Synthesis, crystal structure and biological evaluation of three new Rh(III) complexes incorporating benzimidazole derivatives

被引:6
|
作者
Liu, Jun-Hong [1 ]
Pan, Feng-Hua [2 ]
Wang, Zhen-Feng [2 ]
Wang, Rong [2 ]
Yang, Lin [2 ]
Qin, Qi-Pin [2 ,3 ]
Tan, Ming-Xiong [2 ]
机构
[1] Baotou Iron Steel Vocat Tech Coll, Baotou 014010, Inner Mongolia, Peoples R China
[2] Yulin Normal Univ, Coll Chem & Food Sci, Guangxi Key Lab Agr Resources Chem & Biotechnol, 1303 Jiaoyudong Rd, Yulin 537000, Peoples R China
[3] Guangxi Normal Univ, Sch Chem & Pharm, State Key Lab Chem & Mol Engn Med Resources, 15 Yucai Rd, Guilin 541004, Peoples R China
基金
中国国家自然科学基金;
关键词
Benzimidazole derivatives; Rh(III) complexes; Cell apoptosis; Mitochondrial dysfunction; TUMOR-CELL APOPTOSIS; G-QUADRUPLEX DNA; HIGH IN-VITRO; RUTHENIUM(II) COMPLEXES; MITOCHONDRIAL FUNCTIONS; IRIDIUM(III) COMPLEXES; RHODIUM(III) COMPLEX; TELOMERASE ACTIVITY; ANTITUMOR-ACTIVITY; MOLECULAR DOCKING;
D O I
10.1016/j.inoche.2020.108017
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Three new non-cisplatin analogs [Rh(BID1)(CH3OH)]center dot CH3OH (Rh-1), [Rh(BID2)(CH3OH)]center dot CH3OH (Rh-2) and [Rh(BID3)(CH3OH)]center dot 2CH(3)OH (Rh-3) bearing benzimidazole derivatives (BID1-BID-3) were first prepared as potential anti-tumor compounds. The Rh-3 complex with 8-fluoro group in BID-3 ligand exhibited potential antiproliferative activity against multidrug-resistant human lung adenocarcinoma A549/DDP and cisplatin-resistant human ovarian cancer SK-OV-3/DDP cells, at most 5.0 fold more potent than Rh-1, Rh-2 and cisplatin under the same conditions. Importantly, Rh-1-Rh-3 are more selective for A549/DDP cells versus human normal liver HL-7702 cells. The Rh-2 and Rh-3 caused mitochondrial dysfunction was in the following order: Rh-3 > Rh-2. The different biological behavior of Rh-1-Rh-3 may correlate with different 8-substituted groups in benzimidazole derivatives.
引用
收藏
页数:4
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