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公开(公告)号:US06949563B2
公开(公告)日:2005-09-27
申请号:US10752342
申请日:2004-01-06
申请人: Graham Michael Wynne , Kevin Doyle , Saleh Ahmed , An-Hu Li , John Fraser Keily , Chrystelle Marie Rasamison , Neil Anthony Pegg , Imaad Saba , Claire Thomas , Don Smyth , Shazia Sadiq , Gary Newton , Graham Dawson , Andrew Phillip Crew , Arlindo Lucas Castelhano
发明人: Graham Michael Wynne , Kevin Doyle , Saleh Ahmed , An-Hu Li , John Fraser Keily , Chrystelle Marie Rasamison , Neil Anthony Pegg , Imaad Saba , Claire Thomas , Don Smyth , Shazia Sadiq , Gary Newton , Graham Dawson , Andrew Phillip Crew , Arlindo Lucas Castelhano
IPC分类号: A61K31/381 , A61K31/437 , A61K31/4436 , A61K31/4709 , A61K31/4745 , A61K45/06 , C07D409/12 , C07D409/14 , C07D471/04 , C07D49/02
CPC分类号: C07D409/12 , A61K31/165 , A61K31/22 , A61K31/277 , A61K31/381 , A61K31/437 , A61K31/4436 , A61K31/444 , A61K31/4709 , A61K31/4745 , A61K45/06 , C07D409/14 , C07D471/04 , A61K2300/00
摘要: Compounds represented by Formula (I): or a pharmaceutically acceptable salt or N-oxide thereof, wherein R1 is R2 is and R3 is C0-4alkyl, are useful in the treatment of cancer.
摘要翻译: 由式(I)表示的化合物或其药学上可接受的盐或N-氧化物,其中R1是R2,R3是C0-4-4烷基,可用于治疗癌症。
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2.Aryl-amino substituted pyrrolopyrimidine multi-kinase inhibiting compounds 失效
标题翻译: 芳基 - 氨基取代的吡咯并嘧啶多激酶抑制化合物公开(公告)号:US20060211678A1
公开(公告)日:2006-09-21
申请号:US11194158
申请日:2005-08-01
申请人: Saleh Ahmed , Oscar Barba , Jason Bloxham , Graham Dawson , Wiliam Gattrell , John Kitchin , Neil Anthony Pegg , Imaad Saba , Shazia Sadiq , Colin Peter Sambrook Smith , Don Smyth , Amo Steing , Robin Wilkes , Bijoy Panicker , Paula Tavares , Matthew Cox , An-Hu Li , Hanqing Dong , Lifu Ma , Kenneth Foreman , Qinghua Weng , Kathryn Stolz
发明人: Saleh Ahmed , Oscar Barba , Jason Bloxham , Graham Dawson , Wiliam Gattrell , John Kitchin , Neil Anthony Pegg , Imaad Saba , Shazia Sadiq , Colin Peter Sambrook Smith , Don Smyth , Amo Steing , Robin Wilkes , Bijoy Panicker , Paula Tavares , Matthew Cox , An-Hu Li , Hanqing Dong , Lifu Ma , Kenneth Foreman , Qinghua Weng , Kathryn Stolz
IPC分类号: A61K31/5377 , A61K31/519 , A61K31/496 , A61K31/4745 , C07D487/02 , C07D471/02
CPC分类号: C07D471/02 , C07D487/02 , C07D487/04
摘要: Compounds represented by Formula (I): or stereoisomers or pharmaceutically acceptable salts thereof, are inhibitors of least two of the Abl, Aurora-A, Blk, c-Raf, cSRC, Src, PRK2, FGFR3, Flt3, Lck, Mek1, PDK-1, GSK3β, EGFR, p70S6K, BMX, SGK, CaMKII, Tie-2, IGF-1R, Ron, Ret, and KDR kinases in animals, including humans, for the treatment and/or prevention of various diseases and conditions such as cancer.
摘要翻译: 由式(I)表示的化合物或其立体异构体或其药学上可接受的盐是Abl,Aurora-A,Blk,c-Raf,cSRC,Src,PRK2,FGFR3,Flt3,Lck,Mek1,PDK中的至少两种的抑制剂 -1,GSK3beta,EGFR,p70S6K,BMX,SGK,CaMKII,Tie-2,IGF-1R,Ron,Ret和KDR激酶,用于治疗和/或预防各种疾病和病症, 癌症。
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公开(公告)号:US07465726B2
公开(公告)日:2008-12-16
申请号:US11194158
申请日:2005-08-01
申请人: Saleh Ahmed , Oscar Barba , Jason Bloxham , Graham Dawson , William Gattrell , John Kitchin , Neil Anthony Pegg , Imaad Saba , Shazia Sadiq , Colin Peter Sambrook Smith , Don Smyth , Amo G. Steinig , Robin Wilkes , Bijoy Panicker , Paula Tavares , Matthew Cox , An-Hu Li , Hanqing Dong , Lifu Ma , Kenneth (‘Ken’) Foreman , Qinghua (‘Felix’) Weng , Kathryn Stolz
发明人: Saleh Ahmed , Oscar Barba , Jason Bloxham , Graham Dawson , William Gattrell , John Kitchin , Neil Anthony Pegg , Imaad Saba , Shazia Sadiq , Colin Peter Sambrook Smith , Don Smyth , Amo G. Steinig , Robin Wilkes , Bijoy Panicker , Paula Tavares , Matthew Cox , An-Hu Li , Hanqing Dong , Lifu Ma , Kenneth (‘Ken’) Foreman , Qinghua (‘Felix’) Weng , Kathryn Stolz
IPC分类号: A61K31/437 , A61K31/496 , A61K31/5355 , A61K31/541 , A61K31/5513 , A61K31/551 , C07D471/04 , C07D223/04 , C07D243/08 , C07D241/04 , C07D413/10 , C07D413/06 , C07D413/08 , C07D413/12 , C07D413/14 , C07D417/06 , C07D417/14 , A61K31/04 , A61K31/519 , C07D487/04
CPC分类号: C07D471/02 , C07D487/02 , C07D487/04
摘要: Compounds represented by Formula (I): or stereoisomers or pharmaceutically acceptable salts thereof, are inhibitors of least two of the Abl, Aurora-A, Blk, c-Raf, cSRC, Src, PRK2, FGFR3, Flt3, Lck, Mek1, PDK-1, GSK3β, EGFR, p70S6K, BMX, SGK, CaMKII, Tie-2, IGF-1R, Ron, Ret, and KDR kinases in animals, including humans, for the treatment and/or prevention of various diseases and conditions such as cancer.
摘要翻译: 由式(I)表示的化合物或其立体异构体或其药学上可接受的盐是Abl,Aurora-A,Blk,c-Raf,cSRC,Src,PRK2,FGFR3,Flt3,Lck,Mek1,PDK中的至少两种的抑制剂 -1,GSK3beta,EGFR,p70S6K,BMX,SGK,CaMKII,Tie-2,IGF-1R,Ron,Ret和KDR激酶,用于治疗和/或预防各种疾病和病症, 癌症。
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公开(公告)号:US20060047123A1
公开(公告)日:2006-03-02
申请号:US11218396
申请日:2005-09-02
申请人: Saleh Ahmed , Celine Combet , Scott Cuthill , Graham Dawson , William Gattrell , Mario Lobell , Neil Pegg , Imaad Saba , Simon Swain , Claire Thomas , Graham Wynne
发明人: Saleh Ahmed , Celine Combet , Scott Cuthill , Graham Dawson , William Gattrell , Mario Lobell , Neil Pegg , Imaad Saba , Simon Swain , Claire Thomas , Graham Wynne
IPC分类号: C07D333/22 , C07D277/18 , C07D263/02
CPC分类号: C07D213/40 , C07C323/32 , C07C323/60 , C07C327/32 , C07C2601/02 , C07C2601/14 , C07C2602/08 , C07C2602/10 , C07D209/08 , C07D213/74 , C07D213/75 , C07D215/38 , C07D217/06 , C07D233/54 , C07D235/30 , C07D249/08 , C07D263/10 , C07D277/04 , C07D277/46 , C07D277/62 , C07D285/135 , C07D295/088 , C07D295/135 , C07D295/185 , C07D307/52 , C07D307/81 , C07D309/12 , C07D319/18 , C07D333/20 , C07D409/04 , C07D417/04 , C07D513/04
摘要: Mercaptoamide compounds, represented by Formulas (IA), (IB), (IIA), and (IIB): or a pharmaceutically acceptable salt thereof, inhibit histone deacetylase enzyme and are useful for the treatment and/or prevention of various infections, cancerous diseases, and conditions.
摘要翻译: 由式(IA),(IB),(IIA)和(IIB)表示的巯丙酰胺化合物或其药学上可接受的盐抑制组蛋白脱乙酰酶,并且可用于治疗和/或预防各种感染,癌性疾病 和条件。
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