Methyl divanillate: redox properties and binding affinity with albumin of an antioxidant and potential NADPH oxidase inhibitor

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...

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Veröffentlicht in:RSC advances 2019-06, Vol.9 (35), p.19983-19992
Hauptverfasser: de Vasconcelos, Debora Naliati, Lima, Angélica Nakagawa, Philot, Eric Allison, Scott, Ana Lígia, Ferreira Boza, Izabelle Amorim, de Souza, Aguinaldo Robinson, Morgon, Nelson Henrique, Ximenes, Valdecir Farias
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container_end_page 19992
container_issue 35
container_start_page 19983
container_title RSC advances
container_volume 9
creator de Vasconcelos, Debora Naliati
Lima, Angélica Nakagawa
Philot, Eric Allison
Scott, Ana Lígia
Ferreira Boza, Izabelle Amorim
de Souza, Aguinaldo Robinson
Morgon, Nelson Henrique
Ximenes, Valdecir Farias
description 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 × 10 5 mol −1 L and 2.3 × 10 4 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. Methyl divanillate, a derivative of the vanillic acid (flavouring agent, JECFA number: 959) with promising beneficial biological effects.
doi_str_mv 10.1039/c9ra02465d
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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 × 10 5 mol −1 L and 2.3 × 10 4 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. 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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 × 10 5 mol −1 L and 2.3 × 10 4 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. Methyl divanillate, a derivative of the vanillic acid (flavouring agent, JECFA number: 959) with promising beneficial biological effects.</description><subject>Affinity</subject><subject>Antioxidants</subject><subject>Binding</subject><subject>Biological effects</subject><subject>Chemistry</subject><subject>Computer simulation</subject><subject>Dichroism</subject><subject>Dihedral angle</subject><subject>Dimers</subject><subject>Ferric ions</subject><subject>Free radicals</subject><subject>Inhibitors</subject><subject>Molecular docking</subject><subject>Organic chemistry</subject><subject>Oxidase</subject><subject>Pharmacology</subject><subject>Properties (attributes)</subject><subject>Reduction</subject><subject>Serum albumin</subject><subject>Signal generation</subject><issn>2046-2069</issn><issn>2046-2069</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><recordid>eNp9ks9rFDEUxwdRbKm9eFciXkRYTbJJZtKDsGzVCvUHoueQH2-6KbPJmGRq9-Lfbtyta_VgCLyQ7-c9vnkvTfOQ4BcEz-VLK5PGlAnu7jSHFDMxo1jIu7fOB81xzpe4LsEJFeR-czDnnLAW88Pmx3soq82AnL_SwQ-DLnCCErh4jcYUR0jFQ0Y6OGR8cD5cIN33PviyQd99WSE9mGntA4p9heouPl57V-M2Z4wF6pUe0IfF6acztNUyIB9W3vgS04PmXq-HDMc38aj5-ub1l-XZ7Pzj23fLxfnMMs7KjIMUrSCYUtMaajAXuOOsIwS0NGBakBTA4BZbYbETRlrKWiJ167SFjov5UfNqV3eczBqcra6SHtSY_FqnjYraq7-V4FfqIl4pWZvGMa4Fnt0USPHbBLmotc8WasMCxCkrKqq9jhHWVfTpP-hlnFKoz1OUcsxxyyir1PMdZVPMOUG_N0Ow-jVZtZSfF9vJnlb48W37e_T3HCvwZAekbPfqn6-hRtdX5tH_mPlPShy1aw</recordid><startdate>20190626</startdate><enddate>20190626</enddate><creator>de Vasconcelos, Debora Naliati</creator><creator>Lima, Angélica Nakagawa</creator><creator>Philot, Eric Allison</creator><creator>Scott, Ana Lígia</creator><creator>Ferreira Boza, Izabelle Amorim</creator><creator>de Souza, Aguinaldo Robinson</creator><creator>Morgon, Nelson Henrique</creator><creator>Ximenes, Valdecir Farias</creator><general>Royal Society of Chemistry</general><general>The Royal Society of Chemistry</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7SR</scope><scope>8BQ</scope><scope>8FD</scope><scope>JG9</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0003-2636-3080</orcidid></search><sort><creationdate>20190626</creationdate><title>Methyl divanillate: redox properties and binding affinity with albumin of an antioxidant and potential NADPH oxidase inhibitor</title><author>de Vasconcelos, Debora Naliati ; Lima, Angélica Nakagawa ; Philot, Eric Allison ; Scott, Ana Lígia ; Ferreira Boza, Izabelle Amorim ; de Souza, Aguinaldo Robinson ; Morgon, Nelson Henrique ; Ximenes, Valdecir Farias</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c454t-5e96761022b7b2b0560854811ea9beb7e92eeb070c6c0d6b9c24719a7dace8563</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Affinity</topic><topic>Antioxidants</topic><topic>Binding</topic><topic>Biological effects</topic><topic>Chemistry</topic><topic>Computer simulation</topic><topic>Dichroism</topic><topic>Dihedral angle</topic><topic>Dimers</topic><topic>Ferric ions</topic><topic>Free radicals</topic><topic>Inhibitors</topic><topic>Molecular docking</topic><topic>Organic chemistry</topic><topic>Oxidase</topic><topic>Pharmacology</topic><topic>Properties (attributes)</topic><topic>Reduction</topic><topic>Serum albumin</topic><topic>Signal generation</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>de Vasconcelos, Debora Naliati</creatorcontrib><creatorcontrib>Lima, Angélica Nakagawa</creatorcontrib><creatorcontrib>Philot, Eric Allison</creatorcontrib><creatorcontrib>Scott, Ana Lígia</creatorcontrib><creatorcontrib>Ferreira Boza, Izabelle Amorim</creatorcontrib><creatorcontrib>de Souza, Aguinaldo Robinson</creatorcontrib><creatorcontrib>Morgon, Nelson Henrique</creatorcontrib><creatorcontrib>Ximenes, Valdecir Farias</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>Engineered Materials Abstracts</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>Materials Research Database</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>RSC advances</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>de Vasconcelos, Debora Naliati</au><au>Lima, Angélica Nakagawa</au><au>Philot, Eric Allison</au><au>Scott, Ana Lígia</au><au>Ferreira Boza, Izabelle Amorim</au><au>de Souza, Aguinaldo Robinson</au><au>Morgon, Nelson Henrique</au><au>Ximenes, Valdecir Farias</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Methyl divanillate: redox properties and binding affinity with albumin of an antioxidant and potential NADPH oxidase inhibitor</atitle><jtitle>RSC advances</jtitle><addtitle>RSC Adv</addtitle><date>2019-06-26</date><risdate>2019</risdate><volume>9</volume><issue>35</issue><spage>19983</spage><epage>19992</epage><pages>19983-19992</pages><issn>2046-2069</issn><eissn>2046-2069</eissn><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 × 10 5 mol −1 L and 2.3 × 10 4 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. Methyl divanillate, a derivative of the vanillic acid (flavouring agent, JECFA number: 959) with promising beneficial biological effects.</abstract><cop>England</cop><pub>Royal Society of Chemistry</pub><pmid>35514705</pmid><doi>10.1039/c9ra02465d</doi><tpages>1</tpages><orcidid>https://orcid.org/0000-0003-2636-3080</orcidid><oa>free_for_read</oa></addata></record>
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subjects Affinity
Antioxidants
Binding
Biological effects
Chemistry
Computer simulation
Dichroism
Dihedral angle
Dimers
Ferric ions
Free radicals
Inhibitors
Molecular docking
Organic chemistry
Oxidase
Pharmacology
Properties (attributes)
Reduction
Serum albumin
Signal generation
title Methyl divanillate: redox properties and binding affinity with albumin of an antioxidant and potential NADPH oxidase inhibitor
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