Synthesis and Evaluation of Thiadiazole-based Antileishmanial Agents

Author(s):
Farshid HassanzadehFarshid Hassanzadeh1, Elham JafariElham Jafari1,*, Mozhgan SaeediMozhgan Saeedi1, Sedigheh SaberiSedigheh SaberiSedigheh Saberi ORCID2
1Department of Medicinal Chemistry, Isfahan Pharmaceutical Sciences Research Center, School of Pharmacy and Pharmaceutical Sciences, Isfahan University of Medical Sciences, Isfahan, I.R. Iran
2Department of Mycology and Parasitology, School of Medicine, Isfahan University of Medical Sciences, Isfahan, I.R. Iran
*Corresponding Author: Corresponding author: Department of Medicinal Chemistry and Isfahan Pharmaceutical Sciences Research Center, School of Pharmacy and Pharmaceutical Sciences, Isfahan University of Medical Sciences, Isfahan, I.R. Iran. Email:[email protected]

Journal of Reports in Pharmaceutical Sciences:Vol. 9, issue 2; 189-95
Published online:Oct 07, 2020
Article type:Research Article
Received:Feb 09, 2020
Accepted:May 10, 2020
How to Cite:Hassanzadeh F, Jafari E, Saeedi M, Saberi S. Synthesis and Evaluation of Thiadiazole-based Antileishmanial Agents. J Rep Pharm Sci. 2020;9(2):e147112. doi: https://doi.org/10.4103/jrptps.JRPTPS_3_20

Abstract

Background and Objectives: The 1, 3, 4-thiadiazole scaffold is one of the principal structural components, in a variety of drug categories such as antimicrobial, anti-inflammatory, antineoplastic, and antileishmanial agents. Considering the reported antileishmanial effects of thiadiazole derivatives and the importance of this disease, some of the thiadiazole derivatives with modifications at sulfur atom or amine group attached to the 2-position were synthesized and evaluated for antileishmanial activity. 
Materials and Methods: Derivatives of 1,3,4-thiadiazole including 2-substituted-thio-1,3,4-thiadiazoles bearing (5-(4-nitrobenzylideneamino) or 5-amino (II, IV, V) and one derivative of 2-substituted-amino- 1,3,4-thiadiazole bearing (5- (4-nitrophenyl) (VII) were synthesized and evaluated for their in vitro antileishmanial activity against promastigote and amastigote forms of the Leishmania major. 
Results: The most active compound was found to be compound II after 24-h incubation against promastigotes and amastigotes with the half maximal inhibitory concentration (IC50) values of 44.4 μM and 64.7 μM, respectively. 
Conclusion: All of the synthesized compounds showed good antileishmanial activity against both forms of L. major after 48 and 72 h incubation. 
 

Copyright

© 2020, Author(s). This open-access article is available under the Creative Commons Attribution 4.0 (CC BY 4.0) International License (https://creativecommons.org/licenses/by/4.0/), which allows for unrestricted use, distribution, and reproduction in any medium, provided that the original work is properly cited.

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