Bioorganic and Medicinal Chemistry Letters p. 1511 - 1516 (1999)
Update date:2022-08-03
Topics:
Chen, Huixiong
Roques, Bernard P.
Fournie-Zaluski, Marie-Claude
A series of phosphinic compounds mimicking the transition state of substrates hydrolysed by aminopeptidase N (EC 3.4.11.2) were synthesized. These new compounds have potent inhibitory activities with Ki values in the nanomolar range. These derivatives behave as the most potent APN inhibitors designed to date.
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