
Bioorganic and Medicinal Chemistry Letters p. 379 - 384 (1996)
Update date:2022-08-02
Topics:
Xue, Chu-Biao
He, Xiaohua
Roderick, John
DeGrado, William F.
Decicco, Carl
Copeland, Robert A.
A series of amino-carboxylate inhibitors of matrix metalloproteinases containing different P1 modifications have been synthesized. It was discovered that a toluenesulfonamide-type substituent at the P1 position considerably enhances the binding affinity of inhibitors for stromelysin. Replacements of the P2'-P3' residues with nonpeptide components result in loss of inhibitory activity.
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