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Antioxidant activity of aryltetralone lignans and derivatives from Virola sebifera (Aubl.)
Aryltetralone lignans bearing methylenedioxy groups (1a-b; 2a-b) were isolated from seeds of Virola sebifera. Their antioxidant activities were evaluated by inhibition of lipid peroxidation as indicated by TBARS and chemiluminescence emission (CL) assays. The lignan 1c, 'having a 2′-hydroxy-4′,...
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Published in: | Natural product research 2005-10, Vol.19 (7), p.661-666 |
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creator | Rezende, Kênnia R. Davino, Solange C. Barros, Sílvia B.M. Kato, Massuo J. |
description | Aryltetralone lignans bearing methylenedioxy groups (1a-b; 2a-b) were isolated from seeds of Virola sebifera. Their antioxidant activities were evaluated by inhibition of lipid peroxidation as indicated by TBARS and chemiluminescence emission (CL) assays. The lignan 1c, 'having a 2′-hydroxy-4′,5′-methylenedioxyphenyl group, was the most active compound with TBARS/CL Q
1/2
values of 0.89 and 0.10 µg/mL, respectively. The catechol derivatives 3 and 4, obtained by demethylenation of lignans 1a and 2a, were of similar activity to 1c, and all were much more effective as antioxidants than α-tocopherol. |
doi_str_mv | 10.1080/14786410412331302118 |
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1/2
values of 0.89 and 0.10 µg/mL, respectively. The catechol derivatives 3 and 4, obtained by demethylenation of lignans 1a and 2a, were of similar activity to 1c, and all were much more effective as antioxidants than α-tocopherol.</description><identifier>ISSN: 1478-6419</identifier><identifier>EISSN: 1478-6427</identifier><identifier>DOI: 10.1080/14786410412331302118</identifier><identifier>PMID: 16076635</identifier><language>eng</language><publisher>England: Taylor & Francis Group</publisher><subject>Antioxidant activity ; Antioxidants - pharmacology ; Aryltetralone lignans ; Chemiluminescence emission ; Lignans - chemistry ; Lignans - pharmacology ; Myristicaceae ; Myristicaceae - chemistry ; Seeds - chemistry ; TBARS ; Virola sebifera</subject><ispartof>Natural product research, 2005-10, Vol.19 (7), p.661-666</ispartof><rights>Copyright Taylor & Francis Group, LLC 2005</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c412t-85ab19d2efbc446bfa05e587ca8c9af0a977311e064164c7aa673af9657c80823</citedby><cites>FETCH-LOGICAL-c412t-85ab19d2efbc446bfa05e587ca8c9af0a977311e064164c7aa673af9657c80823</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/16076635$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Rezende, Kênnia R.</creatorcontrib><creatorcontrib>Davino, Solange C.</creatorcontrib><creatorcontrib>Barros, Sílvia B.M.</creatorcontrib><creatorcontrib>Kato, Massuo J.</creatorcontrib><title>Antioxidant activity of aryltetralone lignans and derivatives from Virola sebifera (Aubl.)</title><title>Natural product research</title><addtitle>Nat Prod Res</addtitle><description>Aryltetralone lignans bearing methylenedioxy groups (1a-b; 2a-b) were isolated from seeds of Virola sebifera. Their antioxidant activities were evaluated by inhibition of lipid peroxidation as indicated by TBARS and chemiluminescence emission (CL) assays. The lignan 1c, 'having a 2′-hydroxy-4′,5′-methylenedioxyphenyl group, was the most active compound with TBARS/CL Q
1/2
values of 0.89 and 0.10 µg/mL, respectively. The catechol derivatives 3 and 4, obtained by demethylenation of lignans 1a and 2a, were of similar activity to 1c, and all were much more effective as antioxidants than α-tocopherol.</description><subject>Antioxidant activity</subject><subject>Antioxidants - pharmacology</subject><subject>Aryltetralone lignans</subject><subject>Chemiluminescence emission</subject><subject>Lignans - chemistry</subject><subject>Lignans - pharmacology</subject><subject>Myristicaceae</subject><subject>Myristicaceae - chemistry</subject><subject>Seeds - chemistry</subject><subject>TBARS</subject><subject>Virola sebifera</subject><issn>1478-6419</issn><issn>1478-6427</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2005</creationdate><recordtype>article</recordtype><recordid>eNqFkEFPGzEQha2qqFDoP6gqnyp6CNhrr-3tBUURBaRIXIADl9Ws165ceW1qO0D-PY4StRcEc5nR6HtPMw-hr5ScUKLIKeVSCU4Jpw1jlJGGUvUBHWzWM8Eb-fHfTLt99DnnP6Qybdt-QvtUECkEaw_Q_TwUF5_dCKFg0MU9urLG0WJIa19MSeBjMNi73wFCxhBGPJrkHqGSJmOb4oTvXIoecDaDsyYBPp6vBn_y4wjtWfDZfNn1Q3T76_xmcTlbXl9cLebLma6nl5lqYaDd2Bg7aM7FYIG0plVSg9IdWAKdlIxSQ-ojgmsJICQD24lWakVUww7R963vQ4p_VyaXfnJZG-8hmLjKvVC8lmIV5FtQp5hzMrZ_SG6qj_aU9JtM-9cyrbJvO__VMJnxv2gXYgV-bgEXbEwTPMXkx77A2sdkEwTt8qvOfXkuVXz2rpi9ed8LajiYgA</recordid><startdate>20051001</startdate><enddate>20051001</enddate><creator>Rezende, Kênnia R.</creator><creator>Davino, Solange C.</creator><creator>Barros, Sílvia B.M.</creator><creator>Kato, Massuo J.</creator><general>Taylor & Francis Group</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20051001</creationdate><title>Antioxidant activity of aryltetralone lignans and derivatives from Virola sebifera (Aubl.)</title><author>Rezende, Kênnia R. ; Davino, Solange C. ; Barros, Sílvia B.M. ; Kato, Massuo J.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c412t-85ab19d2efbc446bfa05e587ca8c9af0a977311e064164c7aa673af9657c80823</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2005</creationdate><topic>Antioxidant activity</topic><topic>Antioxidants - pharmacology</topic><topic>Aryltetralone lignans</topic><topic>Chemiluminescence emission</topic><topic>Lignans - chemistry</topic><topic>Lignans - pharmacology</topic><topic>Myristicaceae</topic><topic>Myristicaceae - chemistry</topic><topic>Seeds - chemistry</topic><topic>TBARS</topic><topic>Virola sebifera</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Rezende, Kênnia R.</creatorcontrib><creatorcontrib>Davino, Solange C.</creatorcontrib><creatorcontrib>Barros, Sílvia B.M.</creatorcontrib><creatorcontrib>Kato, Massuo J.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Natural product research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Rezende, Kênnia R.</au><au>Davino, Solange C.</au><au>Barros, Sílvia B.M.</au><au>Kato, Massuo J.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Antioxidant activity of aryltetralone lignans and derivatives from Virola sebifera (Aubl.)</atitle><jtitle>Natural product research</jtitle><addtitle>Nat Prod Res</addtitle><date>2005-10-01</date><risdate>2005</risdate><volume>19</volume><issue>7</issue><spage>661</spage><epage>666</epage><pages>661-666</pages><issn>1478-6419</issn><eissn>1478-6427</eissn><abstract>Aryltetralone lignans bearing methylenedioxy groups (1a-b; 2a-b) were isolated from seeds of Virola sebifera. Their antioxidant activities were evaluated by inhibition of lipid peroxidation as indicated by TBARS and chemiluminescence emission (CL) assays. The lignan 1c, 'having a 2′-hydroxy-4′,5′-methylenedioxyphenyl group, was the most active compound with TBARS/CL Q
1/2
values of 0.89 and 0.10 µg/mL, respectively. The catechol derivatives 3 and 4, obtained by demethylenation of lignans 1a and 2a, were of similar activity to 1c, and all were much more effective as antioxidants than α-tocopherol.</abstract><cop>England</cop><pub>Taylor & Francis Group</pub><pmid>16076635</pmid><doi>10.1080/14786410412331302118</doi><tpages>6</tpages></addata></record> |
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subjects | Antioxidant activity Antioxidants - pharmacology Aryltetralone lignans Chemiluminescence emission Lignans - chemistry Lignans - pharmacology Myristicaceae Myristicaceae - chemistry Seeds - chemistry TBARS Virola sebifera |
title | Antioxidant activity of aryltetralone lignans and derivatives from Virola sebifera (Aubl.) |
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