发明名称 |
Benz-indole and benzo-quinoline derivatives as prodrugs for tumor treatment |
摘要 |
Compounds of the general formula (I) or (IA) in which X is H, Y is a leaving group, R<SUP>1 </SUP>preferably being an aromatic DNA binding subunit are prodrug analogues of duocarmycin. The compounds are expected to be hydroxylated at the carbon atom to which C is joined, by cytochrome P450, in particular by CYP1B1, expressed at high levels in tumours. The prodrug is expected to be activated preferentially in tumour cells, which it will act as a DNA alkylating agent preventing cell division.
|
申请公布号 |
US2007161669(A1) |
申请公布日期 |
2007.07.12 |
申请号 |
US20070710899 |
申请日期 |
2007.02.27 |
申请人 |
SCHOOL OF PHARMACY UNIVERSITY OF LONDON |
发明人 |
SEARCEY MARK;PATTERSON LAURENCE H. |
分类号 |
A61K31/473;C07D221/10;A61K31/40;A61K31/403;A61K31/404;A61K31/4178;A61K31/4184;A61K31/47;A61P35/00;C07D209/60;C07D209/90;C07D401/06;C07D403/02;C07D487/02 |
主分类号 |
A61K31/473 |
代理机构 |
|
代理人 |
|
主权项 |
|
地址 |
|