Keywords
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,Anticancer activity
,Antimicrobial activity
,Bis(pyrazolyl)borate derivatives
,MDA-MB-231
,Metal complexes
,Molecular docking
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Abstract
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Background: The development of the pyrazole-based complexes is greatly enhanced due to
the identification of their structure as medicinal application. Keeping in view therapeutic and
biological activities of pyrazoles based compounds and the potential of transition metals in the
antimicrobial application area, we find it vital to join the chemistry of both moieties in designing
and developing biometal compounds which could aggressively work against various bacterial
species and cancer cells. In this work, we report the synthesis and characterization of copper (II),
nickel (II) and cobalt (II) complexes of dihydrobis(pyrazolyl)borate ligands. Also, antibacterial
activities, MTT assay and molecular docking of these compounds were investigated.
Methods: A bidentate N-donor pyrazole-based ligand abbreviated as K[H2B(PzMe2)2] and corresponding
complexes with Cu(II), Ni(II) and Co(II) were synthesized and characterized. The anticancer activities
of the synthesized compounds were studied against the (MDA-MB-231) cell lines. The antibacterial
investigations of the synthesized compounds against the gram-positive (B. subtilis) and the gram-negative
(S. enterica) bacteria were performed. In addition, molecular docking of the synthesized compounds with
YmaH (PDB ID: 3HSB) protein, ecKAS III (PDB ID:1HNJ) protein and DNA dodecamer (PDB ID: 1BNA)
as the possible targets was studied.
Results: The result showed among the investigated compounds, complex [Cu(H2B(PzMe2)2)2] indicated
the highest cytotoxicity and bacterial inhibition.
Conclusion: In summary, we have synthesized a type of N- donor pyrazole-based ligand and
corresponding metal complexes. In silico molecular docking along with the experimental MTT
assay and antibacterial studies, indicated the metal complexes are more bioactive than free ligand
and can be excellent candidates for further evaluations in the biological area.
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