JP2010513285A5 - - Google Patents

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Publication number
JP2010513285A5
JP2010513285A5 JP2009541404A JP2009541404A JP2010513285A5 JP 2010513285 A5 JP2010513285 A5 JP 2010513285A5 JP 2009541404 A JP2009541404 A JP 2009541404A JP 2009541404 A JP2009541404 A JP 2009541404A JP 2010513285 A5 JP2010513285 A5 JP 2010513285A5
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JP
Japan
Prior art keywords
aliphatic
optionally
independently
cycloaliphatic
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.)
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Application number
JP2009541404A
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English (en)
Japanese (ja)
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JP5406725B2 (ja
JP2010513285A (ja
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Publication date
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Priority claimed from PCT/US2007/025688 external-priority patent/WO2008076392A2/en
Publication of JP2010513285A publication Critical patent/JP2010513285A/ja
Publication of JP2010513285A5 publication Critical patent/JP2010513285A5/ja
Application granted granted Critical
Publication of JP5406725B2 publication Critical patent/JP5406725B2/ja
Expired - Fee Related legal-status Critical Current
Anticipated expiration legal-status Critical

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JP2009541404A 2006-12-14 2007-12-14 タンパク質キナーゼ阻害剤として有用な化合物 Expired - Fee Related JP5406725B2 (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US87487806P 2006-12-14 2006-12-14
US60/874,878 2006-12-14
PCT/US2007/025688 WO2008076392A2 (en) 2006-12-14 2007-12-14 Compounds useful as protein kinase inhibitors

Publications (3)

Publication Number Publication Date
JP2010513285A JP2010513285A (ja) 2010-04-30
JP2010513285A5 true JP2010513285A5 (enExample) 2011-04-14
JP5406725B2 JP5406725B2 (ja) 2014-02-05

Family

ID=39323721

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2009541404A Expired - Fee Related JP5406725B2 (ja) 2006-12-14 2007-12-14 タンパク質キナーゼ阻害剤として有用な化合物

Country Status (12)

Country Link
US (2) US8129387B2 (enExample)
EP (1) EP2102210B1 (enExample)
JP (1) JP5406725B2 (enExample)
CN (1) CN101646671A (enExample)
AT (1) ATE497961T1 (enExample)
AU (1) AU2007334379B2 (enExample)
CA (1) CA2672612A1 (enExample)
DE (1) DE602007012473D1 (enExample)
ES (1) ES2359467T3 (enExample)
MX (1) MX2009006345A (enExample)
NZ (1) NZ577638A (enExample)
WO (1) WO2008076392A2 (enExample)

Families Citing this family (24)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
RU2453548C2 (ru) 2006-01-17 2012-06-20 Вертекс Фармасьютикалз Инкорпорейтед Азаиндолы, полезные в качестве ингибиторов янус-киназ
JP2011515072A (ja) * 2008-02-13 2011-05-19 エラン ファーマ インターナショナル リミテッド α−シヌクレインキナーゼ
CN102076690A (zh) 2008-06-23 2011-05-25 维泰克斯制药公司 蛋白激酶抑制剂
AU2009271663B2 (en) 2008-06-23 2014-04-17 Vertex Pharmaceuticals Incorporated Protein kinase inhibitors
WO2010025073A1 (en) * 2008-08-28 2010-03-04 Takeda Pharmaceutical Company Limited Dihydroimidazo [ 1, 5-f] pteridines as polo-like kinase inhibitors
TWI483941B (zh) 2009-06-17 2015-05-11 Vertex Pharma 流感病毒複製之抑制劑
SG181908A1 (en) * 2009-12-23 2012-08-30 Elan Pharm Inc Pteridinones as inhibitors of polo-like kinase
BR112013008526A2 (pt) * 2010-10-08 2016-07-12 Elan Pharm Inc inibidores de quinase do tipo polo
MX2013006836A (es) 2010-12-16 2013-09-26 Vertex Pharma Inhibidores de la replicacion de los virus de la influenza.
WO2013006634A2 (en) 2011-07-05 2013-01-10 Vertex Pharmaceuticals Incorporated Processes and intermediates for producing azaindoles
UA118010C2 (uk) 2011-08-01 2018-11-12 Вертекс Фармасьютікалз Інкорпорейтед Інгібітори реплікації вірусів грипу
JP6523267B2 (ja) * 2013-06-24 2019-05-29 メルク パテント ゲゼルシャフト ミット ベシュレンクテル ハフツングMerck Patent Gesellschaft mit beschraenkter Haftung Fshrの調節剤としてのイミダゾール化合物及びその使用
SMT201900450T1 (it) 2013-11-13 2019-09-09 Vertex Pharma Inibitori della replicazione di virus dell’influenza
MX2016006200A (es) 2013-11-13 2016-08-08 Vertex Pharma Metodos para preparar inhibidores de la replicacion de virus de influenza.
US9840503B2 (en) 2015-05-11 2017-12-12 Incyte Corporation Heterocyclic compounds and uses thereof
WO2016183120A1 (en) 2015-05-13 2016-11-17 Vertex Pharmaceuticals Incorporated Inhibitors of influenza viruses replication
EP3294717B1 (en) 2015-05-13 2020-07-29 Vertex Pharmaceuticals Inc. Methods of preparing inhibitors of influenza viruses replication
US9708333B2 (en) 2015-08-12 2017-07-18 Incyte Corporation Fused bicyclic 1,2,4-triazine compounds as TAM inhibitors
US10053465B2 (en) 2015-08-26 2018-08-21 Incyte Corporation Pyrrolopyrimidine derivatives as TAM inhibitors
MX2018011792A (es) 2016-03-28 2019-07-04 Incyte Corp Compuestos de pirrolotriazina como inhibidores de tyro3, axl y mer (tam).
EP3687996B1 (en) 2017-09-27 2021-11-03 Incyte Corporation Salts of pyrrolotriazine derivatives useful as tam inhibitors
DK3813800T3 (da) 2018-06-29 2025-06-02 Incyte Corp Formuleringer af en axl/mer-hæmmer
CN111217815B (zh) * 2018-11-27 2021-06-18 沈阳药科大学 含有喋啶酮骨架的化合物及其制备方法和应用
PH12022552347A1 (en) 2020-03-06 2024-01-29 Incyte Corp Combination therapy comprising axl/mer and pd-1/pd-l1 inhibitors

Family Cites Families (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE69940808D1 (de) 1998-03-04 2009-06-10 Bristol Myers Squibb Co Heterocyclen substituierte imidazopyrazine als protein- tyrosin-kinase-inhibitoren
CN101200457A (zh) * 2003-02-26 2008-06-18 贝林格尔英格海姆法玛两合公司 二氢蝶啶酮、其制法及作为药物制剂的用途
US20060074088A1 (en) 2004-08-14 2006-04-06 Boehringer Ingelheim International Gmbh Dihydropteridinones for the treatment of cancer diseases
US7728134B2 (en) 2004-08-14 2010-06-01 Boehringer Ingelheim International Gmbh Hydrates and polymorphs of 4[[(7R)-8-cyclopentyl-7-ethyl-5,6,7,8-tetrahydro-5-methyl-6-oxo-2-pteridinyl]amino]-3-methoxy-N-(1-methyl-4-piperidinyl)-benzamide, process for their manufacture and their use as medicament
US20060058311A1 (en) 2004-08-14 2006-03-16 Boehringer Ingelheim International Gmbh Combinations for the treatment of diseases involving cell proliferation
BRPI0718120A2 (pt) 2006-10-25 2013-11-12 Chroma Therapeutics Ltd Derivados de pteridina como inibidores de cinase do tipo pólo úteis no tratamento de câncer
GB0621203D0 (en) 2006-10-25 2006-12-06 Chroma Therapeutics Ltd PLK inhibitors
RU2339637C1 (ru) 2007-04-05 2008-11-27 Андрей Александрович Иващенко Блокаторы гистаминного рецептора для фармацевтических композиций, обладающих противоаллергическим и аутоиммунным действием
US8541437B2 (en) 2007-04-05 2013-09-24 Alla Chem, Llc Substituted 2,3,4,5-tetrahydro-1H-pyrido[4,3-b]indoles, methods for the production and use thereof

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