Bioorganic and Medicinal Chemistry p. 1989 - 1998 (1997)
Update date:2022-08-03
Topics:
Lee, Kyung Joo
Joo, Keum Chan
Kim, Eun-Jung
Lee, Mijoon
Kim, Dong H.
2-(4-Imidazoyl)hydrocinnamic acid (1) and its congeners (2-4) having different length of alkyl chain spacers between the imidazole ring and the α-carbon to the carboxylate of 1 have been designed, synthesized and evaluated as inhibitors for carboxypeptidase A to show that they are competitive inhibitors for the enzyme. Inhibitor 1 was most potent having the K(i) value of 0.8 μM. The present study demonstrates that imidazole ring is an effective zinc coordinating ligand that can be useful for the design of inhibitors for zinc proteases.
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