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Synthesis and Antiproliferative Activity of Novel Hydrazono Thiazolidene and Thiazole Derivatives Bearing Rhodanine Moiety

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Abstract

Some new fluoro-heterocyclic compounds containing thiazole and pyridine moities have been synthesized and studied for their antiproliferative activity. Thiazole derivatives have been synthesized by the reaction of alpha-halo carbonyl compounds with thiosemicarbazones. Some pyridine derivatives have been synthesized by the reaction of chalcone with cyanothioacetamide and/or malononitrile. Spectroscopic methods have been used for elucidating molecular structures of the products. Cytotoxic activity of several derivatives has been tested against human breast cancer (MCF-7), human colon cancer (HCT-116) and human liver cancer (Hep-G2) by the SRB method. Most of compounds exhibit mild effect on the tested cell lines. One of thiazolidin-4-one derivatives has been characterized by moderate to strong effect on MCF-7 cell line.

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Fig. 1.
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Notes

  1. Method a gave higher yields than method b, lasted for shorter period of time and its procedure was simpler.

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ACKNOWLEDGMENTS

The authors offered a great gratitude to the National Research Center, Egypt for funding this work which is a part of PhD thesis project No 1/6/14. Also the authors are grateful to the Deanship of Scientific Research, king Saud University for funding through Vice Deanship of Scientific Research Chairs.

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Elasasy, M.E.A., Elnaggar, D.H., Hafez, N.A.A. et al. Synthesis and Antiproliferative Activity of Novel Hydrazono Thiazolidene and Thiazole Derivatives Bearing Rhodanine Moiety. Russ J Gen Chem 91, 915–925 (2021). https://doi.org/10.1134/S1070363221050236

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