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Pharm Sci. 2021;27(3): 345-352.
doi: 10.34172/PS.2020.95
  Abstract View: 158
  PDF Download: 41

Research Article

Synthesis, Molecular Docking and Anticancer Activity of Novel 1,3-Thiazolidin-4-Ones

Ramesh Sawant 1* ORCID logo, Jyoti Wadekar 2 ORCID logo, Rushikesh Ukirde 1, Ganesh Barkade 1 ORCID logo

1 Department of Pharmaceutical Chemistry & PG Studies, Dr. Vithalrao Vikhe Patil Foundations College of Pharmacy, Vilad Ghat Ahmednagar-414111, Maharashtra, India.
2 Department of Pharmacognosy, Dr. Vithalrao Vikhe Patil Foundations College of Pharmacy, Vilad Ghat Ahmednagar-414111, Maharashtra, India.

Abstract

Background: Cancer is a major cause of death all over the globe. Controlling cell division byinhibition of mitosis is the most successful clinical strategy for cancer treatment. The developmentof novel anticancer agents is the most important area in medicinal chemistry and drug discoveryresearch. Thiazolidine is the multifunctional nucleus which shows a number of pharmacologicalactivities like anticancer, anti-inflammatory, antioxidant, antibacterial, antifungal, antidiabetic,antihyperlipidemic and antiarthritic.

Methods: In a present study series of 2-substituted-3-(1H-benzimidazole-2-yl)-thiazolidin-4-ones were designed, synthesized by the microwave-assisted system, and characterized bymelting point, IR, 1H NMR, and mass spectroscopy. All the newly synthesized compoundswere examined for their in vitro anticancer activity against breast cancer cell line MCF-7 bySulforhodamine B (SRB) assay.

Results: The compounds AB-12 (GI50: 28.5 μg/ml) and AB-6 (GI50: 50.7 μg/ml) exhibitedsignificant cell growth inhibitory activity.

Conclusion: These results indicate that compound AB-12 and AB-6 as related polo-like kinase1inhibitors compounds could be lead compounds for further development of anticanceragents.

Keywords: Anticancer activity, MCF-7 cell line, Molecular Modelling, Polo like kinase 1 inhibitors, Thiazolidine-4-one, Synthesis
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Submitted: 12 Jun 2020
Revision: 28 Oct 2020
Accepted: 19 Nov 2020
ePublished: 19 Nov 2020
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