
Journal of Medicinal Chemistry p. 625 - 629 (1988)
Update date:2022-08-02
Topics:
Maibaum
Rich
Two new inhibitors, 4 and 5, of the aspartic proteinase porcine pepsin were synthesized. These compounds, which span the P4-P'3 binding subsites of the enzyme, were derived by replacing the Nph-Phe dipeptidyl unit of a good pepsin su
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Doi:10.1021/jm00351a013
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