Synthesis, characterization, biological activity, and 3D-QSAR studies on some novel class of pyrrole derivatives as antitubercular agents
作者:Shrinivas D. Joshi、Uttam A. More、Sheshagiri R. Dixit、Haresh H. Korat、Tejraj M. Aminabhavi、Aravind M. Badiger
DOI:10.1007/s00044-013-0709-y
日期:2014.3
designed, synthesized, and their structures have been elucidated along with the evaluation of antitubercular activity against Mycobacterium tuberculosis H37Rv using the microplate alamar blue assay method and antibacterial activity against Staphylococcus aureus, Bacillus subtilis, Klebsiella pneumoniae, and Escherichia coli by broth micro-dilution assay method. Structural activity relationships and 3D-QSAR
摘要设计,合成了一系列新的吡咯衍生物,并阐明了它们的结构,并使用微孔板阿拉玛蓝法评估了其对结核分枝杆菌H 37 Rv的抗结核活性以及对金黄色葡萄球菌,枯草芽孢杆菌,肺炎克雷伯菌的抗菌活性,以及通过肉汤微稀释法测定的大肠杆菌。结构活性关系和3D-QSAR分析已通过拓扑异构体比较分子场分析(CoMFA)进行。使用42个训练集和8个活性化合物的测试集来开发显示交叉验证相关系数(q 2)为0.815,预测标准误差为0.36,非交叉验证相关系数(r 2)为0.973,六项估计的标准误差为0.14。 图形概要合成; 频谱和3D-QSAR研究;描述了一系列新颖的吡咯衍生物的抗细菌,抗结核和细胞毒性活性。