Synthesis, characterization and anti-proliferative activity of heterocyclic hypervalent organoantimony compounds

被引:52
|
作者
Chen, Yi [1 ,2 ,3 ]
Yu, Kun [3 ]
Tan, Nian-Yuan [3 ]
Qiu, Ren-Hua [3 ]
Liu, Wei [1 ]
Luo, Ning-Lin [3 ]
Tong, Le [2 ]
Au, Chak-Tong [3 ,4 ]
Luo, Zi-Qiang [1 ]
Yin, Shuang-Feng [3 ]
机构
[1] Cent S Univ, Sch Basic Med, Changsha 410013, Hunan, Peoples R China
[2] Hunan Univ Chinese Med, Coll Med, Changsha 410208, Hunan, Peoples R China
[3] Hunan Univ, Coll Chem & Chem Engn, State Key Lab Chemo Biosensing & Chemometr, Changsha 410082, Hunan, Peoples R China
[4] Hong Kong Baptist Univ, Dept Chem, Kowloon, Hong Kong, Peoples R China
基金
中国国家自然科学基金;
关键词
Hypervalent organoantimony; Synthesis; Characterization; Anti-proliferative activity; Cell cycle arrest; Apoptosis; CRYSTAL-STRUCTURES; DIPHENYLANTIMONY(III) DERIVATIVES; IN-VITRO; ANTIMONY; BISMUTH; RADII;
D O I
10.1016/j.ejmech.2014.04.026
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Three heterocyclic hypervalent organoantimony chlorides RN(CH2C6H4)(2)SbCI (2a R = t-Bu, 2b R = Cy, 2c R = Ph) and their chalcogenide derivatives [RN(CH2C6H4)(2)Sb](2)O (3a R = t-Bu, 3b R = Cy, 3c R = Ph) were synthesized and characterized by techniques such as H-1 NMR, C-13 NMR, X-ray diffraction, and elemental analysis. It is found that the anti-proliferative activity detected over these compounds can be attributed to the coordination bond between the antimony and nitrogen atoms of these compounds. Moreover, a preliminary study on mechanistic action suggests that the inhibition effect is ascribable to cell cycle arrest and cell apoptosis. (C)2014 Elsevier Masson SAS. All rights reserved.
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页码:391 / 398
页数:8
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