![用于治疗癌症的作为PLK抑制剂的蝶啶衍生物](/CN/2007/8/7/images/200780039937.jpg)
基本信息:
- 专利标题: 用于治疗癌症的作为PLK抑制剂的蝶啶衍生物
- 专利标题(英):Pteridine derivatives as polo-like kinase inhibitors useful in the treatment of cancer
- 申请号:CN200780039937.8 申请日:2007-10-19
- 公开(公告)号:CN101541800A 公开(公告)日:2009-09-23
- 发明人: D·F·C·莫法特 , S·R·佩特尔 , S·J·戴维斯 , K·W·J·贝克 , O·J·菲利普斯
- 申请人: 色品疗法有限公司
- 申请人地址: 英国牛津郡
- 专利权人: 色品疗法有限公司
- 当前专利权人: 色品疗法有限公司
- 当前专利权人地址: 英国牛津郡
- 代理机构: 上海专利商标事务所有限公司
- 代理人: 陈文青
- 优先权: 0621205.4 2006.10.25 GB; 0715614.4 2007.08.10 GB
- 国际申请: PCT/GB2007/003998 2007.10.19
- 国际公布: WO2008/050096 EN 2008.05.02
- 进入国家日期: 2009-04-27
- 主分类号: C07D475/00
- IPC分类号: C07D475/00 ; A61K31/519 ; A61P35/00
Compound of formula (I) are inhibitors of Polo-like kinases (PLKs), and are useful in treatment of cell proliferative diseases: wherein R1 and R2 are hydrogen, or an optionally substituted (C1-C6)alkyl, (C2- C6)alkenyl, (C2-C6)alkynyl or (C3-C6)cycloalkyl group; R3 and R3' are independently selected from hydrogen, -CN, hydroxyl, halogen, optionally substituted (C1-C6) alkyl, (C2- C6)alkenyl, (C2-C6)alkynyl or (C3-C6)cycloalkyl, -NR5R6 or C1-C4 alkoxy, wherein R5 and R6 are independently hydrogen or optionally substituted (C1-C6)alkyl; ring A is an optionally substituted mono- or bi-cyclic carbocyclic or heterocyclic ring or a ring system having up to 12 ring atoms; T is a radical of formula R-L -Y- wherein R is an alpha amino acid or alpha amino acid ester motif, linked to ring A by linker R-L-Y- as defined in the claims.
IPC结构图谱:
C | 化学;冶金 |
--C07 | 有机化学 |
----C07D | 杂环化合物 |
------C07D475/00 | 含蝶啶环系的杂环化合物 |