JP2022540200A - Lrrk2阻害剤としてのインダゾールおよびアザインダゾール - Google Patents
Lrrk2阻害剤としてのインダゾールおよびアザインダゾール Download PDFInfo
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- JP2022540200A JP2022540200A JP2022501162A JP2022501162A JP2022540200A JP 2022540200 A JP2022540200 A JP 2022540200A JP 2022501162 A JP2022501162 A JP 2022501162A JP 2022501162 A JP2022501162 A JP 2022501162A JP 2022540200 A JP2022540200 A JP 2022540200A
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- Prior art keywords
- alkyl
- cyano
- indazol
- nrcrd
- cycloalkyl
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- BAXOFTOLAUCFNW-UHFFFAOYSA-N 1H-indazole Chemical compound C1=CC=C2C=NNC2=C1 BAXOFTOLAUCFNW-UHFFFAOYSA-N 0.000 title abstract description 4
- QRUDEWIWKLJBPS-UHFFFAOYSA-N benzotriazole Chemical compound C1=CC=C2N[N][N]C2=C1 QRUDEWIWKLJBPS-UHFFFAOYSA-N 0.000 title abstract description 3
- 229940124786 LRRK2 inhibitor Drugs 0.000 title description 5
- 108010020246 Leucine-Rich Repeat Serine-Threonine Protein Kinase-2 Proteins 0.000 claims abstract description 65
- 125000000217 alkyl group Chemical group 0.000 claims description 662
- 125000000475 sulfinyl group Chemical group [*:2]S([*:1])=O 0.000 claims description 449
- 150000001875 compounds Chemical class 0.000 claims description 265
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 claims description 214
- 125000000171 (C1-C6) haloalkyl group Chemical group 0.000 claims description 213
- 125000003601 C2-C6 alkynyl group Chemical group 0.000 claims description 208
- 238000000034 method Methods 0.000 claims description 196
- 125000005843 halogen group Chemical group 0.000 claims description 157
- 125000003118 aryl group Chemical group 0.000 claims description 150
- 125000001424 substituent group Chemical group 0.000 claims description 131
- 125000000592 heterocycloalkyl group Chemical group 0.000 claims description 121
- -1 OR a Inorganic materials 0.000 claims description 106
- 150000003839 salts Chemical class 0.000 claims description 98
- 125000006272 (C3-C7) cycloalkyl group Chemical group 0.000 claims description 72
- 102100032693 Leucine-rich repeat serine/threonine-protein kinase 2 Human genes 0.000 claims description 66
- 125000001313 C5-C10 heteroaryl group Chemical group 0.000 claims description 60
- 125000006376 (C3-C10) cycloalkyl group Chemical group 0.000 claims description 58
- 125000006708 (C5-C14) heteroaryl group Chemical group 0.000 claims description 57
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims description 50
- 229910052739 hydrogen Inorganic materials 0.000 claims description 44
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 41
- 125000004076 pyridyl group Chemical group 0.000 claims description 40
- 229910052799 carbon Inorganic materials 0.000 claims description 39
- 201000010099 disease Diseases 0.000 claims description 34
- 125000002541 furyl group Chemical group 0.000 claims description 34
- 125000001072 heteroaryl group Chemical group 0.000 claims description 31
- 208000018737 Parkinson disease Diseases 0.000 claims description 28
- 125000003226 pyrazolyl group Chemical group 0.000 claims description 27
- 125000006570 (C5-C6) heteroaryl group Chemical group 0.000 claims description 26
- 125000004429 atom Chemical group 0.000 claims description 26
- 125000000842 isoxazolyl group Chemical group 0.000 claims description 26
- 230000000694 effects Effects 0.000 claims description 25
- 125000000714 pyrimidinyl group Chemical group 0.000 claims description 25
- 125000000168 pyrrolyl group Chemical group 0.000 claims description 24
- 125000000335 thiazolyl group Chemical group 0.000 claims description 24
- 229910052757 nitrogen Inorganic materials 0.000 claims description 23
- 125000006568 (C4-C7) heterocycloalkyl group Chemical group 0.000 claims description 22
- 125000002883 imidazolyl group Chemical group 0.000 claims description 22
- 125000001786 isothiazolyl group Chemical group 0.000 claims description 22
- 208000001089 Multiple system atrophy Diseases 0.000 claims description 21
- 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 claims description 18
- 229910052717 sulfur Inorganic materials 0.000 claims description 18
- 229910052760 oxygen Inorganic materials 0.000 claims description 17
- 208000035475 disorder Diseases 0.000 claims description 16
- 230000004770 neurodegeneration Effects 0.000 claims description 16
- 238000006467 substitution reaction Methods 0.000 claims description 16
- 125000001544 thienyl group Chemical group 0.000 claims description 16
- 208000024827 Alzheimer disease Diseases 0.000 claims description 15
- 125000003545 alkoxy group Chemical group 0.000 claims description 15
- 125000003342 alkenyl group Chemical group 0.000 claims description 14
- 208000015122 neurodegenerative disease Diseases 0.000 claims description 14
- 125000002971 oxazolyl group Chemical group 0.000 claims description 14
- 125000004541 benzoxazolyl group Chemical group O1C(=NC2=C1C=CC=C2)* 0.000 claims description 13
- 125000005842 heteroatom Chemical group 0.000 claims description 13
- 125000002098 pyridazinyl group Chemical group 0.000 claims description 13
- 125000006645 (C3-C4) cycloalkyl group Chemical group 0.000 claims description 12
- 201000002832 Lewy body dementia Diseases 0.000 claims description 12
- 229910052801 chlorine Inorganic materials 0.000 claims description 12
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 12
- 125000004765 (C1-C4) haloalkyl group Chemical group 0.000 claims description 11
- 125000004737 (C1-C6) haloalkoxy group Chemical group 0.000 claims description 11
- 229910052794 bromium Inorganic materials 0.000 claims description 11
- 229910052740 iodine Inorganic materials 0.000 claims description 11
- 230000035772 mutation Effects 0.000 claims description 11
- 206010067889 Dementia with Lewy bodies Diseases 0.000 claims description 10
- 229910052731 fluorine Inorganic materials 0.000 claims description 10
- 210000004558 lewy body Anatomy 0.000 claims description 10
- 125000003373 pyrazinyl group Chemical group 0.000 claims description 9
- 125000006163 5-membered heteroaryl group Chemical group 0.000 claims description 8
- 206010012289 Dementia Diseases 0.000 claims description 8
- 125000000304 alkynyl group Chemical group 0.000 claims description 8
- 230000002401 inhibitory effect Effects 0.000 claims description 8
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims description 8
- 208000011580 syndromic disease Diseases 0.000 claims description 8
- 125000001995 cyclobutyl group Chemical group [H]C1([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 claims description 7
- 125000003453 indazolyl group Chemical group N1N=C(C2=C1C=CC=C2)* 0.000 claims description 7
- 125000000555 isopropenyl group Chemical group [H]\C([H])=C(\*)C([H])([H])[H] 0.000 claims description 7
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims description 7
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 7
- 239000008194 pharmaceutical composition Substances 0.000 claims description 7
- 101100310920 Caenorhabditis elegans sra-2 gene Proteins 0.000 claims description 6
- 101100240985 Neurospora crassa (strain ATCC 24698 / 74-OR23-1A / CBS 708.71 / DSM 1257 / FGSC 987) nrc-2 gene Proteins 0.000 claims description 6
- 125000002393 azetidinyl group Chemical group 0.000 claims description 6
- 239000003937 drug carrier Substances 0.000 claims description 6
- 125000001153 fluoro group Chemical group F* 0.000 claims description 6
- 125000002346 iodo group Chemical group I* 0.000 claims description 6
- 125000004588 thienopyridyl group Chemical group S1C(=CC2=C1C=CC=N2)* 0.000 claims description 6
- 125000000876 trifluoromethoxy group Chemical group FC(F)(F)O* 0.000 claims description 6
- 208000009106 Shy-Drager Syndrome Diseases 0.000 claims description 5
- 125000001246 bromo group Chemical group Br* 0.000 claims description 5
- 208000031237 olivopontocerebellar atrophy Diseases 0.000 claims description 5
- 125000003386 piperidinyl group Chemical group 0.000 claims description 5
- 125000004852 dihydrofuranyl group Chemical group O1C(CC=C1)* 0.000 claims description 4
- 125000003566 oxetanyl group Chemical group 0.000 claims description 4
- 125000002943 quinolinyl group Chemical group N1=C(C=CC2=CC=CC=C12)* 0.000 claims description 4
- 125000001412 tetrahydropyranyl group Chemical group 0.000 claims description 4
- 125000001425 triazolyl group Chemical group 0.000 claims description 4
- GBXQPDCOMJJCMJ-UHFFFAOYSA-M trimethyl-[6-(trimethylazaniumyl)hexyl]azanium;bromide Chemical compound [Br-].C[N+](C)(C)CCCCCC[N+](C)(C)C GBXQPDCOMJJCMJ-UHFFFAOYSA-M 0.000 claims description 4
- 125000001309 chloro group Chemical group Cl* 0.000 claims description 3
- GRVDNGHTXZBPIA-UHFFFAOYSA-N 5-cyano-N-[3-(furan-3-yl)-1H-indazol-5-yl]-6-methylpyridine-2-carboxamide Chemical compound C(#N)C=1C=CC(=NC=1C)C(=O)NC=1C=C2C(=NNC2=CC=1)C1=COC=C1 GRVDNGHTXZBPIA-UHFFFAOYSA-N 0.000 claims description 2
- FWDNJDBAKAAWOP-UHFFFAOYSA-N C(#N)C1=CC(=C(C(=O)NC=2C=C3C(=NNC3=CC=2)C)C=C1)C Chemical compound C(#N)C1=CC(=C(C(=O)NC=2C=C3C(=NNC3=CC=2)C)C=C1)C FWDNJDBAKAAWOP-UHFFFAOYSA-N 0.000 claims description 2
- JNCMHMUGTWEVOZ-UHFFFAOYSA-N F[CH]F Chemical compound F[CH]F JNCMHMUGTWEVOZ-UHFFFAOYSA-N 0.000 claims description 2
- 108010081348 HRT1 protein Hairy Proteins 0.000 claims description 2
- 102100021881 Hairy/enhancer-of-split related with YRPW motif protein 1 Human genes 0.000 claims description 2
- 208000003351 Melanosis Diseases 0.000 claims description 2
- 210000001577 neostriatum Anatomy 0.000 claims description 2
- ZLFLGHVRERODIH-UHFFFAOYSA-N C(#N)C=1C=C(C(=NC=1)C(=O)NC1=CC=C2C(=N1)C(=NN2)C1=COC=C1)C Chemical compound C(#N)C=1C=C(C(=NC=1)C(=O)NC1=CC=C2C(=N1)C(=NN2)C1=COC=C1)C ZLFLGHVRERODIH-UHFFFAOYSA-N 0.000 claims 2
- VCPMIICUCIJXEF-UHFFFAOYSA-N 2-bromo-4-cyano-N-[3-(furan-3-yl)-1H-indazol-5-yl]benzamide Chemical compound BrC1=C(C(=O)NC=2C=C3C(=NNC3=CC=2)C2=COC=C2)C=CC(=C1)C#N VCPMIICUCIJXEF-UHFFFAOYSA-N 0.000 claims 1
- IYWJIDQDKVWAGX-UHFFFAOYSA-N 2-chloro-3-cyano-N-[3-(1,3-oxazol-5-yl)-1H-indazol-5-yl]benzamide Chemical compound ClC1=C(C(=O)NC=2C=C3C(=NNC3=CC=2)C2=CN=CO2)C=CC=C1C#N IYWJIDQDKVWAGX-UHFFFAOYSA-N 0.000 claims 1
- QRYPKHSKJYBOIC-UHFFFAOYSA-N 2-chloro-3-cyano-N-[3-[1-(difluoromethyl)pyrazol-4-yl]-1H-indazol-5-yl]benzamide Chemical compound ClC1=C(C(=O)NC=2C=C3C(=NNC3=CC=2)C=2C=NN(C=2)C(F)F)C=CC=C1C#N QRYPKHSKJYBOIC-UHFFFAOYSA-N 0.000 claims 1
- LKGQWGUUIDVACL-UHFFFAOYSA-N 2-chloro-4-cyano-N-[3-(furan-3-yl)-1H-indazol-5-yl]benzamide Chemical compound ClC1=C(C(=O)NC=2C=C3C(=NNC3=CC=2)C2=COC=C2)C=CC(=C1)C#N LKGQWGUUIDVACL-UHFFFAOYSA-N 0.000 claims 1
- FWLUIXSQOWNPJG-UHFFFAOYSA-N 3-cyano-2-fluoro-N-[3-(1,3-oxazol-5-yl)-1H-indazol-5-yl]benzamide Chemical compound C(#N)C=1C(=C(C(=O)NC=2C=C3C(=NNC3=CC=2)C2=CN=CO2)C=CC=1)F FWLUIXSQOWNPJG-UHFFFAOYSA-N 0.000 claims 1
- UUUZFSVCVFBPJS-UHFFFAOYSA-N 3-cyano-2-methoxy-6-methyl-N-[3-(1,3-oxazol-5-yl)-1H-indazol-5-yl]benzamide Chemical compound C(#N)C=1C(=C(C(=O)NC=2C=C3C(=NNC3=CC=2)C2=CN=CO2)C(=CC=1)C)OC UUUZFSVCVFBPJS-UHFFFAOYSA-N 0.000 claims 1
- PWVXDVNDYOAENK-UHFFFAOYSA-N 3-cyano-N-(3-methyl-2H-indazol-5-yl)-2-prop-1-en-2-ylbenzamide Chemical compound C(#N)C=1C(=C(C(=O)NC=2C=C3C(=NNC3=CC=2)C)C=CC=1)C(=C)C PWVXDVNDYOAENK-UHFFFAOYSA-N 0.000 claims 1
- SSRAFCOONRWALQ-UHFFFAOYSA-N 4-cyano-N-[3-(1,2-oxazol-4-yl)-1H-indazol-5-yl]-6,7-dihydro-5H-cyclopenta[c]pyridine-1-carboxamide Chemical compound C(#N)C=1C2=C(C(=NC=1)C(=O)NC=1C=C3C(=NNC3=CC=1)C=1C=NOC=1)CCC2 SSRAFCOONRWALQ-UHFFFAOYSA-N 0.000 claims 1
- OVRXATQVCJVGHY-UHFFFAOYSA-N 4-cyano-N-[3-[1-(difluoromethyl)pyrazol-4-yl]-1H-indazol-5-yl]-2-fluoro-6-methylbenzamide Chemical compound C(#N)C1=CC(=C(C(=O)NC=2C=C3C(=NNC3=CC=2)C=2C=NN(C=2)C(F)F)C(=C1)C)F OVRXATQVCJVGHY-UHFFFAOYSA-N 0.000 claims 1
- RNZCEENXXQWMHR-UHFFFAOYSA-N 5-cyano-1,2-dimethyl-N-(3-phenyl-1H-indazol-5-yl)pyrrole-3-carboxamide Chemical compound C(#N)C1=CC(=C(N1C)C)C(=O)NC=1C=C2C(=NNC2=CC=1)C1=CC=CC=C1 RNZCEENXXQWMHR-UHFFFAOYSA-N 0.000 claims 1
- BVOJEHFDSONNPM-UHFFFAOYSA-N 5-cyano-3,4-dimethyl-N-[3-(1,3-oxazol-2-yl)-1H-indazol-5-yl]pyridine-2-carboxamide Chemical compound C(#N)C=1C(=C(C(=NC=1)C(=O)NC=1C=C2C(=NNC2=CC=1)C=1OC=CN=1)C)C BVOJEHFDSONNPM-UHFFFAOYSA-N 0.000 claims 1
- HWDLFPXGGZPQCR-UHFFFAOYSA-N 5-cyano-3,4-dimethyl-N-[3-(1-methylpyrrol-3-yl)-1H-indazol-5-yl]pyridine-2-carboxamide Chemical compound C(#N)C=1C(=C(C(=NC=1)C(=O)NC=1C=C2C(=NNC2=CC=1)C1=CN(C=C1)C)C)C HWDLFPXGGZPQCR-UHFFFAOYSA-N 0.000 claims 1
- YZIWRQXQMMGTDJ-AATRIKPKSA-N 5-cyano-3,4-dimethyl-N-[3-[(E)-3,3,3-trifluoroprop-1-enyl]-2H-indazol-5-yl]pyridine-2-carboxamide Chemical compound C(#N)C=1C(=C(C(=NC=1)C(=O)NC=1C=C2C(=NNC2=CC=1)\C=C\C(F)(F)F)C)C YZIWRQXQMMGTDJ-AATRIKPKSA-N 0.000 claims 1
- MZPBNIBVEOXKSD-UHFFFAOYSA-N 5-cyano-3,4-dimethyl-N-[3-[1-(1-methylpiperidin-4-yl)pyrazol-4-yl]-1H-indazol-5-yl]pyridine-2-carboxamide Chemical compound C(#N)C=1C(=C(C(=NC=1)C(=O)NC=1C=C2C(=NNC2=CC=1)C=1C=NN(C=1)C1CCN(CC1)C)C)C MZPBNIBVEOXKSD-UHFFFAOYSA-N 0.000 claims 1
- ZHBXZLDCPAEZOH-UHFFFAOYSA-N 5-cyano-3,4-dimethyl-N-[3-[2-(trifluoromethyl)cyclopropyl]-2H-indazol-5-yl]pyridine-2-carboxamide Chemical compound C(#N)C=1C(=C(C(=NC=1)C(=O)NC=1C=C2C(=NNC2=CC=1)C1C(C1)C(F)(F)F)C)C ZHBXZLDCPAEZOH-UHFFFAOYSA-N 0.000 claims 1
- RIDLMEWGSNXREA-UHFFFAOYSA-N 5-cyano-3-fluoro-N-[3-(furan-3-yl)-1H-indazol-5-yl]pyridine-2-carboxamide Chemical compound C(#N)C=1C=C(C(=NC=1)C(=O)NC=1C=C2C(=NNC2=CC=1)C1=COC=C1)F RIDLMEWGSNXREA-UHFFFAOYSA-N 0.000 claims 1
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Classifications
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- A61P25/00—Drugs for disorders of the nervous system
- A61P25/14—Drugs for disorders of the nervous system for treating abnormal movements, e.g. chorea, dyskinesia
- A61P25/16—Anti-Parkinson drugs
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a chain containing hetero atoms as chain links
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- A—HUMAN NECESSITIES
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- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
- A61K31/415—1,2-Diazoles
- A61K31/416—1,2-Diazoles condensed with carbocyclic ring systems, e.g. indazole
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- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/4427—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
- A61K31/4439—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. omeprazole
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- A61P25/28—Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
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- C07D—HETEROCYCLIC COMPOUNDS
- C07D231/00—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
- C07D231/54—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings condensed with carbocyclic rings or ring systems
- C07D231/56—Benzopyrazoles; Hydrogenated benzopyrazoles
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/04—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
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- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
- C07D403/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—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
- C07D405/02—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
- C07D405/04—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 directly linked by a ring-member-to-ring-member bond
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—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
- C07D405/02—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
- 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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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—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
- C07D405/14—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 three or more hetero rings
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
- C07D409/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing three or more hetero rings
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing three or more hetero rings
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—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
- C07D417/14—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 three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
- C07D487/04—Ortho-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D495/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms
- C07D495/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
- C07D495/04—Ortho-condensed systems
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Neurosurgery (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
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- Animal Behavior & Ethology (AREA)
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- Chemical Kinetics & Catalysis (AREA)
- Psychology (AREA)
- Epidemiology (AREA)
- Psychiatry (AREA)
- Hospice & Palliative Care (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Plural Heterocyclic Compounds (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
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| US201962872891P | 2019-07-11 | 2019-07-11 | |
| US62/872,891 | 2019-07-11 | ||
| US201962937979P | 2019-11-20 | 2019-11-20 | |
| US62/937,979 | 2019-11-20 | ||
| PCT/US2020/041506 WO2021007477A1 (en) | 2019-07-11 | 2020-07-10 | Indazoles and azaindazoles as lrrk2 inhibitors |
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| JP2022540200A true JP2022540200A (ja) | 2022-09-14 |
| JP2022540200A5 JP2022540200A5 (https=) | 2023-07-19 |
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| US12435084B2 (en) | 2020-04-09 | 2025-10-07 | Eli Lilly And Company | Indazole derivatives as inhibitors of SARM1 |
| WO2022155419A1 (en) * | 2021-01-15 | 2022-07-21 | ESCAPE Bio, Inc. | Indazoles and azaindazoles as lrrk2 inhibitors |
| WO2022271840A1 (en) * | 2021-06-22 | 2022-12-29 | The Board Of Trustees Of The Leland Stanford Junior University | Selective indazole lrrk2 inhibitors and methods for use thereof |
| WO2025000053A1 (en) * | 2023-06-28 | 2025-01-02 | Psylo Pty Ltd | Compounds |
| CN117186066B (zh) * | 2023-09-08 | 2025-07-22 | 中国药科大学 | 吲唑类alk5抑制剂及其制备方法与用途 |
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| JP3917662B2 (ja) | 1996-02-14 | 2007-05-23 | 日立化成工業株式会社 | 非複屈折性光学用樹脂組成物及びこれを用いた光学用素子 |
| EA002113B1 (ru) | 1996-09-04 | 2001-12-24 | Пфайзер Инк. | Производные индазола и их использование в качестве ингибиторов фосфодиэстеразы (фдэ) типа iv и продуцирования фактора некроза опухоли (фно) |
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| US6133290A (en) | 1998-07-31 | 2000-10-17 | Eli Lilly And Company | 5-HT1F agonists |
| US6995162B2 (en) | 2001-01-12 | 2006-02-07 | Amgen Inc. | Substituted alkylamine derivatives and methods of use |
| US20030134836A1 (en) | 2001-01-12 | 2003-07-17 | Amgen Inc. | Substituted arylamine derivatives and methods of use |
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- 2020-07-10 EP EP20746523.8A patent/EP3997081A1/en not_active Withdrawn
- 2020-07-10 KR KR1020227001361A patent/KR20220045954A/ko not_active Ceased
- 2020-07-10 JP JP2022501162A patent/JP2022540200A/ja active Pending
- 2020-07-10 WO PCT/US2020/041506 patent/WO2021007477A1/en not_active Ceased
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- 2020-07-10 MX MX2021015996A patent/MX2021015996A/es unknown
- 2020-07-10 TW TW109123468A patent/TW202116754A/zh unknown
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| EP3997081A1 (en) | 2022-05-18 |
| TW202116754A (zh) | 2021-05-01 |
| BR112022000325A2 (pt) | 2022-03-15 |
| US11427558B1 (en) | 2022-08-30 |
| MX2021015996A (es) | 2022-06-08 |
| CA3145305A1 (en) | 2021-01-14 |
| US20230077268A1 (en) | 2023-03-09 |
| IL288903A (en) | 2022-02-01 |
| KR20220045954A (ko) | 2022-04-13 |
| CN114450274A (zh) | 2022-05-06 |
| AU2020311940A1 (en) | 2022-02-03 |
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