Literature DB >> 24637077

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

Chetan M Bhalgat1, Pooja V Darda2, Kailash G Bothara3, Shashikant V Bhandari3, Jotsna Gandhi4, B Ramesh5.   

Abstract

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, (1)H NMR, (13)C 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 β-blocker side chain is enhanced by the presence of less bulky aliphatic and heterocyclic tertiary amines.
Copyright © 2014 Elsevier Masson SAS. All rights reserved.

Entities:  

Keywords:  Antiarrhythmic; Antihypertensive; Hybrid; Propanolamine; Thiazolidinone

Mesh:

Substances:

Year:  2014        PMID: 24637077     DOI: 10.1016/j.ejmech.2014.02.048

Source DB:  PubMed          Journal:  Eur J Med Chem        ISSN: 0223-5234            Impact factor:   6.514


  1 in total

1.  The anti-inflammatory activity of 2-iminothiazolidines: evidence for macrophage repolarization.

Authors:  Eduarda Talita Bramorski Mohr; Tainá Larissa Lubschinski; Julia Salvan da Rosa; Guilherme Nicácio Vieira; Mariano Felisberto; Robson Ruan Romualdo; Misael Ferreira; Marcus Mandolesi Sá; Eduardo Monguilhott Dalmarco
Journal:  Inflammopharmacology       Date:  2022-10-22       Impact factor: 5.093

  1 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.