JP2014521620A5 - - Google Patents

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Publication number
JP2014521620A5
JP2014521620A5 JP2014522035A JP2014522035A JP2014521620A5 JP 2014521620 A5 JP2014521620 A5 JP 2014521620A5 JP 2014522035 A JP2014522035 A JP 2014522035A JP 2014522035 A JP2014522035 A JP 2014522035A JP 2014521620 A5 JP2014521620 A5 JP 2014521620A5
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JP
Japan
Prior art keywords
oxo
indazole
carboxamide
dihydro
alkyl
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.)
Granted
Application number
JP2014522035A
Other languages
English (en)
Japanese (ja)
Other versions
JP2014521620A (ja
JP5902299B2 (ja
Filing date
Publication date
Application filed filed Critical
Priority claimed from PCT/EP2012/064054 external-priority patent/WO2013014038A1/en
Publication of JP2014521620A publication Critical patent/JP2014521620A/ja
Publication of JP2014521620A5 publication Critical patent/JP2014521620A5/ja
Application granted granted Critical
Publication of JP5902299B2 publication Critical patent/JP5902299B2/ja
Active legal-status Critical Current
Anticipated expiration legal-status Critical

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JP2014522035A 2011-07-26 2012-07-18 Parp−1阻害剤としての3−オキソ−2,3−ジヒドロ−1h−インダゾール−4−カルボキサミド誘導体 Active JP5902299B2 (ja)

Applications Claiming Priority (5)

Application Number Priority Date Filing Date Title
EP11175355 2011-07-26
EP11175355.4 2011-07-26
EP12167336 2012-05-09
EP12167336.2 2012-05-09
PCT/EP2012/064054 WO2013014038A1 (en) 2011-07-26 2012-07-18 3-oxo-2,3-dihydro-1h-indazole-4-carboxamide derivatives as parp-1 inhibitors

Publications (3)

Publication Number Publication Date
JP2014521620A JP2014521620A (ja) 2014-08-28
JP2014521620A5 true JP2014521620A5 (cg-RX-API-DMAC10.html) 2015-08-20
JP5902299B2 JP5902299B2 (ja) 2016-04-13

Family

ID=46545382

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2014522035A Active JP5902299B2 (ja) 2011-07-26 2012-07-18 Parp−1阻害剤としての3−オキソ−2,3−ジヒドロ−1h−インダゾール−4−カルボキサミド誘導体

Country Status (5)

Country Link
US (1) US9073893B2 (cg-RX-API-DMAC10.html)
EP (1) EP2736896B1 (cg-RX-API-DMAC10.html)
JP (1) JP5902299B2 (cg-RX-API-DMAC10.html)
ES (1) ES2616464T3 (cg-RX-API-DMAC10.html)
WO (1) WO2013014038A1 (cg-RX-API-DMAC10.html)

Families Citing this family (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN104230896A (zh) * 2013-06-17 2014-12-24 上海汇伦生命科技有限公司 苯并咪唑-2-哌嗪杂环类化合物、其药物组合物及其制备方法和用途
WO2016168641A1 (en) 2015-04-17 2016-10-20 Abbvie Inc. Tricyclic modulators of tnf signaling
US20160304496A1 (en) 2015-04-17 2016-10-20 Abbvie Inc. Indazolones as modulators of tnf signaling
US9879016B2 (en) 2015-04-17 2018-01-30 Abbvie Inc. Indazolones as modulators of TNF signaling
WO2023242302A1 (en) 2022-06-15 2023-12-21 Astrazeneca Ab Combination therapy for treating cancer
WO2024231548A1 (en) 2023-05-11 2024-11-14 Astrazeneca Ab Combination of a parp1 inhibitor and a selective estrogen degrader for treating cancer

Family Cites Families (15)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5036083A (en) 1988-07-15 1991-07-30 Ici Pharma Heterocyclic agents
ES2216625T3 (es) * 1998-11-27 2004-10-16 ABBOTT GMBH & CO. KG Bencimidazoles substituidos y su empleo como inhibidores de parp.
DE19918211A1 (de) * 1999-04-22 2000-10-26 Basf Ag Cycloalkylsubstituierte Benzimidazole, deren Herstellung und Anwendung
WO2001021615A1 (fr) * 1999-09-17 2001-03-29 Yamanouchi Pharmaceutical Co., Ltd. Dérivés de benzimidazole
WO2002100833A1 (en) 2001-06-12 2002-12-19 Sumitomo Pharmaceuticals Company, Limited Rho KINASE INHIBITORS
ATE442139T1 (de) * 2003-03-31 2009-09-15 Lilly Co Eli 3-oxo-1,3-dihydro-indazol-2-carbonsäureamid derivate als phospholipase inhibitoren
EP1957477B1 (en) * 2005-09-29 2011-12-07 Abbott Laboratories 1h-benzimidazole-4-carboxamides substituted with phenyl at the 2-position are potent parp inhibitors
CA2628461C (en) * 2005-11-15 2013-09-24 Abbott Laboratories Substituted 1h-benzimidazole-4-carboxamides are potent parp inhibitors
AU2007232297B2 (en) * 2006-04-03 2012-09-20 Msd Italia S.R.L. Amide substituted indazole and benzotriazole derivatives as poly(ADP-ribose)polymerase (PARP) inhibitors
EP2805945B1 (en) * 2007-01-10 2019-04-03 MSD Italia S.r.l. Amide substituted indazoles as poly(ADP-ribose)polymerase (PARP) inhibitors
WO2008141385A1 (en) 2007-05-21 2008-11-27 Biota Scientific Management Pty Ltd Viral polymerase inhibitors
US8067613B2 (en) * 2007-07-16 2011-11-29 Abbott Laboratories Benzimidazole poly(ADP ribose)polymerase inhibitors
TWI499418B (zh) 2009-05-21 2015-09-11 Nerviano Medical Sciences Srl 異喹啉-1(2h)-酮衍生物
US8765972B2 (en) * 2009-07-14 2014-07-01 Nerviano Medical Sciences S.R.L. 3-oxo-2,3-dihydro-1H-isoindole-4-carboxamides with selective PARP-1 inhibition
JP5852958B2 (ja) * 2009-07-14 2016-02-03 ネルビアーノ・メデイカル・サイエンシーズ・エツセ・エルレ・エルレ Parp阻害剤としての3−オキソ−2,3−ジヒドロ−1h−イソインドール−4−カルボキサミド

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