WO2019023147A1 - COMPOUNDS AND COMPOSITIONS FOR THE TREATMENT OF PATHOLOGICAL CONDITIONS ASSOCIATED WITH NLRP ACTIVITY - Google Patents

COMPOUNDS AND COMPOSITIONS FOR THE TREATMENT OF PATHOLOGICAL CONDITIONS ASSOCIATED WITH NLRP ACTIVITY Download PDF

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Publication number
WO2019023147A1
WO2019023147A1 PCT/US2018/043338 US2018043338W WO2019023147A1 WO 2019023147 A1 WO2019023147 A1 WO 2019023147A1 US 2018043338 W US2018043338 W US 2018043338W WO 2019023147 A1 WO2019023147 A1 WO 2019023147A1
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WO
WIPO (PCT)
Prior art keywords
alkyl
hydroxy
optionally substituted
membered
compound
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Ceased
Application number
PCT/US2018/043338
Other languages
English (en)
French (fr)
Inventor
Gary Glick
William R. Roush
Shankar Venkatraman
Dong-Ming Shen
Shomir Ghosh
Jason Katz
Hans Martin Seidel
Luigi Franchi
David Guenther WINKLER
Anthony William OPIPARI JR.
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Novartis Inflammasome Research Inc
Original Assignee
IFM Tre Inc
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Priority to CU2020000004A priority Critical patent/CU24615B1/es
Priority to NZ761026A priority patent/NZ761026A/en
Priority to MX2020000911A priority patent/MX2020000911A/es
Priority to PE2020000150A priority patent/PE20200723A1/es
Priority to CR20200037A priority patent/CR20200037A/es
Priority to CN202310765173.1A priority patent/CN117143042A/zh
Priority to US16/632,849 priority patent/US11203579B2/en
Priority to MA49682A priority patent/MA49682B1/fr
Priority to CA3068836A priority patent/CA3068836A1/en
Priority to CN202311185119.6A priority patent/CN117209447A/zh
Priority to KR1020207004803A priority patent/KR102565167B1/ko
Priority to EP24151235.9A priority patent/EP4349820A3/en
Priority to LTEPPCT/US2018/043338T priority patent/LT3658539T/lt
Priority to PL18752376.6T priority patent/PL3658539T3/pl
Priority to DK18752376.6T priority patent/DK3658539T3/da
Priority to CN201880050915.XA priority patent/CN111094243B/zh
Priority to SI201831090T priority patent/SI3658539T1/sl
Priority to BR112020001476-1A priority patent/BR112020001476A2/pt
Priority to RU2020107727A priority patent/RU2786719C2/ru
Priority to IL271259A priority patent/IL271259B2/en
Priority to EP18752376.6A priority patent/EP3658539B1/en
Application filed by IFM Tre Inc filed Critical IFM Tre Inc
Priority to EA202090353A priority patent/EA202090353A1/ru
Priority to SG11201912166XA priority patent/SG11201912166XA/en
Priority to RS20240513A priority patent/RS65492B1/sr
Priority to AU2018307743A priority patent/AU2018307743C1/en
Priority to HRP20240521TT priority patent/HRP20240521T1/hr
Priority to ES18752376T priority patent/ES2988798T3/es
Priority to FIEP18752376.6T priority patent/FI3658539T3/fi
Priority to JP2020503754A priority patent/JP7412328B2/ja
Publication of WO2019023147A1 publication Critical patent/WO2019023147A1/en
Priority to US16/572,528 priority patent/US10654816B2/en
Priority to ZA2019/08154A priority patent/ZA201908154B/en
Priority to CONC2020/0000527A priority patent/CO2020000527A2/es
Priority to PH12020500127A priority patent/PH12020500127A1/en
Priority to DO2020000012A priority patent/DOP2020000012A/es
Anticipated expiration legal-status Critical
Priority to JOJO/P/2020/0011A priority patent/JOP20200011B1/ar
Priority to US17/496,375 priority patent/US11724992B2/en
Priority to US18/319,630 priority patent/US12084424B2/en
Priority to JP2023218835A priority patent/JP7654767B2/ja
Priority to JP2025044149A priority patent/JP7813931B2/ja
Ceased legal-status Critical Current

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    • C07D317/48—Methylenedioxybenzenes or hydrogenated methylenedioxybenzenes, unsubstituted on the hetero ring
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    • C07C335/42—Sulfonylthioureas; Sulfonylisothioureas
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    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
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    • C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
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    • C07D213/70—Sulfur atoms
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    • C07D405/12—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a chain containing hetero atoms as chain links
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    • C07D409/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
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    • C07D417/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
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    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D471/00—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
    • 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
    • C07D471/04—Ortho-condensed systems

Definitions

  • This disclosure features chemical entities (e.g., a compound that modulates (e.g., antagonizes) NLRP3, or a pharmaceutically acceptable salt, and/or hydrate, and/or cocrystal, and/or drug combination of the compound) that are useful, e.g., for treating a condition, disease or disorder in which a decrease or increase in NLRP3 activity (e.g., an increase, e.g., a condition, disease or disorder associated with NLRP3 signaling) contributes to the pathology and/or symptoms and/or progression of the condition, disease or disorder in a subject (e.g., a human).
  • This disclosure also features compositions as well as other methods of using and making the same.
  • the NLRP3 inflammasome is a component of the inflammatory process and its aberrant activation is pathogenic in inherited disorders such as the cryopyrin associated periodic syndromes (CAPS).
  • CAPS Muckle-Wells syndrome MFS
  • FCAS familial cold autoinflammatory syndrome
  • NOMID neonatal onset multi-system inflammatory disease
  • NLRP3 can form a complex and has been implicated in the pathogenesis of a number of complex diseases, including but not limited to metabolic disorders such as type 2 diabetes, atherosclerosis, obesity and gout, as well as diseases of the central nervous system, such as Alzheimer's disease and multiple sclerosis and Amyotrophic Lateral Sclerosis and Parkinson disease, lung disease, such as asthma and COPD and pulmonary idiopathic fibrosis, liver disease, such as NASH syndrome, viral hepatitis and cirrhosis, pancreatic disease, such as acute and chronic pancreatitis, kidney disease, such as acute and chronic kidney injury, intestinal disease such as Crohn's disease and Ulcerative Colitis, skin disease such as psoriasis, musculoskeletal disease such as scleroderma, vessel disorders, such as giant cell arteritis, disorders of the bones, such as Osteoarthritis , osteoporosis and osteopetrosis disorders eye disease, such as glaucoma and macular degeneration, disease
  • autoimmune disease such as Rheumatoid Arthritis, Systemic Lupus Erythematosus,
  • This disclosure features chemical entities (e.g., a compound that modulates (e.g., antagonizes) NLRP3, or a pharmaceutically acceptable salt, and/or hydrate, and/or cocrystal, and/or drug combination of the compound) that are useful, e.g., for treating a condition, disease or disorder in which a decrease or increase in NLRP3 activity (e.g., an increase, e.g., a condition, disease or disorder associated with NLRP3 signaling).
  • a compound that modulates e.g., antagonizes
  • a pharmaceutically acceptable salt, and/or hydrate, and/or cocrystal, and/or drug combination of the compound e.g., for treating a condition, disease or disorder in which a decrease or increase in NLRP3 activity (e.g., an increase, e.g., a condition, disease or disorder associated with NLRP3 signaling).
  • An "antagonist" of NLRP3 includes compounds that inhibit the ability of NLRP3 to induce the production of IL- ⁇ and/or IL-18 by directly binding to NLRP3, or by inactivating, destabilizing, altering distribution, of LRP3 or otherwise.
  • compositions are featured that include a chemical entity described herein (e.g., a compound described genetically or specifically herein or a pharmaceutically acceptable salt thereof or compositions containing the same) and one or more pharmaceutically acceptable excipients.
  • a chemical entity described herein e.g., a compound described genetically or specifically herein or a pharmaceutically acceptable salt thereof or compositions containing the same
  • one or more pharmaceutically acceptable excipients e.g., a compound described genetically or specifically herein or a pharmaceutically acceptable salt thereof or compositions containing the same.
  • methods for modulating e.g., agonizing, partially agonizing, antagonizing
  • LRP3 activity include contacting LRP3 with a chemical entity described herein (e.g., a compound described generically or specifically herein or a pharmaceutically acceptable salt thereof or compositions containing the same).
  • Methods include in vitro methods, e.g., contacting a sample that includes one or more cells comprising LRP3, as well as in vivo methods.
  • methods of treatment of a disease in which NLRP3 signaling contributes to the pathology and/or symptoms and/or progression of the disease include administering to a subject in need of such treatment an effective amount of a chemical entity described herein (e.g., a compound described generically or specifically herein or a pharmaceutically acceptable salt thereof or compositions containing the same).
  • a chemical entity described herein e.g., a compound described generically or specifically herein or a pharmaceutically acceptable salt thereof or compositions containing the same.
  • methods of treatment include administering to a subject a chemical entity described herein (e.g., a compound described generically or specifically herein or a pharmaceutically acceptable salt thereof or compositions containing the same), wherein the chemical entity is administered in an amount effective to treat a disease in which LRP3 signaling contributes to the pathology and/or symptoms and/or progression of the disease, thereby treating the disease.
  • a chemical entity described herein e.g., a compound described generically or specifically herein or a pharmaceutically acceptable salt thereof or compositions containing the same
  • Embodiments can include one or more of the following features.
  • the chemical entity can be administered in combination with one or more additional therapies with one or more agents suitable for the treatment of the condition, disease or disorder.
  • Examples of the indications that may be treated by the compounds disclosed herein include but are not limited to metabolic disorders such as type 2 diabetes, atherosclerosis, obesity and gout, as well as diseases of the central nervous system, such as Alzheimer's disease and multiple sclerosis and Amyotrophic Lateral Sclerosis and Parkinson disease, lung disease, such as asthma and COPD and pulmonary idiopathic fibrosis, liver disease, such as NASH syndrome, viral hepatitis and cirrhosis, pancreatic disease, such as acute and chronic pancreatitis, kidney disease, such as acute and chronic kidney injury, intestinal disease such as Crohn's disease and Ulcerative Colitis, skin disease such as psoriasis, musculoskeletal disease such as scleroderma, vessel disorders, such as giant cell arteritis, disorders of the bones, such as osteoarthritis , osteoporosis and osteopetrosis disorders, eye disease, such as glaucoma and macular degeneration, diseases caused by viral infection such as HIV and AIDS,
  • the methods can further include identifying the subject.
  • NLRP3 is meant to include, without limitation, nucleic acids, polynucleotides, oligonucleotides, sense and antisense polynucleotide strands, complementary sequences, peptides, polypeptides, proteins, homologous and/or orthologous NLRP3 molecules, isoforms, precursors, mutants, variants, derivatives, splice variants, alleles, different species, and active fragments thereof.
  • an “effective amount” or “therapeutically effective amount,” as used herein, refer to a sufficient amount of a chemical entity (e.g., a compound exhibiting activity as a modulator of LRP3, or a pharmaceutically acceptable salt and/or hydrate and/or cocrystal thereof;) being administered which will relieve to some extent one or more of the symptoms of the disease or condition being treated. The result includes reduction and/or alleviation of the signs, symptoms, or causes of a disease, or any other desired alteration of a biological system.
  • an "effective amount” for therapeutic uses is the amount of the composition comprising a compound as disclosed herein required to provide a clinically significant decrease in disease symptoms.
  • An appropriate "effective" amount in any individual case is determined using any suitable technique, such as a dose escalation study.
  • excipient or “pharmaceutically acceptable excipient” means a pharmaceutically-acceptable material, composition, or vehicle, such as a liquid or solid filler, diluent, carrier, solvent, or encapsulating material.
  • each component is " pharmaceutically acceptable” in the sense of being compatible with the other ingredients of a pharmaceutical formulation, and suitable for use in contact with the tissue or organ of humans and animals without excessive toxicity, irritation, allergic response, immunogenicity, or other problems or complications, commensurate with a reasonable benefit/risk ratio. See, e.g., Remington: The Science and Practice of Pharmacy, 21st ed.; Lippincott Williams & Wilkins: Philadelphia, PA, 2005; Handbook of Pharmaceutical Excipients, 6th ed.
  • pharmaceutically acceptable salt may refer to pharmaceutically acceptable addition salts prepared from pharmaceutically acceptable non-toxic acids including inorganic and organic acids.
  • pharmaceutically acceptable salts are obtained by reacting a compound described herein, with acids such as hydrochloric acid, hydrobromic acid, sulfuric acid, nitric acid, phosphoric acid, methanesulfonic acid, ethanesulfonic acid, p-toluenesulfonic acid, salicylic acid and the like.
  • pharmaceutically acceptable salt may also refer to pharmaceutically acceptable addition salts prepared by reacting a compound having an acidic group with a base to form a salt such as an ammonium salt, an alkali metal salt, such as a sodium or a potassium salt, an alkaline earth metal salt, such as a calcium or a magnesium salt, a salt of organic bases such as dicyclohexylamine, N-methyl-D-glucamine, tris(hydroxymethyl)methylamine, and salts with amino acids such as arginine, lysine, and the like, or by other methods previously determined.
  • a salt such as an ammonium salt, an alkali metal salt, such as a sodium or a potassium salt, an alkaline earth metal salt, such as a calcium or a magnesium salt, a salt of organic bases such as dicyclohexylamine, N-methyl-D-glucamine, tris(hydroxymethyl)methylamine, and salts with amino acids such as arginine, lysine, and the like, or
  • Examples of a salt that the compounds described hereinform with a base include the following: salts thereof with inorganic bases such as sodium, potassium, magnesium, calcium, and aluminum; salts thereof with organic bases such as methylamine, ethylamine and ethanolamine; salts thereof with basic amino acids such as lysine and ornithine; and ammonium salt.
  • the salts may be acid addition salts, which are specifically exemplified by acid addition salts with the following: mineral acids such as hydrochloric acid, hydrobromic acid, hydroiodic acid, sulfuric acid, nitric acid, and phosphoric acid:organic acids such as formic acid, acetic acid, propionic acid, oxalic acid, malonic acid, succinic acid, fumaric acid, maleic acid, lactic acid, malic acid, tartaric acid, citric acid, methanesulfonic acid, and ethanesulfonic acid; acidic amino acids such as aspartic acid and glutamic acid.
  • mineral acids such as hydrochloric acid, hydrobromic acid, hydroiodic acid, sulfuric acid, nitric acid, and phosphoric acid
  • organic acids such as formic acid, acetic acid, propionic acid, oxalic acid, malonic acid, succinic acid, fumaric acid, maleic acid, lactic acid, malic acid, tart
  • composition refers to a mixture of a compound described herein with other chemical components (referred to collectively herein as “excipients”), such as carriers, stabilizers, diluents, dispersing agents, suspending agents, and/or thickening agents.
  • excipients such as carriers, stabilizers, diluents, dispersing agents, suspending agents, and/or thickening agents.
  • the pharmaceutical composition facilitates administration of the compound to an organism. Multiple techniques of administering a compound exist in the art including, but not limited to: rectal, oral, intravenous, aerosol, parenteral, ophthalmic, pulmonary, and topical administration.
  • subject refers to an animal, including, but not limited to, a primate (e.g., human), monkey, cow, pig, sheep, goat, horse, dog, cat, rabbit, rat, or mouse.
  • primate e.g., human
  • monkey cow, pig, sheep, goat
  • horse dog, cat, rabbit, rat
  • patient are used interchangeably herein in reference, for example, to a mammalian subject, such as a human.
  • treat in the context of treating a disease or disorder, are meant to include alleviating or abrogating a disorder, disease, or condition, or one or more of the symptoms associated with the disorder, disease, or condition; or to slowing the progression, spread or worsening of a disease, disorder or condition or of one or more symptoms thereof.
  • halo refers to fluoro (F), chloro (CI), bromo (Br), or iodo (I).
  • alkyl refers to a hydrocarbon chain that may be a straight chain or branched chain, saturated or unsaturated, containing the indicated number of carbon atoms.
  • Ci-io indicates that the group may have from 1 to 10 (inclusive) carbon atoms in it.
  • Non-limiting examples include methyl, ethyl, z ' so-propyl, tert-butyl, /7-hexyl.
  • haloalkyl refers to an alkyl, in which one or more hydrogen atoms is/are replaced with an independently selected halo.
  • alkoxy refers to an -O-alkyl radical (e.g., -OCH3).
  • carbocyclic ring as used herein includes an aromatic or nonaromatic cyclic hydrocarbon group having 3 to 10 carbons, such as 3 to 8 carbons, such as 3 to 7 carbons, which may be optionally substituted.
  • Examples of carbocyclic rings include five-membered, six- membered, and seven-membered carbocyclic rings.
  • heterocyclic ring refers to an aromatic or nonaromatic 5-8 membered monocyclic, 8-12 membered bicyclic, or 1 1-14 membered tricyclic ring system having 1-3 heteroatoms if monocyclic, 1-6 heteroatoms if bicyclic, or 1 -9 heteroatoms if tricyclic, said heteroatoms selected from O, N, or S (e.g., carbon atoms and 1-3, 1-6, or 1-9 heteroatoms of N, O, or S if monocyclic, bicyclic, or tricyclic, respectively), wherein 0, 1, 2, or 3 atoms of each ring may be substituted by a substituent.
  • heterocyclic rings include five-membered, six- membered, and seven-membered heterocyclic rings.
  • cycloalkyl as used herein includes an nonaromatic cyclic, bicylic, fused, or spiro hydrocarbon radical having 3 to 10 carbons, such as 3 to 8 carbons, such as 3 to 7 carbons, wherein the cycloalkyl group which may be optionally substituted.
  • Examples of cycloalkyls include five-membered, six-membered, and seven-membered rings. Examples include cyclopropyl, cyclobutyl, cyclopentyl, cyclopentenyl, cyclohexyl, cyclohexenyl, cycloheptyl, and cyclooctyl.
  • heterocycloalkyl refers to an nonaromatic 5-8 membered monocyclic, 8-12 membered bicyclic, or 1 1-14 membered tricyclic ring, fused, or spiro system radical having 1 -3 heteroatoms if monocyclic, 1-6 heteroatoms if bicyclic, or 1 -9 heteroatoms if tricyclic, said heteroatoms selected from O, N, or S (e.g., carbon atoms and 1-3, 1-6, or 1-9 heteroatoms of N, O, or S if monocyclic, bicyclic, or tricyclic, respectively), wherein 0, 1, 2, or 3 atoms of each ring may be substituted by a substituent.
  • heterocycloalkyls include five-membered, six- membered, and seven-membered heterocyclic rings.
  • Examples include piperazinyl, pyrrolidinyl, dioxanyl, morpholinyl, tetrahydrofuranyl, and the like.
  • aryl is intended to mean an aromatic ring radical containing 6 to 10 ring carbons. Examples include phenyl and naphthyl.
  • heteroaryl is intended to mean an aromatic ring system containing 5 to 14 aromatic ring atoms that may be a single ring, two fused rings or three fused rings wherein at least one aromatic ring atom is a heteroatom selected from, but not limited to, the group consisting of O, S and N.
  • Examples include furanyl, thienyl, pyrrolyl, imidazolyl, oxazolyl, thiazolyl, isoxazolyl, pyrazolyl, isothiazolyl, oxadiazolyl, triazolyl, thiadiazolyl, pyridinyl, pyrazinyl, pyrimidinyl, pyridazinyl, triazinyl and the like.
  • Examples also include carbazolyl, quinolizinyl, quinolinyl, isoquinolinyl, cinnolinyl, phthalazinyl, quinazolinyl, quinoxalinyl, triazinyl, indolyl, isoindolyl, indazolyl, indolizinyl, purinyl, naphthyridinyl, pteridinyl, carbazolyl, acridinyl.
  • hydroxy refers to an OH group.
  • amino refers to an H2 group.
  • oxo refers to O.
  • the terms “the ring B” or “B” are used interchangeably to denote formula AA wherein the bond that is shown as being broken by the wavy line connects B to the NH(CO) group of Formula AA.
  • the term “the optionally substituted ring A” is used to denote
  • the term "the substituted ring B" is used to denote formula AA, wherein the bond that is shown as being broken by the wavy line * connects B to the H(CO) group of Formula AA.
  • atoms making up the compounds of the present embodiments are intended to include all isotopic forms of such atoms.
  • Isotopes include those atoms having the same atomic number but different mass numbers.
  • isotopes of hydrogen include tritium and deuterium
  • isotopes of carbon include 13 C and 14 C.
  • Non-limiting exemplified compounds of the formulae described herein include a stereogenic sulfur atom and optionally one or more stereogenic carbon atoms.
  • This disclosure provides examples of stereoisomer mixtures (e.g., racemic mixture of enantiomers; mixture of diastereomers).
  • This disclosure also describes and exemplifies methods for separating individual components of said stereoisomer mixtures (e.g., resolving the enantiomers of a racemic mixture). In cases of compounds containing only a stereogenic sulfur atom, resolved
  • FIG. 1 depicts ball-and-stick representations of two crystallographically independent molecules of compound 181a in the asymmetrical unit.
  • FIG. 2 depicts ball-and-stick representations of two crystallographically independent molecules of compound 181b in the asymmetrical unit.
  • FIG. 3 depicts the layout of the microplate used in an hTHP-1 assay.
  • n 0, 1, or 2;
  • n 0, 1, or 2;
  • A is a 5-10-membered heteroaryl or a C 6 -Cio aryl
  • B is a 5-10-membered heteroaryl or a C 6 -Cio aryl
  • R 6 is ortho to the bond connecting the B ring to the R 3 (CO) group of Formula AA;
  • R 1 and R 2 are each independently selected from Ci-C 6 alkyl, Ci-C 6 haloalkyl, Ci-C 6 alkoxy, Ci- Ce haloalkoxy, halo, CN, N0 2 , COCi-Ce alkyl, CO-Ce-Cio aryl, CO-(5- to 10-membered heteroaryl), CO2C1-C6 alkyl, CO2C3-C8 cycloalkyl, OCOCi-Ce alkyl, OCOCe-Cio aryl, OCO(5- to 10-membered heteroaryl), OCO(3- to 7-membered heterocycloalkyl), C6-C10 aryl, 5- to 10- membered heteroaryl, H2, NHCi-Ce alkyl, N(Ci-Ce alkyl) 2 , NHCOCi-Ce
  • heterocycloalkyl is optionally substituted with one or more substituents each independently selected from hydroxy, halo, CN, oxo, Ci-Ce alkyl, Ci-Ce alkoxy, COOCi-Ce alkyl, NR 8 R 9 , CONR 8 R 9 , 3- to 7-membered heterocycloalkyl, C6-C10 aryl, 5- to 10-membered heteroaryl, OCOCi-Ce alkyl, OCOCe-Cio aryl, OCO(5- to 10-membered heteroaryl), and OCO(3- to 7- membered heterocycloalkyl), HCOCi-Ce alkyl, HCOCe-Cio aryl, HCO(5- to 10-membered heteroaryl), HCO(3- to 7-membered heterocycloalkyl), and HCOC2-C6 alkynyl;
  • each Ci-C 6 alkyl substituent and each Ci-C 6 alkoxy substituent of the R 1 or R 2 C3-C7 cycloalkyl or of the R 1 or R 2 3- to 7-membered heterocycloalkyl is further optionally independently substituted with one to three hydroxy, halo, or oxo;
  • the 3- to 7-membered heterocycloalkyl, C6-C10 aryl, or 5- to 10-membered heteroaryl, of the R 1 or R 2 Ci-Ce alkyl, the R 1 or R 2 Ci-Ce haloalkyl, the R 1 or R 2 C3-C7 cycloalkyl, or the R 1 or R 2 3- to 7-membered heterocycloalkyl are optionally substituted with one or more substituents independently selected from halo, Ci-C 6 alkyl, oxo, and OCi-Ce alkyl;
  • R 10 is Ci-Ce alkyl
  • each of R 11 and R 12 at each occurrence is independently selected from hydrogen and Ci-C 6 alkyl; each R 3 is inde endentl selected from hydrogen, cyano, hydroxy, Ci-C 6 alkoxy, Ci-C 6 alkyl, alkylene)
  • R 14 is hydrogen, Ci-Ce alkyl, 5-10-membered monocyclic or bicyclic heteroaryl or C 6 -Cio monocyclic or bicyclic aryl, wherein each Ci-Ce alkyl, aryl or heteroaryl is optionally independently substituted with 1, 2, or 3 R 6 ;
  • provided herein is a compound of Formula AA
  • n 0, 1, or 2;
  • n 0, 1, or 2;
  • A is a 5-10-membered heteroaryl or a C 6 -Cio aryl
  • B is a 5-10-membered heteroaryl or a C 6 -Cio aryl
  • R 6 is ortho to the bond connecting the B ring to the R 3 (CO) group of Formula AA;
  • R 1 and R 2 are each independently selected from Ci-C 6 alkyl, Ci-C 6 haloalkyl, Ci-C 6 alkoxy, Ci- Ce haloalkoxy, halo, CN, N0 2 , COCi-Ce alkyl, CO-Ce-Cio aryl, CO-(5- to 10-membered heteroaryl), CO2C1-C6 alkyl, CO2C3-C8 cycloalkyl, OCOCi-Ce alkyl, OCOCe-Cio aryl, OCO(5- to 10-membered heteroaryl), OCO(3- to 7-membered heterocycloalkyl), C6-C10 aryl, 5- to 10- membered heteroaryl, H2, NHCi-Ce alkyl, N(Ci-Ce alkyl) 2 , NHCOCi-Ce
  • HCOC2-C6 alkynyl, HCOOCi-Ce alkyl, H-(C R 13 ) R U R 12 , CO R 8 R 9 , SFs, SCi-Ce alkyl, S(0 2 )Ci-C 6 alkyl, S(0 2 ) R u R 12 , S(0)Ci-Ce alkyl, C3-C7 cycloalkyl, and 3- to 7- membered heterocycloalkyl, wherein the Ci-C 6 alkyl, C1-G5 haloalkyl, C3-C7 cycloalkyl, and 3- to 7-membered heterocycloalkyl is optionally substituted with one or more substituents each independently selected from hydroxy, halo, CN, oxo, Ci-Ce alkyl, Ci-Ce alkoxy, COOCi-Ce alkyl, NR 8 R 9 , CONR 8 R 9 , 3- to 7-membered heterocycloal
  • each Ci-C 6 alkyl substituent and each Ci-C 6 alkoxy substituent of the R 1 or R 2 C3-C7 cycloalkyl or of the R 1 or R 2 3- to 7-membered heterocycloalkyl is further optionally independently substituted with one to three hydroxy, halo, or oxo;
  • the 3- to 7-membered heterocycloalkyl, C6-C10 aryl, or 5- to 10-membered heteroaryl, of the R 1 or R 2 Ci-Ce alkyl, the R 1 or R 2 Ci-Ce haloalkyl, the R 1 or R 2 C3-C7 cycloalkyl, or the R 1 or R 2 3- to 7-membered heterocycloalkyl are optionally substituted with one or more substituents independently selected from halo, Ci-C 6 alkyl, oxo, and OCi-Ce alkyl;
  • R 6 and R 7 are each independently selected from Ci-C 6 alkyl, Ci-C 6 haloalkyl, Ci-C 6 alkoxy, Ci- Ce haloalkoxy, halo, CN, NO2, COCi-Ce alkyl, CO2C1-C6 alkyl, CO2C3-C8 cycloalkyl, OCOCi- Ce alkyl, OCOCe-Cio aryl, OCO(5- to 10-membered heteroaryl), OCO(3- to 7-membered heterocycloalkyl), Ce-Cio aryl, 5- to 10-membered heteroaryl, NH2, NHCi-Ce alkyl, N(Ci-Ce alkyl) 2 , CONR 8 R 9 , SFs, SCi-Ce alkyl, S(0 2 )Ci-C 6 alkyl, C3-C10 cycloalkyl, 3- to 10-membered heterocycloalkyl, and C2-
  • R 10 is Ci-Ce alkyl
  • each of R 11 and R 12 at each occurrence is independently selected from hydrogen and Ci-C 6 alkyl; each R 3 is independently selected from hydrogen, cyano, hydroxy, Ci-Ce alkoxy, Ci-Ce alkyl, alkylene)
  • R 14 is hydrogen, Ci-C 6 alkyl, 5-10-membered monocyclic or bicyclic heteroaryl or C 6 -Cio monocyclic or bicyclic aryl, wherein each Ci-C 6 alkyl, aryl or heteroaryl is optionally independently substituted with 1, 2, or 3 R 6 ;
  • provided herein is a compound of Formula AA
  • n 0, 1, or 2;
  • n 0, 1, or 2;
  • A is a 5-10-membered heteroaryl or a C6-C10 aryl
  • B is a 5-10-membered heteroaryl or a C6-C10 aryl
  • R 6 is ortho to the bond connecting the B ring to the R 3 (CO) group of Formula AA;
  • R 1 and R 2 are each independently selected from Ci-C 6 alkyl, Ci-C 6 haloalkyl, Ci-C 6 alkoxy, Ci- Ce haloalkoxy, halo, CN, NO2, COCi-Ce alkyl, CO-Ce-Cio aryl, CO-(5- to 10-membered heteroaryl), CO2C1-C6 alkyl, CO2C3-C8 cycloalkyl, OCOCi-Ce alkyl, OCOCe-Cio aryl, OCO(5- to 10-membered heteroaryl), OCO(3- to 7-membered heterocycloalkyl), C6-C10 aryl, 5- to 10- membered heteroaryl, H 2 , NHCi-Ce alkyl, N(Ci-Ce alkyl) 2 , NHCOCi-Ce al
  • each Ci-C 6 alkyl substituent and each Ci-C 6 alkoxy substituent of the R 1 or R 2 C3-C7 cycloalkyl or of the R 1 or R 2 3- to 7-membered heterocycloalkyl is further optionally independently substituted with one to three hydroxy, halo, R 8 R 9 , or oxo; wherein the 3- to 7-membered heterocycloalkyl, C6-C10 aryl, 5- to 10-membered heteroaryl, NHCOCe-Cio aryl, HCO(5- to 10-membered heteroaryl) and HCO(3- to 7- membered heterocycloalkyl) are optionally substituted with one or more substituents independently selected from halo, Ci-C 6 alkyl, and OCi-C 6 alkyl;
  • R 6 and R 7 are each independently selected from Ci-C 6 alkyl, Ci-C 6 haloalkyl, C1-G5 alkoxy, Ci- Ce haloalkoxy, halo, CN, NO2, COCi-Ce alkyl, CO2C1-C6 alkyl, CO2C3-C8 cycloalkyl, OCOCi- Ce alkyl, OCOCe-Cio aryl, OCO(5- to 10-membered heteroaryl), OCO(3- to 7-membered heterocycloalkyl), Ce-Cio aryl, 5- to 10-membered heteroaryl, H2, HCi-Ce alkyl, N(Ci-Ce alkyl) 2 , CO R 8 R 9 , SFs, SCi-Ce alkyl, S(0 2 )Ci-C 6 alkyl, C3-C10 cycloalkyl, 3- to 10-membered heterocycloalkyl, and C2-
  • 3- to 7-membered heterocycloalkyl, C6-C10 aryl, 5- to 10-membered heteroaryl, NHCOCe-Cio aryl, HCO(5- to 10-membered heteroaryl) and HCO(3- to 7- membered heterocycloalkyl) are optionally substituted with one or more substituents independently selected from halo, Ci-C 6 alkyl, and OCi-C 6 alkyl;
  • R 10 is Ci-Ce alkyl
  • each of R 11 and R 12 at each occurrence is independently selected from hydrogen and Ci-C 6 alkyl;
  • R 3 is selected from hydrogen, cyano, hydroxy, Ci-C 6 alkoxy, Ci-C 6 alkyl, CO2C1-C6 alkyl, and
  • R 14 is hydrogen, Ci-C 6 alkyl, 5-10-membered monocyclic or bicyclic heteroaryl or C6-C10 monocyclic or bicyclic aryl, wherein each Ci-C 6 alkyl, aryl or heteroaryl is optionally
  • provided herein is a compound of Formula AA
  • n 0, 1, or 2;
  • n 0, 1, or 2;
  • A is a 5- to 10-membered monocyclic or bicyclic heteroaryl or a C6-C10 monocyclic or bicyclic aryl;
  • B is a 5- to 10-membered monocyclic or bicyclic heteroaryl or a C6-C10 monocyclic or bicyclic aryl;
  • R 1 and R 2 are each independently selected from Ci-C 6 alkyl, Ci-C 6 haloalkyl, Ci-C 6 alkoxy, Ci- Ce haloalkoxy, halo, CN, NO2, COCi-Ce alkyl, CO-Ce-Cio aryl, CO(5- to 10-membered heteroaryl), CO2C1-C6 alkyl, CO2C3-C8 cycloalkyl, OCOCi-Ce alkyl, OCOCe-Cio aryl, OCO(5- to 10-membered heteroaryl), OCO(3- to 7-membered heterocycloalkyl), C6-C10 aryl, 5- to 10- membered heteroaryl, H2, NHCi-Ce alkyl, N(Ci-Ce alkyl) 2 , NHCOCi-Ce alkyl
  • each Ci-C 6 alkyl substituent and each Ci-C 6 alkoxy substituent of the R 1 or R 2 C3-C7 cycloalkyl or of the R 1 or R 2 3- to 7-membered heterocycloalkyl is further optionally independently substituted with one to three hydroxy, halo, NR 8 R 9 , or oxo; wherein the 3- to 7-membered heterocycloalkyl, C6-C10 aryl, 5- to 10-membered heteroaryl, NHCOCe-Cio aryl, NHCO(5- to 10-membered heteroaryl) and NHCO(3- to 7- membered heterocycloalkyl) are optionally substituted with one or more substituents independently selected from halo, Ci-C 6 alkyl, and OCi-C 6 alkyl;
  • R 6 and R 7 are each independently selected from Ci-C 6 alkyl, Ci-C 6 haloalkyl, Ci-C 6 alkoxy, Ci- Ce haloalkoxy, halo, CN, NO2, COCi-Ce alkyl, CO2C1-C6 alkyl, CO2C3-C8 cycloalkyl, OCOCi- Ce alkyl, OCOCe-Cio aryl, OCO(5- to 10-membered heteroaryl), OCO(3- to 7-membered heterocycloalkyl), Ce-Cio aryl, 5- to 10-membered heteroaryl, H2, HCi-Ce alkyl, N(Ci-Ce alkyl) 2 , CO R 8 R 9 , SFs, SCi-Ce alkyl, S(0 2 )Ci-C 6 alkyl, C3-C10 cycloalkyl and 3- to 10- membered heterocycloalkyl, and C2-C
  • R 10 is Ci-Ce alkyl; each of R 8 and R 9 at each occurrence is independently selected from hydrogen, Ci-C 6 alkyl,
  • Ci-Ce alkyl is optionally substituted with one or more hydroxy, halo, Ci-C 6 alkoxy, C 6 -Cio aryl, 5- to 10-membered heteroaryl, C3-C7 cycloalkyl or 3- to 7-membered heterocycloalkyl; or R 8 and R 9 taken together with the nitrogen they are attached to form a 3- to 7-membered ring optionally containing one or more heteroatoms in addition to the nitrogen they are attached to;
  • R 13 is Ci-C 6 alkyl, C6-C10 aryl, or 5- to 10-membered heteroaryl;
  • each of R 11 and R 12 at each occurrence is independently selected from hydrogen and Ci-C 6 alkyl; and alkylene)
  • R is selected from hydrogen, cyano, hydroxy, Ci-C 6 alkoxy, Ci-C 6 alkyl, and
  • Ci-C 2 alkylene group is optionally substituted with oxo
  • R 14 is hydrogen, Ci-C 6 alkyl, 5- to 10-membered monocyclic or bicyclic heteroaryl or monocyclic or bicyclic aryl, wherein each Ci-C 6 alkyl, aryl or heteroaryl is optionally
  • provided herein is a compound of Formula AA
  • n 0, 1, or 2;
  • n 0, 1, or 2;
  • A is a 5- to 10-membered monocyclic or bicyclic heteroaryl or a C 6 -Cio monocyclic or bicyclic aryl;
  • B is a 5- to 10-membered monocyclic or bicyclic heteroaryl or a C 6 -Cio monocyclic or bicyclic aryl;
  • R 6 is ortho to the bond connecting the B ring to the H(CO) group of Formula AA;
  • R 1 and R 2 are each independently selected from Ci-C 6 alkyl, Ci-C 6 haloalkyl, Ci-C 6 alkoxy, Ci- Ce haloalkoxy, halo, CN, N0 2 , COCi-Ce alkyl, CO-Ce-Cio aryl; CO(5- to 10-membered heteroaryl); CO2C1-C6 alkyl, CO2C3-C8 cycloalkyl, OCOCi-Ce alkyl, OCOCe-Cio aryl, OCO(5- to 10-membered heteroaryl), OCO(3- to 7-membered heterocycloalkyl), C6-C10 aryl, 5- to 10- membered heteroaryl, H2, NHCi-Ce alkyl, N(Ci-Ce alkyl) 2 , NHCOCi-Ce alky
  • each Ci-C 6 alkyl substituent and each Ci-C 6 alkoxy substituent of the R 1 or R 2 C3-C7 cycloalkyl or of the R 1 or R 2 3- to 7-membered heterocycloalkyl is further optionally independently substituted with one to three hydroxy, halo, NR 8 R 9 , or oxo; wherein the 3- to 7-membered heterocycloalkyl, C6-C10 aryl, 5- to 10-membered heteroaryl, NHCOCe-Cio aryl, NHCO(5- to 10-membered heteroaryl) and NHCO(3- to 7- membered heterocycloalkyl) are optionally substituted with one or more substituents independently selected from halo, Ci-C 6 alkyl, and OCi-C 6 alkyl; or at least one pair of R 1 and R 2 on adjacent atoms, taken together with the atoms connecting them, independently form at least one C4-C8 carbocyclic
  • heterocycloalkyl and a C2-C6 alkenyl
  • R 10 is Ci-Ce alkyl
  • each of R 11 and R 12 at each occurrence is independently selected from hydrogen and Ci-C 6 alkyl;
  • R 3 is selected from hydrogen, cyano, hydroxy, Ci-C 6 alkoxy, Ci-C 6 alkyl, and
  • Ci-C 2 alkylene group is optionally substituted by oxo
  • R 14 is hydrogen, Ci-C 6 alkyl, 5- to 10-membered monocyclic or bicyclic heteroaryl or C6-C10 monocyclic or bicyclic aryl , wherein each Ci-C 6 alkyl, aryl or heteroaryl is optionally independently substituted with 1 or 2 R 6 ;
  • n 0, 1, or 2;
  • n 0, 1, or 2;
  • A is a 5- to 10-membered monocyclic or bicyclic heteroaryl or a C 6 -Cio monocyclic or bicyclic aryl;
  • B is a 5-membered heteroaryl, a 7-10 membered monocyclic or bicyclic heteroaryl, or a C 6 -Cio monocyclic or bicyclic aryl;
  • R 1 and R 2 are each independently selected from Ci-C 6 alkyl, Ci-C 6 haloalkyl, Ci-C 6 alkoxy, Ci- Ce haloalkoxy, halo, CN, NO2, COCi-Ce alkyl, CO-Ce-Cio aryl; CO(5- to 10-membered heteroaryl); CO2C1-C6 alkyl, CO2C3-C8 cycloalkyl, OCOCi-Ce alkyl, OCOCe-Cio aryl, OCO(5- to 10-membered heteroaryl), OCO(3- to 7-membered heterocycloalkyl), C6-C10 aryl, 5- to 10- membered heteroaryl, H2, HCi-Ce alkyl, N(Ci-Ce alkyl) 2 , HCOCi-Ce alkyl
  • each Ci-C 6 alkyl substituent and each Ci-C 6 alkoxy substituent of the R 1 or R 2 C3-C7 cycloalkyl or of the R 1 or R 2 3- to 7-membered heterocycloalkyl is further optionally independently substituted with one to three hydroxy, halo, NR 8 R 9 , or oxo; wherein the 3- to 7-membered heterocycloalkyl, C6-C10 aryl, 5- to 10-membered heteroaryl, NHCOCe-Cio aryl, NHCO(5- to 10-membered heteroaryl) and NHCO(3- to 7- membered heterocycloalkyl) are optionally substituted with one or more substituents independently selected from halo, Ci-C 6 alkyl, and OCi-C 6 alkyl;
  • R 6 and R 7 are each independently selected from Ci-C 6 alkyl, Ci-C 6 haloalkyl, Ci-C 6 alkoxy, Ci- Ce haloalkoxy, halo, CN, NO2, COCi-Ce alkyl, CO2C1-C6 alkyl, CO2C3-C8 cycloalkyl, OCOCi- Ce alkyl, OCOCe-Cio aryl, OCO(5- to 10-membered heteroaryl), OCO(3- to 7-membered heterocycloalkyl), Ce-Cio aryl, 5- to 10-membered heteroaryl, H2, HCi-Ce alkyl, N(Ci-Ce alkyl) 2 , CO R 8 R 9 , SFs, S(0 2 )Ci-C 6 alkyl, C3-C10 cycloalkyl and 3- to 10-membered
  • heterocycloalkyl and a C2-C6 alkenyl
  • each of R 11 and R 12 at each occurrence is independently selected from hydrogen and Ci-C 6 alkyl;
  • R is selected from hydrogen, cyano, hydroxy, Ci-C 6 alkoxy, Ci-C 6 alkyl, and
  • Ci-C 2 alkylene group is optionally substituted by oxo
  • R 14 is hydrogen, Ci-C 6 alkyl, 5- to 10-membered monocyclic or bicyclic heteroaryl or monocyclic or bicyclic aryl , wherein each Ci-C 6 alkyl, aryl or heteroaryl is optionally independently substituted with 1 or 2 R 6 ;
  • n 0, 1, or 2.
  • n 0 or 2.
  • n 0.
  • n ⁇ .
  • n ⁇ 2.
  • n 0
  • n 0
  • n 1
  • A is a 5- to 10-membered (e.g., 5- to 6-membered) monocyclic or bicyclic heteroaryl or a C 6 -Cio (e.g., C 6 ) monocyclic or bicyclic aryl, such as phenyl.
  • A is a 5- to 10-membered (e.g., 5- to 6-membered) monocyclic or bicyclic heteroaryl.
  • A is a 5-membered heteroaryl containing a sulfur and optionally one or more nitrogens.
  • A is a C 6 -Cio monocyclic or bicyclic aryl.
  • A is phenyl optionally substituted with 1 or 2 R 1 and optionally substituted with 1 or 2 R 2 .
  • A is naphthyl optionally substituted with 1 or 2 R 1 and optionally substituted with 1 or 2 R 2 .
  • A is furanyl optionally substituted with 1 or 2 R 1 and optionally substituted with 1 R 2 .
  • A is furanyl optionally substituted with 1 R 1 and optionally substituted with 1 or 2 R 2 .
  • A is thiophenyl optionally substituted with 1 or 2 R 1 and optionally substituted with 1 or 2 R 2 .
  • A is oxazolyl optionally substituted with 1 or 2 R 1 and optionally substituted with 1 or 2 R 2 .
  • A is thiazolyl optionally substituted with 1 or 2 R 1 and optionally substituted with 1 or 2 R 2 . In some embodiments, A is oxazolyl optionally substituted with 2 R 1 or optionally substituted with 2 R 2 .
  • A is thiazolyl optionally substituted with 2 R 1 or optionally substituted with 2 R 2 .
  • A is pyrazolyl optionally substituted with 1 or 2 R 1 and optionally substituted with 1 or 2 R 2 .
  • A is pyrazolyl optionally substituted with 1 R 1 and optionally substituted with 1 or 2 R 2 .
  • A is pyrazolyl optionally substituted with 1 or 2 R 1 and optionally substituted with 1 R 2 .
  • A is pyridyl optionally substituted with 1 or 2 R 1 and optionally substituted with 1 or 2 R 2 .
  • A is indazolyl optionally substituted with 1 or 2 R 1 and optionally substituted with 1 or 2 R 2 .
  • A is phenyl substituted with 1 R 1 and optionally substituted with 1 R 2 .
  • A is naphthyl substituted with 1 R 1 and optionally substituted with 1 R 2 .
  • A is furanyl substituted with 1 R 1 and optionally substituted with 1 R 2 .
  • A is thiophenyl substituted with 1 R 1 and optionally substituted with 1 R 2 .
  • A is oxazolyl substituted with 1 R 1 and optionally substituted with 1 R 2 . In some embodiments, A is thiazolyl substituted with 1 R 1 and optionally substituted with 1 R 2 .
  • A is pyrazolyl substituted with 1 R 1 and optionally substituted with 1 R 2 .
  • A is pyridyl substituted with 1 R 1 and optionally substituted with 1 R 2 .
  • A is indazolyl optionally substituted with 1 R 1 and optionally substituted with 1 R 2 .
  • A is phenyl substituted with 1 R 1 and substituted with 1 R 2 .
  • A is furanyl substituted with 1 R 1 and substituted with 1 R 2 .
  • A is thiophenyl substituted with 1 R 1 and substituted with 1 R 2 .
  • A is oxazolyl substituted with 1 R 1 and substituted with 1 R 2 .
  • A is thiazolyl substituted with 1 R 1 and substituted with 1 R 2 .
  • A is pyrazolyl substituted with 1 R 1 and substituted with 1 R 2 .
  • A is pyridyl substituted with 1 R 1 and substituted with 1 R 2 .
  • A is phenyl, m is 0 or 1, and n is 0, 1, or 2.
  • A is furanyl, m is 0 or 1, and n is 0, 1, or 2.
  • A is thiophenyl
  • m is 0 or 1
  • n is 0, 1, or 2.
  • A is oxazolyl
  • m is 0 or 1
  • n is 0, 1, or 2.
  • A is thiazolyl
  • m is 0 or 1
  • n is 0, 1, or 2.
  • A is pyrazolyl
  • m is 0 or 1
  • n is 0, 1, or 2.
  • A is pyridyl
  • m is 0 or 1
  • n is 0, 1, or 2.
  • A is indazolyl, m is 0 or 1, and n is 0, 1, or 2.
  • A is phenyl, m is 0, and n is 0 or 1.
  • A is furanyl, m is 0, and n is 0 or 1.
  • A is thiophenyl, m is 0, and n is 0 or 1.
  • A is oxazolyl, m is 0, and n is 0 or 1.
  • A is thiazolyl, m is 0, and n is 0 or 1.
  • A is pyrazolyl, m is 0, and n is 0 or 1.
  • A is pyridyl, m is 0, and n is 0 or 1.
  • the optionally substituted ring A (a)
  • the optionally substituted ring A is In some embodiments, the optionally substituted ring A is
  • the optionally substituted ring A is
  • the optionally substituted ring A is
  • the optionally substituted ring A is In some embodiments, the optionally substituted ring A is
  • the optionally substituted ring A is
  • the optionally substituted ring A is
  • the optionally substituted ring A is In some embodiments, the optionally substituted ring A is
  • the optionally substituted ring A is
  • the optionally substituted ring A is In some embodiments, the optionally substituted ring A is
  • the optionally substituted ring A is
  • the optionally substituted ring A is
  • the optionally substituted ring A is
  • the optionally substituted ring A is
  • the optionally substituted ring A is
  • the optionally substituted ring A is
  • the optionally substituted ring A is
  • the optionally substituted ring A is
  • the optionally substituted ring A is R
  • the optionally substituted ring A is s *
  • the optionally substituted ring A is
  • the optionally substituted ring A is N
  • the optionally substituted ring A is
  • the optionally substituted ring A is
  • the optionally substituted ring A is
  • the optionally substituted ring A is
  • the optionally substituted ring A is
  • the optionally substituted ring A is
  • the optionally substituted ring A is
  • the optionally substituted ring A is
  • the optionally substituted ring A is In some embodiments, the optionally substituted ring A
  • the optionally substituted ring A is optionally substituted
  • the optionally substituted ring A is optionally substituted
  • the optionally substituted ring A is optionally substituted
  • the optionally substituted ring A is optionally substituted
  • the optionally substituted ring A is optionally substituted
  • the optionally substituted ring A is optionally substituted
  • the optionally substituted ring A is optionally substituted
  • the optionally substituted ring A i s In some embodiments, the optionally substituted ring A is
  • the optionally substituted ring A is
  • the optionally substituted ring A is optionally substituted
  • the optionally substituted ring A is optionally substituted
  • the optionally substituted ring A is optionally substituted
  • the optionally substituted ring A is optionally substituted
  • the optionally substituted ring A is optionally substituted
  • the optionally substituted ring A is optionally substituted
  • the optionally substituted ring A In some embodiments, the optionally substituted ring A is
  • the optionally substituted ring A is
  • the optionally substituted ring A is
  • the optionally substituted ring A is
  • the optionally substituted ring A is
  • the optionally substituted ring A is
  • the optionally substituted ring A is
  • the optionally substituted ring A is
  • the optionally substituted ring A is In some embodiments, the optionally substituted ring A is
  • the optionally substituted ring A is
  • the optionally substituted ring A is
  • the optionally substituted ring A is In some embodiments, the optionally substituted ring A is
  • the optionally substituted ring A is
  • the optionally substituted ring A is
  • the optionally substituted ring A is
  • the optionally substituted ring A is In some embodiments, the optionally substituted ring
  • the optionally substituted ring is optionally substituted
  • the optionally substituted ring is optionally substituted
  • the optionally substituted ring is optionally substituted
  • the optionally substituted ring is optionally substituted
  • R 1 and R 2 are each independently selected from Ci-C 6 alkyl, Ci-C 6 haloalkyl, Ci-C 6 alkoxy, Ci- Ce haloalkoxy, halo, CN, NO2, COCi-Ce alkyl, CO-Ce-Cio aryl, CO(5- to 10-membered heteroaryl), CO2C1-C6 alkyl, CO2C3-C8 cycloalkyl, OCOCi-Ce alkyl, OCOCe-Cio aryl, OCO(5- to 10-membered heteroaryl), OCO(3- to 7-membered heterocycloalkyl), C6-C10 aryl, 5- to 10- membered heteroaryl, H2, NHCi-Ce alkyl, N(Ci-Ce alkyl) 2 , CO R 8 R 9 , SFs, SCi-Ce alkyl, S(0 2 )Ci-C 6 alkyl, S(0
  • each Ci-C 6 alkyl substituent and each Ci-C 6 alkoxy substituent of the R 1 or R 2 C3-C7 cycloalkyl or of the R 1 or R 2 3- to 7-membered heterocycloalkyl is further optionally independently substituted with one to three hydroxy, halo, R 8 R 9 , or oxo; wherein the 3- to 7-membered heterocycloalkyl, C6-C10 aryl, and 5- to 10-membered heteroaryl are optionally substituted with one or more substituents independently selected from halo, Ci-C 6 alkyl, and OCi-C 6 alkyl;
  • R 1 and R 2 are each independently selected from Ci-C 6 alkyl, Ci-C 6 haloalkyl, Ci-C 6 alkoxy, Ci- Ce haloalkoxy, halo, CN, NO2, COCi-Ce alkyl, CO-Ce-Cio aryl; CO(5- to 10-membered heteroaryl); CO2C1-C6 alkyl, CO2C3-C8 cycloalkyl, OCOCi-Ce alkyl, OCOCe-Cio aryl, OCO(5- to 10-membered heteroaryl), OCO(3- to 7-membered heterocycloalkyl), C6-C10 aryl, 5- to 10- membered heteroaryl, H2, HCi-Ce alkyl, N(Ci-Ce alkyl) 2 , CO R 8 R 9 , SFs, SCi-Ce alkyl, S(0 2 )Ci-C 6 alkyl, S(0
  • R 1 and R 2 are each independently selected from Ci-C 6 haloalkyl, Ci-C 6 alkoxy, Ci-C 6 haloalkoxy, halo, CN, NO2, COCi-Ce alkyl, CO-Ce-Cio aryl, CO(5- to 10-membered heteroaryl), CO2C1-C6 alkyl, CO2C3-C8 cycloalkyl, OCOCi-Ce alkyl, OCOCe-Cio aryl, OCO(5- to 10- membered heteroaryl), OCO(3- to 7-membered heterocycloalkyl), C6-C10 aryl, 5- to 10- membered heteroaryl, H2, HCi-Ce alkyl, N(Ci-Ce alkyl) 2 , CO R 8 R 9 , SFs, SCi-Ce alkyl, S(0 2 )Ci-C 6 alkyl, S(0 2 ) R u R
  • heterocycloalkyl NHCOCi-Ce alkyl, NHCOCe-Cio aryl, NHCO(5- to 10-membered heteroaryl), NHCO(3- to 7-membered heterocycloalkyl), and NHCOC2-Ce alkynyl; wherein each Ci-C 6 alkyl substituent and each Ci-C 6 alkoxy substituent of the R 1 or R 2 C3-C7 cycloalkyl or of the R 1 or R 2 3- to 7-membered heterocycloalkyl is further optionally independently substituted with one to three hydroxy, halo, R 8 R 9 , or oxo; wherein the 3- to 7-membered heterocycloalkyl, C6-C10 aryl, 5- to 10-membered heteroaryl, HCOCe-Cio aryl, HCO(5- to 10-membered heteroaryl) and HCO(3- to 7- membered heterocycloalkyl) are optionally substituted
  • R 1 and R 2 are each independently selected from Ci-Ce alkyl, halo, CN, NO2, COCi-Ce alkyl, CO- Ce-Cio aryl, CO(5- to 10-membered heteroaryl), CO2C1-C6 alkyl, OCOCi-Ce alkyl, OCOCe-Cio aryl, OCO(5- to 10-membered heteroaryl), OCO(3- to 7-membered heterocycloalkyl), C6-C10 aryl, 5- to 10-membered heteroaryl, NH2, NHCi-Ce alkyl, N(Ci-Ce alkyl) 2 , CONR 8 R 9 , SFs, SCi- Ce alkyl, S(0 2 )Ci-C 6 alkyl, S(0 2 )NR u R 12 , S(0)Ci-Ce alkyl, C3-C7 cycloalkyl and 3- to 7- membered heterocycloal
  • each Ci-C 6 alkyl substituent and each Ci-C 6 alkoxy substituent of the R 1 or R 2 C3-C7 cycloalkyl or of the R 1 or R 2 3- to 7-membered heterocycloalkyl is further optionally independently substituted with one to three hydroxy, halo, NR 8 R 9 , or oxo; wherein the 3- to 7-membered heterocycloalkyl, C 6 -Cio aryl, 5- to 10-membered heteroaryl, HCOCe-Cio aryl, HCO(5- to 10-membered heteroaryl) and HCO(3- to 7- membered heterocycloalkyl) are optionally substituted with one or more substituents independently selected from halo, Ci-C 6 alkyl, and OCi-C 6 alkyl;
  • R 1 and R 2 are each independently selected from Ci-C 6 alkyl, Ci-C 6 haloalkyl, Ci-C 6 alkoxy, Ci- Ce haloalkoxy, halo, CN, N0 2 , COCi-Ce alkyl, CO-Ce-Cio aryl, CO(5- to 10-membered heteroaryl), CO2C1-C6 alkyl, CO2C3-C8 cycloalkyl, OCOCi-Ce alkyl, OCOCe-Cio aryl, OCO(5- to 10-membered heteroaryl), OCO(3- to 7-membered heterocycloalkyl), C6-C10 aryl, 5- to 10- membered heteroaryl, H2, HCi-Ce alkyl, N(Ci-Ce alkyl) 2 , CO R 8 R 9 , SFs, SCi-Ce alkyl, S(0 2 )Ci-C 6 alkyl,
  • each Ci-C 6 alkyl substituent and each Ci-C 6 alkoxy substituent of the R 1 or R 2 C3-C7 cycloalkyl or of the R 1 or R 2 3- to 7-membered heterocycloalkyl is further optionally independently substituted with one to three hydroxy, halo, or oxo;
  • 3- to 7-membered heterocycloalkyl, C6-C10 aryl, 5- to 10-membered heteroaryl, NHCOCe-Cio aryl, NHCO(5- to 10-membered heteroaryl) and NHCO(3- to 7- membered heterocycloalkyl) are optionally substituted with one or more substituents independently selected from halo, Ci-C 6 alkyl, and OCi-C 6 alkyl;
  • R 1 and R 2 are each independently selected from Ci-C 6 alkyl, Ci-C 6 haloalkyl, Ci-C 6 alkoxy, Ci- Ce haloalkoxy, halo, CN, NO2, COCi-Ce alkyl, CO-Ce-Cio aryl, CO(5- to 10-membered heteroaryl), CO2C1-C6 alkyl, CO2C3-C8 cycloalkyl, OCOCi-Ce alkyl, OCOCe-Cio aryl, OCO(5- to 10-membered heteroaryl), OCO(3- to 7-membered heterocycloalkyl), C6-C10 aryl, 5- to 10- membered heteroaryl, H2, HCi-Ce alkyl, N(Ci-Ce alkyl) 2 , CO R 8 R 9 , SFs, SCi-Ce alkyl, S(0 2 )Ci-C 6 alkyl, S(0
  • 3- to 7-membered heterocycloalkyl, C6-C10 aryl, 5- to 10-membered heteroaryl, NHCOCe-Cio aryl, NHCO(5- to 10-membered heteroaryl) and NHCO(3- to 7- membered heterocycloalkyl) are optionally substituted with one or more substituents independently selected from halo, Ci-C 6 alkyl, and OCi-C 6 alkyl.
  • R 1 and R 2 are each independently selected from Ci-C 6 alkyl, Ci-C 6 haloalkyl, C1-G5 alkoxy, Ci- Ce haloalkoxy, halo, CN, NO2, COCi-Ce alkyl, CO-Ce-Cio aryl, CO(5- to 10-membered heteroaryl), CO2C1-C6 alkyl, CO2C3-C8 cycloalkyl, OCOCi-Ce alkyl, OCOCe-Cio aryl, OCO(5- to 10-membered heteroaryl), OCO(3- to 7-membered heterocycloalkyl), C6-C10 aryl, 5- to 10- membered heteroaryl, NH 2 , NHCi-Ce alkyl, N(Ci-Ce alkyl) 2 , CONR 8 R 9 , SFs, SCi-Ce alkyl, S(0 2 )Ci-C 6 alkyl
  • R 1 and R 2 are each independently selected from Ci-C 6 alkyl, halo, CN, COC1-C6 alkyl, CO2C1- C 6 alkyl, C6-C10 aryl, S(0)Ci-C 6 alkyl, 5- to 10-membered heteroaryl, and 3- to 7-membered heterocycloalkyl,
  • Ci-C 6 alkyl and 3- to 7-membered heterocycloalkyl is optionally substituted with one or more substituents each independently selected from hydroxy and oxo.
  • R 1 is selected from Ci-C 6 alkyl, Ci-C 6 haloalkyl, Ci-C 6 alkoxy, Ci-C 6 haloalkoxy, halo, CN, NO2, COCi-Ce alkyl, CO-Ce-Cio aryl, CO(5- to 10-membered heteroaryl), CO2C1-C6 alkyl, CO2C3-C8 cycloalkyl, OCOCi-Ce alkyl, OCOCe-Cio aryl, OCO(5- to 10-membered heteroaryl), OCO(3- to 7-membered heterocycloalkyl), C6-C10 aryl, 5- to 10-membered heteroaryl, NH2, NHCi-Ce alkyl, N(Ci-Ce alkyl) 2 , CONR 8 R 9 , SFs, SCi-Ce alkyl, S(0 2 )Ci-C 6 alkyl, S(0 2 )
  • 3- to 7-membered heterocycloalkyl, C6-C10 aryl, 5- to 10-membered heteroaryl, NHCOCe-Cio aryl, NHCO(5- to 10-membered heteroaryl) and NHCO(3- to 7- membered heterocycloalkyl) are optionally substituted with one or more substituents independently selected from halo, Ci-C 6 alkyl, and OCi-C 6 alkyl.
  • n l ; and,
  • R 1 is selected from Ci-Ce alkyl, halo, CN, COCi-Ce alkyl, CO2C1-C6 alkyl, Ce-Cio aryl, 5- to 10- membered heteroaryl, S(0)Ci-C 6 alkyl, and 3- to 7-membered heterocycloalkyl,
  • Ci-Ce alkyl and 3- to 7-membered heterocycloalkyl is optionally substituted with one or more substituents each independently selected from hydroxy and oxo.
  • R 1 and R 2 are each independently selected from Ci-C 6 alkyl, Ci-C 6 haloalkyl, Ci-Ce alkoxy, Ci- Ce haloalkoxy, halo, CN, N0 2 , COCi-Ce alkyl, CO-Ce-Cio aryl, CO(5- to 10-membered heteroaryl), CO2C1-C6 alkyl, CO2C3-C8 cycloalkyl, OCOCi-Ce alkyl, OCOCe-Cio aryl, OCO(5- to 10-membered heteroaryl), OCO(3- to 7-membered heterocycloalkyl), C6-C10 aryl, 5- to 10- membered heteroaryl, NH2, NHCi-Ce alkyl, N(Ci-Ce alkyl) 2 , CONR 8 R 9 , SFs, SCi-Ce alkyl, S(0 2 )Ci-C 6 alkyl
  • 3- to 7-membered heterocycloalkyl, C6-C10 aryl, 5- to 10-membered heteroaryl, NHCOCe-Cio aryl, NHCO(5- to 10-membered heteroaryl) and NHCO(3- to 7-membered heterocycloalkyl) are optionally substituted with one or more substituents independently selected from halo, C1-G5 alkyl, and OCi-C 6 alkyl;
  • R 1 and R 2 are each independently selected from Ci-C 6 alkyl, halo, CN, COCi-C 6 alkyl, CO2C1- C 6 alkyl, C 6 -Cio aryl, 5- to 10-membered heteroaryl, S(0)Ci-C 6 alkyl, and 3- to 7-membered heterocycloalkyl,
  • Ci-Ce alkyl and 3- to 7-membered heterocycloalkyl is optionally substituted with one or more substituents each independently selected from hydroxy and oxo.
  • n l ;
  • n l ;
  • n l ;
  • R 1 and R 2 are on adjacent atoms, and taken together with the atoms connecting them, form a C5 carbocyclic ring or a 5- to-6-membered heterocyclic ring containing 1 or 2 heteroatoms independently selected from O, N, and S, wherein the carbocyclic ring or heterocyclic ring is optionally independently substituted with one or more substituents independently selected from hydroxy, halo, oxo, Ci-Ce alkyl, Ci-Ce alkoxy, COOCi-Ce alkyl, Ce-Cio aryl, and CO R 8 R 9 .
  • m l
  • n l
  • R 1 and R 2 are on adjacent atoms, and taken together with the atoms connecting them, form a C 4 - C 8 carbocyclic ring or a 5- to 8-membered heterocyclic ring containing 1 or 2 heteroatoms independently selected from O, N, and S, wherein the carbocyclic ring or heterocyclic ring is unsubstituted.
  • R 1 s Ci-C 6 alkyl optionally substituted with one or more hydroxy, n some embodiments, R 1 s l-hydroxy-2-methylpropan-2-yl.
  • R 1 s 2-hydroxy ethyl. n some embodiments, R 1 s Ci-Ce alkyl.
  • R 1 s isopropyl.
  • R 1 s isopropyl.
  • R 1 s 2-hydroxy-2-propyl.
  • R 1 s hydroxymethyl
  • R 1 s C3-C7 cycloalkyl substituted with hydroxy at the carbon directly connected to ring A.
  • R 1 is 1 -hydroxy- 1-cyclopropyl.
  • R 1 is 1 -hydroxy- 1-cyclobutyl.
  • R 1 is 1 -hydroxy- 1-cyclopentyl.
  • R 1 is 1 -hydroxy- 1-cyclohexyl.
  • R 1 is 3- to 7-membered heterocycloalkyl optionally substituted with one or more hydroxy.
  • R 1 is 3- to 7-membered heterocycloalkyl.
  • R 1 is morpholinyl (e.g., 1-morpholinyl).
  • R 1 is l,3-dioxolan-2-yl.
  • R 1 is 3- to 7-membered heterocycloalkyl optionally substituted with one or more Ci-C 6 alkyl.
  • R 1 is l-methylpyrrolidin-2-yl.
  • R 1 is 3- to 7-membered heterocycloalkyl substituted with hydroxy at the carbon directly connected to ring A.
  • R 1 is Ci-Ce alkyl optionally substituted with one or more oxo.
  • R 1 is COCH3.
  • R 1 is COCH2CH3.
  • R 1 is C3-C7 cycloalkyl optionally substituted with one or more oxo.
  • R 1 is 3- to 7-membered heterocycloalkyl optionally substituted with one or more oxo.
  • R 1 is Ci-C 6 alkyl optionally substituted with one or more Ci-C 6 alkoxy. In some embodiments, R 1 is 2-methoxy-2-propyl.
  • R 1 is methoxymethyl
  • R 1 is C3-C7 cycloalkyl optionally substituted with one or more Ci-C 6 alkoxy.
  • R 1 is 3- to 7-membered heterocycloalkyl optionally substituted with one or more Ci-C 6 alkoxy.
  • R 1 is Ci-C 6 alkyl optionally substituted with one or more R 8 R 9 .
  • R 1 is Ci-C 6 alkyl substituted with R 8 R 9 at the carbon directly connected to ring A. In some embodiments, R 1 is (methylamino)methyl .
  • R 1 is (dimethylamino)methyl.
  • R 1 is aminomethyl
  • R 1 is N-methylacetamidom ethyl.
  • R 1 is 1 -(dimethylamino)eth- 1 -yl .
  • R 1 is 2-(dimethylamino)prop-2-yl.
  • R 1 is (2-methoxy-eth- 1 -yl)(methyl)aminom ethyl .
  • R 1 is (methyl)(acetyl)aminom ethyl .
  • R 1 is (methyl)(cyclopropylmethyl)aminomethyl.
  • R 1 is (methyl)(2,2-difluoroeth- 1 -yl)aminomethyl
  • R 1 is C3-C7 cycloalkyl optionally substituted with one or more R 8 R 9 . In some embodiments, R 1 is 3- to 7-membered heterocycloalkyl optionally substituted with one or more R 8 R 9 .
  • R 1 is Ci-C 6 haloalkyl optionally substituted with one or more hydroxy. In some embodiments, R 1 is Ci-Ce alkoxy.
  • R 1 is Ci-C 6 haloalkoxy.
  • R 1 is Ci-C 6 alkyl optionally substituted with 3- to 7-membered heterocycloalkyl, wherein the 3- to 7-membered heterocycloalkyl is further optionally substituted as defined elsewhere herein.
  • R 1 is pyrrolidinylmethyl (e.g., pyrrolidin-l-ylmethyl).
  • R 1 is optionally substituted pyrrolidinylmethyl (e.g., 3,3- difluoropyrrolidin- 1 -ylmethyl).
  • R 1 is azetidinylmethyl (e.g., azeti din- 1 -ylmethyl).
  • R 1 is optionally substituted azetidinylmethyl (e.g., 3-methoxyazetidin-l- ylmethyl).
  • R 1 is morpholinylmethyl (e.g., morpholin-4-ylmethyl). In some embodiments, R 1 is halo.
  • R 1 is fluoro. In some embodiments, R is chloro.
  • R is CN
  • R is COCi-Ce alkyl.
  • R is CO-Ce-Cio aryl.
  • R is CO(5- to 10-membered heteroaryl).
  • R is CO2C1-C6 alkyl.
  • R is CO2C3-C8 cycloalkyl.
  • R is OCOCi-Ce alkyl.
  • R is OCOCe-Cio aryl.
  • R s C6-C10 aryl.
  • R s phenyl In some embodiments, R s phenyl.
  • R s 5- to 10-membered heteroaryl.
  • R s pyridyl e.g., 4-pyridyl
  • R s pyrazolyl (e.g., 1-pyrazolyl).
  • R s H 2 In some embodiments, R s H 2 .
  • R s HCi-Ce alkyl In some embodiments, R s HCi-Ce alkyl.
  • R s N(Ci-Ce alkyl) 2 In some embodiments, R s N(Ci-Ce alkyl) 2 .
  • R s CO R 8 R 9 In some embodiments, R s CO R 8 R 9 .
  • R s SFs In some embodiments, R s SFs.
  • R s S(0 2 )Ci-C 6 alkyl.
  • R 1 s S(0 2 )CH 3 .
  • R 1 s S(0 2 )N(CH 3 ) 2 .
  • R 1 s S(0)Ci-Ce alkyl.
  • R 1 s S(0)CH 3 .
  • R 1 s attached to a carbon of an aryl ring A.
  • R 1 is Ci-C 6 alkyl optionally substituted with one or more hydroxy
  • R 2 is Ci-C 6 alkyl optionally substituted with one or more hydroxy
  • R 1 is l-hydroxy-2-methylpropan-2-yl
  • R 2 is methyl
  • R 1 is 2-hydroxy-2-propyl and R 2 is methyl.
  • R 1 is 2-hydroxy-2-propyl and R 2 is isopropyl.
  • R 1 is 2-hydroxy-2-propyl and R 2 is 2-hydroxy-2-propyl.
  • R 1 is 2-hydroxy-2-propyl and R 2 is 1 -hydroxy ethyl.
  • R 1 is hydroxymethyl and R 2 is methyl.
  • R 1 is 1 -hydroxy ethyl and R 2 is methyl.
  • R 1 is 2-hydroxy ethyl and R 2 is methyl.
  • R 1 is l-hydroxy-2-propyl and R 2 is methyl.
  • R 1 is Ci-Ce alkyl optionally substituted with one or more hydroxy
  • R 2 is C 6 -Cio aryl.
  • R 1 is 2-hydroxy-2-propyl and R 2 is phenyl.
  • R 1 is Ci-C 6 alkyl optionally substituted with one or more hydroxy
  • R 2 is 5- to 10-membered heteroaryl.
  • R 1 is 2-hydroxy-2-propyl and R 2 is pyridyl.
  • R 1 is 2-hydroxy-2-propyl and R 2 is pyrazolyl.
  • R 1 is Ci-C 6 alkyl optionally substituted with one or more hydroxy
  • R 2 is SFs.
  • R 1 is Ci-C 6 alkyl optionally substituted with one or more hydroxy
  • R 2 is SCi-Ce alkyl
  • R 1 is Ci-C 6 alkyl optionally substituted with one or more hydroxy
  • R 2 is S(0 2 )Ci-C 6 alkyl.
  • R 1 is Ci-C 6 alkyl optionally substituted with one or more hydroxy
  • R 2 is S(0 2 )CH 3 .
  • R 1 is Ci-C 6 alkyl optionally substituted with one or more hydroxy, and R 2 is halo. n some embodiments, R s 2-hydroxy-2-propyl and R 2 is chloro.
  • R s 2-hydroxy-2-propyl and R 2 is fluoro.
  • R s C3-C7 cycloalkyl optionally substituted with one or more hydroxy
  • R 2 is Ci-Ce alkyl
  • R s 1 -hydroxy- 1-cyclopropyl, and R 2 is methyl
  • R s 1 -hydroxy- 1-cyclobutyl, and R 2 is methyl
  • R s 1 -hydroxy- 1-cyclopentyl, and R 2 is methyl
  • R s 1 -hydroxy- 1-cyclohexyl, and R 2 is methyl.
  • R s 3- to 7-membered heterocycloalkyl optionally substituted with one or more hydroxy, and R 2 Ci-C 6 alkyl.
  • R s morpholinyl, and R 2 is methyl.
  • R s l,3-dioxolan-2-yl, and R 2 is methyl.
  • R s 3- to 7-membered heterocycloalkyl optionally substituted with one or more hydroxy, and R 2 halo.
  • R s l,3-dioxolan-2-yl, and R 2 is fluoro.
  • R s l,3-dioxolan-2-yl, and R 2 is chloro.
  • R s Ci-C 6 alkyl optionally substituted with one or more oxo, and R 2 is methyl.
  • R s COCH3, and R 2 is methyl.
  • R s Ci-C 6 alkyl optionally substituted with one or more Ci-Ce alkoxy, and R 2 is Ci-Ce alkyl.
  • R s 2-methoxy-2-propyl, and R 2 is methyl.
  • R s Ci-C 6 alkyl optionally substituted with one or more R 8 R 9 , and R 2 s Ci-Ce alkyl.
  • R s (dimethylamino)methyl, and R 2 is methyl.
  • R s Ci-C 6 alkyl optionally substituted with one or more R 8 R 9 , and R 2 s halo.
  • R s (dimethylamino)methyl, and R 2 is fluoro.
  • R s (dimethylamino)methyl, and R 2 is fluoro.
  • R s (methylamino)methyl, and R 2 is fluoro.
  • R 1 is aminomethyl, and R 2 is fluoro.
  • R 1 is Ci-C 6 alkyl
  • R 2 is Ci-Ce alkyl
  • R 1 is methyl
  • R 2 is methyl
  • R 2 is l-hydroxy-2-methylpropan-2-yl
  • R 1 is methyl
  • R 2 is 2-hydroxy-2-propyl and R 1 is methyl.
  • R 2 is 2-hydroxy-2-propyl and R 1 is isopropyl.
  • R 2 is 2-hydroxy-2-propyl and R 1 is 1 -hydroxy ethyl.
  • R 2 is hydroxymethyl and R 1 is methyl.
  • R 2 is 1 -hydroxy ethyl and R 1 is methyl.
  • R 2 is 2-hydroxy ethyl and R 1 is methyl.
  • R 2 is l-hydroxy-2-propyl and R 1 is methyl.
  • R 2 is Ci-C 6 alkyl optionally substituted with one or more hydroxy
  • R 1 is C 6 -Cio aryl.
  • R 2 is 2-hydroxy-2-propyl and R 1 is phenyl.
  • R 2 is Ci-C 6 alkyl optionally substituted with one or more hydroxy
  • R 1 is 5- to 10-membered heteroaryl.
  • R 2 is 2-hydroxy-2-propyl and R 1 is pyridyl.
  • R 2 is 2-hydroxy-2-propyl and R 1 is pyrazolyl.
  • R 2 is Ci-C 6 alkyl optionally substituted with one or more hydroxy
  • R 1 is SFs.
  • R 2 is Ci-C 6 alkyl optionally substituted with one or more hydroxy
  • R 1 is SCi-Ce alkyl.
  • R 2 is Ci-C 6 alkyl optionally substituted with one or more hydroxy
  • R 1 is S(0 2 )Ci-C 6 alkyl.
  • R 2 is Ci-C 6 alkyl optionally substituted with one or more hydroxy
  • R 1 is S(0 2 )CH 3 .
  • R 2 is Ci-C 6 alkyl optionally substituted with one or more hydroxy, and R 1 is halo.
  • R 2 is 2-hydroxy-2-propyl and R 1 is chloro.
  • R 2 is 2-hydroxy-2-propyl and R 1 is fluoro. In some embodiments, R 2 is C3-C7 cycloalkyl optionally substituted with one or more hydroxy, and R 1 is Ci-Ce alkyl.
  • R 2 is 1 -hydroxy- 1-cyclopropyl, and R 1 is methyl.
  • R 2 is 1 -hydroxy- 1-cyclobutyl, and R 1 is methyl.
  • R 2 is 1 -hydroxy- 1-cyclopentyl, and R 1 is methyl.
  • R 2 is 1 -hydroxy- 1-cyclohexyl, and R 1 is methyl.
  • R 2 is 3- to 7-membered heterocycloalkyl optionally substituted with one or more hydroxy
  • R 1 is Ci-C 6 alkyl.
  • R 2 is morpholinyl, and R 1 is methyl.
  • R 2 is l,3-dioxolan-2-yl, and R 1 is methyl.
  • R 2 is 3- to 7-membered heterocycloalkyl optionally substituted with one or more hydroxy, and R 1 is halo.
  • R 2 is l,3-dioxolan-2-yl, and R 1 is fluoro.
  • R 2 is l,3-dioxolan-2-yl, and R 1 is chloro.
  • R 2 is Ci-Ce alkyl optionally substituted with one or more oxo, and R 1 is methyl.
  • R 2 is COCH3, and R 1 is methyl.
  • R 2 is Ci-Ce alkyl optionally substituted with one or more Ci-Ce alkoxy, and R 1 is Ci-Ce alkyl.
  • R 2 is 2-methoxy-2-propyl
  • R 1 is methyl
  • R 2 is Ci-Ce alkyl optionally substituted with one or more R 8 R 9
  • R 1 is Ci-Ce alkyl.
  • R 2 is (dimethylamino)methyl, and R 1 is methyl.
  • R 2 is Ci-Ce alkyl optionally substituted with one or more R 8 R 9 , and R 1 is halo.
  • R 2 is (dimethylamino)methyl, and R 1 is fluoro.
  • R 2 is (methylamino)methyl, and R 1 is fluoro.
  • R 2 is aminomethyl, and R 1 is fluoro.
  • R 2 is Ci-Ce alkoxy, and R 1 is Ci-Ce alkyl optionally substituted with one or more R 8 R 9 .
  • R 2 is methoxy, and R 1 is (dimethylamino)methyl.
  • R 1 and R 2 are each attached to a carbon of an aryl ring A.
  • R 1 and R 2 are each attached to a carbon of a heteroaryl ring A.
  • R 1 is attached to a carbon and R 2 is attached to a nitrogen of a heteroaryl ring A.
  • R 2 is attached to a carbon and R 1 is attached to a nitrogen of a heteroaryl ring A.
  • R 1 and R 2 are on adjacent atoms, and taken together with the atoms connecting them, form a Cs aliphatic carbocyclic ring.
  • R 1 and R 2 are on adjacent atoms, and taken together with the atoms connecting them, form a C 6 aliphatic carbocyclic ring.
  • R 1 and R 2 are on adjacent atoms, and taken together with the atoms connecting them, form a C 6 aromatic carbocyclic ring.
  • R 1 and R 2 are on adjacent atoms, and taken together with the atoms connecting them, form a 5-membered aliphatic heterocyclic ring containing 1 or 2 heteroatoms independently selected from O, N, and S. In some embodiments, R 1 and R 2 are on adjacent atoms, and taken together with the atoms connecting them, form a 5-membered heteroaromatic ring containing 1 or 2 heteroatoms independently selected from O, N, and S.
  • R 1 and R 2 are on adjacent atoms, and taken together with the atoms connecting them, form a 6-membered aliphatic heterocyclic ring containing 1 or 2 heteroatoms independently selected from O, N, and S.
  • R 1 and R 2 are on adjacent atoms, and taken together with the atoms connecting them, form a 6-membered heteroaromatic ring containing 1 or 2 heteroatoms independently selected from O, N, and S.
  • R 1 and R 2 are different.
  • R 1 and R 2 are different, and R 2 comprises a carbonyl group.
  • R 1 and R 2 are different, and R 2 comprises 1 or 2 (e.g., 1) nitrogen atoms
  • R 1 and R 2 are different, and R 2 comprises 1 or 2 (e.g., 1) oxygen atoms.
  • R 1 and R 2 are different, and R 2 comprises a sulfur atom.
  • R 2 and R 1 are different, and R 2 comprises a carbonyl group.
  • R 2 and R 1 are different, and R 2 comprises 1 or 2 (e.g., 1) nitrogen atoms
  • R 2 and R 1 are different, and R 2 comprises 1 or 2 (e.g., 1) oxygen atoms.
  • R 2 and R 1 are different, and R 2 comprises a sulfur atom.
  • R 1 and R 2 are the same.
  • R 1 is para or meta to R 2 .
  • R 1 is para or ortho to R 2 .
  • R 1 is ortho or meta to R 2 . In some embodiments, R 1 is para to R 2 .
  • R 1 is meta to R 2 .
  • R 1 is ortho to R 2 .
  • the variables o and p are ortho to R 1 .
  • B is a 5- to 10-membered monocyclic or bicyclic heteroaryl or a C 6 -Cio monocyclic or bicyclic aryl, such as phenyl.
  • B is a 5- to 6-membered monocyclic heteroaryl or a C 6 monocyclic aryl. In some embodiments, B is a 5- to 10-membered monocyclic or bicyclic heteroaryl.
  • B is a C 6 -Cio monocyclic or bicyclic aryl.
  • B is a 5-membered heteroaryl.
  • B is a 7-10 membered monocyclic or bicyclic heteroaryl.
  • B is phenyl substituted with 1 or 2 R 6 and optionally substituted with 1, 2, or 3 R 7 .
  • B is pyridyl substituted with 1 or 2 R 6 and optionally substituted with 1, 2, or 3 R 7 .
  • B is indazolyl substituted with 1 or 2 R 6 and optionally substituted with 1, 2, or 3 R 7 . In some embodiments, B is pyrazolyl substituted with 1 or 2 R 6 and optionally substituted with 1 or 2 R 7 .
  • B is phenyl, o is 1 or 2, and p is 0, 1, 2, or 3.
  • B is phenyl, o is 1, and p is 0, 1, 2, or 3.
  • B is phenyl, o is 2, and p is 0, 1, 2, or 3.
  • B is one of the rings disclosed hereinbelow, substituted as disclosed hereinbelow, wherein in each case the bond that is shown as being broken by the wavy line / connects B to the H(CO)group of Formula AA.
  • the substituted ring B is the substituted ring B
  • the substituted ring B is the substituted ring B
  • the substituted ring B is the substituted ring B
  • the substituted ring B is the substituted ring B
  • the substituted ring B is the substituted ring B
  • the substituted ring B is In some embodiments, the substituted ring B is
  • the substituted ring B is
  • the substituted ring B is In some embodiments, the substituted ring B is
  • the substituted ring B is
  • the substituted ring B is the substituted ring B
  • the substituted ring B is the substituted ring B
  • the substituted ring B is In some embodiments, the substituted ring B is
  • the substituted ring B is
  • the substituted ring B is
  • the substituted ring B is
  • the substituted ring B is
  • the substituted ring B is
  • the substituted ring B is
  • the substituted ring B is
  • the substituted ring B is In some embodiments, the substituted ring B is
  • the substituted ring B is
  • the substituted ring B is
  • the substituted ring B is
  • the substituted ring B is
  • the substituted ring B is
  • the substituted ring B is
  • the substituted ring B is In some embodiments, the substituted ring B is
  • the substituted ring B is
  • the substituted ring B is
  • the substituted ring B is
  • the substituted ring B is
  • the substituted ring B is
  • the substituted ring B is
  • the substituted ring B is In some embodiments, the substituted ring B is
  • the substituted ring B is
  • the substituted ring B is
  • the substituted ring B is In some embodiments, the substituted ring B is
  • the substituted ring B is
  • the substituted ring B is
  • the substituted ring B is In some embodiments, the substituted ring B is
  • the substituted ring B is
  • the substituted ring B is
  • R 6 and R 7 are each independently selected from Ci-C 6 alkyl, Ci-C 6 haloalkyl, Ci-C 6 alkoxy, Ci- Ce haloalkoxy, halo, CN, NO2, COCi-Ce alkyl, CO2C1-C6 alkyl, CO2C3-C8 cycloalkyl, OCOCi- Ce alkyl, OCOCe-Cio aryl, OCO(5- to 10-membered heteroaryl), OCO(3- to 7-membered heterocycloalkyl), Ce-Cio aryl, 5- to 10-membered heteroaryl, H2, HCi-Ce alkyl, N(Ci-Ce alkyl) 2 , CO R 8 R 9 , SFs, S(0 2 )Ci-C 6 alkyl, C3-C10 cycloalkyl and 3- to 10-membered
  • heterocycloalkyl and a C2-C6 alkenyl
  • R 6 and R 7 are each optionally substituted with one or more substituents independently selected from
  • heterocycloalkyl NHCOCi-Ce alkyl, NHCOCe-Cio aryl, NHCO(5- to 10-membered heteroaryl), NHCO(3- to 7-membered heterocycloalkyl), NHCOC2-C6 alkynyl,
  • Ci-C 6 alkyl or Ci-C 6 alkoxy that R 6 or R 7 is substituted with is optionally substituted with one or more hydroxyl, C6-C10 aryl or NR 8 R 9 , or wherein R 6 or R 7 is optionally fused to a five- to -seven-membered carbocyclic ring or heterocyclic ring containing one or two heteroatoms independently selected from oxygen, sulfur and nitrogen;
  • 3- to 7-membered heterocycloalkyl, C 6 -Cio aryl, 5- to 10-membered heteroaryl, HCOCe-Cio aryl, HCO(5- to 10-membered heteroaryl) and HCO(3- to 7- membered heterocycloalkyl) are optionally substituted with one or more substituents independently selected from halo, Ci-C 6 alkyl, and OCi-C 6 alkyl;
  • R 6 and R 7 are each independently selected from Ci-C 6 alkyl, Ci-C 6 haloalkyl, Ci-C 6 alkoxy, Ci- Ce haloalkoxy, halo, CN, N0 2 , COCi-Ce alkyl, C0 2 Ci-Ce alkyl, C0 2 C 3 -C 8 cycloalkyl, OCOCi- Ce alkyl, OCOCe-Cio aryl, OCO(5- to 10-membered heteroaryl), OCO(3- to 7-membered heterocycloalkyl), Ce-Cio aryl, 5- to 10-membered heteroaryl, H 2 , HCi-Ce alkyl, N(Ci-Ce alkyl) 2 , CO R 8 R 9 , SFs, S(0 2 )Ci-Ce alkyl, C 3 -Cio cycloalkyl and 3- to 10-membered
  • heterocycloalkyl and a C 2 -C 6 alkenyl
  • R 6 and R 7 are each optionally substituted with one or more substituents independently selected from
  • heterocycloalkyl NHCOCi-Ce alkyl, NHCOCe-Cio aryl, NHCO(5- to 10-membered heteroaryl), NHCO(3- to 7-membered heterocycloalkyl), NHCOC 2 -Ce alkynyl,
  • Ci-C 6 alkyl or Ci-C 6 alkoxy that R 6 or R 7 is substituted with is optionally substituted with one or more hydroxyl, C 6 -Cio aryl or NR 8 R 9 , or wherein R 6 or R 7 is optionally fused to a five- to -seven-membered carbocyclic ring or heterocyclic ring containing one or two heteroatoms independently selected from oxygen, sulfur and nitrogen;
  • 3- to 7-membered heterocycloalkyl, C 6 -Cio aryl, 5- to 10-membered heteroaryl, HCOCe-Cio aryl, HCO(5- to 10-membered heteroaryl) and HCO(3- to 7- membered heterocycloalkyl) are optionally substituted with one or more substituents independently selected from halo, Ci-C 6 alkyl, and OCi-C 6 alkyl;
  • R 6 and R 7 are each independently selected from Ci-C 6 alkyl, Ci-C 6 haloalkyl, C1-G5 alkoxy, Ci- Ce haloalkoxy, halo, CN, N0 2 , COCi-Ce alkyl, C0 2 Ci-Ce alkyl, C0 2 C 3 -C 8 cycloalkyl, OCOCi- Ce alkyl, OCOCe-Cio aryl, OCO(5- to 10-membered heteroaryl), OCO(3- to 7-membered heterocycloalkyl), Ce-Cio aryl, 5- to 10-membered heteroaryl, H 2 , HCi-Ce alkyl, N(Ci-Ce alkyl) 2 , CO R 8 R 9 , SFs, SCi-Ce alkyl, S(0 2 )Ci-Ce alkyl, C 3 -C 7 cycloalkyl and 3- to 7-membered hetero
  • 3- to 7-membered heterocycloalkyl, C6-C10 aryl, 5- to 10-membered heteroaryl, NHCOCe-Cio aryl, NHCO(5- to 10-membered heteroaryl) and NHCO(3- to 7- membered heterocycloalkyl) are optionally substituted with one or more substituents independently selected from halo, Ci-C 6 alkyl, and OCi-C 6 alkyl;
  • R 6 and R 7 are each independently selected from Ci-C 6 haloalkyl, Ci-C 6 alkoxy, Ci-C 6 haloalkoxy, halo, CN, N0 2 , COCi-Ce alkyl, C0 2 Ci-Ce alkyl, C0 2 C 3 -C 8 cycloalkyl, OCOCi-Ce alkyl, OCOCe-Cio aryl, OCO(5- to 10-membered heteroaryl), OCO(3- to 7-membered heterocycloalkyl), Ce-Cio aryl, 5- to 10-membered heteroaryl, H 2 , HCi-Ce alkyl, N(Ci-Ce alkyl) 2 , CO R 8 R 9 , SFs, SCi-Ce alkyl, S(0 2 )Ci-Ce alkyl, C 3 -C 7 cycloalkyl and 3- to 7-membered heterocycloalkyl,
  • heterocycloalkyl NHCOCi-Ce alkyl, NHCOCe-Cio aryl, NHCO(5- to 10-membered heteroaryl), NHCO(3- to 7-membered heterocycloalkyl), and NHCOC 2 -Ce alkynyl;
  • 3- to 7-membered heterocycloalkyl, C6-C10 aryl, 5- to 10-membered heteroaryl, NHCOCe-Cio aryl, NHCO(5- to 10-membered heteroaryl) and NHCO(3- to 7- membered heterocycloalkyl) are optionally substituted with one or more substituents independently selected from halo, Ci-C 6 alkyl, and OCi-C 6 alkyl;
  • R 6 and R 7 are each independently selected from Ci-Ce alkyl, halo, CN, N0 2 , COCi-Ce alkyl, C0 2 Ci-Ce alkyl, OCOCi-Ce alkyl, OCOCe-Cio aryl, OCO(5- to 10-membered heteroaryl), OCO(3- to 7-membered heterocycloalkyl), C 6 -Cio aryl, 5- to 10-membered heteroaryl, NH 2 , NHCi-Ce alkyl, N(Ci-Ce alkyl) 2 , CONR 8 R 9 , SFs, SCi-Ce alkyl, S(0 2 )Ci-Ce alkyl, C3-C7 cycloalkyl and 3- to 7-membered heterocycloalkyl,
  • 3- to 7-membered heterocycloalkyl, C6-C10 aryl, 5- to 10-membered heteroaryl, NHCOCe-Cio aryl, NHCO(5- to 10-membered heteroaryl) and NHCO(3- to 7- membered heterocycloalkyl) are optionally substituted with one or more substituents independently selected from halo, Ci-C 6 alkyl, and OCi-C 6 alkyl;
  • R 6 and R 7 are each independently selected from Ci-C 6 alkyl, Ci-C 6 haloalkyl, Ci-C 6 alkoxy, Ci- Ce haloalkoxy, halo, CN, N0 2 , COCi-Ce alkyl, C0 2 Ci-Ce alkyl, C0 2 C 3 -C 8 cycloalkyl, OCOCi- Ce alkyl, OCOCe-Cio aryl, OCO(5- to 10-membered heteroaryl), OCO(3- to 7-membered heterocycloalkyl), Ce-Cio aryl, 5- to 10-membered heteroaryl, H2, HCi-Ce alkyl, N(Ci-Ce alkyl) 2 , CO R 8 R 9 , SFs, SCi-Ce alkyl, S(0 2 )Ci-C 6 alkyl, C3-C7 cycloalkyl and 3- to 7-membered heterocycloalky
  • R 6 and R 7 are each independently selected from Ci-C 6 alkyl, Ci-C 6 haloalkyl, Ci-C 6 alkoxy, Ci- Ce haloalkoxy, halo, CN, NO2, COCi-Ce alkyl, CO2C1-C6 alkyl, CO2C3-C8 cycloalkyl, OCOCi- Ce alkyl, OCOCe-Cio aryl, OCO(5- to 10-membered heteroaryl), OCO(3- to 7-membered heterocycloalkyl), Ce-Cio aryl, 5- to 10-membered heteroaryl, NH 2 , NHCi-Ce alkyl, N(Ci-Ce alkyl) 2 , CONR 8 R 9 , SFs, SCi-Ce alkyl, S(0 2 )Ci-C 6 alkyl, C3-C7 cycloalkyl and 3- to 7-membered heterocycloalkyl,
  • Ci-C 6 alkyl, C3-C7 cycloalkyl and 3- to 7-membered heterocycloalkyl are each unsubstituted;
  • R 6 is independently selected from Ci-C 6 alkyl, C3-C7 cycloalkyl, Ci-C 6 haloalkyl, Ci-C 6 alkoxy, Ci-C 6 haloalkoxy, halo, CN, C6-C10 aryl, 5- to 10-membered heteroaryl, CO-C1-C6 alkyl;
  • R 7 is independently selected from Ci-C 6 alkyl, Ci-C 6 haloalkyl, Ci-C 6 alkoxy, Ci-C 6 haloalkoxy, halo, CN, COCi-Ce alkyl, C0 2 Ci-Ce alkyl, C0 2 C 3 -Ce cycloalkyl, OCOCi-Ce alkyl, OCOCe-Cio aryl, OCO(5- to 10-membered heteroaryl), OCO(3- to 7-membered heterocycloalkyl), Ce-Cio aryl, 5- to 10-membered heteroaryl, CONR 8 R 9 , SFs, S(0 2 )Ci-
  • Ci-C 6 alkyl C3-C7 cycloalkyl and 4- to 6-membered heterocycloalkyl, wherein the Ci-C 6 alkyl is optionally substituted with one to two Ci-C 6 alkoxy;
  • R 6 and R 7 are each independently selected from Ci-C 6 alkyl, Ci-C 6 alkoxy, halo, CN, NO2, COCi-Ce alkyl, CO2C1-C6 alkyl, Ce-Cio aryl, 5- to 10-membered heteroaryl, CO R 8 R 9 , and 3- to 7-membered heterocycloalkyl,
  • Ci-C 6 alkyl and 3- to 7-membered heterocycloalkyl is optionally substituted with one or more substituents each independently selected from hydroxy or oxo,
  • R 6 and R 7 on adjacent atoms taken together with the atoms connecting them, independently form at least one C4-C8 carbocyclic ring, wherein the carbocyclic ring is optionally independently substituted with one or more hydroxy or oxo.
  • R 6 and R 7 are each independently selected from Ci-C 6 alkyl, Ci-C 6 alkoxy, halo, CN, NO2, COCi-Ce alkyl, CO2C1-C6 alkyl, Ce-Cio aryl, 5- to 10-membered heteroaryl, CONR 8 R 9 , and 3- to 7-membered heterocycloalkyl,
  • Ci-C 6 alkyl and 3- to 7-membered heterocycloalkyl is optionally substituted with one or more substituents each independently selected from hydroxy or oxo,
  • R 6 and R 7 on adjacent atoms taken together with the atoms connecting them, independently form at least one C4-C6 aliphatic carbocyclic ring, wherein the carbocyclic ring is optionally independently substituted with one or more hydroxy or oxo.
  • R 6 and R 7 are each independently selected from Ci-C 6 alkyl, Ci-C 6 alkoxy, halo, CN, NO2, COCi-Ce alkyl, CO2C1-C6 alkyl, Ce-Cio aryl, 5- to 10-membered heteroaryl, CONR 8 R 9 , and 3- to 7-membered heterocycloalkyl,
  • Ci-C 6 alkyl and 3- to 7-membered heterocycloalkyl is optionally substituted with one or more substituents each independently selected from hydroxy or oxo,
  • R 6 and R 7 on adjacent atoms taken together with the atoms connecting them, independently form at least one 5-to 8-membered heterocyclic ring containing 1 or 2 heteroatoms independently selected from O, N, and S, wherein the heterocyclic ring is optionally independently substituted with one or more hydroxy or oxo.
  • the heterocyclic ring is optionally independently substituted with one or more hydroxy or oxo.
  • R 6 and R 7 are each independently selected from Ci-C 6 alkyl, Ci-C 6 alkoxy, halo, CN, NO2, COCi-Ce alkyl, CO2C1-C6 alkyl, Ce-Cio aryl, 5- to 10-membered heteroaryl, CO R 8 R 9 , and 3- to 7-membered heterocycloalkyl,
  • Ci-C 6 alkyl and 3- to 7-membered heterocycloalkyl is optionally substituted with one or more substituents each independently selected from hydroxy or oxo,
  • R 6 and R 7 on adjacent atoms taken together with the atoms connecting them, independently form at least one C4-C8 carbocyclic ring, wherein the carbocyclic ring is optionally independently substituted with one or more hydroxy or oxo.
  • R 6 and R 7 on adjacent atoms taken together with the atoms connecting them, independently form at least one C 6 aliphatic carbocyclic ring, wherein the carbocyclic ring is optionally independently substituted with one or more hydroxy or oxo.
  • R 6 and R 7 on adjacent atoms taken together with the atoms connecting them, independently form at least one 5-to 6-membered heterocyclic ring containing 1 heteroatom independently selected from O, N, and S, wherein the heterocyclic ring is optionally
  • R 6 and R 7 on adjacent atoms taken together with the atoms connecting them, independently form at least one 5-to 6-membered heterocyclic ring containing 1 heteroatom independently selected from O, N, and S, wherein the heterocyclic ring is optionally
  • R 6 is selected from Ci-C 6 alkyl, Ci-Ce haloalkyl, Ci-C 6 alkoxy, Ci-C 6 haloalkoxy, halo, CN,
  • 3- to 7-membered heterocycloalkyl, C6-C10 aryl, 5- to 10-membered heteroaryl, NHCOCe-Cio aryl, NHCO(5- to 10-membered heteroaryl) and NHCO(3- to 7- membered heterocycloalkyl) are optionally substituted with one or more substituents independently selected from halo, Ci-C 6 alkyl, and OCi-C 6 alkyl.
  • o l
  • p l
  • R 6 and R 7 are each independently selected from Ci-C 6 alkyl, Ci-C 6 alkoxy, halo, CN, NO2, COCi-Ce alkyl, CO2C1-C6 alkyl, Ce-Cio aryl, 5- to 10-membered heteroaryl, CONR 8 R 9 , and 3- to 7-membered heterocycloalkyl,
  • C1-C5 alkyl and 3- to 7-membered heterocycloalkyl is optionally substituted with one or more substituents each independently selected from hydroxy or oxo,
  • R 6 and R 7 on adjacent atoms taken together with the atoms connecting them, independently form at least one C4-C8 carbocyclic ring, wherein the carbocyclic ring is optionally independently substituted with one or more hydroxy or oxo.
  • o l or 2
  • p l, 2, or 3
  • R 6 and R 7 are each independently selected from Ci-C 6 alkyl, Ci-C 6 haloalkyl, Ci-C 6 alkoxy, Ci- Ce haloalkoxy, halo, CN, NO2, COCi-Ce alkyl, CO2C1-C6 alkyl, CO2C3-C8 cycloalkyl, OCOCi- Ce alkyl, OCOCe-Cio aryl, OCO(5- to 10-membered heteroaryl), OCO(3- to 7-membered heterocycloalkyl), Ce-Cio aryl, 5- to 10-membered heteroaryl, NH2, NHCi-Ce alkyl, N(Ci-Ce alkyl) 2 , CONR 8 R 9 , SFs, SCi-Ce alkyl, S(0 2 )Ci-C 6 alkyl, C3-C7 cycloalkyl and 3- to 7-membered heterocycloalkyl,
  • 3- to 7-membered heterocycloalkyl, C6-C10 aryl, 5- to 10-membered heteroaryl, NHCOCe-Cio aryl, HCO(5- to 10-membered heteroaryl) and HCO(3- to 7- membered heterocycloalkyl) are optionally substituted with one or more substituents independently selected from halo, Ci-C 6 alkyl, and OCi-C 6 alkyl.
  • each R 6 is independently selected from Ci-C 6 alkyl, C3-C7 cycloalkyl, C1-C5 haloalkyl, Ci-Ce alkoxy, Ci-C 6 haloalkoxy, halo, CN, C6-C10 aryl, 5- to 10-membered heteroaryl, CO-C1-C6 alkyl; CONR 8 R 9 , and 4- to 6-membered heterocycloalkyl,
  • R 7 is independently selected from Ci-C 6 alkyl, Ci-C 6 haloalkyl, Ci-C 6 alkoxy, Ci-C 6 haloalkoxy, halo, CN, COCi-Ce alkyl, CO2C1-C6 alkyl, CO2C3-C6 cycloalkyl, OCOCi-Ce alkyl, OCOCe-Cio aryl, OCO(5- to 10-membered heteroaryl), OCO(3- to 7-membered heterocycloalkyl), Ce-Cio aryl, 5- to 10-membered heteroaryl, CONR 8 R 9 , SFs, S(0 2 )Ci- C 6 alkyl, C3-C7 cycloalkyl and 4- to 6-membered heterocycloalkyl, wherein the Ci-C 6 alkyl is optionally substituted with one to two Ci-C 6 alkoxy;
  • each R 6 is independently selected from Ci-C 6 alkyl, C3-C7 cycloalkyl, C1-C5 haloalkyl, Ci-C 6 alkoxy, Ci-C 6 haloalkoxy, halo, CN, C 6 -Cio aryl, 5- to 10-membered heteroaryl, CO-C1-C6 alkyl; CO R 8 R 9 , and 4- to 6-membered heterocycloalkyl,
  • each R 7 is independently selected from Ci-C 6 alkyl, Ci-C 6 haloalkyl, Ci-C 6 alkoxy, Ci-Ce haloalkoxy, halo, CN, COCi-Ce alkyl, CO2C1-C6 alkyl, CO2C3-C6 cycloalkyl, OCOCi-Ce alkyl, OCOCe-Cio aryl, OCO(5- to 10-membered heteroaryl),
  • C4-C7 e.g., C4-C 6
  • carbocyclic ring e.
  • o l or 2
  • p l, 2, or 3
  • R 6 and R 7 are each independently selected from Ci-C 6 alkyl, Ci-C 6 alkoxy, halo, CN, NO2, COCi-Ce alkyl, CO2C1-C6 alkyl, Ce-Cio aryl, 5- to 10-membered heteroaryl, CONR 8 R 9 , and 3- to 7-membered heterocycloalkyl, wherein the Ci-C 6 alkyl and 3- to 7-membered heterocycloalkyl is optionally substituted with one or more substituents each independently selected from hydroxy or oxo,
  • R 6 and R 7 on adjacent atoms taken together with the atoms connecting them, independently form at least one C4-C8 carbocyclic ring, wherein the carbocyclic ring is optionally independently substituted with one or more hydroxy or oxo.
  • o l or 2
  • p l, 2, or 3
  • R 6 and R 7 are each independently selected from Ci-C 6 alkyl, Ci-C 6 alkoxy, halo, CN, NO2, COCi-Ce alkyl, CO2C1-C6 alkyl, Ce-Cio aryl, 5- to 10-membered heteroaryl, CO R 8 R 9 , and 3- to 7-membered heterocycloalkyl,
  • Ci-C 6 alkyl and 3- to 7-membered heterocycloalkyl is optionally substituted with one or more substituents each independently selected from hydroxy or oxo.
  • o l or 2
  • p l, 2, or 3
  • o l or 2
  • p l, 2, or 3
  • R 6 and one R 7 are on adjacent atoms, and each pair of one R 6 and one R 7 taken together with the atoms connecting them independently form a C 4 -Cs carbocyclic ring or a 5- to 8-membered heterocyclic ring containing 1 or 2 heteroatoms independently selected from O, N, and S, wherein the carbocyclic ring or heterocyclic ring is unsubstituted.
  • R 6 is Ci-Ce alkyl.
  • R 6 is isopropyl.
  • R 6 is ethyl
  • R 6 is methyl
  • R 6 is Ci-C 6 alkyl substituted with one or more halo
  • R 6 is trifluoromethyl.
  • R 6 is trifluoromethoxy
  • R 6 is C3-C7 cycloalkyl.
  • R 6 is cyclopropyl
  • R 6 is halo
  • R 6 is chloro
  • R 6 is fluoro
  • R 6 is cyano
  • R 6 is attached to a carbon of an aryl ring B.
  • R 6 is attached to a carbon of a heteroaryl ring B.
  • R 6 is attached to a nitrogen of a heteroaryl ring B.
  • At least one R 6 is Ci-C 6 alkyl
  • at least one R 7 is Ci-C 6 alkyl optionally substituted with one or more halo.
  • At least one R 6 is Ci-C 6 alkyl and at least one R 7 is Ci-C 6 alkyl.
  • At least one R 6 is isopropyl and at least one R 7 is methyl.
  • At least one R 6 is isopropyl and at least one R 7 is isopropyl.
  • At least one R 6 is Ci-C 6 alkyl
  • at least one R 7 is Ci-C 6 alkyl substituted with one or more halo.
  • At least one R 6 is isopropyl and at least one R 7 is trifluoromethyl.
  • At least one R 6 is Ci-C 6 alkyl, and at least one R 7 is C3-C7 cycloalkyl. In some embodiments, at least one R 6 is isopropyl and at least one R 7 is cyclopropyl.
  • At least one R 6 is isopropyl and at least one R 7 is halo.
  • At least one R 6 is isopropyl and at least one R 7 is chloro.
  • At least one R 6 is isopropyl and at least one R 7 is fluoro.
  • At least one R 6 is Ci-C 6 alkyl, and at least one R 7 is cyano.
  • At least one R 6 is isopropyl and at least one R 7 is cyano.
  • At least one R 6 is C3-C7 cycloalkyl, and at least one R 7 is C3-C7 ycloalkyl.
  • At least one R 6 is cyclopropyl, and at least one R 7 is cyclopropyl.
  • At least one R 6 is C3-C7 cycloalkyl, and at least one R 7 is halo, n some embodiments. at least one R 6 is cyclopropyl and at least one R 7 is halo,
  • At least one R 6 is cyclopropyl and at least one R 7 is chloro.
  • At least one R 6 is cyclopropyl and at least one R 7 is fluoro.
  • At least one R 6 is Ci-C 6 alkyl, and at least one R 7 is Ci-C 6 alkoxy optionally substituted with one or more halo. In some embodiments, at least one R 6 is isopropyl, and at least one R 7 is Ci-C 6 alkoxy.
  • At least one R 6 is isopropyl, and at least one R 7 is methoxy.
  • At least one R 6 is Ci-C 6 alkyl, and at least one R 7 is Ci-C 6 alkoxy substituted with one or more halo.
  • At least one R 6 is isopropyl, and at least one R 7 is trifluoromethoxy.
  • At least one R 6 is isopropyl, and at least one R 7 is difluoromethoxy.
  • At least one R 6 is halo
  • at least one R 7 is Ci-C 6 haloalkyl optionally sub stituted with hydroxy .
  • At least one R 6 is halo
  • at least one R 7 is Ci-C 6 haloalkoxy.
  • At least one R 6 is chloro, and at least one R 7 is trifluoromethoxy.
  • At least one R 6 is Ci-C 6 alkoxy; and at least one R 7 is halo.
  • At least one R 7 is Ci-C 6 alkyl, and at least one R 6 is Ci-C 6 alkyl optionally substituted with one or more halo.
  • At least one R 7 is isopropyl and at least one R 6 is methyl.
  • At least one R 7 is Ci-C 6 alkyl, and at least one R 6 is Ci-C 6 alkyl substituted with one or more halo.
  • At least one R 7 is isopropyl and at least one R 6 is trifluoromethyl.
  • At least one R 7 is Ci-C 6 alkyl, and at least one R 6 is C3-C7 cycloalkyl. In some embodiments, at least one R 7 is isopropyl and at least one R 6 is cyclopropyl.
  • At least one R 7 is Ci-C 6 alkyl, and at least one R 6 is halo.
  • At least one R 7 is isopropyl and at least one R 6 is halo.
  • At least one R 7 is isopropyl and at least one R 6 is chloro.
  • At least one R 7 is isopropyl and at least one R 6 is fluoro.
  • At least one R 7 is Ci-C 6 alkyl, and at least one R 6 is cyano.
  • At least one R 7 is isopropyl and at least one R 6 is cyano.
  • At least one R 7 is C3-C7 cycloalkyl, and at least one R 6 is C3-C7 cycloalkyl.
  • At least one R 7 is cyclopropyl, and at least one R 6 is cyclopropyl.
  • At least one R 7 is C3-C7 cycloalkyl, and at least one R 6 is halo.
  • At least one R 7 is cyclopropyl and at least one R 6 is halo.
  • At least one R 7 is cyclopropyl and at least one R 6 is chloro.
  • At least one R 7 is cyclopropyl and at least one R 6 is fluoro.
  • At least one R 7 is Ci-C 6 alkyl, and at least one R 6 is Ci-C 6 alkoxy optionally substituted with one or more halo.
  • At least one R 7 is isopropyl, and at least one R 6 is Ci-C 6 alkoxy.
  • At least one R 7 is isopropyl, and at least one R 6 is methoxy.
  • At least one R 7 is Ci-C 6 alkyl, and at least one R 6 is Ci-C 6 alkoxy substituted with one or more halo.
  • At least one R 7 is isopropyl, and at least one R 6 is trifluoromethoxy. In some embodiments, at least one R 7 is halo, and at least one R 6 is Ci-C 6 haloalkyl optionally substituted with one or more hydroxy.
  • At least one R 7 is halo, and at least one R 6 is Ci-C 6 haloalkoxy.
  • At least one R 7 is chloro, and at least one R 6 is trifluoromethoxy.
  • At least one R 7 is Ci-C 6 alkoxy; and at least one R 6 is halo.
  • R 6 and R 7 are each attached to a carbon of a heteroaryl ring B.
  • R 6 is attached to a carbon and R 7 is attached to a nitrogen of a heteroaryl ring B.
  • R 7 is attached to a carbon and R 6 is attached to a nitrogen of a heteroaryl ring B.
  • R 6 and R 7 are on adjacent atoms, and taken together with the atoms connecting them, form a Cs aliphatic carbocyclic ring.
  • R 6 and R 7 are on adjacent atoms, and taken together with the atoms connecting them, form a C 6 aliphatic carbocyclic ring.
  • R 6 and R 7 are on adjacent atoms, and taken together with the atoms connecting them, form a 5-membered aliphatic heterocyclic ring containing 1 or 2 heteroatoms independently selected from O, N, and S.
  • R 6 and R 7 are on adjacent atoms, and taken together with the atoms connecting them, form a 5-membered heteroaromatic ring containing 1 or 2 heteroatoms independently selected from O, N, and S.
  • R 6 and R 7 are on adjacent atoms, and taken together with the atoms connecting them, form a 6-membered aliphatic heterocyclic ring containing 1 or 2 heteroatoms independently selected from O, N, and S.
  • R 6 and R 7 are on adjacent atoms, and taken together with the atoms connecting them, form a 6-membered heteroaromatic ring containing 1 or 2 heteroatoms independently selected from O, N, and S.
  • one R 6 and one R 7 are on adjacent atoms, and taken together with the atoms connecting them, form a C4-Cs carbocyclic ring or a 5- to 8-membered heterocyclic ring containing 1 or 2 heteroatoms independently selected from O, N, and S,
  • one pair of one R 6 and one R 7 are on adjacent atoms; and said pair of one R 6 and one R 7 taken together with the atoms connecting them form form a C4-Cs carbocyclic ring or a 5- to 8- membered heterocyclic ring containing 1 or 2 heteroatoms independently selected from O, N, and S,
  • one pair of one R 6 and one R 7 are on adjacent atoms; and said pair of one R 6 and one R 7 taken together with the atoms connecting them form form a Cs aliphatic carbocyclic ring.
  • one pair of one R 6 and one R 7 are on adjacent atoms; and said pair of one R 6 and one R 7 taken together with the atoms connecting them form form a Cs aliphatic carbocyclic ring.
  • each of one R 6 and one R 7 are on adjacent atoms; one pair of one R 6 and one R 7 taken together with the atoms connecting them form a C 4 aliphatic carbocyclic ring and the other pair of one R 6 and one R 7 taken together with the atoms connecting them form a Cs aliphatic carbocyclic ring.
  • each of one R 6 and one R 7 are on adjacent atoms, and each pair of one R 6 and one R 7 taken together with the atoms connecting them form a Cs carbocyclic ring optionally
  • each of one R 6 and one R 7 are on adjacent atoms, and each pair of one R 6 and one R 7 taken together with the atoms connecting them form a Cs aliphatic carbocyclic ring.
  • each of one R 6 and one R 7 are on adjacent atoms, and each pair of one R 6 and one R 7 taken together with the atoms connecting them form a C 6 aliphatic carbocyclic ring.
  • each of one R 6 and one R 7 are on adjacent atoms, and each pair of one R 6 and one R 7 taken together with the atoms connecting them form a C 6 aromatic carbocyclic ring.
  • each of one R 6 and one R 7 are on adjacent atoms, and each pair of one R 6 and one R 7 taken together with the atoms connecting them form a 5-membered aliphatic heterocyclic ring containing 1 or 2 heteroatoms independently selected from O, N, and S.
  • each of one R 6 and one R 7 are on adjacent atoms, and each pair of one R 6 and one R 7 taken together with the atoms connecting them form a 5-membered heteroaromatic ring containing 1 or 2 heteroatoms independently selected from O, N, and S.
  • each of one R 6 and one R 7 are on adjacent atoms, and each pair of one R 6 and one R 7 taken together with the atoms connecting them form a 6-membered aliphatic heterocyclic ring containing 1 or 2 heteroatoms independently selected from O, N, and S.
  • each of one R 6 and one R 7 are on adjacent atoms, and each pair of one R 6 and one R 7 taken together with the atoms connecting them form a 6-membered heteroaromatic ring containing 1 or 2 heteroatoms independently selected from O, N, and S.
  • each of one R 6 and one R 7 are on adjacent atoms; one pair of one R 6 and one R 7 taken together with the atoms connecting them form a C5 aliphatic carbocyclic ring and the other pair of one R 6 and one R 7 taken together with the atoms connecting them form a 5-membered aliphatic heterocyclic ring containing 1 or 2 heteroatoms independently selected from O, N, and S.
  • each of one R 6 and one R 7 are on adjacent atoms; one pair of one R 6 and one R 7 taken together with the atoms connecting them form a Cs aliphatic carbocyclic ring and the other pair of one R 6 and one R 7 taken together with the atoms connecting them form a 5-membered aliphatic heterocyclic ring containing 1 or 2 heteroatoms independently selected from O, N, and S.
  • each of one R 6 and one R 7 are on adjacent atoms, and each pair of one R 6 and one R 7 taken together with the atoms connecting them independently form a C4-Cs carbocyclic ring or a 5- to 8-membered heterocyclic ring containing 1 or 2 heteroatoms independently selected from 0, N, and S,
  • one of the two rings is fused to the B ring at the 2- and 3- positions relative to the bond connecting the B ring to the NR 3 (CO) group, and the other of the two rings is fused to the B ring at the 5- and 6- positions relative to the bond connecting the B ring to the H(CO) group.
  • each of one R 6 and one R 7 are on adjacent atoms, and each pair of one R 6 and one R 7 taken together with the atoms connecting them independently form a C4-Cs carbocyclic ring or a 5- to 8-membered heterocyclic ring containing 1 or 2 heteroatoms independently selected from O, N, and S,
  • one of the two rings is fused to the B ring at the 2- and 3- positions relative to the bond connecting the B ring to the R 3 (CO) group, and the other of the two rings is fused to the B ring at the 4- and 5- positions relative to the bond connecting the B ring to the H(CO) group.
  • each of one R 6 and one R 7 are on adjacent atoms, and each pair of one R 6 and one R 7 taken together with the atoms connecting them form a Cs aliphatic carbocyclic ring.
  • each of one R 6 and one R 7 are on adjacent atoms, and each pair of one R 6 and one R 7 taken together with the atoms connecting them form a C 4 aliphatic carbocyclic ring.
  • each of one R 6 and one R 7 are on adjacent atoms, one pair of one R 6 and one R 7 taken together with the atoms connecting them form a Cs aliphatic carbocyclic ring, and the other pair of one R 6 and one R 7 taken together with the atoms connecting them form a 5-membered heterocyclic ring containing 1 or 2 heteroatoms independently selected from O, N, and S.
  • each of one R 6 and one R 7 are on adjacent atoms, and each pair of one R 6 and one R 7 taken together with the atoms connecting them form a Cs aliphatic carbocyclic ring; and one R 7 is halo (e.g., CI or F).
  • each of one R 6 and one R 7 are on adjacent atoms, and each pair of one R 6 and one R 7 taken together with the atoms connecting them form a Cs aliphatic carbocyclic ring; and one R 7 is CN.

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EP18752376.6A EP3658539B1 (en) 2017-07-24 2018-07-23 Compounds and compositions for treating conditions associated with nlrp activity
MX2020000911A MX2020000911A (es) 2017-07-24 2018-07-23 Compuestos y composiciones para tratar afecciones asociadas con la actividad nlrp.
PE2020000150A PE20200723A1 (es) 2017-07-24 2018-07-23 Compuestos y composiciones para tratar afecciones asociadas con la actividad nlrp
CR20200037A CR20200037A (es) 2017-07-24 2018-07-23 Compuestos y composiciones para tratar afecciones asociadas con la actividad nlrp
CN202310765173.1A CN117143042A (zh) 2017-07-24 2018-07-23 用于治疗与nlrp活性相关的病症的化合物和组合物
US16/632,849 US11203579B2 (en) 2017-07-24 2018-07-23 Compounds and compositions for treating conditions associated with NLRP activity
MA49682A MA49682B1 (fr) 2017-07-24 2018-07-23 Composés et compositions destinés au traitement d'états pathologiques associés à une activité de nlrp
CA3068836A CA3068836A1 (en) 2017-07-24 2018-07-23 Compounds and compositions for treating conditions associated with nlrp activity
CN202311185119.6A CN117209447A (zh) 2017-07-24 2018-07-23 用于治疗与nlrp活性相关的病症的化合物和组合物
KR1020207004803A KR102565167B1 (ko) 2017-07-24 2018-07-23 Nlrp 활성과 관련된 병태를 치료하기 위한 화합물 및 조성물
EP24151235.9A EP4349820A3 (en) 2017-07-24 2018-07-23 Compounds and compositions for treating conditions associated with nlrp activity
LTEPPCT/US2018/043338T LT3658539T (lt) 2017-07-24 2018-07-23 Su nlrp veikla susijusių ligų gydymui skirti junginiai ir kompozicijos
PL18752376.6T PL3658539T3 (pl) 2017-07-24 2018-07-23 Związki i kompozycje do leczenia stanów związanych z aktywnością nlrp
DK18752376.6T DK3658539T3 (da) 2017-07-24 2018-07-23 Forbindelser og sammensætninger til behandling af tilstande, som er forbundet med nlrp-aktivitet
CN201880050915.XA CN111094243B (zh) 2017-07-24 2018-07-23 用于治疗与nlrp活性相关的病症的化合物和组合物
SI201831090T SI3658539T1 (sl) 2017-07-24 2018-07-23 Spojine in sestavki za zdravljenje stanj, povezanih z delovanjem nlrp
EA202090353A EA202090353A1 (ru) 2017-10-18 2018-07-23 Соединения и композиции для лечения состояний, ассоциированных с активностью nlrp
RU2020107727A RU2786719C2 (ru) 2017-07-24 2018-07-23 Соединения и композиции для лечения состояний, ассоциированных с активностью nlrp
IL271259A IL271259B2 (en) 2017-07-24 2018-07-23 Compounds and compositions for treating conditions associated with nlrp activity
CU2020000004A CU24615B1 (es) 2017-07-24 2018-07-23 Compuestos para tratar afecciones asociadas con la actividad nlrp
BR112020001476-1A BR112020001476A2 (pt) 2017-07-24 2018-07-23 compostos e composições para tratar condições associadas à atividade nlrp
NZ761026A NZ761026A (en) 2017-07-24 2018-07-23 Compounds and compositions for treating conditions associated with nlrp activity
SG11201912166XA SG11201912166XA (en) 2017-07-24 2018-07-23 Compounds and compositions for treating conditions associated with nlrp activity
RS20240513A RS65492B1 (sr) 2017-07-24 2018-07-23 Jedinjenja i kompozicije za lečenje stanja povezanih sa aktivnošću nlrp
AU2018307743A AU2018307743C1 (en) 2017-07-24 2018-07-23 Compounds and compositions for treating conditions associated with NLRP activity
HRP20240521TT HRP20240521T1 (hr) 2017-07-24 2018-07-23 Spojevi i pripravci za liječenje stanja povezanih s aktivnošću nlrp
ES18752376T ES2988798T3 (es) 2017-07-24 2018-07-23 Compuestos y composiciones para el tratamiento de afecciones asociadas a la actividad de NLRP
FIEP18752376.6T FI3658539T3 (fi) 2017-07-24 2018-07-23 Yhdisteitä ja koostumuksia nlrp-aktiivisuuteen liittyvien tilojen hoitamiseksi
JP2020503754A JP7412328B2 (ja) 2017-07-24 2018-07-23 Ｎｌｒｐ活性に関連する状態を治療するための化合物及び組成物
US16/572,528 US10654816B2 (en) 2017-07-24 2019-09-16 Compounds and compositions for treating conditions associated with NLRP activity
ZA2019/08154A ZA201908154B (en) 2017-07-24 2019-12-09 Compounds and compositions for treating conditions associated with nlrp activity
CONC2020/0000527A CO2020000527A2 (es) 2017-07-24 2020-01-17 Compuestos y composiciones para tratar afecciones asociadas con la actividad nlrp
PH12020500127A PH12020500127A1 (en) 2017-07-24 2020-01-17 Compounds and compositions for treating conditions associated with nlrp activity
DO2020000012A DOP2020000012A (es) 2017-07-24 2020-01-23 Compuestos y composiciones para tratar afecciones asociadas con la actividad nlrp
JOJO/P/2020/0011A JOP20200011B1 (ar) 2017-07-24 2020-01-26 مركبات وتركيبات لمعالجة حالات مرضية مرتبطة بنشاط nlrp
US17/496,375 US11724992B2 (en) 2017-07-24 2021-10-07 Compounds and compositions for treating conditions associated with NLRP activity
US18/319,630 US12084424B2 (en) 2017-07-24 2023-05-18 Compounds and compositions for treating conditions associated with NLRP activity
JP2023218835A JP7654767B2 (ja) 2017-07-24 2023-12-26 Ｎｌｒｐ活性に関連する状態を治療するための化合物及び組成物
JP2025044149A JP7813931B2 (ja) 2017-07-24 2025-03-18 Ｎｌｒｐ活性に関連する状態を治療するための化合物及び組成物

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Cited By (54)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2018225018A1 (en) 2017-06-09 2018-12-13 Cadila Healthcare Limited Novel substituted sulfoximine compounds
WO2019068772A1 (en) 2017-10-03 2019-04-11 Inflazome Limited NEW COMPOUNDS
CN110590576A (zh) * 2019-08-15 2019-12-20 安徽金禾实业股份有限公司 一种4-多氟代甲氧基邻苯二胺的制备方法
WO2020010118A1 (en) * 2018-07-03 2020-01-09 Novartis Inflammasome Research, Inc. Methods of treating or selecting a treatment for a subject resistant to tnf inhibitor using a nlrp3 antagonist
WO2020018975A1 (en) * 2018-07-20 2020-01-23 Genentech, Inc. Sulfonimidamide compounds as inhibitors of interleukin-1 activity
WO2020035466A1 (en) 2018-08-15 2020-02-20 Inflazome Limited Novel sulfoneurea compounds
WO2020035465A1 (en) 2017-08-15 2020-02-20 Inflazome Limited Novel sulfoneurea compounds
WO2020035464A1 (en) 2018-08-15 2020-02-20 Inflazome Limited Novel sulfonamideurea compounds
US10654816B2 (en) 2017-07-24 2020-05-19 Novartis Inflammasome Research, Inc. Compounds and compositions for treating conditions associated with NLRP activity
WO2020102576A1 (en) * 2018-11-16 2020-05-22 Novartis Inflammasome Research, Inc. Compounds and compositions for treating conditions associated with nlrp activity
WO2020102096A1 (en) * 2018-11-13 2020-05-22 Novartis Inflammasome Research, Inc. Compounds and compositions for treating conditions associated with nlrp activity
WO2020104657A1 (en) 2018-11-23 2020-05-28 Inflazome Limited Nlrp3 inhibitors
WO2020148619A1 (en) 2019-01-14 2020-07-23 Cadila Healthcare Limited Novel substituted sulfonylurea derivatives
WO2020154499A1 (en) * 2019-01-23 2020-07-30 Novartis Inflammasome Research, Inc. Sulfonimidamide compounds and compositions for treating conditions associated with nlrp activity
WO2020208249A1 (en) 2019-04-12 2020-10-15 Inflazome Limited Nlrp3 inflammasome inhibition
WO2020254697A1 (en) 2019-06-21 2020-12-24 Ac Immune Sa Fused 1,2 thiazoles and 1,2 thiazines which act as nl3p3 modulators
WO2021002887A1 (en) 2019-07-02 2021-01-07 Novartis Inflammasome Research, Inc. Gut-targeted nlrp3 antagonists and their use in therapy
WO2021032588A1 (en) 2019-08-16 2021-02-25 Inflazome Limited Macrocyclic sulfonylamide derivatives useful as nlrp3 inhibitors
WO2021032591A1 (en) 2019-08-16 2021-02-25 Inflazome Limited Macrocyclic sulfonylurea derivatives useful as nlrp3 inhibitors
WO2021043966A1 (en) 2019-09-06 2021-03-11 Inflazome Limited Nlrp3 inhibitors
WO2021093820A1 (zh) * 2019-11-12 2021-05-20 成都百裕制药股份有限公司 酰胺衍生物及其制备方法和在医药上的应用
WO2021150574A1 (en) * 2020-01-22 2021-07-29 Genentech, Inc. Sulfonimidamide compounds as nlrp3 modulators
WO2021165245A1 (en) 2020-02-18 2021-08-26 Inflazome Limited Compounds
WO2021255279A1 (en) 2020-06-19 2021-12-23 Ac Immune Sa D i h yd rooxazo le and thiourea derivatives modulating the nlrp3 inflammasome pathway
WO2022023907A1 (en) 2020-07-31 2022-02-03 Novartis Ag Methods of selecting and treating patients at elevated risk of major adverse cardiac events
WO2022051582A1 (en) 2020-09-04 2022-03-10 NodThera Limited Sulphamoyl urea derivatives containing alkyl-oxacycloalkyl moiety and uses thereof
WO2022105852A1 (zh) 2020-11-20 2022-05-27 江苏恒瑞医药股份有限公司 三嗪二酮类衍生物、其制备方法及其在医药上的应用
CN114989058A (zh) * 2022-06-02 2022-09-02 中国科学院成都生物研究所 一种手性氯代砜亚胺类化合物及其衍生物的制备方法
WO2022219546A1 (en) 2021-04-16 2022-10-20 Novartis Ag Heteroaryl aminopropanol derivatives as inhibitors of lta4h
US11542255B2 (en) 2017-08-15 2023-01-03 Inflazome Limited Sulfonylureas and sulfonylthioureas as NLRP3 inhibitors
WO2023002399A1 (en) 2021-07-23 2023-01-26 Novartis Ag Dosing regimen for an nlrp3 inhibitor in the treatment of osteoarthritis
WO2023118521A1 (en) 2021-12-22 2023-06-29 Ac Immune Sa Dihydro-oxazol derivative compounds
JP2023528968A (ja) * 2020-06-11 2023-07-06 メッドシャイン ディスカバリー インコーポレイテッド ジメチルスルホキシミン誘導体
WO2024013395A1 (en) 2022-07-14 2024-01-18 Ac Immune Sa Pyrrolotriazine and imidazotriazine derivatives as modulators of the nlrp3 inflammasome pathway
WO2024023696A1 (en) 2022-07-27 2024-02-01 Novartis Ag Dosing regimen for a nlrp3 inhibitor
WO2024023266A1 (en) 2022-07-28 2024-02-01 Ac Immune Sa Novel compounds
US11905252B2 (en) 2018-03-02 2024-02-20 Inflazome Limited Compounds
US11926600B2 (en) 2017-08-15 2024-03-12 Inflazome Limited Sulfonylureas and sulfonylthioureas as NLRP3 inhibitors
US12012392B2 (en) 2017-11-09 2024-06-18 Inflazome Limited Sulfonamide carboxamide compounds
US12012397B2 (en) 2017-12-18 2024-06-18 NodThera Limited Sulphonyl urea derivatives as NLRP3 inflammasome modulators
US12054461B2 (en) 2019-06-12 2024-08-06 NodThera Limited Sulfonylurea derivatives and uses thereof
US12134611B2 (en) 2018-11-13 2024-11-05 Novartis Ag Compounds and compositions for treating conditions associated with NLRP activity
WO2024249539A1 (en) 2023-06-02 2024-12-05 Merck Sharp & Dohme Llc 5,6 unsaturated bicyclic heterocyles useful as inhibitors of nod-like receptor protein 3
US12167995B2 (en) 2019-06-10 2024-12-17 Axalbion Sa [((1R,2S,5R)-2-isopropyl-5-methyl-cyclohexanecarbonyl)-amino]-acetic acid isopropyl ester for treatment of chronic cough
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US12421223B2 (en) 2018-11-13 2025-09-23 Novartis Ag Compounds and compositions for treating conditions associated with NLRP activity
WO2026057747A1 (en) 2024-09-11 2026-03-19 Ac Immune Sa Therapeutic use of nlrp3 inflammasome pathway inhibitor compounds
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Citations (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0173498A1 (en) 1984-08-08 1986-03-05 E.I. Du Pont De Nemours And Company Herbicidal sulphonimidamide compounds
EP0552553A1 (en) * 1991-12-20 1993-07-28 Eli Lilly And Company Sulfonimidamides as antineoplastic agents
EP2314593A1 (en) * 2001-08-02 2011-04-27 Portola Pharmaceuticals, Inc. Platelet ADP receptor inhibitors
EP2927214A1 (en) * 2012-11-30 2015-10-07 Kyowa Hakko Kirin Co., Ltd. Nitrogen-containing heterocyclic compound
WO2016131098A1 (en) * 2015-02-16 2016-08-25 The University Of Queensland Sulfonylureas and related compounds and use of same
WO2017184624A1 (en) * 2016-04-18 2017-10-26 Ifm Therapeutics, Inc Compounds and compositions for treating conditions associated with nlrp activity
WO2017184604A1 (en) * 2016-04-18 2017-10-26 Ifm Therapeutics, Inc Compounds and compositions for treating conditions associated with nlrp activity

Family Cites Families (20)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5258406A (en) 1991-12-20 1993-11-02 Eli Lilly And Company Sulfonimidamides
US5169860A (en) 1992-03-13 1992-12-08 Eli Lilly And Company Antitumor compositions and methods of treatment
PT1270565E (pt) 1997-01-29 2004-09-30 Pfizer Furano-2-sulfonamida 4-substituida e sua utilizacao na preparacao de derivados de sulfonilureia
EP1214087A1 (en) 1999-09-14 2002-06-19 Pfizer Products Inc. Combination treatment with il-1ra and compounds that inhibit il-1 processing and release
CA2369967A1 (en) 2001-02-12 2002-08-12 Joseph Anthony Cornicelli Methods of treating nuclear factor-kappa b mediated diseases and disorders
BRPI1006380B1 (pt) 2009-04-16 2021-04-06 Koninklijke Philips N.V. Método para comunicação em uma rede de uma primeira estação a uma segunda estação e estação de rádio
EP3436432B1 (en) 2016-03-30 2021-01-27 Genentech, Inc. Substituted benzamides and methods of use thereof
CA3021349A1 (en) 2016-04-19 2017-10-26 Innate Tumor Immunity, Inc. Nlrp3 modulators
EP3571187B1 (en) 2017-01-23 2023-11-22 Genentech, Inc. Chemical compounds as inhibitors of interleukin-1 activity
TWI674261B (zh) 2017-02-17 2019-10-11 美商英能腫瘤免疫股份有限公司 Nlrp3 調節劑
WO2018225018A1 (en) 2017-06-09 2018-12-13 Cadila Healthcare Limited Novel substituted sulfoximine compounds
NZ760129A (en) 2017-07-07 2025-12-19 Inflazome Ltd Novel sulfonamide carboxamide compounds
ES2988798T3 (es) * 2017-07-24 2024-11-21 Novartis Ag Compuestos y composiciones para el tratamiento de afecciones asociadas a la actividad de NLRP
JP7349981B2 (ja) 2017-07-24 2023-09-25 ノバルティス アーゲー Ｎｌｒｐ活性に関連する状態を治療するための化合物及び組成物
EP3668840A1 (en) 2017-08-15 2020-06-24 Inflazome Limited Novel sulfonamide carboxamide compounds
EP3692020A1 (en) * 2017-10-03 2020-08-12 Inflazome Limited Novel compounds
CA3105521A1 (en) 2018-07-20 2020-01-23 F. Hoffmann-La Roche Ag Sulfonimidamide compounds as inhibitors of interleukin-1 activity
GB201902327D0 (en) 2019-02-20 2019-04-03 Inflazome Ltd Novel compounds
BR112021003665A2 (pt) 2018-09-13 2021-05-18 Bayer Aktiengesellschaft derivados de heterocicleno como agentes de controle de pragas
EP3911323A4 (en) 2019-01-18 2022-11-16 Nuvation Bio Inc. HETEROCYCLIC COMPOUNDS AS ADENOSINE ANTAGONISTS

Patent Citations (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0173498A1 (en) 1984-08-08 1986-03-05 E.I. Du Pont De Nemours And Company Herbicidal sulphonimidamide compounds
US4666506A (en) 1984-08-08 1987-05-19 E. I. Du Pont De Nemours And Company Herbicidal pyrimidines
EP0552553A1 (en) * 1991-12-20 1993-07-28 Eli Lilly And Company Sulfonimidamides as antineoplastic agents
EP2314593A1 (en) * 2001-08-02 2011-04-27 Portola Pharmaceuticals, Inc. Platelet ADP receptor inhibitors
EP2927214A1 (en) * 2012-11-30 2015-10-07 Kyowa Hakko Kirin Co., Ltd. Nitrogen-containing heterocyclic compound
WO2016131098A1 (en) * 2015-02-16 2016-08-25 The University Of Queensland Sulfonylureas and related compounds and use of same
WO2017184624A1 (en) * 2016-04-18 2017-10-26 Ifm Therapeutics, Inc Compounds and compositions for treating conditions associated with nlrp activity
WO2017184623A1 (en) * 2016-04-18 2017-10-26 Ifm Therapeutics, Inc Compounds and compositions for treating conditions associated with nlrp activity
WO2017184604A1 (en) * 2016-04-18 2017-10-26 Ifm Therapeutics, Inc Compounds and compositions for treating conditions associated with nlrp activity

Non-Patent Citations (9)

* Cited by examiner, † Cited by third party
Title
"Handbook of Pharmaceutical Additives", 2007, GOWER PUBLISHING COMPANY
"Handbook of Pharmaceutical Excipients", 2009, THE PHARMACEUTICAL PRESS AND THE AMERICAN PHARMACEUTICAL ASSOCIATION
"Pharmaceutical Preformulation and Formulation", 2009, CRC PRESS LLC
"Remington: The Science and Practice of Pharmacy", 2005, LIPPINCOTT WILLIAMS & WILKINS
SAXENA A ET AL: "Estimation of antitumor activity of sulphonaimidamide analogs of oncolytic sulphonylureas", OXIDATION COMMUNICATIONS, vol. 26, no. 1, 2003, pages 9 - 13, XP009507954, ISSN: 0209-4541 *
SCOZZAFAVA A ET AL: "Arylsulfonyl-N,N-diethyl-dithiocarbamates: a novel class of antitumor agents", BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, vol. 10, no. 16, 21 August 2000 (2000-08-21), pages 1887 - 1891, XP004216023, ISSN: 0960-894X, DOI: 10.1016/S0960-894X(00)00375-9 *
SUPURAN C T ET AL: "Carbonic anhydrase inhibitors - Part 94. 1,3,4-Thiadiazole-2-sulfonamide derivatives as antitumor agents?", EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY, vol. 35, no. 9, 1 September 2000 (2000-09-01), pages 867 - 874, XP004331220, ISSN: 0223-5234, DOI: 10.1016/S0223-5234(00)00169-0 *
TOTH J E ET AL: "Sulfonimidamide Analogs of Oncolytic Sulfonylureas", JOURNAL OF MEDICINAL CHEMISTRY, vol. 40, no. 6, 14 March 1997 (1997-03-14), pages 1018 - 1025, XP000926714, ISSN: 0022-2623, DOI: 10.1021/JM960673L *
TOTH J E ET AL: "Synthesis and resolution of sulfonimidamide analogs of sulfonylureas", JOURNAL OF ORGANIC CHEMISTRY, vol. 58, no. 12, 1 June 1993 (1993-06-01), pages 3469 - 3472, XP055499492, ISSN: 0022-3263, DOI: 10.1021/jo00064a044 *

Cited By (80)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2018225018A1 (en) 2017-06-09 2018-12-13 Cadila Healthcare Limited Novel substituted sulfoximine compounds
US11236045B2 (en) 2017-06-09 2022-02-01 Cadila Healthcare Limited Substituted sulfoximine compounds
EP3634951B1 (en) * 2017-06-09 2024-07-10 Zydus Lifesciences Limited Novel substituted sulfoximine compounds
US11724992B2 (en) 2017-07-24 2023-08-15 Novartis Ag Compounds and compositions for treating conditions associated with NLRP activity
US10654816B2 (en) 2017-07-24 2020-05-19 Novartis Inflammasome Research, Inc. Compounds and compositions for treating conditions associated with NLRP activity
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US11203579B2 (en) 2017-07-24 2021-12-21 Novartis Ag Compounds and compositions for treating conditions associated with NLRP activity
WO2020035465A1 (en) 2017-08-15 2020-02-20 Inflazome Limited Novel sulfoneurea compounds
US11542255B2 (en) 2017-08-15 2023-01-03 Inflazome Limited Sulfonylureas and sulfonylthioureas as NLRP3 inhibitors
US11613542B2 (en) 2017-08-15 2023-03-28 Inflazome Limited Sulfonylureas and sulfonylthioureas as NLRP3 inhibitors
US11926600B2 (en) 2017-08-15 2024-03-12 Inflazome Limited Sulfonylureas and sulfonylthioureas as NLRP3 inhibitors
WO2019068772A1 (en) 2017-10-03 2019-04-11 Inflazome Limited NEW COMPOUNDS
US11623922B2 (en) 2017-10-03 2023-04-11 Inflazome Limited Compounds
US12012392B2 (en) 2017-11-09 2024-06-18 Inflazome Limited Sulfonamide carboxamide compounds
US12221434B2 (en) 2017-11-09 2025-02-11 Inflazome Limited Sulfonamide carboxamide compounds
US12012397B2 (en) 2017-12-18 2024-06-18 NodThera Limited Sulphonyl urea derivatives as NLRP3 inflammasome modulators
US12459925B2 (en) 2017-12-18 2025-11-04 NodThera Limited Sulphonyl urea derivatives as NLRP3 inflammasome modulators
US11905252B2 (en) 2018-03-02 2024-02-20 Inflazome Limited Compounds
WO2020010118A1 (en) * 2018-07-03 2020-01-09 Novartis Inflammasome Research, Inc. Methods of treating or selecting a treatment for a subject resistant to tnf inhibitor using a nlrp3 antagonist
WO2020018975A1 (en) * 2018-07-20 2020-01-23 Genentech, Inc. Sulfonimidamide compounds as inhibitors of interleukin-1 activity
CN112513048A (zh) * 2018-07-20 2021-03-16 豪夫迈·罗氏有限公司 作为白细胞介素-1活性抑制剂的磺酰亚胺酰胺类化合物
US12234245B2 (en) 2018-07-20 2025-02-25 Genentech, Inc. Sulfonimidamide compounds as inhibitors of interleukin-1 activity
WO2020035464A1 (en) 2018-08-15 2020-02-20 Inflazome Limited Novel sulfonamideurea compounds
WO2020035466A1 (en) 2018-08-15 2020-02-20 Inflazome Limited Novel sulfoneurea compounds
US12134611B2 (en) 2018-11-13 2024-11-05 Novartis Ag Compounds and compositions for treating conditions associated with NLRP activity
WO2020102096A1 (en) * 2018-11-13 2020-05-22 Novartis Inflammasome Research, Inc. Compounds and compositions for treating conditions associated with nlrp activity
EP4667054A3 (en) * 2018-11-13 2026-02-18 Novartis AG Compounds and compositions for treating conditions associated with nlrp activity
AU2019379109B2 (en) * 2018-11-13 2022-07-07 Novartis Ag Compounds and compositions for treating conditions associated with NLRP activity
US12421223B2 (en) 2018-11-13 2025-09-23 Novartis Ag Compounds and compositions for treating conditions associated with NLRP activity
WO2020102576A1 (en) * 2018-11-16 2020-05-22 Novartis Inflammasome Research, Inc. Compounds and compositions for treating conditions associated with nlrp activity
WO2020104657A1 (en) 2018-11-23 2020-05-28 Inflazome Limited Nlrp3 inhibitors
US12084416B2 (en) 2019-01-14 2024-09-10 Zydus Lifesciences Limited Substituted sulfonylurea derivatives
WO2020148619A1 (en) 2019-01-14 2020-07-23 Cadila Healthcare Limited Novel substituted sulfonylurea derivatives
CN113329998A (zh) * 2019-01-23 2021-08-31 诺华股份有限公司 用于治疗与nlrp活性相关的病症的磺酰亚胺酰胺化合物和组合物
WO2020154499A1 (en) * 2019-01-23 2020-07-30 Novartis Inflammasome Research, Inc. Sulfonimidamide compounds and compositions for treating conditions associated with nlrp activity
WO2020208249A1 (en) 2019-04-12 2020-10-15 Inflazome Limited Nlrp3 inflammasome inhibition
US12167995B2 (en) 2019-06-10 2024-12-17 Axalbion Sa [((1R,2S,5R)-2-isopropyl-5-methyl-cyclohexanecarbonyl)-amino]-acetic acid isopropyl ester for treatment of chronic cough
US12054461B2 (en) 2019-06-12 2024-08-06 NodThera Limited Sulfonylurea derivatives and uses thereof
WO2020254697A1 (en) 2019-06-21 2020-12-24 Ac Immune Sa Fused 1,2 thiazoles and 1,2 thiazines which act as nl3p3 modulators
WO2021002887A1 (en) 2019-07-02 2021-01-07 Novartis Inflammasome Research, Inc. Gut-targeted nlrp3 antagonists and their use in therapy
CN110590576A (zh) * 2019-08-15 2019-12-20 安徽金禾实业股份有限公司 一种4-多氟代甲氧基邻苯二胺的制备方法
WO2021032588A1 (en) 2019-08-16 2021-02-25 Inflazome Limited Macrocyclic sulfonylamide derivatives useful as nlrp3 inhibitors
WO2021032591A1 (en) 2019-08-16 2021-02-25 Inflazome Limited Macrocyclic sulfonylurea derivatives useful as nlrp3 inhibitors
WO2021043966A1 (en) 2019-09-06 2021-03-11 Inflazome Limited Nlrp3 inhibitors
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JP2023502171A (ja) * 2019-11-12 2023-01-20 成都百裕制薬股▲ふん▼有限公司 アミド誘導体及びその調製方法並びに医薬における応用
JP7392169B2 (ja) 2019-11-12 2023-12-05 成都百裕制薬股▲ふん▼有限公司 アミド誘導体及びその調製方法並びに医薬における応用
CN112851607B (zh) * 2019-11-12 2026-04-28 康百达（四川）生物医药科技有限公司 酰胺衍生物及其制备方法和在医药上的应用
KR102797670B1 (ko) 2019-11-12 2025-04-18 캉바이다 (시추안) 바이오테크놀로지 씨오. 엘티디. 아마이드 유도체 및 그 제조방법과 의학적 응용
KR20220115557A (ko) * 2019-11-12 2022-08-17 청두 바이위 파머수티컬 씨오., 엘티디 아마이드 유도체 및 그 제조방법과 의학적 응용
AU2020383646B2 (en) * 2019-11-12 2023-10-12 Kangbaida (Sichuan) Biotechnology Co., Ltd. Amide derivative and preparation method therefore and use thereof in medicine
CN112851607A (zh) * 2019-11-12 2021-05-28 成都百裕制药股份有限公司 酰胺衍生物及其制备方法和在医药上的应用
US11976054B2 (en) 2019-11-12 2024-05-07 Chengdu Baiyu Pharmaceutical Co., Ltd. Amide derivative and preparation method therefore and use thereof in medicine
WO2021093820A1 (zh) * 2019-11-12 2021-05-20 成都百裕制药股份有限公司 酰胺衍生物及其制备方法和在医药上的应用
WO2021150574A1 (en) * 2020-01-22 2021-07-29 Genentech, Inc. Sulfonimidamide compounds as nlrp3 modulators
WO2021165245A1 (en) 2020-02-18 2021-08-26 Inflazome Limited Compounds
JP7504234B2 (ja) 2020-06-11 2024-06-21 シーセン ファーマシューティカル カンパニー リミテッド ジメチルスルホキシミン誘導体
JP2023528968A (ja) * 2020-06-11 2023-07-06 メッドシャイン ディスカバリー インコーポレイテッド ジメチルスルホキシミン誘導体
US12428391B2 (en) 2020-06-11 2025-09-30 Cisen Pharmaceutical Co., Ltd Dimethylsulfoximine derivative
WO2021255279A1 (en) 2020-06-19 2021-12-23 Ac Immune Sa D i h yd rooxazo le and thiourea derivatives modulating the nlrp3 inflammasome pathway
WO2022023907A1 (en) 2020-07-31 2022-02-03 Novartis Ag Methods of selecting and treating patients at elevated risk of major adverse cardiac events
WO2022051582A1 (en) 2020-09-04 2022-03-10 NodThera Limited Sulphamoyl urea derivatives containing alkyl-oxacycloalkyl moiety and uses thereof
WO2022105852A1 (zh) 2020-11-20 2022-05-27 江苏恒瑞医药股份有限公司 三嗪二酮类衍生物、其制备方法及其在医药上的应用
EP4628163A1 (en) 2021-04-16 2025-10-08 Novartis AG Novel heteroaryl aminopropanol derivatives
WO2022219546A1 (en) 2021-04-16 2022-10-20 Novartis Ag Heteroaryl aminopropanol derivatives as inhibitors of lta4h
WO2023002399A1 (en) 2021-07-23 2023-01-26 Novartis Ag Dosing regimen for an nlrp3 inhibitor in the treatment of osteoarthritis
WO2023118521A1 (en) 2021-12-22 2023-06-29 Ac Immune Sa Dihydro-oxazol derivative compounds
CN114989058A (zh) * 2022-06-02 2022-09-02 中国科学院成都生物研究所 一种手性氯代砜亚胺类化合物及其衍生物的制备方法
CN114989058B (zh) * 2022-06-02 2024-04-16 中国科学院成都生物研究所 一种手性氯代砜亚胺类化合物及其衍生物的制备方法
WO2024013395A1 (en) 2022-07-14 2024-01-18 Ac Immune Sa Pyrrolotriazine and imidazotriazine derivatives as modulators of the nlrp3 inflammasome pathway
WO2024023696A1 (en) 2022-07-27 2024-02-01 Novartis Ag Dosing regimen for a nlrp3 inhibitor
WO2024023266A1 (en) 2022-07-28 2024-02-01 Ac Immune Sa Novel compounds
WO2024249539A1 (en) 2023-06-02 2024-12-05 Merck Sharp & Dohme Llc 5,6 unsaturated bicyclic heterocyles useful as inhibitors of nod-like receptor protein 3
WO2025068958A1 (en) 2023-09-29 2025-04-03 Novartis Ag Nlrp3 inhibitor for use in lowering the risk of cardiovascular diseases
WO2025133307A1 (en) 2023-12-22 2025-06-26 Ac Immune Sa Heterocyclic modulators of the nlrp3 inflammasome pathway
WO2025153532A1 (en) 2024-01-16 2025-07-24 NodThera Limited Nlrp3 inhibitors and glp-1 agonists combination therapies
WO2025153624A1 (en) 2024-01-17 2025-07-24 Ac Immune Sa Imidazo[1,2-d][1,2,4]triazine derivatives for use as inhibitors of the nlrp3 inflammasome pathway
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WO2025163069A1 (en) 2024-01-31 2025-08-07 Ac Immune Sa Novel compounds
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