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N-halo derivatives VI: Microbiological and chemical evaluations of 3-chloro-2-oxazolidinones

โœ Scribed by Masanori Kosugi; James J. Kaminski; Sally H. Selk; Ian H. Pitman; Nicolae Bodor; Takeru Higuchi


Publisher
John Wiley and Sons
Year
1976
Tongue
English
Weight
471 KB
Volume
65
Category
Article
ISSN
0022-3549

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โœฆ Synopsis


Comparative antimicrobial activity of 3-chloro-2-oxazolidinone (I), 3-chloro-4-methyl-2-oxazolidinone (II), 3-chloro-4,4-dimethyl-2-oxazolidinone (III), and N-chlorosuccinimide (IV) was evaluated in aqueous buffers in the absence and presence of 5% horse serum. All four compounds had similar bactericidal activity in the absence of horse serum, but I and III had superior activity relative to IV when serum was present. Compound III was considerably more stable with respect ot loss of positive chlorine and bactericidal activity than I and II when stored in 0.1 M sodium dihydrogen phosphate buffered to pH 7.0 at 40 degrees. Thus, III is potentially the most useful bactericidal agent of those evaluated. The chlorine potentials of I, II, and III, the rate constants for transfer of positive chlorine from I and III to morpholine in aqueous solutions, and the hydrolytic stabilities of I and III with respect to loss of positive chlorine were evaluated. These data, together with previously calculated data for IV, are used to rationalize the observed bactericidal activities.


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