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 (cg-RX-API-DMAC7.html) 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 (cg-RX-API-DMAC7.html)
EP (1) EP2424843B1 (cg-RX-API-DMAC7.html)
JP (1) JP2012525367A (cg-RX-API-DMAC7.html)
KR (1) KR20120004542A (cg-RX-API-DMAC7.html)
CN (1) CN102803225A (cg-RX-API-DMAC7.html)
AU (1) AU2010243353B2 (cg-RX-API-DMAC7.html)
BR (1) BRPI1016190A2 (cg-RX-API-DMAC7.html)
CA (1) CA2759083A1 (cg-RX-API-DMAC7.html)
EA (1) EA020017B1 (cg-RX-API-DMAC7.html)
ES (1) ES2458872T3 (cg-RX-API-DMAC7.html)
MX (1) MX2011011516A (cg-RX-API-DMAC7.html)
PL (1) PL2424843T3 (cg-RX-API-DMAC7.html)
PT (1) PT2424843E (cg-RX-API-DMAC7.html)
WO (1) WO2010125402A1 (cg-RX-API-DMAC7.html)

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AU2011240735B2 (en) 2010-04-13 2015-01-29 Novartis Ag Combination comprising a cyclin dependent kinase 4 or cyclin dependent kinase (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
EP3243515B1 (en) * 2011-08-30 2019-10-16 CHDI Foundation, Inc. Kynurenine-3-monooxygenase inhibitors, pharmaceutical compositions, and methods of use thereof
AU2013234451A1 (en) * 2012-03-21 2014-09-25 Bayer Intellectual Property Gmbh Use of (RS)-S-cyclopropyl-S-(4-{[4-{[1R, 2R)-2-hydroxy-1-methylpropyl]oxy}-5-(trifluoromethyl)pyrimidin-2-yl] amino}phenyl)sulfoximide for treating specific tumours
SG11201405477XA (en) * 2012-04-06 2014-11-27 Pfizer Diacylglycerol acyltransferase 2 inhibitors
DK3023100T3 (da) * 2013-07-18 2019-05-27 Taiho Pharmaceutical Co Ltd Antitumorlægemiddel til intermitterende administration af fgfr-hæmmer
JP6084292B2 (ja) 2013-07-18 2017-02-22 大鵬薬品工業株式会社 Fgfr阻害剤耐性癌の治療薬
PE20170770A1 (es) 2014-07-17 2017-07-04 Chdi Foundation Inc Metodos y composiciones para tratar trastornos relacionados con vih
JP6190079B2 (ja) 2015-03-31 2017-08-30 大鵬薬品工業株式会社 3,5−二置換ベンゼンアルキニル化合物の結晶
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
US20180344646A1 (en) * 2015-11-25 2018-12-06 Patheon Development Services Inc. Amorphous dispersion granules and oral dosage forms
US11883404B2 (en) 2016-03-04 2024-01-30 Taiho Pharmaceuticals Co., Ltd. Preparation and composition for treatment of malignant tumors
JP7085985B2 (ja) 2016-03-04 2022-06-17 大鵬薬品工業株式会社 悪性腫瘍治療用製剤及び組成物
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
KR102473372B1 (ko) 2018-03-19 2022-12-05 다이호야쿠힌고교 가부시키가이샤 알킬황산나트륨을 포함하는 의약 조성물
EP3849968B1 (en) * 2018-09-13 2022-12-21 Bristol-Myers Squibb Company 1h-indazole carboxamides as receptor-interacting protein kinase 1 inhibitors (ripk1)

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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
PL341984A1 (en) 1998-01-28 2001-05-07 Shionogi & Co Novel tricycle compounds
WO2001000579A1 (en) 1999-06-30 2001-01-04 Tularik Inc. COMPOUNDS FOR THE MODULATION OF PPARη ACTIVITY
MXPA02001160A (es) 1999-08-04 2002-07-02 Millennium Pharm Inc Compuestos que se unen a los receptores para melanocortina-4, y metodo de uso de estos.
US6780858B2 (en) 2000-01-13 2004-08-24 Tularik Inc. Antibacterial agents
WO2002000647A1 (en) 2000-06-23 2002-01-03 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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BRPI0417543A (pt) 2003-12-12 2007-03-27 Wyeth Corp quinolinas úteis no tratamento de doença cardiovascular
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CA2658887C (en) 2006-07-28 2016-08-23 University Of Connecticut Fatty acid amide hydrolase inhibitors
JP5528807B2 (ja) * 2006-10-12 2014-06-25 アステックス、セラピューティックス、リミテッド 複合薬剤
MY150032A (en) * 2007-07-19 2013-11-29 Merck Sharp & Dohme Heterocyclic amide compounds as protein kinase inhibitors

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