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)
- Biomedical Technology (AREA)
- Neurosurgery (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 | 2009-04-14 | ||
| US12/423,299 US7863291B2 (en) | 2008-04-23 | 2009-04-14 | Quinuclidine compounds as alpha-7 nicotinic acetylcholine receptor ligands |
| 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 (84)
| 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 |
| HUE038946T2 (hu) | 2008-04-23 | 2018-12-28 | Gilead Sciences Inc | 1'-szubsztituált carba-nukleozid analógok antivirális kezelésre |
| KR20110092266A (ko) * | 2008-08-04 | 2011-08-17 | 씨에이치디아이 파운데이션, 인코포레이티드 | 소정 키누레닌-3-모노옥시게나아제 억제제, 약학적 조성물, 및 그의 사용 방법 |
| 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 |
| JP5767643B2 (ja) | 2009-09-21 | 2015-08-19 | ギリード・サイエンシズ・インコーポレーテッド | 1’−置換カルバヌクレオシド類似体の調製のためのプロセスおよび中間体 |
| 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 |
| JP2013509417A (ja) * | 2009-10-28 | 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アザ二環式化合物 |
| BR112012017484A2 (pt) * | 2010-01-14 | 2020-08-25 | Sanofi | "derivados de oxazolopirimidina 2,5-substituídos" |
| JP2013525457A (ja) | 2010-04-30 | 2013-06-20 | ブリストル−マイヤーズ スクイブ カンパニー | アルファ−7ニコチン性アセチルコリン受容体リガンドプロドラッグとしてのアザ−二環式アミンn−オキシド化合物 |
| PL2589592T3 (pl) | 2010-06-30 | 2019-03-29 | Fujifilm Corporation | Nowe pochodne nikotynamidu lub ich sole |
| KR101995598B1 (ko) | 2010-07-19 | 2019-07-02 | 길리애드 사이언시즈, 인코포레이티드 | 부분입체 이성질성으로 순수한 포스포라미데이트 전구약물의 제조 방법 |
| PE20130400A1 (es) | 2010-07-22 | 2013-04-10 | Gilead Sciences Inc | Metodos y compuestos para tratar infecciones virales por paramyxoviridae |
| WO2012088266A2 (en) | 2010-12-22 | 2012-06-28 | Incyte Corporation | Substituted imidazopyridazines and benzimidazoles as inhibitors of fgfr3 |
| TWI565709B (zh) | 2011-07-19 | 2017-01-11 | 英菲尼提製藥股份有限公司 | 雜環化合物及其用途 |
| MY166890A (en) | 2011-08-30 | 2018-07-24 | Chdi Foundation Inc | Kynurenine-3-monooxygenase inhibitors, pharmaceutical compositions, and methods of use thereof |
| SI2766359T1 (sl) | 2011-10-14 | 2016-09-30 | Ambit Biosciences Corporation | Heterociklične spojine in njihova uporaba kot modulatorjev receptorja tirozin kinaze tipa III |
| 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 |
| EP2855471B1 (en) | 2012-05-24 | 2017-11-15 | 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 |
| SI2861595T1 (sl) | 2012-06-13 | 2017-04-26 | Incyte Holdings Corporation | Substituirane triciklične spojine kot inhibitorji fgfr |
| 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 |
| HUE043398T2 (hu) | 2013-03-14 | 2019-08-28 | Merck Patent Gmbh | Glikozidáz inhibítorok |
| LT2986610T (lt) | 2013-04-19 | 2018-04-10 | Incyte Holdings Corporation | Bicikliniai heterociklai, kaip fgfr inhibitoriai |
| KR102408261B1 (ko) | 2014-02-03 | 2022-06-10 | 비타이 파마슈티컬즈, 엘엘씨 | Ror-감마의 디하이드로피롤로피리딘 저해제 |
| 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 |
| JP2017520610A (ja) | 2014-07-17 | 2017-07-27 | シーエイチディーアイ ファウンデーション,インコーポレーテッド | Hiv関連障害を治療するための方法及び組成物 |
| KR102043337B1 (ko) | 2014-08-28 | 2019-11-11 | 아셰뉴론 에스아 | 글리코시다제 저해제 |
| UA118989C2 (uk) | 2014-10-14 | 2019-04-10 | Вітае Фармасьютікалс, Інк. | Дигідропіролопіридинові інгібітори ror-гамма |
| 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 |
| EP3215512A1 (en) | 2014-11-04 | 2017-09-13 | Bristol-Myers Squibb Company | Quinuclidine compounds as alpha-7 nicotinic acetylcholine receptor ligands |
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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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