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Arch Pharm (Weinheim) ; 337(1): 25-34, 2004 Jan.
Article in English | MEDLINE | ID: mdl-14760625

ABSTRACT

Several substituted 3-aryl-1-(4-aryl-2-thiazolyl)-5-(3-pyridyl)-2-pyrazolines were synthesized by reacting substituted 3-aryl-5-(3-pyridyl)-1-thiocarbamoyl-2-pyrazolines with phenacyl bromide in ethanol. The structures of all compounds were confirmed by IR, (1)H-NMR, mass spectral data and elemental analyses. The antihypertensive activity of compounds was examined by the tail-cuff method and compared with clonidine. Compounds 24-28 showed significant antihypertensive activity.


Subject(s)
Antihypertensive Agents/chemical synthesis , Antihypertensive Agents/pharmacokinetics , Pyrazoles/chemical synthesis , Pyrazoles/pharmacokinetics , Thiazoles/chemical synthesis , Thiazoles/pharmacokinetics , Animals , Antihypertensive Agents/administration & dosage , Blood Pressure/drug effects , Clonidine/administration & dosage , Clonidine/pharmacokinetics , Hypotension/chemically induced , Injections, Intraperitoneal , Male , Molecular Structure , Pyrazoles/administration & dosage , Quantitative Structure-Activity Relationship , Rats , Rats, Sprague-Dawley , Thiazoles/administration & dosage
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