Bioorganic and Medicinal Chemistry Letters p. 1521 - 1524 (1998)
Update date:2022-08-04
Topics:
Rodriguez, Chester E.
Holmes, H. Michael
Mlodnosky, Karyn L.
Lam, Vinh Q.
Berkman, Clifford E.
Several putative, phosphorus-containing inhibitors of γ-glutamyl hydrolase were synthesized and evaluated for inhibitory activity. The phosphonamidoic acids were shown to be weak competitive inhibitors while both a phosphoramidate diester and a phosphonamidate ester were shown to be potent time-dependent inactivators, presumably through irreversible phosphorylation of an active site nucleophile.
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