WillowV1, Main, Corpus, bibRecord, 001449

9,10-seco-9,19-cyclolanostane triterpene from Salix caprea L. (goat willow).

Identifieur interne : 001449 ( Main/Corpus ); précédent : 001448; suivant : 001450

9,10-seco-9,19-cyclolanostane triterpene from Salix caprea L. (goat willow).

Auteurs : Mudasir A. Tantry ; Saba Shah ; Mohammad Y. Dar ; Mohammad M. Mir ; Khalid Ghazanfar ; Faheem A. Sheikh ; Mohammad A. Khuroo ; Seema Akbar

Source :

Natural product research [ 1478-6427 ] ; 2013.

RBID : pubmed:22401597

English descriptors

KwdEn :
- Chloroform (MeSH), Chromatography (MeSH), Flowers (chemistry), Magnetic Resonance Spectroscopy (MeSH), Microbial Sensitivity Tests (MeSH), Molecular Structure (MeSH), Plant Extracts (analysis), Plant Extracts (isolation & purification), Plant Extracts (pharmacology), Plasmodium falciparum (drug effects), Salix (chemistry), Triterpenes (analysis), Triterpenes (isolation & purification), Triterpenes (pharmacology).
MESH :
- chemical , analysis : Plant Extracts, Triterpenes.
- chemical , isolation & purification : Plant Extracts, Triterpenes.
- chemical , pharmacology : Plant Extracts, Triterpenes.
- chemical : Chloroform.
- chemistry : Flowers, Salix.
- drug effects : Plasmodium falciparum.
- Chromatography, Magnetic Resonance Spectroscopy, Microbial Sensitivity Tests, Molecular Structure.

Abstract

Chemical investigation of low polar solvent extract of Salix caprea through chromatographic techniques led to the isolation of new triterpene as 1α,3β,25-trihydroxy-9(11)-ene-16-one-9,10-seco-9,19-cyclolanostane (1) along with fatty alcohols. The structure of compound 1 was established by IR, HRESI/MS and NMR including 1D and 2D experiments. The compound 1 showed moderate in vitro antiplasmodial activity.

DOI: 10.1080/14786419.2012.665912
PubMed: 22401597

Links to Exploration step

pubmed:22401597

Le document en format XML

<record><TEI><teiHeader><fileDesc><titleStmt><title xml:lang="en">9,10-seco-9,19-cyclolanostane triterpene from Salix caprea L. (goat willow).</title>
<author><name sortKey="Tantry, Mudasir A" sort="Tantry, Mudasir A" uniqKey="Tantry M" first="Mudasir A" last="Tantry">Mudasir A. Tantry</name>
<affiliation><nlm:affiliation>National Center for Natural Products Research, Research Institute of Pharmaceutical Sciences, School of Pharmacy, The University of Mississippi, University, MS 38677, USA. mtantry@olemiss.edu</nlm:affiliation>
</affiliation>
</author>
<author><name sortKey="Shah, Saba" sort="Shah, Saba" uniqKey="Shah S" first="Saba" last="Shah">Saba Shah</name>
</author>
<author><name sortKey="Dar, Mohammad Y" sort="Dar, Mohammad Y" uniqKey="Dar M" first="Mohammad Y" last="Dar">Mohammad Y. Dar</name>
</author>
<author><name sortKey="Mir, Mohammad M" sort="Mir, Mohammad M" uniqKey="Mir M" first="Mohammad M" last="Mir">Mohammad M. Mir</name>
</author>
<author><name sortKey="Ghazanfar, Khalid" sort="Ghazanfar, Khalid" uniqKey="Ghazanfar K" first="Khalid" last="Ghazanfar">Khalid Ghazanfar</name>
</author>
<author><name sortKey="Sheikh, Faheem A" sort="Sheikh, Faheem A" uniqKey="Sheikh F" first="Faheem A" last="Sheikh">Faheem A. Sheikh</name>
</author>
<author><name sortKey="Khuroo, Mohammad A" sort="Khuroo, Mohammad A" uniqKey="Khuroo M" first="Mohammad A" last="Khuroo">Mohammad A. Khuroo</name>
</author>
<author><name sortKey="Akbar, Seema" sort="Akbar, Seema" uniqKey="Akbar S" first="Seema" last="Akbar">Seema Akbar</name>
</author>
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<publicationStmt><idno type="wicri:source">PubMed</idno>
<date when="2013">2013</date>
<idno type="RBID">pubmed:22401597</idno>
<idno type="pmid">22401597</idno>
<idno type="doi">10.1080/14786419.2012.665912</idno>
<idno type="wicri:Area/Main/Corpus">001449</idno>
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<sourceDesc><biblStruct><analytic><title xml:lang="en">9,10-seco-9,19-cyclolanostane triterpene from Salix caprea L. (goat willow).</title>
<author><name sortKey="Tantry, Mudasir A" sort="Tantry, Mudasir A" uniqKey="Tantry M" first="Mudasir A" last="Tantry">Mudasir A. Tantry</name>
<affiliation><nlm:affiliation>National Center for Natural Products Research, Research Institute of Pharmaceutical Sciences, School of Pharmacy, The University of Mississippi, University, MS 38677, USA. mtantry@olemiss.edu</nlm:affiliation>
</affiliation>
</author>
<author><name sortKey="Shah, Saba" sort="Shah, Saba" uniqKey="Shah S" first="Saba" last="Shah">Saba Shah</name>
</author>
<author><name sortKey="Dar, Mohammad Y" sort="Dar, Mohammad Y" uniqKey="Dar M" first="Mohammad Y" last="Dar">Mohammad Y. Dar</name>
</author>
<author><name sortKey="Mir, Mohammad M" sort="Mir, Mohammad M" uniqKey="Mir M" first="Mohammad M" last="Mir">Mohammad M. Mir</name>
</author>
<author><name sortKey="Ghazanfar, Khalid" sort="Ghazanfar, Khalid" uniqKey="Ghazanfar K" first="Khalid" last="Ghazanfar">Khalid Ghazanfar</name>
</author>
<author><name sortKey="Sheikh, Faheem A" sort="Sheikh, Faheem A" uniqKey="Sheikh F" first="Faheem A" last="Sheikh">Faheem A. Sheikh</name>
</author>
<author><name sortKey="Khuroo, Mohammad A" sort="Khuroo, Mohammad A" uniqKey="Khuroo M" first="Mohammad A" last="Khuroo">Mohammad A. Khuroo</name>
</author>
<author><name sortKey="Akbar, Seema" sort="Akbar, Seema" uniqKey="Akbar S" first="Seema" last="Akbar">Seema Akbar</name>
</author>
</analytic>
<series><title level="j">Natural product research</title>
<idno type="eISSN">1478-6427</idno>
<imprint><date when="2013" type="published">2013</date>
</imprint>
</series>
</biblStruct>
</sourceDesc>
</fileDesc>
<profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Chloroform (MeSH)</term>
<term>Chromatography (MeSH)</term>
<term>Flowers (chemistry)</term>
<term>Magnetic Resonance Spectroscopy (MeSH)</term>
<term>Microbial Sensitivity Tests (MeSH)</term>
<term>Molecular Structure (MeSH)</term>
<term>Plant Extracts (analysis)</term>
<term>Plant Extracts (isolation & purification)</term>
<term>Plant Extracts (pharmacology)</term>
<term>Plasmodium falciparum (drug effects)</term>
<term>Salix (chemistry)</term>
<term>Triterpenes (analysis)</term>
<term>Triterpenes (isolation & purification)</term>
<term>Triterpenes (pharmacology)</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="analysis" xml:lang="en"><term>Plant Extracts</term>
<term>Triterpenes</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="isolation & purification" xml:lang="en"><term>Plant Extracts</term>
<term>Triterpenes</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="pharmacology" xml:lang="en"><term>Plant Extracts</term>
<term>Triterpenes</term>
</keywords>
<keywords scheme="MESH" type="chemical" xml:lang="en"><term>Chloroform</term>
</keywords>
<keywords scheme="MESH" qualifier="chemistry" xml:lang="en"><term>Flowers</term>
<term>Salix</term>
</keywords>
<keywords scheme="MESH" qualifier="drug effects" xml:lang="en"><term>Plasmodium falciparum</term>
</keywords>
<keywords scheme="MESH" xml:lang="en"><term>Chromatography</term>
<term>Magnetic Resonance Spectroscopy</term>
<term>Microbial Sensitivity Tests</term>
<term>Molecular Structure</term>
</keywords>
</textClass>
</profileDesc>
</teiHeader>
<front><div type="abstract" xml:lang="en">Chemical investigation of low polar solvent extract of Salix caprea through chromatographic techniques led to the isolation of new triterpene as 1α,3β,25-trihydroxy-9(11)-ene-16-one-9,10-seco-9,19-cyclolanostane (1) along with fatty alcohols. The structure of compound 1 was established by IR, HRESI/MS and NMR including 1D and 2D experiments. The compound 1 showed moderate in vitro antiplasmodial activity.</div>
</front>
</TEI>
<pubmed><MedlineCitation Status="MEDLINE" Owner="NLM"><PMID Version="1">22401597</PMID>
<DateCompleted><Year>2013</Year>
<Month>06</Month>
<Day>19</Day>
</DateCompleted>
<DateRevised><Year>2013</Year>
<Month>11</Month>
<Day>21</Day>
</DateRevised>
<Article PubModel="Print-Electronic"><Journal><ISSN IssnType="Electronic">1478-6427</ISSN>
<JournalIssue CitedMedium="Internet"><Volume>27</Volume>
<Issue>2</Issue>
<PubDate><Year>2013</Year>
</PubDate>
</JournalIssue>
<Title>Natural product research</Title>
<ISOAbbreviation>Nat Prod Res</ISOAbbreviation>
</Journal>
<ArticleTitle>9,10-seco-9,19-cyclolanostane triterpene from Salix caprea L. (goat willow).</ArticleTitle>
<Pagination><MedlinePgn>171-5</MedlinePgn>
</Pagination>
<ELocationID EIdType="doi" ValidYN="Y">10.1080/14786419.2012.665912</ELocationID>
<Abstract><AbstractText>Chemical investigation of low polar solvent extract of Salix caprea through chromatographic techniques led to the isolation of new triterpene as 1α,3β,25-trihydroxy-9(11)-ene-16-one-9,10-seco-9,19-cyclolanostane (1) along with fatty alcohols. The structure of compound 1 was established by IR, HRESI/MS and NMR including 1D and 2D experiments. The compound 1 showed moderate in vitro antiplasmodial activity.</AbstractText>
</Abstract>
<AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Tantry</LastName>
<ForeName>Mudasir A</ForeName>
<Initials>MA</Initials>
<AffiliationInfo><Affiliation>National Center for Natural Products Research, Research Institute of Pharmaceutical Sciences, School of Pharmacy, The University of Mississippi, University, MS 38677, USA. mtantry@olemiss.edu</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Shah</LastName>
<ForeName>Saba</ForeName>
<Initials>S</Initials>
</Author>
<Author ValidYN="Y"><LastName>Dar</LastName>
<ForeName>Mohammad Y</ForeName>
<Initials>MY</Initials>
</Author>
<Author ValidYN="Y"><LastName>Mir</LastName>
<ForeName>Mohammad M</ForeName>
<Initials>MM</Initials>
</Author>
<Author ValidYN="Y"><LastName>Ghazanfar</LastName>
<ForeName>Khalid</ForeName>
<Initials>K</Initials>
</Author>
<Author ValidYN="Y"><LastName>Sheikh</LastName>
<ForeName>Faheem A</ForeName>
<Initials>FA</Initials>
</Author>
<Author ValidYN="Y"><LastName>Khuroo</LastName>
<ForeName>Mohammad A</ForeName>
<Initials>MA</Initials>
</Author>
<Author ValidYN="Y"><LastName>Akbar</LastName>
<ForeName>Seema</ForeName>
<Initials>S</Initials>
</Author>
</AuthorList>
<Language>eng</Language>
<PublicationTypeList><PublicationType UI="D016428">Journal Article</PublicationType>
<PublicationType UI="D013485">Research Support, Non-U.S. Gov't</PublicationType>
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<ArticleDate DateType="Electronic"><Year>2012</Year>
<Month>03</Month>
<Day>08</Day>
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</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="C557046">9,10-seco-9,19-cyclolanostane xyloside</NameOfSubstance>
</Chemical>
<Chemical><RegistryNumber>0</RegistryNumber>
<NameOfSubstance UI="D010936">Plant Extracts</NameOfSubstance>
</Chemical>
<Chemical><RegistryNumber>0</RegistryNumber>
<NameOfSubstance UI="D014315">Triterpenes</NameOfSubstance>
</Chemical>
<Chemical><RegistryNumber>7V31YC746X</RegistryNumber>
<NameOfSubstance UI="D002725">Chloroform</NameOfSubstance>
</Chemical>
</ChemicalList>
<CitationSubset>IM</CitationSubset>
<MeshHeadingList><MeshHeading><DescriptorName UI="D002725" MajorTopicYN="N">Chloroform</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D002845" MajorTopicYN="N">Chromatography</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D035264" MajorTopicYN="N">Flowers</DescriptorName>
<QualifierName UI="Q000737" MajorTopicYN="Y">chemistry</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D009682" MajorTopicYN="N">Magnetic Resonance Spectroscopy</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D008826" MajorTopicYN="N">Microbial Sensitivity Tests</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D015394" MajorTopicYN="N">Molecular Structure</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D010936" MajorTopicYN="N">Plant Extracts</DescriptorName>
<QualifierName UI="Q000032" MajorTopicYN="Y">analysis</QualifierName>
<QualifierName UI="Q000302" MajorTopicYN="N">isolation & purification</QualifierName>
<QualifierName UI="Q000494" MajorTopicYN="N">pharmacology</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D010963" MajorTopicYN="N">Plasmodium falciparum</DescriptorName>
<QualifierName UI="Q000187" MajorTopicYN="N">drug effects</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D032108" MajorTopicYN="N">Salix</DescriptorName>
<QualifierName UI="Q000737" MajorTopicYN="Y">chemistry</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D014315" MajorTopicYN="N">Triterpenes</DescriptorName>
<QualifierName UI="Q000032" MajorTopicYN="Y">analysis</QualifierName>
<QualifierName UI="Q000302" MajorTopicYN="N">isolation & purification</QualifierName>
<QualifierName UI="Q000494" MajorTopicYN="N">pharmacology</QualifierName>
</MeshHeading>
</MeshHeadingList>
</MedlineCitation>
<PubmedData><History><PubMedPubDate PubStatus="entrez"><Year>2012</Year>
<Month>3</Month>
<Day>10</Day>
<Hour>6</Hour>
<Minute>0</Minute>
</PubMedPubDate>
<PubMedPubDate PubStatus="pubmed"><Year>2012</Year>
<Month>3</Month>
<Day>10</Day>
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<Minute>0</Minute>
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<PubMedPubDate PubStatus="medline"><Year>2013</Year>
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<Day>20</Day>
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<PublicationStatus>ppublish</PublicationStatus>
<ArticleIdList><ArticleId IdType="pubmed">22401597</ArticleId>
<ArticleId IdType="doi">10.1080/14786419.2012.665912</ArticleId>
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9,10-seco-9,19-cyclolanostane triterpene from Salix caprea L. (goat willow).

9,10-seco-9,19-cyclolanostane triterpene from Salix caprea L. (goat willow).

Source :

English descriptors

Abstract

Links to Exploration step

Le document en format XML

Pour manipuler ce document sous Unix (Dilib)

Pour mettre un lien sur cette page dans le réseau Wicri

Pour générer des pages wiki