2017
DOI: 10.1039/c7nj01273j
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Unpredicted formation of copper(ii) complexes containing 2-thiophen-2-yl-1-thiophen-2-ylmethyl-1H-benzoimidazole and their most promising in vitro cytotoxicity in MCF-7 and HeLa cell lines over cisplatin

Abstract: An in situ reaction of CuCl2·2H2O, o-phenylenediamine, thiophene-2-carbaldehyde and sodium azide in methanol afforded complex 1a.

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Cited by 23 publications
(9 citation statements)
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“…As observed in Figure , the UV–Vis absorption spectrum of the complex underwent a red shift in relation to the free dppb as a consequence of the ligand coordination. A similar behavior was observed for other copper(II) complexes bearing benzimidazole as ligand . Moreover, the electronic spectrum of the complex, measured in dmso solution at 5 m m (inset in Figure ), reveals a single broad band centered at 748 nm due to d–d transition with ε = 80 M −1 cm −1 .…”
Section: Resultssupporting
confidence: 81%
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“…As observed in Figure , the UV–Vis absorption spectrum of the complex underwent a red shift in relation to the free dppb as a consequence of the ligand coordination. A similar behavior was observed for other copper(II) complexes bearing benzimidazole as ligand . Moreover, the electronic spectrum of the complex, measured in dmso solution at 5 m m (inset in Figure ), reveals a single broad band centered at 748 nm due to d–d transition with ε = 80 M −1 cm −1 .…”
Section: Resultssupporting
confidence: 81%
“…Moreover, under the same experimental conditions, the commercially available drugs cisplatin (IC 50 = 1.1 ± 0.2 μ m ) and carboplatin (IC 50 = 10 ± 1 μ m ) exhibit cytotoxic activity in the same order of magnitude as the newly synthesized compound . Similarly, previous studies of copper‐based complexes containing benzimidazole derivatives have demonstrated that the antineoplastic potential of benzimidazoles enhance upon copper(II) coordination …”
Section: Resultssupporting
confidence: 62%
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“…The Stern–Volmer equation (I 0 /I = Ksv[Q] + 1) was used to analyse the quenching constant. This indicated that the ligand and complex could replace EB in the DNA–EB system . The K SV values were obtained as a slope from the plot of I 0 / I vs. [ Q ] evaluated for the ligand and complex as shown in Figure and Table , where I 0 is the emission intensity in the absence of the compound, I corr is the corrected emission intensity in the presence of the compound, K SV is the quenching constant and [ Q ] is the concentration of the compound.…”
Section: Resultsmentioning
confidence: 99%