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

Author:

Nguyen Van-Thanh1,Huynh Thi-Kim-Chi12,Ho Gia-Thien-Thanh13,Nguyen Thi-Hong-An1ORCID,Le Anh Nguyen Thi4,Dao Duy Quang4,Mai Tam V. T.567,Huynh Lam K.68ORCID,Hoang Thi-Kim-Dung12ORCID

Affiliation:

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

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

3. Ton Duc Thang University, 19 Nguyen Huu Tho Street, Tan Phong Ward, District 7, Ho Chi Minh City 700000, Vietnam

4. Institute of Research and Development, Duy Tan University, Da Nang 50000, Vietnam

5. Institute for Computational Science and Technology, SBI Building, Quang Trung Software City, Tan Chanh Hiep Ward, District 12, Ho Chi Minh City 700000, Vietnam

6. University of Science, Ho Chi Minh City, 227 Nguyen Van Cu Street, Ward 4, District 5, Ho Chi Minh City 700000, Vietnam

7. Vietnam National University, Ho Chi Minh City 700000, Vietnam

8. International University, Block 6, Linh Trung Ward, Thu Duc District, Ho Chi Minh City 700000, Vietnam

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 H -benzimidazole-2-yl)-phenol derivatives and corresponding metal salt solutions. The compound structures were identified by FT-IR, 1 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 50 < 10.4 µM, complexes C 1 , C 3 and C 14 could be considered potential multi-targeted anti-cancer agents.

Publisher

The Royal Society

Subject

Multidisciplinary

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