| Literature DB >> 3086556 |
J M Girodeau, C Agouridas, M Masson, R Pineau, F Le Goffic.
Abstract
Unsaturated analogues of diaminopimelic acid have been synthesized. The amino acids were designed so that they would be reversible or irreversible inhibitors of both of the two last enzymes of the lysine pathway. The compounds were tested with meso-diaminopimelate decarboxylase. trans-3,4-Didehydrodiaminopimelic acid (2) was found to be the most potent inhibitor. The antibacterial activities did not correlate with enzyme inhibiting activities. 4-Methylenediaminopimelic acid 4 showed strong antibacterial properties. It is suggested that L,L-diaminopimelate epimerase could be the target enzyme.Entities:
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Year: 1986 PMID: 3086556 DOI: 10.1021/jm00156a021
Source DB: PubMed Journal: J Med Chem ISSN: 0022-2623 Impact factor: 7.446