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Design, synthesis and biological evaluation of novel indolin-2-ones as potent anticancer compounds.


ABSTRACT: The indolin-2-one core is a privileged structure for antitumor agents, especially kinase inhibitors. Twenty-three novel indolin-2-ones were designed by molecular dissection of the anticancer drug indirubin. Seventeen of them exhibited significant inhibition against the tested cell lines, and two of them (1c and 1h) showed IC50 values at the submicromolar level against HCT-116 cells. Compounds 1c and 2c were also potent inhibitors of the triple-negative breast cancer (TNBC) cell line MDA-MB-231. Flow cytometry was utilized to explore the antitumor mechanism of 1c and 2c with MDA-MB-231 cells, and distinct effects were observed on 2c. Furthermore, immunocytochemical examination of 1c suggested a destabilization of microtubules, which was significantly different from the effect of IM, an indirubin derivative.

SUBMITTER: Zhou A 

PROVIDER: S-EPMC6432916 | biostudies-literature | 2017 Aug

REPOSITORIES: biostudies-literature

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Design, synthesis and biological evaluation of novel indolin-2-ones as potent anticancer compounds.

Zhou Andong A   Yan Lei L   Lai Fangfang F   Chen Xiaoguang X   Goto Masuo M   Lee Kuo-Hsiung KH   Xiao Zhiyan Z  

Bioorganic & medicinal chemistry letters 20170607 15


The indolin-2-one core is a privileged structure for antitumor agents, especially kinase inhibitors. Twenty-three novel indolin-2-ones were designed by molecular dissection of the anticancer drug indirubin. Seventeen of them exhibited significant inhibition against the tested cell lines, and two of them (1c and 1h) showed IC<sub>50</sub> values at the submicromolar level against HCT-116 cells. Compounds 1c and 2c were also potent inhibitors of the triple-negative breast cancer (TNBC) cell line M  ...[more]

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