Discovery of podophyllotoxins

被引:374
作者
Imbert, TF [1 ]
机构
[1] Ctr Rech Pierre Fabre, Div Med Chem, F-81106 Castres, France
关键词
podophyllotoxin; etoposide; teniposide; tubulin; topoisomerase;
D O I
10.1016/S0300-9084(98)80004-7
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 [生物化学与分子生物学]; 081704 [应用化学];
摘要
This review deals with the historical discovery of particularly important lignan derivatives used in cancer chemotherapy. From isolation of the naturally occurring podophyllotoxin, an inhibitor of microtubule assembly, to hemisynthesis of the clinically important anticancer drugs etoposide and teniposide, it will be demonstrated how the activities and the ability of this class of compounds to inhibit topoisomerase II were discovered by different research teams. By virtue of these discoveries, new hemisynthetic derivatives, with different mechanisms of action, are bringing improvements in the ability to treat cancer. ((C) Society francaise de biochimie et biologie moleculaire / Elsevier, Paris).
引用
收藏
页码:207 / 222
页数:16
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