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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JP2015524450A (ja
JP6247294B2 (ja
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Publication date
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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)

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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
US9193689B2 (en) 2012-03-07 2015-11-24 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
JP6456392B2 (ja) 2013-09-11 2019-01-23 インスティチュート オブ キャンサー リサーチ:ロイヤル キャンサー ホスピタル 3−アリール−5−置換イソキノリン−1−オン化合物及びその治療的使用
UY36060A (es) 2014-04-02 2015-10-30 Bayer Pharma AG Compuestos de azol sustituidos con amida
CN106459057B (zh) * 2014-04-10 2019-06-07 湖北生物医药产业技术研究院有限公司 作为PARP抑制剂的4H-吡唑并[1,5-α]苯并咪唑化合物的类似物
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
WO2017055313A1 (en) 2015-10-01 2017-04-06 Bayer Pharma Aktiengesellschaft Amido-substituted azole compounds
WO2017055316A1 (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
WO2017160898A1 (en) * 2016-03-15 2017-09-21 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
US10875860B2 (en) 2016-12-22 2020-12-29 Purdue Research Foundation Azaindenoisoquinoline compounds and uses thereof
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

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GB9624482D0 (en) 1995-12-18 1997-01-15 Zeneca Phaema S A Chemical compounds
SK285141B6 (sk) 1996-02-13 2006-07-07 Astrazeneca Uk Limited Použitie chinazolínového derivátu, chinazolínový derivát, spôsob jeho prípravy a farmaceutická kompozícia, ktorá ho obsahuje
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
AU9298098A (en) 1997-09-03 1999-03-22 Guilford Pharmaceuticals Inc. Amino-substituted compounds, methods, and compositions for inhibiting parp activity
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
US6340759B1 (en) 1997-10-02 2002-01-22 Eisai Co., Ltd. Fused pyridine derivatives
WO2000009504A1 (en) * 1998-08-11 2000-02-24 Pfizer Products Inc. Substituted 1,8-naphthyridin-4(1h)-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
MXPA02011770A (es) 2000-05-31 2003-04-10 Astrazeneca Ab Derivados de indol con actividad de dano vascular.
US20050277627A1 (en) 2000-07-07 2005-12-15 Arnould Jean C Colchinol derivatives as vascular damaging agents
KR20030022264A (ko) 2000-07-07 2003-03-15 앤지오젠 파마슈티칼스 리미티드 신생 혈관 형성 억제제인 콜치놀 유도체
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
KR101444489B1 (ko) 2007-02-01 2014-09-24 리스버로직스 코퍼레이션 심혈관 질환을 예방 및 치료하기 위한 화합물
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
US9193689B2 (en) * 2012-03-07 2015-11-24 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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