Journal
EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY
Volume 76, Issue -, Pages 580-588Publisher
ELSEVIER FRANCE-EDITIONS SCIENTIFIQUES MEDICALES ELSEVIER
DOI: 10.1016/j.ejmech.2014.02.048
Keywords
Thiazolidinone; Propanolamine; Hybrid; Antihypertensive; Antiarrhythmic
Categories
Ask authors/readers for more resources
In the present study, fourteen derivatives comprising of 5-benzylidene-2-(phenylimino)-thiazolidin-4-one moiety were synthesized. The structures of synthesized compounds were established by elemental analysis, IR, H-1 NMR, C-13 NMR and mass spectral data and tested for electrocardiographic, antiarrhythmic and antihypertensive activities. Compound 11 was found to be most potent in this series. The pharmacological results suggested that, the antiarrhythmic effects of these compounds were related to their Ca++ ion channel antagonistic properties, which are believed to be due to the presence of 5-benzilidine-2-(phenylimino)-thiazolidin-4-one moiety. The antihypertensive effect of beta-blocker side chain is enhanced by the presence of less bulky aliphatic and heterocyclic tertiary amines. (C) 2014 Elsevier Masson SAS. All rights reserved.
Authors
I am an author on this paper
Click your name to claim this paper and add it to your profile.
Reviews
Recommended
No Data Available