[Chemical constituents of Salix matsudana leaf].
Identifieur interne : 001060 ( Main/Corpus ); précédent : 001059; suivant : 001061[Chemical constituents of Salix matsudana leaf].
Auteurs : Fei-Hong Zuo ; Guo-Jiang Wu ; Jin-Jin Li ; Guo-Ping Zhou ; Hui-Zheng Fu ; Yuan-Yue LiaoSource :
- Zhong yao cai = Zhongyaocai = Journal of Chinese medicinal materials [ 1001-4454 ] ; 2013.
English descriptors
- KwdEn :
- Chromatography, High Pressure Liquid (MeSH), Drugs, Chinese Herbal (chemistry), Drugs, Chinese Herbal (isolation & purification), Glucosides (chemistry), Glucosides (isolation & purification), Luteolin (chemistry), Luteolin (isolation & purification), Molecular Structure (MeSH), Plant Leaves (chemistry), Salix (chemistry), Sitosterols (chemistry), Sitosterols (isolation & purification).
- MESH :
- chemical , chemistry : Drugs, Chinese Herbal, Glucosides, Luteolin, Sitosterols.
- chemical , isolation & purification : Drugs, Chinese Herbal, Glucosides, Luteolin, Sitosterols.
- chemistry : Plant Leaves, Salix.
- Chromatography, High Pressure Liquid, Molecular Structure.
Abstract
OBJECTIVE
To study the chemical constituents of the leaf of Salix matsudana.
METHODS
The chemical constituents were isolated by column chromatography on silica gel, Sephadex LH-20 and MPLC. Their structures were elucidated on the basis of spectral analysis.
RESULTS
Eight compounds were isolated and their structures were identified as beta-Sitosterol(1),5,7-Dihydroxychromone-7-O-beta-D-glucopyranoside(2), (2S)-Helichrysin A(3), (2R)-Helichrysin A(4), Luteolin-7-O-beta-D-glucoside(5), Salicin(6), Apigenin-7-O-beta-D-glucopyranside(7), Lutelion-3'-methylether-7-O-f-D-glucopyranside(8).
CONCLUSION
Compounds 1-4 are isolated from this plant for the first time.
PubMed: 25090681
Links to Exploration step
pubmed:25090681Le document en format XML
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Their structures were elucidated on the basis of spectral analysis.</p></div><div type="abstract" xml:lang="en"><p><b>RESULTS</b></p><p>Eight compounds were isolated and their structures were identified as beta-Sitosterol(1),5,7-Dihydroxychromone-7-O-beta-D-glucopyranoside(2), (2S)-Helichrysin A(3), (2R)-Helichrysin A(4), Luteolin-7-O-beta-D-glucoside(5), Salicin(6), Apigenin-7-O-beta-D-glucopyranside(7), Lutelion-3'-methylether-7-O-f-D-glucopyranside(8).</p></div><div type="abstract" xml:lang="en"><p><b>CONCLUSION</b></p><p>Compounds 1-4 are isolated from this plant for the first time.</p></div></front></TEI><pubmed><MedlineCitation Status="MEDLINE" Owner="NLM"><PMID Version="1">25090681</PMID><DateCompleted><Year>2014</Year><Month>12</Month><Day>22</Day></DateCompleted><DateRevised><Year>2017</Year><Month>11</Month><Day>16</Day></DateRevised><Article PubModel="Print"><Journal><ISSN IssnType="Print">1001-4454</ISSN><JournalIssue CitedMedium="Print"><Volume>36</Volume><Issue>12</Issue><PubDate><Year>2013</Year><Month>Dec</Month></PubDate></JournalIssue><Title>Zhong yao cai = Zhongyaocai = Journal of Chinese medicinal materials</Title><ISOAbbreviation>Zhong Yao Cai</ISOAbbreviation></Journal><ArticleTitle>[Chemical constituents of Salix matsudana leaf].</ArticleTitle><Pagination><MedlinePgn>1959-62</MedlinePgn></Pagination><Abstract><AbstractText Label="OBJECTIVE" NlmCategory="OBJECTIVE">To study the chemical constituents of the leaf of Salix matsudana.</AbstractText><AbstractText Label="METHODS" NlmCategory="METHODS">The chemical constituents were isolated by column chromatography on silica gel, Sephadex LH-20 and MPLC. Their structures were elucidated on the basis of spectral analysis.</AbstractText><AbstractText Label="RESULTS" NlmCategory="RESULTS">Eight compounds were isolated and their structures were identified as beta-Sitosterol(1),5,7-Dihydroxychromone-7-O-beta-D-glucopyranoside(2), (2S)-Helichrysin A(3), (2R)-Helichrysin A(4), Luteolin-7-O-beta-D-glucoside(5), Salicin(6), Apigenin-7-O-beta-D-glucopyranside(7), Lutelion-3'-methylether-7-O-f-D-glucopyranside(8).</AbstractText><AbstractText Label="CONCLUSION" NlmCategory="CONCLUSIONS">Compounds 1-4 are isolated from this plant for the first time.</AbstractText></Abstract><AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Zuo</LastName><ForeName>Fei-hong</ForeName><Initials>FH</Initials></Author><Author ValidYN="Y"><LastName>Wu</LastName><ForeName>Guo-jiang</ForeName><Initials>GJ</Initials></Author><Author ValidYN="Y"><LastName>Li</LastName><ForeName>Jin-jin</ForeName><Initials>JJ</Initials></Author><Author ValidYN="Y"><LastName>Zhou</LastName><ForeName>Guo-ping</ForeName><Initials>GP</Initials></Author><Author ValidYN="Y"><LastName>Fu</LastName><ForeName>Hui-zheng</ForeName><Initials>HZ</Initials></Author><Author ValidYN="Y"><LastName>Liao</LastName><ForeName>Yuan-yue</ForeName><Initials>YY</Initials></Author></AuthorList><Language>chi</Language><PublicationTypeList><PublicationType UI="D016428">Journal Article</PublicationType></PublicationTypeList></Article><MedlineJournalInfo><Country>China</Country><MedlineTA>Zhong Yao Cai</MedlineTA><NlmUniqueID>9426370</NlmUniqueID><ISSNLinking>1001-4454</ISSNLinking></MedlineJournalInfo><ChemicalList><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance UI="D004365">Drugs, Chinese Herbal</NameOfSubstance></Chemical><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance UI="D005960">Glucosides</NameOfSubstance></Chemical><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance UI="D012855">Sitosterols</NameOfSubstance></Chemical><Chemical><RegistryNumber>5LI01C78DD</RegistryNumber><NameOfSubstance UI="C025473">gamma-sitosterol</NameOfSubstance></Chemical><Chemical><RegistryNumber>98J6XDS46I</RegistryNumber><NameOfSubstance UI="C066408">luteolin-7-glucoside</NameOfSubstance></Chemical><Chemical><RegistryNumber>KUX1ZNC9J2</RegistryNumber><NameOfSubstance UI="D047311">Luteolin</NameOfSubstance></Chemical></ChemicalList><CitationSubset>IM</CitationSubset><MeshHeadingList><MeshHeading><DescriptorName UI="D002851" MajorTopicYN="N">Chromatography, High Pressure Liquid</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D004365" MajorTopicYN="N">Drugs, Chinese Herbal</DescriptorName><QualifierName UI="Q000737" MajorTopicYN="Y">chemistry</QualifierName><QualifierName UI="Q000302" MajorTopicYN="N">isolation & purification</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D005960" MajorTopicYN="N">Glucosides</DescriptorName><QualifierName UI="Q000737" MajorTopicYN="N">chemistry</QualifierName><QualifierName UI="Q000302" MajorTopicYN="N">isolation & purification</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D047311" MajorTopicYN="N">Luteolin</DescriptorName><QualifierName UI="Q000737" MajorTopicYN="N">chemistry</QualifierName><QualifierName UI="Q000302" MajorTopicYN="N">isolation & purification</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D015394" MajorTopicYN="N">Molecular Structure</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D018515" MajorTopicYN="N">Plant Leaves</DescriptorName><QualifierName UI="Q000737" MajorTopicYN="Y">chemistry</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D032108" MajorTopicYN="N">Salix</DescriptorName><QualifierName UI="Q000737" MajorTopicYN="Y">chemistry</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D012855" MajorTopicYN="N">Sitosterols</DescriptorName><QualifierName UI="Q000737" MajorTopicYN="N">chemistry</QualifierName><QualifierName UI="Q000302" MajorTopicYN="N">isolation & purification</QualifierName></MeshHeading></MeshHeadingList></MedlineCitation><PubmedData><History><PubMedPubDate PubStatus="entrez"><Year>2014</Year><Month>8</Month><Day>6</Day><Hour>6</Hour><Minute>0</Minute></PubMedPubDate><PubMedPubDate PubStatus="pubmed"><Year>2014</Year><Month>8</Month><Day>6</Day><Hour>6</Hour><Minute>0</Minute></PubMedPubDate><PubMedPubDate PubStatus="medline"><Year>2014</Year><Month>12</Month><Day>23</Day><Hour>6</Hour><Minute>0</Minute></PubMedPubDate></History><PublicationStatus>ppublish</PublicationStatus><ArticleIdList><ArticleId IdType="pubmed">25090681</ArticleId></ArticleIdList></PubmedData></pubmed></record>Pour manipuler ce document sous Unix (Dilib)
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