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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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 |
format | Article |
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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><identifier>ISSN: 2046-2069</identifier><identifier>EISSN: 2046-2069</identifier><identifier>DOI: 10.1039/c9ra02465d</identifier><identifier>PMID: 35514705</identifier><language>eng</language><publisher>England: Royal Society of Chemistry</publisher><subject>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</subject><ispartof>RSC advances, 2019-06, Vol.9 (35), p.19983-19992</ispartof><rights>This journal is © The Royal Society of Chemistry.</rights><rights>Copyright Royal Society of Chemistry 2019</rights><rights>This journal is © The Royal Society of Chemistry 2019 The Royal Society of Chemistry</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c454t-5e96761022b7b2b0560854811ea9beb7e92eeb070c6c0d6b9c24719a7dace8563</citedby><cites>FETCH-LOGICAL-c454t-5e96761022b7b2b0560854811ea9beb7e92eeb070c6c0d6b9c24719a7dace8563</cites><orcidid>0000-0003-2636-3080</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC9065500/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC9065500/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,860,881,27901,27902,53766,53768</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/35514705$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><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><title>Methyl divanillate: redox properties and binding affinity with albumin of an antioxidant and potential NADPH oxidase inhibitor</title><title>RSC advances</title><addtitle>RSC Adv</addtitle><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.</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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