Inhibitors of P-glycoprotein - Lead identification and optimisation

被引:34
作者
Pleban, K [1 ]
Ecker, GF [1 ]
机构
[1] Univ Vienna, Dept Pharmaceut Chem, A-1090 Vienna, Austria
关键词
inhibitors of P-glycoprotein; multidrug resistance; QSAR; pharmacophore models;
D O I
10.2174/1389557053402729
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
The membrane bound drug efflux pump P-glycoprotein (P-gp) transports a wide variety of functionally and structurally diverse cytotoxic drugs out of tumour cells. Overexpression of P-glycoprotein is one of the predominant mechanisms responsible for development of multiple drug resistance in tumour therapy. Thus, inhibition of P-gp represents a promising approach for treatment of multidrug resistant tumours. This review highlights concepts for identification and optimization of new inhibitors of P-glycoprotein.
引用
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页码:153 / 163
页数:11
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