JP5389905B2 - α−7ニコチン性アセチルコリン受容体リガンドとしてのキヌクリジン化合物 - Google Patents
α−7ニコチン性アセチルコリン受容体リガンドとしてのキヌクリジン化合物 Download PDFInfo
- Publication number
- JP5389905B2 JP5389905B2 JP2011506374A JP2011506374A JP5389905B2 JP 5389905 B2 JP5389905 B2 JP 5389905B2 JP 2011506374 A JP2011506374 A JP 2011506374A JP 2011506374 A JP2011506374 A JP 2011506374A JP 5389905 B2 JP5389905 B2 JP 5389905B2
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- JP
- Japan
- Prior art keywords
- mmol
- methyl
- amine
- pyrimidinyl
- octane
- 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.)
- Expired - Fee Related
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- 0 *NC1=NCC2(C(CC3)CCN3C2)O1 Chemical compound *NC1=NCC2(C(CC3)CCN3C2)O1 0.000 description 6
- SWSXXHXILWJNBY-KRWDZBQOSA-N Cc(cc1)cc2c1cnc(N/C(/O[C@@H]1C(CC3)CCN3C1)=N/C)c2 Chemical compound Cc(cc1)cc2c1cnc(N/C(/O[C@@H]1C(CC3)CCN3C1)=N/C)c2 SWSXXHXILWJNBY-KRWDZBQOSA-N 0.000 description 2
- ZGDMABRZZLIIIM-NSHDSACASA-N C/N=C(/Nc(cc1)nc(Cl)c1Cl)\O[C@@H]1C(CC2)CCN2C1 Chemical compound C/N=C(/Nc(cc1)nc(Cl)c1Cl)\O[C@@H]1C(CC2)CCN2C1 ZGDMABRZZLIIIM-NSHDSACASA-N 0.000 description 1
- ZLFBHBYXUCELQF-HNNXBMFYSA-N C/N=C(/Nc(cc1)nc2c1cncc2)\O[C@@H]1C(CC2)CCN2C1 Chemical compound C/N=C(/Nc(cc1)nc2c1cncc2)\O[C@@H]1C(CC2)CCN2C1 ZLFBHBYXUCELQF-HNNXBMFYSA-N 0.000 description 1
- HLRZGHGMGMZKEL-HNNXBMFYSA-N C/N=C(/Nc(nc1)nc(-c2cnccc2)c1Br)\O[C@@H]1C(CC2)CCN2C1 Chemical compound C/N=C(/Nc(nc1)nc(-c2cnccc2)c1Br)\O[C@@H]1C(CC2)CCN2C1 HLRZGHGMGMZKEL-HNNXBMFYSA-N 0.000 description 1
- UTZXQBGOSZRSMT-KRWDZBQOSA-N C/N=C(/Nc1cc(-c2cccnc2OC)ccn1)\O[C@@H]1C(CC2)CCN2C1 Chemical compound C/N=C(/Nc1cc(-c2cccnc2OC)ccn1)\O[C@@H]1C(CC2)CCN2C1 UTZXQBGOSZRSMT-KRWDZBQOSA-N 0.000 description 1
- KUVIMLPMUMDFCV-JTQLQIEISA-N C/N=C(/Nc1nc(c(OC)ncn2)c2[s]1)\O[C@@H]1C(CC2)CCN2C1 Chemical compound C/N=C(/Nc1nc(c(OC)ncn2)c2[s]1)\O[C@@H]1C(CC2)CCN2C1 KUVIMLPMUMDFCV-JTQLQIEISA-N 0.000 description 1
- ARXKQMOFRRPMFB-AWEZNQCLSA-N C/N=C(/Nc1ncc(N2CCCC2)nc1)\O[C@@H]1C(CC2)CCN2C1 Chemical compound C/N=C(/Nc1ncc(N2CCCC2)nc1)\O[C@@H]1C(CC2)CCN2C1 ARXKQMOFRRPMFB-AWEZNQCLSA-N 0.000 description 1
- UUKUVVDEABNKOV-NSHDSACASA-N C/N=C(/Nc1ncnc(SC)c1)\O[C@@H]1C(CC2)CCN2C1 Chemical compound C/N=C(/Nc1ncnc(SC)c1)\O[C@@H]1C(CC2)CCN2C1 UUKUVVDEABNKOV-NSHDSACASA-N 0.000 description 1
- KEEAZYDQOLFVOL-UHFFFAOYSA-N C1N=C(Nc2cccnc2)OC11C(CC2)CCN2C1 Chemical compound C1N=C(Nc2cccnc2)OC11C(CC2)CCN2C1 KEEAZYDQOLFVOL-UHFFFAOYSA-N 0.000 description 1
- LVWWSYBLTZWGDR-HNNXBMFYSA-N C1N=C(Nc2nnc3[n]2cccc3)O[C@@]11C(CC2)CCN2C1 Chemical compound C1N=C(Nc2nnc3[n]2cccc3)O[C@@]11C(CC2)CCN2C1 LVWWSYBLTZWGDR-HNNXBMFYSA-N 0.000 description 1
- WLYKLHKTDTYDLH-INIZCTEOSA-N CC(C)Oc1cc(NC2=NC[C@]3(C(CC4)CCN4C3)O2)ncn1 Chemical compound CC(C)Oc1cc(NC2=NC[C@]3(C(CC4)CCN4C3)O2)ncn1 WLYKLHKTDTYDLH-INIZCTEOSA-N 0.000 description 1
- ALXSIRQDCFMONG-HNNXBMFYSA-N CC(Nc(cc1)cc2c1nc(N/C(/O[C@@H]1C(CC3)CCN3C1)=N/C)[s]2)=O Chemical compound CC(Nc(cc1)cc2c1nc(N/C(/O[C@@H]1C(CC3)CCN3C1)=N/C)[s]2)=O ALXSIRQDCFMONG-HNNXBMFYSA-N 0.000 description 1
- DJEQZVQFEPKLOY-UHFFFAOYSA-N CCCCN(C)C Chemical compound CCCCN(C)C DJEQZVQFEPKLOY-UHFFFAOYSA-N 0.000 description 1
- YFTDVJGEFLMGSW-SECBINFHSA-N CCCC[C@H](CN)OCCNC Chemical compound CCCC[C@H](CN)OCCNC YFTDVJGEFLMGSW-SECBINFHSA-N 0.000 description 1
- VFWYAHMMJNOYRO-ICIURTGMSA-N CCCNC[C@@H](CN=[IH](C)N[I]1N[C@@H]2C=CC[C@H](C)C2N1)O Chemical compound CCCNC[C@@H](CN=[IH](C)N[I]1N[C@@H]2C=CC[C@H](C)C2N1)O VFWYAHMMJNOYRO-ICIURTGMSA-N 0.000 description 1
- XAFPGZLOVLGDRT-CFCGPWAMSA-N CCN(C1)[C@H](C2)C2[C@@H]1OCC Chemical compound CCN(C1)[C@H](C2)C2[C@@H]1OCC XAFPGZLOVLGDRT-CFCGPWAMSA-N 0.000 description 1
- QIFXAGNEEIACEB-UHFFFAOYSA-N CCNCCC(C)CN Chemical compound CCNCCC(C)CN QIFXAGNEEIACEB-UHFFFAOYSA-N 0.000 description 1
- RGUIBKYPRDGCTL-UHFFFAOYSA-N CCOC(NC(Nc(nc1)ccc1OC)=S)=O Chemical compound CCOC(NC(Nc(nc1)ccc1OC)=S)=O RGUIBKYPRDGCTL-UHFFFAOYSA-N 0.000 description 1
- FKZUMAMNRPWLKP-UHFFFAOYSA-N CCOC(Nc1nc2cnc(N(C)C)nc2[s]1)=O Chemical compound CCOC(Nc1nc2cnc(N(C)C)nc2[s]1)=O FKZUMAMNRPWLKP-UHFFFAOYSA-N 0.000 description 1
- RSAYOWHRLDBGBO-UHFFFAOYSA-N CCc1nnc(N=C(SC)SC)[o]1 Chemical compound CCc1nnc(N=C(SC)SC)[o]1 RSAYOWHRLDBGBO-UHFFFAOYSA-N 0.000 description 1
- KHPLUUNNXFOJKR-IHWYPQMZSA-N CN/C=C\CNC[N]#CS Chemical compound CN/C=C\CNC[N]#CS KHPLUUNNXFOJKR-IHWYPQMZSA-N 0.000 description 1
- AJKKVOSELKCXDM-PEHGTWAWSA-N CN1[C@@H](CCCCOCN)C1 Chemical compound CN1[C@@H](CCCCOCN)C1 AJKKVOSELKCXDM-PEHGTWAWSA-N 0.000 description 1
- TUWLYFAEAPMOJS-UHFFFAOYSA-N COCc1ncnc(O)c1 Chemical compound COCc1ncnc(O)c1 TUWLYFAEAPMOJS-UHFFFAOYSA-N 0.000 description 1
- YJZQFLXZZGZDKK-UHFFFAOYSA-N COc(cc1)cc(nc2)c1nc2NCc(c(OC)c1)ccc1OC Chemical compound COc(cc1)cc(nc2)c1nc2NCc(c(OC)c1)ccc1OC YJZQFLXZZGZDKK-UHFFFAOYSA-N 0.000 description 1
- MFDBYMJQLWCZKY-UHFFFAOYSA-N COc(nc1)ncc1-c1cc(N=C=S)ncn1 Chemical compound COc(nc1)ncc1-c1cc(N=C=S)ncn1 MFDBYMJQLWCZKY-UHFFFAOYSA-N 0.000 description 1
- KBFBGQUDRKPWIP-UHFFFAOYSA-N COc1cc2nc(N=C=S)cnc2cc1 Chemical compound COc1cc2nc(N=C=S)cnc2cc1 KBFBGQUDRKPWIP-UHFFFAOYSA-N 0.000 description 1
- ACSARTICULWGBY-UHFFFAOYSA-N CSC(SC)=Nc1n[n](ccnc2)c2n1 Chemical compound CSC(SC)=Nc1n[n](ccnc2)c2n1 ACSARTICULWGBY-UHFFFAOYSA-N 0.000 description 1
- FAMZBJTVMUQZHO-CAWKVTGQSA-N C[C@H]([C@H](C)/C1=N/CCCNCCNC)C2=C[C@H]2C[C@H]1N Chemical compound C[C@H]([C@H](C)/C1=N/CCCNCCNC)C2=C[C@H]2C[C@H]1N FAMZBJTVMUQZHO-CAWKVTGQSA-N 0.000 description 1
- CCTVXOHNMVDSII-HNNXBMFYSA-N Cc1cc(N/C(/O[C@@H]2C(CC3)CCN3C2)=N/C)nc(C)c1C#N Chemical compound Cc1cc(N/C(/O[C@@H]2C(CC3)CCN3C2)=N/C)nc(C)c1C#N CCTVXOHNMVDSII-HNNXBMFYSA-N 0.000 description 1
- WTTQQWHDRLGJSP-UHFFFAOYSA-N Cc1nc(N=C=S)ccc1C#N Chemical compound Cc1nc(N=C=S)ccc1C#N WTTQQWHDRLGJSP-UHFFFAOYSA-N 0.000 description 1
- RHTUMZMNPADJLE-AWEZNQCLSA-N Clc1cccc(NC2=NC[C@]3(C(CC4)CCN4C3)O2)n1 Chemical compound Clc1cccc(NC2=NC[C@]3(C(CC4)CCN4C3)O2)n1 RHTUMZMNPADJLE-AWEZNQCLSA-N 0.000 description 1
- PUXOOQNLQPZQFB-UHFFFAOYSA-N Nc([s]c1c2)nc1ccc2OC(F)F Chemical compound Nc([s]c1c2)nc1ccc2OC(F)F PUXOOQNLQPZQFB-UHFFFAOYSA-N 0.000 description 1
- VZKIMVYWEBBKGS-UHFFFAOYSA-N Nc([s]c1n2)nc1ccc2OCc1ccccc1 Chemical compound Nc([s]c1n2)nc1ccc2OCc1ccccc1 VZKIMVYWEBBKGS-UHFFFAOYSA-N 0.000 description 1
- ILDRNIDSVAZBMZ-UHFFFAOYSA-N Nc1cnc(C(F)(F)F)cn1 Chemical compound Nc1cnc(C(F)(F)F)cn1 ILDRNIDSVAZBMZ-UHFFFAOYSA-N 0.000 description 1
- UUYSQAYUTMLLBO-UHFFFAOYSA-N Nc1n[n](ccnc2)c2n1 Chemical compound Nc1n[n](ccnc2)c2n1 UUYSQAYUTMLLBO-UHFFFAOYSA-N 0.000 description 1
- DKHLVVSSFRDDKS-UHFFFAOYSA-N S=C=Nc(ncc(Cl)c1)c1Cl Chemical compound S=C=Nc(ncc(Cl)c1)c1Cl DKHLVVSSFRDDKS-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- 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
- C07D498/12—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 three hetero rings
- C07D498/20—Spiro-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
- A61P25/18—Antipsychotics, i.e. neuroleptics; Drugs for mania or schizophrenia
-
- 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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D519/00—Heterocyclic compounds containing more than one system of two or more relevant hetero rings condensed among themselves or condensed with a common carbocyclic ring system not provided for in groups C07D453/00 or C07D455/00
Landscapes
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Public Health (AREA)
- Medicinal Chemistry (AREA)
- Neurosurgery (AREA)
- Biomedical Technology (AREA)
- Neurology (AREA)
- Psychiatry (AREA)
- Hospice & Palliative Care (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Pyridine Compounds (AREA)
Applications Claiming Priority (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US4721108P | 2008-04-23 | 2008-04-23 | |
| US61/047,211 | 2008-04-23 | ||
| US12/423,299 US7863291B2 (en) | 2008-04-23 | 2009-04-14 | Quinuclidine compounds as alpha-7 nicotinic acetylcholine receptor ligands |
| US12/423,299 | 2009-04-14 | ||
| PCT/US2009/041076 WO2009131926A1 (en) | 2008-04-23 | 2009-04-20 | Quinuclidine compounds as alpha-7 nicotinic acetylcholine receptor ligands |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2011518831A JP2011518831A (ja) | 2011-06-30 |
| JP2011518831A5 JP2011518831A5 (enExample) | 2012-05-17 |
| JP5389905B2 true JP5389905B2 (ja) | 2014-01-15 |
Family
ID=41215599
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2011506374A Expired - Fee Related JP5389905B2 (ja) | 2008-04-23 | 2009-04-20 | α−7ニコチン性アセチルコリン受容体リガンドとしてのキヌクリジン化合物 |
Country Status (27)
| Country | Link |
|---|---|
| US (1) | US7863291B2 (enExample) |
| EP (1) | EP2271650B1 (enExample) |
| JP (1) | JP5389905B2 (enExample) |
| KR (1) | KR20110015565A (enExample) |
| CN (1) | CN102066384B (enExample) |
| AR (1) | AR071215A1 (enExample) |
| AU (1) | AU2009239575B2 (enExample) |
| BR (1) | BRPI0911542A2 (enExample) |
| CA (1) | CA2722325A1 (enExample) |
| CL (1) | CL2009000975A1 (enExample) |
| CO (1) | CO6300941A2 (enExample) |
| CY (1) | CY1117045T1 (enExample) |
| DK (1) | DK2271650T3 (enExample) |
| EA (1) | EA017628B1 (enExample) |
| ES (1) | ES2553753T3 (enExample) |
| HR (1) | HRP20151111T1 (enExample) |
| HU (1) | HUE028302T2 (enExample) |
| IL (1) | IL208673A (enExample) |
| MX (1) | MX2010011374A (enExample) |
| NZ (1) | NZ588649A (enExample) |
| PE (1) | PE20091977A1 (enExample) |
| PL (1) | PL2271650T3 (enExample) |
| PT (1) | PT2271650E (enExample) |
| SI (1) | SI2271650T1 (enExample) |
| TW (1) | TWI431007B (enExample) |
| WO (1) | WO2009131926A1 (enExample) |
| ZA (1) | ZA201007527B (enExample) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2013509405A (ja) * | 2009-10-29 | 2013-03-14 | ブリストル−マイヤーズ スクイブ カンパニー | α7ニコチン性アセチルコリン受容体リガンドとしてのキヌクリジン化合物 |
Families Citing this family (85)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US8309577B2 (en) * | 2008-04-23 | 2012-11-13 | Bristol-Myers Squibb Company | Quinuclidine compounds as α-7 nicotinic acetylcholine receptor ligands |
| PL2280973T3 (pl) | 2008-04-23 | 2013-05-31 | Gilead Sciences Inc | Analogi karba-nukleozydowe do leczenia przeciwwirusowego |
| BRPI0916576A2 (pt) * | 2008-08-04 | 2017-06-27 | Chdi Inc | pelo menos uma entidade química, composição farmacêutica, e, método para tratar uma condição ou distúrbio. |
| TWI453207B (zh) * | 2008-09-08 | 2014-09-21 | Signal Pharm Llc | 胺基三唑并吡啶,其組合物及使用其之治療方法 |
| NZ599404A (en) | 2009-09-21 | 2014-02-28 | Gilead Sciences Inc | Processes and intermediates for the preparation of 1’-substituted carba-nucleoside analogs |
| US8278320B2 (en) * | 2009-10-28 | 2012-10-02 | Bristol-Myers Squibb Company | Azabicyclo[2.2.1]heptane compounds as alpha-7 nicotinic acetylcholine receptor ligands |
| US8507516B2 (en) | 2009-10-28 | 2013-08-13 | Bristol-Myers Squibb Company | Azabicyclic compounds as alpha-7 nicotinic acetylcholine receptor ligands |
| TWI544926B (zh) | 2010-01-14 | 2016-08-11 | 賽諾菲阿凡提斯公司 | 2,5-經取代之唑并嘧啶衍生物類 |
| CN103025744A (zh) * | 2010-04-30 | 2013-04-03 | 百时美施贵宝公司 | 作为α-7烟碱乙酰胆碱受体配体前药的氮杂二环胺N-氧化物化合物 |
| JP5744021B2 (ja) | 2010-06-30 | 2015-07-01 | 富士フイルム株式会社 | 新規なニコチンアミド誘導体またはその塩 |
| EA025311B1 (ru) | 2010-07-19 | 2016-12-30 | Гайлид Сайэнсиз, Инк. | Способы получения диастереомерно чистых фосфорамидатных пролекарств |
| PT2595980E (pt) | 2010-07-22 | 2014-11-27 | Gilead Sciences Inc | Métodos e compostos para tratar infeções pelo vírus da família paramyxoviridae |
| WO2012088266A2 (en) | 2010-12-22 | 2012-06-28 | Incyte Corporation | Substituted imidazopyridazines and benzimidazoles as inhibitors of fgfr3 |
| US9056877B2 (en) | 2011-07-19 | 2015-06-16 | Infinity Pharmaceuticals, Inc. | Heterocyclic compounds and uses thereof |
| SG2014012926A (en) | 2011-08-30 | 2014-06-27 | Chdi Foundation Inc | Kynurenine-3-monooxygenase inhibitors, pharmaceutical compositions, and methods of use thereof |
| KR102066297B1 (ko) | 2011-10-14 | 2020-01-14 | 암비트 바이오사이언시즈 코포레이션 | 헤테로사이클릭 화합물 및 이의 유형 3 수용체 티로신 키나아제의 조절인자로서의 용도 |
| AR090037A1 (es) | 2011-11-15 | 2014-10-15 | Xention Ltd | Derivados de tieno y/o furo-pirimidinas y piridinas inhibidores de los canales de potasio |
| US9458179B2 (en) | 2012-05-24 | 2016-10-04 | Bristol-Myers Squibb Company | Quinuclidine, 1-azabicyclo[2.2.1]heptane, 1-azabicyclo [3.2.1]octane, and 1-azabicyclo[3.2.2]nonane compounds as alpha-7 nicotinic acetylcholine receptor ligands |
| CA2876689C (en) | 2012-06-13 | 2022-04-26 | Incyte Corporation | Substituted tricyclic compounds as fgfr inhibitors |
| US9388185B2 (en) | 2012-08-10 | 2016-07-12 | Incyte Holdings Corporation | Substituted pyrrolo[2,3-b]pyrazines as FGFR inhibitors |
| US9266892B2 (en) | 2012-12-19 | 2016-02-23 | Incyte Holdings Corporation | Fused pyrazoles as FGFR inhibitors |
| WO2014159234A1 (en) | 2013-03-14 | 2014-10-02 | Merck Patent Gmbh | Glycosidase inhibitors |
| PH12015502383B1 (en) | 2013-04-19 | 2023-02-03 | Incyte Holdings Corp | Bicyclic heterocycles as fgfr inhibitors |
| DK3102576T3 (da) | 2014-02-03 | 2019-07-22 | Vitae Pharmaceuticals Llc | Dihydropyrrolopyridininhibitorer af ror-gamma |
| JP5714745B2 (ja) * | 2014-04-28 | 2015-05-07 | ブリストル−マイヤーズ スクイブ カンパニーBristol−Myers Squibb Company | α7ニコチン性アセチルコリン受容体リガンドとしてのキヌクリジン化合物 |
| MX372995B (es) | 2014-07-17 | 2020-04-13 | Chdi Foundation Inc | Metodos y composiciones para el tratamiento de trastornos relacionados con vih. |
| MX381417B (es) | 2014-08-28 | 2025-03-12 | Asceneuron Sa | Inhibidores de glucosidasa. |
| SI3207043T1 (sl) | 2014-10-14 | 2019-04-30 | Vitae Pharmaceuticals, Inc. | Dihidropirolopiridinovi inhibitorji za ROR-gama |
| US10851105B2 (en) | 2014-10-22 | 2020-12-01 | Incyte Corporation | Bicyclic heterocycles as FGFR4 inhibitors |
| TWI698444B (zh) | 2014-10-29 | 2020-07-11 | 美商基利科學股份有限公司 | 製備核糖苷的方法 |
| US10174052B2 (en) | 2014-11-04 | 2019-01-08 | Bristol-Myers Squibb Company | Quinuclidine compounds as α-7 nicotinic acetylcholine receptor ligands |
| US9663515B2 (en) | 2014-11-05 | 2017-05-30 | Vitae Pharmaceuticals, Inc. | Dihydropyrrolopyridine inhibitors of ROR-gamma |
| US9845308B2 (en) | 2014-11-05 | 2017-12-19 | Vitae Pharmaceuticals, Inc. | Isoindoline inhibitors of ROR-gamma |
| CA2976790C (en) | 2015-02-20 | 2024-02-27 | Incyte Corporation | Bicyclic heterocycles as fgfr inhibitors |
| US9580423B2 (en) | 2015-02-20 | 2017-02-28 | Incyte Corporation | Bicyclic heterocycles as FGFR4 inhibitors |
| MA41551A (fr) | 2015-02-20 | 2017-12-26 | Incyte Corp | Hétérocycles bicycliques utilisés en tant qu'inhibiteurs de fgfr4 |
| EP3331876B1 (en) | 2015-08-05 | 2020-10-07 | Vitae Pharmaceuticals, LLC | Modulators of ror-gamma |
| DK3349758T3 (da) | 2015-09-16 | 2022-06-13 | Gilead Sciences Inc | Fremgangsmåder til behandling af arenaviridae-virusinfektioner |
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| Publication number | Priority date | Publication date | Assignee | Title |
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| JP2013509405A (ja) * | 2009-10-29 | 2013-03-14 | ブリストル−マイヤーズ スクイブ カンパニー | α7ニコチン性アセチルコリン受容体リガンドとしてのキヌクリジン化合物 |
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