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J Med Chem. 1991 Sep;34(9):2692-701.

Design and synthesis of P2-P1'-linked macrocyclic human renin inhibitors.

Author information

1
Merck Sharp and Dohme Research Laboratories, Rahway, New Jersey 07065.

Abstract

Using a computer model of the active site of human renin developed at Merck, we designed a series of novel P2-P1'-linked, macrocyclic renin inhibitors 3-10. These unique inhibitors incorporate a transition-state isostere within a 13- or 14-membered ring. The three most active compounds in this family were 13-membered-ring glutamine-derived inhibitor 3, 14-membered-ring diaminopropionic acid derived inhibitor 6, and 13-membered-ring diol 9 (IC50 0.61, 0.59, 0.65 microM, respectively). Modification of inhibitor 3 at P4 led to 56 nM macrocyclic renin inhibitor 39. This study shows the viability of renin inhibitor designs which incorporate a scissile-bond replacement within a macrocycle.

PMID:
1895289
DOI:
10.1021/jm00113a005
[Indexed for MEDLINE]

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