2016
DOI: 10.1016/j.saa.2015.07.037
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Synthesis of a novel 4H-pyran analog as minor groove binder to DNA using ethidium bromide as fluorescence probe

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Cited by 47 publications
(19 citation statements)
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“…DNA binding studies of the final products have been performed by viscosity measurements, circular dichroism, UV-visible absorption and fluorescence spectroscopy. These studies allow to conclude that the synthesized 4H-pyrans bind to DNA through the minor groove rather than to major groove or by intercalation, with a higher K b than those previously reported for a 4H-pyran 78,79 . This work represents one of the scarce studies carried out with pyrans and their DNA binding interactions, thus opening the door for the future development of these scaffolds as promising drugs.…”
Section: Resultsmentioning
confidence: 52%
See 1 more Smart Citation
“…DNA binding studies of the final products have been performed by viscosity measurements, circular dichroism, UV-visible absorption and fluorescence spectroscopy. These studies allow to conclude that the synthesized 4H-pyrans bind to DNA through the minor groove rather than to major groove or by intercalation, with a higher K b than those previously reported for a 4H-pyran 78,79 . This work represents one of the scarce studies carried out with pyrans and their DNA binding interactions, thus opening the door for the future development of these scaffolds as promising drugs.…”
Section: Resultsmentioning
confidence: 52%
“…Based on our own experience in this field 76 , 77 , the plausible DNA interactions of 4 H -pyrans synthesized in this work have been studied because of their wide range of biological properties 78 , 79 . Thus, the interaction effect of 4 H -pyrans 3 , 6–9 towards calf thymus DNA (ctDNA) was investigated.…”
Section: Resultsmentioning
confidence: 99%
“…Fluorescence intensity of EB increases upon interaction with DNA due to the intercalation of the planar phenenthridinium ring between adjacent base pairs on the double helix. [ 29–31 ] Incremental additions of ZnS NPs (2 to 20 μM) to the EB–CT DNA complex, caused a reduction in the fluorescence intensity, without altering the peak position (Figure 4a). The extent of decrease in the fluorescence intensity (quenching), without any changes in the wavelength of maximum emission, may be due to the following possible reasons: (i) ZnS NPs may bind to EB, causing fluorescence quenching; (ii) ZnS NPs might replace EB from EB–CT DNA complex, decreasing the EB concentration; and (iii) the formation of a new complex (ZnS NP–CT DNA–EB) due to interaction of ZnS NPs with the CT DNA–EB system.…”
Section: Resultsmentioning
confidence: 99%
“…The extent of decrease in the fluorescence intensity (quenching), without any changes in the wavelength of maximum emission, may be due to the following possible reasons: (i) ZnS NPs may bind to EB, causing fluorescence quenching; (ii) ZnS NPs might replace EB from EB–CT DNA complex, decreasing the EB concentration; and (iii) the formation of a new complex (ZnS NP–CT DNA–EB) due to interaction of ZnS NPs with the CT DNA–EB system. [ 30,32 ]…”
Section: Resultsmentioning
confidence: 99%
“…This can also be attributed to the formation of the ground-state DNA-complex adduct due to the cationic metal complexes binding with the negatively charged oxygen of the phosphodiester of DNA, where the contraction of DNA drives a few EB molecules out of the DNA base pairs. 28 DNA binding parameters by electrochemical analysis. Cyclic voltammetry is an essential tool to investigate the electrontransfer reactions of complexes.…”
Section: Dna/bsa Interaction Studiesmentioning
confidence: 99%