Synthesis, structure and anticancer activities of Zn(II), Cd(II) complexes with 5,7-dichloro-8-hydroxyquinoline-2-carboxaldehyde-4-methyl-3-thiosemicarbazone

Giang Ninh Thi Minh, Ngoc Nguyen Thi Bich, Hai Le Thi Hong

Abstract


Two new complexes [Zn(QMS)] and [Cd(QMS)] were synthesized by reaction between MCl2(M = Zn, Cd) with  5,7-dichloro-8-hydroxyquinoline-2-carboxaldehyde-4-methyl-3-thiosemicarbazone (H2QMS). Their structures were determined by ESI-MS, IR and 1H NMR spectroscopies. The results showed that in these complexes the ratio of M(II) : H2QMS ligand is  1 : 1, M(II) is bound to H2QMS ligand through O, Nquinoline, Nthiosemicarbazide and S atoms. The complexes were tested for cell in vitro cytotoxicity on human cancer cells including KB, Hep-G2, LU and MCF-7. The results showed that ZnQMS complex exhibits high antitumor activities on KB, Hep-G2, Lu cancer cell lines with IC50 values 9,41; 5,53 and 6,73 μM respectively. CdQMS complex gives a high activity against on LU cancer cell line with IC50 value 4,54 μM.

Keywords


Structure; Zn(II); Cd(II) complexes; 5;7-dichloro-8-hydroxyquinoline-2-carboxaldehyde-4-methyl-3-thiosemicarbazone; anticancer

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References


L. T. H. Hai, N. T. N. Vinh, L. T. Tuyen, L. V. Meervelt, T. T. Da, Journal of Coordination Chemistry, 72 (2019) 1637-1651. https://doi.org/10.1080/00958972.2019.1608359

N. T. T. Chi, T. T. C. Mai, P. V Thong, N. Long, N. H My and L. V. Meervelt, Acta Cryst., C73 (2017) 1030–1037. https://doi.org/10.1107/S2053229617015200

D. Rogolino, A. Cavazzoni, A. Gatti, M. Tegoni, G. Pelosi,V. Verdolino, European Journal of Medicinal Chemistry, 128 (2017) 140–153. DOI: 10.1016/j.ejmech.2017.01.031

C. Molinaro, A. Martoriati, L. Pelinski and K. Cailliau, Cancers, 12 (2020), 2863. doi: 10.3390/cancers12102863

A. Kotian, V. Kamat, K. Naik, D. G. Kokare, K. Kumara, K. L. Neratur, V. Kumbar, K. Bhat, V. K. Revankar, Bioorganic Chemisty, 112 (2021) 104962. DOI:10.1016/j.bioorg.2021.104962

S. A. Andres, K. Bajaj, N. S. Vishnosky, M. A. Peterson, M. S. Mashuta, R. M. Buchanan, P. J. Bates and C. A. Grapperhaus, Inorganic Chemistry, 59 (2020) 4924–4935. https://doi.org/10.1021/acs.inorgchem.0c00182

S. H. Chan, C. H. Chui, S. W. Chan, S. H. L. Kok , D. Chan, M. Y. T. Tsoi, P. H. M. Leung, A. K. Y. Lam, A. S. C. Chan, K. H. Lam, J. C. O. Tang, ACS Med. Chem. Lett, 4 (2013). 170–174. DOI: 10.1021/ml300238z

S. Rubino, R. Busà, A. Attanzio, R. Alduina, V. D. Stefano, M. A. Girasolo, S. Orecchio, L. Tesoriere, Bioorganic & Medicinal Chemistry, 25 (2017) 2378–2386. DOI: 10.1016/j.bmc.2017.02.067

F. Liu, Z. Zhou, S. Gou, J. Zhao, F. Chen, Journal of Coordination Chemistry, 67 (2014), 2858–2866. https://doi.org/10.1080/00958972.2014.951638




DOI: https://doi.org/10.51316/jca.2021.107

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