Abstract
Summary
1. The bacteriostatic and bactericidal activity of a series of N-substituted p-aminobenzoic acid derivatives have been determined.
2. Among the acids the order of decreasing activity is as follows: p-butylaminobenzoic acid > p-ethylaminobenzoic acid > p-aminobenzoic acid.
3. Of 2 procaine hydrochloride (U.S.P.) derivatives, the N-butyl derivative displays greater antibacterial action than the N-ethyl.
4. Among the methyl and ethyl esters of p-aminobenzoic acid, the N-propyl derivatives display more activity than the N-ethyl or N-butyl compounds. The latter 2 were approximately equal in respect to antibacterial action.
5. The order of decreasing activity among the p-alkylaminobenzamides was: butyl > propyl > ethyl.
6. Diethylaminoethyl-p-n-butylaminobenzate hydrochloride and p-n-butylaminobenzamide were not antagonized by the presence of p-aminobenzoic acid when tested in trypticase soy broth against Streptococcus pyogenes (C203).
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