Appl Environ Microbiol. 1971 April; 21(4): 565-568
Copyright © 1971 American Society for Microbiology. All Rights Reserved.
Department of Pharmacy, University of Sydney, Sydney, N.S.W. 2006, Australia
ABSTRACT
The activities are reported of sodium salts of several n-alkylsalicylic acids against Staphylococcus aureus, Pseudomonas aeruginosa, Mycobacterium phlei, and Candida albicans. The acids had alkyl substituents of 1 to 18 carbon atoms in the 3, 4, or 5 positions relative to the carboxyl group of salicylic acid. Generally, the antimicrobial properties were typical of anionic surface-active agents although the salicylates are more potent than most of these, particularly against S. aureus.
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