JP2010536842A5 - - Google Patents

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Publication number
JP2010536842A5
JP2010536842A5 JP2010521488A JP2010521488A JP2010536842A5 JP 2010536842 A5 JP2010536842 A5 JP 2010536842A5 JP 2010521488 A JP2010521488 A JP 2010521488A JP 2010521488 A JP2010521488 A JP 2010521488A JP 2010536842 A5 JP2010536842 A5 JP 2010536842A5
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JP
Japan
Prior art keywords
alkyl
pharmaceutically acceptable
independently
tautomer
membered
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
JP2010521488A
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English (en)
Japanese (ja)
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JP2010536842A (ja
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Publication date
Priority claimed from GBGB0716532.7A external-priority patent/GB0716532D0/en
Application filed filed Critical
Publication of JP2010536842A publication Critical patent/JP2010536842A/ja
Publication of JP2010536842A5 publication Critical patent/JP2010536842A5/ja
Pending legal-status Critical Current

Links

JP2010521488A 2007-08-24 2008-08-21 ポリ(adp−リボース)ポリメラーゼ(parp)阻害剤としてのキノリン−4−オン及び4−オキソジヒドロシンノリン誘導体 Pending JP2010536842A (ja)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
GBGB0716532.7A GB0716532D0 (en) 2007-08-24 2007-08-24 Therapeutic compounds
PCT/GB2008/050731 WO2009027730A1 (en) 2007-08-24 2008-08-21 Quinolin-4-one and 4-oxodihydrocinnoline derivatives as inhibitors of poly(adp-ribose)polymerase (parp)

Publications (2)

Publication Number Publication Date
JP2010536842A JP2010536842A (ja) 2010-12-02
JP2010536842A5 true JP2010536842A5 (https=) 2011-09-22

Family

ID=38599210

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2010521488A Pending JP2010536842A (ja) 2007-08-24 2008-08-21 ポリ(adp−リボース)ポリメラーゼ(parp)阻害剤としてのキノリン−4−オン及び4−オキソジヒドロシンノリン誘導体

Country Status (7)

Country Link
US (1) US8354413B2 (https=)
EP (1) EP2193121A1 (https=)
JP (1) JP2010536842A (https=)
AU (1) AU2008291905A1 (https=)
CA (1) CA2697971A1 (https=)
GB (1) GB0716532D0 (https=)
WO (1) WO2009027730A1 (https=)

Families Citing this family (15)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP5654001B2 (ja) * 2009-04-29 2015-01-14 グラクソ グループ リミテッドGlaxo Group Limited P2X7調節因子としての5,6,7,8−テトラヒドロ[1,2,4]トリアゾロ[4,3−a]ピラジン誘導体
CA2829123C (en) 2011-03-14 2016-04-12 Eternity Bioscience Inc. Quinazolinediones and their use
TWI527800B (zh) 2011-04-01 2016-04-01 南京英派藥業有限公司 作為聚(二磷酸腺苷酸-核醣)聚合酶(parp)之抑制劑之1-(芳基甲基)喹唑啉-2,4(1h,3h)-二酮及其應用
TWI735416B (zh) 2014-10-06 2021-08-11 美商維泰克斯製藥公司 囊腫纖維化症跨膜傳導調節蛋白之調節劑
ES2946970T3 (es) 2016-03-31 2023-07-28 Vertex Pharma Regulador de conductancia transmembrana de moduladores de fibrosis quística
SI3519401T1 (sl) 2016-09-30 2022-01-31 Vertex Pharmaceuticals Incorporated Modulator regulatorja transmembranske prevodnosti pri cistični fibrozi, farmacevtski sestavki, postopki zdravljenja in proces za izdelavo modulatorja
CN110267948B (zh) 2016-12-09 2023-12-08 弗特克斯药品有限公司 囊性纤维化跨膜传导调控剂的调节剂、药物组合物、治疗方法和制备所述调节剂的方法
AU2018279646B2 (en) 2017-06-08 2023-04-06 Vertex Pharmaceuticals Incorporated Methods of treatment for cystic fibrosis
MA49631A (fr) 2017-07-17 2020-05-27 Vertex Pharma Méthodes de traitement de la fibrose kystique
TWI799435B (zh) 2017-08-02 2023-04-21 美商維泰克斯製藥公司 製備化合物之製程
US10654829B2 (en) 2017-10-19 2020-05-19 Vertex Pharmaceuticals Incorporated Crystalline forms and compositions of CFTR modulators
KR102716244B1 (ko) 2017-12-08 2024-10-14 버텍스 파마슈티칼스 인코포레이티드 낭포성 섬유증 막횡단 전도 조절자의 조정제의 제조 방법
TWI810243B (zh) 2018-02-05 2023-08-01 美商維泰克斯製藥公司 用於治療囊腫纖化症之醫藥組合物
EP3774825A1 (en) 2018-04-13 2021-02-17 Vertex Pharmaceuticals Incorporated Modulators of cystic fibrosis transmembrane conductance regulator, pharmaceutical compositions, methods of treatment, and process for making the modulator
CN110845425B (zh) * 2019-11-07 2023-09-08 合肥工业大学 一种酞嗪衍生物及其制备方法和应用

Family Cites Families (16)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0343574B1 (en) 1988-05-24 1994-07-27 Kirin Beer Kabushiki Kaisha 4(1H)-quinolone derivatives
IL100555A (en) 1991-02-07 2000-08-31 Hoechst Marion Roussel Inc N-substituted quinoline derivatives their preparation their use for the preparation of medicaments and the pharmaceutical compositions containing them
US5753674A (en) 1991-10-22 1998-05-19 Octamer, Inc. Adenosine diphosphoribose polymerase binding nitroso aromatic compounds useful as retroviral inactivating agents, anti-retroviral agents, anti-retroviral agents and anti-tumor agents
ATE198623T1 (de) 1994-08-12 2001-01-15 Myriad Genetics Inc Verfahren zum nachweis von prädisposition von ovarial- und brustkrebs
US5589483A (en) 1994-12-21 1996-12-31 Geron Corporation Isoquinoline poly (ADP-ribose) polymerase inhibitors to treat skin diseases associated with cellular senescence
ES2108641B1 (es) * 1995-07-31 1998-08-16 Menarini Lab Sulfonimidas quinolonicas con accion antagonista de los leucotrienos.
EP1309594B1 (fr) 2000-08-08 2004-12-15 Sanofi-Aventis Derives de benzimidazole, leur preparation et leur application en therapeutique
HU228960B1 (hu) 2000-10-30 2013-07-29 Kudos Pharm Ltd Ftalazinon-származékok
WO2002090334A1 (en) 2001-05-08 2002-11-14 Kudos Pharmaceuticals Limited Isoquinolinone derivatives as parp inhibitors
WO2003051879A1 (en) 2001-12-14 2003-06-26 Altana Pharma Ag Known and novel 4,5-dihydro-imidazo[4,5,1-ij]quinolin-6-ones useful as poly(adp-ribose)polymerase inhibitors
DE60335359D1 (de) 2002-04-30 2011-01-27 Kudos Pharm Ltd Phthalazinonderivate
PL1633724T3 (pl) * 2003-03-12 2011-10-31 Kudos Pharm Ltd Pochodne ftalazynonu
WO2005023246A1 (en) 2003-09-04 2005-03-17 Aventis Pharmaceuticals Inc. Substituted indoles as inhibitors of poly (adp-ribose) polymerase (parp)
US20050228007A1 (en) 2004-02-26 2005-10-13 Prakash Jagtap Isoquinoline derivatives and methods of use thereof
JP2008510783A (ja) 2004-08-26 2008-04-10 クドス ファーマシューティカルズ リミテッド 4−ヘテロアリールメチル置換フタラジノン誘導体
DK1954274T3 (da) * 2005-11-10 2011-01-31 Chemocentryx Inc Substituerede quinoloner og fremgangsmåder til anvendelse

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