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Bioorg Med Chem Lett ; 12(15): 1967-71, 2002 Aug 05.
Article in English | MEDLINE | ID: mdl-12113820

ABSTRACT

Three novel metabolites of the angiotensin-II (A-II) receptor antagonist tasosartan have been identified in humans, and the syntheses and pharmacologic profiling of these metabolites are reported. Each metabolite bound the human A-II receptor with IC(50)s between 20 and 45nM. The in vivo effects of these compounds in attenuating the pressor response to angiotensin-II challenge in anesthetized rats were also investigated. An unsaturated diol metabolite exhibited in vivo efficacy at intravenous doses of 1 and 3mg/kg, while the other metabolites, both carboxylic acids, had no significant effect at the same doses.


Subject(s)
Angiotensin Receptor Antagonists , Pyrimidines/metabolism , Pyrimidines/pharmacology , Tetrazoles/metabolism , Tetrazoles/pharmacology , Animals , Blood Pressure/drug effects , Dose-Response Relationship, Drug , Heart Rate/drug effects , Humans , Inhibitory Concentration 50 , Injections, Intravenous , Pyrimidines/chemistry , Rats , Receptors, Angiotensin/metabolism , Structure-Activity Relationship , Tetrazoles/chemistry
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