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具有抗血吸虫活性的吡喹酮衍生物:芳环修饰。

Praziquantel derivatives with antischistosomal activity: aromatic ring modification.

机构信息

College of Pharmaceutical Science, Soochow University, 199 RenAi Road, Suzhou 215123, Jiangsu, China.

出版信息

Chem Biol Drug Des. 2013 Aug;82(2):216-25. doi: 10.1111/cbdd.12153. Epub 2013 Jun 29.

Abstract

A series of aromatic ring-modified praziquantel derivatives were prepared and evaluated against juvenile and adult stage of Schistosoma japonicumin. Several analogs comparable in activity to the drug praziquantel have been identified based on in vitro and in vivo japonuicum schistosomes worm viability assay. Structure and activity relationship of these praziquantel aromatic ring-modified compounds was revealed. Specifically, a compound in which a bromine has been introduced in the aromatic ring of praziquantel demonstrated close antischistosomal activity to praziquantel in vivo.

摘要

一系列芳香环修饰的吡喹酮衍生物被制备出来,并对日本血吸虫的幼体和成虫阶段进行了评估。根据体外和体内日本血吸虫虫体活力测定,已经确定了几种与药物吡喹酮活性相当的类似物。这些吡喹酮芳香环修饰化合物的结构与活性关系得到了揭示。具体来说,在吡喹酮的芳环中引入溴原子的化合物在体内具有与吡喹酮相近的抗血吸虫活性。

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