首页> 外文期刊>European Journal of Medicinal Chemistry: Chimie Therapeutique >Synthesis, antifungal activities and 3D-QSAR study of N-(5-substituted-1,3,4-thiadiazol-2-yl)cyclopropanecarboxamides.
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Synthesis, antifungal activities and 3D-QSAR study of N-(5-substituted-1,3,4-thiadiazol-2-yl)cyclopropanecarboxamides.

机译:N-(5-取代的1,3,4-噻二唑-2-基)环丙烷甲酰胺的合成,抗真菌活性和3D-QSAR研究。

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摘要

A series of cyclopropanecarboxamide were prepared and tested for antifungal activity in vivo. The preliminary bioassays indicated that some compounds are comparable to the commercial fungicides. To further explore the comprehensive structure-activity relationship on the basis of fungicidal activity data, comparative molecular field analysis (CoMFA) was performed, and a statistically reliable model with good predictive power (r(2)=0.8, q(2)=0.516) was achieved. Based on the CoMFA, compound 7p was designed and synthesized, which was found to display a good antifungal activity (79.38%) as 7g and 7h.
机译:制备了一系列环丙烷甲酰胺并在体内测试其抗真菌活性。初步的生物测定表明,某些化合物与商业杀菌剂相当。为了进一步根据杀真菌活性数据探索全面的构效关系,进行了比较分子场分析(CoMFA),并建立了具有可靠预测能力的统计可靠模型(r(2)= 0.8,q(2)= 0.516 ) 已实现。基于CoMFA,设计并合成了化合物7p,发现7g和7h显示出良好的抗真菌活性(79.38%)。

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