Please use this identifier to cite or link to this item: https://scidar.kg.ac.rs/handle/123456789/10917
Title: Synthesis and anticancer activity of chalcone analogues with sulfonyl groups
Authors: Muškinja, Jovana
Burmudz̃ija A.
Baskić D.
Popovic, Suzana
Todorovic, Danijela
Zaric, Milan
Ratković, Zoran
Journal: Medicinal Chemistry Research
Issue Date: 15-Mar-2019
Abstract: © 2019, Springer Science+Business Media, LLC, part of Springer Nature. Three series of sulfonyl esters were synthesized in reactions of sulfonyl chlorides with three different phenolic chalcone analogues (dehydrozingerone (4-(4-hydroxy-3-methoxyphenyl)-3-buten-2-one), (E)-1-(4-hydroxy-3-methoxyphenyl)pent-1-en-3-one, and (E)-1-(4-hydroxy-3-methoxyphenyl)-5-methylhex-1-en-3-one). The structures of the new compounds were determined by IR, MS, and NMR methods. Screening of the new sulfonyl esters’ in vitro cytotoxic activities against human epithelial cervical carcinoma (HeLa) and normal human fibroblast (MRC-5) cell lines by the MTT method was performed. The five most active were selected and further tested on HeLa, MRC-5, and MCF-7 (breast carcinoma) cell lines. The examined compounds exhibit strong in vitro anticancer activities with moderate-to-high selectivity, inducing apoptotic cell death and cell cycle arrest in both HeLa and MCF-7 cell lines, but have little to no effect on the non-cancerous MRC-5 cell line.
URI: https://scidar.kg.ac.rs/handle/123456789/10917
Type: journal article
DOI: 10.1007/s00044-018-02283-4
ISSN: 10542523
SCOPUS: 85059674977
Appears in Collections:Faculty of Medical Sciences, Kragujevac
Faculty of Science, Kragujevac
Institute for Information Technologies, Kragujevac

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