Literature DB >> 17869511

Quantitative structure-activity relationship studies for prediction of antimicrobial activity of synthesized 2,4-hexadienoic acid derivatives.

Balasubramanian Narasimhan1, Vikramjeet Judge, Rakesh Narang, Ruchita Ohlan, Sucheta Ohlan.   

Abstract

A new series of 2,4-hexadienoic acid derivatives (S(1)-S(42)) has been synthesized and evaluated as antimicrobial agents against Staphylococcus aureus, Bacillus subtilis, Escherichia coli, Candida albicans, and Aspergillus niger. Quantitative structure-activity relationship (QSAR) investigation using Hansch analysis was applied to find out correlation between antimicrobial activities with physicochemical properties of the synthesized compounds. Various physicochemical descriptors and experimentally determined minimum inhibitory concentration values for different microorganisms were used as independent and dependent variables, respectively. The QSAR revealed that topological parameters especially molecular connectivity indices (chi(2), (0)chi(v), (2)chi(v)) were found to have overall significant correlation with antimicrobial activity of 2,4-hexadienoic acid derivatives. The statistical results of training set, cross-validated r(2) and conventional r values gave reliability to the prediction of molecules with activity using QSAR models.

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Year:  2007        PMID: 17869511     DOI: 10.1016/j.bmcl.2007.08.037

Source DB:  PubMed          Journal:  Bioorg Med Chem Lett        ISSN: 0960-894X            Impact factor:   2.823


  5 in total

1.  Synthesis and quantitative structure activity relationship (QSAR) of arylidene (benzimidazol-1-yl)acetohydrazones as potential antibacterial agents.

Authors:  Yeldez El-Kilany; Nariman M Nahas; Mariam A Al-Ghamdi; Mohamed E I Badawy; El Sayed H El Ashry
Journal:  World J Microbiol Biotechnol       Date:  2014-10-11       Impact factor: 3.312

2.  Structure-activity relationship investigation of tertiary amine derivatives of cinnamic acid as acetylcholinesterase and butyrylcholinesterase inhibitors: compared with that of phenylpropionic acid, sorbic acid and hexanoic acid.

Authors:  Xiaohui Gao; Jingjing Tang; Haoran Liu; Linbo Liu; Lu Kang; Wen Chen
Journal:  J Enzyme Inhib Med Chem       Date:  2018-12       Impact factor: 5.051

3.  Benzylidene/2-chlorobenzylidene hydrazides: synthesis, antimicrobial activity, QSAR studies and antiviral evaluation.

Authors:  Davinder Kumar; Vikramjeet Judge; Rakesh Narang; Sonia Sangwan; Erik De Clercq; Jan Balzarini; Balasubramanian Narasimhan
Journal:  Eur J Med Chem       Date:  2010-03-07       Impact factor: 6.514

4.  4-[1-(Substituted aryl/alkyl carbonyl)-benzoimidazol-2-yl]-benzenesulfonic acids: synthesis, antimicrobial activity, QSAR studies, and antiviral evaluation.

Authors:  Snehlata Yadav; Pradeep Kumar; Erik De Clercq; Jan Balzarini; Christophe Pannecouque; Sharwan Kumar Dewan; Balasubramanian Narasimhan
Journal:  Eur J Med Chem       Date:  2010-10-07       Impact factor: 6.514

5.  N'-[4-[(Substituted imino)methyl]benzylidene]-substituted benzohydrazides: synthesis, antimicrobial, antiviral, and anticancer evaluation, and QSAR studies.

Authors:  Pradeep Kumar; Balasubramanian Narasimhan; Kalavathy Ramasamy; Vasudevan Mani; Rakesh Kumar Mishra; Abu Bakar Abdul Majeed; Erik De Clercq
Journal:  Monatsh Chem       Date:  2012-12-01       Impact factor: 1.451

  5 in total

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