Title : N-formyl hydroxylamine containing dipeptides: generation of a new class of vasopeptidase inhibitors.

Pub. Date : 2000 Feb 7

PMID : 10698448






2 Functional Relationships(s)
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Compound Name
Protein Name
Organism
1 Four primary zinc-binding pharmacophores (thiols, carboxylates, phosphorus acids, and hydroxamates) have been utilized in generating inhibitors of zinc metalloproteases such as ACE, NEP, the MMPs, and ECE. Sulfhydryl Compounds angiotensin I converting enzyme Homo sapiens
2 Although compounds which inhibit the activity of both ACE and NEP (vasopeptidase inhibitors, VPIs) have been reported which incorporate a thiol, carboxylate, or phosphorus acid pharmacophore, the generation of hydroxamate based vasopeptidase inhibitors has remained elusive. Sulfhydryl Compounds angiotensin I converting enzyme Homo sapiens