A new lignan glycoside and phenylethanoid glycosides from Strobilanthes cusia BREMEK.
Identifieur interne : 002B30 ( PubMed/Corpus ); précédent : 002B29; suivant : 002B31A new lignan glycoside and phenylethanoid glycosides from Strobilanthes cusia BREMEK.
Auteurs : Tomonori Tanaka ; Tsuyoshi Ikeda ; Miho Kaku ; Xing-Hua Zhu ; Masafumi Okawa ; Kazumi Yokomizo ; Masaru Uyeda ; Toshihiro NoharaSource :
- Chemical & pharmaceutical bulletin [ 0009-2363 ] ; 2004.
English descriptors
- KwdEn :
- Acanthaceae, Animals, Antiviral Agents (chemistry), Antiviral Agents (isolation & purification), Antiviral Agents (pharmacology), Chlorocebus aethiops, Drugs, Chinese Herbal (chemistry), Drugs, Chinese Herbal (isolation & purification), Drugs, Chinese Herbal (pharmacology), Glycosides (chemistry), Glycosides (isolation & purification), Glycosides (pharmacology), Herpesvirus 1, Human (drug effects), Lignans (chemistry), Lignans (isolation & purification), Lignans (pharmacology), Magnetic Resonance Spectroscopy, Phenylpropionates (chemistry), Phenylpropionates (isolation & purification), Phenylpropionates (pharmacology), Plant Roots, Stereoisomerism, Vero Cells.
- MESH :
- chemical , chemistry : Antiviral Agents, Drugs, Chinese Herbal, Glycosides, Lignans, Phenylpropionates.
- chemical , isolation & purification : Antiviral Agents, Drugs, Chinese Herbal, Glycosides, Lignans, Phenylpropionates.
- chemical , pharmacology : Antiviral Agents, Drugs, Chinese Herbal, Glycosides, Lignans, Phenylpropionates.
- drug effects : Herpesvirus 1, Human.
- Acanthaceae, Animals, Chlorocebus aethiops, Magnetic Resonance Spectroscopy, Plant Roots, Stereoisomerism, Vero Cells.
Abstract
The root of Strobilanthes cusia BREMEK. (Acanthaceae), popularly known as Da-Ching-Yeh, has been commonly used in traditional Chinese medicine. It is used to treat influenza, epidemic cerebrospinal meningitis, encephalitis B, viral pneumonia, mumps, and severe acute respiratory syndrome (SARS). In this study, we found a new lignan glycoside (6) and two new phenylethanoid glycosides (7, 8) together with five known compounds as chemical constituents of Strobilanthes cusia root. Some samples were examined for anti-herpes simplex virus type-1 (HSV-1) activity. Among the tested samples, lupeol showed anti-HSV-1 activity (EC(50): 11.7 microM) and showed 100% inhibition of virus plaque formation at 58.7 microM.
DOI: 10.1248/cpb.52.1242
PubMed: 15467245
Links to Exploration step
pubmed:15467245Le document en format XML
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sortKey="Yokomizo, Kazumi" sort="Yokomizo, Kazumi" uniqKey="Yokomizo K" first="Kazumi" last="Yokomizo">Kazumi Yokomizo</name></author><author><name sortKey="Uyeda, Masaru" sort="Uyeda, Masaru" uniqKey="Uyeda M" first="Masaru" last="Uyeda">Masaru Uyeda</name></author><author><name sortKey="Nohara, Toshihiro" sort="Nohara, Toshihiro" uniqKey="Nohara T" first="Toshihiro" last="Nohara">Toshihiro Nohara</name></author></titleStmt><publicationStmt><idno type="wicri:source">PubMed</idno><date when="2004">2004</date><idno type="RBID">pubmed:15467245</idno><idno type="pmid">15467245</idno><idno type="doi">10.1248/cpb.52.1242</idno><idno type="wicri:Area/PubMed/Corpus">002B30</idno><idno type="wicri:explorRef" wicri:stream="PubMed" wicri:step="Corpus" wicri:corpus="PubMed">002B30</idno></publicationStmt><sourceDesc><biblStruct><analytic><title xml:lang="en">A new lignan glycoside and phenylethanoid glycosides from Strobilanthes cusia BREMEK.</title><author><name sortKey="Tanaka, Tomonori" sort="Tanaka, Tomonori" uniqKey="Tanaka T" first="Tomonori" last="Tanaka">Tomonori Tanaka</name><affiliation><nlm:affiliation>Faculty of Medical and Pharmaceutical Sciences, Kumamoto University, Kumamoto, Japan.</nlm:affiliation></affiliation></author><author><name sortKey="Ikeda, Tsuyoshi" sort="Ikeda, Tsuyoshi" uniqKey="Ikeda T" first="Tsuyoshi" last="Ikeda">Tsuyoshi Ikeda</name></author><author><name sortKey="Kaku, Miho" sort="Kaku, Miho" uniqKey="Kaku M" first="Miho" last="Kaku">Miho Kaku</name></author><author><name sortKey="Zhu, Xing Hua" sort="Zhu, Xing Hua" uniqKey="Zhu X" first="Xing-Hua" last="Zhu">Xing-Hua Zhu</name></author><author><name sortKey="Okawa, Masafumi" sort="Okawa, Masafumi" uniqKey="Okawa M" first="Masafumi" last="Okawa">Masafumi Okawa</name></author><author><name sortKey="Yokomizo, Kazumi" sort="Yokomizo, Kazumi" uniqKey="Yokomizo K" first="Kazumi" last="Yokomizo">Kazumi Yokomizo</name></author><author><name sortKey="Uyeda, Masaru" sort="Uyeda, Masaru" uniqKey="Uyeda M" first="Masaru" last="Uyeda">Masaru Uyeda</name></author><author><name sortKey="Nohara, Toshihiro" sort="Nohara, Toshihiro" uniqKey="Nohara T" first="Toshihiro" last="Nohara">Toshihiro Nohara</name></author></analytic><series><title level="j">Chemical & pharmaceutical bulletin</title><idno type="ISSN">0009-2363</idno><imprint><date when="2004" type="published">2004</date></imprint></series></biblStruct></sourceDesc></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Acanthaceae</term><term>Animals</term><term>Antiviral Agents (chemistry)</term><term>Antiviral Agents (isolation & purification)</term><term>Antiviral Agents (pharmacology)</term><term>Chlorocebus aethiops</term><term>Drugs, Chinese Herbal (chemistry)</term><term>Drugs, Chinese Herbal (isolation & purification)</term><term>Drugs, Chinese Herbal (pharmacology)</term><term>Glycosides (chemistry)</term><term>Glycosides (isolation & purification)</term><term>Glycosides (pharmacology)</term><term>Herpesvirus 1, Human (drug effects)</term><term>Lignans (chemistry)</term><term>Lignans (isolation & purification)</term><term>Lignans (pharmacology)</term><term>Magnetic Resonance Spectroscopy</term><term>Phenylpropionates (chemistry)</term><term>Phenylpropionates (isolation & purification)</term><term>Phenylpropionates (pharmacology)</term><term>Plant Roots</term><term>Stereoisomerism</term><term>Vero Cells</term></keywords><keywords scheme="MESH" type="chemical" qualifier="chemistry" xml:lang="en"><term>Antiviral Agents</term><term>Drugs, Chinese Herbal</term><term>Glycosides</term><term>Lignans</term><term>Phenylpropionates</term></keywords><keywords scheme="MESH" type="chemical" qualifier="isolation & purification" xml:lang="en"><term>Antiviral Agents</term><term>Drugs, Chinese Herbal</term><term>Glycosides</term><term>Lignans</term><term>Phenylpropionates</term></keywords><keywords scheme="MESH" type="chemical" qualifier="pharmacology" xml:lang="en"><term>Antiviral Agents</term><term>Drugs, Chinese Herbal</term><term>Glycosides</term><term>Lignans</term><term>Phenylpropionates</term></keywords><keywords scheme="MESH" qualifier="drug effects" xml:lang="en"><term>Herpesvirus 1, Human</term></keywords><keywords scheme="MESH" xml:lang="en"><term>Acanthaceae</term><term>Animals</term><term>Chlorocebus aethiops</term><term>Magnetic Resonance Spectroscopy</term><term>Plant Roots</term><term>Stereoisomerism</term><term>Vero Cells</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">The root of Strobilanthes cusia BREMEK. (Acanthaceae), popularly known as Da-Ching-Yeh, has been commonly used in traditional Chinese medicine. It is used to treat influenza, epidemic cerebrospinal meningitis, encephalitis B, viral pneumonia, mumps, and severe acute respiratory syndrome (SARS). In this study, we found a new lignan glycoside (6) and two new phenylethanoid glycosides (7, 8) together with five known compounds as chemical constituents of Strobilanthes cusia root. Some samples were examined for anti-herpes simplex virus type-1 (HSV-1) activity. Among the tested samples, lupeol showed anti-HSV-1 activity (EC(50): 11.7 microM) and showed 100% inhibition of virus plaque formation at 58.7 microM.</div></front></TEI><pubmed><MedlineCitation Status="MEDLINE" Owner="NLM"><PMID Version="1">15467245</PMID><DateCompleted><Year>2005</Year><Month>02</Month><Day>25</Day></DateCompleted><DateRevised><Year>2019</Year><Month>12</Month><Day>10</Day></DateRevised><Article PubModel="Print"><Journal><ISSN IssnType="Print">0009-2363</ISSN><JournalIssue CitedMedium="Print"><Volume>52</Volume><Issue>10</Issue><PubDate><Year>2004</Year><Month>Oct</Month></PubDate></JournalIssue><Title>Chemical & pharmaceutical bulletin</Title><ISOAbbreviation>Chem. Pharm. Bull.</ISOAbbreviation></Journal><ArticleTitle>A new lignan glycoside and phenylethanoid glycosides from Strobilanthes cusia BREMEK.</ArticleTitle><Pagination><MedlinePgn>1242-5</MedlinePgn></Pagination><Abstract><AbstractText>The root of Strobilanthes cusia BREMEK. (Acanthaceae), popularly known as Da-Ching-Yeh, has been commonly used in traditional Chinese medicine. It is used to treat influenza, epidemic cerebrospinal meningitis, encephalitis B, viral pneumonia, mumps, and severe acute respiratory syndrome (SARS). In this study, we found a new lignan glycoside (6) and two new phenylethanoid glycosides (7, 8) together with five known compounds as chemical constituents of Strobilanthes cusia root. Some samples were examined for anti-herpes simplex virus type-1 (HSV-1) activity. Among the tested samples, lupeol showed anti-HSV-1 activity (EC(50): 11.7 microM) and showed 100% inhibition of virus plaque formation at 58.7 microM.</AbstractText></Abstract><AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Tanaka</LastName><ForeName>Tomonori</ForeName><Initials>T</Initials><AffiliationInfo><Affiliation>Faculty of Medical and Pharmaceutical Sciences, Kumamoto University, Kumamoto, Japan.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Ikeda</LastName><ForeName>Tsuyoshi</ForeName><Initials>T</Initials></Author><Author ValidYN="Y"><LastName>Kaku</LastName><ForeName>Miho</ForeName><Initials>M</Initials></Author><Author ValidYN="Y"><LastName>Zhu</LastName><ForeName>Xing-Hua</ForeName><Initials>XH</Initials></Author><Author ValidYN="Y"><LastName>Okawa</LastName><ForeName>Masafumi</ForeName><Initials>M</Initials></Author><Author ValidYN="Y"><LastName>Yokomizo</LastName><ForeName>Kazumi</ForeName><Initials>K</Initials></Author><Author ValidYN="Y"><LastName>Uyeda</LastName><ForeName>Masaru</ForeName><Initials>M</Initials></Author><Author ValidYN="Y"><LastName>Nohara</LastName><ForeName>Toshihiro</ForeName><Initials>T</Initials></Author></AuthorList><Language>eng</Language><PublicationTypeList><PublicationType UI="D016428">Journal Article</PublicationType></PublicationTypeList></Article><MedlineJournalInfo><Country>Japan</Country><MedlineTA>Chem Pharm Bull (Tokyo)</MedlineTA><NlmUniqueID>0377775</NlmUniqueID><ISSNLinking>0009-2363</ISSNLinking></MedlineJournalInfo><ChemicalList><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance UI="D000998">Antiviral Agents</NameOfSubstance></Chemical><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance UI="D004365">Drugs, Chinese Herbal</NameOfSubstance></Chemical><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance UI="D006027">Glycosides</NameOfSubstance></Chemical><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance 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