4.7 Article

Synthesis and pharmacological screening of some novel antihypertensive agents possessing 5-Benzylidene-2-(phenylimino)-thiazolidin-4-one ring

Journal

EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY
Volume 76, Issue -, Pages 580-588

Publisher

ELSEVIER FRANCE-EDITIONS SCIENTIFIQUES MEDICALES ELSEVIER
DOI: 10.1016/j.ejmech.2014.02.048

Keywords

Thiazolidinone; Propanolamine; Hybrid; Antihypertensive; Antiarrhythmic

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

Primary Rating

4.7
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available