JP6082409B2 - 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 - Google Patents

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 Download PDF

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JP6082409B2
JP6082409B2 JP2014560442A JP2014560442A JP6082409B2 JP 6082409 B2 JP6082409 B2 JP 6082409B2 JP 2014560442 A JP2014560442 A JP 2014560442A JP 2014560442 A JP2014560442 A JP 2014560442A JP 6082409 B2 JP6082409 B2 JP 6082409B2
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JP2015512885A (ja
JP2015512885A5 (enExample
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アッシュワース,アラン
ジェイムズ ロード,クリストファー
ジェイムズ ロード,クリストファー
ジェイムズ ローランド エリオット,リチャード
ジェイムズ ローランド エリオット,リチャード
ニクレスク−ドゥバツ,ダン
ポーター,ロデリック
ジョン ボッフェイ,レイモンド
ジョン ボッフェイ,レイモンド
ジェイン ベイフォード,メラニー
ジェイン ベイフォード,メラニー
ファース−クラーク,スチュアート
ニコラス ジャービス,アシュリー
ニコラス ジャービス,アシュリー
ロバート ペリオー,トレバー
ロバート ペリオー,トレバー
エリザベス キー,レベカー
エリザベス キー,レベカー
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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
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
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    • C07D217/24Oxygen atoms
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  • Plural Heterocyclic Compounds (AREA)
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JP2014560442A 2012-03-07 2013-03-07 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 Expired - Fee Related JP6082409B2 (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US201261607680P 2012-03-07 2012-03-07
US61/607,680 2012-03-07
PCT/GB2013/050561 WO2013132253A1 (en) 2012-03-07 2013-03-07 3-aryl-5-substituted-isoquinolin-1-one compounds and their therapeutic use

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JP2015512885A JP2015512885A (ja) 2015-04-30
JP2015512885A5 JP2015512885A5 (enExample) 2016-03-31
JP6082409B2 true JP6082409B2 (ja) 2017-02-15

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US (1) US9193689B2 (enExample)
EP (1) EP2822656B1 (enExample)
JP (1) JP6082409B2 (enExample)
KR (1) KR102104144B1 (enExample)
CN (1) CN104302358B (enExample)
AU (1) AU2013229229B2 (enExample)
CA (1) CA2865511A1 (enExample)
DK (1) DK2822656T3 (enExample)
ES (1) ES2611504T3 (enExample)
IN (1) IN2014MN01875A (enExample)
MX (1) MX346147B (enExample)
RU (1) RU2696572C2 (enExample)
WO (1) WO2013132253A1 (enExample)

Families Citing this family (31)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
MX346147B (es) 2012-03-07 2017-03-09 Inst Of Cancer Research: Royal Cancer Hospital (The) Compuestos de 3-aril-5-substituido-isoquinolin-1-ona y su uso terapeutico.
EP2882714B1 (en) * 2012-08-08 2019-11-13 Merck Patent GmbH (aza-)isoquinolinone derivatives
WO2015036759A1 (en) 2013-09-11 2015-03-19 Institute Of Cancer Research: Royal Cancer Hospital (The) 3-aryl-5-substituted-isoquinolin-1-one compounds and their therapeutic use
CA3038280A1 (en) * 2015-09-30 2017-04-06 Max-Planck-Gesellschaft Zur Forderung Der Wissenschaften E.V. - Generalverwaltung Heteroaryl derivatives as sepiapterin reductase inhibitors
BR112018011053A2 (pt) 2015-12-02 2018-11-21 Syngenta Participations Ag derivados de oxadiazol microbiocidas
UY37623A (es) 2017-03-03 2018-09-28 Syngenta Participations Ag Derivados de oxadiazol tiofeno fungicidas
US11447481B2 (en) 2017-06-02 2022-09-20 Syngenta Participations Ag Microbiocidal oxadiazole derivatives
WO2018219773A1 (en) 2017-06-02 2018-12-06 Syngenta Participations Ag Fungicidal compositions
KR20200022452A (ko) 2017-06-28 2020-03-03 신젠타 파티서페이션즈 아게 살진균 조성물
WO2019011928A1 (en) 2017-07-11 2019-01-17 Syngenta Participations Ag MICROBIOCIDE OXADIAZOLE DERIVATIVES
BR112020000456A2 (pt) 2017-07-11 2020-07-21 Syngenta Participations Ag derivados oxadiazol microbiocidas
BR112020000465B1 (pt) 2017-07-11 2024-02-20 Syngenta Participations Ag Derivados oxadiazol microbiocidas
WO2019011926A1 (en) 2017-07-11 2019-01-17 Syngenta Participations Ag MICROBIOCIDE OXADIAZOLE DERIVATIVES
WO2019012011A1 (en) 2017-07-12 2019-01-17 Syngenta Participations Ag MICROBIOCIDE OXADIAZOLE DERIVATIVES
WO2019012003A1 (en) 2017-07-13 2019-01-17 Syngenta Participations Ag MICROBIOCIDE OXADIAZOLE DERIVATIVES
US12402885B2 (en) 2017-09-23 2025-09-02 Universität Zürich Medical occlusion device
EP3459469A1 (en) 2017-09-23 2019-03-27 Universität Zürich Medical occluder device
AR114136A1 (es) 2017-10-10 2020-07-29 Hoffmann La Roche Compuestos heterocíclicos
WO2020016180A1 (en) 2018-07-16 2020-01-23 Syngenta Crop Protection Ag Microbiocidal oxadiazole derivatives
JP7598875B2 (ja) 2019-04-12 2024-12-12 リボサイエンス リミティド ライアビリティ カンパニー エクトヌクレオチドピロホスファターゼホスホジエステラーゼ1阻害剤としての二環式ヘテロアリール誘導体
AR118673A1 (es) 2019-04-18 2021-10-20 Syngenta Crop Protection Ag Procedimiento para la preparación de derivados de oxadiazol microbiocidas
CN114641242B (zh) 2019-09-26 2025-11-18 苏黎世大学 左心耳闭塞装置
JP7512380B2 (ja) * 2019-10-30 2024-07-08 ディグムバイオ.インコーポレイテッド イソキノリノン誘導体、その製造方法及びそれを有効成分として含有するポリ(adp-リボース)ポリメラーゼ-1(parp-1)関連疾患の予防又は治療用薬学的組成物
US11972017B2 (en) 2020-10-21 2024-04-30 Verint Americas Inc. System and method of automated determination of use of sensitive information and corrective action for improper use
CN117043302A (zh) 2021-03-18 2023-11-10 默克专利有限公司 用于有机电致发光器件的杂芳族化合物
US20240246903A1 (en) * 2021-05-04 2024-07-25 Board Of Regents, The University Of Texas System Indanone and tetraloneketo or hydroxyl oximes as cancel therapeutics
EP4674841A2 (en) * 2022-02-16 2026-01-07 Duke Street Bio Limited Pharmaceutical compound
CN115572262B (zh) * 2022-10-27 2024-08-27 厦门沃克沃德医药科技有限公司 一种异喹啉衍生物及其制备方法
WO2024238871A1 (en) * 2023-05-18 2024-11-21 Rectify Pharmaceuticals, Inc. Aryl sulfonamide compounds and their use in treating medical conditions
GB2634228A (en) * 2023-10-02 2025-04-09 Duke Street Bio Ltd PARP1 inhibitor compounds
WO2025136936A1 (en) * 2023-12-19 2025-06-26 Merck Sharp & Dohme Llc Agonists of trem2 activity

Family Cites Families (67)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2851458A (en) 1955-06-08 1958-09-09 Burroughs Wellcome Co Diquaternary compounds and the manufacture thereof
US3464563A (en) 1967-02-06 1969-09-02 American Air Filter Co Liquid filter apparatus
US4678500A (en) 1984-06-29 1987-07-07 E. I. Du Pont De Nemours And Company Herbicidal 2,6-disubstituted benzylsulfonamides and benzenesulfamates
US5177075A (en) 1988-08-19 1993-01-05 Warner-Lambert Company Substituted dihydroisoquinolinones and related compounds as potentiators of the lethal effects of radiation and certain chemotherapeutic agents; selected compounds, analogs and process
US4942163A (en) 1989-03-07 1990-07-17 E. I. Du Pont De Nemours And Company 1(2H)-isoquinolinones and 1-isoquinolineamines as cancer chemotherapeutic agents
DE69839887D1 (de) 1997-10-02 2008-09-25 Eisai R&D Man Co Ltd Kondensierte pyridinderivate
US6878714B2 (en) 2001-01-12 2005-04-12 Amgen Inc. Substituted alkylamine derivatives and methods of use
US20040176361A1 (en) 2001-05-23 2004-09-09 Masakazu Fujio Fused heterocyclic compound and medicinal use thereof
KR100909141B1 (ko) 2001-09-21 2009-07-23 브리스톨-마이어스스퀴브컴파니 인자 Xa 억제제로서의 락탐-함유 화합물 및 그의 유도체
MY140680A (en) 2002-05-20 2010-01-15 Bristol Myers Squibb Co Hepatitis c virus inhibitors
EP1544194A4 (en) 2002-07-24 2009-01-21 Kyorin Seiyaku Kk DERIVATIVE 4- (ARYL SUBSTITUTED) -5-HYDROXYISOQUINOLINONE
DK1557414T3 (da) 2002-10-01 2012-05-29 Mitsubishi Tanabe Pharma Corp IsoquinoIin-forbindelser og medicinsk anvendelse deraf
PL376769A1 (pl) 2002-10-23 2006-01-09 Glenmark Pharmaceuticals Ltd. Nowe związki tricykliczne użyteczne w leczeniu chorób zapalnych i alergicznych, sposób ich wytwarzania i kompozycje farmaceutyczne je zawierające
DE60335911D1 (de) 2002-12-20 2011-03-10 Daiichi Sankyo Co Ltd Isochinolinonderivate und deren verwendung als medikamente
ES2320771T3 (es) 2003-04-16 2009-05-28 Bristol-Myers Squibb Company Inhibidores peptidicos de isoquinolina macrociclicos del virus de la hepatitis c.
TW200536830A (en) 2004-02-06 2005-11-16 Chugai Pharmaceutical Co Ltd 1-(2H)-isoquinolone derivative
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
WO2005113540A1 (ja) 2004-05-20 2005-12-01 Mitsubishi Pharma Corporation イソキノリン化合物及びその医薬用途
EP2332527A3 (en) 2004-10-20 2011-11-16 Resverlogix Corp. Flavanoids and Isoflavanoids for the prevention and treatment of cardiovascular diseases
BRPI0516947A (pt) 2004-10-22 2008-09-23 Janssen Pharmaceutica Nv inibidores de quinase c-fms
EP1828134B1 (en) 2004-12-16 2008-10-29 F.Hoffmann-La Roche Ag Piperazinyl pyridine derivatives as anti-obesity agents
TWI389897B (zh) 2005-02-22 2013-03-21 Chugai Pharmaceutical Co Ltd 1- (2H) -isoquinolinone derivatives
CA2603185C (en) 2005-03-31 2011-07-26 Astellas Pharma Inc. Propane-1,3-dione derivative or salt thereof
CN101365446B (zh) 2005-07-29 2013-05-22 雷斯弗洛吉克斯公司 预防和治疗复杂疾病的药物组合物及其经由可植入医药装置的递送
EP1937268A4 (en) * 2005-08-24 2009-07-22 Inotek Pharmaceuticals Corp INDENOISOCHINOLINONE ANALOGUES AND METHOD OF USE THEREOF
CA2662112A1 (en) 2006-09-05 2008-03-13 Kyowa Hakko Kirin Co., Ltd. Imidazole derivatives and their use as cannabinoid type 2 (cb2) receptor modulators
US7772180B2 (en) 2006-11-09 2010-08-10 Bristol-Myers Squibb Company Hepatitis C virus inhibitors
NZ579355A (en) 2007-02-01 2012-03-30 Resverlogix Corp 2-(Aryl)-4-oxo-quinazoline derivatives
FR2919286A1 (fr) 2007-07-27 2009-01-30 Sanofi Aventis Sa Derives de derives de 1-oxo-1,2-dihydroisoquinoleine-5- carboxamides et de 4-oxo-3,4-dihydroquinazoline-8- carboxamides,leur preparation et leur application en therapeutique.
US20090054392A1 (en) 2007-08-20 2009-02-26 Wyeth Naphthylpyrimidine, naphthylpyrazine and naphthylpyridazine analogs and their use as agonists of the wnt-beta-catenin cellular messaging system
WO2009027650A1 (en) 2007-08-24 2009-03-05 The Institute Of Cancer: Royal Cancer Hospital Materials and methods for exploiting synthetic lethality in brca-associated cancers
CA2704648A1 (en) 2007-11-05 2009-05-14 Novartis Ag Methods and compositions for measuring wnt activation and for treating wnt-related cancers
DE102008019838A1 (de) 2008-04-19 2009-12-10 Boehringer Ingelheim International Gmbh Neue Arylsulfonylglycin-Derivate, deren Herstellung und deren Verwendung als Arzneimittel
CA2722035C (en) 2008-04-22 2016-10-11 Janssen Pharmaceutica Nv Quinoline or isoquinoline substituted p2x7 antagonists
US8697685B2 (en) 2008-11-20 2014-04-15 Glaxosmithkline Llc Chemical compounds
SG174252A1 (en) 2009-03-06 2011-10-28 Hoffmann La Roche Heterocyclic antiviral compounds
CN105859639A (zh) 2009-03-18 2016-08-17 雷斯韦洛吉克斯公司 新的抗炎剂
JP5813626B2 (ja) 2009-04-22 2015-11-17 レスバーロジックス コーポレイション 新規抗炎症剤
TWI499418B (zh) 2009-05-21 2015-09-11 Nerviano Medical Sciences Srl 異喹啉-1(2h)-酮衍生物
BR112012008518A2 (pt) 2009-10-13 2016-04-05 Msd Oss Bv derivado heterocíclico, e, composição farmacêutica
AU2011255218B2 (en) 2010-05-21 2015-03-12 Infinity Pharmaceuticals, Inc. Chemical compounds, compositions and methods for kinase modulation
EP2582680A1 (en) 2010-06-17 2013-04-24 Novartis AG Biphenyl substituted 1,3-dihydro-benzoimidazol-2-ylideneamine derivatives
EA201490272A1 (ru) 2011-07-13 2014-05-30 Новартис Аг Новые 4-пиперидинильные соединения для применения в качестве ингибиторов танкиразы
CN103781776A (zh) 2011-07-13 2014-05-07 诺华股份有限公司 用作端锚聚合酶抑制剂的新的2-哌啶-1-基-乙酰胺化合物
CN103814032A (zh) 2011-07-13 2014-05-21 诺华股份有限公司 用作端锚聚合酶抑制剂的4-氧代-3,5,7,8-四氢-4H-吡喃并[4,3-d]嘧啶基化合物
JP6106182B2 (ja) 2011-11-25 2017-03-29 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−1阻害剤としての3−フェニル−イソキノリン−1(2h)−オン誘導体
NZ624063A (en) 2011-12-31 2016-09-30 Beigene Ltd Fused tetra or penta-cyclic dihydrodiazepinocarbazolones as parp inhibitors
AU2011384859B2 (en) 2011-12-31 2016-03-17 Beigene, Ltd. Fused tetra or penta-cyclic pyridophthalazinones as PARP inhibitors
AU2013212175B2 (en) 2012-01-28 2017-03-02 Cancer Research Technology Limited Azaheterocyclic compounds
US9174980B2 (en) 2012-01-31 2015-11-03 Boehringer Ingelheim International Gmbh Heterocyclic compounds as inhibitors of leukotriene production
MX349736B (es) 2012-02-09 2017-08-10 Merck Patent Gmbh Derivados de tetrahidro-quinazolinona como inhibidores de tankirasas y poli(adp-ribosa) polimerasa.
EP2822944A1 (en) 2012-03-05 2015-01-14 Amgen, Inc. Oxazolidinone compounds and derivatives thereof
MX346147B (es) 2012-03-07 2017-03-09 Inst Of Cancer Research: Royal Cancer Hospital (The) Compuestos de 3-aril-5-substituido-isoquinolin-1-ona y su uso terapeutico.
NZ630489A (en) 2012-03-28 2016-04-29 Merck Patent Gmbh Bicyclic pyrazinone derivatives
US20130281397A1 (en) 2012-04-19 2013-10-24 Rvx Therapeutics Inc. Treatment of diseases by epigenetic regulation
SI2844659T1 (sl) 2012-05-04 2016-10-28 Merck Patent Gmbh Pirolotriazinonski derivati
WO2013177349A2 (en) 2012-05-25 2013-11-28 Glaxosmithkline Llc Quinazolinediones as tankyrase inhibitors
MX2014014582A (es) 2012-06-07 2015-05-11 Hoffmann La Roche Inhibidores pirazolopirimidona y pirazolopiridona de tanquirasa.
HK1202112A1 (en) 2012-06-07 2015-09-18 霍夫曼-拉罗奇有限公司 Pyrrolopyrimidone and pyrrolopyridone inhibitors of tankyrase
JP2015520205A (ja) 2012-06-20 2015-07-16 エフ・ホフマン−ラ・ロシュ・アクチェンゲゼルシャフト タンキラーゼのピロロピラゾン阻害剤
MX2014015345A (es) 2012-06-20 2015-03-05 Hoffmann La Roche Inhibidores piranopiridona de tanquirasa.
EP2882714B1 (en) 2012-08-08 2019-11-13 Merck Patent GmbH (aza-)isoquinolinone derivatives
WO2014036022A1 (en) 2012-08-29 2014-03-06 Amgen Inc. Quinazolinone compounds and derivatives thereof
WO2014045101A1 (en) 2012-09-21 2014-03-27 Cellzome Gmbh Tetrazolo quinoxaline derivatives as tankyrase inhibitors
AR092211A1 (es) 2012-09-24 2015-04-08 Merck Patent Ges Mit Beschränkter Haftung Derivados de hidropirrolopirrol
US9388142B2 (en) 2012-09-26 2016-07-12 Merck Patent Gmbh Quinazolinone derivatives as PARP inhibitors
WO2014087165A1 (en) 2012-12-06 2014-06-12 University Of Bath Tankyrase inhibitors

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CA2865511A1 (en) 2013-09-12
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