细胞毒性
赫拉
化学
布雷菲尔德A
细胞凋亡
细胞培养
癌细胞
转移
癌症研究
药理学
乳腺癌
癌症
体外
立体化学
细胞
生物化学
内科学
生物
医学
高尔基体
遗传学
作者
Mingying Wang,Baojia Sun,Tao Ye,Yanbing Wang,Yonglian Hou,Siyuan Wang,Huaqi Pan,Hui‐Ming Hua,Dahong Li
标识
DOI:10.1016/j.bmc.2023.117380
摘要
27 novel 5-(4-hydroxyphenyl)-3H-1,2-dithiole-3-thione derivatives of brefeldin A were designed and synthesized to make them more conducive to the cancer treatment. The antiproliferative activity of all the target compounds was tested against six human cancer cell lines and one human normal cell line. Compound 10d exhibited nearly the most potent cytotoxicity with IC50 values of 0.58, 0.69, 1.82, 0.85, 0.75, 0.33 and 1.75 μM against A549, DU-145, A375, HeLa, HepG2, MDA-MB-231 and L-02 cell lines. Moreover, 10d inhibited metastasis and induced apoptosis of MDA-MB-231 cells in a dose-dependent manner. The potent anticancer effects of 10d were prompted based on the aforementioned results, the therapeutic potential of 10d for breast cancer was worth further exploration.
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