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The schematic representation of HOMOs of the species in the proposed mechanism for the electrocatalytic reduction of CO2 by the Ru(II) complex.
A proposed photocatalytic cycle for the reduction of CO2 to CO
(A) Perspective of molecular docking of the Ni(II) complex with the major groove side of DNA by UCSF chimera, (B) two-dimensional interactions generated by LIGPLOT+.
(A) The ligand docked in binding pocket of BSA. (B) The hydrophobic and hydrophilic amino acid residues surrounding the ligand. (C) The hydrogen bonding interaction distance between ligand and SER 201
The upper panel shows microscopic photographs of the MCF-7 cancer cells in the absence (C) and presence of different concentrations of the Ni(II) complex (indicated by the number inside each photo).
(a) Molecular docking of the Rh(III) complex with DNA. (b) The bases of DNA with dominant interactions with the complex in the active site
(A) Perspective of molecular docking of the Cu(II) complex with the major groove side of DNA by MVD chimera, (B) two-dimensional interactions generated by LIGPLOT+.
Treatment of K562 cells with the various metal salts showed different inhibition effects in a concentration dependent manner. The cell inhibition was measured after 48 h by the MTT assay. Each data point represents the mean for three separate experiments
Molecular docking of trans-[Cu(cip)2(OH)2] with DNA (A) and BSA (B).
ZN-Aminoacid
Zn-BSA
Zn-DNA
TPY
Quenchine
Ru-BSA
TPTZ
Photocatalyst
Fe-BSA
Fe-DNA
FTS
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