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Bioorg Med Chem Lett ; 12(9): 1275-8, 2002 May 06.
Article in English | MEDLINE | ID: mdl-11965369

ABSTRACT

A novel non-peptidyl endothelin converting enzyme inhibitor was obtained through a pharmacophore analysis of known inhibitors and three-dimensional structure database search. Analogues of the new inhibitor were designed using the structure-activity relationship of known inhibitors and synthesized. In anesthetized rats, intraperitoneal administration of the analogues suppressed the pressor responses induced by big endothelin-1.


Subject(s)
Aspartic Acid Endopeptidases/chemistry , Aspartic Acid Endopeptidases/pharmacology , Enzyme Inhibitors/chemical synthesis , Enzyme Inhibitors/pharmacology , Formazans/chemistry , Formazans/pharmacology , Tetrazoles/chemistry , Tetrazoles/pharmacology , Animals , Aspartic Acid Endopeptidases/chemical synthesis , Endothelin-Converting Enzymes , Formazans/chemical synthesis , Hydrogen Bonding , Metalloendopeptidases , Models, Molecular , Rats , Tetrazoles/chemical synthesis
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