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Journal of Zhejiang University SCIENCE B

ISSN 1673-1581(Print), 1862-1783(Online), Monthly

Quantitative structure-activity relationships of antimicrobial fatty acids and derivatives against Staphylococcus aureus

Abstract: Fatty acids and derivatives (FADs) are resources for natural antimicrobials. In order to screen for additional potent antimicrobial agents, the antimicrobial activities of FADs against Staphylococcus aureus were examined using a microplate assay. Monoglycerides of fatty acids were the most potent class of fatty acids, among which monotridecanoin possessed the most potent antimicrobial activity. The conventional quantitative structure-activity relationship (QSAR) and comparative molecular field analysis (CoMFA) were performed to establish two statistically reliable models (conventional QSAR: R2=0.942, Q2LOO=0.910; CoMFA: R2=0.979, Q2=0.588, respectively). Improved forecasting can be achieved by the combination of these two models that provide a good insight into the structure-activity relationships of the FADs and that may be useful to design new FADs as antimicrobial agents.

Key words: Fatty acid derivatives, Quantitative structure-activity relationship, Comparative molecular field analysis, Antimicrobial activity


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DOI:

10.1631/jzus.B1100049

CLC number:

TS221

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Downloaded:

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Cited:

12

On-line Access:

2012-01-18

Received:

2011-02-20

Revision Accepted:

2011-07-27

Crosschecked:

2011-12-07

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