Synthesis of 4-(4-methylidene-4H-3,1-benzothiazin-2-yl)benzene1,3-diols and their antiproliferative activity against human cancer cell lines


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One-step synthesis of novel biologically active 4- or 6-(4-methylidene-4H-3,1-benzothiazin-2yl)benzene-1,3-diols is described. The target compounds were prepared by the reaction of aryl-modified sulfinylbis[(2,4-dihydroxyphenyl)methanethione]s with 1-(2-aminophenyl)ethanones. Newly synthesized compounds were characterized by IR, 1H NMR, and mass spectral data. Their antiproliferative potency against human cancer cell lines was determined. Some descriptors were calculated to find the relationship between the structure and activity. It is revealed that the presence of hydrophobic substituents in the benzenediol ring intensifies the biological potency.

作者简介

J. Matysiak

Department of Chemistry

编辑信件的主要联系方式.
Email: joanna.matysiak@up.lublin.pl
波兰, Akademicka 15, Lublin, 20-950

A. Skrzypek

Department of Chemistry

Email: joanna.matysiak@up.lublin.pl
波兰, Akademicka 15, Lublin, 20-950

A. Niewiadomy

Department of Chemistry; Institute of Industrial Organic Chemistry

Email: joanna.matysiak@up.lublin.pl
波兰, Akademicka 15, Lublin, 20-950; Annopol 6, Warsaw, 03-236

M. Karpińska

Institute of Industrial Organic Chemistry

Email: joanna.matysiak@up.lublin.pl
波兰, Annopol 6, Warsaw, 03-236

J. Wietrzyk

Department of Experimental Oncology

Email: joanna.matysiak@up.lublin.pl
波兰, R. Weigla 12, Wroclaw, 53-114

B. Paw

Medical University of Lublin

Email: joanna.matysiak@up.lublin.pl
波兰, Jaczewskiego 4, Lublin, 20-090

D. Kłopotowska

Department of Experimental Oncology

Email: joanna.matysiak@up.lublin.pl
波兰, R. Weigla 12, Wroclaw, 53-114

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