Bioorganic and Medicinal Chemistry Letters p. 945 - 950 (1998)
Update date:2022-07-30
Topics:
Cox, Russell J.
Schouten, James A.
Stentiford, Rosie A.
Wareing, Katrina J.
Dipeptide substrates of N-Succinyl Diaminopimelic Acid Aminotransferase (DAP-AT) were converted to hydrazines by treatment with hydrazine and cyanoborohydride. These compounds were tested in vitro as inhibitors of DAP- AT from E. coli and in vivo as antibiotics. The hydrazinodipeptides showed potent slow binding inhibition of DAP-AT as well as antimicrobial activity.
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