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Synthesis of Marine Cyclopeptide Galaxamide Analogues as Potential Anticancer Agents.


ABSTRACT: In this paper, eight new galaxamide analogues (Z-1~Z-8) were synthesized and evaluated for their cytotoxic activities against five cancer cell lines, MCF-7, MD-MBA-231, HepG2, Hela, and A549, using MTT assays. The modified analogue Z-6 displayed broad spectrum cytotoxic activity toward each tested cell line with IC50 values of 1.65 ± 0.30 (MCF-7), 2.91 ± 0.17 (HepG2), 4.59 ± 0.27 (MD-MBA-231), 5.69 ± 0.37 (Hela), and 5.96 ± 0.41 (A549) μg/mL, respectively. The galaxamides Z-3 and Z-6 induced concentration-dependent apoptosis of the MCF-7 cells after 72 h as evaluated by the flow cytometry experiment. The results showed that these compounds could induce MCF-7 cell apoptosis by arresting the G0/G1 phase of the cell cycle and finally achieving the effect of inhibiting the proliferation of MCF-7 cells.

SUBMITTER: Li D 

PROVIDER: S-EPMC8949366 | biostudies-literature | 2022 Feb

REPOSITORIES: biostudies-literature

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Synthesis of Marine Cyclopeptide Galaxamide Analogues as Potential Anticancer Agents.

Li Daichun D   Liao Xiaojian X   Zhong Shenghui S   Zhao Bingxin B   Xu Shihai S  

Marine drugs 20220222 3


In this paper, eight new galaxamide analogues (<b>Z-1</b>~<b>Z-8</b>) were synthesized and evaluated for their cytotoxic activities against five cancer cell lines, MCF-7, MD-MBA-231, HepG2, Hela, and A549, using MTT assays. The modified analogue <b>Z-6</b> displayed broad spectrum cytotoxic activity toward each tested cell line with IC<sub>50</sub> values of 1.65 ± 0.30 (MCF-7), 2.91 ± 0.17 (HepG2), 4.59 ± 0.27 (MD-MBA-231), 5.69 ± 0.37 (Hela), and 5.96 ± 0.41 (A549) μg/mL, respectively. The gal  ...[more]

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