CJ-12,954 and its congeners, new anti-Helicobacter pylori compounds produced by Phanerochaete velutina: fermentation, isolation, structural elucidation and biological activities.
Identifieur interne : 000C22 ( Main/Exploration ); précédent : 000C21; suivant : 000C23CJ-12,954 and its congeners, new anti-Helicobacter pylori compounds produced by Phanerochaete velutina: fermentation, isolation, structural elucidation and biological activities.
Auteurs : K A Dekker [Japon] ; T. Inagaki ; T D Gootz ; K. Kaneda ; E. Nomura ; T. Sakakibara ; S. Sakemi ; Y. Sugie ; Y. Yamauchi ; N. Yoshikawa ; N. KojimaSource :
- The Journal of antibiotics [ 0021-8820 ] ; 1997.
Descripteurs français
- KwdFr :
- Anti-infectieux (composition chimique), Anti-infectieux (métabolisme), Anti-infectieux (pharmacologie), Antibactériens (MeSH), Basidiomycota (composition chimique), Basidiomycota (métabolisme), Benzofuranes (composition chimique), Benzofuranes (métabolisme), Benzofuranes (pharmacologie), Fermentation (MeSH), Helicobacter pylori (effets des médicaments et des substances chimiques), Relation structure-activité (MeSH), Spiranes (composition chimique), Spiranes (métabolisme), Spiranes (pharmacologie), Structure moléculaire (MeSH), Tests de sensibilité microbienne (MeSH).
- MESH :
- composition chimique : Anti-infectieux, Basidiomycota, Benzofuranes, Spiranes.
- effets des médicaments et des substances chimiques : Helicobacter pylori.
- métabolisme : Anti-infectieux, Basidiomycota, Benzofuranes, Spiranes.
- pharmacologie : Anti-infectieux, Benzofuranes, Spiranes.
- Antibactériens, Fermentation, Relation structure-activité, Structure moléculaire, Tests de sensibilité microbienne.
English descriptors
- KwdEn :
- Anti-Bacterial Agents (MeSH), Anti-Infective Agents (chemistry), Anti-Infective Agents (metabolism), Anti-Infective Agents (pharmacology), Basidiomycota (chemistry), Basidiomycota (metabolism), Benzofurans (chemistry), Benzofurans (metabolism), Benzofurans (pharmacology), Fermentation (MeSH), Helicobacter pylori (drug effects), Microbial Sensitivity Tests (MeSH), Molecular Structure (MeSH), Spiro Compounds (chemistry), Spiro Compounds (metabolism), Spiro Compounds (pharmacology), Structure-Activity Relationship (MeSH).
- MESH :
- chemical , chemistry : Anti-Infective Agents, Benzofurans, Spiro Compounds.
- chemical , metabolism : Anti-Infective Agents, Benzofurans, Spiro Compounds.
- chemical , pharmacology : Anti-Infective Agents, Benzofurans, Spiro Compounds.
- chemical : Anti-Bacterial Agents.
- chemistry : Basidiomycota.
- drug effects : Helicobacter pylori.
- metabolism : Basidiomycota.
- Fermentation, Microbial Sensitivity Tests, Molecular Structure, Structure-Activity Relationship.
Abstract
Seven new phthalide compounds with anti-Helicobacter pylori activities were isolated from the basidiomycete Phanerochaete velutina CL6387. The two most potent phthalide compounds, CJ-12,954 and CJ-13,014, have MICs of 5 ng/ml. The structure-activity relationship shows that the presence of a spiroketal part in addition to the phthalide part, greatly enhances the activity. The phthalide compounds appear to be specific for H. pylori, since they did not show antibacterial activities when tested against a panel of other microorganisms.
DOI: 10.7164/antibiotics.50.833
PubMed: 9402988
Affiliations:
Links toward previous steps (curation, corpus...)
Le document en format XML
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Inagaki</name></author><author><name sortKey="Gootz, T D" sort="Gootz, T D" uniqKey="Gootz T" first="T D" last="Gootz">T D Gootz</name></author><author><name sortKey="Kaneda, K" sort="Kaneda, K" uniqKey="Kaneda K" first="K" last="Kaneda">K. Kaneda</name></author><author><name sortKey="Nomura, E" sort="Nomura, E" uniqKey="Nomura E" first="E" last="Nomura">E. Nomura</name></author><author><name sortKey="Sakakibara, T" sort="Sakakibara, T" uniqKey="Sakakibara T" first="T" last="Sakakibara">T. Sakakibara</name></author><author><name sortKey="Sakemi, S" sort="Sakemi, S" uniqKey="Sakemi S" first="S" last="Sakemi">S. Sakemi</name></author><author><name sortKey="Sugie, Y" sort="Sugie, Y" uniqKey="Sugie Y" first="Y" last="Sugie">Y. Sugie</name></author><author><name sortKey="Yamauchi, Y" sort="Yamauchi, Y" uniqKey="Yamauchi Y" first="Y" last="Yamauchi">Y. Yamauchi</name></author><author><name sortKey="Yoshikawa, N" sort="Yoshikawa, N" uniqKey="Yoshikawa N" first="N" last="Yoshikawa">N. 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Inagaki</name></author><author><name sortKey="Gootz, T D" sort="Gootz, T D" uniqKey="Gootz T" first="T D" last="Gootz">T D Gootz</name></author><author><name sortKey="Kaneda, K" sort="Kaneda, K" uniqKey="Kaneda K" first="K" last="Kaneda">K. Kaneda</name></author><author><name sortKey="Nomura, E" sort="Nomura, E" uniqKey="Nomura E" first="E" last="Nomura">E. Nomura</name></author><author><name sortKey="Sakakibara, T" sort="Sakakibara, T" uniqKey="Sakakibara T" first="T" last="Sakakibara">T. Sakakibara</name></author><author><name sortKey="Sakemi, S" sort="Sakemi, S" uniqKey="Sakemi S" first="S" last="Sakemi">S. Sakemi</name></author><author><name sortKey="Sugie, Y" sort="Sugie, Y" uniqKey="Sugie Y" first="Y" last="Sugie">Y. Sugie</name></author><author><name sortKey="Yamauchi, Y" sort="Yamauchi, Y" uniqKey="Yamauchi Y" first="Y" last="Yamauchi">Y. Yamauchi</name></author><author><name sortKey="Yoshikawa, N" sort="Yoshikawa, N" uniqKey="Yoshikawa N" first="N" last="Yoshikawa">N. Yoshikawa</name></author><author><name sortKey="Kojima, N" sort="Kojima, N" uniqKey="Kojima N" first="N" last="Kojima">N. Kojima</name></author></analytic><series><title level="j">The Journal of antibiotics</title><idno type="ISSN">0021-8820</idno><imprint><date when="1997" type="published">1997</date></imprint></series></biblStruct></sourceDesc></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Anti-Bacterial Agents (MeSH)</term><term>Anti-Infective Agents (chemistry)</term><term>Anti-Infective Agents (metabolism)</term><term>Anti-Infective Agents (pharmacology)</term><term>Basidiomycota (chemistry)</term><term>Basidiomycota (metabolism)</term><term>Benzofurans (chemistry)</term><term>Benzofurans (metabolism)</term><term>Benzofurans (pharmacology)</term><term>Fermentation (MeSH)</term><term>Helicobacter pylori (drug effects)</term><term>Microbial Sensitivity Tests (MeSH)</term><term>Molecular Structure (MeSH)</term><term>Spiro Compounds (chemistry)</term><term>Spiro Compounds (metabolism)</term><term>Spiro Compounds (pharmacology)</term><term>Structure-Activity Relationship (MeSH)</term></keywords><keywords scheme="KwdFr" xml:lang="fr"><term>Anti-infectieux (composition chimique)</term><term>Anti-infectieux (métabolisme)</term><term>Anti-infectieux (pharmacologie)</term><term>Antibactériens (MeSH)</term><term>Basidiomycota (composition chimique)</term><term>Basidiomycota (métabolisme)</term><term>Benzofuranes (composition chimique)</term><term>Benzofuranes (métabolisme)</term><term>Benzofuranes (pharmacologie)</term><term>Fermentation (MeSH)</term><term>Helicobacter pylori (effets des médicaments et des substances chimiques)</term><term>Relation structure-activité (MeSH)</term><term>Spiranes (composition chimique)</term><term>Spiranes (métabolisme)</term><term>Spiranes (pharmacologie)</term><term>Structure moléculaire (MeSH)</term><term>Tests de sensibilité microbienne (MeSH)</term></keywords><keywords scheme="MESH" type="chemical" qualifier="chemistry" xml:lang="en"><term>Anti-Infective Agents</term><term>Benzofurans</term><term>Spiro Compounds</term></keywords><keywords scheme="MESH" type="chemical" qualifier="metabolism" xml:lang="en"><term>Anti-Infective Agents</term><term>Benzofurans</term><term>Spiro Compounds</term></keywords><keywords scheme="MESH" type="chemical" qualifier="pharmacology" xml:lang="en"><term>Anti-Infective Agents</term><term>Benzofurans</term><term>Spiro Compounds</term></keywords><keywords scheme="MESH" type="chemical" xml:lang="en"><term>Anti-Bacterial Agents</term></keywords><keywords scheme="MESH" qualifier="chemistry" xml:lang="en"><term>Basidiomycota</term></keywords><keywords scheme="MESH" qualifier="composition chimique" xml:lang="fr"><term>Anti-infectieux</term><term>Basidiomycota</term><term>Benzofuranes</term><term>Spiranes</term></keywords><keywords scheme="MESH" qualifier="drug effects" xml:lang="en"><term>Helicobacter pylori</term></keywords><keywords scheme="MESH" qualifier="effets des médicaments et des substances chimiques" xml:lang="fr"><term>Helicobacter pylori</term></keywords><keywords scheme="MESH" qualifier="metabolism" xml:lang="en"><term>Basidiomycota</term></keywords><keywords scheme="MESH" qualifier="métabolisme" xml:lang="fr"><term>Anti-infectieux</term><term>Basidiomycota</term><term>Benzofuranes</term><term>Spiranes</term></keywords><keywords scheme="MESH" qualifier="pharmacologie" xml:lang="fr"><term>Anti-infectieux</term><term>Benzofuranes</term><term>Spiranes</term></keywords><keywords scheme="MESH" xml:lang="en"><term>Fermentation</term><term>Microbial Sensitivity Tests</term><term>Molecular Structure</term><term>Structure-Activity Relationship</term></keywords><keywords scheme="MESH" xml:lang="fr"><term>Antibactériens</term><term>Fermentation</term><term>Relation structure-activité</term><term>Structure moléculaire</term><term>Tests de sensibilité microbienne</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">Seven new phthalide compounds with anti-Helicobacter pylori activities were isolated from the basidiomycete Phanerochaete velutina CL6387. The two most potent phthalide compounds, CJ-12,954 and CJ-13,014, have MICs of 5 ng/ml. The structure-activity relationship shows that the presence of a spiroketal part in addition to the phthalide part, greatly enhances the activity. The phthalide compounds appear to be specific for H. pylori, since they did not show antibacterial activities when tested against a panel of other microorganisms.</div></front></TEI><pubmed><MedlineCitation Status="MEDLINE" Owner="NLM"><PMID Version="1">9402988</PMID><DateCompleted><Year>1998</Year><Month>01</Month><Day>20</Day></DateCompleted><DateRevised><Year>2019</Year><Month>07</Month><Day>23</Day></DateRevised><Article PubModel="Print"><Journal><ISSN IssnType="Print">0021-8820</ISSN><JournalIssue CitedMedium="Print"><Volume>50</Volume><Issue>10</Issue><PubDate><Year>1997</Year><Month>Oct</Month></PubDate></JournalIssue><Title>The Journal of antibiotics</Title><ISOAbbreviation>J Antibiot (Tokyo)</ISOAbbreviation></Journal><ArticleTitle>CJ-12,954 and its congeners, new anti-Helicobacter pylori compounds produced by Phanerochaete velutina: fermentation, isolation, structural elucidation and biological activities.</ArticleTitle><Pagination><MedlinePgn>833-9</MedlinePgn></Pagination><Abstract><AbstractText>Seven new phthalide compounds with anti-Helicobacter pylori activities were isolated from the basidiomycete Phanerochaete velutina CL6387. The two most potent phthalide compounds, CJ-12,954 and CJ-13,014, have MICs of 5 ng/ml. The structure-activity relationship shows that the presence of a spiroketal part in addition to the phthalide part, greatly enhances the activity. The phthalide compounds appear to be specific for H. pylori, since they did not show antibacterial activities when tested against a panel of other microorganisms.</AbstractText></Abstract><AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Dekker</LastName><ForeName>K A</ForeName><Initials>KA</Initials><AffiliationInfo><Affiliation>Central Research Division, Pfizer Pharmaceuticals, Inc., Aichi, Japan.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Inagaki</LastName><ForeName>T</ForeName><Initials>T</Initials></Author><Author ValidYN="Y"><LastName>Gootz</LastName><ForeName>T D</ForeName><Initials>TD</Initials></Author><Author ValidYN="Y"><LastName>Kaneda</LastName><ForeName>K</ForeName><Initials>K</Initials></Author><Author ValidYN="Y"><LastName>Nomura</LastName><ForeName>E</ForeName><Initials>E</Initials></Author><Author ValidYN="Y"><LastName>Sakakibara</LastName><ForeName>T</ForeName><Initials>T</Initials></Author><Author ValidYN="Y"><LastName>Sakemi</LastName><ForeName>S</ForeName><Initials>S</Initials></Author><Author ValidYN="Y"><LastName>Sugie</LastName><ForeName>Y</ForeName><Initials>Y</Initials></Author><Author ValidYN="Y"><LastName>Yamauchi</LastName><ForeName>Y</ForeName><Initials>Y</Initials></Author><Author ValidYN="Y"><LastName>Yoshikawa</LastName><ForeName>N</ForeName><Initials>N</Initials></Author><Author ValidYN="Y"><LastName>Kojima</LastName><ForeName>N</ForeName><Initials>N</Initials></Author></AuthorList><Language>eng</Language><PublicationTypeList><PublicationType UI="D016428">Journal Article</PublicationType></PublicationTypeList></Article><MedlineJournalInfo><Country>Japan</Country><MedlineTA>J Antibiot (Tokyo)</MedlineTA><NlmUniqueID>0151115</NlmUniqueID><ISSNLinking>0021-8820</ISSNLinking></MedlineJournalInfo><ChemicalList><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance UI="D000900">Anti-Bacterial Agents</NameOfSubstance></Chemical><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance UI="D000890">Anti-Infective Agents</NameOfSubstance></Chemical><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance UI="D001572">Benzofurans</NameOfSubstance></Chemical><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance UI="C109706">CJ 12954</NameOfSubstance></Chemical><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance UI="C109705">CJ 13014</NameOfSubstance></Chemical><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance UI="D013141">Spiro Compounds</NameOfSubstance></Chemical><Chemical><RegistryNumber>8VV922U86J</RegistryNumber><NameOfSubstance UI="C082022">phthalide</NameOfSubstance></Chemical></ChemicalList><CitationSubset>IM</CitationSubset><MeshHeadingList><MeshHeading><DescriptorName UI="D000900" MajorTopicYN="N">Anti-Bacterial Agents</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D000890" MajorTopicYN="N">Anti-Infective Agents</DescriptorName><QualifierName UI="Q000737" MajorTopicYN="Y">chemistry</QualifierName><QualifierName UI="Q000378" MajorTopicYN="N">metabolism</QualifierName><QualifierName UI="Q000494" MajorTopicYN="Y">pharmacology</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D001487" MajorTopicYN="N">Basidiomycota</DescriptorName><QualifierName UI="Q000737" MajorTopicYN="N">chemistry</QualifierName><QualifierName UI="Q000378" MajorTopicYN="Y">metabolism</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D001572" MajorTopicYN="N">Benzofurans</DescriptorName><QualifierName UI="Q000737" MajorTopicYN="N">chemistry</QualifierName><QualifierName UI="Q000378" MajorTopicYN="N">metabolism</QualifierName><QualifierName UI="Q000494" MajorTopicYN="N">pharmacology</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D005285" MajorTopicYN="N">Fermentation</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D016480" MajorTopicYN="N">Helicobacter pylori</DescriptorName><QualifierName UI="Q000187" MajorTopicYN="Y">drug effects</QualifierName></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="D013141" MajorTopicYN="N">Spiro Compounds</DescriptorName><QualifierName UI="Q000737" MajorTopicYN="N">chemistry</QualifierName><QualifierName UI="Q000378" MajorTopicYN="N">metabolism</QualifierName><QualifierName UI="Q000494" MajorTopicYN="N">pharmacology</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D013329" MajorTopicYN="N">Structure-Activity Relationship</DescriptorName></MeshHeading></MeshHeadingList></MedlineCitation><PubmedData><History><PubMedPubDate PubStatus="pubmed"><Year>1997</Year><Month>12</Month><Day>24</Day></PubMedPubDate><PubMedPubDate PubStatus="medline"><Year>1997</Year><Month>12</Month><Day>24</Day><Hour>0</Hour><Minute>1</Minute></PubMedPubDate><PubMedPubDate PubStatus="entrez"><Year>1997</Year><Month>12</Month><Day>24</Day><Hour>0</Hour><Minute>0</Minute></PubMedPubDate></History><PublicationStatus>ppublish</PublicationStatus><ArticleIdList><ArticleId IdType="pubmed">9402988</ArticleId><ArticleId IdType="doi">10.7164/antibiotics.50.833</ArticleId></ArticleIdList></PubmedData></pubmed><affiliations><list><country><li>Japon</li></country></list><tree><noCountry><name sortKey="Gootz, T D" sort="Gootz, T D" uniqKey="Gootz T" first="T D" last="Gootz">T D Gootz</name><name sortKey="Inagaki, T" sort="Inagaki, T" uniqKey="Inagaki T" first="T" last="Inagaki">T. Inagaki</name><name sortKey="Kaneda, K" sort="Kaneda, K" uniqKey="Kaneda K" first="K" last="Kaneda">K. Kaneda</name><name sortKey="Kojima, N" sort="Kojima, N" uniqKey="Kojima N" first="N" last="Kojima">N. Kojima</name><name sortKey="Nomura, E" sort="Nomura, E" uniqKey="Nomura E" first="E" last="Nomura">E. Nomura</name><name sortKey="Sakakibara, T" sort="Sakakibara, T" uniqKey="Sakakibara T" first="T" last="Sakakibara">T. Sakakibara</name><name sortKey="Sakemi, S" sort="Sakemi, S" uniqKey="Sakemi S" first="S" last="Sakemi">S. Sakemi</name><name sortKey="Sugie, Y" sort="Sugie, Y" uniqKey="Sugie Y" first="Y" last="Sugie">Y. Sugie</name><name sortKey="Yamauchi, Y" sort="Yamauchi, Y" uniqKey="Yamauchi Y" first="Y" last="Yamauchi">Y. Yamauchi</name><name sortKey="Yoshikawa, N" sort="Yoshikawa, N" uniqKey="Yoshikawa N" first="N" last="Yoshikawa">N. Yoshikawa</name></noCountry><country name="Japon"><noRegion><name sortKey="Dekker, K A" sort="Dekker, K A" uniqKey="Dekker K" first="K A" last="Dekker">K A Dekker</name></noRegion></country></tree></affiliations></record>Pour manipuler ce document sous Unix (Dilib)
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