2016
DOI: 10.1016/j.jphotobiol.2016.09.016
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In vitro DNA binding profile of enantiomeric dinuclear Cu(II)/Ni(II) complexes derived from l–/d–histidine–terepthaldehyde reduced Schiff base as potential chemotherapeutic agents

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Cited by 23 publications
(7 citation statements)
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“…8,48 The increased fluorescence intensity of EB gets markedly quenched upon addition of another molecule either by the displacement of the EB or by acquiring the excited-state electron of EB through a photoelectron-transfer mechanism. 45 Therefore, an EB displacement technique provides a collateral evidence for the modes of DNA binding. 16 In Figure 8, the increased concentration of complexes to DNA-bound EB did not exhibit any change on the fluorescence intensity.…”
Section: Resultsmentioning
confidence: 85%
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“…8,48 The increased fluorescence intensity of EB gets markedly quenched upon addition of another molecule either by the displacement of the EB or by acquiring the excited-state electron of EB through a photoelectron-transfer mechanism. 45 Therefore, an EB displacement technique provides a collateral evidence for the modes of DNA binding. 16 In Figure 8, the increased concentration of complexes to DNA-bound EB did not exhibit any change on the fluorescence intensity.…”
Section: Resultsmentioning
confidence: 85%
“…DNA binding analysis is considered to be one of the most crucial factors to examine the feasibility of a number of anticancer drugs as it is the vital transporter of genetic data related to the most cancers occurring via DNA damage. 45 The binding of metal to DNA could occur by two processes: either via covalent bonding in which the nitrogen base of DNA replaces the labile metal ion or by noncovalent interactions (electrostatic, intercalative, or groove binding of complexes to DNA helix). 43 Therefore, the interaction of drug−DNA is vital for the coherent designing and development of new DNAtargeted drugs.…”
Section: Resultsmentioning
confidence: 99%
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