2019
DOI: 10.1039/c9nj01815h
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In vitrocytotoxicity and catalytic evaluation of dioxidovanadium(v) complexes in an azohydrazone ligand environment

Abstract: Synthesis, characterization, in vitro cytotoxicity and catalytic potential of the dioxidovanadium(v) complexes of azohydrazones.

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Cited by 41 publications
(25 citation statements)
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“…In continuation of our previous work on the synthesis, characterization, and biological studies of vanadium(V/IV) complexes [8,13,[31][32][33][34][35][36][37][38][39][40][41][42][43][44][45], here we report a new mononuclear dioxidovanadium(V) (1) as well as an oxido-bridged dinuclear oxidovanadium(V) (2) complex, each with a tridentate ONO donor Schiff base ligand derived from 2,4-dihydroxybenzaldehyde and 2-amino-4-nitrophenol. Considering the therapeutic potential of the synthesized polyphenolic ligand molecule [27,30,46], corresponding oxidovanadium(V) complexes were synthesized to further investigate their pharmacological activities such as DNA interaction and anticancer activities.…”
Section: Introductionmentioning
confidence: 60%
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“…In continuation of our previous work on the synthesis, characterization, and biological studies of vanadium(V/IV) complexes [8,13,[31][32][33][34][35][36][37][38][39][40][41][42][43][44][45], here we report a new mononuclear dioxidovanadium(V) (1) as well as an oxido-bridged dinuclear oxidovanadium(V) (2) complex, each with a tridentate ONO donor Schiff base ligand derived from 2,4-dihydroxybenzaldehyde and 2-amino-4-nitrophenol. Considering the therapeutic potential of the synthesized polyphenolic ligand molecule [27,30,46], corresponding oxidovanadium(V) complexes were synthesized to further investigate their pharmacological activities such as DNA interaction and anticancer activities.…”
Section: Introductionmentioning
confidence: 60%
“…The spectrum of H 2 L exhibits two compounds connected via intermolecular hydrogen bonding as shown in Figure S2 due to which two equivalent sets of protons obtained in the NMR. The 1 H NMR spectra of H 2 L show singlet resonances in the downfield region in the range δ = 10.92-8.95, and 8.21 ppm due to -OH, and -CH (azomethine) protons, respectively [42]. The aromatic protons were observed in the expected range between δ = 8.20-6.27 ppm [37].…”
Section: Nmr Spectramentioning
confidence: 96%
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