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苯并咪唑衍生物金属配合物作为潜在抗癌剂:合成、表征、实验与计算相结合的研究

Metal complexes of benzimidazole-derived as potential anti-cancer agents: synthesis, characterization, combined experimental and computational studies.

作者信息

Nguyen Van-Thanh, Huynh Thi-Kim-Chi, Ho Gia-Thien-Thanh, Nguyen Thi-Hong-An, Le Anh Nguyen Thi, Dao Duy Quang, Mai Tam V T, Huynh Lam K, Hoang Thi-Kim-Dung

机构信息

Institute of Chemical Technology - VAST, 1A Thanh Loc 29 Street, Thanh Loc Ward, District 12, Ho Chi Minh City 700000, Vietnam.

Graduate University of Science and Technology - VAST, 18 Hoang Quoc Viet Street, Nghia Do Ward, Cau Giay District, Hanoi 100000, Vietnam.

出版信息

R Soc Open Sci. 2022 Sep 21;9(9):220659. doi: 10.1098/rsos.220659. eCollection 2022 Sep.

Abstract

In this study, a series of 14 Cu (II), Zn (II), Ni (II) and Ag (I) complexes containing bis-benzimidazole derivatives were successfully designed and synthesized from 2-(1-benzimidazole-2-yl)-phenol derivatives and corresponding metal salt solutions. The compound structures were identified by FT-IR, H-NMR, powder X-ray diffraction and ESI-MS analyses, and the presence of the metal in the complexes was confirmed by ultraviolet-visible spectroscopy and ICP optical emission spectrometry. Electronic structure calculations were also carried out to describe the detailed structures in addition to the electronic absorption spectra of the ligands. The cytotoxic activity of the complexes was evaluated against three human cancer cell lines: lung (A549), breast (MDA-MB-231) and prostate (PC3) cancer cells. All complexes inhibited anti-proliferative cancer cells better than free ligands, especially Zn (II) and Ag (I) complexes, which are most sensitive to MDA-MB-231 cells. In addition, showing the growth inhibition of three cancer cell lines with IC < 10.4 µM, complexes , and could be considered potential multi-targeted anti-cancer agents.

摘要

在本研究中,由2-(1-苯并咪唑-2-基)-苯酚衍生物和相应的金属盐溶液成功设计并合成了一系列14种含双苯并咪唑衍生物的铜(II)、锌(II)、镍(II)和银(I)配合物。通过傅里叶变换红外光谱(FT-IR)、氢核磁共振谱(H-NMR)、粉末X射线衍射和电喷雾电离质谱(ESI-MS)分析确定了化合物结构,并通过紫外可见光谱和电感耦合等离子体发射光谱法确认了配合物中金属的存在。除了配体的电子吸收光谱外,还进行了电子结构计算以描述详细结构。评估了这些配合物对三种人类癌细胞系的细胞毒性活性:肺癌(A549)、乳腺癌(MDA-MB-231)和前列腺癌(PC3)细胞。所有配合物对癌细胞的抗增殖抑制作用均优于游离配体,尤其是锌(II)和银(I)配合物,它们对MDA-MB-231细胞最为敏感。此外,配合物 、 和 对三种癌细胞系均表现出生长抑制作用,其半数抑制浓度(IC)<10.4 μM,可被认为是潜在的多靶点抗癌剂。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fba8/9490329/029d9807b0cb/rsos220659f03.jpg

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