Synthesis and activity against multidrug resistance in Chinese hamster ovary cells of new acridone-4-carboxamides

…, B Dumaitre, A Daugan, P Pianetti

文献索引：Dodic, Nerina; Dumaitre, Bernard; Daugan, Alain; Pianetti, Pascal Journal of Medicinal Chemistry, 1995 , vol. 38, # 13 p. 2418 - 2426

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被引用次数: 58

摘要

A number of tricyclic carboxamides have been synthesized and tested to evaluate their ability to reverse multidrug resistance in the CHRC/5 cell line. Among them the acridone derivatives were the most potent. A key feature is the presence of a dimethoxybenzyl or phenethylamine cationic site, separated from the tricyclic lipophilic part by a carbamoylphenyl chain. Optimization led to compounds 2 orders of magnitude more ...