JP2009536617A5 - - Google Patents

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Publication number
JP2009536617A5
JP2009536617A5 JP2009505430A JP2009505430A JP2009536617A5 JP 2009536617 A5 JP2009536617 A5 JP 2009536617A5 JP 2009505430 A JP2009505430 A JP 2009505430A JP 2009505430 A JP2009505430 A JP 2009505430A JP 2009536617 A5 JP2009536617 A5 JP 2009536617A5
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JP
Japan
Prior art keywords
aliphatic
compound
disease
formula
halo
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.)
Pending
Application number
JP2009505430A
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English (en)
Japanese (ja)
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JP2009536617A (ja
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Publication date
Application filed filed Critical
Priority claimed from PCT/US2007/008819 external-priority patent/WO2007117692A2/en
Publication of JP2009536617A publication Critical patent/JP2009536617A/ja
Publication of JP2009536617A5 publication Critical patent/JP2009536617A5/ja
Pending legal-status Critical Current

Links

JP2009505430A 2006-04-11 2007-04-11 タンパク質キナーゼの阻害剤として有用なチアゾール、イミダゾール、およびピラゾール Pending JP2009536617A (ja)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US79108306P 2006-04-11 2006-04-11
PCT/US2007/008819 WO2007117692A2 (en) 2006-04-11 2007-04-11 Thiazoles, imidazoles, and pyrazoles useful as inhibitors of protein kinases

Publications (2)

Publication Number Publication Date
JP2009536617A JP2009536617A (ja) 2009-10-15
JP2009536617A5 true JP2009536617A5 (https=) 2011-05-12

Family

ID=38508761

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2009505430A Pending JP2009536617A (ja) 2006-04-11 2007-04-11 タンパク質キナーゼの阻害剤として有用なチアゾール、イミダゾール、およびピラゾール

Country Status (9)

Country Link
US (3) US7589214B2 (https=)
EP (1) EP2007732B1 (https=)
JP (1) JP2009536617A (https=)
CN (1) CN101460466B (https=)
AT (1) ATE534632T1 (https=)
AU (1) AU2007235237B2 (https=)
CA (1) CA2648923A1 (https=)
ES (1) ES2376765T3 (https=)
WO (1) WO2007117692A2 (https=)

Families Citing this family (22)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2007117692A2 (en) * 2006-04-11 2007-10-18 Vertex Pharmaceuticals Incorporated Thiazoles, imidazoles, and pyrazoles useful as inhibitors of protein kinases
RU2528231C2 (ru) * 2009-04-24 2014-09-10 Тиботек Фармасьютикалз Диариловые эфиры
US8735417B2 (en) 2009-12-17 2014-05-27 Merck Sharp & Dohme Corp. Aminopyrimidines as Syk inhibitors
WO2011075517A1 (en) 2009-12-17 2011-06-23 Merck Sharp & Dohme Corp. Aminopyrimidines as syk inhibitors
MX2013013090A (es) 2011-05-10 2013-12-16 Merck Sharp & Dohme Aminopirimidinas como inhibidores de tirosina cinaza del bazo.
US9145391B2 (en) 2011-05-10 2015-09-29 Merck Sharp & Dohme Corp. Bipyridylaminopyridines as Syk inhibitors
EP2707357B1 (en) 2011-05-10 2017-01-18 Merck Sharp & Dohme Corp. Pyridyl aminopyridines as syk inhibitors
JP6170944B2 (ja) 2011-12-28 2017-07-26 ヤンセン・サイエンシズ・アイルランド・ユーシー Hcv阻害剤としてのヘテロ−二環式誘導体
SG11201500499TA (en) 2012-08-10 2015-03-30 Boehringer Ingelheim Int Heteroaromatic compounds as bruton's tyrosine kinase (btk) inhibitors
JP6178861B2 (ja) 2012-11-02 2017-08-09 ファイザー・インク ブルトン型チロシンキナーゼ阻害剤
CN103848810A (zh) 2012-11-30 2014-06-11 北京赛林泰医药技术有限公司 鲁顿酪氨酸激酶抑制剂
JP6403751B2 (ja) * 2013-03-14 2018-10-10 ベーリンガー インゲルハイム インターナショナル ゲゼルシャフト ミット ベシュレンクテル ハフツング 5−チアゾールカルボキサミン誘導体及びbtk阻害剤としてのその使用
WO2014152114A1 (en) 2013-03-15 2014-09-25 Boehringer Ingelheim International Gmbh Heteroaromatic compounds as btk inhibitors
JP6615752B2 (ja) * 2013-09-30 2019-12-04 グアンジョウ・イノケア・ファーマ・テク・カンパニー・リミテッド Btkの置換ニコチンイミド阻害剤およびそれらの調製、ならびにがん、炎症および自己免疫疾患の治療における使用
BR112016013540B1 (pt) 2013-12-13 2021-03-02 F. Hoffmann-La Roche Ag inibidores de tirosina quinase de bruton
WO2015116485A1 (en) * 2014-01-29 2015-08-06 Boehringer Ingelheim International Gmbh Pyrazole compounds as btk inhibitors
CN105085474B (zh) * 2014-05-07 2018-05-18 北京赛林泰医药技术有限公司 鲁顿酪氨酸激酶抑制剂
TW201607930A (zh) * 2014-07-18 2016-03-01 百濟神州有限公司 作為t790m/wt-egfr的選擇性和不可逆的激酶抑制劑的5-氨基-4-氨甲醯基-吡唑化合物及其用途
US9975882B2 (en) 2015-12-16 2018-05-22 Boehringer Ingelheim International Gmbh Heteroaromatic compounds as BTK inhibitors
US10570118B2 (en) 2016-01-13 2020-02-25 Boehringer Ingelheim International Gmbh Isoquinolones as BTK inhibitors
WO2020173407A1 (en) * 2019-02-25 2020-09-03 Beijing Innocare Pharma Tech Co., Ltd. Process for preparing 6- (1-acryloylpiperidin-4-yl) -2- (4-phenoxyphenyl) nicotinamide
WO2022012550A1 (en) * 2020-07-13 2022-01-20 Henan Normal University Substituted 1h-imidazo [1, 2-b] pyrazole-3-carboxamide as bruton's tyrosine kinase inhibitors

Family Cites Families (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB9608435D0 (en) * 1996-04-24 1996-06-26 Celltech Therapeutics Ltd Chemical compounds
US6288061B1 (en) * 1997-12-26 2001-09-11 Welfide Corporation Imidazole derivatives
EP1317450B1 (en) * 2000-09-15 2006-11-22 Vertex Pharmaceuticals Incorporated Pyrazole compounds useful as protein kinase inhibitors
WO2002064136A2 (en) * 2001-01-26 2002-08-22 Chugai Seiyaku Kabushiki Kaisha Malonyl-coa decarboxylase inhibitors useful as metabolic modulators
PL2256106T3 (pl) * 2003-07-22 2015-08-31 Astex Therapeutics Ltd Związki 3,4-pochodne 1h-pirazolu i ich zastosowanie jako kinazy zależne od cyklin (cdk) i modulatory kinazy syntazy glikogenu-3 (gsk-3)
WO2005123671A1 (ja) * 2004-06-22 2005-12-29 Taisho Pharmaceutical Co., Ltd. ピロール誘導体
FR2881426B1 (fr) 2005-02-03 2007-03-30 Aventis Pharma Sa Pyrolles et imidazoles substitues, compositions les contenant, procede de frabrication et utilisation
WO2007117692A2 (en) * 2006-04-11 2007-10-18 Vertex Pharmaceuticals Incorporated Thiazoles, imidazoles, and pyrazoles useful as inhibitors of protein kinases

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