IN VITRO CYTOTOXIC ACTIVITIES OF PLATINUM(II) COMPLEXES CONTAINING 1H-BENZO[d]IMIDAZOLE AND 1H-1,3-DIAZOLE DERIVATIVES

Q4 Pharmacology, Toxicology and Pharmaceutics
Tuğçe Yılmaz, Elif Ergin, Hatice Oruç Demirbağ, Semra Utku
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引用次数: 0

Abstract

Objective: This study aimed to synthesize and evaluate the cytotoxic activities of four platinum(II) complexes with 2-substituted or nonsubstituted 1H-benzo[d]imidazole and 1H-1,3-diazole derivatives as carrier ligands (L1-L4), which may have potent cytotoxic activity and low side effects. Material and Method: K1-K4 complexes were synthesized by heating and mixing K2PtCl4 and the appropriate L1-L4. The chemical structures of K1-K4 were elucidated by Infrared and 1H Nuclear Magnetic Resonance spectroscopic methods. In vitro, cytotoxic effects of K1-K4 complexes against prostate (DU-145), endometrial adenocarcinoma (Ishikawa), and breast cancer (MCF-7) cell lines were tested by the MTT method. Result and Discussion: According to the IC50 values of the tested cell lines, K1 and K2 derivatives bearing unsubstituted 1H-benzo[d]imidazole (L1) and 1H-1,3-diazole (L2) were found to be the most effective compounds among these synthesized complexes.
含有 1H-苯并[d]偶氮唑和 1H-1,3-二偶氮唑衍生物的铂(II) 复合物的体外毒性作用
研究目的本研究旨在合成四种以 2-取代或非取代 1H-苯并[d]咪唑和 1H-1,3-二唑衍生物为载体配体(L1-L4)的铂(II)配合物,并评估其细胞毒活性:通过加热并混合 K2PtCl4 和适当的 L1-L4 合成 K1-K4 复合物。通过红外光谱和 1H 核磁共振光谱方法阐明了 K1-K4 的化学结构。在体外,用 MTT 法测试了 K1-K4 复合物对前列腺癌(DU-145)、子宫内膜腺癌(石川)和乳腺癌(MCF-7)细胞株的细胞毒性作用。结果与讨论:根据受试细胞株的 IC50 值,发现含有未取代的 1H-苯并[d]咪唑(L1)和 1H-1,3-二唑(L2)的 K1 和 K2 衍生物是这些合成复合物中最有效的化合物。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Ankara Universitesi Eczacilik Fakultesi Dergisi
Ankara Universitesi Eczacilik Fakultesi Dergisi Pharmacology, Toxicology and Pharmaceutics-Pharmaceutical Science
CiteScore
0.80
自引率
0.00%
发文量
70
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