Abstract
Novel triazole substituted pyrazolyl-methylenehydrazinyl-5-arylidene thiazolidinone derivatives 6a–n and 7a–l were synthesized and characterized by Fourier transform infrared, 1H and 13C nuclear magnetic resonance, mass spectrometry and elemental (CHN) analysis. The in vitro antibacterial (6a–n and 7a–l) and cytotoxic (6a–n) activities were evaluated for these compounds. The results revealed that the compounds 6b, 6i, 6k, 7b, 7h displayed good antibacterial activity. The compounds 6c (IC50 = 5.4 μM), 6l (IC50 = 6.3 μM) and 6f (IC50 = 9.85 μM) were effective for inhibition of human breast cancer cell line MCF-7. Similarly, the compounds 6b (IC50 = 8.7 μM) and 6c (IC50 = 9.06 μM) were shown to have effective inhibition on human cervical cancer cell line Hela.
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Acknowledgements
S. B. thanks the MHRD, India for the Research Seed Grant (RSG). V. P. thanks the MHRD, India for the fellowship. S.B. and V.P. thank Director, National Institute of Technology Warangal, India for providing research facilities.
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Pogaku, V., Eslavath, R.K., Dayakar, G. et al. Synthesis and biological evaluation of novel triazole substituted pyrazolyl-methylenehydrazinyl-5-arylidene thiazolidinone derivatives as antibacterial and cytotoxic agents. Res Chem Intermed 43, 6079–6098 (2017). https://doi.org/10.1007/s11164-017-2978-4
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DOI: https://doi.org/10.1007/s11164-017-2978-4