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2-甲基-3-[2-(2-甲基-1-丙烯基)-1H-苯并咪唑-1-基]嘧啶并[1,2-a]苯并咪唑-4(3H)-酮作为潜在抗菌剂的 QSAR 模型的合成与探索。

Synthesis and exploration of QSAR model of 2-methyl-3-[2-(2-methylprop-1-en-1-yl)-1H-benzimidazol-1-yl]pyrimido[1,2-a]benzimidazol-4(3H)-one as potential antibacterial agents.

机构信息

School of Chemical Sciences, Devi Ahilya University, Takshashila Campus, Khandwa Road, Indore, India.

出版信息

J Enzyme Inhib Med Chem. 2012 Apr;27(2):294-301. doi: 10.3109/14756366.2011.587814. Epub 2011 Jun 23.

Abstract

Present communication deals with the synthesis of novel 2-methyl-3-[2-(2-methylprop-1-en-1-yl)-1H-benzimidazol-1-yl]pyrimido[1,2-a]benzimidazol-4(3H)-one derivatives under phase transfer catalysis (PTC) conditions using benzyl triethyl ammonium chloride (BTEAC) as PTC. It also elicits the studies on in vitro antimicrobial evaluation of synthesized compounds against a representative genera of gram-negative and gram-positive bacteria i.e., Bacillus subtilis, Staphylococcus aureus, Pseudomonas diminuta and Escherichia coli. All the compounds have been found to manifest profound antimicrobial activity. Moreover, extensive quantitative structure-activity relationship (QSAR) studies have been performed to deduce a correlation between molecular descriptors under consideration and the elicited biological activity. A tri-parametric QSAR model has been generated upon rigorous statistical treatment.

摘要

本通讯涉及在相转移催化(PTC)条件下使用苄基三乙基氯化铵(BTEAC)作为 PTC 合成新型 2-甲基-3-[2-(2-甲基-1-丙烯-1-基)-1H-苯并咪唑-1-基]嘧啶并[1,2-a]苯并咪唑-4(3H)-酮衍生物。它还研究了合成化合物对革兰氏阴性和革兰氏阳性细菌代表属即枯草芽孢杆菌、金黄色葡萄球菌、微小假单胞菌和大肠杆菌的体外抗菌评价。所有化合物都表现出很强的抗菌活性。此外,还进行了广泛的定量构效关系(QSAR)研究,以推断所考虑的分子描述符与所产生的生物活性之间的相关性。经过严格的统计处理,生成了一个三参数 QSAR 模型。

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