Chemical composition of propolis from Canada, its antiradical activity and plant origin.
Identifieur interne : 003E49 ( Main/Exploration ); précédent : 003E48; suivant : 003E50Chemical composition of propolis from Canada, its antiradical activity and plant origin.
Auteurs : Roumen Christov [Canada] ; Boryana Trusheva ; Milena Popova ; Vassya Bankova ; Michel BertrandSource :
- Natural product research [ 1478-6419 ] ; 2006.
Descripteurs français
- KwdFr :
- Acides coumariques (analyse), Acétophénones (analyse), Anti-infectieux (analyse), Arbres (MeSH), Chalcone (analogues et dérivés), Chalcone (analyse), Chalcones (MeSH), Chromatographie gazeuse-spectrométrie de masse (MeSH), Cinnamates (analyse), Colombie-Britannique (MeSH), Dérivés du biphényle (composition chimique), Hydrazines (composition chimique), Hydroxybenzoates (analyse), Picrates (MeSH), Piégeurs de radicaux libres (analyse), Propionates (MeSH), Propolis (analyse), Québec (MeSH).
- MESH :
- analogues et dérivés : Chalcone.
- analyse : Acides coumariques, Acétophénones, Anti-infectieux, Chalcone, Cinnamates, Hydroxybenzoates, Piégeurs de radicaux libres, Propolis.
- composition chimique : Dérivés du biphényle, Hydrazines.
- Arbres, Chalcones, Chromatographie gazeuse-spectrométrie de masse, Colombie-Britannique, Picrates, Propionates, Québec.
English descriptors
- KwdEn :
- Acetophenones (analysis), Anti-Infective Agents (analysis), Biphenyl Compounds (chemistry), British Columbia (MeSH), Chalcone (analogs & derivatives), Chalcone (analysis), Chalcones (MeSH), Cinnamates (analysis), Coumaric Acids (analysis), Free Radical Scavengers (analysis), Gas Chromatography-Mass Spectrometry (MeSH), Hydrazines (chemistry), Hydroxybenzoates (analysis), Picrates (MeSH), Propionates (MeSH), Propolis (analysis), Quebec (MeSH), Trees (MeSH).
- MESH :
- chemical , analogs & derivatives : Chalcone.
- chemical , analysis : Acetophenones, Anti-Infective Agents, Chalcone, Cinnamates, Coumaric Acids, Free Radical Scavengers, Hydroxybenzoates, Propolis.
- chemical , chemistry : Biphenyl Compounds, Hydrazines.
- British Columbia, Chalcones, Gas Chromatography-Mass Spectrometry, Picrates, Propionates, Quebec, Trees.
Abstract
The chemical composition of propolis from two regions in Canada was studied: Boreal forest and Pacific coastal forest that lay outside the area of distribution of Aigeiros poplars, the usual propolis source plants. In the sample from Victoria, p-hydroxyacetophenone, benzyl hydroxybenzoate and cinnamic acid were the major components, accompanied by significant amounts of dihydrochalcones, which allowed the identification of its plant source: Populus trichocarpa of Section Tacamahaca. Three dihydrochalcones were new for propolis. The sample from Richmond was characterized by large amounts of p-coumaric and cinnamic acid, typical for poplars of Section Leuce, subsection Trepidae, its plant source was identified as P. tremuloides. Both samples showed good radical scavenging activity against DPPH. Obviously, Northern type propolis is a promising potential source of biologically active substances and deserves further investigation.
DOI: 10.1080/14786410500056918
PubMed: 16835083
Affiliations:
Links toward previous steps (curation, corpus...)
Le document en format XML
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Popova</name></author><author><name sortKey="Bankova, Vassya" sort="Bankova, Vassya" uniqKey="Bankova V" first="Vassya" last="Bankova">Vassya Bankova</name></author><author><name sortKey="Bertrand, Michel" sort="Bertrand, Michel" uniqKey="Bertrand M" first="Michel" last="Bertrand">Michel Bertrand</name></author></titleStmt><publicationStmt><idno type="wicri:source">PubMed</idno><date when="2006">2006</date><idno type="RBID">pubmed:16835083</idno><idno type="pmid">16835083</idno><idno type="doi">10.1080/14786410500056918</idno><idno type="wicri:Area/Main/Corpus">003D71</idno><idno type="wicri:explorRef" wicri:stream="Main" wicri:step="Corpus" wicri:corpus="PubMed">003D71</idno><idno type="wicri:Area/Main/Curation">003D71</idno><idno type="wicri:explorRef" wicri:stream="Main" wicri:step="Curation">003D71</idno><idno type="wicri:Area/Main/Exploration">003D71</idno></publicationStmt><sourceDesc><biblStruct><analytic><title xml:lang="en">Chemical composition of propolis from Canada, its 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Bankova</name></author><author><name sortKey="Bertrand, Michel" sort="Bertrand, Michel" uniqKey="Bertrand M" first="Michel" last="Bertrand">Michel Bertrand</name></author></analytic><series><title level="j">Natural product research</title><idno type="ISSN">1478-6419</idno><imprint><date when="2006" type="published">2006</date></imprint></series></biblStruct></sourceDesc></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Acetophenones (analysis)</term><term>Anti-Infective Agents (analysis)</term><term>Biphenyl Compounds (chemistry)</term><term>British Columbia (MeSH)</term><term>Chalcone (analogs & derivatives)</term><term>Chalcone (analysis)</term><term>Chalcones (MeSH)</term><term>Cinnamates (analysis)</term><term>Coumaric Acids (analysis)</term><term>Free Radical Scavengers (analysis)</term><term>Gas Chromatography-Mass Spectrometry (MeSH)</term><term>Hydrazines (chemistry)</term><term>Hydroxybenzoates (analysis)</term><term>Picrates (MeSH)</term><term>Propionates (MeSH)</term><term>Propolis (analysis)</term><term>Quebec (MeSH)</term><term>Trees (MeSH)</term></keywords><keywords scheme="KwdFr" xml:lang="fr"><term>Acides coumariques (analyse)</term><term>Acétophénones (analyse)</term><term>Anti-infectieux (analyse)</term><term>Arbres (MeSH)</term><term>Chalcone (analogues et dérivés)</term><term>Chalcone (analyse)</term><term>Chalcones (MeSH)</term><term>Chromatographie gazeuse-spectrométrie de masse (MeSH)</term><term>Cinnamates (analyse)</term><term>Colombie-Britannique (MeSH)</term><term>Dérivés du biphényle (composition chimique)</term><term>Hydrazines (composition chimique)</term><term>Hydroxybenzoates (analyse)</term><term>Picrates (MeSH)</term><term>Piégeurs de radicaux libres (analyse)</term><term>Propionates (MeSH)</term><term>Propolis (analyse)</term><term>Québec (MeSH)</term></keywords><keywords scheme="MESH" type="chemical" qualifier="analogs & derivatives" xml:lang="en"><term>Chalcone</term></keywords><keywords scheme="MESH" type="chemical" qualifier="analysis" xml:lang="en"><term>Acetophenones</term><term>Anti-Infective Agents</term><term>Chalcone</term><term>Cinnamates</term><term>Coumaric Acids</term><term>Free Radical Scavengers</term><term>Hydroxybenzoates</term><term>Propolis</term></keywords><keywords scheme="MESH" type="chemical" qualifier="chemistry" xml:lang="en"><term>Biphenyl Compounds</term><term>Hydrazines</term></keywords><keywords scheme="MESH" qualifier="analogues et dérivés" xml:lang="fr"><term>Chalcone</term></keywords><keywords scheme="MESH" qualifier="analyse" xml:lang="fr"><term>Acides coumariques</term><term>Acétophénones</term><term>Anti-infectieux</term><term>Chalcone</term><term>Cinnamates</term><term>Hydroxybenzoates</term><term>Piégeurs de radicaux libres</term><term>Propolis</term></keywords><keywords scheme="MESH" qualifier="composition chimique" xml:lang="fr"><term>Dérivés du biphényle</term><term>Hydrazines</term></keywords><keywords scheme="MESH" xml:lang="en"><term>British Columbia</term><term>Chalcones</term><term>Gas Chromatography-Mass Spectrometry</term><term>Picrates</term><term>Propionates</term><term>Quebec</term><term>Trees</term></keywords><keywords scheme="MESH" xml:lang="fr"><term>Arbres</term><term>Chalcones</term><term>Chromatographie gazeuse-spectrométrie de masse</term><term>Colombie-Britannique</term><term>Picrates</term><term>Propionates</term><term>Québec</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">The chemical composition of propolis from two regions in Canada was studied: Boreal forest and Pacific coastal forest that lay outside the area of distribution of Aigeiros poplars, the usual propolis source plants. In the sample from Victoria, p-hydroxyacetophenone, benzyl hydroxybenzoate and cinnamic acid were the major components, accompanied by significant amounts of dihydrochalcones, which allowed the identification of its plant source: Populus trichocarpa of Section Tacamahaca. Three dihydrochalcones were new for propolis. The sample from Richmond was characterized by large amounts of p-coumaric and cinnamic acid, typical for poplars of Section Leuce, subsection Trepidae, its plant source was identified as P. tremuloides. Both samples showed good radical scavenging activity against DPPH. Obviously, Northern type propolis is a promising potential source of biologically active substances and deserves further investigation.</div></front></TEI><pubmed><MedlineCitation Status="MEDLINE" Owner="NLM"><PMID Version="1">16835083</PMID><DateCompleted><Year>2006</Year><Month>08</Month><Day>29</Day></DateCompleted><DateRevised><Year>2017</Year><Month>11</Month><Day>16</Day></DateRevised><Article PubModel="Print"><Journal><ISSN IssnType="Print">1478-6419</ISSN><JournalIssue CitedMedium="Print"><Volume>20</Volume><Issue>6</Issue><PubDate><Year>2006</Year><Month>May</Month><Day>20</Day></PubDate></JournalIssue><Title>Natural product research</Title><ISOAbbreviation>Nat Prod Res</ISOAbbreviation></Journal><ArticleTitle>Chemical composition of propolis from Canada, its antiradical activity and plant origin.</ArticleTitle><Pagination><MedlinePgn>531-6</MedlinePgn></Pagination><Abstract><AbstractText>The chemical composition of propolis from two regions in Canada was studied: Boreal forest and Pacific coastal forest that lay outside the area of distribution of Aigeiros poplars, the usual propolis source plants. In the sample from Victoria, p-hydroxyacetophenone, benzyl hydroxybenzoate and cinnamic acid were the major components, accompanied by significant amounts of dihydrochalcones, which allowed the identification of its plant source: Populus trichocarpa of Section Tacamahaca. Three dihydrochalcones were new for propolis. The sample from Richmond was characterized by large amounts of p-coumaric and cinnamic acid, typical for poplars of Section Leuce, subsection Trepidae, its plant source was identified as P. tremuloides. Both samples showed good radical scavenging activity against DPPH. Obviously, Northern type propolis is a promising potential source of biologically active substances and deserves further investigation.</AbstractText></Abstract><AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Christov</LastName><ForeName>Roumen</ForeName><Initials>R</Initials><AffiliationInfo><Affiliation>Regional Center for Mass Spectrometry, Department of Chemistry, University of Montreal, Quebec, Canada.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Trusheva</LastName><ForeName>Boryana</ForeName><Initials>B</Initials></Author><Author ValidYN="Y"><LastName>Popova</LastName><ForeName>Milena</ForeName><Initials>M</Initials></Author><Author ValidYN="Y"><LastName>Bankova</LastName><ForeName>Vassya</ForeName><Initials>V</Initials></Author><Author ValidYN="Y"><LastName>Bertrand</LastName><ForeName>Michel</ForeName><Initials>M</Initials></Author></AuthorList><Language>eng</Language><PublicationTypeList><PublicationType UI="D016428">Journal Article</PublicationType></PublicationTypeList></Article><MedlineJournalInfo><Country>England</Country><MedlineTA>Nat Prod Res</MedlineTA><NlmUniqueID>101167924</NlmUniqueID><ISSNLinking>1478-6419</ISSNLinking></MedlineJournalInfo><ChemicalList><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance UI="D000098">Acetophenones</NameOfSubstance></Chemical><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance UI="D000890">Anti-Infective Agents</NameOfSubstance></Chemical><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance UI="D001713">Biphenyl Compounds</NameOfSubstance></Chemical><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance UI="D047188">Chalcones</NameOfSubstance></Chemical><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance UI="D002934">Cinnamates</NameOfSubstance></Chemical><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance UI="D003373">Coumaric Acids</NameOfSubstance></Chemical><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance UI="D016166">Free Radical Scavengers</NameOfSubstance></Chemical><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance UI="D006834">Hydrazines</NameOfSubstance></Chemical><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance UI="D062385">Hydroxybenzoates</NameOfSubstance></Chemical><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance UI="D010851">Picrates</NameOfSubstance></Chemical><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance UI="D011422">Propionates</NameOfSubstance></Chemical><Chemical><RegistryNumber>5S5A2Q39HX</RegistryNumber><NameOfSubstance UI="D002599">Chalcone</NameOfSubstance></Chemical><Chemical><RegistryNumber>9009-62-5</RegistryNumber><NameOfSubstance UI="D011429">Propolis</NameOfSubstance></Chemical><Chemical><RegistryNumber>DFD3H4VGDH</RegistryNumber><NameOfSubstance UI="C004931">1,1-diphenyl-2-picrylhydrazyl</NameOfSubstance></Chemical><Chemical><RegistryNumber>G1L3HT4CMH</RegistryNumber><NameOfSubstance UI="C031335">4-hydroxyacetophenone</NameOfSubstance></Chemical><Chemical><RegistryNumber>H5W525SX7Q</RegistryNumber><NameOfSubstance UI="C015812">dihydrochalcone</NameOfSubstance></Chemical><Chemical><RegistryNumber>IBS9D1EU3J</RegistryNumber><NameOfSubstance UI="C495469">trans-3-(4'-hydroxyphenyl)-2-propenoic acid</NameOfSubstance></Chemical><Chemical><RegistryNumber>U14A832J8D</RegistryNumber><NameOfSubstance UI="C029010">cinnamic acid</NameOfSubstance></Chemical></ChemicalList><CitationSubset>IM</CitationSubset><MeshHeadingList><MeshHeading><DescriptorName UI="D000098" MajorTopicYN="N">Acetophenones</DescriptorName><QualifierName UI="Q000032" MajorTopicYN="N">analysis</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D000890" MajorTopicYN="N">Anti-Infective Agents</DescriptorName><QualifierName UI="Q000032" MajorTopicYN="N">analysis</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D001713" MajorTopicYN="N">Biphenyl Compounds</DescriptorName><QualifierName UI="Q000737" MajorTopicYN="N">chemistry</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D001955" MajorTopicYN="N">British Columbia</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D002599" MajorTopicYN="N">Chalcone</DescriptorName><QualifierName UI="Q000031" MajorTopicYN="N">analogs & derivatives</QualifierName><QualifierName UI="Q000032" MajorTopicYN="N">analysis</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D047188" MajorTopicYN="N">Chalcones</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D002934" MajorTopicYN="N">Cinnamates</DescriptorName><QualifierName UI="Q000032" MajorTopicYN="N">analysis</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D003373" MajorTopicYN="N">Coumaric Acids</DescriptorName><QualifierName UI="Q000032" 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MajorTopicYN="N">Propolis</DescriptorName><QualifierName UI="Q000032" MajorTopicYN="Y">analysis</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D011792" MajorTopicYN="N">Quebec</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D014197" MajorTopicYN="N">Trees</DescriptorName></MeshHeading></MeshHeadingList></MedlineCitation><PubmedData><History><PubMedPubDate PubStatus="pubmed"><Year>2006</Year><Month>7</Month><Day>13</Day><Hour>9</Hour><Minute>0</Minute></PubMedPubDate><PubMedPubDate PubStatus="medline"><Year>2006</Year><Month>8</Month><Day>30</Day><Hour>9</Hour><Minute>0</Minute></PubMedPubDate><PubMedPubDate PubStatus="entrez"><Year>2006</Year><Month>7</Month><Day>13</Day><Hour>9</Hour><Minute>0</Minute></PubMedPubDate></History><PublicationStatus>ppublish</PublicationStatus><ArticleIdList><ArticleId IdType="pubmed">16835083</ArticleId><ArticleId IdType="pii">P61025R72024QMP7</ArticleId><ArticleId IdType="doi">10.1080/14786410500056918</ArticleId></ArticleIdList></PubmedData></pubmed><affiliations><list><country><li>Canada</li></country></list><tree><noCountry><name sortKey="Bankova, Vassya" sort="Bankova, Vassya" uniqKey="Bankova V" first="Vassya" last="Bankova">Vassya Bankova</name><name sortKey="Bertrand, Michel" sort="Bertrand, Michel" uniqKey="Bertrand M" first="Michel" last="Bertrand">Michel Bertrand</name><name sortKey="Popova, Milena" sort="Popova, Milena" uniqKey="Popova M" first="Milena" last="Popova">Milena Popova</name><name sortKey="Trusheva, Boryana" sort="Trusheva, Boryana" uniqKey="Trusheva B" first="Boryana" last="Trusheva">Boryana Trusheva</name></noCountry><country name="Canada"><noRegion><name sortKey="Christov, Roumen" sort="Christov, Roumen" uniqKey="Christov R" first="Roumen" last="Christov">Roumen Christov</name></noRegion></country></tree></affiliations></record>Pour manipuler ce document sous Unix (Dilib)
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