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Synthesis,anti-fungal activity evaluation and QSAR studies on podophyllotoxin derivatives

机译:鬼臼毒素衍生物的合成,抗真菌活性评价和QSAR研究

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The anti-fungal and cytotoxic activites of podophyllotoxin and seven C-4 substituted podophyllotoxin ester derivatives,viz:trans-cinnamyl,cis-cinnamyl,o-methoxy cinnamyl,dimethyl acrylyl,p-methoxy phenyl acetyl,3,4-dimethoxy phenyl acetyl and 2,5-dimethoxy phenyl acetyl esters were evaluated on four fungi,viz:Macrophomina phaseolina,Fusarium oxysporum,Myrrothecium verrucarria and Asperigillus candidus,The podophyllotoxin derivatives were synthesised and their structures were elucidated.Quantitative structure activity relationships were developed between the activity of these compounds against the four fungi and molecular descriptors.The linear regression models developed had one to two descriptors.For all the cases the r~2 was in the range of 0.73 to 0.96,indicating good data fit and q~2 was in the range of 0.60 to 0.68,indicating that the predictive capabilities of the models were acceptable.Solvent accessible surface area(namely the partial positive solvent-accessible surface area),A log P,highest occupied molecular orbital and conformational energy were identified as important descriptors.
机译:鬼臼毒素和7种C-4取代鬼臼毒素酯衍生物的抗真菌和细胞毒性活性,即:反式肉桂基,顺式肉桂基,邻甲氧基肉桂基,二甲基丙烯酰基,对甲氧基苯基乙酰基,3,4-二甲氧基苯基乙酰基分别对菜豆大麦蛾,尖孢镰刀菌,疣状肉孢菌和念珠菌四种真菌进行了评价,并用2,5-二甲氧基苯基乙酰酯进行了合成,并合成了鬼臼毒素衍生物并阐明了它们的结构。这些化合物针对四种真菌和分子描述子。所建立的线性回归模型具有一到两个描述子。在所有情况下,r〜2在0.73至0.96的范围内,表明数据拟合良好,q〜2在该范围内。从0.60到0.68,表明模型的预测能力是可以接受的。溶剂可及表面积(即部分正溶剂可及表面积),A log P,最高占据分子轨道和构象能被认为是重要的描述子。

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