JP5651681B2 - 代謝型グルタミン酸受容体5介在障害の治療のための化合物、およびその使用方法 - Google Patents
代謝型グルタミン酸受容体5介在障害の治療のための化合物、およびその使用方法 Download PDFInfo
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- JP5651681B2 JP5651681B2 JP2012503692A JP2012503692A JP5651681B2 JP 5651681 B2 JP5651681 B2 JP 5651681B2 JP 2012503692 A JP2012503692 A JP 2012503692A JP 2012503692 A JP2012503692 A JP 2012503692A JP 5651681 B2 JP5651681 B2 JP 5651681B2
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Classifications
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- 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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
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Landscapes
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| PCT/US2010/029575 WO2010114971A1 (en) | 2009-04-03 | 2010-04-01 | Compounds for treating disorders mediated by metabotropic glutamate receptor 5, and methods of use thereof |
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| EA019980B1 (ru) | 2009-12-18 | 2014-07-30 | Янссен Фармацевтика Нв | БИЦИКЛИЧЕСКИЕ ТИАЗОЛЫ В КАЧЕСТВЕ АЛЛОСТЕРИЧЕСКИХ МОДУЛЯТОРОВ РЕЦЕПТОРОВ mGluR5 |
| WO2011073347A1 (en) | 2009-12-18 | 2011-06-23 | Janssen Pharmaceutica Nv | Bicyclic thiazoles as allosteric modulators of mglur5 receptors |
| USRE48301E1 (en) | 2010-07-09 | 2020-11-10 | Abbvie B.V. | Fused heterocyclic derivatives as S1P modulators |
| WO2012031024A1 (en) | 2010-08-31 | 2012-03-08 | Vanderbilt University | Bicyclic oxazole and thiazole compounds and their use as allosteric modulators of mglur5 receptors |
| EP2648723A4 (en) * | 2010-12-08 | 2014-04-02 | Univ Vanderbilt | Bicyclic pyrazole compounds as allergic Mglur5 receptor modulators |
| WO2012083224A1 (en) * | 2010-12-17 | 2012-06-21 | Vanderbilt University | Bicyclic triazole and pyrazole lactams as allosteric modulators of mglur5 receptors |
| US8975276B2 (en) | 2011-06-29 | 2015-03-10 | Bristol-Myers Squibb Company | Inhibitors of PDE10 |
| JP6068464B2 (ja) * | 2011-07-15 | 2017-01-25 | ヤンセン ファーマシューティカルズ,インコーポレーテッド | γ−セクレターゼ調節剤としての新規な置換インドール誘導体 |
| MY188000A (en) | 2011-12-28 | 2021-11-08 | Fujifilm Corp | Novel nicotinamide derivative or salt thereof |
| KR20150023822A (ko) * | 2012-06-20 | 2015-03-05 | 벤더르빌트 유니버시티 | Mglur5 수용체의 알로스테릭 조절물질로서 치환된 바이사이클릭 알콕시 피라졸 유사체 |
| JP2015525241A (ja) | 2012-06-22 | 2015-09-03 | イー・アイ・デュポン・ドウ・ヌムール・アンド・カンパニーE.I.Du Pont De Nemours And Company | 殺菌・殺カビ性ヘテロ環式化合物 |
| JP2016011257A (ja) * | 2012-10-23 | 2016-01-21 | 大日本住友製薬株式会社 | テトラヒドロオキサゾロピリジン誘導体 |
| CA2889249C (en) | 2012-12-20 | 2021-02-16 | Francois Paul Bischoff | Tricyclic 3,4-dihydro-2h-pyrido[1,2-a]pyrazine-1,6-dione derivatives as gamma secretase modulators |
| AU2014206834B2 (en) | 2013-01-17 | 2017-06-22 | Janssen Pharmaceutica Nv | Novel substituted pyrido-piperazinone derivatives as gamma secretase modulators |
| GB201321749D0 (en) * | 2013-12-09 | 2014-01-22 | Ucb Pharma Sa | Therapeutic agents |
| US10562897B2 (en) | 2014-01-16 | 2020-02-18 | Janssen Pharmaceutica Nv | Substituted 3,4-dihydro-2H-pyrido[1,2-a]pyrazine-1,6-diones as gamma secretase modulators |
| SG11201705355VA (en) * | 2014-12-29 | 2017-08-30 | Recordati Ireland Ltd | Heterocyclylalkyne derivatives and their use as modulators of mglur5 receptors |
| WO2016171181A1 (ja) * | 2015-04-21 | 2016-10-27 | 大日本住友製薬株式会社 | 2位置換縮合ピラゾール誘導体 |
| US10100049B2 (en) | 2015-11-03 | 2018-10-16 | Theravance Biopharma R&D Ip, Llc | JAK kinase inhibitor compounds for treatment of respiratory disease |
| EP3559005A1 (en) | 2016-12-21 | 2019-10-30 | Biotheryx Inc. | Thienopyrrole derivatives for use in targeting proteins, compositions, methods, and uses thereof |
| CN110461839B (zh) | 2017-03-09 | 2022-08-23 | 施万生物制药研发Ip有限责任公司 | 含有4元杂环酰胺的jak抑制剂 |
| AR111495A1 (es) | 2017-05-01 | 2019-07-17 | Theravance Biopharma R&D Ip Llc | Compuestos de imidazo-piperidina fusionada como inhibidores de jak |
| JP7096268B2 (ja) | 2017-05-01 | 2022-07-05 | セラヴァンス バイオファーマ アール&ディー アイピー, エルエルシー | Jak阻害剤化合物の結晶形態 |
| CA3059785A1 (en) | 2017-05-01 | 2018-11-08 | Theravance Biopharma R&D Ip, Llc | Methods of treatment using a jak inhibitor compound |
| MX2020004839A (es) | 2017-11-02 | 2020-10-16 | Aicuris Gmbh & Co Kg | Nuevas indol-2-carboxamidas sustituidas con amino-tiazol, de alta actividad, activas contra el virus de la hepatitis b (vhb). |
| MX2021002273A (es) | 2018-09-04 | 2021-05-27 | Theravance Biopharma R&D Ip Llc | Proceso para preparar inhibidores de las jak y productos intermedios de estos. |
| PL3837258T3 (pl) | 2018-09-04 | 2024-09-16 | Theravance Biopharma R&D Ip, Llc | Amidy dimetyloaminoazetydyny jako inhibitory jak |
| EA202190686A1 (ru) | 2018-09-04 | 2021-07-23 | ТЕРЕВАНС БАЙОФАРМА Ар энд Ди АйПи, ЭлЭлСи | 5-7-членные гетероциклические амиды в качестве ингибиторов jak |
| AU2019373059A1 (en) | 2018-10-29 | 2021-05-06 | Theravance Biopharma R&D Ip, Llc | 2-azabicyclo hexane compound as JAK inhibitor |
| TW202144343A (zh) | 2020-03-02 | 2021-12-01 | 美商施萬生物製藥研發 Ip有限責任公司 | Jak抑制劑化合物之結晶水合物 |
| CN113880843B (zh) * | 2020-07-03 | 2023-03-10 | 武汉朗来科技发展有限公司 | 一种杂环化合物及其应用 |
| CA3223194A1 (en) | 2021-06-25 | 2022-12-29 | Theravance Biopharma R&D Ip, Llc | Imidazolo indazole compounds as jak inhibitors |
| US20250099442A1 (en) * | 2021-12-10 | 2025-03-27 | Prothena Biosciences Limited | Compounds for use in treating neurological disorders |
| EP4596554A4 (en) * | 2022-09-29 | 2025-12-10 | Suzhou Arkbiopharmaceutical Co Ltd | Fused AZA Cyclic Compound, its Preparation Process and its Use in Medicine |
Family Cites Families (9)
| Publication number | Priority date | Publication date | Assignee | Title |
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| DE1620508A1 (de) * | 1965-07-23 | 1969-09-18 | Thomae Gmbh Dr K | Verfahren zur Herstellung neuer 4,5,6,7-Tetrahydrothiazolo-[5,4-c]-pyridine |
| US3503990A (en) * | 1967-01-31 | 1970-03-31 | Endo Lab | 6-aryl-4,5,6,7-tetrahydro-4-oxoindole derivatives |
| US3621027A (en) * | 1968-03-18 | 1971-11-16 | Endo Lab | 1-aminoalkyl-2,6-diaryl 4,5,6,7 tetrahydro-4-oxindales |
| PL1636217T3 (pl) * | 2003-05-13 | 2009-02-27 | Hoffmann La Roche | 1-Imidazobenzotiazole jako ligandy receptora adenozynowego |
| JP2007523181A (ja) * | 2004-02-18 | 2007-08-16 | アストラゼネカ アクチボラグ | ポリヘテロ環式化合物、および、代謝型グルタミン酸受容体アンタゴニストとしてのそれらの使用 |
| US7585881B2 (en) * | 2004-02-18 | 2009-09-08 | Astrazeneca Ab | Additional heteropolycyclic compounds and their use as metabotropic glutamate receptor antagonists |
| TW200800204A (en) * | 2005-08-15 | 2008-01-01 | Astrazeneca Ab | Bicyclic piperazines as metabotropic glutatmate receptor antagonists |
| GB0622202D0 (en) * | 2006-11-07 | 2006-12-20 | Addex Pharmaceuticals Sa | Novel compounds |
| CA2710474A1 (en) * | 2008-01-24 | 2009-07-30 | Ucb Pharma, S.A. | Compounds comprising a cyclobutoxy group |
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| WO2010114971A1 (en) | 2010-10-07 |
| EP2414340A1 (en) | 2012-02-08 |
| CA2756989A1 (en) | 2010-10-07 |
| US20120029190A1 (en) | 2012-02-02 |
| JP2012522793A (ja) | 2012-09-27 |
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