Synthesis of 7-Substituted Fluoroquinolone Derivatives Contain- ing Triazolidine Dione Moiety and In Vitro Evaluation of their Cytotoxic Effects

Authors

Hadi Adibi1,*, Leila Hosseinzadeh1, Maryam Mahdian2, Alireza Foroumadi3, Mohammad Ali Zolfigol4, Shadpour Mallakpour5
1Novel Drug Delivery Research Center, Faculty of Pharmacy, Kermanshah University of Medical Sciences, Kermanshah, Iran
2Student's Research Committee, Kermanshah University of Medical Sciences, Kermanshah, Iran
3Department of Medicinal Chemistry, Faculty of Pharmacy & Pharmaceutical Sciences Research Center, Tehran University of Medical Sciences, Tehran, Iran
4Faculty of Chemistry, Bu-Ali Sina University, Hamedan, Iran
5Organic Polymer Chemistry Research Laboratory, Department of Chemistry, Isfahan University of Technology, Isfahan, Iran
*Corresponding Author: Corresponding author: Novel Drug Delivery Research Center, Faculty of Pharmacy, Kermanshah University of Medical Sciences, Kermanshah, Iran. Email:[email protected]

Journal of Reports in Pharmaceutical Sciences:Vol. 2, issue 1; 75-82
Published online:Feb 25, 2013
Article type:Rapid Communication
Received:Jan 19, 2013
Accepted:Feb 18, 2013
How to Cite:Adibi H, Hosseinzadeh L, Mahdian M, Foroumadi A, Zolfigol MA, et al. Synthesis of 7-Substituted Fluoroquinolone Derivatives Contain- ing Triazolidine Dione Moiety and In Vitro Evaluation of their Cytotoxic Effects. J Rep Pharm Sci. 2013;2(1):e147764. doi:

Abstract

A series of fluoroquinolone derivatives holding triazolidine dione moieties have been synthesized and proved to be cytotoxic agents in vitro particularly against cancer cell lines (SKNMC, MCF7, A2780-CP, SW48, A549, KB, HT-29, HepG2). The cytotoxic activity was assessed using MTT colorimetric assay. Our compounds showed less cytotoxicity than doxorubicin in all studied cell lines. The best results was obtained for the compound 3a on A549 cell line (IC50 = 34.5 μM) and the compound 3b on SW48 (IC50 = 42 μM) and A2780-CP (IC50 = 43 μM) cell lines. The compound 3b that has the phenyl urazole moiety at C-7 position, showed better anticancer effect than the compound 3a on SW48, A2780-CP and MCF7 cell lines. 

Highlights

Copyright

© 2013, 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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