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Design, synthesis and biological evaluation of a series of new resveratrol analogues as potential anti-cancer agents.

ABSTRACT: A series of novel resveratrol derivatives were designed, synthesized and evaluated as anti-cancer agents. Most of the compounds showed significant anti-proliferative activities against three human cancer cell lines (HepG2, A549 and Hela). Among these compounds, compound r displayed the most potent inhibitory activity and showed low cytotoxic activity. Cell apoptosis and cell cycle assays demonstrated that compound r significantly induced apoptosis (p < 0.001) and arrested cell cycle at S phase. Immunofluorescence microscopy analysis showed compound r disrupted the tubulin network. Docking simulations supported the pharmacological results of compound r. It is believed that this work would be very useful for designing a new series of tubulin inhibitors.

SUBMITTER: Yang L

PROVIDER: S-EPMC6774960 | biostudies-literature | 2019 Sep

REPOSITORIES: biostudies-literature

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Design, synthesis and biological evaluation of a series of new resveratrol analogues as potential anti-cancer agents.

Yang Lifang L Qin Xuemei X Liu Hongcun H Wei Yanye Y Zhu Hailiang H Jiang Mingguo M

Royal Society open science 20190904 9

A series of novel resveratrol derivatives were designed, synthesized and evaluated as anti-cancer agents. Most of the compounds showed significant anti-proliferative activities against three human cancer cell lines (HepG2, A549 and Hela). Among these compounds, compound r displayed the most potent inhibitory activity and showed low cytotoxic activity. Cell apoptosis and cell cycle assays demonstrated that compound r significantly induced apoptosis (p < 0.001) and arrested ce ...[more]

PMID: 31598278

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