A new paclitaxel prodrug for use in ADEPT strategy

被引:39
作者
Bouvier, E [1 ]
Thirot, S [1 ]
Schmidt, F [1 ]
Monneret, C [1 ]
机构
[1] Inst Curie, UMR CNRS 176, Sect Rech, F-75248 Paris 05, France
关键词
D O I
10.1039/b306236h
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
A new paclitaxel prodrug intended for use in Antibody-Directed Prodrug Therapy ( ADEPT) or Prodrug Monotherapy (PMT) has been prepared. This prodrug was originally designed to be activated into the drug by human beta-glucuronidase. In order to enhance the liberation rate of paclitaxel, an elongated spacer system including a nitro-aromatic derivative and a N,N'-methylethylenediamine was incorporated between the sugar moiety and the drug. Indeed, this new prodrug proved to be activated significantly faster than a former paclitaxel prodrug containing a conventional spacer.
引用
收藏
页码:3343 / 3352
页数:10
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