2012
DOI: 10.1016/j.jinorgbio.2012.07.006
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Copper(II) thiosemicarbazonate molecular modifications modulate apoptotic and oxidative effects on U937 cell line

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Cited by 23 publications
(22 citation statements)
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References 31 publications
(34 reference statements)
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“…Lipid peroxidation was evaluated by ‘‘Thiobarbituric Acid Reactive Substances” (TBARS) method, as previously described [ 28 ], using Malondialdehyde as a standard for the calibration curve (range 0–10 μM). In preliminary experiments, we documented that cells treated with H 2 O 2 50μM for 30 min displayed substantial increases (about 2-fold) in TBARS when compared to untreated cells, thereby validating the use of TBARS as a “footprint” of increased oxidative stress in our experimental setting..…”
Section: Characterization Of Tio 2 and Co mentioning
confidence: 99%
“…Lipid peroxidation was evaluated by ‘‘Thiobarbituric Acid Reactive Substances” (TBARS) method, as previously described [ 28 ], using Malondialdehyde as a standard for the calibration curve (range 0–10 μM). In preliminary experiments, we documented that cells treated with H 2 O 2 50μM for 30 min displayed substantial increases (about 2-fold) in TBARS when compared to untreated cells, thereby validating the use of TBARS as a “footprint” of increased oxidative stress in our experimental setting..…”
Section: Characterization Of Tio 2 and Co mentioning
confidence: 99%
“…Thiosemicarbazones (TSCs) are sulfur-containing organic substances whose biological properties have been extensively studied [1][2][3][4][5][6][7][8], in particular their activities against microbial diseases as malaria, small-pot, influenza, leishmaniasis or chagas [9][10][11][12][13][14], neurological pathologies [15,16] and cancer [17][18][19][20][21][22][23][24][25][26][27][28][29][30][31][32][33][34][35][36]. Different biological targets have been identified, like DNA [37][38][39], RNA [40] and several enzymes as RNA-dependent DNA polymerases [41], xanthine oxidoreductase [42], thioredoxin reductase [43,44], topoisomerase IIa [45][46][47] or s...…”
Section: -Introductionmentioning
confidence: 99%
“…From this perspective, hydrazones seem promising, because of their well-known coordinating abilities and biological properties [4][5][6][7][8][9][10][11][13][14][15][16]. We have focused our attention on the o-vanillin acylhydrazone scaffold: the potentially tetradentate ligand H 2 L shows a great versatility.…”
Section: Discussionmentioning
confidence: 99%
“…Acylhydrazone-based ligands and their transition metal complexes are widely studied in catalysis [1], as building blocks in supramolecular chemistry [2,3], as anticancer agents [4,5], and, particularly interesting for our research, antiviral molecules [6,7]. They are often used to build multinuclear metal complexes since they are versatile ligands and their coordination properties can be easily tuned from an electronic and a steric point of view [8][9][10].…”
Section: Introductionmentioning
confidence: 99%