JP2008531599A5 - - Google Patents

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Publication number
JP2008531599A5
JP2008531599A5 JP2007557244A JP2007557244A JP2008531599A5 JP 2008531599 A5 JP2008531599 A5 JP 2008531599A5 JP 2007557244 A JP2007557244 A JP 2007557244A JP 2007557244 A JP2007557244 A JP 2007557244A JP 2008531599 A5 JP2008531599 A5 JP 2008531599A5
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JP
Japan
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alkyl
aryl
independently
halo
group
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JP2007557244A
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English (en)
Japanese (ja)
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JP2008531599A (ja
JP4377942B2 (ja
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Priority claimed from PCT/US2006/006988 external-priority patent/WO2006091963A1/en
Publication of JP2008531599A publication Critical patent/JP2008531599A/ja
Publication of JP2008531599A5 publication Critical patent/JP2008531599A5/ja
Application granted granted Critical
Publication of JP4377942B2 publication Critical patent/JP4377942B2/ja
Expired - Fee Related legal-status Critical Current
Anticipated expiration legal-status Critical

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JP2007557244A 2005-02-25 2006-02-27 テトラヒドロインドロン及びテトラヒドロインダゾロン誘導体 Expired - Fee Related JP4377942B2 (ja)

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
US65623005P 2005-02-25 2005-02-25
US70571505P 2005-08-04 2005-08-04
US72796505P 2005-10-18 2005-10-18
PCT/US2006/006988 WO2006091963A1 (en) 2005-02-25 2006-02-27 Tetrahydroindolone and tetrahydroindazolone derivatives

Publications (3)

Publication Number Publication Date
JP2008531599A JP2008531599A (ja) 2008-08-14
JP2008531599A5 true JP2008531599A5 (enExample) 2009-05-14
JP4377942B2 JP4377942B2 (ja) 2009-12-02

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ID=36581601

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2007557244A Expired - Fee Related JP4377942B2 (ja) 2005-02-25 2006-02-27 テトラヒドロインドロン及びテトラヒドロインダゾロン誘導体

Country Status (24)

Country Link
US (8) US7358370B2 (enExample)
EP (2) EP1856057B1 (enExample)
JP (1) JP4377942B2 (enExample)
KR (3) KR101617774B1 (enExample)
CN (1) CN101180275B (enExample)
AR (1) AR054186A1 (enExample)
AU (2) AU2006216441B2 (enExample)
BR (1) BRPI0607739A2 (enExample)
CA (1) CA2598993C (enExample)
DK (1) DK1856057T3 (enExample)
EA (1) EA013521B1 (enExample)
ES (1) ES2527770T3 (enExample)
GE (1) GEP20104994B (enExample)
IL (1) IL185280A (enExample)
MA (1) MA29713B1 (enExample)
MX (1) MX2007010227A (enExample)
NO (1) NO20074274L (enExample)
NZ (2) NZ560685A (enExample)
PL (1) PL1856057T3 (enExample)
PT (1) PT1856057E (enExample)
SI (1) SI1856057T1 (enExample)
TW (1) TWI382015B (enExample)
UA (1) UA92907C2 (enExample)
WO (1) WO2006091963A1 (enExample)

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FR2955323B1 (fr) * 2010-01-19 2015-01-16 Sanofi Aventis Nouveaux derives d'indazole inhibiteurs d'hsp90, compositions les contenant et utilisation
FR2943341B1 (fr) * 2009-03-19 2011-03-11 Sanofi Aventis Nouveaux derives d'indazole inhibiteurs d'hsp90,compositions les contenant et utilisation
EP3578664B1 (en) * 2009-03-30 2024-10-30 Nordic Bioscience A/S Collagen iv neo-epitope fibrosis assay
AR077405A1 (es) 2009-07-10 2011-08-24 Sanofi Aventis Derivados del indol inhibidores de hsp90, composiciones que los contienen y utilizacion de los mismos para el tratamiento del cancer
FR2949467B1 (fr) 2009-09-03 2011-11-25 Sanofi Aventis Nouveaux derives de 5,6,7,8-tetrahydroindolizine inhibiteurs d'hsp90, compositions les contenant et utilisation
US9205086B2 (en) 2010-04-19 2015-12-08 Synta Pharmaceuticals Corp. Cancer therapy using a combination of a Hsp90 inhibitory compounds and a EGFR inhibitor
GB201009853D0 (en) 2010-06-11 2010-07-21 Chroma Therapeutics Ltd HSP90 inhibitors
CN101872359B (zh) * 2010-06-11 2013-08-14 北京邮电大学 实现演变点发现的社会网络演化分析方法及系统
CN102311389A (zh) * 2010-06-29 2012-01-11 王小龙 一种氮芳香取代吡唑衍生物、及其合成和抗癌应用
CN101967125B (zh) 2010-10-08 2012-07-04 广州暨南生物医药研究开发基地有限公司 一种Hsp90抑制剂Xbj-B16-1及其制备方法与应用
CN101955461B (zh) * 2010-10-08 2012-11-21 广州暨南生物医药研究开发基地有限公司 一种Hsp90抑制剂Xbj-B11及其制备方法与应用
MX2013010524A (es) 2011-03-15 2013-12-06 Univ British Columbia Combinacion de oligonucleotido anti-clusterina con inhibidor hsp90 para el tratamiento de cancer de prostata.
CN102675288B (zh) * 2011-03-18 2014-01-01 北京师范大学 2-((2-(双(2-吡啶甲基)氨基)乙基)氨基)-4-(3,6,6-三甲基-4-氧-4,5,6,7-四氢吲唑基)苯甲酰胺及制备、应用
CA2853799A1 (en) 2011-11-02 2013-05-10 Synta Pharmaceuticals Corp. Cancer therapy using a combination of hsp90 inhibitors with topoisomerase i inhibitors
WO2013067165A1 (en) 2011-11-02 2013-05-10 Synta Pharmaceuticals Corp. Combination therapy of hsp90 inhibitors with platinum-containing agents
US9402831B2 (en) 2011-11-14 2016-08-02 Synta Pharmaceutical Corp. Combination therapy of HSP90 inhibitors with BRAF inhibitors
EP2879675B1 (en) 2012-08-06 2019-11-13 Duke University Compounds and methods for targeting hsp90
CN103467356B (zh) * 2013-08-12 2015-04-01 绍兴文理学院 一种四氢吲哚化合物及其制备方法与应用
WO2016020288A1 (en) 2014-08-04 2016-02-11 Nuevolution A/S Optionally fused heterocyclyl-substituted derivatives of pyrimidine useful for the treatment of inflammatory, metabolic, oncologic and autoimmune diseases
US10246421B2 (en) * 2014-09-11 2019-04-02 Esanex, Inc. Indazolyl- and indolyl-benzamide derivatives
US20160143884A1 (en) * 2014-11-26 2016-05-26 Esanex, Inc. Use of tetrahydroindazolylbenzamide and tetrahydroindolylbenzamide derivatives for the treatment of human immunodeficiency virus (hiv) and acquired immune deficiency syndrome (aids)
CN104592203A (zh) * 2015-01-30 2015-05-06 广州暨南生物医药研究开发基地有限公司 一种2-氨基-4-四氢吲唑取代的苯甲酰胺化合物及其在制备抗肿瘤药物中的应用
CN104592230B (zh) * 2015-01-30 2017-02-01 广州暨南生物医药研究开发基地有限公司 一种2‑(石榴皮烷‑3‑氨基)‑4‑四氢吲唑取代的苯甲酰胺化合物及其应用
WO2016191412A1 (en) * 2015-05-26 2016-12-01 University Of South Florida Antimicrobial compositions, methods of use, and methods of treatment of infections
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US11261187B2 (en) 2016-04-22 2022-03-01 Duke University Compounds and methods for targeting HSP90
US20190134003A1 (en) * 2016-05-18 2019-05-09 Esanex, Inc. Combination therapies using indazolylbenzamide derivatives for the treatment of cancer
KR20190064602A (ko) 2016-09-23 2019-06-10 에사넥스, 인코포레이티드 암의 치료를 위한 인다졸릴벤즈아미드 유도체를 사용한 조합 요법
JP6594570B2 (ja) 2017-03-20 2019-10-23 フォーマ セラピューティクス,インコーポレイテッド ピルビン酸キナーゼ(pkr)活性化剤としてのピロロピロール組成物
WO2020061378A1 (en) 2018-09-19 2020-03-26 Forma Therapeutics, Inc. Treating sickle cell disease with a pyruvate kinase r activating compound
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