Please use this identifier to cite or link to this item: http://repositorio.unicamp.br/jspui/handle/REPOSIP/339074
Type: Artigo
Title: Methyl divanillate: redox properties and binding affinity with albumin of an antioxidant and potential NADPH oxidase inhibitor
Author: Vasconcelos, Debora Naliati de
Lima, Angélica Nakagawa
Philot, Eric Allison
Scott, Ana Lígia
Amorim, Izabelle
Boza, Ferreira
Souza, Aguinaldo Robinson de
Morgon, Nelson Henrique
Ximenes, Valdecir Farias
Abstract: Vanillic acid is a widely used food additive (flavouring agent, JECFA number: 959) with many reported beneficial biological effects. The same is true for its ester derivative (methyl vanillate, JECFA number: 159). Based on the increasing evidence that diapocynin, the dimer of apocynin (NADPH oxidase inhibitor), has some improved pharmacological properties compared to its monomer, here the dimer of methyl vanillate (MV), i.e., methyl divanillate (dimer of methyl vanillate, DMV) was synthesized and studied in the context of its redox properties and binding affinity with human serum albumin (HSA). We found that the antioxidant potency of DMV was significantly increased compared to MV. In this regard, the reduction of 2,2-diphenyl-1-picrylhydrazyl (DPPH) free radical by DMV was 30-fold more effective compared to MV. Ferric ion reduction was 4-fold higher and peroxyl radical reduction was 2.7-fold higher. The interaction with HSA was significantly improved (Stern–Vomer constants, 3.8 × 105 mol−1 L and 2.3 × 104 mol−1 L, for DMV and MV, respectively). The complexation between DMV and HSA was also evidenced by induced circular dichroism (ICD) signal generation in the former due to its fixation in the asymmetric protein pocket. Density-functional calculations (TD-DFT) showed that the ICD spectrum was related to a DMV conformation bearing a dihedral angle of approximately −60°. Similar dihedral angles were obtained in the lowest and most populated DMV cluster poses obtained by molecular docking simulations. The computational studies and experimental displacement studies revealed that DMV binds preferentially at site I. In conclusion, besides being a powerful antioxidant, DMV is also a strong ligand of HSA. This is the first study on the chemical and biophysical properties of DMV, a compound with potential beneficial biological effects
Subject: Metilação
Oxirredução
Albumina
NADPH oxidase
Country: Estados Unidos
Editor: Royal Society of Chemistry
Rights: Aberto
Identifier DOI: 10.1039/c9ra02465d
Address: https://pubs.rsc.org/en/content/articlelanding/2019/ra/c9ra02465d
Date Issue: 2019
Appears in Collections:IQ - Artigos e Outros Documentos

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