JP2015524450A5 - - Google Patents

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Publication number
JP2015524450A5
JP2015524450A5 JP2015525763A JP2015525763A JP2015524450A5 JP 2015524450 A5 JP2015524450 A5 JP 2015524450A5 JP 2015525763 A JP2015525763 A JP 2015525763A JP 2015525763 A JP2015525763 A JP 2015525763A JP 2015524450 A5 JP2015524450 A5 JP 2015524450A5
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JP
Japan
Prior art keywords
atoms
compound
het
pharmaceutically acceptable
formula
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JP2015525763A
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English (en)
Japanese (ja)
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JP6247294B2 (ja
JP2015524450A (ja
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Priority claimed from PCT/EP2013/002085 external-priority patent/WO2014023390A2/en
Publication of JP2015524450A publication Critical patent/JP2015524450A/ja
Publication of JP2015524450A5 publication Critical patent/JP2015524450A5/ja
Application granted granted Critical
Publication of JP6247294B2 publication Critical patent/JP6247294B2/ja
Expired - Fee Related legal-status Critical Current
Anticipated expiration legal-status Critical

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JP2015525763A 2012-08-08 2013-07-12 (アザ−)イソキノリノン誘導体 Expired - Fee Related JP6247294B2 (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
EP12005752.6 2012-08-08
EP12005752 2012-08-08
PCT/EP2013/002085 WO2014023390A2 (en) 2012-08-08 2013-07-12 (aza-)isoquinolinone derivatives

Related Child Applications (1)

Application Number Title Priority Date Filing Date
JP2017142160A Division JP6333450B2 (ja) 2012-08-08 2017-07-21 (アザ−)イソキノリノン誘導体

Publications (3)

Publication Number Publication Date
JP2015524450A JP2015524450A (ja) 2015-08-24
JP2015524450A5 true JP2015524450A5 (enExample) 2016-09-01
JP6247294B2 JP6247294B2 (ja) 2017-12-13

Family

ID=48793165

Family Applications (2)

Application Number Title Priority Date Filing Date
JP2015525763A Expired - Fee Related JP6247294B2 (ja) 2012-08-08 2013-07-12 (アザ−)イソキノリノン誘導体
JP2017142160A Expired - Fee Related JP6333450B2 (ja) 2012-08-08 2017-07-21 (アザ−)イソキノリノン誘導体

Family Applications After (1)

Application Number Title Priority Date Filing Date
JP2017142160A Expired - Fee Related JP6333450B2 (ja) 2012-08-08 2017-07-21 (アザ−)イソキノリノン誘導体

Country Status (23)

Country Link
US (1) US9376433B2 (enExample)
EP (1) EP2882714B1 (enExample)
JP (2) JP6247294B2 (enExample)
KR (1) KR102083154B1 (enExample)
CN (1) CN104507912B (enExample)
AR (1) AR092366A1 (enExample)
AU (1) AU2013301870B2 (enExample)
BR (1) BR112015002601A2 (enExample)
CA (1) CA2881330C (enExample)
DK (1) DK2882714T3 (enExample)
ES (1) ES2773272T3 (enExample)
HR (1) HRP20200180T1 (enExample)
HU (1) HUE047608T2 (enExample)
IL (1) IL237072B (enExample)
LT (1) LT2882714T (enExample)
MX (1) MX362939B (enExample)
PL (1) PL2882714T3 (enExample)
PT (1) PT2882714T (enExample)
RS (1) RS59921B1 (enExample)
RU (1) RU2654216C2 (enExample)
SG (1) SG11201500732TA (enExample)
SI (1) SI2882714T1 (enExample)
WO (1) WO2014023390A2 (enExample)

Families Citing this family (19)

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Publication number Priority date Publication date Assignee Title
JP2942847B2 (ja) 1990-06-22 1999-08-30 ダイセル化学工業株式会社 液晶性ポリマーフィルムの製造装置とそれを用いた液晶性ポリマーフィルムの製造方法
EP2822656B1 (en) 2012-03-07 2016-10-19 Institute of Cancer Research: Royal Cancer Hospital (The) 3-aryl-5-substituted-isoquinolin-1-one compounds and their therapeutic use
WO2014087165A1 (en) * 2012-12-06 2014-06-12 University Of Bath Tankyrase inhibitors
US9611223B2 (en) 2013-09-11 2017-04-04 Institute Of Cancer Research: Royal Cancer Hospital (The) 3-aryl-5-substituted-isoquinolin-1-one compounds and their therapeutic use
UY36060A (es) 2014-04-02 2015-10-30 Bayer Pharma AG Compuestos de azol sustituidos con amida
AU2015245786B2 (en) * 2014-04-10 2018-03-15 Hubei Bio-Pharmaceutical Industrial Technological Institute Inc. Analogues of 4H-pyrazolo[1,5-a]benzimidazole compound as PARP inhibitors
CN105153156B (zh) * 2015-09-22 2017-07-28 徐峰 一种4‑苯基‑2,7‑萘啶‑1(2h)‑酮的制备方法
WO2017055316A1 (en) 2015-10-01 2017-04-06 Bayer Pharma Aktiengesellschaft Amido-substituted azole compounds
WO2017055313A1 (en) 2015-10-01 2017-04-06 Bayer Pharma Aktiengesellschaft Amido-substituted azole compounds
WO2017156350A1 (en) 2016-03-09 2017-09-14 K-Gen, Inc. Methods of cancer treatment
US10759795B2 (en) 2016-03-15 2020-09-01 Purdue Research Foundation Aza-A-ring indenoisoquinoline topoisomerase I poisons
WO2018078005A1 (en) 2016-10-29 2018-05-03 Bayer Pharma Aktiengesellschaft Amido-substituted azaspiro derivatives as tankyrase inhibitors
WO2018078009A1 (en) 2016-10-29 2018-05-03 Bayer Pharma Aktiengesellschaft Amido-substituted cyclohexane derivatives
WO2018087126A1 (en) 2016-11-09 2018-05-17 Bayer Pharma Aktiengesellschaft Amido-substituted cyclohexane derivatives as inhibitors of tankyrase
CN110167936A (zh) 2016-12-22 2019-08-23 珀杜研究基金会 氮杂茚并异喹啉化合物及其用途
US10899733B2 (en) 2017-08-23 2021-01-26 Oregon Health & Science University Inhibitors of PARPs that catalyze mono-ADP-ribosylation
RU2709928C1 (ru) * 2019-02-21 2019-12-24 Федеральное государственное бюджетное научное учреждение "Институт природно-технических систем" (ИПТС) Датчик удельной электропроводности
JPWO2024029583A1 (enExample) * 2022-08-05 2024-02-08
GB2634228A (en) * 2023-10-02 2025-04-09 Duke Street Bio Ltd PARP1 inhibitor compounds

Family Cites Families (25)

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Publication number Priority date Publication date Assignee Title
GB9624482D0 (en) 1995-12-18 1997-01-15 Zeneca Phaema S A Chemical compounds
JP4471404B2 (ja) 1996-02-13 2010-06-02 アストラゼネカ ユーケイ リミテッド Vegfインヒビターとしてのキナゾリン誘導体
ATE211134T1 (de) 1996-03-05 2002-01-15 4-anilinochinazolin derivate
GB9718972D0 (en) 1996-09-25 1997-11-12 Zeneca Ltd Chemical compounds
GB9714249D0 (en) 1997-07-08 1997-09-10 Angiogene Pharm Ltd Vascular damaging agents
US6197785B1 (en) * 1997-09-03 2001-03-06 Guilford Pharmaceuticals Inc. Alkoxy-substituted compounds, methods, and compositions for inhibiting PARP activity
WO1999011622A1 (en) 1997-09-03 1999-03-11 Guilford Pharmaceuticals Inc. Amino-substituted compounds, methods, and compositions for inhibiting parp activity
WO1999018077A1 (en) 1997-10-02 1999-04-15 Eisai Co., Ltd. Fused pyridine derivatives
JP3989102B2 (ja) * 1997-10-02 2007-10-10 エーザイ・アール・アンド・ディー・マネジメント株式会社 縮合ピリジン誘導体
OA11591A (en) * 1998-08-11 2004-07-30 Pfizer Prod Inc Substituted 1,8-naphthyridin-4(H)-ones as phosphodiesterase 4 inhibitors.
GB9900334D0 (en) 1999-01-07 1999-02-24 Angiogene Pharm Ltd Tricylic vascular damaging agents
GB9900752D0 (en) 1999-01-15 1999-03-03 Angiogene Pharm Ltd Benzimidazole vascular damaging agents
NZ522074A (en) 2000-05-31 2004-06-25 Astrazeneca Ab Indole derivatives with vascular damaging activity
CA2410562A1 (en) 2000-07-07 2002-01-31 Angiogene Pharmaceuticals Limited Colchinol derivatives as angiogenesis inhibitors
JP2004502766A (ja) 2000-07-07 2004-01-29 アンギオジェン・ファーマシューティカルズ・リミテッド 血管損傷剤としてのコルヒノール誘導体
MY140680A (en) 2002-05-20 2010-01-15 Bristol Myers Squibb Co Hepatitis c virus inhibitors
WO2005075432A1 (ja) * 2004-02-06 2005-08-18 Chugai Seiyaku Kabushiki Kaisha 1−(2h)−イソキノロン誘導体およびその抗ガン剤としての使用
US7772180B2 (en) * 2006-11-09 2010-08-10 Bristol-Myers Squibb Company Hepatitis C virus inhibitors
MX2009008099A (es) 2007-02-01 2009-12-14 Resverlogix Corp Compuestos para la prevencion y tratamiento de enfermedades cardiovasculares.
SI2134691T1 (sl) 2007-03-08 2012-06-29 Janssen Pharmaceutica Nv Derivati kvinolina kot PARP in TANK inhibitorji
TWI499418B (zh) 2009-05-21 2015-09-11 Nerviano Medical Sciences Srl 異喹啉-1(2h)-酮衍生物
FR2956816B1 (fr) 2010-03-01 2012-05-18 Univ Joseph Fourier Utilisation de quinolones pour la preparation de medicaments, nouvelles quinolones et leur procede de synthese
US8957203B2 (en) 2011-05-05 2015-02-17 Bristol-Myers Squibb Company Hepatitis C virus inhibitors
EP2822656B1 (en) * 2012-03-07 2016-10-19 Institute of Cancer Research: Royal Cancer Hospital (The) 3-aryl-5-substituted-isoquinolin-1-one compounds and their therapeutic use
US20130311482A1 (en) 2012-05-17 2013-11-21 Tagged, Inc. Multi-user timeline for facilitating social discovery in social networking environments

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