| Literature DB >> 4995846 |
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.Entities:
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Year: 1971 PMID: 4995846 PMCID: PMC377231 DOI: 10.1128/am.21.4.565-568.1971
Source DB: PubMed Journal: Appl Microbiol ISSN: 0003-6919