Design, synthesis and biological evaluation of novel benzothiazole derivatives bearing semicarbazone moiety as antitumor agents

Junjie Ma , Gang Hu , Lijun Xie , Lei Chen , Boxuan Xu , Ping Gong

Chemical Research in Chinese Universities ›› 2015, Vol. 31 ›› Issue (6) : 958 -963.

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Chemical Research in Chinese Universities ›› 2015, Vol. 31 ›› Issue (6) : 958 -963. DOI: 10.1007/s40242-015-5034-1
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Design, synthesis and biological evaluation of novel benzothiazole derivatives bearing semicarbazone moiety as antitumor agents

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Abstract

A series of novel benzothiazole derivatives bearing semicarbazone as a linker was designed and synthesized, and their in vitro antitumor activities were evaluated against four cancer cell lines(HT29, H460, A549 and MDA-MB-231). Most of them showed moderate to excellent activity against all the tested cell lines. Among them, compounds 12a―12i with fluoro-substituted benzyl-1H-indole moiety displayed more potent activity than those with phenyl moiety. The most promising compound 12d exhibited excellent antitumor activity with IC50 values of 0.015, 0.28, 1.53 and 0.68 μmol/L against the four tested cell lines respectively.

Keywords

Benzothiazole / Semicarbazone / Antitumor activity

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Junjie Ma, Gang Hu, Lijun Xie, Lei Chen, Boxuan Xu, Ping Gong. Design, synthesis and biological evaluation of novel benzothiazole derivatives bearing semicarbazone moiety as antitumor agents. Chemical Research in Chinese Universities, 2015, 31(6): 958-963 DOI:10.1007/s40242-015-5034-1

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