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A new generation of bradykinin antagonists.
Stewart, J M; Gera, L; Hanson, W; Zuzack, J S; Burkard, M; McCullough, R; Whalley, E T.
Afiliação
  • Stewart JM; Department of Biochemistry, University of Colorado School of Medicine, Denver 80262, USA.
Immunopharmacology ; 33(1-3): 51-60, 1996 Jun.
Article em En | MEDLINE | ID: mdl-8856115
ABSTRACT
Bradykinin B2 receptors are constitutively expressed, and require the entire peptide chain of bradykinin for recognition. Expression of B1 receptors is induced in inflammation; they recognize BK-(1-8). Heretofore blockade of all the actions of bradykinin required two different antagonists, one for each class of receptors. The new antagonists described here are full chain antagonists having high potency on B2 receptors, but they are also very potent antagonists for B1 receptors. They are highly resistant to kininases and show very long action in vivo. These antagonists contain the novel amino acid alpha-(2-indanyl)glycine (IgI) at positions 5 and 7. The peptide DArg-Arg-Pro-Hyp-Gly-Igl-Ser-DIgl-Oic-Arg (designated B9430) shows all these desirable characteristics. It represents a new class of bradykinin antagonist peptides.
Assuntos
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Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Oligopeptídeos / Bradicinina Limite: Animals / Female / Humans / Male Idioma: En Revista: Immunopharmacology Ano de publicação: 1996 Tipo de documento: Article País de afiliação: Estados Unidos
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Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Oligopeptídeos / Bradicinina Limite: Animals / Female / Humans / Male Idioma: En Revista: Immunopharmacology Ano de publicação: 1996 Tipo de documento: Article País de afiliação: Estados Unidos
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