JP2010526145A - [6,6]および[6,7]−二環式gpr119gタンパク質結合受容体アゴニスト - Google Patents
[6,6]および[6,7]−二環式gpr119gタンパク質結合受容体アゴニスト Download PDFInfo
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- JP2010526145A JP2010526145A JP2010507528A JP2010507528A JP2010526145A JP 2010526145 A JP2010526145 A JP 2010526145A JP 2010507528 A JP2010507528 A JP 2010507528A JP 2010507528 A JP2010507528 A JP 2010507528A JP 2010526145 A JP2010526145 A JP 2010526145A
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- Prior art keywords
- alkyl
- aryl
- heteroaryl
- cycloalkyl
- independently
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- 0 *c(c(*)c1N)c(*)c(Br)c1O Chemical compound *c(c(*)c1N)c(*)c(Br)c1O 0.000 description 12
- ZWEMMWOGJIDHRN-UHFFFAOYSA-N CC(C)(C)OC(N(CC1)CCC1N1c(ncnc2Nc(cccn3)c3OC)c2OCCC1)=O Chemical compound CC(C)(C)OC(N(CC1)CCC1N1c(ncnc2Nc(cccn3)c3OC)c2OCCC1)=O ZWEMMWOGJIDHRN-UHFFFAOYSA-N 0.000 description 1
- HQWPHPCMDSQUAD-UHFFFAOYSA-N CC(C)(C)OC(N(CC1)CCC1N1c2cccc(Nc(cc3)ccc3S(C)(=O)=O)c2OCC1)=O Chemical compound CC(C)(C)OC(N(CC1)CCC1N1c2cccc(Nc(cc3)ccc3S(C)(=O)=O)c2OCC1)=O HQWPHPCMDSQUAD-UHFFFAOYSA-N 0.000 description 1
- ZRLROXAIZWXOQB-UHFFFAOYSA-N CC(C)(C)OC(N(CC1)CCC1Nc1nc(C)nc(Cl)c1O)=O Chemical compound CC(C)(C)OC(N(CC1)CCC1Nc1nc(C)nc(Cl)c1O)=O ZRLROXAIZWXOQB-UHFFFAOYSA-N 0.000 description 1
- WUVKJRATEDNTIE-UHFFFAOYSA-N CC(C)OC(N(CC1)CCC1N(CCC1)c2c1c(Nc(c(Cl)cnc1)c1Cl)ncn2)=O Chemical compound CC(C)OC(N(CC1)CCC1N(CCC1)c2c1c(Nc(c(Cl)cnc1)c1Cl)ncn2)=O WUVKJRATEDNTIE-UHFFFAOYSA-N 0.000 description 1
- OFVOOVXRDWVUDL-UHFFFAOYSA-N CC(C)OC(N(CC1)CCC1N1c(cccc2Nc(ccc(S(C)(=O)=O)c3)c3Cl)c2OCC1)=O Chemical compound CC(C)OC(N(CC1)CCC1N1c(cccc2Nc(ccc(S(C)(=O)=O)c3)c3Cl)c2OCC1)=O OFVOOVXRDWVUDL-UHFFFAOYSA-N 0.000 description 1
- SOGXTEJVWVBQAT-UHFFFAOYSA-N CC(C)OC(N(CC1)CCC1N1c(nc[n]c2Nc(ccc(S(C)(=O)=O)c3)c3F)c2NCC1)=O Chemical compound CC(C)OC(N(CC1)CCC1N1c(nc[n]c2Nc(ccc(S(C)(=O)=O)c3)c3F)c2NCC1)=O SOGXTEJVWVBQAT-UHFFFAOYSA-N 0.000 description 1
- VQULWPOSYVCNII-UHFFFAOYSA-N CC(C)OC(N(CC1)CCC1N1c(ncnc2Nc(cc(cc3)C#N)c3Cl)c2OCC1)=O Chemical compound CC(C)OC(N(CC1)CCC1N1c(ncnc2Nc(cc(cc3)C#N)c3Cl)c2OCC1)=O VQULWPOSYVCNII-UHFFFAOYSA-N 0.000 description 1
- JUMYKIGTQOLNGH-UHFFFAOYSA-N CC(C)OC(N(CC1)CCC1N1c(ncnc2Nc3c(C)c(C(OC)=O)ccc3)c2OCC1)=O Chemical compound CC(C)OC(N(CC1)CCC1N1c(ncnc2Nc3c(C)c(C(OC)=O)ccc3)c2OCC1)=O JUMYKIGTQOLNGH-UHFFFAOYSA-N 0.000 description 1
- RTCGVPVOMRZZHJ-UHFFFAOYSA-N CC(C)OC(N(CC1)CCC1N1c2ncnc(Cl)c2OCCC1)=O Chemical compound CC(C)OC(N(CC1)CCC1N1c2ncnc(Cl)c2OCCC1)=O RTCGVPVOMRZZHJ-UHFFFAOYSA-N 0.000 description 1
- ZBGMWBBBOXADCH-UHFFFAOYSA-N COc(cccc1)c1OC(N(CC1)CCC1N1c(ncnc2Nc(c(F)c3)ccc3C#N)c2OCC1)=O Chemical compound COc(cccc1)c1OC(N(CC1)CCC1N1c(ncnc2Nc(c(F)c3)ccc3C#N)c2OCC1)=O ZBGMWBBBOXADCH-UHFFFAOYSA-N 0.000 description 1
- CSSVBYYMRPJLFD-UHFFFAOYSA-N CS(c(cc1)cc(F)c1Nc1c2OCCN(C3CCNCC3)c2ncn1)(=O)=O Chemical compound CS(c(cc1)cc(F)c1Nc1c2OCCN(C3CCNCC3)c2ncn1)(=O)=O CSSVBYYMRPJLFD-UHFFFAOYSA-N 0.000 description 1
- AUAUXGHKVMBOCU-UHFFFAOYSA-N CS(c(cc1)cc(F)c1Nc1ncnc2c1OCCN2C(CC1)CCN1c1ncccn1)(=O)=O Chemical compound CS(c(cc1)cc(F)c1Nc1ncnc2c1OCCN2C(CC1)CCN1c1ncccn1)(=O)=O AUAUXGHKVMBOCU-UHFFFAOYSA-N 0.000 description 1
- QGDCAAAIQWLPLQ-UHFFFAOYSA-N Cc(nc1Cl)nc(Cl)c1OC Chemical compound Cc(nc1Cl)nc(Cl)c1OC QGDCAAAIQWLPLQ-UHFFFAOYSA-N 0.000 description 1
- KHNRACJEMJPQRH-UHFFFAOYSA-N Cc(nc1O)nc(O)c1OC Chemical compound Cc(nc1O)nc(O)c1OC KHNRACJEMJPQRH-UHFFFAOYSA-N 0.000 description 1
- GRJDOERHQLHPLF-UHFFFAOYSA-N Cc(nccc1)c1Nc1cccc2c1OCCN2C(CC1)CCN1c1ncccn1 Chemical compound Cc(nccc1)c1Nc1cccc2c1OCCN2C(CC1)CCN1c1ncccn1 GRJDOERHQLHPLF-UHFFFAOYSA-N 0.000 description 1
- VHLWDKINXSAVLV-UHFFFAOYSA-N N#Cc(cc1)cc(F)c1Nc1c2OCCN(C3CCNCC3)c2ncn1 Chemical compound N#Cc(cc1)cc(F)c1Nc1c2OCCN(C3CCNCC3)c2ncn1 VHLWDKINXSAVLV-UHFFFAOYSA-N 0.000 description 1
Classifications
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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
- C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
- C07D413/04—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms 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
- 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
-
- 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
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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
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- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Diabetes (AREA)
- Hematology (AREA)
- Obesity (AREA)
- Biomedical Technology (AREA)
- Neurology (AREA)
- Neurosurgery (AREA)
- Physical Education & Sports Medicine (AREA)
- Heart & Thoracic Surgery (AREA)
- Cardiology (AREA)
- Ophthalmology & Optometry (AREA)
- Endocrinology (AREA)
- Urology & Nephrology (AREA)
- Virology (AREA)
- Emergency Medicine (AREA)
- Oncology (AREA)
- Communicable Diseases (AREA)
- Tropical Medicine & Parasitology (AREA)
- Dermatology (AREA)
- Vascular Medicine (AREA)
- AIDS & HIV (AREA)
- Psychiatry (AREA)
- Child & Adolescent Psychology (AREA)
- Hospice & Palliative Care (AREA)
- Molecular Biology (AREA)
- Orthopedic Medicine & Surgery (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US91594407P | 2007-05-04 | 2007-05-04 | |
| PCT/US2008/061928 WO2008137435A1 (en) | 2007-05-04 | 2008-04-30 | [6,6] and [6,7]-bicyclic gpr119 g protein-coupled receptor agonists |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2010526145A true JP2010526145A (ja) | 2010-07-29 |
| JP2010526145A5 JP2010526145A5 (en:Method) | 2011-05-12 |
Family
ID=39705174
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2010507528A Withdrawn JP2010526145A (ja) | 2007-05-04 | 2008-04-30 | [6,6]および[6,7]−二環式gpr119gタンパク質結合受容体アゴニスト |
Country Status (10)
| Country | Link |
|---|---|
| US (4) | US7910583B2 (en:Method) |
| EP (1) | EP2144902B1 (en:Method) |
| JP (1) | JP2010526145A (en:Method) |
| CN (1) | CN101668756A (en:Method) |
| AR (1) | AR066437A1 (en:Method) |
| CL (1) | CL2008001271A1 (en:Method) |
| ES (1) | ES2388967T3 (en:Method) |
| PE (1) | PE20090222A1 (en:Method) |
| TW (1) | TW200848055A (en:Method) |
| WO (1) | WO2008137435A1 (en:Method) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2012043505A1 (ja) * | 2010-09-28 | 2012-04-05 | 興和株式会社 | 新規なピペリジン誘導体及びこれを含有する医薬 |
| JP2013545791A (ja) * | 2010-12-17 | 2013-12-26 | ベーリンガー インゲルハイム インターナショナル ゲゼルシャフト ミット ベシュレンクテル ハフツング | 糖尿病、肥満および関連疾患の治療のためのgpr119モジュレーターとしての縮合ジヒドロピラン |
Families Citing this family (64)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US7407955B2 (en) | 2002-08-21 | 2008-08-05 | Boehringer Ingelheim Pharma Gmbh & Co., Kg | 8-[3-amino-piperidin-1-yl]-xanthines, the preparation thereof and their use as pharmaceutical compositions |
| DE102004054054A1 (de) | 2004-11-05 | 2006-05-11 | Boehringer Ingelheim Pharma Gmbh & Co. Kg | Verfahren zur Herstellung chiraler 8-(3-Amino-piperidin-1-yl)-xanthine |
| EP1852108A1 (en) | 2006-05-04 | 2007-11-07 | Boehringer Ingelheim Pharma GmbH & Co.KG | DPP IV inhibitor formulations |
| NZ573360A (en) | 2006-05-04 | 2012-08-31 | Boehringer Ingelheim Int | Polymorphic forms of 1-[(4-methyl-quinazolin-2-yl)methyl]-3-methyl-7-(2-butyn-1-yl)-8-(3-(R)-amino-piperidin-1-yl)-xanthine |
| PE20080251A1 (es) | 2006-05-04 | 2008-04-25 | Boehringer Ingelheim Int | Usos de inhibidores de dpp iv |
| CA2693444A1 (en) * | 2007-07-17 | 2009-01-22 | Bristol-Myers Squibb Company | Method for modulating gpr119 g protein-coupled receptor and selected compounds |
| PE20140960A1 (es) | 2008-04-03 | 2014-08-15 | Boehringer Ingelheim Int | Formulaciones que comprenden un inhibidor de dpp4 |
| US8188098B2 (en) | 2008-05-19 | 2012-05-29 | Hoffmann-La Roche Inc. | GPR119 receptor agonists |
| JP2011528365A (ja) | 2008-07-16 | 2011-11-17 | シェーリング コーポレイション | Gpr119モジュレーターとしての二環式ヘテロ環誘導体およびそれらの使用方法 |
| TW201006821A (en) * | 2008-07-16 | 2010-02-16 | Bristol Myers Squibb Co | Pyridone and pyridazone analogues as GPR119 modulators |
| US8815876B2 (en) | 2008-07-16 | 2014-08-26 | Merck Sharp & Dohme Corp. | Bicyclic heterocycle derivatives and methods of use thereof |
| AU2009270983A1 (en) * | 2008-07-16 | 2010-01-21 | Schering Corporation | Bicyclic heterocycle derivatives and their use as GPCR modulators |
| KR20200118243A (ko) | 2008-08-06 | 2020-10-14 | 베링거 인겔하임 인터내셔날 게엠베하 | 메트포르민 요법이 부적합한 환자에서의 당뇨병 치료 |
| US20200155558A1 (en) | 2018-11-20 | 2020-05-21 | Boehringer Ingelheim International Gmbh | Treatment for diabetes in patients with insufficient glycemic control despite therapy with an oral antidiabetic drug |
| MX2011006713A (es) | 2008-12-23 | 2011-07-13 | Boehringer Ingelheim Int | Formas salinas de compuesto organico. |
| WO2010075273A1 (en) * | 2008-12-23 | 2010-07-01 | Schering Corporation | Bicyclic heterocycle derivatives and methods of use thereof |
| JPWO2010084944A1 (ja) * | 2009-01-22 | 2012-07-19 | 田辺三菱製薬株式会社 | 新規ピロロ[2,3−d]ピリミジン化合物 |
| WO2010088518A2 (en) * | 2009-01-31 | 2010-08-05 | Kalypsys, Inc. | Heterocyclic modulators of gpr119 for treatment of disease |
| US8410089B2 (en) | 2009-02-18 | 2013-04-02 | Takeda Pharmaceutical Company Limited | Fused heterocyclic ring compound |
| US8580807B2 (en) | 2009-04-03 | 2013-11-12 | Merck Sharp & Dohme Corp. | Bicyclic piperidine and piperazine derivatives as GPCR modulators for the treatment of obesity, diabetes and other metabolic disorders |
| AR077215A1 (es) | 2009-06-24 | 2011-08-10 | Boehringer Ingelheim Int | Derivados de piperidina, composiciones farmaceuticas y metodos relacionados con ellos |
| US8481731B2 (en) | 2009-06-24 | 2013-07-09 | Boehringer Ingelheim International Gmbh | Compounds, pharmaceutical composition and methods relating thereto |
| AU2010323068B2 (en) | 2009-11-27 | 2015-09-03 | Boehringer Ingelheim International Gmbh | Treatment of genotyped diabetic patients with DPP-IV inhibitors such as linagliptin |
| WO2011107494A1 (de) | 2010-03-03 | 2011-09-09 | Sanofi | Neue aromatische glykosidderivate, diese verbindungen enthaltende arzneimittel und deren verwendung |
| WO2011113947A1 (en) | 2010-03-18 | 2011-09-22 | Boehringer Ingelheim International Gmbh | Combination of a gpr119 agonist and the dpp-iv inhibitor linagliptin for use in the treatment of diabetes and related conditions |
| US8415367B2 (en) | 2010-04-08 | 2013-04-09 | Bristol-Myers Squibb Company | Pyrimidinylpiperidinyloxypyridinone analogues as GPR119 modulators |
| KR101927068B1 (ko) | 2010-05-05 | 2018-12-10 | 베링거 인겔하임 인터내셔날 게엠베하 | 체중 감소 치료에 후속하는 dpp-4 억제제에 의한 순차적 병용 요법 |
| WO2011140161A1 (en) | 2010-05-06 | 2011-11-10 | Bristol-Myers Squibb Company | Benzofuranyl analogues as gpr119 modulators |
| BR112012028445A2 (pt) | 2010-05-06 | 2016-07-19 | Bristol Myers Squibb Co | compostos de heteroarila bicíclica como moduladores de gpr119 |
| TW201202230A (en) * | 2010-05-24 | 2012-01-16 | Mitsubishi Tanabe Pharma Corp | Novel quinazoline compound |
| US8530413B2 (en) | 2010-06-21 | 2013-09-10 | Sanofi | Heterocyclically substituted methoxyphenyl derivatives with an oxo group, processes for preparation thereof and use thereof as medicaments |
| WO2011161161A1 (en) | 2010-06-24 | 2011-12-29 | Boehringer Ingelheim International Gmbh | Diabetes therapy |
| TW201215388A (en) | 2010-07-05 | 2012-04-16 | Sanofi Sa | (2-aryloxyacetylamino)phenylpropionic acid derivatives, processes for preparation thereof and use thereof as medicaments |
| TW201215387A (en) | 2010-07-05 | 2012-04-16 | Sanofi Aventis | Spirocyclically substituted 1,3-propane dioxide derivatives, processes for preparation thereof and use thereof as a medicament |
| TW201221505A (en) | 2010-07-05 | 2012-06-01 | Sanofi Sa | Aryloxyalkylene-substituted hydroxyphenylhexynoic acids, process for preparation thereof and use thereof as a medicament |
| CA2812061A1 (en) | 2010-09-22 | 2012-03-29 | Arena Pharmaceuticals, Inc. | Modulators of the gpr119 receptor and the treatment of disorders related thereto |
| US9034883B2 (en) | 2010-11-15 | 2015-05-19 | Boehringer Ingelheim International Gmbh | Vasoprotective and cardioprotective antidiabetic therapy |
| EP2661438A4 (en) * | 2011-01-03 | 2014-06-11 | Hanmi Pharm Ind Co Ltd | NEW BICYCLIC COMPOUND FOR MODULATING G-PROTEIN-COUPLED RECEPTORS |
| CN102617548A (zh) * | 2011-01-31 | 2012-08-01 | 北京赛林泰医药技术有限公司 | 作为gpr受体激动剂的双环杂芳基化合物及其组合物和应用 |
| EP2718279B1 (en) | 2011-06-09 | 2016-08-10 | Rhizen Pharmaceuticals SA | Novel compounds as modulators of gpr-119 |
| WO2013010964A1 (en) | 2011-07-15 | 2013-01-24 | Boehringer Ingelheim International Gmbh | Substituted quinazolines, the preparation thereof and the use thereof in pharmaceutical compositions |
| WO2013037390A1 (en) | 2011-09-12 | 2013-03-21 | Sanofi | 6-(4-hydroxy-phenyl)-3-styryl-1h-pyrazolo[3,4-b]pyridine-4-carboxylic acid amide derivatives as kinase inhibitors |
| EP2760862B1 (en) | 2011-09-27 | 2015-10-21 | Sanofi | 6-(4-hydroxy-phenyl)-3-alkyl-1h-pyrazolo[3,4-b]pyridine-4-carboxylic acid amide derivatives as kinase inhibitors |
| US9555001B2 (en) | 2012-03-07 | 2017-01-31 | Boehringer Ingelheim International Gmbh | Pharmaceutical composition and uses thereof |
| EP2849755A1 (en) | 2012-05-14 | 2015-03-25 | Boehringer Ingelheim International GmbH | A xanthine derivative as dpp -4 inhibitor for use in the treatment of podocytes related disorders and/or nephrotic syndrome |
| EP2849754B1 (en) | 2012-05-14 | 2022-09-14 | Boehringer Ingelheim International GmbH | Linagliptin, a xanthine derivative as dpp-4 inhibitor, for use in the treatment of sirs and/or sepsis |
| EP2850073B1 (en) | 2012-05-16 | 2017-07-19 | Bristol-Myers Squibb Company | Pyrimidinylpiperidinyloxypyridone analogues as gpr119 modulators |
| WO2013174767A1 (en) | 2012-05-24 | 2013-11-28 | Boehringer Ingelheim International Gmbh | A xanthine derivative as dpp -4 inhibitor for use in modifying food intake and regulating food preference |
| CA2878625A1 (en) | 2012-07-11 | 2014-01-16 | Elcelyx Therapeutics, Inc. | Compositions comprising statins, biguanides and further agents for reducing cardiometabolic risk |
| ES2950384T3 (es) | 2014-02-28 | 2023-10-09 | Boehringer Ingelheim Int | Uso médico de un inhibidor de DPP-4 |
| US9832059B2 (en) * | 2014-06-02 | 2017-11-28 | Marvell World Trade Ltd. | High efficiency orthogonal frequency division multiplexing (OFDM) physical layer (PHY) |
| CN105218561B (zh) * | 2014-06-25 | 2018-10-30 | 上海艾力斯医药科技有限公司 | 稠合嘧啶环衍生物、其制备方法及应用 |
| MX386419B (es) | 2015-01-06 | 2025-03-18 | Arena Pharm Inc | Metodos de condiciones de tratamiento relacionadas con el receptor s1p1. |
| MA42807A (fr) | 2015-06-22 | 2018-07-25 | Arena Pharm Inc | Sel l-arginine cristallin d'acide (r)-2-(7-(4-cyclopentyl-3-(trifluorométhyl)benzyloxy)-1,2,3,4-tétrahydrocyclo-penta[b]indol-3-yl)acétique (composé 1) pour une utilisation dans des troubles associés au récepteur de s1p1 |
| JP2019517542A (ja) | 2016-06-10 | 2019-06-24 | ベーリンガー インゲルハイム インターナショナル ゲゼルシャフト ミット ベシュレンクテル ハフツング | リナグリプチンおよびメトホルミンの組合せ |
| KR20190116416A (ko) | 2017-02-16 | 2019-10-14 | 아레나 파마슈티칼스, 인크. | 원발 담즙성 담관염을 치료하기 위한 화합물 및 방법 |
| KR102859841B1 (ko) | 2018-06-06 | 2025-09-12 | 아레나 파마슈티칼스, 인크. | S1p1 수용체와 관련된 병태의 치료 방법 |
| AU2021228729A1 (en) | 2020-02-28 | 2022-09-22 | Kallyope, Inc. | GPR40 agonists |
| UY39222A (es) | 2020-05-19 | 2021-11-30 | Kallyope Inc | Activadores de la ampk |
| AU2021297323A1 (en) | 2020-06-26 | 2023-02-16 | Kallyope, Inc. | AMPK activators |
| WO2023178130A1 (en) * | 2022-03-16 | 2023-09-21 | Biotheryx, Inc. | Sos1 protein degraders, pharmaceutical compositions, and therapeutic applications |
| CN114969044B (zh) * | 2022-05-30 | 2024-10-11 | 北京火山引擎科技有限公司 | 一种基于数据湖的物化列创建方法以及数据查询方法 |
| CN115160340B (zh) * | 2022-06-07 | 2023-07-21 | 四川大学华西医院 | 一种具有ack1抑制活性的小分子化合物及其应用 |
| WO2025175258A1 (en) * | 2024-02-17 | 2025-08-21 | Padarn Therapeutics, Inc. | Inhibitors of cdk2 |
Family Cites Families (32)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3826643A (en) * | 1967-08-07 | 1974-07-30 | American Cyanamid Co | Method of controlling undesirable plant species using 3-nitropyridines |
| US5776983A (en) * | 1993-12-21 | 1998-07-07 | Bristol-Myers Squibb Company | Catecholamine surrogates useful as β3 agonists |
| US5488064A (en) * | 1994-05-02 | 1996-01-30 | Bristol-Myers Squibb Company | Benzo 1,3 dioxole derivatives |
| US5612359A (en) * | 1994-08-26 | 1997-03-18 | Bristol-Myers Squibb Company | Substituted biphenyl isoxazole sulfonamides |
| US5491134A (en) * | 1994-09-16 | 1996-02-13 | Bristol-Myers Squibb Company | Sulfonic, phosphonic or phosphiniic acid β3 agonist derivatives |
| US5541204A (en) * | 1994-12-02 | 1996-07-30 | Bristol-Myers Squibb Company | Aryloxypropanolamine β 3 adrenergic agonists |
| US5620997A (en) | 1995-05-31 | 1997-04-15 | Warner-Lambert Company | Isothiazolones |
| AU6966696A (en) | 1995-10-05 | 1997-04-28 | Warner-Lambert Company | Method for treating and preventing inflammation and atherosclerosis |
| US5770615A (en) * | 1996-04-04 | 1998-06-23 | Bristol-Myers Squibb Company | Catecholamine surrogates useful as β3 agonists |
| US6566384B1 (en) * | 1996-08-07 | 2003-05-20 | Darwin Discovery Ltd. | Hydroxamic and carboxylic acid derivatives having MMP and TNF inhibitory activity |
| TW536540B (en) * | 1997-01-30 | 2003-06-11 | Bristol Myers Squibb Co | Endothelin antagonists: N-[[2'-[[(4,5-dimethyl-3-isoxazolyl)amino]sulfonyl]-4-(2-oxazolyl)[1,1'-biphenyl]-2-yl]methyl]-N,3,3-trimethylbutanamide and N-(4,5-dimethyl-3-isoxazolyl)-2'-[(3,3-dimethyl-2-oxo-1-pyrrolidinyl)methyl]-4'-(2-oxazolyl)[1,1'-biphe |
| UA57811C2 (uk) | 1997-11-21 | 2003-07-15 | Пфайзер Продактс Інк. | Фармацевтична композиція, що містить інгібітор альдозоредуктази та інгібітор глікогенфосфорилази (варіанти), комплект, який її включає, та способи лікування ссавців зі станом інсулінорезистентності |
| TR200100149T2 (tr) | 1998-07-06 | 2001-10-22 | Bristol-Myers Squibb Company | Dual anjiyotensin endotelin alıcı antagonistleri olarak bifenil-sülfonamitler |
| EP1140862A4 (en) | 1998-12-23 | 2004-07-28 | Bristol Myers Squibb Pharma Co | THROMBIN OR Xa FACTOR INHIBITORS |
| CA2413241A1 (en) | 2000-06-29 | 2002-01-10 | Bristol-Myers Squibb Pharma Company | Thrombin or factor xa inhibitors |
| DE60125227T2 (de) | 2000-12-01 | 2007-09-20 | Astellas Pharma Inc. | Verfahren zum screening von diabetes-heilverfahren |
| US7482366B2 (en) * | 2001-12-21 | 2009-01-27 | X-Ceptor Therapeutics, Inc. | Modulators of LXR |
| CA2469435A1 (en) * | 2001-12-21 | 2003-07-24 | X-Ceptor Therapeutics, Inc. | Modulators of lxr |
| AU2004205642C1 (en) | 2003-01-14 | 2012-01-12 | Arena Pharmaceuticals, Inc. | 1,2,3-trisubstituted aryl and heteroaryl derivatives as modulators of metabolism and the prophylaxis and treatment of disorders related thereto such as diabetes and hyperglycemia |
| KR20050106033A (ko) | 2003-02-24 | 2005-11-08 | 아레나 파마슈티칼스, 인크. | 글루코스 대사 조절제로서의 페닐- 및피리딜피페리딘-유도체 |
| SE0301010D0 (sv) | 2003-04-07 | 2003-04-07 | Astrazeneca Ab | Novel compounds |
| AR045047A1 (es) | 2003-07-11 | 2005-10-12 | Arena Pharm Inc | Derivados arilo y heteroarilo trisustituidos como moduladores del metabolismo y de la profilaxis y tratamiento de desordenes relacionados con los mismos |
| BRPI0412689A (pt) | 2003-07-14 | 2006-10-03 | Arena Pharm Inc | derivados de heteroarila e arila fundida como moduladores de metabolismo e a profilaxia e tratamento de distúrbios relacionados a ele |
| US20070088163A1 (en) | 2003-09-12 | 2007-04-19 | Kemia, Inc. | Modulators of calcitonin and amylin activity |
| US20080269114A1 (en) | 2004-03-17 | 2008-10-30 | 7Tm Pharma A/S | Y4 Selective Receptor Agonists For Thereapeutic Interventions |
| MXPA06012683A (es) * | 2004-05-03 | 2007-01-16 | Hoffmann La Roche | Derivados de indolilo como moduladores de receptor x del higado. |
| WO2005121121A2 (en) | 2004-06-04 | 2005-12-22 | Arena Pharmaceuticals, Inc. | Substituted aryl and heteroaryl derivatives as modulators of metabolism and the prophylaxis and treatment of disorders related thereto |
| WO2006067532A1 (en) | 2004-12-24 | 2006-06-29 | Prosidion Ltd | G-protein coupled receptor agonists |
| MY148521A (en) * | 2005-01-10 | 2013-04-30 | Arena Pharm Inc | Substituted pyridinyl and pyrimidinyl derivatives as modulators of metabolism and the treatment of disorders related thereto |
| JP5349960B2 (ja) * | 2005-06-23 | 2013-11-20 | エモリー ユニバーシティー | 腫瘍画像化のためのアミノ酸類似体の立体選択的合成 |
| JP2010526146A (ja) | 2007-05-04 | 2010-07-29 | ブリストル−マイヤーズ スクイブ カンパニー | [6,5]−二環式gpr119gタンパク質結合受容体アゴニスト |
| CA2693444A1 (en) | 2007-07-17 | 2009-01-22 | Bristol-Myers Squibb Company | Method for modulating gpr119 g protein-coupled receptor and selected compounds |
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- 2011-11-04 US US13/289,375 patent/US8314095B2/en active Active
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Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2012043505A1 (ja) * | 2010-09-28 | 2012-04-05 | 興和株式会社 | 新規なピペリジン誘導体及びこれを含有する医薬 |
| JP2013545791A (ja) * | 2010-12-17 | 2013-12-26 | ベーリンガー インゲルハイム インターナショナル ゲゼルシャフト ミット ベシュレンクテル ハフツング | 糖尿病、肥満および関連疾患の治療のためのgpr119モジュレーターとしての縮合ジヒドロピラン |
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| CL2008001271A1 (es) | 2008-09-12 |
| CN101668756A (zh) | 2010-03-10 |
| US8076322B2 (en) | 2011-12-13 |
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| US8513265B2 (en) | 2013-08-20 |
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| TW200848055A (en) | 2008-12-16 |
| PE20090222A1 (es) | 2009-03-27 |
| EP2144902B1 (en) | 2012-05-16 |
| EP2144902A1 (en) | 2010-01-20 |
| WO2008137435A1 (en) | 2008-11-13 |
| US7910583B2 (en) | 2011-03-22 |
| US20130116237A1 (en) | 2013-05-09 |
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