发明名称 HYDROXYBENZAMIDE DERIVATIVES AND THEIR USE AS INHIBITORS OF HSP90
摘要 The invention provides compounds of the formula (I): or salts, tautomers, solvates and N-oxides thereof; wherein R<SUP>1</SUP> is hydroxy or hydrogen; R<SUP>2</SUP> is hydroxy; methoxy or hydrogen; provided that at least one of R<SUP>1</SUP> and R<SUP>2</SUP> is hydroxy; R<SUP>3</SUP> is selected from hydrogen; halogen; cyano; optionally substituted C<SUB>1-5 </SUB>hydrocarbyl and optionally substituted C<SUB>1-5</SUB>hydrocarbyloxy; R4 is selected from hydrogen; a group -(O)n-R<SUP>7</SUP> where n is 0 or 1 and R<SUP>7</SUP> is an optionally substituted acyclic C<SUB>1-5</SUB>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-C<SUB>1-5</SUB> hydrocarbyl- amino; or R<SUP>3</SUP> and R<SUP>4</SUP> together form a monocyclic carbocyclic or heterocyclic ring of 5 to 7 ring members; and NR<SUP>5</SUP>R<SUP>6</SUP> 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.
申请公布号 WO2006109085(A8) 申请公布日期 2007.05.18
申请号 WO2006GB01382 申请日期 2006.04.13
申请人 ASTEX THERAPEUTICS LIMITED;CHESSARI, GIANNI;CONGREVE, MILES, STUART;NAVARRO, EVA, FIGUEROA;FREDERICKSON, MARTYN;MURRAY, CHRISTOPHER;WOOLFORD, ALISON, JO-ANNE;CARR, MARIA, GRAZIA;DOWNHAM, ROBERT;O'BRIEN, MICHAEL, ALISTAIR;PHILLIPS, THERESA, RACHEL;WOODHEAD, ANDREW, JAMES 发明人 CHESSARI, GIANNI;CONGREVE, MILES, STUART;NAVARRO, EVA, FIGUEROA;FREDERICKSON, MARTYN;MURRAY, CHRISTOPHER;WOOLFORD, ALISON, JO-ANNE;CARR, MARIA, GRAZIA;DOWNHAM, ROBERT;O'BRIEN, MICHAEL, ALISTAIR;PHILLIPS, THERESA, RACHEL;WOODHEAD, ANDREW, JAMES
分类号 C07D209/44;A61K31/403;A61K31/438;A61K31/439;C07D209/08;C07D215/08;C07D401/04;C07D401/12;C07D471/04;C07D471/10;C07D491/08;C07D491/10 主分类号 C07D209/44
代理机构 代理人
主权项
地址