A novel antioxidant phenyl disaccharide from Populus tremula knotwood.
Identifieur interne : 003C55 ( Main/Exploration ); précédent : 003C54; suivant : 003C56A novel antioxidant phenyl disaccharide from Populus tremula knotwood.
Auteurs : Madalina Neacsu [Roumanie] ; Vicente Micol ; Laura Pérez-Fons ; Stefan Willför ; Bjarne Holmbom ; Ricardo MallaviaSource :
- Molecules (Basel, Switzerland) [ 1420-3049 ] ; 2007.
Descripteurs français
- KwdFr :
- Antioxydants (pharmacologie), Arbres (composition chimique), Bois (MeSH), Chromatographie en phase gazeuse (MeSH), Chromatographie en phase liquide à haute performance (MeSH), Diholoside (composition chimique), Diholoside (pharmacologie), Extraits de plantes (composition chimique), Extraits de plantes (pharmacologie), Peroxydation lipidique (effets des médicaments et des substances chimiques), Peroxydes (composition chimique), Phénols (composition chimique), Phénols (pharmacologie), Piégeurs de radicaux libres (composition chimique), Populus (composition chimique), Spectrométrie de masse (MeSH), Spectrophotométrie UV (MeSH), Superoxydes (composition chimique).
- MESH :
- composition chimique : Arbres, Diholoside, Extraits de plantes, Peroxydes, Phénols, Piégeurs de radicaux libres, Populus, Superoxydes.
- effets des médicaments et des substances chimiques : Peroxydation lipidique.
- pharmacologie : Antioxydants, Diholoside, Extraits de plantes, Phénols.
- Bois, Chromatographie en phase gazeuse, Chromatographie en phase liquide à haute performance, Spectrométrie de masse, Spectrophotométrie UV.
English descriptors
- KwdEn :
- Antioxidants (pharmacology), Chromatography, Gas (MeSH), Chromatography, High Pressure Liquid (MeSH), Disaccharides (chemistry), Disaccharides (pharmacology), Free Radical Scavengers (chemistry), Lipid Peroxidation (drug effects), Mass Spectrometry (MeSH), Peroxides (chemistry), Phenols (chemistry), Phenols (pharmacology), Plant Extracts (chemistry), Plant Extracts (pharmacology), Populus (chemistry), Spectrophotometry, Ultraviolet (MeSH), Superoxides (chemistry), Trees (chemistry), Wood (MeSH).
- MESH :
- chemical , chemistry : Disaccharides, Free Radical Scavengers, Peroxides, Phenols, Plant Extracts, Superoxides.
- chemical , pharmacology : Antioxidants, Disaccharides, Phenols, Plant Extracts.
- chemistry : Populus, Trees.
- drug effects : Lipid Peroxidation.
- Chromatography, Gas, Chromatography, High Pressure Liquid, Mass Spectrometry, Spectrophotometry, Ultraviolet, Wood.
Abstract
The complete characterization of two compounds obtained from the acetone extract of Populus tremula knotwood has been was achieved using LC-DAD-MS, MS/MS, IR and NMR. The new compounds were unequivocally identified as a mixture of the ester isomers of the (E) and (Z) p-coumarate of 1-O-rutinose. The isomers showed the capacity to inhibit lipid peroxidation induced by tert-butylhydroperoxide and to trap peroxyl radicals, as determined by a chemiluminescence method. These new phenyl disaccharides also showed a significant ORAC (oxygen radical absorbance capacity) value, i.e. 11.7 microM TE (Trolox Equivalents).
DOI: 10.3390/12020205
PubMed: 17846571
PubMed Central: PMC6149441
Affiliations:
Links toward previous steps (curation, corpus...)
Le document en format XML
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uniqKey="Perez Fons L" first="Laura" last="Pérez-Fons">Laura Pérez-Fons</name></author><author><name sortKey="Willfor, Stefan" sort="Willfor, Stefan" uniqKey="Willfor S" first="Stefan" last="Willför">Stefan Willför</name></author><author><name sortKey="Holmbom, Bjarne" sort="Holmbom, Bjarne" uniqKey="Holmbom B" first="Bjarne" last="Holmbom">Bjarne Holmbom</name></author><author><name sortKey="Mallavia, Ricardo" sort="Mallavia, Ricardo" uniqKey="Mallavia R" first="Ricardo" last="Mallavia">Ricardo Mallavia</name></author></titleStmt><publicationStmt><idno type="wicri:source">PubMed</idno><date when="2007">2007</date><idno type="RBID">pubmed:17846571</idno><idno type="pmid">17846571</idno><idno type="pmc">PMC6149441</idno><idno type="doi">10.3390/12020205</idno><idno type="wicri:Area/Main/Corpus">003A79</idno><idno type="wicri:explorRef" wicri:stream="Main" wicri:step="Corpus" wicri:corpus="PubMed">003A79</idno><idno type="wicri:Area/Main/Curation">003A79</idno><idno 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uniqKey="Micol V" first="Vicente" last="Micol">Vicente Micol</name></author><author><name sortKey="Perez Fons, Laura" sort="Perez Fons, Laura" uniqKey="Perez Fons L" first="Laura" last="Pérez-Fons">Laura Pérez-Fons</name></author><author><name sortKey="Willfor, Stefan" sort="Willfor, Stefan" uniqKey="Willfor S" first="Stefan" last="Willför">Stefan Willför</name></author><author><name sortKey="Holmbom, Bjarne" sort="Holmbom, Bjarne" uniqKey="Holmbom B" first="Bjarne" last="Holmbom">Bjarne Holmbom</name></author><author><name sortKey="Mallavia, Ricardo" sort="Mallavia, Ricardo" uniqKey="Mallavia R" first="Ricardo" last="Mallavia">Ricardo Mallavia</name></author></analytic><series><title level="j">Molecules (Basel, Switzerland)</title><idno type="eISSN">1420-3049</idno><imprint><date when="2007" type="published">2007</date></imprint></series></biblStruct></sourceDesc></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Antioxidants (pharmacology)</term><term>Chromatography, Gas (MeSH)</term><term>Chromatography, High Pressure Liquid (MeSH)</term><term>Disaccharides (chemistry)</term><term>Disaccharides (pharmacology)</term><term>Free Radical Scavengers (chemistry)</term><term>Lipid Peroxidation (drug effects)</term><term>Mass Spectrometry (MeSH)</term><term>Peroxides (chemistry)</term><term>Phenols (chemistry)</term><term>Phenols (pharmacology)</term><term>Plant Extracts (chemistry)</term><term>Plant Extracts (pharmacology)</term><term>Populus (chemistry)</term><term>Spectrophotometry, Ultraviolet (MeSH)</term><term>Superoxides (chemistry)</term><term>Trees (chemistry)</term><term>Wood (MeSH)</term></keywords><keywords scheme="KwdFr" xml:lang="fr"><term>Antioxydants (pharmacologie)</term><term>Arbres (composition chimique)</term><term>Bois (MeSH)</term><term>Chromatographie en phase gazeuse (MeSH)</term><term>Chromatographie en phase liquide à haute performance (MeSH)</term><term>Diholoside (composition chimique)</term><term>Diholoside (pharmacologie)</term><term>Extraits de plantes (composition chimique)</term><term>Extraits de plantes (pharmacologie)</term><term>Peroxydation lipidique (effets des médicaments et des substances chimiques)</term><term>Peroxydes (composition chimique)</term><term>Phénols (composition chimique)</term><term>Phénols (pharmacologie)</term><term>Piégeurs de radicaux libres (composition chimique)</term><term>Populus (composition chimique)</term><term>Spectrométrie de masse (MeSH)</term><term>Spectrophotométrie UV (MeSH)</term><term>Superoxydes (composition chimique)</term></keywords><keywords scheme="MESH" type="chemical" qualifier="chemistry" xml:lang="en"><term>Disaccharides</term><term>Free Radical Scavengers</term><term>Peroxides</term><term>Phenols</term><term>Plant Extracts</term><term>Superoxides</term></keywords><keywords scheme="MESH" type="chemical" qualifier="pharmacology" xml:lang="en"><term>Antioxidants</term><term>Disaccharides</term><term>Phenols</term><term>Plant Extracts</term></keywords><keywords scheme="MESH" qualifier="chemistry" xml:lang="en"><term>Populus</term><term>Trees</term></keywords><keywords scheme="MESH" qualifier="composition chimique" xml:lang="fr"><term>Arbres</term><term>Diholoside</term><term>Extraits de plantes</term><term>Peroxydes</term><term>Phénols</term><term>Piégeurs de radicaux libres</term><term>Populus</term><term>Superoxydes</term></keywords><keywords scheme="MESH" qualifier="drug effects" xml:lang="en"><term>Lipid Peroxidation</term></keywords><keywords scheme="MESH" qualifier="effets des médicaments et des substances chimiques" xml:lang="fr"><term>Peroxydation lipidique</term></keywords><keywords scheme="MESH" qualifier="pharmacologie" xml:lang="fr"><term>Antioxydants</term><term>Diholoside</term><term>Extraits de plantes</term><term>Phénols</term></keywords><keywords scheme="MESH" xml:lang="en"><term>Chromatography, Gas</term><term>Chromatography, High Pressure Liquid</term><term>Mass Spectrometry</term><term>Spectrophotometry, Ultraviolet</term><term>Wood</term></keywords><keywords scheme="MESH" xml:lang="fr"><term>Bois</term><term>Chromatographie en phase gazeuse</term><term>Chromatographie en phase liquide à haute performance</term><term>Spectrométrie de masse</term><term>Spectrophotométrie UV</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">The complete characterization of two compounds obtained from the acetone extract of Populus tremula knotwood has been was achieved using LC-DAD-MS, MS/MS, IR and NMR. The new compounds were unequivocally identified as a mixture of the ester isomers of the (E) and (Z) p-coumarate of 1-O-rutinose. The isomers showed the capacity to inhibit lipid peroxidation induced by tert-butylhydroperoxide and to trap peroxyl radicals, as determined by a chemiluminescence method. These new phenyl disaccharides also showed a significant ORAC (oxygen radical absorbance capacity) value, i.e. 11.7 microM TE (Trolox Equivalents).</div></front></TEI><pubmed><MedlineCitation Status="MEDLINE" Owner="NLM"><PMID Version="1">17846571</PMID><DateCompleted><Year>2007</Year><Month>10</Month><Day>23</Day></DateCompleted><DateRevised><Year>2019</Year><Month>06</Month><Day>08</Day></DateRevised><Article PubModel="Electronic"><Journal><ISSN IssnType="Electronic">1420-3049</ISSN><JournalIssue CitedMedium="Internet"><Volume>12</Volume><Issue>2</Issue><PubDate><Year>2007</Year><Month>Feb</Month><Day>19</Day></PubDate></JournalIssue><Title>Molecules (Basel, Switzerland)</Title><ISOAbbreviation>Molecules</ISOAbbreviation></Journal><ArticleTitle>A novel antioxidant phenyl disaccharide from Populus tremula knotwood.</ArticleTitle><Pagination><MedlinePgn>205-17</MedlinePgn></Pagination><Abstract><AbstractText>The complete characterization of two compounds obtained from the acetone extract of Populus tremula knotwood has been was achieved using LC-DAD-MS, MS/MS, IR and NMR. The new compounds were unequivocally identified as a mixture of the ester isomers of the (E) and (Z) p-coumarate of 1-O-rutinose. The isomers showed the capacity to inhibit lipid peroxidation induced by tert-butylhydroperoxide and to trap peroxyl radicals, as determined by a chemiluminescence method. These new phenyl disaccharides also showed a significant ORAC (oxygen radical absorbance capacity) value, i.e. 11.7 microM TE (Trolox Equivalents).</AbstractText></Abstract><AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Neacsu</LastName><ForeName>Madalina</ForeName><Initials>M</Initials><AffiliationInfo><Affiliation>Department of Chemistry and Biochemistry, University of Agricultural Sciences and Veterinary Medicine, Manastur 3-5, 400372 Cluj, Napoca, Romania. neacsumro@yahoo.com</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Micol</LastName><ForeName>Vicente</ForeName><Initials>V</Initials></Author><Author ValidYN="Y"><LastName>Pérez-Fons</LastName><ForeName>Laura</ForeName><Initials>L</Initials></Author><Author ValidYN="Y"><LastName>Willför</LastName><ForeName>Stefan</ForeName><Initials>S</Initials></Author><Author ValidYN="Y"><LastName>Holmbom</LastName><ForeName>Bjarne</ForeName><Initials>B</Initials></Author><Author ValidYN="Y"><LastName>Mallavia</LastName><ForeName>Ricardo</ForeName><Initials>R</Initials></Author></AuthorList><Language>eng</Language><PublicationTypeList><PublicationType UI="D016428">Journal Article</PublicationType><PublicationType UI="D013485">Research Support, Non-U.S. Gov't</PublicationType></PublicationTypeList><ArticleDate DateType="Electronic"><Year>2007</Year><Month>02</Month><Day>19</Day></ArticleDate></Article><MedlineJournalInfo><Country>Switzerland</Country><MedlineTA>Molecules</MedlineTA><NlmUniqueID>100964009</NlmUniqueID><ISSNLinking>1420-3049</ISSNLinking></MedlineJournalInfo><ChemicalList><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance UI="D000975">Antioxidants</NameOfSubstance></Chemical><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance UI="D004187">Disaccharides</NameOfSubstance></Chemical><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance UI="D016166">Free Radical 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MajorTopicYN="N">chemistry</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D010636" MajorTopicYN="N">Phenols</DescriptorName><QualifierName UI="Q000737" MajorTopicYN="Y">chemistry</QualifierName><QualifierName UI="Q000494" MajorTopicYN="N">pharmacology</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D010936" MajorTopicYN="N">Plant Extracts</DescriptorName><QualifierName UI="Q000737" MajorTopicYN="Y">chemistry</QualifierName><QualifierName UI="Q000494" MajorTopicYN="N">pharmacology</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D032107" MajorTopicYN="N">Populus</DescriptorName><QualifierName UI="Q000737" MajorTopicYN="Y">chemistry</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D013056" MajorTopicYN="N">Spectrophotometry, Ultraviolet</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D013481" MajorTopicYN="N">Superoxides</DescriptorName><QualifierName UI="Q000737" 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IdType="pubmed">11599998</ArticleId></ArticleIdList></Reference></ReferenceList></PubmedData></pubmed><affiliations><list><country><li>Roumanie</li></country></list><tree><noCountry><name sortKey="Holmbom, Bjarne" sort="Holmbom, Bjarne" uniqKey="Holmbom B" first="Bjarne" last="Holmbom">Bjarne Holmbom</name><name sortKey="Mallavia, Ricardo" sort="Mallavia, Ricardo" uniqKey="Mallavia R" first="Ricardo" last="Mallavia">Ricardo Mallavia</name><name sortKey="Micol, Vicente" sort="Micol, Vicente" uniqKey="Micol V" first="Vicente" last="Micol">Vicente Micol</name><name sortKey="Perez Fons, Laura" sort="Perez Fons, Laura" uniqKey="Perez Fons L" first="Laura" last="Pérez-Fons">Laura Pérez-Fons</name><name sortKey="Willfor, Stefan" sort="Willfor, Stefan" uniqKey="Willfor S" first="Stefan" last="Willför">Stefan Willför</name></noCountry><country name="Roumanie"><noRegion><name sortKey="Neacsu, Madalina" sort="Neacsu, Madalina" uniqKey="Neacsu M" first="Madalina" last="Neacsu">Madalina 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