5-(4-Hydroxyphenyl)-3H-1,2-dithiole-3-thione derivatives of brefeldin A: Design, synthesis and cytotoxicity in MDA-MB-231 human breast cancer cells

被引:1
作者
Wang, Mingying [1 ,2 ]
Sun, Baojia [3 ]
Ye, Tao [1 ,2 ]
Wang, Yanbing [4 ]
Hou, Yonglian [1 ,2 ]
Wang, Siyuan [5 ]
Pan, Huaqi [6 ]
Hua, Huiming [1 ,2 ]
Li, Dahong [1 ,2 ]
机构
[1] Shenyang Pharmaceut Univ, Minist Educ, Key Lab Struct Based Drug Design & Discovery, 103 Wenhua Rd, Shenyang 110016, Peoples R China
[2] Shenyang Pharmaceut Univ, Sch Tradit Chinese Mat Med, 103 Wenhua Rd, Shenyang 110016, Peoples R China
[3] Yantai Valiant Pharmaceut Co Ltd, 60 Taiyuan Rd,Dajijia Ind Pk, Yeda Yantai 264006, Shandong, Peoples R China
[4] Shenyang Pharmaceut Univ, Sch Life Sci & Biopharmaceut, Shenyang 110016, Peoples R China
[5] Shenzhen Technol Univ, Coll Pharm, Shenzhen 518118, Peoples R China
[6] Chinese Acad Sci, Inst Appl Ecol, Shenyang 110016, Peoples R China
关键词
Brefeldin A; 5-(4-Hydroxyphenyl)-3H-1; 2-Dithiole-3-thione; Breast cancer; Apoptosis; Metastasis; GROWTH;
D O I
10.1016/j.bmc.2023.117380
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
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 & mu;M 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.
引用
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页数:14
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