JP7148518B2 - β－セクレターゼ阻害剤としての二環式チアジンおよびオキサジン誘導体ならびに使用方法 - Google Patents
β－セクレターゼ阻害剤としての二環式チアジンおよびオキサジン誘導体ならびに使用方法 Download PDFInfo
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- JP7148518B2 JP7148518B2 JP2019531734A JP2019531734A JP7148518B2 JP 7148518 B2 JP7148518 B2 JP 7148518B2 JP 2019531734 A JP2019531734 A JP 2019531734A JP 2019531734 A JP2019531734 A JP 2019531734A JP 7148518 B2 JP7148518 B2 JP 7148518B2
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- fluoro
- thiazin
- compound
- tautomer
- fluorophenyl
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- 238000000034 method Methods 0.000 title description 59
- AGIJRRREJXSQJR-UHFFFAOYSA-N 2h-thiazine Chemical compound N1SC=CC=C1 AGIJRRREJXSQJR-UHFFFAOYSA-N 0.000 title 1
- 239000002439 beta secretase inhibitor Substances 0.000 title 1
- 125000002619 bicyclic group Chemical group 0.000 title 1
- 150000004893 oxazines Chemical class 0.000 title 1
- 150000001875 compounds Chemical class 0.000 claims description 401
- 150000003839 salts Chemical class 0.000 claims description 103
- 238000002360 preparation method Methods 0.000 claims description 91
- -1 2-propynyloxy Chemical group 0.000 claims description 75
- 208000024827 Alzheimer disease Diseases 0.000 claims description 72
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 claims description 46
- 229920002554 vinyl polymer Polymers 0.000 claims description 46
- 125000000217 alkyl group Chemical group 0.000 claims description 42
- 239000008194 pharmaceutical composition Substances 0.000 claims description 36
- 210000004556 brain Anatomy 0.000 claims description 32
- QALHEGSMUNUVRR-IDUWFGFVSA-N 2-amino-7a-[2-fluoro-5-[(Z)-2-fluoro-2-(5-prop-2-ynoxypyrazin-2-yl)ethenyl]phenyl]-4,4a,5,7-tetrahydropyrrolo[3,4-d][1,3]thiazine-6-carboxylic acid Chemical compound NC1=NC2(CN(CC2CS1)C(O)=O)c1cc(\C=C(/F)c2cnc(OCC#C)cn2)ccc1F QALHEGSMUNUVRR-IDUWFGFVSA-N 0.000 claims description 31
- 206010012289 Dementia Diseases 0.000 claims description 31
- DZHSAHHDTRWUTF-SIQRNXPUSA-N amyloid-beta polypeptide 42 Chemical compound C([C@@H](C(=O)N[C@@H](C)C(=O)N[C@@H](CCC(O)=O)C(=O)N[C@@H](CC(O)=O)C(=O)N[C@H](C(=O)NCC(=O)N[C@@H](CO)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H](CCCCN)C(=O)NCC(=O)N[C@@H](C)C(=O)N[C@H](C(=O)N[C@@H]([C@@H](C)CC)C(=O)NCC(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCSC)C(=O)N[C@@H](C(C)C)C(=O)NCC(=O)NCC(=O)N[C@@H](C(C)C)C(=O)N[C@@H](C(C)C)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](C)C(O)=O)[C@@H](C)CC)C(C)C)NC(=O)[C@H](CC=1C=CC=CC=1)NC(=O)[C@@H](NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CC=1N=CNC=1)NC(=O)[C@H](CC=1N=CNC=1)NC(=O)[C@@H](NC(=O)[C@H](CCC(O)=O)NC(=O)[C@H](CC=1C=CC(O)=CC=1)NC(=O)CNC(=O)[C@H](CO)NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](CC=1N=CNC=1)NC(=O)[C@H](CCCNC(N)=N)NC(=O)[C@H](CC=1C=CC=CC=1)NC(=O)[C@H](CCC(O)=O)NC(=O)[C@H](C)NC(=O)[C@@H](N)CC(O)=O)C(C)C)C(C)C)C1=CC=CC=C1 DZHSAHHDTRWUTF-SIQRNXPUSA-N 0.000 claims description 26
- 210000001175 cerebrospinal fluid Anatomy 0.000 claims description 25
- 125000003545 alkoxy group Chemical group 0.000 claims description 23
- 208000010877 cognitive disease Diseases 0.000 claims description 23
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 claims description 23
- 239000003814 drug Substances 0.000 claims description 22
- 238000011282 treatment Methods 0.000 claims description 22
- 125000001424 substituent group Chemical group 0.000 claims description 21
- WADGHWKXQZVKFK-UHFFFAOYSA-N thiazin-2-amine Chemical compound NN1SC=CC=C1 WADGHWKXQZVKFK-UHFFFAOYSA-N 0.000 claims description 19
- 229910052736 halogen Inorganic materials 0.000 claims description 16
- 150000002367 halogens Chemical class 0.000 claims description 16
- 229910052739 hydrogen Inorganic materials 0.000 claims description 14
- 239000000546 pharmaceutical excipient Substances 0.000 claims description 14
- 208000005145 Cerebral amyloid angiopathy Diseases 0.000 claims description 13
- 208000027061 mild cognitive impairment Diseases 0.000 claims description 13
- BCOHSRWZBPAAFJ-XOYQDKGISA-N 6-[(Z)-2-[3-[(4aR,5S,7aS)-2-amino-5-(trifluoromethyl)-4,4a,5,7-tetrahydrofuro[3,4-d][1,3]oxazin-7a-yl]-4-fluorophenyl]-1-fluoroethenyl]pyridine-3-carbonitrile Chemical compound NC=1OC[C@H]2[C@@](N=1)(CO[C@@H]2C(F)(F)F)C=1C=C(C=CC=1F)\C=C(/F)\C1=NC=C(C#N)C=C1 BCOHSRWZBPAAFJ-XOYQDKGISA-N 0.000 claims description 12
- GWEZIKZYIWTLEB-ANUQTDGMSA-N 6-[(Z)-2-[3-[(4aS,5S,7aS)-2-amino-5-(fluoromethyl)-4,4a,5,7-tetrahydrofuro[3,4-d][1,3]thiazin-7a-yl]-4-fluorophenyl]-1-fluoroethenyl]pyridine-3-carbonitrile Chemical compound NC=1SC[C@H]2[C@@](N=1)(CO[C@@H]2CF)C=1C=C(C=CC=1F)\C=C(/F)\C1=NC=C(C#N)C=C1 GWEZIKZYIWTLEB-ANUQTDGMSA-N 0.000 claims description 12
- 229910052799 carbon Inorganic materials 0.000 claims description 12
- 229910052731 fluorine Inorganic materials 0.000 claims description 10
- 230000007505 plaque formation Effects 0.000 claims description 10
- 230000009467 reduction Effects 0.000 claims description 10
- LEWBFBGKCXJOCQ-JDSUTPELSA-N (4aR,7aS)-7a-[2-fluoro-5-[(Z)-2-fluoro-2-(5-methoxypyrazin-2-yl)ethenyl]phenyl]-6-(5-fluoropyrimidin-2-yl)-4,4a,5,7-tetrahydropyrrolo[3,4-d][1,3]thiazin-2-amine Chemical compound FC1=C(C=C(C=C1)\C=C(\C1=NC=C(N=C1)OC)/F)[C@@]12N=C(SC[C@@H]1CN(C2)C1=NC=C(C=N1)F)N LEWBFBGKCXJOCQ-JDSUTPELSA-N 0.000 claims description 9
- QWWBKEHWUIMNGN-IRHUPWNQSA-N (4aR,7aS)-7a-[5-[(Z)-2-(5-chloropyridin-2-yl)-2-fluoroethenyl]-2-fluorophenyl]-6-(5-fluoropyrimidin-2-yl)-4,4a,5,7-tetrahydropyrrolo[3,4-d][1,3]thiazin-2-amine Chemical compound NC1=N[C@]2(CN(C[C@H]2CS1)C1=NC=C(F)C=N1)C1=C(F)C=CC(\C=C(/F)C2=NC=C(Cl)C=C2)=C1 QWWBKEHWUIMNGN-IRHUPWNQSA-N 0.000 claims description 9
- QWWBKEHWUIMNGN-XBWNKMOUSA-N (4aS,7aR)-7a-[5-[(Z)-2-(5-chloropyridin-2-yl)-2-fluoroethenyl]-2-fluorophenyl]-6-(5-fluoropyrimidin-2-yl)-4,4a,5,7-tetrahydropyrrolo[3,4-d][1,3]thiazin-2-amine Chemical compound NC1=N[C@@]2(CN(C[C@@H]2CS1)C1=NC=C(F)C=N1)C1=C(F)C=CC(\C=C(/F)C2=NC=C(Cl)C=C2)=C1 QWWBKEHWUIMNGN-XBWNKMOUSA-N 0.000 claims description 9
- WHIUBCKUVNJKKI-LETVZAPESA-N 6-[(Z)-2-[3-[(4aS,5S,7aS)-2-amino-5-(difluoromethyl)-4,4a,5,7-tetrahydrofuro[3,4-d][1,3]thiazin-7a-yl]-4-fluorophenyl]-1-fluoroethenyl]pyridine-3-carbonitrile Chemical compound NC=1SC[C@H]2[C@@](N=1)(CO[C@@H]2C(F)F)C=1C=C(C=CC=1F)\C=C(/F)\C1=NC=C(C#N)C=C1 WHIUBCKUVNJKKI-LETVZAPESA-N 0.000 claims description 9
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims description 9
- 125000004307 pyrazin-2-yl group Chemical group [H]C1=C([H])N=C(*)C([H])=N1 0.000 claims description 9
- 125000003373 pyrazinyl group Chemical group 0.000 claims description 9
- 125000004076 pyridyl group Chemical group 0.000 claims description 9
- YVNTYZHIQCBZIN-XKMNTDACSA-N (4aS,5S,7aS)-7a-[2-fluoro-5-[(Z)-2-fluoro-2-[5-(trifluoromethoxy)pyridin-2-yl]ethenyl]phenyl]-5-(trifluoromethyl)-4,4a,5,7-tetrahydrofuro[3,4-d][1,3]thiazin-2-amine Chemical compound NC1=N[C@]2(CO[C@@H]([C@H]2CS1)C(F)(F)F)C1=C(F)C=CC(\C=C(/F)C2=NC=C(OC(F)(F)F)C=C2)=C1 YVNTYZHIQCBZIN-XKMNTDACSA-N 0.000 claims description 8
- ZOLASYMXTWTSAU-AIELCWNPSA-N 6-[(Z)-2-[3-[(4aR,7aS)-2-amino-6-(5-fluoro-4-methoxy-6-methylpyrimidin-2-yl)-4,4a,5,7-tetrahydropyrrolo[3,4-d][1,3]thiazin-7a-yl]-4-fluorophenyl]-1-fluoroethenyl]pyridine-3-carbonitrile Chemical compound COC1=C(F)C(C)=NC(=N1)N1C[C@H]2CSC(N)=N[C@]2(C1)C1=C(F)C=CC(\C=C(/F)C2=CC=C(C=N2)C#N)=C1 ZOLASYMXTWTSAU-AIELCWNPSA-N 0.000 claims description 8
- BCOHSRWZBPAAFJ-YIHKTLQQSA-N 6-[(Z)-2-[3-[(4aS,5R,7aR)-2-amino-5-(trifluoromethyl)-4,4a,5,7-tetrahydrofuro[3,4-d][1,3]oxazin-7a-yl]-4-fluorophenyl]-1-fluoroethenyl]pyridine-3-carbonitrile Chemical compound NC=1OC[C@@H]2[C@](N=1)(CO[C@H]2C(F)(F)F)C=1C=C(C=CC=1F)\C=C(/F)\C1=NC=C(C#N)C=C1 BCOHSRWZBPAAFJ-YIHKTLQQSA-N 0.000 claims description 8
- WYLKDBUCNHBXCP-XOYQDKGISA-N 6-[(Z)-2-[3-[(4aS,5S,7aS)-2-amino-5-(trifluoromethyl)-4,4a,5,7-tetrahydrofuro[3,4-d][1,3]thiazin-7a-yl]-4-fluorophenyl]-1-fluoroethenyl]pyridine-3-carbonitrile Chemical compound NC1=N[C@]2(CO[C@@H]([C@H]2CS1)C(F)(F)F)c1cc(\C=C(/F)c2ccc(cn2)C#N)ccc1F WYLKDBUCNHBXCP-XOYQDKGISA-N 0.000 claims description 8
- 208000028698 Cognitive impairment Diseases 0.000 claims description 8
- 201000010374 Down Syndrome Diseases 0.000 claims description 8
- 208000012902 Nervous system disease Diseases 0.000 claims description 8
- 206010044688 Trisomy 21 Diseases 0.000 claims description 8
- 125000001072 heteroaryl group Chemical group 0.000 claims description 8
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims description 8
- GKKLJUXLRFAZSA-NZEFLHGSSA-N (4aR,7aS)-7a-[2-fluoro-5-[(Z)-2-fluoro-2-[5-(2,2,3,3-tetrafluoropropoxy)pyrazin-2-yl]ethenyl]phenyl]-6-(5-fluoropyrimidin-2-yl)-4,4a,5,7-tetrahydropyrrolo[3,4-d][1,3]thiazin-2-amine Chemical compound FC1=C(C=C(C=C1)\C=C(\C1=NC=C(N=C1)OCC(C(F)F)(F)F)/F)[C@@]12N=C(SC[C@@H]1CN(C2)C1=NC=C(C=N1)F)N GKKLJUXLRFAZSA-NZEFLHGSSA-N 0.000 claims description 7
- OHBAMRDCYITIKZ-ZAULRJFKSA-N (4aR,7aS)-7a-[5-[(Z)-2-(5-but-2-ynoxypyrazin-2-yl)-2-fluoroethenyl]-2-fluorophenyl]-6-(5-fluoropyrimidin-2-yl)-4,4a,5,7-tetrahydropyrrolo[3,4-d][1,3]thiazin-2-amine Chemical compound CC#CCOC1=NC=C(N=C1)C(\F)=C\C1=CC(=C(F)C=C1)[C@]12CN(C[C@H]1CSC(N)=N2)C1=NC=C(F)C=N1 OHBAMRDCYITIKZ-ZAULRJFKSA-N 0.000 claims description 7
- OCOWEWOMRYUXLY-NZEFLHGSSA-N (4aR,7aS)-7a-[5-[(Z)-2-[5-(2,2-difluoroethoxy)pyrazin-2-yl]-2-fluoroethenyl]-2-fluorophenyl]-6-(5-fluoropyrimidin-2-yl)-4,4a,5,7-tetrahydropyrrolo[3,4-d][1,3]thiazin-2-amine Chemical compound NC1=N[C@]2(CN(C[C@H]2CS1)C1=NC=C(F)C=N1)C1=C(F)C=CC(\C=C(/F)C2=CN=C(OCC(F)F)C=N2)=C1 OCOWEWOMRYUXLY-NZEFLHGSSA-N 0.000 claims description 7
- JXIRZJRQKBJGGS-QDKFJWRJSA-N (4aR,7aS)-7a-[5-[(Z)-2-[5-[(2S)-but-3-yn-2-yl]oxypyrazin-2-yl]-2-fluoroethenyl]-2-fluorophenyl]-6-(5-fluoropyrimidin-2-yl)-4,4a,5,7-tetrahydropyrrolo[3,4-d][1,3]thiazin-2-amine Chemical compound C[C@H](OC1=NC=C(N=C1)C(\F)=C\C1=CC(=C(F)C=C1)[C@]12CN(C[C@H]1CSC(N)=N2)C1=NC=C(F)C=N1)C#C JXIRZJRQKBJGGS-QDKFJWRJSA-N 0.000 claims description 7
- KRDTZIZUJNTCAC-PFXPYRGJSA-N (4aS,5S,7aS)-7a-[2-fluoro-5-[(Z)-2-fluoro-2-(5-methoxypyrazin-2-yl)ethenyl]phenyl]-5-(trifluoromethyl)-4,4a,5,7-tetrahydrofuro[3,4-d][1,3]thiazin-2-amine Chemical compound COC1=NC=C(N=C1)C(\F)=C\C1=CC(=C(F)C=C1)[C@]12CO[C@@H]([C@H]1CSC(N)=N2)C(F)(F)F KRDTZIZUJNTCAC-PFXPYRGJSA-N 0.000 claims description 7
- ZIKMCSQBXXNAMM-CUWGKCGESA-N (4aS,5S,7aS)-7a-[2-fluoro-5-[(Z)-2-fluoro-2-(5-prop-2-ynoxypyrazin-2-yl)ethenyl]phenyl]-5-(trifluoromethyl)-4,4a,5,7-tetrahydrofuro[3,4-d][1,3]thiazin-2-amine Chemical compound NC1=N[C@]2(CO[C@@H]([C@H]2CS1)C(F)(F)F)C1=C(F)C=CC(\C=C(/F)C2=CN=C(OCC#C)C=N2)=C1 ZIKMCSQBXXNAMM-CUWGKCGESA-N 0.000 claims description 7
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- NVNVYXHMZVSSEQ-WUXFZBHOSA-N (4aS,5S,7aS)-7a-[5-[(Z)-2-[3-chloro-5-(trifluoromethyl)pyridin-2-yl]-2-fluoroethenyl]-2-fluorophenyl]-5-(trifluoromethyl)-4,4a,5,7-tetrahydrofuro[3,4-d][1,3]thiazin-2-amine Chemical compound NC1=N[C@]2(CO[C@@H]([C@H]2CS1)C(F)(F)F)c1cc(\C=C(/F)c2ncc(cc2Cl)C(F)(F)F)ccc1F NVNVYXHMZVSSEQ-WUXFZBHOSA-N 0.000 claims description 7
- YIQUYGRGOCRWFL-QFMRXCROSA-N 5-[(Z)-2-[3-[(4aR,7aS)-2-amino-6-(5-fluoropyrimidin-2-yl)-4,4a,5,7-tetrahydropyrrolo[3,4-d][1,3]thiazin-7a-yl]-4-fluorophenyl]-1-fluoroethenyl]pyrazine-2-carbonitrile Chemical compound NC1=N[C@]2(CN(C[C@H]2CS1)C1=NC=C(F)C=N1)C1=C(F)C=CC(\C=C(/F)C2=NC=C(N=C2)C#N)=C1 YIQUYGRGOCRWFL-QFMRXCROSA-N 0.000 claims description 7
- BUJQZBNDSOLLBU-QFWLKESYSA-N 5-[(Z)-2-[3-[(4aS,5S,7aS)-2-amino-5-(trifluoromethyl)-4,4a,5,7-tetrahydrofuro[3,4-d][1,3]thiazin-7a-yl]-4-fluorophenyl]-1-fluoroethenyl]pyrazine-2-carbonitrile Chemical compound NC1=N[C@]2(CO[C@@H]([C@H]2CS1)C(F)(F)F)C1=C(F)C=CC(\C=C(/F)C2=NC=C(N=C2)C#N)=C1 BUJQZBNDSOLLBU-QFWLKESYSA-N 0.000 claims description 7
- GWEZIKZYIWTLEB-WJDPGPTFSA-N 6-[(Z)-2-[3-[(4aR,5R,7aR)-2-amino-5-(fluoromethyl)-4,4a,5,7-tetrahydrofuro[3,4-d][1,3]thiazin-7a-yl]-4-fluorophenyl]-1-fluoroethenyl]pyridine-3-carbonitrile Chemical compound NC1=N[C@@]2(CO[C@@H](CF)[C@@H]2CS1)C1=C(F)C=CC(\C=C(/F)C2=CC=C(C=N2)C#N)=C1 GWEZIKZYIWTLEB-WJDPGPTFSA-N 0.000 claims description 7
- WYLKDBUCNHBXCP-YIHKTLQQSA-N 6-[(Z)-2-[3-[(4aR,5R,7aR)-2-amino-5-(trifluoromethyl)-4,4a,5,7-tetrahydrofuro[3,4-d][1,3]thiazin-7a-yl]-4-fluorophenyl]-1-fluoroethenyl]pyridine-3-carbonitrile Chemical compound NC1=N[C@@]2(CO[C@H]([C@@H]2CS1)C(F)(F)F)c1cc(\C=C(/F)c2ccc(cn2)C#N)ccc1F WYLKDBUCNHBXCP-YIHKTLQQSA-N 0.000 claims description 7
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- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D513/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00
- C07D513/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00 in which the condensed system contains two hetero rings
- C07D513/04—Ortho-condensed systems
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D498/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D498/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
- C07D498/04—Ortho-condensed systems
Landscapes
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Neurosurgery (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Biomedical Technology (AREA)
- Neurology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Life Sciences & Earth Sciences (AREA)
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- General Health & Medical Sciences (AREA)
- Psychiatry (AREA)
- Hospice & Palliative Care (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen- Or Sulfur-Containing Heterocyclic Ring Compounds With Rings Of Six Or More Members (AREA)
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| PCT/US2017/066180 WO2018112084A1 (en) | 2016-12-15 | 2017-12-13 | Bicyclic thiazine and oxazine derivatives as beta-secretase inhibitors and methods of use |
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| US8999980B2 (en) † | 2009-12-11 | 2015-04-07 | Shionogi & Co., Ltd. | Oxazine derivatives |
| US11548903B2 (en) | 2016-12-15 | 2023-01-10 | Amgen Inc. | Bicyclic thiazine and oxazine derivatives as beta-secretase inhibitors and methods of use |
| EP3555084B1 (en) | 2016-12-15 | 2022-03-16 | Amgen Inc. | Thiazine derivatives as beta-secretase inhibitors and methods of use |
| AU2017376446B2 (en) | 2016-12-15 | 2021-10-14 | Amgen Inc. | 1,4-thiazine dioxide and 1,2,4-thiadiazine dioxide derivatives as beta-secretase inhibitors and methods of use |
| AU2017378316B2 (en) | 2016-12-15 | 2021-04-01 | Amgen Inc. | Cyclopropyl fused thiazine derivatives as beta-secretase inhibitors and methods of use |
Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
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| WO2010038686A1 (ja) | 2008-09-30 | 2010-04-08 | エーザイ・アール・アンド・ディー・マネジメント株式会社 | 新規な縮合アミノジヒドロチアジン誘導体 |
| JP2012533603A (ja) | 2009-07-22 | 2012-12-27 | エーザイ・アール・アンド・ディー・マネジメント株式会社 | 縮合アミノジヒドロ−オキサジン誘導体 |
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| US5441870A (en) | 1992-04-15 | 1995-08-15 | Athena Neurosciences, Inc. | Methods for monitoring cellular processing of β-amyloid precursor protein |
| SI9300303A (en) | 1993-06-08 | 1994-12-31 | Krka Tovarna Zdravil | Process for isolation of hypolipemic effective substance |
| EP0871720A2 (en) | 1995-06-07 | 1998-10-21 | Athena Neurosciences, Inc. | Beta-secretase, antibodies to beta-secretase, and assays for detecting beta-secretase inhibition |
| EP1115874B1 (en) | 1998-09-24 | 2009-01-07 | Pharmacia & Upjohn Company LLC | Alzheimer's disease secretase |
| KR101052122B1 (ko) | 2005-10-25 | 2011-07-26 | 시오노기세야쿠 가부시키가이샤 | 아미노디히드로티아진 유도체 |
| MX2009011498A (es) | 2007-04-24 | 2009-11-10 | Shionogi & Co | Derivados de aminodihidrotiazina sustituida con un grupo ciclico. |
| WO2008133273A1 (ja) | 2007-04-24 | 2008-11-06 | Shionogi & Co., Ltd. | アルツハイマー症治療用医薬組成物 |
| US20100317850A1 (en) | 2008-01-18 | 2010-12-16 | Yuichi Suzuki | Condensed aminodihydrothiazine derivative |
| TWI431004B (zh) | 2008-05-02 | 2014-03-21 | Lilly Co Eli | Ｂａｃｅ抑制劑 |
| AU2009258496B8 (en) | 2008-06-13 | 2014-06-26 | Shionogi & Co., Ltd. | Sulfur-containing heterocyclic derivative having beta-secretase-inhibiting activity |
| AU2009277485B2 (en) | 2008-07-28 | 2013-05-02 | Eisai R&D Management Co., Ltd. | Spiroaminodihydrothiazine derivatives |
| WO2010013302A1 (ja) | 2008-07-28 | 2010-02-04 | エーザイ・アール・アンド・ディー・マネジメント株式会社 | スピロアミノジヒドロチアジン誘導体 |
| AR077277A1 (es) | 2009-07-09 | 2011-08-17 | Lilly Co Eli | Compuestos de biciclo (1,3)tiazin-2-amina formulacion farmaceutica que lo comprende y su uso para la manufactura de un medicamento util para el tratamiento de la enfermedad de alzheimer |
| US20110065695A1 (en) | 2009-09-11 | 2011-03-17 | Jeremy Beauchamp | Use of aminodihydrothiazines for the treatment or prevention of diabetes |
| UA108363C2 (uk) | 2009-10-08 | 2015-04-27 | Похідні імінотіадіазиндіоксиду як інгібітори bace, композиція на їх основі і їх застосування | |
| US20120238557A1 (en) | 2009-11-13 | 2012-09-20 | Shionogi & Co., Ltd. | Aminothiazine or aminooxazine derivative having amino linker |
| WO2011070781A1 (ja) | 2009-12-09 | 2011-06-16 | 塩野義製薬株式会社 | 置換アミノチアジン誘導体 |
| US8999980B2 (en) | 2009-12-11 | 2015-04-07 | Shionogi & Co., Ltd. | Oxazine derivatives |
| UA103272C2 (uk) | 2009-12-11 | 2013-09-25 | Ф. Хоффманн-Ля Рош Аг | 2-аміно-5,5-дифтор-5,6-дигідро-4h-оксазини як інгібітори bace1 і/або bace2 |
| EA201391029A1 (ru) | 2011-01-12 | 2014-01-30 | Новартис Аг | Производные оксазина и их применение при лечении неврологических нарушений |
| KR101569260B1 (ko) | 2011-01-13 | 2015-11-13 | 노파르티스 아게 | 신규 헤테로시클릭 유도체 및 신경계 장애의 치료에서의 그의 용도 |
| GB201101140D0 (en) | 2011-01-21 | 2011-03-09 | Eisai Ltd | Fused aminodihydrothiazine derivatives |
| GB201101139D0 (en) | 2011-01-21 | 2011-03-09 | Eisai Ltd | Fused aminodihydrothiazine derivatives |
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| JP2020503293A (ja) * | 2016-12-15 | 2020-01-30 | アムジエン・インコーポレーテツド | β−セクレターゼ阻害剤としてのオキサジン誘導体および使用方法 |
| JP7177773B2 (ja) | 2016-12-15 | 2022-11-24 | アムジエン・インコーポレーテツド | β－セクレターゼ阻害剤としてのオキサジン誘導体および使用方法 |
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| JP2020503294A (ja) | 2020-01-30 |
| MX2019007100A (es) | 2019-12-16 |
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| CA3047285A1 (en) | 2018-06-21 |
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| EP3555106A1 (en) | 2019-10-23 |
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| MA54101A (fr) | 2021-10-27 |
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| US20200199153A1 (en) | 2020-06-25 |
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