发明申请
US20090215772A1 Hydroxybenzamide derivatives and their use as inhibitors of HSP90
有权
羟基苯甲酰胺衍生物及其作为HSP90抑制剂的用途
- 专利标题: Hydroxybenzamide derivatives and their use as inhibitors of HSP90
- 专利标题(中): 羟基苯甲酰胺衍生物及其作为HSP90抑制剂的用途
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申请号: US11911490申请日: 2006-04-13
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公开(公告)号: US20090215772A1公开(公告)日: 2009-08-27
- 发明人: Gianni Chessari , Miles Stuart Congreve , Eva Figueroa Navarro , Martyn Frederickson , Christopher Murray , Alison Jo-Anne Woolford , Maria Grazia Carr , Michael Alistair O'Brien , Andrew James Woodhead , Robert Downham , Theresa Rachel Phillips
- 申请人: Gianni Chessari , Miles Stuart Congreve , Eva Figueroa Navarro , Martyn Frederickson , Christopher Murray , Alison Jo-Anne Woolford , Maria Grazia Carr , Michael Alistair O'Brien , Andrew James Woodhead , Robert Downham , Theresa Rachel Phillips
- 申请人地址: UK Cambridge
- 专利权人: Astex Therapeutics Limited
- 当前专利权人: Astex Therapeutics Limited
- 当前专利权人地址: UK Cambridge
- 优先权: GB0507474.5 20050413; GB0604111.5 20060301
- 国际申请: PCT/GB06/01382 WO 20060413
- 主分类号: A61K31/5377
- IPC分类号: A61K31/5377 ; C07D209/44 ; A61K31/403 ; A61K31/454 ; C07D401/02 ; C07D403/02 ; A61K31/497 ; C07D413/14
摘要:
The invention provides compounds of the formula (I): or salts, tautomers, solvates and N-oxides thereof; wherein R1 is hydroxy or hydrogen; R2 is hydroxy; methoxy or hydrogen; provided that at least one of R1 and R2 is hydroxy; R3 is selected from hydrogen; halogen; cyano; optionally substituted C1-5 hydrocarbyl and optionally substituted C1-5 hydrocarbyloxy; R4 is selected from hydrogen; a group —(O)n—R7 where n is 0 or 1 and R7 is an optionally substituted acyclic C1-5 hydrocarbyl group or a monocyclic carbocyclic or heterocyclic group having 3 to 7 ring members; halogen; cyano; hydroxy; amino; and optionally substituted mono- or di-C1-5 hydrocarbylamino; or R3 and R4 together form a monocyclic carbocyclic or heterocyclic ring of 5 to 7 ring members; and NR5R6 forms an optionally substituted bicyclic heterocyclic group having 8 to 12 ring members of which up to 5 ring members are heteroatoms selected from oxygen, nitrogen and sulphur.The compounds have activity as Hsp90 inhibitors.
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