JP2012525367A5 - - Google Patents

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Publication number
JP2012525367A5
JP2012525367A5 JP2012507826A JP2012507826A JP2012525367A5 JP 2012525367 A5 JP2012525367 A5 JP 2012525367A5 JP 2012507826 A JP2012507826 A JP 2012507826A JP 2012507826 A JP2012507826 A JP 2012507826A JP 2012525367 A5 JP2012525367 A5 JP 2012525367A5
Authority
JP
Japan
Prior art keywords
pyridin
benzimidazol
methanone
piperidin
dimethylamino
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.)
Ceased
Application number
JP2012507826A
Other languages
English (en)
Japanese (ja)
Other versions
JP2012525367A (ja
Filing date
Publication date
Application filed filed Critical
Priority claimed from PCT/GB2010/050725 external-priority patent/WO2010125402A1/en
Publication of JP2012525367A publication Critical patent/JP2012525367A/ja
Publication of JP2012525367A5 publication Critical patent/JP2012525367A5/ja
Ceased legal-status Critical Current

Links

JP2012507826A 2009-04-30 2010-04-30 イミダゾール誘導体およびサイクリン依存性キナーゼ類のモジュレーターとしてのその使用 Ceased JP2012525367A (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US17429309P 2009-04-30 2009-04-30
US61/174,293 2009-04-30
PCT/GB2010/050725 WO2010125402A1 (en) 2009-04-30 2010-04-30 Imidazole derivatives and their use as modulators of cyclin dependent kinases

Publications (2)

Publication Number Publication Date
JP2012525367A JP2012525367A (ja) 2012-10-22
JP2012525367A5 true JP2012525367A5 (Direct) 2014-10-02

Family

ID=42315726

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2012507826A Ceased JP2012525367A (ja) 2009-04-30 2010-04-30 イミダゾール誘導体およびサイクリン依存性キナーゼ類のモジュレーターとしてのその使用

Country Status (14)

Country Link
US (1) US8598217B2 (Direct)
EP (1) EP2424843B1 (Direct)
JP (1) JP2012525367A (Direct)
KR (1) KR20120004542A (Direct)
CN (1) CN102803225A (Direct)
AU (1) AU2010243353B2 (Direct)
BR (1) BRPI1016190A2 (Direct)
CA (1) CA2759083A1 (Direct)
EA (1) EA020017B1 (Direct)
ES (1) ES2458872T3 (Direct)
MX (1) MX2011011516A (Direct)
PL (1) PL2424843T3 (Direct)
PT (1) PT2424843E (Direct)
WO (1) WO2010125402A1 (Direct)

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EP2558092B1 (en) 2010-04-13 2018-06-27 Novartis AG Combination comprising a cyclin dependent kinase 4 or cyclin dependent kinase 6 (cdk4/6) inhibitor and an mtor inhibitor for treating cancer
BR122021002201A8 (pt) * 2011-02-25 2023-04-11 Merck Sharp & Dohme Composto, composição, uso de um composto, e, método de tratamento de um distúrbio, condição ou doença
HRP20170928T1 (hr) 2011-08-30 2017-09-22 Chdi Foundation, Inc. Inhibitori kinurenin-3-monooksigenaze, farmaceutski pripravci, i postupci za njihovu upotrebu
US20150051232A1 (en) * 2012-03-21 2015-02-19 Bayer Intellectual Property Gmbh Use of (rs)-s-cyclopropyl-s-(4--5-(trifluoromethyl)pyrimidin-2-yl]amino}phenyl)sulfoximide for treating specific tumours
HK1206735A1 (en) * 2012-04-06 2016-01-15 辉瑞公司 Diacylglycerol acyltransferase 2 inhibitors
JP6084291B2 (ja) * 2013-07-18 2017-02-22 大鵬薬品工業株式会社 Fgfr阻害剤の間歇投与用抗腫瘍剤
EP3023101B1 (en) 2013-07-18 2020-08-19 Taiho Pharmaceutical Co., Ltd. Therapeutic agent for fgfr inhibitor-resistant cancer
CR20170061A (es) 2014-07-17 2017-07-17 Chdi Foundation Inc Métodos y composiciones para el tratamiento de trastornos relacionados con vih
EP3279202B1 (en) 2015-03-31 2020-06-24 Taiho Pharmaceutical Co., Ltd. Crystal of 3,5-disubstituted benzene alkynyl compound
CN105218459B (zh) * 2015-11-03 2019-02-15 广东电网有限责任公司电力科学研究院 苯并咪唑类金属钝化剂及其制备方法和应用
EP3380079A4 (en) * 2015-11-25 2019-08-21 Patheon Development Services Inc. AMORPHOUS DISPERSION GRANULES AND PHARMACEUTICAL FORMS FOR ORAL USE
KR102793563B1 (ko) 2016-03-04 2025-04-11 다이호야쿠힌고교 가부시키가이샤 악성 종양 치료용 제제 및 조성물
US11883404B2 (en) 2016-03-04 2024-01-30 Taiho Pharmaceuticals Co., Ltd. Preparation and composition for treatment of malignant tumors
JP7365332B2 (ja) * 2017-08-07 2023-10-19 ジョイント・ストック・カンパニー “バイオキャド” Cdk8/19阻害薬としての新規ヘテロ環式化合物
FI3769765T3 (fi) 2018-03-19 2024-05-15 Taiho Pharmaceutical Co Ltd Natriumalkyylisulfaattia sisältävä farmaseuttinen koostumus
ES2936481T3 (es) 2018-09-13 2023-03-17 Bristol Myers Squibb Co 1H-Indazol-carboxamidas como inhibidores de la proteína cinasa 1 que interactúa con el receptor (RIPK1)

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Publication number Priority date Publication date Assignee Title
JPH05331163A (ja) 1991-03-26 1993-12-14 Kumiai Chem Ind Co Ltd ピリジン誘導体及び除草剤
DE4142075A1 (de) 1991-12-19 1993-06-24 Hoechst Ag Carbocyclische fuenfringverbindungen, verfahren zu ihrer herstellung und ihre verwendung als pharmazeutika
JP3217848B2 (ja) 1992-03-25 2001-10-15 クミアイ化学工業株式会社 ピリジン誘導体及び除草剤
CA2318368C (en) 1998-01-28 2007-09-11 Shionogi & Co., Ltd. Novel tricyclic compound
DK1192137T3 (da) 1999-06-30 2013-11-11 Amgen Inc Forbindelser til modulering af PPAR-gamma aktivitet
CA2381008A1 (en) 1999-08-04 2001-02-15 Millennium Pharmaceuticals, Inc. Melanocortin-4 receptor binding compounds and methods of use thereof
CA2397575A1 (en) 2000-01-13 2001-07-19 Tularik Inc. Antibacterial agents
EP1296977A1 (en) 2000-06-23 2003-04-02 Bristol-Myers Squibb Pharma Company Heteroaryl-phenyl substituted factor xa inhibitors
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US6603000B2 (en) 2001-07-11 2003-08-05 Boehringer Ingelheim Pharmaceuticals, Inc. Synthesis for heteroarylamine compounds
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BRPI0707315A2 (pt) * 2006-01-27 2011-05-03 Hoffmann La Roche uso de 2-imidazol substituìdo de derivados de imidazolina
WO2008013963A2 (en) 2006-07-28 2008-01-31 University Of Connecticut Fatty acid amide hydrolase inhibitors
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EP2178861B1 (en) * 2007-07-19 2014-08-20 Merck Sharp & Dohme Corp. Heterocyclic amide compounds as protein kinase inhibitors

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