently C 2-9 heterocycloalkyl substituted with one, two, or three R 20k . In some embodiments (e.g., including Formulae (XI), (XII), (XIII), and/or (XIV); or sub-formulae thereof), R 12 is independently -CH 2 -C 2-9 heterocycloalkyl substituted with one, two, or three R 20k .
• R 12 is independently C 6-10 aryl substituted with one, two, or three R 20k . In some embodiments (e.g., including Formulae (XI), (XII), (XIII), and/or (XIV); or sub-formulae thereof), R 12 is independently -CH 2 -C 6-10 aryl substituted with one, two, or three R 20k .
• R 12 is independently C 1-9 heteroaryl substituted with one, two, or three R 20k .
• R 12a is independently hydrogen.
• R 12a is independently C 1-6 alkyl.
• R 12a is independently C 2-6 alkenyl. In some embodiments (e.g., including Formulae (XI), (XII), (XIII), and/or (XIV); or sub-formulae thereof), R 12a is independently C 2-6 alkynyl. In some embodiments (e.g., including Formulae (XI), (XII), (XIII), and/or (XIV); or sub-formulae thereof), R 12a is independently C 3-6 cycloalkyl.
• R 12a is independently -CH 2 -C 3-6 cycloalkyl. In some embodiments (e.g., including Formulae (XI), (XII), (XIII), and/or (XIV); or sub-formulae thereof), R 12a is independently -CH 2 -C 2-9 heterocycloalkyl. In some embodiments (e.g., including Formulae (XI), (XII), (XIII), and/or (XIV); or sub-formulae thereof), R 12a is independently C 6-10 aryl.
• R 12a is independently -CH 2 -C 6-10 aryl. In some embodiments (e.g., including Formulae (XI), (XII), (XIII), and/or (XIV); or sub-formulae thereof), R 12a is independently C 1-9 heteroaryl. In some embodiments (e.g., including Formulae (XI), (XII), (XIII), and/or (XIV); or sub-formulae thereof), R 12a is independently C 1-6 alkyl substituted with one, two, or three R 20k .
• R 12a is independently C 2-6 alkenyl substituted with one, two, or three R 20k . In some embodiments (e.g., including Formulae (XI), (XII), (XIII), and/or (XIV); or sub-formulae thereof), R 12a is independently C 2-6 alkynyl substituted with one, two, or three R 20k .
• R 12a is independently C 3-6 cycloalkyl substituted with one, two, or three R 20k .
• R 12a is independently -CH 2 -C 3-6 cycloalkyl substituted with one, two, or three R 20k .
• R 12a is independently -CH 2 -C 2-9 heterocycloalkyl substituted with one, two, or three R 20k .
• R 12a is independently C 6-10 aryl substituted with one, two, or three R 20k .
• R 12a is independently -CH 2 -C 6-10 aryl substituted with one, two, or three R 20k . In some embodiments (e.g., including Formulae (XI), (XII), (XIII), and/or (XIV); or sub-formulae thereof), R 12a is independently C 1-9 heteroaryl substituted with one, two, or three R 20k .
• R 13 is independently hydrogen. In some embodiments (e.g., including Formulae (XI), (XII), (XIII), and/or (XIV); or sub-formulae thereof), R 13 is independently C 1-6 alkyl. In some embodiments (e.g., including Formulae (XI), (XII), (XIII), and/or (XIV); or sub-formulae thereof), R 13 is independently C 1-6 haloalkyl.
• R 12 and R 13 together with the nitrogen to which they are attached, form a C 2-9 heterocycloalkyl ring.
• R 12 and R 13 together with the nitrogen to which they are attached, form a C 2-9 heterocycloalkyl ring substituted with one, two, or three R 20k .
• R 14 is independently hydrogen. In some embodiments (e.g., including Formulae (XI), (XII), (XIII), and/or (XIV); or sub-formulae thereof), R 14 is independently C 1-6 alkyl. In some embodiments (e.g., including Formulae (XI), (XII), (XIII), and/or (XIV); or sub-formulae thereof), R 14 is independently C 1-6 haloalkyl.
• R 15 is independently C 1-6 alkyl. In some embodiments (e.g., including Formulae (XI), (XII), (XIII), and/or (XIV); or sub-formulae thereof), R 15 is independently C 2-6 alkenyl. In some embodiments (e.g., including Formulae (XI), (XII), (XIII), and/or (XIV); or sub-formulae thereof), R 15 is independently C 2-6 alkynyl.
• R 15 is independently C 3-6 cycloalkyl. In some embodiments (e.g., including Formulae (XI), (XII), (XIII), and/or (XIV); or sub-formulae thereof), R 15 is independently C 1-6 heteroalkyl. In some embodiments (e.g., including Formulae (XI), (XII), (XIII), and/or (XIV); or sub-formulae thereof), R 15 is independently C 2-9 heterocycloalkyl.
• R 15 is independently C 6-10 aryl. In some embodiments (e.g., including Formulae (XI), (XII), (XIII), and/or (XIV); or sub-formulae thereof), R 15 is independently C 1- 9 heteroaryl. In some embodiments (e.g., including Formulae (XI), (XII), (XIII), and/or (XIV); or sub-formulae thereof), R 15 is independently C 1-6 alkyl substituted with one, two, or three R 20k .
• R 15 is independently C 2-6 alkenyl substituted with one, two, or three R 20k . In some embodiments (e.g., including Formulae (XI), (XII), (XIII), and/or (XIV); or sub-formulae thereof), R 15 is independently C 2-6 alkynyl substituted with one, two, or three R 20k .
• R 15 is independently C 3-6 cycloalkyl substituted with one, two, or three R 20k . In some embodiments (e.g., including Formulae (XI), (XII), (XIII), and/or (XIV); or sub-formulae thereof), R 15 is independently C 1-6 heteroalkyl substituted with one, two, or three R 20k .
• R 15 is independently C 2-9 heterocycloalkyl substituted with one, two, or three R 20k . In some embodiments (e.g., including Formulae (XI), (XII), (XIII), and/or (XIV); or sub-formulae thereof), R 15 is independently C 6-10 aryl substituted with one, two, or three R 20k .
• R 15 is independently C 1-9 heteroaryl substituted with one, two, or three R 20k .
• R 15 is independently selected C 1-6 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 3-6 cycloalkyl, C 2 - 9 heterocycloalkyl, C 6-10 aryl, and C 1-9 heteroaryl, wherein C 1-6 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 3-6 cycloalkyl, C 2 - 9 heterocycloalkyl, C 6-10 aryl, and C 1-9 heteroaryl are optionally substituted with one, two, or three R 20k .
• R 15 is independently selected C 1-6 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 3-6 cycloalkyl, C 2-9 heterocycloalkyl, C 6-10 aryl, and C 1 - 9 heteroaryl.
• R 15 is independently selected from C 1-6 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 3-6 cycloalkyl, C 2-9 heterocycloalkyl, C 6-10 aryl, and C 1-9 heteroaryl substituted with one, two, or three R 20k .
• R 16 is independently -C 1-6 alkylene-OP(O)(OR 16a )(OR 16b ).
• R 16 is independently -C 1-6 alkylene-OP(O)(OR 16a )(OR 16b ), wherein the C 1-6 alkylene is substituted with one, two, or three R 20l .
• R 16 is independently -P(O)(OR 16a )(OR 16b ).
• R 16 is independently -C 1 alkylene-OP(O)(OR 16a )(OR 16b ).
• R 16 is independently -C 1 alkylene-OP(O)(OR 16a )(OR 16b ), wherein the C 1 alkylene is substituted with one or two R 20l .
• R 16 is independently -C 2 alkylene-OP(O)(OR 16a )(OR 16b ).
• R 16 is independently -C 2 alkylene-OP(O)(OR 16a )(OR 16b ), wherein the C 2 alkylene is substituted with one, two, or three R 20l .
• R 16 is independently -C3alkylene-OP(O)(OR 16a )(OR 16b ).
• R 16 is independently -C 3 alkylene-OP(O)(OR 16a )(OR 16b ), wherein the C 3 alkylene is substituted with one, two, or three R 20l .
• R 16 is independently -C 4 alkylene-OP(O)(OR 16a )(OR 16b ).
• R 16 is independently -C 4 alkylene-OP(O)(OR 16a )(OR 16b ), wherein the C 4 alkylene is substituted with one, two, or three R 20l .
• R 16 is independently -C 5 alkylene-OP(O)(OR 16a )(OR 16b ).
• R 16 is independently -C 5 alkylene-OP(O)(OR 16a )(OR 16b ), wherein the C 5 alkylene is substituted with one, two, or three R 20l .
• R 16 is independently -C 6 alkylene-OP(O)(OR 16a )(OR 16b ).
• R 16 is independently -C 6 alkylene-OP(O)(OR 16a )(OR 16b ), wherein the C 6 alkylene is substituted with one, two, or three R 20l .
• R 16a is independently hydrogen.
• R 16a is independently C 1-6 alkyl. In some embodiments (e.g., including Formulae (XI), (XII), (XIII), and/or (XIV); or sub-formulae thereof), R 16a is independently C 2-6 alkenyl. In some embodiments (e.g., including Formulae (XI), (XII), (XIII), and/or (XIV); or sub-formulae thereof), R 16a is independently C 2-6 alkynyl.
• R 16a is independently C 3-6 cycloalkyl. In some embodiments (e.g., including Formulae (XI), (XII), (XIII), and/or (XIV); or sub-formulae thereof), R 16a is independently -CH 2 -C 3-6 cycloalkyl. In some embodiments (e.g., including Formulae (XI), (XII), (XIII), and/or (XIV); or sub-formulae thereof), R 16a is independently -CH 2 -C 2-9 heterocycloalkyl.
• R 16a is independently C 6-10 aryl. In some embodiments (e.g., including Formulae (XI), (XII), (XIII), and/or (XIV); or sub-formulae thereof), R 16a is independently -CH 2 -C 6-10 aryl. In some embodiments (e.g., including Formulae (XI), (XII), (XIII), and/or (XIV); or sub-formulae thereof), R 16a is independently C 1-9 heteroaryl.
• R 16a is independently C 1-6 alkyl substituted with one, two, or three R 20m . In some embodiments (e.g., including Formulae (XI), (XII), (XIII), and/or (XIV); or sub-formulae thereof), R 16a is independently C 2-6 alkenyl substituted with one, two, or three R 20m .
• R 16a is independently C 2-6 alkynyl substituted with one, two, or three R 20m . In some embodiments (e.g., including Formulae (XI), (XII), (XIII), and/or (XIV); or sub-formulae thereof), R 16a is independently C 3-6 cycloalkyl substituted with one, two, or three R 20m .
• R 16a is independently -CH 2 -C 3-6 cycloalkyl substituted with one, two, or three R 20m .
• R 16a is independently -CH 2 -C 2-9 heterocycloalkyl substituted with one, two, or three R 20m .
• R 16a is independently C 6-10 aryl substituted with one, two, or three R 20m . In some embodiments (e.g., including Formulae (XI), (XII), (XIII), and/or (XIV); or sub-formulae thereof), R 16a is independently -CH 2 -C 6-10 aryl substituted with one, two, or three R 20m .
• R 16a is independently C 1-9 heteroaryl substituted with one, two, or three R 20m .
• R 16b is independently hydrogen.
• R 16b is independently C 1-6 alkyl.
• R 16b is independently C 2-6 alkenyl. In some embodiments (e.g., including Formulae (XI), (XII), (XIII), and/or (XIV); or sub-formulae thereof), R 16b is independently C 2-6 alkynyl. In some embodiments (e.g., including Formulae (XI), (XII), (XIII), and/or (XIV); or sub-formulae thereof), R 16b is independently C 3-6 cycloalkyl.
• R 16b is independently -CH 2 -C 3-6 cycloalkyl. In some embodiments (e.g., including Formulae (XI), (XII), (XIII), and/or (XIV); or sub-formulae thereof), R 16b is independently -CH 2 -C 2-9 heterocycloalkyl. In some embodiments (e.g., including Formulae (XI), (XII), (XIII), and/or (XIV); or sub-formulae thereof), R 16b is independently C 6-10 aryl.
• R 16b is independently -CH 2 -C 6-10 aryl. In some embodiments (e.g., including Formulae (XI), (XII), (XIII), and/or (XIV); or sub-formulae thereof), R 16b is independently C 1-9 heteroaryl. In some embodiments (e.g., including Formulae (XI), (XII), (XIII), and/or (XIV); or sub-formulae thereof), R 16b is independently C 1-6 alkyl substituted with one, two, or three R 20m .
• R 16b is independently C 2-6 alkenyl substituted with one, two, or three R 20m . In some embodiments (e.g., including Formulae (XI), (XII), (XIII), and/or (XIV); or sub-formulae thereof), R 16b is independently C 2-6 alkynyl substituted with one, two, or three R 20m .
• R 16b is independently C 3-6 cycloalkyl substituted with one, two, or three R 20m .
• R 16b is independently -CH 2 -C 3-6 cycloalkyl substituted with one, two, or three R 20m .
• R 16b is independently -CH 2 -C 2-9 heterocycloalkyl substituted with one, two, or three R 20m .
• R 16b is independently C 6-10 aryl substituted with one, two, or three R 20m .
• R 16b is independently -CH 2 -C 6-10 aryl substituted with one, two, or three R 20m . In some embodiments (e.g., including Formulae (XI), (XII), (XIII), and/or (XIV); or sub-formulae thereof), R 16b is independently C 1-9 heteroaryl substituted with one, two, or three R 20m .
• Sub-formulae of Formula I, II, III, and/or IV are those formula having the same number as the parent formula (e.g., I, II, III, and/or IV) followed by one or more letters and/or apostrophes and/or numbers.
• sub-formulae of Formula I include I-3, Ia-3, Ib-3, Ic-3, Ig-3, Ih-3, Ii-3, I’, Ia’, Ib’, Ic’, Ia’-1, Ib’-1, Ic’- 1, Ia’-2, Ib’-2, Ic’-2, I’‘, Ia’‘, Ib’‘, Ic’‘, Ia’‘-1, Ib’‘-1, Ic’‘-1, Ia’‘-2, Ib’‘-2, Ic’‘-2, I’‘, Ia’‘’‘, Ib’‘‘, Ic’‘‘, Ia’‘‘-1, Ib’‘‘- 1, Ic’‘‘-1, Ia’‘‘-2, Ib’‘‘’’’‘-2, Ic’‘‘‘-2,Ia, Ib, Ic, Id, Ie, If, Ig, Ih, Ii, Ij, Ik, Il, Im, In, Io, Ioa, Io
• sub-formulae of Formula II include II-3, IIa, IIb, IIc, IId, IIe, IIf, IIg, IIh, IIi, IIj, and IIk.
• sub-formulae of Formula III Include III-3, III’, IIIa’, IIIb’, IIIc’, IIIa’-1, IIIb’-1, IIIc’-1, IIIa’-2, IIIb’-2, IIIc’-2, III’‘, IIIa’‘, IIIb’‘, IIIc’‘, IIIa’‘-1, IIIb’‘-1, IIIc’‘-1, IIIa’‘-2, IIIb’‘-2, IIIc’‘-2, III’‘‘, IIIa’‘‘, IIIb’‘‘, IIIc’‘’‘, IIIa’‘‘-1, IIIb’‘‘-1, IIIc’‘‘-1, IIIa’‘’‘-2, IIIb’‘‘-2, IIIc’‘-2, IIIa 4 , IIIa 4 , IIIb 4 , IIIc 4 , IIIa 4 , III
• sub-formulae of Formula IV include IVa, IVb, IVc, IVd, IVe, IVf, IVg, IVh, IVi, IVj, IVk, IVl, IVm, IVn, and IVo.
• a compound of Formulae (XI) or sub-formulae thereof is understood to include a formula selected from Formulae I-3, Ia-3, Ib-3, Ic-3, Ig-3, Ih-3, Ii-3, I, I’, Ia’, Ib’, Ic’, Ia’-1, Ib’-1, Ic’-1, Ia’-2, Ib’-2, Ic’-2, I’‘, Ia’‘, Ib’‘, Ic’‘, Ia’‘-1, Ib’‘-1, Ic’‘-1, Ia’‘-2, Ib’‘-2, Ic’‘-2, I’‘, Ia’‘, Ia’‘, Ib’‘-2, Ic’‘-2, I’‘, Ia’‘, Ia’
• a compound of Formulae (XII) or sub-formulae thereof is understood to include a formula selected from Formulae II-3, II, IIa, IIb, IIc, IId, IIe, IIf, IIg, IIh, IIi, IIj, and IIk.
• a compound of Formulae (XIII) or sub-formulae thereof is understood to include a formula selected from Formulae III-3, III, III’, IIIa’, IIIb’, IIIc’, IIIa’-1, IIIb’-1, IIIc’-1, IIIa’-2, IIIb’-2, IIIc’-2, III’‘, IIIa’‘, IIIb’‘, IIIc’‘, IIIa’‘-1, IIIb’‘-1, IIIc’‘-1, IIIa’‘-2, IIIb’‘-2, IIIc’‘-2, III’‘, IIIa’‘‘, IIIb’‘‘, IIIc’‘‘, IIIa’‘‘-1, IIIb’‘‘- 1, IIIc’‘‘-1, IIIa’‘‘-2, IIIb’‘‘-2, IIIc’‘‘-2, III4, IIIa4, IIIb4, IIIc4, IIIa4-1, IIIb4-1, IIIc4-1, IIIa4-2, IIIb4-2, IIIc4-2, III5, IIIa 5
• a compound of Formulae (XIV) or sub-formulae thereof is understood to include a formula selected from Formulae IV, IVa, IVb, IVc, IVd, IVe, IVf, IVg, IVh, IVi, IVj, IVk, IVl, IVm, IVn, and IVo.
• the compound is a compound described herein, including a compound of any one of Formulae XI, XII, XIII, or XIV; a sub-formulae of any of the foregoing; an embodiment of any of the foregoing; or a compound described in a figure, table, aspect, embodiment, or claim herein.
• the method may include (e.g., use, implementation, or administration) any compound described herein, including a compound of any one of Formulae XI, XII, XIII, or XIV; a sub-formulae of any of the foregoing; or an embodiment of any of the foregoing; or a compound described in a figure, table, aspect, embodiment, or claim herein.
• the compound has the formula: and R 2 is as described herein.
• the compound has the formula: and R 2 is as described herein.
• the compound has the formula: and R 2 is as described herein.
• the compound has the formula: and R 2 and R 4 are as described herein. In some embodiments, the compound has the formula: and R 2 and R 4 are as described herein. In some embodiments, the compound has the formula: and R 2 and R 4 are as described herein. In some embodiments, the compound has the formula: and R 2 is as described herein. In some embodiments, the compound has the formula: and R 2 is as described herein. In some embodiments, the compound has the formula: and R 2 is as described herein. In some embodiments, the compound has the formula: and R 2 is as described herein. In some embodiments, the compound has the formula: and R 2 is as described herein. In some embodiments, the compound has the formula: and R 2 is as described herein. In some embodiments, the compound has the formula: and R 2 is as described herein. In some embodiments, the compound has the formula: and R 2 is as described herein. In some embodiments, the compound has the formula: and R 2 is as described herein. In some embodiments, the compound has the formula
• the compound has the formula: and R 2 is as described herein. In some embodiments, the compound has the formula: and R 2 is as described herein. In some embodiments, the compound has the formula: and R 2 is as described herein. In some embodiments, the compound has the formula: and R 2 is as described herein. In some embodiments, the compound has the formula: and R 2 is as described herein. In some embodiments, the compound has the formula: and R 2 is as described herein. In some embodiments, the compound has the formula: and R 2 is as described herein. In some embodiments, the compound has the formula: and R 2 is as described herein. In some embodiments, the compound has the formula: and R 2 is as described herein. In some embodiments, the compound has the formula: and R 2 is as described herein. In some embodiments, the compound has the formula: and R 2 is as described herein. In some embodiments, the compound has the formula: and R 2 is as described herein. In some embodiments, the compound has the formula: and R 2 is as described herein
• each R 20a , R 20b , R 20c , R 20d , R 20e , R 20f , R 20g , R 20h , R 20i , R 20j , R 20k , R 20l , and R 20m is independently selected from halogen, -CN, C 1-6 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 3-6 cycloalkyl, -CH 2 -C 3-6 cycloalkyl, C 2-9 heterocycloalkyl, -CH 2 -C 2-9 heterocycloalkyl, C 6-10 aryl, -CH 2 -C 6-10 aryl, C 1-9 heteroaryl, -OR 21 ,
• R 20a is independently oxo. In some embodiments R 20a is independently -CN. In some embodiments R 20a is independently halogen. In some embodiments R 20a is independently -CN. In some embodiments R 20a is independently C 1-6 alkyl. In some embodiments R 20a is independently C 2-6 alkenyl. In some embodiments R 20a is independently C 2-6 alkynyl. In some embodiments R 20a is independently C 3-6 cycloalkyl. In some embodiments R 20a is independently -CH 2 -C 3-6 cycloalkyl. In some embodiments R 20a is independently C 1- 6 heteroalkyl. In some embodiments R 20a is independently C 2-9 heterocycloalkyl.
• R 20a is independently -CH 2 -C 2-9 heterocycloalkyl. In some embodiments R 20a is independently C 6-10 aryl. In some embodiments R 20a is independently -CH 2 -C 6-10 aryl. In some embodiments R 20a is independently C 1-9 heteroaryl. In some embodiments R 20a is independently -OR 21 . In some embodiments R 20a is independently -SR 21 . In some embodiments R 20a is independently -N(R 22 )(R 23 ). In some embodiments R 20a is independently -C(O)OR 22 . In some embodiments R 20a is independently -C(O)N(R 22 )(R 23 ).
• R 20a is independently - C(O)C(O)N(R 22 )(R 23 ). In some embodiments R 20a is independently -OC(O)N(R 22 )(R 23 ). In some embodiments R 20a is independently -N(R 24 )C(O)N(R 22 )(R 23 ). In some embodiments R 20a is independently -N(R 24 )C(O)OR 22 . In some embodiments R 20a is independently -N(R 24 )C(O)R 25 . In some embodiments R 20a is independently -N(R 24 )S(O) 2 R 25 . In some embodiments R 20a is independently -C(O)R 25 .
• R 20a is independently -S(O) 2 R 25 . In some embodiments R 20a is independently -S(O) 2 N(R 22 )(R 23 ) . In some embodiments R 20a is independently - OCH 2 C(O)OR 22 . In some embodiments R 20a is independently -OC(O)R 25 .
• R 20a is independently C 1-6 alkyl substituted with one, two, or three groups independently selected from halogen, oxo, -CN, C 1-6 alkyl, C 1-6 haloalkyl, C 1-6 alkoxy, C 1-6 haloalkoxy, -OR 21 , -SR 21 , -N(R 22 )(R 23 ), -C(O)OR 22 , -C(O)N(R 22 )(R 23 ), - C(O)C(O)N(R 22 )(R 23 ), -OC(O)N(R 22 )(R 23 ), -N(R 24 )C(O)N(R 22 )(R 23 ), -N(R 24 )C(O)OR 25 , -N(R 24 )C(O)R 25 , - N(R 24 )S(O) 2 R 25 , -C(O)R 25 , -S(O) 2 R 25 ,
• R 20a is independently C 2-6 alkenyl substituted with one, two, or three groups independently selected from halogen, oxo, -CN, C 1-6 alkyl, C 1-6 haloalkyl, C 1-6 alkoxy, C 1-6 haloalkoxy, -OR 21 , -SR 21 , -N(R 22 )(R 23 ), -C(O)OR 22 , -C(O)N(R 22 )(R 23 ), - C(O)C(O)N(R 22 )(R 23 ), -OC(O)N(R 22 )(R 23 ), -N(R 24 )C(O)N(R 22 )(R 23 ), -N(R 24 )C(O)OR 25 , -N(R 24 )C(O)R 25 , - N(R 24 )S(O) 2 R 25 , -C(O)R 25 , -S(O) 2 R 25
• R 20a is independently C 2-6 alkynyl substituted with one, two, or three groups independently selected from halogen, oxo, -CN, C 1-6 alkyl, C 1-6 haloalkyl, C 1-6 alkoxy, C 1-6 haloalkoxy, -OR 21 , -SR 21 , -N(R 22 )(R 23 ), -C(O)OR 22 , -C(O)N(R 22 )(R 23 ), - C(O)C(O)N(R 22 )(R 23 ), -OC(O)N(R 22 )(R 23 ), -N(R 24 )C(O)N(R 22 )(R 23 ), -N(R 24 )C(O)OR 25 , -N(R 24 )C(O)R 25 , - N(R 24 )S(O) 2 R 25 , -C(O)R 25 , -S(O) 2 R 25
• R 20a is independently C 3-6 cycloalkyl substituted with one, two, or three groups independently selected from halogen, oxo, - CN, C 1-6 alkyl, C 1-6 haloalkyl, C 1-6 alkoxy, C 1-6 haloalkoxy, -OR 21 , -SR 21 , -N(R 22 )(R 23 ), -C(O)OR 22 , -C(O)N(R 22 )(R 23 ), -C(O)C(O)N(R 22 )(R 23 ), -OC(O)N(R 22 )(R 23 ), -N(R 24 )C(O)N(R 22 )(R 23 ), -N(R 24 )C(O)OR 25 , -N(R 24 )C(O)R 25 , - N(R 24 )S(O) 2 R 25 , -C(O)R 25 , -S(O) 2
• R 20a is independently -CH 2 -C 3-6 cycloalkyl substituted with one, two, or three groups independently selected from halogen, oxo, -CN, C 1-6 alkyl, C 1-6 haloalkyl, C 1-6 alkoxy, C 1-6 haloalkoxy, -OR 21 , -SR 21 , -N(R 22 )(R 23 ), -C(O)OR 22 , - C(O)N(R 22 )(R 23 ), -C(O)C(O)N(R 22 )(R 23 ), -OC(O)N(R 22 )(R 23 ), -N(R 24 )C(O)N(R 22 )(R 23 ), -N(R 24 )C(O)OR 25 , - N(R 24 )C(O)R 25 , -N(R 24 )S(O) 2 R 25 , -C(O)R 25 , -
• R 20a is independently C 1-6 heteroalkyl substituted with one, two, or three groups independently selected from halogen, oxo, -CN, C 1-6 alkyl, C 1-6 haloalkyl, C 1-6 alkoxy, C 1-6 haloalkoxy, -OR 21 , -SR 21 , -N(R 22 )(R 23 ), -C(O)OR 22 , - C(O)N(R 22 )(R 23 ), -C(O)C(O)N(R 22 )(R 23 ), -OC(O)N(R 22 )(R 23 ), -N(R 24 )C(O)N(R 22 )(R 23 ), -N(R 24 )C(O)OR 25 , - N(R 24 )C(O)R 25 , -N(R 24 )S(O) 2 R 25 , -C(O)R 25 , -S(O) 2
• R 20a is independently C 2-9 heterocycloalkyl substituted with one, two, or three groups independently selected from halogen, oxo, -CN, C 1-6 alkyl, C 1-6 haloalkyl, C 1-6 alkoxy, C 1-6 haloalkoxy, -OR 21 , -SR 21 , -N(R 22 )(R 23 ), -C(O)OR 22 , - C(O)N(R 22 )(R 23 ), -C(O)C(O)N(R 22 )(R 23 ), -OC(O)N(R 22 )(R 23 ), -N(R 24 )C(O)N(R 22 )(R 23 ), -N(R 24 )C(O)OR 25 , - N(R 24 )C(O)R 25 , -N(R 24 )S(O) 2 R 25 , -C(O)R 25 , -S(O)OR 25
• R 20a is independently -CH 2 -C 2-9 heterocycloalkyl substituted with one, two, or three groups independently selected from halogen, oxo, -CN, C 1-6 alkyl, C 1-6 haloalkyl, C 1-6 alkoxy, C 1-6 haloalkoxy, -OR 21 , -SR 21 , -N(R 22 )(R 23 ), - C(O)OR 22 , -C(O)N(R 22 )(R 23 ), -C(O)C(O)N(R 22 )(R 23 ), -OC(O)N(R 22 )(R 23 ), -N(R 24 )C(O)N(R 22 )(R 23 ), - N(R 24 )C(O)OR 25 , -N(R 24 )C(O)R 25 , -N(R 24 )S(O) 2 R 25 , -C(O)R 25 , -
• R 20a is independently C 6-10 aryl substituted with one, two, or three groups independently selected from halogen, oxo, -CN, C 1-6 alkyl, C 1-6 haloalkyl, C 1-6 alkoxy, C 1-6 haloalkoxy, -OR 21 , -SR 21 , -N(R 22 )(R 23 ), - C(O)OR 22 , -C(O)N(R 22 )(R 23 ), -C(O)C(O)N(R 22 )(R 23 ), -OC(O)N(R 22 )(R 23 ), -N(R 24 )C(O)N(R 22 )(R 23 ), - N(R 24 )C(O)OR 25 , -N(R 24 )C(O)R 25 , -N(R 24 )S(O) 2 R 25 , -C(O)R 25 , -S(O) 2 R 25 ,
• R 20a is independently -CH 2 -C 6-10 aryl substituted with one, two, or three groups independently selected from halogen, oxo, -CN, C 1-6 alkyl, C 1-6 haloalkyl, C 1-6 alkoxy, C 1-6 haloalkoxy, -OR 21 , -SR 21 , -N(R 22 )(R 23 ), - C(O)OR 22 , -C(O)N(R 22 )(R 23 ), -C(O)C(O)N(R 22 )(R 23 ), -OC(O)N(R 22 )(R 23 ), -N(R 24 )C(O)N(R 22 )(R 23 ), - N(R 24 )C(O)OR 25 , -N(R 24 )C(O)R 25 , -N(R 24 )S(O) 2 R 25 , -C(O)R 25 , -N(R
• R 20a is independently C 1-9 heteroaryl substituted with one, two, or three groups independently selected from halogen, oxo, -CN, C 1-6 alkyl, C 1-6 haloalkyl, C 1-6 alkoxy, C 1-6 haloalkoxy, -OR 21 , -SR 21 , -N(R 22 )(R 23 ), - C(O)OR 22 , -C(O)N(R 22 )(R 23 ), -C(O)C(O)N(R 22 )(R 23 ), -OC(O)N(R 22 )(R 23 ), -N(R 24 )C(O)N(R 22 )(R 23 ), - N(R 24 )C(O)OR 25 , -N(R 24 )C(O)R 25 , -N(R 24 )S(O) 2 R 25 , -C(O)R 25 , -S(O) 2 R 25 ,
• R 20a is independently selected from oxo, -CN, halogen, -CN, C 1-6 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 3-6 cycloalkyl, -CH 2 -C 3-6 cycloalkyl, C 2-9 heterocycloalkyl, -CH 2 -C 2-9 heterocycloalkyl, C 6-10 aryl, -CH 2 -C 6-10 aryl, C 1 - 9 heteroaryl, -OR 21 , -SR 21 , -N(R 22 )(R 23 ), -C(O)OR 22 , -C(O)N(R 22 )(R 23 ), -C(O)C(O)N(R 22 )(R 23 ), -OC(O)N(R 22 )(R 23 ), - N(R 24 )C(O)N(R 22 )(R 23 ), -N(R 24 )C(O)
• R 20b is independently oxo. In some embodiments R 20b is independently -CN. In some embodiments R 20b is independently halogen. In some embodiments R 20b is independently -CN. In some embodiments R 20b is independently C 1-6 alkyl. In some embodiments R 20b is independently C 2-6 alkenyl. In some embodiments R 20b is independently C 2-6 alkynyl. In some embodiments R 20b is independently C 3-6 cycloalkyl. In some embodiments R 20b is independently -CH 2 -C 3-6 cycloalkyl. In some embodiments R 20b is independently C 1- 6 heteroalkyl. In some embodiments R 20b is independently C 2-9 heterocycloalkyl.
• R 20b is independently -CH 2 -C 2-9 heterocycloalkyl. In some embodiments R 20b is independently C 6-10 aryl. In some embodiments R 20b is independently -CH 2 -C 6-10 aryl. In some embodiments R 20b is independently C 1-9 heteroaryl. In some embodiments R 20b is independently -OR 21 . In some embodiments R 20b is independently -SR 21 . In some embodiments R 20b is independently -N(R 22 )(R 23 ). In some embodiments R 20b is independently -C(O)OR 22 . In some embodiments R 20b is independently -C(O)N(R 22 )(R 23 ).
• R 20b is independently - C(O)C(O)N(R 22 )(R 23 ). In some embodiments R 20b is independently -OC(O)N(R 22 )(R 23 ). In some embodiments R 20b is independently -N(R 24 )C(O)N(R 22 )(R 23 ). In some embodiments R 20b is independently -N(R 24 )C(O)OR 22 . In some embodiments R 20b is independently -N(R 24 )C(O)R 25 . In some embodiments R 20b is independently -N(R 24 )S(O) 2 R 25 . In some embodiments R 20b is independently -C(O)R 25 .
• R 20b is independently -S(O) 2 R 25 . In some embodiments R 20b is independently -S(O) 2 N(R 22 )(R 23 ) . In some embodiments R 20b is independently - OCH 2 C(O)OR 22 . In some embodiments R 20b is independently -OC(O)R 25 .
• R 20b is independently C 1-6 alkyl substituted with one, two, or three groups independently selected from halogen, oxo, -CN, C 1-6 alkyl, C 1-6 haloalkyl, C 1-6 alkoxy, C 1-6 haloalkoxy, -OR 21 , -SR 21 , -N(R 22 )(R 23 ), -C(O)OR 22 , -C(O)N(R 22 )(R 23 ), - C(O)C(O)N(R 22 )(R 23 ), -OC(O)N(R 22 )(R 23 ), -N(R 24 )C(O)N(R 22 )(R 23 ), -N(R 24 )C(O)OR 25 , -N(R 24 )C(O)R 25 , - N(R 24 )S(O) 2 R 25 , -C(O)R 25 , -S(O) 2 R 25 ,
• R 20b is independently C 2-6 alkenyl substituted with one, two, or three groups independently selected from halogen, oxo, -CN, C 1-6 alkyl, C 1-6 haloalkyl, C 1-6 alkoxy, C 1-6 haloalkoxy, -OR 21 , -SR 21 , -N(R 22 )(R 23 ), -C(O)OR 22 , -C(O)N(R 22 )(R 23 ), - C(O)C(O)N(R 22 )(R 23 ), -OC(O)N(R 22 )(R 23 ), -N(R 24 )C(O)N(R 22 )(R 23 ), -N(R 24 )C(O)OR 25 , -N(R 24 )C(O)R 25 , - N(R 24 )S(O) 2 R 25 , -C(O)R 25 , -S(O) 2 R 25
• R 20b is independently C 2-6 alkynyl substituted with one, two, or three groups independently selected from halogen, oxo, -CN, C 1-6 alkyl, C 1-6 haloalkyl, C 1-6 alkoxy, C 1-6 haloalkoxy, -OR 21 , -SR 21 , -N(R 22 )(R 23 ), -C(O)OR 22 , -C(O)N(R 22 )(R 23 ), - C(O)C(O)N(R 22 )(R 23 ), -OC(O)N(R 22 )(R 23 ), -N(R 24 )C(O)N(R 22 )(R 23 ), -N(R 24 )C(O)OR 25 , -N(R 24 )C(O)R 25 , - N(R 24 )S(O) 2 R 25 , -C(O)R 25 , -S(O) 2 R 25
• R 20b is independently C 3-6 cycloalkyl substituted with one, two, or three groups independently selected from halogen, oxo, - CN, C 1-6 alkyl, C 1-6 haloalkyl, C 1-6 alkoxy, C 1-6 haloalkoxy, -OR 21 , -SR 21 , -N(R 22 )(R 23 ), -C(O)OR 22 , -C(O)N(R 22 )(R 23 ), -C(O)C(O)N(R 22 )(R 23 ), -OC(O)N(R 22 )(R 23 ), -N(R 24 )C(O)N(R 22 )(R 23 ), -N(R 24 )C(O)OR 25 , -N(R 24 )C(O)R 25 , - N(R 24 )S(O) 2 R 25 , -C(O)R 25 , -S(O) 2
• R 20b is independently -CH 2 -C 3-6 cycloalkyl substituted with one, two, or three groups independently selected from halogen, oxo, -CN, C 1-6 alkyl, C 1-6 haloalkyl, C 1-6 alkoxy, C 1-6 haloalkoxy, -OR 21 , -SR 21 , -N(R 22 )(R 23 ), -C(O)OR 22 , - C(O)N(R 22 )(R 23 ), -C(O)C(O)N(R 22 )(R 23 ), -OC(O)N(R 22 )(R 23 ), -N(R 24 )C(O)N(R 22 )(R 23 ), -N(R 24 )C(O)OR 25 , - N(R 24 )C(O)R 25 , -N(R 24 )S(O) 2 R 25 , -C(O)R 25 , -
• R 20b is independently C 1-6 heteroalkyl substituted with one, two, or three groups independently selected from halogen, oxo, -CN, C 1-6 alkyl, C 1-6 haloalkyl, C 1-6 alkoxy, C 1-6 haloalkoxy, -OR 21 , -SR 21 , -N(R 22 )(R 23 ), -C(O)OR 22 , - C(O)N(R 22 )(R 23 ), -C(O)C(O)N(R 22 )(R 23 ), -OC(O)N(R 22 )(R 23 ), -N(R 24 )C(O)N(R 22 )(R 23 ), -N(R 24 )C(O)OR 25 , - N(R 24 )C(O)R 25 , -N(R 24 )S(O) 2 R 25 , -C(O)R 25 , -S(O) 2
• R 20b is independently C 2-9 heterocycloalkyl substituted with one, two, or three groups independently selected from halogen, oxo, -CN, C 1-6 alkyl, C 1-6 haloalkyl, C 1-6 alkoxy, C 1-6 haloalkoxy, -OR 21 , -SR 21 , -N(R 22 )(R 23 ), -C(O)OR 22 , - C(O)N(R 22 )(R 23 ), -C(O)C(O)N(R 22 )(R 23 ), -OC(O)N(R 22 )(R 23 ), -N(R 24 )C(O)N(R 22 )(R 23 ), -N(R 24 )C(O)OR 25 , - N(R 24 )C(O)R 25 , -N(R 24 )S(O) 2 R 25 , -C(O)R 25 , -S(O)OR 25
• R 20b is independently -CH 2 -C 2-9 heterocycloalkyl substituted with one, two, or three groups independently selected from halogen, oxo, -CN, C 1-6 alkyl, C 1-6 haloalkyl, C 1-6 alkoxy, C 1-6 haloalkoxy, -OR 21 , -SR 21 , -N(R 22 )(R 23 ), - C(O)OR 22 , -C(O)N(R 22 )(R 23 ), -C(O)C(O)N(R 22 )(R 23 ), -OC(O)N(R 22 )(R 23 ), -N(R 24 )C(O)N(R 22 )(R 23 ), - N(R 24 )C(O)OR 25 , -N(R 24 )C(O)R 25 , -N(R 24 )S(O) 2 R 25 , -C(O)R 25 , -
• R 20b is independently C 6-10 aryl substituted with one, two, or three groups independently selected from halogen, oxo, -CN, C 1-6 alkyl, C 1-6 haloalkyl, C 1-6 alkoxy, C 1-6 haloalkoxy, -OR 21 , -SR 21 , -N(R 22 )(R 23 ), - C(O)OR 22 , -C(O)N(R 22 )(R 23 ), -C(O)C(O)N(R 22 )(R 23 ), -OC(O)N(R 22 )(R 23 ), -N(R 24 )C(O)N(R 22 )(R 23 ), - N(R 24 )C(O)OR 25 , -N(R 24 )C(O)R 25 , -N(R 24 )S(O) 2 R 25 , -C(O)R 25 , -S(O) 2 R 25 ,
• R 20b is independently -CH 2 -C 6-10 aryl substituted with one, two, or three groups independently selected from halogen, oxo, -CN, C 1-6 alkyl, C 1-6 haloalkyl, C 1-6 alkoxy, C 1-6 haloalkoxy, -OR 21 , -SR 21 , -N(R 22 )(R 23 ), - C(O)OR 22 , -C(O)N(R 22 )(R 23 ), -C(O)C(O)N(R 22 )(R 23 ), -OC(O)N(R 22 )(R 23 ), -N(R 24 )C(O)N(R 22 )(R 23 ), - N(R 24 )C(O)OR 25 , -N(R 24 )C(O)R 25 , -N(R 24 )S(O) 2 R 25 , -C(O)R 25 , -N(R
• R 20b is independently C 1-9 heteroaryl substituted with one, two, or three groups independently selected from halogen, oxo, -CN, C 1-6 alkyl, C 1-6 haloalkyl, C 1-6 alkoxy, C 1-6 haloalkoxy, -OR 21 , -SR 21 , -N(R 22 )(R 23 ), - C(O)OR 22 , -C(O)N(R 22 )(R 23 ), -C(O)C(O)N(R 22 )(R 23 ), -OC(O)N(R 22 )(R 23 ), -N(R 24 )C(O)N(R 22 )(R 23 ), - N(R 24 )C(O)OR 25 , -N(R 24 )C(O)R 25 , -N(R 24 )S(O) 2 R 25 , -C(O)R 25 , -S(O) 2 R 25 ,
• R 20b is independently selected from oxo, -CN, halogen, -CN, C 1-6 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 3-6 cycloalkyl, -CH 2 -C 3-6 cycloalkyl, C 2-9 heterocycloalkyl, -CH 2 -C 2-9 heterocycloalkyl, C 6-10 aryl, -CH 2 -C 6-10 aryl, C 1- 9 heteroaryl, -OR 21 , -SR 21 , -N(R 22 )(R 23 ), -C(O)OR 22 , -C(O)N(R 22 )(R 23 ), -C(O)C(O)N(R 22 )(R 23 ), -OC(O)N(R 22 )(R 23 ), - N(R 24 )C(O)N(R 22 )(R 23 ), -N(R 24 )C(O)N(
• R 20c is independently oxo. In some embodiments R 20c is independently -CN. In some embodiments R 20c is independently halogen. In some embodiments R 20c is independently -CN. In some embodiments R 20c is independently C 1-6 alkyl. In some embodiments R 20c is independently C 2-6 alkenyl. In some embodiments R 20c is independently C 2-6 alkynyl. In some embodiments R 20c is independently C 3-6 cycloalkyl. In some embodiments R 20c is independently -CH 2 -C 3-6 cycloalkyl. In some embodiments R 20c is independently C 1- 6 heteroalkyl. In some embodiments R 20c is independently C 2-9 heterocycloalkyl.
• R 20c is independently -CH 2 -C 2-9 heterocycloalkyl. In some embodiments R 20c is independently C 6-10 aryl. In some embodiments R 20c is independently -CH 2 -C 6-10 aryl. In some embodiments R 20c is independently C 1-9 heteroaryl. In some embodiments R 20c is independently -OR 21 . In some embodiments R 20c is independently -SR 21 . In some embodiments R 20c is independently -N(R 22 )(R 23 ). In some embodiments R 20c is independently -C(O)OR 22 . In some embodiments R 20c is independently -C(O)N(R 22 )(R 23 ).
• R 20c is independently - C(O)C(O)N(R 22 )(R 23 ). In some embodiments R 20c is independently -OC(O)N(R 22 )(R 23 ). In some embodiments R 20c is independently -N(R 24 )C(O)N(R 22 )(R 23 ). In some embodiments R 20c is independently -N(R 24 )C(O)OR 22 . In some embodiments R 20c is independently -N(R 24 )C(O)R 25 . In some embodiments R 20c is independently -N(R 24 )S(O) 2 R 25 . In some embodiments R 20c is independently -C(O)R 25 .
• R 20c is independently -S(O) 2 R 25 . In some embodiments R 20c is independently -S(O) 2 N(R 22 )(R 23 ) . In some embodiments R 20c is independently - OCH 2 C(O)OR 22 . In some embodiments R 20c is independently -OC(O)R 25 .
• R 20c is independently C 1-6 alkyl substituted with one, two, or three groups independently selected from halogen, oxo, -CN, C 1-6 alkyl, C 1-6 haloalkyl, C 1-6 alkoxy, C 1-6 haloalkoxy, -OR 21 , -SR 21 , -N(R 22 )(R 23 ), -C(O)OR 22 , -C(O)N(R 22 )(R 23 ), - C(O)C(O)N(R 22 )(R 23 ), -OC(O)N(R 22 )(R 23 ), -N(R 24 )C(O)N(R 22 )(R 23 ), -N(R 24 )C(O)OR 25 , -N(R 24 )C(O)R 25 , - N(R 24 )S(O) 2 R 25 , -C(O)R 25 , -S(O) 2 R 25 ,
• R 20c is independently C 2-6 alkenyl substituted with one, two, or three groups independently selected from halogen, oxo, -CN, C 1-6 alkyl, C 1-6 haloalkyl, C 1-6 alkoxy, C 1-6 haloalkoxy, -OR 21 , -SR 21 , -N(R 22 )(R 23 ), -C(O)OR 22 , -C(O)N(R 22 )(R 23 ), - C(O)C(O)N(R 22 )(R 23 ), -OC(O)N(R 22 )(R 23 ), -N(R 24 )C(O)N(R 22 )(R 23 ), -N(R 24 )C(O)OR 25 , -N(R 24 )C(O)R 25 , - N(R 24 )S(O) 2 R 25 , -C(O)R 25 , -S(O) 2 R 25
• R 20c is independently C 2-6 alkynyl substituted with one, two, or three groups independently selected from halogen, oxo, -CN, C 1-6 alkyl, C 1-6 haloalkyl, C 1-6 alkoxy, C 1-6 haloalkoxy, -OR 21 , -SR 21 , -N(R 22 )(R 23 ), -C(O)OR 22 , -C(O)N(R 22 )(R 23 ), - C(O)C(O)N(R 22 )(R 23 ), -OC(O)N(R 22 )(R 23 ), -N(R 24 )C(O)N(R 22 )(R 23 ), -N(R 24 )C(O)OR 25 , -N(R 24 )C(O)R 25 , - N(R 24 )S(O) 2 R 25 , -C(O)R 25 , -S(O) 2 R 25
• R 20c is independently C 3-6 cycloalkyl substituted with one, two, or three groups independently selected from halogen, oxo, - CN, C 1-6 alkyl, C 1-6 haloalkyl, C 1-6 alkoxy, C 1-6 haloalkoxy, -OR 21 , -SR 21 , -N(R 22 )(R 23 ), -C(O)OR 22 , -C(O)N(R 22 )(R 23 ), -C(O)C(O)N(R 22 )(R 23 ), -OC(O)N(R 22 )(R 23 ), -N(R 24 )C(O)N(R 22 )(R 23 ), -N(R 24 )C(O)OR 25 , -N(R 24 )C(O)R 25 , - N(R 24 )S(O) 2 R 25 , -C(O)R 25 , -S(O) 2
• R 20c is independently -CH 2 -C 3-6 cycloalkyl substituted with one, two, or three groups independently selected from halogen, oxo, -CN, C 1-6 alkyl, C 1-6 haloalkyl, C 1-6 alkoxy, C 1-6 haloalkoxy, -OR 21 , -SR 21 , -N(R 22 )(R 23 ), -C(O)OR 22 , - C(O)N(R 22 )(R 23 ), -C(O)C(O)N(R 22 )(R 23 ), -OC(O)N(R 22 )(R 23 ), -N(R 24 )C(O)N(R 22 )(R 23 ), -N(R 24 )C(O)OR 25 , - N(R 24 )C(O)R 25 , -N(R 24 )S(O) 2 R 25 , -C(O)R 25 , -
• R 20c is independently C 1-6 heteroalkyl substituted with one, two, or three groups independently selected from halogen, oxo, -CN, C 1-6 alkyl, C 1-6 haloalkyl, C 1-6 alkoxy, C 1-6 haloalkoxy, -OR 21 , -SR 21 , -N(R 22 )(R 23 ), -C(O)OR 22 , - C(O)N(R 22 )(R 23 ), -C(O)C(O)N(R 22 )(R 23 ), -OC(O)N(R 22 )(R 23 ), -N(R 24 )C(O)N(R 22 )(R 23 ), -N(R 24 )C(O)OR 25 , - N(R 24 )C(O)R 25 , -N(R 24 )S(O) 2 R 25 , -C(O)R 25 , -S(O) 2
• R 20c is independently C 2-9 heterocycloalkyl substituted with one, two, or three groups independently selected from halogen, oxo, -CN, C 1-6 alkyl, C 1-6 haloalkyl, C 1-6 alkoxy, C 1-6 haloalkoxy, -OR 21 , -SR 21 , -N(R 22 )(R 23 ), -C(O)OR 22 , - C(O)N(R 22 )(R 23 ), -C(O)C(O)N(R 22 )(R 23 ), -OC(O)N(R 22 )(R 23 ), -N(R 24 )C(O)N(R 22 )(R 23 ), -N(R 24 )C(O)OR 25 , - N(R 24 )C(O)R 25 , -N(R 24 )S(O) 2 R 25 , -C(O)R 25 , -S(O)OR 25
• R 20c is independently -CH 2 -C 2-9 heterocycloalkyl substituted with one, two, or three groups independently selected from halogen, oxo, -CN, C 1-6 alkyl, C 1-6 haloalkyl, C 1-6 alkoxy, C 1-6 haloalkoxy, -OR 21 , -SR 21 , -N(R 22 )(R 23 ), - C(O)OR 22 , -C(O)N(R 22 )(R 23 ), -C(O)C(O)N(R 22 )(R 23 ), -OC(O)N(R 22 )(R 23 ), -N(R 24 )C(O)N(R 22 )(R 23 ), - N(R 24 )C(O)OR 25 , -N(R 24 )C(O)R 25 , -N(R 24 )S(O) 2 R 25 , -C(O)R 25 , -
• R 20c is independently C 6-10 aryl substituted with one, two, or three groups independently selected from halogen, oxo, -CN, C 1-6 alkyl, C 1-6 haloalkyl, C 1-6 alkoxy, C 1-6 haloalkoxy, -OR 21 , -SR 21 , -N(R 22 )(R 23 ), - C(O)OR 22 , -C(O)N(R 22 )(R 23 ), -C(O)C(O)N(R 22 )(R 23 ), -OC(O)N(R 22 )(R 23 ), -N(R 24 )C(O)N(R 22 )(R 23 ), - N(R 24 )C(O)OR 25 , -N(R 24 )C(O)R 25 , -N(R 24 )S(O) 2 R 25 , -C(O)R 25 , -S(O) 2 R 25 ,
• R 20c is independently -CH 2 -C 6-10 aryl substituted with one, two, or three groups independently selected from halogen, oxo, -CN, C 1-6 alkyl, C 1-6 haloalkyl, C 1-6 alkoxy, C 1-6 haloalkoxy, -OR 21 , -SR 21 , -N(R 22 )(R 23 ), - C(O)OR 22 , -C(O)N(R 22 )(R 23 ), -C(O)C(O)N(R 22 )(R 23 ), -OC(O)N(R 22 )(R 23 ), -N(R 24 )C(O)N(R 22 )(R 23 ), - N(R 24 )C(O)OR 25 , -N(R 24 )C(O)R 25 , -N(R 24 )S(O) 2 R 25 , -C(O)R 25 , -N(R
• R 20c is independently C 1-9 heteroaryl substituted with one, two, or three groups independently selected from halogen, oxo, -CN, C 1-6 alkyl, C 1-6 haloalkyl, C 1-6 alkoxy, C 1-6 haloalkoxy, -OR 21 , -SR 21 , -N(R 22 )(R 23 ), - C(O)OR 22 , -C(O)N(R 22 )(R 23 ), -C(O)C(O)N(R 22 )(R 23 ), -OC(O)N(R 22 )(R 23 ), -N(R 24 )C(O)N(R 22 )(R 23 ), - N(R 24 )C(O)OR 25 , -N(R 24 )C(O)R 25 , -N(R 24 )S(O) 2 R 25 , -C(O)R 25 , -S(O) 2 R 25 ,
• R 20c is independently selected from oxo, -CN, halogen, -CN, C 1-6 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 3-6 cycloalkyl, -CH 2 -C 3-6 cycloalkyl, C 2-9 heterocycloalkyl, -CH 2 -C 2-9 heterocycloalkyl, C 6-10 aryl, -CH 2 -C 6-10 aryl, C 1- 9 heteroaryl, -OR 21 , -SR 21 , -N(R 22 )(R 23 ), -C(O)OR 22 , -C(O)N(R 22 )(R 23 ), -C(O)C(O)N(R 22 )(R 23 ), -OC(O)N(R 22 )(R 23 ), - N(R 24 )C(O)N(R 22 )(R 23 ), -N(R 24 )C(O)N(
• R 20d is independently oxo. In some embodiments R 20d is independently -CN. In some embodiments R 20d is independently halogen. In some embodiments R 20d is independently -CN. In some embodiments R 20d is independently C 1-6 alkyl. In some embodiments R 20d is independently C 2-6 alkenyl. In some embodiments R 20d is independently C 2-6 alkynyl. In some embodiments R 20d is independently C 3-6 cycloalkyl. In some embodiments R 20d is independently -CH 2 -C 3-6 cycloalkyl. In some embodiments R 20d is independently C 1 - 6 heteroalkyl. In some embodiments R 20d is independently C 2-9 heterocycloalkyl.
• R 20d is independently -CH 2 -C 2-9 heterocycloalkyl. In some embodiments R 20d is independently C 6-10 aryl. In some embodiments R 20d is independently -CH 2 -C 6-10 aryl. In some embodiments R 20d is independently C 1-9 heteroaryl. In some embodiments R 20d is independently -OR 21 . In some embodiments R 20d is independently -SR 21 . In some embodiments R 20d is independently -N(R 22 )(R 23 ). In some embodiments R 20d is independently -C(O)OR 22 . In some embodiments R 20d is independently -C(O)N(R 22 )(R 23 ).
• R 20d is independently - C(O)C(O)N(R 22 )(R 23 ). In some embodiments R 20d is independently -OC(O)N(R 22 )(R 23 ). In some embodiments R 20d is independently -N(R 24 )C(O)N(R 22 )(R 23 ). In some embodiments R 20d is independently -N(R 24 )C(O)OR 22 . In some embodiments R 20d is independently -N(R 24 )C(O)R 25 . In some embodiments R 20d is independently -N(R 24 )S(O) 2 R 25 . In some embodiments R 20d is independently -C(O)R 25 .
• R 20d is independently -S(O) 2 R 25 . In some embodiments R 20d is independently -S(O) 2 N(R 22 )(R 23 ) . In some embodiments R 20d is independently - OCH 2 C(O)OR 22 . In some embodiments R 20d is independently -OC(O)R 25 .
• R 20d is independently C 1-6 alkyl substituted with one, two, or three groups independently selected from halogen, oxo, -CN, C 1-6 alkyl, C 1-6 haloalkyl, C 1-6 alkoxy, C 1-6 haloalkoxy, -OR 21 , -SR 21 , -N(R 22 )(R 23 ), -C(O)OR 22 , -C(O)N(R 22 )(R 23 ), - C(O)C(O)N(R 22 )(R 23 ), -OC(O)N(R 22 )(R 23 ), -N(R 24 )C(O)N(R 22 )(R 23 ), -N(R 24 )C(O)OR 25 , -N(R 24 )C(O)R 25 , - N(R 24 )S(O) 2 R 25 , -C(O)R 25 , -S(O) 2 R 25 ,
• R 20d is independently C 2-6 alkenyl substituted with one, two, or three groups independently selected from halogen, oxo, -CN, C 1-6 alkyl, C 1-6 haloalkyl, C 1-6 alkoxy, C 1-6 haloalkoxy, -OR 21 , -SR 21 , -N(R 22 )(R 23 ), -C(O)OR 22 , -C(O)N(R 22 )(R 23 ), - C(O)C(O)N(R 22 )(R 23 ), -OC(O)N(R 22 )(R 23 ), -N(R 24 )C(O)N(R 22 )(R 23 ), -N(R 24 )C(O)OR 25 , -N(R 24 )C(O)R 25 , - N(R 24 )S(O) 2 R 25 , -C(O)R 25 , -S(O) 2 R 25
• R 20d is independently C 2-6 alkynyl substituted with one, two, or three groups independently selected from halogen, oxo, -CN, C 1-6 alkyl, C 1-6 haloalkyl, C 1-6 alkoxy, C 1-6 haloalkoxy, -OR 21 , -SR 21 , -N(R 22 )(R 23 ), -C(O)OR 22 , -C(O)N(R 22 )(R 23 ), - C(O)C(O)N(R 22 )(R 23 ), -OC(O)N(R 22 )(R 23 ), -N(R 24 )C(O)N(R 22 )(R 23 ), -N(R 24 )C(O)OR 25 , -N(R 24 )C(O)R 25 , - N(R 24 )S(O) 2 R 25 , -C(O)R 25 , -S(O) 2 R 25
• R 20d is independently C 3-6 cycloalkyl substituted with one, two, or three groups independently selected from halogen, oxo, - CN, C 1-6 alkyl, C 1-6 haloalkyl, C 1-6 alkoxy, C 1-6 haloalkoxy, -OR 21 , -SR 21 , -N(R 22 )(R 23 ), -C(O)OR 22 , -C(O)N(R 22 )(R 23 ), -C(O)C(O)N(R 22 )(R 23 ), -OC(O)N(R 22 )(R 23 ), -N(R 24 )C(O)N(R 22 )(R 23 ), -N(R 24 )C(O)OR 25 , -N(R 24 )C(O)R 25 , - N(R 24 )S(O) 2 R 25 , -C(O)R 25 , -S(O) 2
• R 20d is independently -CH 2 -C 3-6 cycloalkyl substituted with one, two, or three groups independently selected from halogen, oxo, -CN, C 1-6 alkyl, C 1-6 haloalkyl, C 1-6 alkoxy, C 1-6 haloalkoxy, -OR 21 , -SR 21 , -N(R 22 )(R 23 ), -C(O)OR 22 , - C(O)N(R 22 )(R 23 ), -C(O)C(O)N(R 22 )(R 23 ), -OC(O)N(R 22 )(R 23 ), -N(R 24 )C(O)N(R 22 )(R 23 ), -N(R 24 )C(O)OR 25 , - N(R 24 )C(O)R 25 , -N(R 24 )S(O) 2 R 25 , -C(O)R 25 , -
• R 20d is independently C 1-6 heteroalkyl substituted with one, two, or three groups independently selected from halogen, oxo, -CN, C 1-6 alkyl, C 1-6 haloalkyl, C 1-6 alkoxy, C 1-6 haloalkoxy, -OR 21 , -SR 21 , -N(R 22 )(R 23 ), -C(O)OR 22 , - C(O)N(R 22 )(R 23 ), -C(O)C(O)N(R 22 )(R 23 ), -OC(O)N(R 22 )(R 23 ), -N(R 24 )C(O)N(R 22 )(R 23 ), -N(R 24 )C(O)OR 25 , - N(R 24 )C(O)R 25 , -N(R 24 )S(O) 2 R 25 , -C(O)R 25 , -S(O) 2
• R 20d is independently C 2-9 heterocycloalkyl substituted with one, two, or three groups independently selected from halogen, oxo, -CN, C 1-6 alkyl, C 1-6 haloalkyl, C 1-6 alkoxy, C 1-6 haloalkoxy, -OR 21 , -SR 21 , -N(R 22 )(R 23 ), -C(O)OR 22 , - C(O)N(R 22 )(R 23 ), -C(O)C(O)N(R 22 )(R 23 ), -OC(O)N(R 22 )(R 23 ), -N(R 24 )C(O)N(R 22 )(R 23 ), -N(R 24 )C(O)OR 25 , - N(R 24 )C(O)R 25 , -N(R 24 )S(O) 2 R 25 , -C(O)R 25 , -S(O)OR 25
• R 20d is independently -CH 2 -C 2-9 heterocycloalkyl substituted with one, two, or three groups independently selected from halogen, oxo, -CN, C 1-6 alkyl, C 1-6 haloalkyl, C 1-6 alkoxy, C 1-6 haloalkoxy, -OR 21 , -SR 21 , -N(R 22 )(R 23 ), - C(O)OR 22 , -C(O)N(R 22 )(R 23 ), -C(O)C(O)N(R 22 )(R 23 ), -OC(O)N(R 22 )(R 23 ), -N(R 24 )C(O)N(R 22 )(R 23 ), - N(R 24 )C(O)OR 25 , -N(R 24 )C(O)R 25 , -N(R 24 )S(O) 2 R 25 , -C(O)R 25 , -
• R 20d is independently C 6-10 aryl substituted with one, two, or three groups independently selected from halogen, oxo, -CN, C 1-6 alkyl, C 1-6 haloalkyl, C 1-6 alkoxy, C 1-6 haloalkoxy, -OR 21 , -SR 21 , -N(R 22 )(R 23 ), - C(O)OR 22 , -C(O)N(R 22 )(R 23 ), -C(O)C(O)N(R 22 )(R 23 ), -OC(O)N(R 22 )(R 23 ), -N(R 24 )C(O)N(R 22 )(R 23 ), - N(R 24 )C(O)OR 25 , -N(R 24 )C(O)R 25 , -N(R 24 )S(O) 2 R 25 , -C(O)R 25 , -S(O) 2 R 25 ,
• R 20d is independently -CH 2 -C 6-10 aryl substituted with one, two, or three groups independently selected from halogen, oxo, -CN, C 1-6 alkyl, C 1-6 haloalkyl, C 1-6 alkoxy, C 1-6 haloalkoxy, -OR 21 , -SR 21 , -N(R 22 )(R 23 ), - C(O)OR 22 , -C(O)N(R 22 )(R 23 ), -C(O)C(O)N(R 22 )(R 23 ), -OC(O)N(R 22 )(R 23 ), -N(R 24 )C(O)N(R 22 )(R 23 ), - N(R 24 )C(O)OR 25 , -N(R 24 )C(O)R 25 , -N(R 24 )S(O) 2 R 25 , -C(O)R 25 , -N(R
• R 20d is independently C 1-9 heteroaryl substituted with one, two, or three groups independently selected from halogen, oxo, -CN, C 1-6 alkyl, C 1-6 haloalkyl, C 1-6 alkoxy, C 1-6 haloalkoxy, -OR 21 , -SR 21 , -N(R 22 )(R 23 ), - C(O)OR 22 , -C(O)N(R 22 )(R 23 ), -C(O)C(O)N(R 22 )(R 23 ), -OC(O)N(R 22 )(R 23 ), -N(R 24 )C(O)N(R 22 )(R 23 ), - N(R 24 )C(O)OR 25 , -N(R 24 )C(O)R 25 , -N(R 24 )S(O) 2 R 25 , -C(O)R 25 , -S(O) 2 R 25 ,
• R 20d is independently selected from oxo, -CN, halogen, -CN, C 1-6 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 3-6 cycloalkyl, -CH 2 -C 3-6 cycloalkyl, C 2-9 heterocycloalkyl, -CH 2 -C 2-9 heterocycloalkyl, C 6-10 aryl, -CH 2 -C 6-10 aryl, C 1 - 9 heteroaryl, -OR 21 , -SR 21 , -N(R 22 )(R 23 ), -C(O)OR 22 , -C(O)N(R 22 )(R 23 ), -C(O)C(O)N(R 22 )(R 23 ), -OC(O)N(R 22 )(R 23 ), - N(R 24 )C(O)N(R 22 )(R 23 ), -N(R 24 )C(O)
• R 20e is independently oxo. In some embodiments R 20e is independently -CN. In some embodiments R 20e is independently halogen. In some embodiments R 20e is independently -CN. In some embodiments R 20e is independently C 1-6 alkyl. In some embodiments R 20e is independently C 2-6 alkenyl. In some embodiments R 20e is independently C 2-6 alkynyl. In some embodiments R 20e is independently C 3-6 cycloalkyl. In some embodiments R 20e is independently -CH 2 -C 3-6 cycloalkyl. In some embodiments R 20e is independently C 1 - 6 heteroalkyl. In some embodiments R 20e is independently C 2-9 heterocycloalkyl.
• R 20e is independently -CH 2 -C 2-9 heterocycloalkyl. In some embodiments R 20e is independently C 6-10 aryl. In some embodiments R 20e is independently -CH 2 -C 6-10 aryl. In some embodiments R 20e is independently C 1-9 heteroaryl. In some embodiments R 20e is independently -OR 21 . In some embodiments R 20e is independently -SR 21 . In some embodiments R 20e is independently -N(R 22 )(R 23 ). In some embodiments R 20e is independently -C(O)OR 22 . In some embodiments R 20e is independently -C(O)N(R 22 )(R 23 ).
• R 20e is independently - C(O)C(O)N(R 22 )(R 23 ). In some embodiments R 20e is independently -OC(O)N(R 22 )(R 23 ). In some embodiments R 20e is independently -N(R 24 )C(O)N(R 22 )(R 23 ). In some embodiments R 20e is independently -N(R 24 )C(O)OR 22 . In some embodiments R 20e is independently -N(R 24 )C(O)R 25 . In some embodiments R 20e is independently -N(R 24 )S(O) 2 R 25 . In some embodiments R 20e is independently -C(O)R 25 .
• R 20e is independently -S(O) 2 R 25 . In some embodiments R 20e is independently -S(O) 2 N(R 22 )(R 23 ) . In some embodiments R 20e is independently - OCH 2 C(O)OR 22 . In some embodiments R 20e is independently -OC(O)R 25 .
• R 20e is independently C 1-6 alkyl substituted with one, two, or three groups independently selected from halogen, oxo, -CN, C 1-6 alkyl, C 1-6 haloalkyl, C 1-6 alkoxy, C 1-6 haloalkoxy, -OR 21 , -SR 21 , -N(R 22 )(R 23 ), -C(O)OR 22 , -C(O)N(R 22 )(R 23 ), - C(O)C(O)N(R 22 )(R 23 ), -OC(O)N(R 22 )(R 23 ), -N(R 24 )C(O)N(R 22 )(R 23 ), -N(R 24 )C(O)OR 25 , -N(R 24 )C(O)R 25 , - N(R 24 )S(O) 2 R 25 , -C(O)R 25 , -S(O) 2 R 25 ,
• R 20e is independently C 2-6 alkenyl substituted with one, two, or three groups independently selected from halogen, oxo, -CN, C 1-6 alkyl, C 1-6 haloalkyl, C 1-6 alkoxy, C 1-6 haloalkoxy, -OR 21 , -SR 21 , -N(R 22 )(R 23 ), -C(O)OR 22 , -C(O)N(R 22 )(R 23 ), - C(O)C(O)N(R 22 )(R 23 ), -OC(O)N(R 22 )(R 23 ), -N(R 24 )C(O)N(R 22 )(R 23 ), -N(R 24 )C(O)OR 25 , -N(R 24 )C(O)R 25 , - N(R 24 )S(O) 2 R 25 , -C(O)R 25 , -S(O) 2 R 25
• R 20e is independently C 2-6 alkynyl substituted with one, two, or three groups independently selected from halogen, oxo, -CN, C 1-6 alkyl, C 1-6 haloalkyl, C 1-6 alkoxy, C 1-6 haloalkoxy, -OR 21 , -SR 21 , -N(R 22 )(R 23 ), -C(O)OR 22 , -C(O)N(R 22 )(R 23 ), - C(O)C(O)N(R 22 )(R 23 ), -OC(O)N(R 22 )(R 23 ), -N(R 24 )C(O)N(R 22 )(R 23 ), -N(R 24 )C(O)OR 25 , -N(R 24 )C(O)R 25 , - N(R 24 )S(O) 2 R 25 , -C(O)R 25 , -S(O) 2 R 25
• R 20e is independently C 3-6 cycloalkyl substituted with one, two, or three groups independently selected from halogen, oxo, - CN, C 1-6 alkyl, C 1-6 haloalkyl, C 1-6 alkoxy, C 1-6 haloalkoxy, -OR 21 , -SR 21 , -N(R 22 )(R 23 ), -C(O)OR 22 , -C(O)N(R 22 )(R 23 ), -C(O)C(O)N(R 22 )(R 23 ), -OC(O)N(R 22 )(R 23 ), -N(R 24 )C(O)N(R 22 )(R 23 ), -N(R 24 )C(O)OR 25 , -N(R 24 )C(O)R 25 , - N(R 24 )S(O) 2 R 25 , -C(O)R 25 , -S(O) 2
• R 20e is independently -CH 2 -C 3-6 cycloalkyl substituted with one, two, or three groups independently selected from halogen, oxo, -CN, C 1-6 alkyl, C 1-6 haloalkyl, C 1-6 alkoxy, C 1-6 haloalkoxy, -OR 21 , -SR 21 , -N(R 22 )(R 23 ), -C(O)OR 22 , - C(O)N(R 22 )(R 23 ), -C(O)C(O)N(R 22 )(R 23 ), -OC(O)N(R 22 )(R 23 ), -N(R 24 )C(O)N(R 22 )(R 23 ), -N(R 24 )C(O)OR 25 , - N(R 24 )C(O)R 25 , -N(R 24 )S(O) 2 R 25 , -C(O)R 25 , -
• R 20e is independently C 1-6 heteroalkyl substituted with one, two, or three groups independently selected from halogen, oxo, -CN, C 1-6 alkyl, C 1-6 haloalkyl, C 1-6 alkoxy, C 1-6 haloalkoxy, -OR 21 , -SR 21 , -N(R 22 )(R 23 ), -C(O)OR 22 , - C(O)N(R 22 )(R 23 ), -C(O)C(O)N(R 22 )(R 23 ), -OC(O)N(R 22 )(R 23 ), -N(R 24 )C(O)N(R 22 )(R 23 ), -N(R 24 )C(O)OR 25 , - N(R 24 )C(O)R 25 , -N(R 24 )S(O) 2 R 25 , -C(O)R 25 , -S(O) 2
• R 20e is independently C 2-9 heterocycloalkyl substituted with one, two, or three groups independently selected from halogen, oxo, -CN, C 1-6 alkyl, C 1-6 haloalkyl, C 1-6 alkoxy, C 1-6 haloalkoxy, -OR 21 , -SR 21 , -N(R 22 )(R 23 ), -C(O)OR 22 , - C(O)N(R 22 )(R 23 ), -C(O)C(O)N(R 22 )(R 23 ), -OC(O)N(R 22 )(R 23 ), -N(R 24 )C(O)N(R 22 )(R 23 ), -N(R 24 )C(O)OR 25 , - N(R 24 )C(O)R 25 , -N(R 24 )S(O) 2 R 25 , -C(O)R 25 , -S(O)OR 25
• R 20e is independently -CH 2 -C 2-9 heterocycloalkyl substituted with one, two, or three groups independently selected from halogen, oxo, -CN, C 1-6 alkyl, C 1-6 haloalkyl, C 1-6 alkoxy, C 1-6 haloalkoxy, -OR 21 , -SR 21 , -N(R 22 )(R 23 ), - C(O)OR 22 , -C(O)N(R 22 )(R 23 ), -C(O)C(O)N(R 22 )(R 23 ), -OC(O)N(R 22 )(R 23 ), -N(R 24 )C(O)N(R 22 )(R 23 ), - N(R 24 )C(O)OR 25 , -N(R 24 )C(O)R 25 , -N(R 24 )S(O) 2 R 25 , -C(O)R 25 , -
• R 20e is independently C 6-10 aryl substituted with one, two, or three groups independently selected from halogen, oxo, -CN, C 1-6 alkyl, C 1-6 haloalkyl, C 1-6 alkoxy, C 1-6 haloalkoxy, -OR 21 , -SR 21 , -N(R 22 )(R 23 ), - C(O)OR 22 , -C(O)N(R 22 )(R 23 ), -C(O)C(O)N(R 22 )(R 23 ), -OC(O)N(R 22 )(R 23 ), -N(R 24 )C(O)N(R 22 )(R 23 ), - N(R 24 )C(O)OR 25 , -N(R 24 )C(O)R 25 , -N(R 24 )S(O) 2 R 25 , -C(O)R 25 , -S(O) 2 R 25 ,
• R 20e is independently -CH 2 -C 6-10 aryl substituted with one, two, or three groups independently selected from halogen, oxo, -CN, C 1-6 alkyl, C 1-6 haloalkyl, C 1-6 alkoxy, C 1-6 haloalkoxy, -OR 21 , -SR 21 , -N(R 22 )(R 23 ), - C(O)OR 22 , -C(O)N(R 22 )(R 23 ), -C(O)C(O)N(R 22 )(R 23 ), -OC(O)N(R 22 )(R 23 ), -N(R 24 )C(O)N(R 22 )(R 23 ), - N(R 24 )C(O)OR 25 , -N(R 24 )C(O)R 25 , -N(R 24 )S(O) 2 R 25 , -C(O)R 25 , -N(R
• R 20e is independently C 1-9 heteroaryl substituted with one, two, or three groups independently selected from halogen, oxo, -CN, C 1-6 alkyl, C 1-6 haloalkyl, C 1-6 alkoxy, C 1-6 haloalkoxy, -OR 21 , -SR 21 , -N(R 22 )(R 23 ), - C(O)OR 22 , -C(O)N(R 22 )(R 23 ), -C(O)C(O)N(R 22 )(R 23 ), -OC(O)N(R 22 )(R 23 ), -N(R 24 )C(O)N(R 22 )(R 23 ), - N(R 24 )C(O)OR 25 , -N(R 24 )C(O)R 25 , -N(R 24 )S(O) 2 R 25 , -C(O)R 25 , -S(O) 2 R 25 ,
• R 20e is independently selected from oxo, -CN, halogen, -CN, C 1-6 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 3-6 cycloalkyl, -CH 2 -C 3-6 cycloalkyl, C 2-9 heterocycloalkyl, -CH 2 -C 2-9 heterocycloalkyl, C 6-10 aryl, -CH 2 -C 6-10 aryl, C 1- 9 heteroaryl, -OR 21 , -SR 21 , -N(R 22 )(R 23 ), -C(O)OR 22 , -C(O)N(R 22 )(R 23 ), -C(O)C(O)N(R 22 )(R 23 ), -OC(O)N(R 22 )(R 23 ), - N(R 24 )C(O)N(R 22 )(R 23 ), -N(R 24 )C(O)N(
• R 20f is independently oxo. In some embodiments R 20f is independently -CN. In some embodiments R 20f is independently halogen. In some embodiments R 20f is independently -CN. In some embodiments R 20f is independently C 1-6 alkyl. In some embodiments R 20f is independently C 2-6 alkenyl. In some embodiments R 20f is independently C 2-6 alkynyl. In some embodiments R 20f is independently C 3-6 cycloalkyl. In some embodiments R 20f is independently -CH 2 -C 3-6 cycloalkyl. In some embodiments R 20f is independently C 1- 6 heteroalkyl. In some embodiments R 20f is independently C 2-9 heterocycloalkyl.
• R 20f is independently -CH 2 -C 2-9 heterocycloalkyl. In some embodiments R 20f is independently C 6-10 aryl. In some embodiments R 20f is independently -CH 2 -C 6-10 aryl. In some embodiments R 20f is independently C 1-9 heteroaryl. In some embodiments R 20f is independently -OR 21 . In some embodiments R 20f is independently -SR 21 . In some embodiments R 20f is independently -N(R 22 )(R 23 ). In some embodiments R 20f is independently -C(O)OR 22 . In some embodiments R 20f is independently -C(O)N(R 22 )(R 23 ).
• R 20f is independently - C(O)C(O)N(R 22 )(R 23 ). In some embodiments R 20f is independently -OC(O)N(R 22 )(R 23 ). In some embodiments R 20f is independently -N(R 24 )C(O)N(R 22 )(R 23 ). In some embodiments R 20f is independently -N(R 24 )C(O)OR 22 . In some embodiments R 20f is independently -N(R 24 )C(O)R 25 . In some embodiments R 20f is independently -N(R 24 )S(O) 2 R 25 . In some embodiments R 20f is independently -C(O)R 25 .
• R 20f is independently -S(O) 2 R 25 . In some embodiments R 20f is independently -S(O) 2 N(R 22 )(R 23 ) . In some embodiments R 20f is independently - OCH 2 C(O)OR 22 . In some embodiments R 20f is independently -OC(O)R 25 .
• R 20f is independently C 1-6 alkyl substituted with one, two, or three groups independently selected from halogen, oxo, -CN, C 1-6 alkyl, C 1-6 haloalkyl, C 1-6 alkoxy, C 1-6 haloalkoxy, -OR 21 , -SR 21 , -N(R 22 )(R 23 ), -C(O)OR 22 , -C(O)N(R 22 )(R 23 ), - C(O)C(O)N(R 22 )(R 23 ), -OC(O)N(R 22 )(R 23 ), -N(R 24 )C(O)N(R 22 )(R 23 ), -N(R 24 )C(O)OR 25 , -N(R 24 )C(O)R 25 , - N(R 24 )S(O) 2 R 25 , -C(O)R 25 , -S(O) 2 R 25 ,
• R 20f is independently C 2-6 alkenyl substituted with one, two, or three groups independently selected from halogen, oxo, -CN, C 1-6 alkyl, C 1-6 haloalkyl, C 1-6 alkoxy, C 1-6 haloalkoxy, -OR 21 , -SR 21 , -N(R 22 )(R 23 ), -C(O)OR 22 , -C(O)N(R 22 )(R 23 ), - C(O)C(O)N(R 22 )(R 23 ), -OC(O)N(R 22 )(R 23 ), -N(R 24 )C(O)N(R 22 )(R 23 ), -N(R 24 )C(O)OR 25 , -N(R 24 )C(O)R 25 , - N(R 24 )S(O) 2 R 25 , -C(O)R 25 , -S(O) 2 R 25
• R 20f is independently C 2-6 alkynyl substituted with one, two, or three groups independently selected from halogen, oxo, -CN, C 1-6 alkyl, C 1-6 haloalkyl, C 1-6 alkoxy, C 1-6 haloalkoxy, -OR 21 , -SR 21 , -N(R 22 )(R 23 ), -C(O)OR 22 , -C(O)N(R 22 )(R 23 ), - C(O)C(O)N(R 22 )(R 23 ), -OC(O)N(R 22 )(R 23 ), -N(R 24 )C(O)N(R 22 )(R 23 ), -N(R 24 )C(O)OR 25 , -N(R 24 )C(O)R 25 , - N(R 24 )S(O) 2 R 25 , -C(O)R 25 , -S(O) 2 R 25
• R 20f is independently C 3-6 cycloalkyl substituted with one, two, or three groups independently selected from halogen, oxo, - CN, C 1-6 alkyl, C 1-6 haloalkyl, C 1-6 alkoxy, C 1-6 haloalkoxy, -OR 21 , -SR 21 , -N(R 22 )(R 23 ), -C(O)OR 22 , -C(O)N(R 22 )(R 23 ), -C(O)C(O)N(R 22 )(R 23 ), -OC(O)N(R 22 )(R 23 ), -N(R 24 )C(O)N(R 22 )(R 23 ), -N(R 24 )C(O)OR 25 , -N(R 24 )C(O)R 25 , - N(R 24 )S(O) 2 R 25 , -C(O)R 25 , -S(O) 2
• R 20f is independently -CH 2 -C 3-6 cycloalkyl substituted with one, two, or three groups independently selected from halogen, oxo, -CN, C 1-6 alkyl, C 1-6 haloalkyl, C 1-6 alkoxy, C 1-6 haloalkoxy, -OR 21 , -SR 21 , -N(R 22 )(R 23 ), -C(O)OR 22 , - C(O)N(R 22 )(R 23 ), -C(O)C(O)N(R 22 )(R 23 ), -OC(O)N(R 22 )(R 23 ), -N(R 24 )C(O)N(R 22 )(R 23 ), -N(R 24 )C(O)OR 25 , - N(R 24 )C(O)R 25 , -N(R 24 )S(O) 2 R 25 , -C(O)R 25 , -
• R 20f is independently C 1-6 heteroalkyl substituted with one, two, or three groups independently selected from halogen, oxo, -CN, C 1-6 alkyl, C 1-6 haloalkyl, C 1-6 alkoxy, C 1-6 haloalkoxy, -OR 21 , -SR 21 , -N(R 22 )(R 23 ), -C(O)OR 22 , - C(O)N(R 22 )(R 23 ), -C(O)C(O)N(R 22 )(R 23 ), -OC(O)N(R 22 )(R 23 ), -N(R 24 )C(O)N(R 22 )(R 23 ), -N(R 24 )C(O)OR 25 , - N(R 24 )C(O)R 25 , -N(R 24 )S(O) 2 R 25 , -C(O)R 25 , -S(O) 2
• R 20f is independently C 2-9 heterocycloalkyl substituted with one, two, or three groups independently selected from halogen, oxo, -CN, C 1-6 alkyl, C 1-6 haloalkyl, C 1-6 alkoxy, C 1-6 haloalkoxy, -OR 21 , -SR 21 , -N(R 22 )(R 23 ), -C(O)OR 22 , - C(O)N(R 22 )(R 23 ), -C(O)C(O)N(R 22 )(R 23 ), -OC(O)N(R 22 )(R 23 ), -N(R 24 )C(O)N(R 22 )(R 23 ), -N(R 24 )C(O)OR 25 , - N(R 24 )C(O)R 25 , -N(R 24 )S(O) 2 R 25 , -C(O)R 25 , -S(O)OR 25
• R 20f is independently -CH 2 -C 2-9 heterocycloalkyl substituted with one, two, or three groups independently selected from halogen, oxo, -CN, C 1-6 alkyl, C 1-6 haloalkyl, C 1-6 alkoxy, C 1-6 haloalkoxy, -OR 21 , -SR 21 , -N(R 22 )(R 23 ), - C(O)OR 22 , -C(O)N(R 22 )(R 23 ), -C(O)C(O)N(R 22 )(R 23 ), -OC(O)N(R 22 )(R 23 ), -N(R 24 )C(O)N(R 22 )(R 23 ), - N(R 24 )C(O)OR 25 , -N(R 24 )C(O)R 25 , -N(R 24 )S(O) 2 R 25 , -C(O)R 25 , -
• R 20f is independently C 6-10 aryl substituted with one, two, or three groups independently selected from halogen, oxo, -CN, C 1-6 alkyl, C 1-6 haloalkyl, C 1-6 alkoxy, C 1-6 haloalkoxy, -OR 21 , -SR 21 , -N(R 22 )(R 23 ), - C(O)OR 22 , -C(O)N(R 22 )(R 23 ), -C(O)C(O)N(R 22 )(R 23 ), -OC(O)N(R 22 )(R 23 ), -N(R 24 )C(O)N(R 22 )(R 23 ), - N(R 24 )C(O)OR 25 , -N(R 24 )C(O)R 25 , -N(R 24 )S(O) 2 R 25 , -C(O)R 25 , -S(O) 2 R 25 ,
• R 20f is independently -CH 2 -C 6-10 aryl substituted with one, two, or three groups independently selected from halogen, oxo, -CN, C 1-6 alkyl, C 1-6 haloalkyl, C 1-6 alkoxy, C 1-6 haloalkoxy, -OR 21 , -SR 21 , -N(R 22 )(R 23 ), - C(O)OR 22 , -C(O)N(R 22 )(R 23 ), -C(O)C(O)N(R 22 )(R 23 ), -OC(O)N(R 22 )(R 23 ), -N(R 24 )C(O)N(R 22 )(R 23 ), - N(R 24 )C(O)OR 25 , -N(R 24 )C(O)R 25 , -N(R 24 )S(O) 2 R 25 , -C(O)R 25 , -N(R
• R 20f is independently C 1-9 heteroaryl substituted with one, two, or three groups independently selected from halogen, oxo, -CN, C 1-6 alkyl, C 1-6 haloalkyl, C 1-6 alkoxy, C 1-6 haloalkoxy, -OR 21 , -SR 21 , -N(R 22 )(R 23 ), - C(O)OR 22 , -C(O)N(R 22 )(R 23 ), -C(O)C(O)N(R 22 )(R 23 ), -OC(O)N(R 22 )(R 23 ), -N(R 24 )C(O)N(R 22 )(R 23 ), - N(R 24 )C(O)OR 25 , -N(R 24 )C(O)R 25 , -N(R 24 )S(O) 2 R 25 , -C(O)R 25 , -S(O) 2 R 25 ,
• R 20f is independently selected from oxo, -CN, halogen, -CN, C 1-6 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 3-6 cycloalkyl, -CH 2 -C 3-6 cycloalkyl, C 2-9 heterocycloalkyl, -CH 2 -C 2-9 heterocycloalkyl, C 6-10 aryl, -CH 2 -C 6-10 aryl, C 1- 9 heteroaryl, -OR 21 , -SR 21 , -N(R 22 )(R 23 ), -C(O)OR 22 , -C(O)N(R 22 )(R 23 ), -C(O)C(O)N(R 22 )(R 23 ), -OC(O)N(R 22 )(R 23 ), - N(R 24 )C(O)N(R 22 )(R 23 ), -N(R 24 )C(O)N(
• R 20g is independently oxo. In some embodiments R 20g is independently -CN. In some embodiments R 20g is independently halogen. In some embodiments R 20g is independently -CN. In some embodiments R 20g is independently C 1-6 alkyl. In some embodiments R 20g is independently C 2-6 alkenyl. In some embodiments R 20g is independently C 2-6 alkynyl. In some embodiments R 20g is independently C 3-6 cycloalkyl. In some embodiments R 20g is independently -CH 2 -C 3-6 cycloalkyl. In some embodiments R 20g is independently C 1 - 6 heteroalkyl. In some embodiments R 20g is independently C 2-9 heterocycloalkyl.
• R 20g is independently -CH 2 -C 2-9 heterocycloalkyl. In some embodiments R 20g is independently C 6-10 aryl. In some embodiments R 20g is independently -CH 2 -C 6-10 aryl. In some embodiments R 20g is independently C 1-9 heteroaryl. In some embodiments R 20g is independently -OR 21 . In some embodiments R 20g is independently -SR 21 . In some embodiments R 20g is independently -N(R 22 )(R 23 ). In some embodiments R 20g is independently -C(O)OR 22 . In some embodiments R 20g is independently -C(O)N(R 22 )(R 23 ).
• R 20g is independently - C(O)C(O)N(R 22 )(R 23 ). In some embodiments R 20g is independently -OC(O)N(R 22 )(R 23 ). In some embodiments R 20g is independently -N(R 24 )C(O)N(R 22 )(R 23 ). In some embodiments R 20g is independently -N(R 24 )C(O)OR 22 . In some embodiments R 20g is independently -N(R 24 )C(O)R 25 . In some embodiments R 20g is independently -N(R 24 )S(O) 2 R 25 . In some embodiments R 20g is independently -C(O)R 25 .
• R 20g is independently -S(O) 2 R 25 . In some embodiments R 20g is independently -S(O) 2 N(R 22 )(R 23 ) . In some embodiments R 20g is independently - OCH 2 C(O)OR 22 . In some embodiments R 20g is independently -OC(O)R 25 .
• R 20g is independently C 1-6 alkyl substituted with one, two, or three groups independently selected from halogen, oxo, -CN, C 1-6 alkyl, C 1-6 haloalkyl, C 1-6 alkoxy, C 1-6 haloalkoxy, -OR 21 , -SR 21 , -N(R 22 )(R 23 ), -C(O)OR 22 , -C(O)N(R 22 )(R 23 ), - C(O)C(O)N(R 22 )(R 23 ), -OC(O)N(R 22 )(R 23 ), -N(R 24 )C(O)N(R 22 )(R 23 ), -N(R 24 )C(O)OR 25 , -N(R 24 )C(O)R 25 , - N(R 24 )S(O) 2 R 25 , -C(O)R 25 , -S(O) 2 R 25 ,
• R 20g is independently C 2-6 alkenyl substituted with one, two, or three groups independently selected from halogen, oxo, -CN, C 1-6 alkyl, C 1-6 haloalkyl, C 1-6 alkoxy, C 1-6 haloalkoxy, -OR 21 , -SR 21 , -N(R 22 )(R 23 ), -C(O)OR 22 , -C(O)N(R 22 )(R 23 ), - C(O)C(O)N(R 22 )(R 23 ), -OC(O)N(R 22 )(R 23 ), -N(R 24 )C(O)N(R 22 )(R 23 ), -N(R 24 )C(O)OR 25 , -N(R 24 )C(O)R 25 , - N(R 24 )S(O) 2 R 25 , -C(O)R 25 , -S(O) 2 R 25
• R 20g is independently C 2-6 alkynyl substituted with one, two, or three groups independently selected from halogen, oxo, -CN, C 1-6 alkyl, C 1-6 haloalkyl, C 1-6 alkoxy, C 1-6 haloalkoxy, -OR 21 , -SR 21 , -N(R 22 )(R 23 ), -C(O)OR 22 , -C(O)N(R 22 )(R 23 ), - C(O)C(O)N(R 22 )(R 23 ), -OC(O)N(R 22 )(R 23 ), -N(R 24 )C(O)N(R 22 )(R 23 ), -N(R 24 )C(O)OR 25 , -N(R 24 )C(O)R 25 , - N(R 24 )S(O) 2 R 25 , -C(O)R 25 , -S(O) 2 R 25
• R 20g is independently C 3-6 cycloalkyl substituted with one, two, or three groups independently selected from halogen, oxo, - CN, C 1-6 alkyl, C 1-6 haloalkyl, C 1-6 alkoxy, C 1-6 haloalkoxy, -OR 21 , -SR 21 , -N(R 22 )(R 23 ), -C(O)OR 22 , -C(O)N(R 22 )(R 23 ), -C(O)C(O)N(R 22 )(R 23 ), -OC(O)N(R 22 )(R 23 ), -N(R 24 )C(O)N(R 22 )(R 23 ), -N(R 24 )C(O)OR 25 , -N(R 24 )C(O)R 25 , - N(R 24 )S(O) 2 R 25 , -C(O)R 25 , -S(O) 2

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