New platinum(II) complexes of CCC-pincer N-heterocyclic carbene ligand: Synthesis, characterization, cytotoxicity and antileishmanial activity

被引:13
|
作者
Tabrizi, Leila [1 ]
Chiniforoshan, Hossein [1 ]
机构
[1] Isfahan Univ Technol, Dept Chem, Esfahan 8415683111, Iran
关键词
Carbene ligand; Pt(II) complex; Antileishmanial activity; Cytotoxicity; Lipophilicity; IRIDIUM COMPLEXES; ORGANOMETALLIC COMPOUNDS; ANTICANCER DRUGS; PALLADIUM; THERAPY; GOLD; FUNCTIONALIZATION; HYDROGENATION; COORDINATION; MECHANISMS;
D O I
10.1016/j.jorganchem.2016.06.013
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Five new CCC-pincer N-heterocyclic carbene Pt(II) complexes, [Pt((CCC)-C-TMP)X] (X - Cl (1), O2C(CH3) (2), O2C(CH2CH3) (3), O2C(CH2CH2CH3) (4), O2C(CH(CH3)(2)) (5)) ((CCC)-C-TMP = 1,1'-(1,3-phenylene)bis(3-(2,4,6-trimethoxyphenyl)-1H-benzo[d]imidazol-2-ylidene) were synthesized and characterized by elemental analysis, IR, (C-13, H-1) NMR and ESI-MS spectroscopies. Complexes 1-5 showed varying degree of antileishmanial activities with IC50 values ranging between 0.02 and 3.41 mu M. Complex 5 significantly showed the best antiproliferative activity against Leishmania species essayed more active than the reference drug amphotericin B. The antiproliferative effects of 1-5 were assessed on a panel of four human tumor cell lines including human ovarian (SKOV3, inherently resistant to cisplatin), human breast cancer (MCF-7), human colon adenocarcinoma (HT29) and lung adenocarcinoma (A549) cells. Complex 5 was 16 times as cytotoxic as cisplatin in the same cell line. (C) 2016 Elsevier B.V. All rights reserved.
引用
收藏
页码:98 / 105
页数:8
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