JP2015514806A5 - - Google Patents

Download PDF

Info

Publication number
JP2015514806A5
JP2015514806A5 JP2015509093A JP2015509093A JP2015514806A5 JP 2015514806 A5 JP2015514806 A5 JP 2015514806A5 JP 2015509093 A JP2015509093 A JP 2015509093A JP 2015509093 A JP2015509093 A JP 2015509093A JP 2015514806 A5 JP2015514806 A5 JP 2015514806A5
Authority
JP
Japan
Prior art keywords
alkyl
alkoxy
halo
group
independently selected
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
JP2015509093A
Other languages
English (en)
Japanese (ja)
Other versions
JP2015514806A (ja
JP6101343B2 (ja
Filing date
Publication date
Application filed filed Critical
Priority claimed from PCT/US2013/037884 external-priority patent/WO2013163241A1/en
Publication of JP2015514806A publication Critical patent/JP2015514806A/ja
Publication of JP2015514806A5 publication Critical patent/JP2015514806A5/ja
Application granted granted Critical
Publication of JP6101343B2 publication Critical patent/JP6101343B2/ja
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

JP2015509093A 2012-04-26 2013-04-24 血小板凝集を治療するためのプロテアーゼ活性化受容体4(par4)阻害剤としてのイミダゾチアジアゾールおよびイミダゾピリダジン誘導体 Active JP6101343B2 (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US201261638567P 2012-04-26 2012-04-26
US61/638,567 2012-04-26
PCT/US2013/037884 WO2013163241A1 (en) 2012-04-26 2013-04-24 Imidazothiadiazole and imidazopyridazine derivatives as protease activated receptor 4 (par4) inhibitors for treating platelet aggregation

Publications (3)

Publication Number Publication Date
JP2015514806A JP2015514806A (ja) 2015-05-21
JP2015514806A5 true JP2015514806A5 (cg-RX-API-DMAC10.html) 2016-03-17
JP6101343B2 JP6101343B2 (ja) 2017-03-22

Family

ID=48225151

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2015509093A Active JP6101343B2 (ja) 2012-04-26 2013-04-24 血小板凝集を治療するためのプロテアーゼ活性化受容体4(par4)阻害剤としてのイミダゾチアジアゾールおよびイミダゾピリダジン誘導体

Country Status (14)

Country Link
US (1) US9518064B2 (cg-RX-API-DMAC10.html)
EP (1) EP2855489B1 (cg-RX-API-DMAC10.html)
JP (1) JP6101343B2 (cg-RX-API-DMAC10.html)
KR (1) KR20150003766A (cg-RX-API-DMAC10.html)
CN (1) CN104640869B (cg-RX-API-DMAC10.html)
AU (1) AU2013251680A1 (cg-RX-API-DMAC10.html)
BR (1) BR112014026651A8 (cg-RX-API-DMAC10.html)
CA (1) CA2871599A1 (cg-RX-API-DMAC10.html)
EA (1) EA201491954A1 (cg-RX-API-DMAC10.html)
ES (1) ES2617879T3 (cg-RX-API-DMAC10.html)
IL (1) IL235141A0 (cg-RX-API-DMAC10.html)
MX (1) MX2014012741A (cg-RX-API-DMAC10.html)
SG (1) SG11201406733QA (cg-RX-API-DMAC10.html)
WO (1) WO2013163241A1 (cg-RX-API-DMAC10.html)

Families Citing this family (24)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN104583218B (zh) 2012-04-26 2018-04-24 百时美施贵宝公司 作为蛋白酶活化受体4(par4)抑制剂用于治疗血小板聚集的咪唑并噻二唑和咪唑并吡嗪的衍生物
CN104540835B (zh) * 2012-04-26 2017-08-08 百时美施贵宝公司 用于治疗血小板聚集的作为蛋白酶激活受体4(par4)抑制剂的咪唑并噻二唑衍生物
WO2015124570A1 (en) 2014-02-18 2015-08-27 INSERM (Institut National de la Santé et de la Recherche Médicale) Methods and pharmaceutical composition for the treatment of influenza a virus infection
WO2015144571A1 (en) 2014-03-24 2015-10-01 Bayer Cropscience Ag Phenylpiperidinecarboxamide derivatives as fungicides
US9598419B1 (en) 2014-06-24 2017-03-21 Universite De Montreal Imidazotriazine and imidazodiazine compounds
US9617279B1 (en) 2014-06-24 2017-04-11 Bristol-Myers Squibb Company Imidazooxadiazole compounds
US10214544B2 (en) 2015-02-26 2019-02-26 Universite De Montreal Imidazopyridazine and imidazothiadiazole compounds
WO2016138199A1 (en) 2015-02-26 2016-09-01 Bristol-Myers Squibb Company Benzothiazole and benzothiophne compounds
US9789087B2 (en) 2015-08-03 2017-10-17 Thomas Jefferson University PAR4 inhibitor therapy for patients with PAR4 polymorphism
US10329307B2 (en) 2015-10-19 2019-06-25 Universite De Montreal Heterocyclic compounds as inhibitors of platelet aggregation
WO2017184520A1 (en) * 2016-04-18 2017-10-26 Vanderbilt University Substituted and fused 6-membered protease activated receptor 4 (par-4) antagonists
US20190315774A1 (en) 2016-07-14 2019-10-17 Bristol-Myers Squibb Company Tricyclic heteroaryl-substituted quinoline and azaquinoline compounds as par4 inhibitors
JP7102388B2 (ja) 2016-07-14 2022-07-19 ブリストル-マイヤーズ スクイブ カンパニー 単環式ヘテロアリール置換化合物
KR102494647B1 (ko) 2016-07-14 2023-01-31 브리스톨-마이어스 스큅 컴퍼니 비시클릭 헤테로아릴 치환된 화합물
JP7058256B2 (ja) 2016-07-14 2022-04-21 ブリストル-マイヤーズ スクイブ カンパニー 二環式ヘテロアリール置換化合物
LT3559010T (lt) * 2016-12-23 2022-10-10 Minoryx Therapeutics S.L. 5-[[4-[2-[5-(1-hidroksietil)-2-piridinil]etoksi]fenil]metil]-2,4-tiazolidindiono ir jo druskų gavimo būdas
WO2019149205A1 (zh) * 2018-01-31 2019-08-08 江苏恒瑞医药股份有限公司 苯并杂芳基类衍生物、其制备方法及其在医药上的应用
CN110218218B (zh) * 2018-03-01 2022-04-08 江苏恒瑞医药股份有限公司 苯并呋喃类衍生物、其制备方法及其在医药上的应用
WO2019218957A1 (zh) * 2018-05-16 2019-11-21 深圳信立泰药业股份有限公司 作为用于治疗血小板聚集的蛋白酶激活受体4(par4)抑制剂的化合物
WO2019218955A1 (zh) * 2018-05-16 2019-11-21 深圳信立泰药业股份有限公司 作为用于治疗血小板聚集的蛋白酶激活受体4(par4)抑制剂的化合物
CN110627817B (zh) * 2018-06-25 2022-03-29 中国药科大学 咪唑并环类par4拮抗剂及其医药用途
CN111349105B (zh) * 2018-12-24 2023-04-07 江苏恒瑞医药股份有限公司 苯并呋喃类衍生物、其制备方法及其在医药上的应用
CN109651126A (zh) * 2019-01-17 2019-04-19 杭州师范大学 一种四苯乙烯基羧酸有机配体及其配合物的制备方法
CN113150005B (zh) * 2021-04-09 2022-08-30 中国药科大学 喹喔啉类化合物、制备方法及其在医药上的应用

Family Cites Families (46)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE2823686A1 (de) 1978-05-31 1979-12-06 Bayer Ag Imidazo eckige klammer auf 2.1-b eckige klammer zu eckige klammer auf 1.3.4 eckige klammer zu -thiadiazole
DE3020421A1 (de) 1980-05-29 1981-12-10 Bayer Ag, 5090 Leverkusen Imidazoazolalkensaeureamide, neue zwischenprodukte zu ihrer herstellung, ihre herstellung und ihre verwendung in arzneimitteln
NO811630L (no) 1980-05-29 1981-11-30 Bayer Ag Imidazoazolalkensyreamider, nye mellomprodukter for deres fremstilling, deres fremstilling og deres anvendelse som legemiddel
DE3446778A1 (de) * 1984-12-21 1986-07-03 Dr. Karl Thomae Gmbh, 7950 Biberach Neue imidazoderivate, ihre herstellung und diese verbindungen enthaltende arzneimittel
US4925849A (en) 1987-06-15 1990-05-15 Fujisawa Pharmaceutical Company, Ltd. Pharmaceutically useful pyrazolopyridines
GB8901423D0 (en) 1989-01-23 1989-03-15 Fujisawa Pharmaceutical Co Pyrazolopyridine compound and processes for preparation thereof
ATE211384T1 (de) 1991-01-29 2002-01-15 Fujisawa Pharmaceutical Co Verwendung von adenosinantagonisten zur vorbeugung und behandlung von pankreatitis und ulcera
JP2928079B2 (ja) 1994-02-14 1999-07-28 永信薬品工業股▲ふん▼有限公司 1−(置換ベンジル)−3−(置換アリール)縮合ピラゾール類、その製造法及びその用途
DE69941777D1 (de) 1998-03-10 2010-01-21 Ono Pharmaceutical Co Carbonsäurederivate und medikamente die diese als aktiven wirkstoff enthalten
CZ20021242A3 (cs) 1999-10-08 2002-08-14 Grünenthal GmbH Bicyklické deriváty imidazo-5-yl-aminu, způsob jejich výroby, jejich pouľití a léčiva tyto látky obsahující
DE19948434A1 (de) 1999-10-08 2001-06-07 Gruenenthal Gmbh Substanzbibliothek enthaltend bicyclische Imidazo-5-amine und/oder bicyclische Imidazo-3-amine
DE10019714A1 (de) 2000-04-20 2002-01-10 Gruenenthal Gmbh Salze von bicyclischen, N-acylierten Imidazo-3-aminen und Imidazo-5-aminen
US6387942B2 (en) 2000-06-19 2002-05-14 Yung Shin Pharmaceutical Ind. Co. Ltd Method of treating disorders related to protease-activated receptors-induced cell activation
US6673815B2 (en) 2001-11-06 2004-01-06 Bristol-Myers Squibb Company Substituted acid derivatives useful as antidiabetic and antiobesity agents and method
CA2364985A1 (en) * 2001-12-14 2003-06-14 John W. Gillard Imidazo(2,1-b)thiadiazole sulfonamides
EP1582516B1 (en) 2003-01-10 2013-07-17 Idemitsu Kosan Co., Ltd. Nitrogenous heterocyclic derivative and organic electroluminescent element employing the same
US20070112043A1 (en) 2003-06-13 2007-05-17 Jaquith James B Acylated and non-acylated imidazo[2,1-b]-1,3,4,-thiadiazole-2-sulfonamides, and uses thereof
US20060135571A1 (en) 2003-06-13 2006-06-22 Jaquith James B Imidazo(2,1-b)-1,3,4-thiadiazole sulfoxides and sulfones
US20050267182A1 (en) 2003-11-13 2005-12-01 Ambit Biosciences Corporation Urea derivatives as FLT-3 modulators
CA2555263A1 (en) 2004-02-12 2005-09-01 Neurogen Corporation Imidazo-pyridazines, triazolo-pyridazines and related benzodiazepine receptor ligands
CA2617319A1 (en) 2005-06-24 2007-01-04 The Trustees Of The University Of Pennsylvania Radiolabeled-pegylation of ligands for use as imaging agents
WO2007039177A2 (en) 2005-09-29 2007-04-12 Sanofi-Aventis Phenyl- and pyridinyl- 1, 2 , 4 - oxadiazolone derivatives, processes for their preparation and their use as pharmaceuticals
NL2000397C2 (nl) 2006-01-05 2007-10-30 Pfizer Prod Inc Bicyclische heteroarylverbindingen als PDE10 inhibitoren.
JP2009530281A (ja) 2006-03-14 2009-08-27 アムジエン・インコーポレーテツド 代謝障害の治療に有用である二環式カルボン酸誘導体
BRPI0710133A2 (pt) 2006-04-13 2012-10-30 Aegera Therapeutics Inc uso de compostos de imidazo[2,1-b]-1,3,4-tiadiazol-2-sulfonamida para tratar dor neuropática
DE102006054757A1 (de) 2006-11-21 2008-05-29 Bayer Healthcare Ag Neue aza-bicyclische Verbindungen und ihre Verwendung
US7638541B2 (en) 2006-12-28 2009-12-29 Metabolex Inc. 5-ethyl-2-{4-[4-(4-tetrazol-1-yl-phenoxymethyl)-thiazol-2-yl]-piperidin-1-yl}-pyrimidine
EP1964841A1 (en) 2007-02-28 2008-09-03 sanofi-aventis Imidazo[1,2-a]azine and their use as pharmaceuticals
JP2010526836A (ja) 2007-05-10 2010-08-05 ジーイー・ヘルスケア・リミテッド カンナビノイドCB2レセプターに対して活性を有するイミダゾール(1,2−a)ピリジン及び関連化合物
WO2009017954A1 (en) 2007-08-01 2009-02-05 Phenomix Corporation Inhibitors of jak2 kinase
CA2695989A1 (en) 2007-08-10 2009-02-19 Glaxosmithkline Llc Certain nitrogen containing bicyclic chemical entities for treating viral infections
WO2009027733A1 (en) 2007-08-24 2009-03-05 Astrazeneca Ab (2-pyridin-3-ylimidazo[1,2-b]pyridazin-6-yl) urea derivatives as antibacterial agents
GB0718735D0 (en) 2007-09-25 2007-11-07 Prolysis Ltd Antibacterial agents
JP2011506487A (ja) 2007-12-21 2011-03-03 ザ・ユニバーシティ・オブ・シドニー トランスロケータータンパク質リガンド
CA2713554C (en) * 2008-02-05 2016-09-06 Sanofi-Aventis Imidazopyridazines as par1 inhibitors, production thereof, and use as medicaments
CA2719507C (en) 2008-03-31 2018-03-27 Metabolex, Inc. Oxymethylene aryl compounds and uses thereof
EP2331530B8 (en) 2008-09-26 2013-12-25 National Health Research Institutes Fused multicyclic compounds as protein kinase inhibitors
CA2740193A1 (en) 2008-12-23 2010-07-01 Abbott Laboratories Anti-viral compounds
FR2948521B1 (fr) 2009-07-21 2012-01-27 Dxo Labs Procede d'estimation d'un defaut d'un systeme de capture d'images et systemes associes
TWI450894B (zh) 2009-12-18 2014-09-01 Mitsubishi Tanabe Pharma Corp 新穎抗血小板藥
CN102372701A (zh) 2010-08-10 2012-03-14 江苏恒瑞医药股份有限公司 氮杂双环己烷类衍生物、其制备方法及其在医药上的应用
US8796268B2 (en) 2010-08-11 2014-08-05 Millennium Pharmaceuticals, Inc. Heteroaryls and uses thereof
EP2747769B1 (en) 2011-08-22 2017-08-02 Merck Sharp & Dohme Corp. 2-spiro-substituted iminothiazines and their mono-and dioxides as bace inhibitors, compositions and their use
CN104583218B (zh) 2012-04-26 2018-04-24 百时美施贵宝公司 作为蛋白酶活化受体4(par4)抑制剂用于治疗血小板聚集的咪唑并噻二唑和咪唑并吡嗪的衍生物
CN104540835B (zh) 2012-04-26 2017-08-08 百时美施贵宝公司 用于治疗血小板聚集的作为蛋白酶激活受体4(par4)抑制剂的咪唑并噻二唑衍生物
BR112015001201B1 (pt) 2012-07-18 2022-02-22 University Of Notre Dame Du Lac Compostos anti-infecciosos 5,5-heteroaromáticos e composição

Similar Documents

Publication Publication Date Title
JP2015514806A5 (cg-RX-API-DMAC10.html)
JP2015514808A5 (cg-RX-API-DMAC10.html)
CY1119771T1 (el) Ενωσεις αμινοπυριμιδινυλιου ως αναστολεις toy jak
PH12020551315A1 (en) Benzoxazepin oxazolidinone compounds and methods of use
JP2016506369A5 (cg-RX-API-DMAC10.html)
JP2016516699A5 (cg-RX-API-DMAC10.html)
JP2019518766A5 (cg-RX-API-DMAC10.html)
HK1254469A1 (zh) 稠合双环嘧啶衍生物及其用途
HRP20171453T1 (hr) Derivati imidazotiadiazola i imidazopirazina kao inhibitori proteazom aktiviranog receptora 4 (par4) za liječenje agregacije trombocita
EA201890888A1 (ru) Новые спиро[3h-индол-3,2'-пирролидин]-2(1h)-оновые соединения и производные в качестве ингибиторов mdm2-p53
JP2016506958A5 (cg-RX-API-DMAC10.html)
WO2016160617A3 (en) Inhibitors of cyclin-dependent kinases
WO2016105528A3 (en) Inhibitors of cyclin-dependent kinase 7 (cdk7)
JP2019509291A5 (cg-RX-API-DMAC10.html)
JP2014518882A5 (cg-RX-API-DMAC10.html)
JP2017509586A5 (cg-RX-API-DMAC10.html)
JP2016530259A5 (cg-RX-API-DMAC10.html)
HRP20221207T1 (hr) Supstituirani biciklički heterociklički spojevi kao inhibitori prmt5
JP2016517878A5 (cg-RX-API-DMAC10.html)
JP2016532715A5 (cg-RX-API-DMAC10.html)
JP2017528467A5 (cg-RX-API-DMAC10.html)
JP2014511892A5 (cg-RX-API-DMAC10.html)
JP2020500182A5 (cg-RX-API-DMAC10.html)
JP2017509689A5 (cg-RX-API-DMAC10.html)
JP2017524013A5 (cg-RX-API-DMAC10.html)