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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JP4377942B2 (ja
JP2008531599A (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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EP1991525A1 (en) * 2006-02-27 2008-11-19 Serenex, Inc. Cyclohexylamino, benzene, pyridine, and pyridazine derivatives
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US20080119457A1 (en) * 2006-08-24 2008-05-22 Serenex, Inc. Benzene, Pyridine, and Pyridazine Derivatives
WO2008024961A1 (en) * 2006-08-24 2008-02-28 Serenex, Inc. Dihydropyridazine, tetrahydropyridine, chromanone, and dihydronaphthalenone derivatives as heat-shock protein 90 inhibitors
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US20080070933A1 (en) * 2006-08-24 2008-03-20 Huang Kenneth H Purine, Pyrimidine, and Azaindole Derivatives
WO2008024980A2 (en) * 2006-08-24 2008-02-28 Serenex, Inc. Pyrrole, thiophene, furan, imidazole, oxazole, and thiazole derivatives
FR2907453B1 (fr) 2006-10-24 2008-12-26 Sanofi Aventis Sa Nouveaux derives du fluorene,compositions les contenant et utilisation
US20100280032A1 (en) * 2006-10-26 2010-11-04 Synta Pharmaceuticals Corp. Method for treating inflammatory disorders
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WO2009051244A1 (ja) 2007-10-18 2009-04-23 Takeda Pharmaceutical Company Limited 複素環化合物
CA2755660A1 (fr) * 2009-03-19 2010-09-23 Sanofi 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
FR2955323B1 (fr) * 2010-01-19 2015-01-16 Sanofi Aventis Nouveaux derives d'indazole inhibiteurs d'hsp90, compositions les contenant et utilisation
ES2635494T3 (es) * 2009-03-30 2017-10-04 Nordic Bioscience A/S Ensayo de biomarcador de fibrosis
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
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
GB201009853D0 (en) 2010-06-11 2010-07-21 Chroma Therapeutics Ltd HSP90 inhibitors
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
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
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
US9457045B2 (en) 2011-03-15 2016-10-04 The University Of British Columbia Combination of anti-clusterin oligonucleotide with Hsp90 inhibitor for the treatment of prostate cancer
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
EP2776025A1 (en) 2011-11-02 2014-09-17 Synta Pharmaceuticals Corp. Combination therapy of hsp90 inhibitors with platinum-containing agents
JP2014532712A (ja) 2011-11-02 2014-12-08 シンタ ファーマシューティカルズ コーポレーション トポイソメラーゼi阻害剤とhsp90阻害剤の組合せを使用する癌療法
EP2780010A1 (en) 2011-11-14 2014-09-24 Synta Pharmaceuticals 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
MY194204A (en) 2014-08-04 2022-11-21 Nuevolution As Optionally fused heterocyclyl-substituted derivatives of pyrimidine useful for the treatment of inflammatory, metabolic, oncologic and autoimmune diseases
WO2016040809A1 (en) * 2014-09-11 2016-03-17 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
WO2017059434A1 (en) 2015-10-02 2017-04-06 Esanex, Inc. Use of tetrahydroindazolylbenzamide and tetrahydroindolylbenzamide derivatives for the treatment of cancer
CA3000803C (en) * 2015-10-13 2020-03-24 Nihon Nohyaku Co., Ltd. Oxime group-containing condensed heterocyclic compound or salt thereof, agricultural and horticultural insecticide comprising the compound, and method for using the insecticide
US11261187B2 (en) 2016-04-22 2022-03-01 Duke University Compounds and methods for targeting HSP90
CA3022882A1 (en) * 2016-05-18 2017-11-23 Esanex, Inc. Combination therapies using indazolylbenzamide derivatives for the treatment of cancer
CN110035752A (zh) 2016-09-23 2019-07-19 埃萨内克斯股份有限公司 使用吲唑基苯甲酰胺衍生物治疗癌症的组合疗法
SMT201900517T1 (it) 2017-03-20 2019-11-13 Forma Therapeutics Inc Composizioni di pirrolopirrolo come attivatori di piruvato chinasi (pkr)
CN113166060B (zh) 2018-09-19 2024-01-09 诺沃挪第克健康护理股份公司 用丙酮酸激酶激活化合物治疗镰状细胞病
US11001588B2 (en) 2018-09-19 2021-05-11 Forma Therapeutics, Inc. Activating pyruvate kinase R and mutants thereof
CA3151612A1 (en) 2019-09-19 2021-03-25 George P. Luke Pyruvate kinase r (pkr) activating compositions
PE20230240A1 (es) 2019-12-20 2023-02-07 Nuevolution As Compuestos activos frente a receptores nucleares
JP2021098692A (ja) 2019-12-20 2021-07-01 ヌエヴォリューション・アクティーゼルスカブNuevolution A/S 核内受容体に対して活性の化合物
WO2021198955A1 (en) 2020-03-31 2021-10-07 Nuevolution A/S Compounds active towards nuclear receptors
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