Synthesis, characterization, and investigation of antiproliferative activity of novel Ag (I)-N-Heterocyclic Carbene (NHC) compounds

被引:16
|
作者
Cevik-Yildiz, Esranur [1 ]
Sahin, Neslihan [2 ,3 ,4 ]
Sahin-Bolukbasi, Serap [1 ]
机构
[1] Sivas Cumhuriyet Univ, Fac Pharm, Dept Biochem, TR-58140 Sivas, Turkey
[2] Sivas Cumhuriyet Univ, Fac Educ, Dept Basic Educ, TR-58140 Sivas, Turkey
[3] Inonu Univ, Fac Sci & Art, Dept Chem, TR-44280 Malatya, Turkey
[4] Inonu Univ, Catalysis Res & Applicat Ctr, TR-44280 Malatya, Turkey
关键词
N-Heterocyclic carbene; Silver complex; Antiproliferative activity; Breast cancer; Prostate cancer; CRYSTAL-STRUCTURES; SILVER(I) COMPLEXES; BIOLOGICAL EVALUATION; ANTICANCER ACTIVITY; BENZIMIDAZOLE; ANTIBACTERIAL; STABILIZATION; DERIVATIVES; INHIBITION; ACTIVATION;
D O I
10.1016/j.molstruc.2019.126987
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The aim of this study was to present the synthesis, characterization, and investigation of the antiproliferative activity of new metal N-Heterocyclic Carbene (NHC) salts (1a-c) and their Ag(I) complexes (2a-c). All synthesized compounds were characterized using elemental analysis, LC-MS, FT-IR,H- 1 NMR, and C-13 NMR spectroscopy techniques. Salts and complexes were tested for antiproliferative activities on human breast and prostate cancer cell lines (MCF-7, MDA-MB-23, DU-145) and L-929 normal cells for 24 h, 48 h and 72 h using MTT assays. The Ag(I)-NHC complexes (2a c) showed dose and time-dependent cytotoxic activity against all cell lines. MDA-MB-231 and MCF-7 human breast carcinoma cells were the most sensitive to displaying IC50 lower than 1 mu M at all time points for 2a and 2b complexes respectively. The IC(50)s for Ag(I)-NHC were higher in normal cells especially compared to the breast cancer cells, suggesting that complexes possessed noteworthy selectivity for human breast cancer cells. Complex 2a showed high selectivity (>= 13-fold) for MDA-MB-231 breast cancer cells at all time points. These results also demonstrated that complex 2b has 4-7-fold selectivity against MCF-7 breast cancer cells. (C) 2019 Published by Elsevier B.V.
引用
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页数:9
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