Synthesis and biological activity of novel zingerone–thiohydantoin hybrids Scientific paper

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Katarina Virijević
https://orcid.org/0000-0003-2703-8829
Petar Stanić
https://orcid.org/0000-0002-3655-6452
Jovana Muškinja
https://orcid.org/0000-0002-0638-3423
Jelena Katanić Stanković
https://orcid.org/0000-0002-2997-9588
Nikola Srećković
https://orcid.org/0000-0002-0216-5816
Marko Živanović
https://orcid.org/0000-0002-8833-8035
Biljana Šmit
http://orcid.org/0000-0001-9799-4723

Abstract

A series of zingerone–thiohydantoin hybrids were synthesized from O-alkyl zingerone derivatives by cyclocondensation with thiosemicarbazide in a two-step reaction. The obtained new potentially bioactive compounds were structurally characterized by IR and NMR spectroscopy, as well as by elemen­tal and HRMS analysis. In addition, their antimicrobial and in vitro anticancer activities were tested. The tested compounds showed low to moderate antimic­robial activity. Zingerone–thiohydantoin hybrid with an O-butyl substituent exerted the significant cytotoxic activity on colon HCT-116 cancer cells, with­out toxicity on healthy MRC-5 cells.

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How to Cite
[1]
K. Virijević, “Synthesis and biological activity of novel zingerone–thiohydantoin hybrids: Scientific paper”, J. Serb. Chem. Soc., vol. 87, no. 12, pp. 1349–1358, Aug. 2022.
Section
Organic Chemistry

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