Open Chemistry Journal




ISSN: 1874-8422 ― Volume 6, 2019

Synthesis and Evaluation of New 2-Iminothiazolidin-4-one and Thiazolidin-2,4-dione Derivatives as Antimicrobial and Anti-inflammatory Agents



Waleed A. Bayoumi1, *, Shaymaa H. Abdel-Rhman2, Mohamed E. Shaker3
1 Department of Pharmaceutical Organic Chemistry, Faculty of Pharmacy, University of Mansoura, Mansoura 35516, Egypt;
2 Department of Microbiology, Faculty of Pharmacy, University of Mansoura, Mansoura 35516, Egypt;
3 Department of Pharmacology and Toxicology, Faculty of Pharmacy, University of Mansoura, Mansoura 35516, Egypt

Abstract

A new series of 2-iminothiazolidin-4-ones and thiazolidin-2,4-diones were designed and synthesized. The target compounds were evaluated for antimicrobial and anti-inflammatory activities, aiming to find a candidate carrying dual activities. The antibacterial activity was determined by cup-diffusion technique and NCCLS broth dilution method. The MICs were determined using 96-well microtitre plates, while the anti-inflammatory activity was determined using carrageenan- induced rat paw edema model. The results revealed that target compounds showed no antifungal activity towards tested Fungi, whereas the antibacterial activity was mainly on Gram-positive bacteria. The anti-inflammatory activity was observed in compounds belonging to the thiazolidin-2,4-dione series. The structures of the newly synthesized compounds were confirmed by physical and spectral data.

Keywords:: 2-iminothiazolidin-4-ones, anti-inflammatory, antimicrobial, synthesis, thiazolidin-2,4-diones.


Article Information


Identifiers and Pagination:

Year: 2014
Volume: 1
First Page: 33
Last Page: 38
Publisher Id: CHEM-1-33
DOI: 10.2174/1874842201401010033

Article History:

Received Date: 24/9/2014
Revision Received Date: 26/11/2014
Acceptance Date: 27/11/2014
Electronic publication date: 31/12/2014
Collection year: 2014

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© Bayoumi et al.; Licensee Bentham Open.

open-access license: This is an open access article licensed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted, non-commercial use, distribution and reproduction in any medium, provided the work is properly cited.


* Address correspondence to this author at the Department of Pharmaceutical Organic Chemistry, Faculty of Pharmacy, University of Mansoura, Mansoura 35516, Egypt; Tel: +20 111 5633 722; Fax: +20 5022 4749; E-mail: waleedbayoumi@mans.edu.eg


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