dc.contributorUniversidade Estadual Paulista (Unesp)
dc.date.accessioned2014-05-27T11:28:37Z
dc.date.accessioned2022-10-05T18:45:21Z
dc.date.available2014-05-27T11:28:37Z
dc.date.available2022-10-05T18:45:21Z
dc.date.created2014-05-27T11:28:37Z
dc.date.issued2013-03-01
dc.identifierMolecules, v. 18, n. 3, p. 2821-2839, 2013.
dc.identifier1420-3049
dc.identifierhttp://hdl.handle.net/11449/74759
dc.identifier10.3390/molecules18032821
dc.identifierWOS:000316611700028
dc.identifier2-s2.0-84875625176
dc.identifier2-s2.0-84875625176.pdf
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/3923710
dc.description.abstractApocynin is the most employed inhibitor of NADPH oxidase (NOX), a multienzymatic complex capable of catalyzing the one-electron reduction of molecular oxygen to the superoxide anion. Despite controversies about its selectivity, apocynin has been used as one of the most promising drugs in experimental models of inflammatory and neurodegenerative diseases. Here, we aimed to study the chemical and biophysical properties of apocynin. The oxidation potential was determined by cyclic voltammetry (Epa = 0.76V), the hydrophobicity index was calculated (logP = 0.83) and the molar absorption coefficient was determined (ε275nm = 1.1 × 104 M-1 cm-1). Apocynin was a weak free radical scavenger (as measured using the DPPH, peroxyl radical and nitric oxide assays) when compared to protocatechuic acid, used here as a reference antioxidant. On the other hand, apocynin was more effective than protocatechuic acid as scavenger of the non-radical species hypochlorous acid. Apocynin reacted promptly with the non-radical reactive species H2O2 only in the presence of peroxidase. This finding is relevant, since it represents a new pathway for depleting H2O2 in cellular experimental models, besides the direct inhibition of NADPH oxidase. This could be relevant for its application as an inhibitor of NOX4, since this isoform produces H 2O2 and not superoxide anion. The binding parameters calculated by fluorescence quenching showed that apocynin binds to human serum albumin (HSA) with a binding affinity of 2.19 × 104 M -1. The association did not alter the secondary and tertiary structure of HSA, as verified by synchronous fluorescence and circular dichroism. The displacement of fluorescent probes suggested that apocynin binds to site I and site II of HSA. Considering the current biomedical applications of this phytochemical, the dissemination of these chemical and biophysical properties can be very helpful for scientists and physicians interested in the use of apocynin.
dc.languageeng
dc.relationMolecules
dc.relation3.098
dc.relation0,855
dc.rightsAcesso aberto
dc.sourceScopus
dc.subjectAlbumin
dc.subjectApocynin
dc.subjectBinding constant
dc.subjectHydrogen peroxide
dc.subjectNADPH oxidase
dc.subjectacetophenone derivative
dc.subjectapocynin
dc.subjectenzyme inhibitor
dc.subjecthydrogen peroxide
dc.subjecthypochlorous acid
dc.subjectreduced nicotinamide adenine dinucleotide phosphate oxidase
dc.subjectscavenger
dc.subjectchemical phenomena
dc.subjectchemistry
dc.subjectdrug antagonism
dc.subjectkinetics
dc.subjectoxidation reduction reaction
dc.subjectpH
dc.subjectAcetophenones
dc.subjectEnzyme Inhibitors
dc.subjectFree Radical Scavengers
dc.subjectHydrogen Peroxide
dc.subjectHydrogen-Ion Concentration
dc.subjectHydrophobic and Hydrophilic Interactions
dc.subjectHypochlorous Acid
dc.subjectKinetics
dc.subjectNADPH Oxidase
dc.subjectOxidation-Reduction
dc.titleApocynin: Chemical and biophysical properties of a NADPH oxidase inhibitor
dc.typeArtigo


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