Cytotoxicity, anti‐microbial studies of M( II )‐dithiocarbamate complexes, and molecular docking study against SARS COV2 RNA ‐dependent RNA polymerase

Abstract Ten transition metal dithiocarbamate (DTC)complexes of the type [M(κ2‐Et2DT)2] (1–5), and [M(κ2‐PyDT)2] (6–10) (where M = Co, Ni, Cu, Pd, and Pt; Et2DT = diethyl dithiocarbamate; PyDT = pyrrolidine dithiocarbamate) were synthesized and characterized by different methods. The dithiocarbamate acted as bidentate chelating ligands to afford a tetrahedral complexes with Co(II) ion and square planner with other transition metal ions. The dithiocarbamate complexes showed good activity against the pathogen bacteria species. The results showed the Pt‐dithiocarbamate complexes are more active against all the tested bacteria than the Pd‐dithiocarbamate complex. The dithiocarbamate complexes displayed the maximum inhibition zone against E. coli bacteria, whereas the lowest activity of the dithiocarbamate against Salmonella typhimurium bacteria. The cytotoxicity of the Pd(II) and Pt(II) complexes was screened against the MCF‐7 breast cancer cell line and the complexes showed moderate activity compared with the cis‐platin. The results indicated that the MCF7 cells treated with 500 μg\ml of ligands and Pd(II) and Pt(II) complexes after 24 hr exposure showed intercellular space and dead cells. Finally, molecular docking studies were carried out to examine the binding mode of the synthesized compounds against the proposed target; SARS COV2 RNA‐dependent RNA polymerase.