JP2009507079A5 - - Google Patents

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Publication number
JP2009507079A5
JP2009507079A5 JP2008530175A JP2008530175A JP2009507079A5 JP 2009507079 A5 JP2009507079 A5 JP 2009507079A5 JP 2008530175 A JP2008530175 A JP 2008530175A JP 2008530175 A JP2008530175 A JP 2008530175A JP 2009507079 A5 JP2009507079 A5 JP 2009507079A5
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JP
Japan
Prior art keywords
optionally substituted
group
lower alkyl
heteroaryl
optionally
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.)
Pending
Application number
JP2008530175A
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English (en)
Japanese (ja)
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JP2009507079A (ja
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Publication date
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Priority claimed from PCT/US2006/034747 external-priority patent/WO2007030559A2/en
Publication of JP2009507079A publication Critical patent/JP2009507079A/ja
Publication of JP2009507079A5 publication Critical patent/JP2009507079A5/ja
Pending legal-status Critical Current

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JP2008530175A 2005-09-07 2006-09-06 Ppar活性化合物 Pending JP2009507079A (ja)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US71532705P 2005-09-07 2005-09-07
PCT/US2006/034747 WO2007030559A2 (en) 2005-09-07 2006-09-06 1, 3-disubstituted indole derivatives for use as ppar modulators

Publications (2)

Publication Number Publication Date
JP2009507079A JP2009507079A (ja) 2009-02-19
JP2009507079A5 true JP2009507079A5 (enExample) 2009-11-05

Family

ID=37685960

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2008530175A Pending JP2009507079A (ja) 2005-09-07 2006-09-06 Ppar活性化合物

Country Status (17)

Country Link
US (1) US20070072904A1 (enExample)
EP (1) EP1943245A2 (enExample)
JP (1) JP2009507079A (enExample)
KR (1) KR20080047591A (enExample)
CN (1) CN101304992A (enExample)
AU (1) AU2006287513A1 (enExample)
BR (1) BRPI0615929A2 (enExample)
CA (1) CA2621474A1 (enExample)
CR (1) CR9868A (enExample)
EC (1) ECSP088352A (enExample)
IL (1) IL189776A0 (enExample)
NO (1) NO20081041L (enExample)
NZ (1) NZ567162A (enExample)
RU (1) RU2419618C2 (enExample)
SG (1) SG165362A1 (enExample)
WO (1) WO2007030559A2 (enExample)
ZA (1) ZA200802007B (enExample)

Families Citing this family (44)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CA2644809A1 (en) 2006-03-02 2007-09-07 Astellas Pharma Inc. 17 .beta. hsd type 5 inhibitor
EP2079466B1 (en) 2006-09-29 2014-01-15 GlaxoSmithKline LLC Substituted indole compounds
WO2008063888A2 (en) 2006-11-22 2008-05-29 Plexxikon, Inc. Compounds modulating c-fms and/or c-kit activity and uses therefor
PE20090159A1 (es) * 2007-03-08 2009-02-21 Plexxikon Inc COMPUESTOS DERIVADOS DE ACIDO INDOL-PROPIONICO COMO MODULADORES PPARs
MX2009009290A (es) * 2007-03-08 2009-09-10 Plexxikon Inc Compuestos activos en ppar.
CA2682135A1 (en) * 2007-04-17 2008-10-30 Baxter International Inc. Nucleic acid microparticles for pulmonary delivery
CA2695004C (en) 2007-07-17 2016-01-19 Plexxikon, Inc. Compounds and methods for kinase modulation, and indications therefor
WO2009143018A2 (en) 2008-05-19 2009-11-26 Plexxikon, Inc. Compounds and methods for kinase modulation, and indications therefor
FR2950053B1 (fr) * 2009-09-11 2014-08-01 Fournier Lab Sa Utilisation de derives d'indole benzoique comme activateurs de nurr-1, pour le traitement de la maladie de parkinson
KR20120097512A (ko) 2009-11-18 2012-09-04 플렉시콘, 인코퍼레이티드 키나제 조절을 위한 화합물 및 방법, 및 그에 대한 적응증
EP2516438A4 (en) 2009-12-23 2013-06-12 Plexxikon Inc COMPOUNDS AND METHODS FOR KINASE MODULATION AND DISPLAYS THEREFOR
TWI510487B (zh) 2010-04-21 2015-12-01 Plexxikon Inc 用於激酶調節的化合物和方法及其適應症
TR201816421T4 (tr) 2011-02-07 2018-11-21 Plexxikon Inc Kinaz modülasyonu için bileşikler ve metotlar ve bunların endikasyonları.
RU2631487C2 (ru) 2011-05-17 2017-09-22 Плексксикон Инк. Модуляция киназ и показания к её применению
US9358235B2 (en) 2012-03-19 2016-06-07 Plexxikon Inc. Kinase modulation, and indications therefor
AU2013312477B2 (en) 2012-09-06 2018-05-31 Plexxikon Inc. Compounds and methods for kinase modulation, and indications therefor
CA2886117C (en) * 2012-10-05 2022-05-31 Merck Sharp & Dohme Corp. Indoline compounds and their use as aldosterone synthase inhibitors
SG11201504754QA (en) 2012-12-21 2015-07-30 Plexxikon Inc Compounds and methods for kinase modulation, and indications therefor
PT2970265T (pt) 2013-03-15 2018-10-23 Plexxikon Inc Compostos heterocíclicos e suas utilizações
US20140303121A1 (en) 2013-03-15 2014-10-09 Plexxikon Inc. Heterocyclic compounds and uses thereof
WO2014194127A1 (en) 2013-05-30 2014-12-04 Plexxikon Inc. Compounds for kinase modulation, and indications therefor
US9771369B2 (en) 2014-03-04 2017-09-26 Plexxikon Inc. Compounds and methods for kinase modulation, and indications therefor
KR101585605B1 (ko) * 2014-03-20 2016-01-21 현대약품 주식회사 Pparg에 결합하되 증진제로 작용하지 않는 화합물 및 이를 유효성분으로 함유하는 pparg 관련 질병의 치료용 약학적 조성물
HUE046293T2 (hu) 2014-06-13 2020-02-28 Inventiva PPAR vegyületek fibrotikus betegségek kezelésében történõ alkalmazásra
EP3194392B1 (en) 2014-09-15 2020-01-01 Plexxikon, Inc. Heterocyclic compounds and uses thereof
US10160755B2 (en) 2015-04-08 2018-12-25 Plexxikon Inc. Compounds and methods for kinase modulation, and indications therefor
WO2017019804A2 (en) 2015-07-28 2017-02-02 Plexxikon Inc. Compounds and methods for kinase modulation, and indications therefor
EP4071149A3 (en) 2015-09-21 2023-01-25 Opna Immuno Oncology, SA Heterocyclic compounds and uses thereof
BR112018011475A2 (pt) 2015-12-07 2018-12-04 Plexxikon Inc compostos e métodos para modulação de quinase e indicação para a mesma
SG11201805237TA (en) 2015-12-21 2018-07-30 Council Scient Ind Res Novel 1,2,3 triazole-thiazole compounds, process for preparation and use thereof
EP3430005B1 (en) 2016-03-16 2021-12-08 Plexxikon Inc. Compounds and methods for kinase modulation and indications therefore
TW201815766A (zh) 2016-09-22 2018-05-01 美商普雷辛肯公司 用於ido及tdo調節之化合物及方法以及其適應症
US10703757B2 (en) 2016-12-23 2020-07-07 Plexxikon Inc. Compounds and methods for CDK8 modulation and indications therefor
WO2018165501A1 (en) * 2017-03-10 2018-09-13 Lycera Corporation INDOLINYL SULFONAMIDE AND RELATED COMPOUNDS FOR USE AS AGONISTS OF RORγ AND THE TREATMENT OF DISEASE
US10577366B2 (en) 2017-03-20 2020-03-03 Plexxikon Inc. Crystalline forms of a compound that inhibits bromodomain
WO2018226846A1 (en) 2017-06-07 2018-12-13 Plexxikon Inc. Compounds and methods for kinase modulation
TWI805599B (zh) 2017-07-25 2023-06-21 美商第一三共公司 激酶調節化合物之調配物
AU2018348241B2 (en) 2017-10-13 2023-01-12 Opna Bio SA Solid forms of a compound for modulating kinases
CA3080197C (en) 2017-10-27 2023-12-19 Plexxikon Inc. Formulations of a compound modulating kinases
CN112119072A (zh) 2018-03-20 2020-12-22 普莱希科公司 用于ido和tdo调节的化合物和方法,以及其适应症
JP2023524465A (ja) 2020-04-29 2023-06-12 プレキシコン インコーポレイティド 複素環式化合物の合成
KR102772169B1 (ko) * 2021-05-28 2025-02-26 서울대학교산학협력단 신규 인돌 감마 락탐 화합물 및 이를 유효성분으로 포함하는 저아디포넥틴혈증 관련 질환의 예방, 개선 또는 치료용 조성물
CN115504925B (zh) * 2021-06-22 2024-03-12 广东药科大学 一类ppar激动剂、其制备方法及其作为药物的用途
WO2025019330A1 (en) 2023-07-14 2025-01-23 Pleiogenix Inc. Methods of treating fibrotic liver diseases or conditions with indeglitazar

Family Cites Families (34)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3489767A (en) * 1966-01-12 1970-01-13 Sumitomo Chemical Co 1-(phenylsulfonyl)-3-indolyl aliphatic acid derivatives
US3557142A (en) * 1968-02-20 1971-01-19 Sterling Drug Inc 4,5,6,7-tetrahydro-indole-lower-alkanoic acids and esters
GB1573212A (en) * 1976-04-15 1980-08-20 Technicon Instr Immunoassay for gentamicin
DE3246932A1 (de) * 1982-12-16 1984-06-20 Schering AG, 1000 Berlin und 4709 Bergkamen Substituierte 5h-pyrimido(5,4-b)indole
US4568649A (en) * 1983-02-22 1986-02-04 Immunex Corporation Immediate ligand detection assay
US4626513A (en) * 1983-11-10 1986-12-02 Massachusetts General Hospital Method and apparatus for ligand detection
GB8707051D0 (en) * 1986-04-15 1987-04-29 Ici America Inc Heterocyclic carboxamides
US5688655A (en) * 1988-02-10 1997-11-18 Ict Pharmaceuticals, Inc. Method of screening for protein inhibitors and activators
EP0610793A1 (en) * 1993-02-08 1994-08-17 Takeda Chemical Industries, Ltd. Tetracyclic morpholine derivatives and their use or analgesics
DE69434998T2 (de) * 1993-05-27 2008-03-13 Aventis Pharmaceuticals Inc. Topologisch getrennte, kodierende Festphasen-Bibliotheken
US5840485A (en) * 1993-05-27 1998-11-24 Selectide Corporation Topologically segregated, encoded solid phase libraries
DK0753511T3 (da) * 1994-03-30 2001-09-24 Zeria Pharm Co Ltd 4-indol-1-ylsmørsyrederivater, deres fremstilling og deres anvendelse som inhibitorer af alfa 1-adrenerge receptorer og testosteron-5alfa-reduktaser
US5763198A (en) * 1994-07-22 1998-06-09 Sugen, Inc. Screening assays for compounds
US5747276A (en) * 1995-09-15 1998-05-05 The Scripps Research Institute Screening methods for the identification of novel antibiotics
US6294330B1 (en) * 1997-01-31 2001-09-25 Odyssey Pharmaceuticals Inc. Protein fragment complementation assays for the detection of biological or drug interactions
EP0972071A4 (en) * 1997-03-07 2004-04-21 Tropix Inc TEST ARRANGEMENT FOR PROTEAS INHIBITORS
US6178384B1 (en) * 1997-09-29 2001-01-23 The Trustees Of Columbia University In The City Of New York Method and apparatus for selecting a molecule based on conformational free energy
IL136954A0 (en) * 1997-12-24 2001-06-14 Aventis Pharma Gmbh Indole derivatives as inhibitors of factor xa
US6331537B1 (en) * 1998-06-03 2001-12-18 Gpi Nil Holdings, Inc. Carboxylic acids and carboxylic acid isosteres of N-heterocyclic compounds
US6288234B1 (en) * 1998-06-08 2001-09-11 Advanced Medicine, Inc. Multibinding inhibitors of microsomal triglyceride transferase protein
TNSN99224A1 (fr) * 1998-12-01 2005-11-10 Inst For Pharm Discovery Inc Methodes de reduction des niveaux de glucose et triglyceride en serum et pour suppression de l'antigenese utilisant les acides la indolealkanoique
CZ20013833A3 (cs) * 1999-04-28 2002-02-13 Aventis Pharma Deutschland Gmbh Deriváty kyselin se dvěma arylovými zbytky jako ligandy receptorů PPAR a farmaceutické prostředky, které je obsahují
US6939090B1 (en) * 1999-08-17 2005-09-06 Mitsubishi Materials Corporation Throwaway tip and throwaway-type cutting tool
IL149883A0 (en) * 1999-12-03 2002-11-10 Kyoto Pharma Ind Heterocyclic compounds and pharmaceutical compositions containing the same
US6608059B1 (en) * 2000-06-27 2003-08-19 Smithkline Beecham Corporation Fatty acid synthase inhibitors
CZ20033394A3 (cs) * 2001-06-12 2005-03-16 Wellstat Therapeutics Corporation Sloučeniny pro léčení metabolických poruch a způsob jejich přípravy
CA2460313C (en) * 2001-09-14 2011-03-08 Tularik Inc. Bisphenylsulfanyl and sulphonate compounds and use thereof for elevating hdl cholesterol levels
JP2005528346A (ja) * 2002-02-25 2005-09-22 イーライ・リリー・アンド・カンパニー ペルオキシソーム増殖因子活性化受容体調節物質
US6806265B2 (en) * 2002-05-16 2004-10-19 Boehringer Ingelheim International Gmbh Non-nucleoside reverse transcriptase inhibitors
KR20120104412A (ko) * 2002-09-06 2012-09-20 인설트 테라페틱스, 인코퍼레이티드 공유결합된 치료제 전달을 위한 사이클로덱스트린-기초 중합체
US7268174B2 (en) * 2003-07-11 2007-09-11 Siemens Power Generation, Inc. Homogeneous alumoxane-LCT-epoxy polymers and methods for making the same
JP4845730B2 (ja) * 2003-07-17 2011-12-28 プレキシコン,インコーポレーテッド Ppar活性化合物
US7348338B2 (en) * 2003-07-17 2008-03-25 Plexxikon, Inc. PPAR active compounds
US20050203151A1 (en) * 2003-12-19 2005-09-15 Kalypsys, Inc. Novel compounds, compositions and uses thereof for treatment of metabolic disorders and related conditions

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