Trichothecrotocins A-C, Antiphytopathogenic Agents from Potato Endophytic Fungus Trichothecium crotocinigenum.
Identifieur interne : 000625 ( Main/Exploration ); précédent : 000624; suivant : 000626Trichothecrotocins A-C, Antiphytopathogenic Agents from Potato Endophytic Fungus Trichothecium crotocinigenum.
Auteurs : Hui-Xiang Yang [République populaire de Chine] ; Hong-Lian Ai [République populaire de Chine] ; Tao Feng [République populaire de Chine] ; Wen-Xuan Wang [République populaire de Chine] ; Bin Wu [République populaire de Chine] ; Yong-Sheng Zheng [République populaire de Chine] ; Huan Sun [République populaire de Chine] ; Juan He [République populaire de Chine] ; Zheng-Hui Li [République populaire de Chine] ; Ji-Kai Liu [République populaire de Chine]Source :
- Organic letters [ 1523-7052 ] ; 2018.
Descripteurs français
- KwdFr :
- Alternaria (effets des médicaments et des substances chimiques), Antifongiques (composition chimique), Antifongiques (isolement et purification), Antifongiques (pharmacologie), Ascomycota (composition chimique), Conformation moléculaire (MeSH), Fongicides industriels (composition chimique), Fongicides industriels (isolement et purification), Fongicides industriels (pharmacologie), Fusarium (effets des médicaments et des substances chimiques), Phytophthora infestans (effets des médicaments et des substances chimiques), Relation dose-effet des médicaments (MeSH), Relation structure-activité (MeSH), Rhizoctonia (effets des médicaments et des substances chimiques), Tests de sensibilité microbienne (MeSH).
- MESH :
- composition chimique : Antifongiques, Ascomycota, Fongicides industriels.
- effets des médicaments et des substances chimiques : Alternaria, Fusarium, Phytophthora infestans, Rhizoctonia.
- isolement et purification : Antifongiques, Fongicides industriels.
- pharmacologie : Antifongiques, Fongicides industriels.
- Conformation moléculaire, Relation dose-effet des médicaments, Relation structure-activité, Tests de sensibilité microbienne.
English descriptors
- KwdEn :
- Alternaria (drug effects), Antifungal Agents (chemistry), Antifungal Agents (isolation & purification), Antifungal Agents (pharmacology), Ascomycota (chemistry), Dose-Response Relationship, Drug (MeSH), Fungicides, Industrial (chemistry), Fungicides, Industrial (isolation & purification), Fungicides, Industrial (pharmacology), Fusarium (drug effects), Microbial Sensitivity Tests (MeSH), Molecular Conformation (MeSH), Phytophthora infestans (drug effects), Rhizoctonia (drug effects), Structure-Activity Relationship (MeSH).
- MESH :
- chemical , chemistry : Antifungal Agents, Fungicides, Industrial.
- chemistry : Ascomycota.
- drug effects : Alternaria, Fusarium, Phytophthora infestans, Rhizoctonia.
- chemical , isolation & purification : Antifungal Agents, Fungicides, Industrial.
- chemical , pharmacology : Antifungal Agents, Fungicides, Industrial.
- Dose-Response Relationship, Drug, Microbial Sensitivity Tests, Molecular Conformation, Structure-Activity Relationship.
Abstract
Two trichothecene sesquiterpenoids, trichothecrotocins A (1) and B (2), and a merosesquiterpenoid racemate, (±)-trichothecrotocin C (3), were obtained from potato endophytic fungus Trichothecium crotocinigenum by bioguided isolation. Their structures were elucidated by extensive spectroscopic methods, electronic circular dichroism calculations, and single-crystal X-ray diffraction. Compounds 1 and 2 are trichothecenes possessing new ring systems. Compound 3 possesses a novel 6/6-5/5/5 fused ring system. Compounds 1-3 showed antiphytopathogenic activities with MIC values of 8-128 μg/mL.
DOI: 10.1021/acs.orglett.8b03735
PubMed: 30540193
Affiliations:
Links toward previous steps (curation, corpus...)
Le document en format XML
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<term>Antifungal Agents (pharmacology)</term>
<term>Ascomycota (chemistry)</term>
<term>Dose-Response Relationship, Drug (MeSH)</term>
<term>Fungicides, Industrial (chemistry)</term>
<term>Fungicides, Industrial (isolation & purification)</term>
<term>Fungicides, Industrial (pharmacology)</term>
<term>Fusarium (drug effects)</term>
<term>Microbial Sensitivity Tests (MeSH)</term>
<term>Molecular Conformation (MeSH)</term>
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<term>Antifongiques (pharmacologie)</term>
<term>Ascomycota (composition chimique)</term>
<term>Conformation moléculaire (MeSH)</term>
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<term>Fongicides industriels (isolement et purification)</term>
<term>Fongicides industriels (pharmacologie)</term>
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<term>Phytophthora infestans (effets des médicaments et des substances chimiques)</term>
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<front><div type="abstract" xml:lang="en">Two trichothecene sesquiterpenoids, trichothecrotocins A (1) and B (2), and a merosesquiterpenoid racemate, (±)-trichothecrotocin C (3), were obtained from potato endophytic fungus Trichothecium crotocinigenum by bioguided isolation. Their structures were elucidated by extensive spectroscopic methods, electronic circular dichroism calculations, and single-crystal X-ray diffraction. Compounds 1 and 2 are trichothecenes possessing new ring systems. Compound 3 possesses a novel 6/6-5/5/5 fused ring system. Compounds 1-3 showed antiphytopathogenic activities with MIC values of 8-128 μg/mL.</div>
</front>
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<DateCompleted><Year>2019</Year>
<Month>07</Month>
<Day>15</Day>
</DateCompleted>
<DateRevised><Year>2019</Year>
<Month>07</Month>
<Day>15</Day>
</DateRevised>
<Article PubModel="Print-Electronic"><Journal><ISSN IssnType="Electronic">1523-7052</ISSN>
<JournalIssue CitedMedium="Internet"><Volume>20</Volume>
<Issue>24</Issue>
<PubDate><Year>2018</Year>
<Month>12</Month>
<Day>21</Day>
</PubDate>
</JournalIssue>
<Title>Organic letters</Title>
<ISOAbbreviation>Org Lett</ISOAbbreviation>
</Journal>
<ArticleTitle>Trichothecrotocins A-C, Antiphytopathogenic Agents from Potato Endophytic Fungus Trichothecium crotocinigenum.</ArticleTitle>
<Pagination><MedlinePgn>8069-8072</MedlinePgn>
</Pagination>
<ELocationID EIdType="doi" ValidYN="Y">10.1021/acs.orglett.8b03735</ELocationID>
<Abstract><AbstractText>Two trichothecene sesquiterpenoids, trichothecrotocins A (1) and B (2), and a merosesquiterpenoid racemate, (±)-trichothecrotocin C (3), were obtained from potato endophytic fungus Trichothecium crotocinigenum by bioguided isolation. Their structures were elucidated by extensive spectroscopic methods, electronic circular dichroism calculations, and single-crystal X-ray diffraction. Compounds 1 and 2 are trichothecenes possessing new ring systems. Compound 3 possesses a novel 6/6-5/5/5 fused ring system. Compounds 1-3 showed antiphytopathogenic activities with MIC values of 8-128 μg/mL.</AbstractText>
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<AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Yang</LastName>
<ForeName>Hui-Xiang</ForeName>
<Initials>HX</Initials>
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</AffiliationInfo>
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<Author ValidYN="Y"><LastName>Ai</LastName>
<ForeName>Hong-Lian</ForeName>
<Initials>HL</Initials>
<AffiliationInfo><Affiliation>School of Pharmaceutical Sciences , South-Central University for Nationalities , Wuhan 430074 , China.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Feng</LastName>
<ForeName>Tao</ForeName>
<Initials>T</Initials>
<Identifier Source="ORCID">0000-0002-1977-9857</Identifier>
<AffiliationInfo><Affiliation>School of Pharmaceutical Sciences , South-Central University for Nationalities , Wuhan 430074 , China.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Wang</LastName>
<ForeName>Wen-Xuan</ForeName>
<Initials>WX</Initials>
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</AffiliationInfo>
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<Author ValidYN="Y"><LastName>Wu</LastName>
<ForeName>Bin</ForeName>
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</AffiliationInfo>
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<Author ValidYN="Y"><LastName>Zheng</LastName>
<ForeName>Yong-Sheng</ForeName>
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<AffiliationInfo><Affiliation>School of Pharmaceutical Sciences , South-Central University for Nationalities , Wuhan 430074 , China.</Affiliation>
</AffiliationInfo>
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<Author ValidYN="Y"><LastName>Sun</LastName>
<ForeName>Huan</ForeName>
<Initials>H</Initials>
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</AffiliationInfo>
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<Author ValidYN="Y"><LastName>He</LastName>
<ForeName>Juan</ForeName>
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<ForeName>Zheng-Hui</ForeName>
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<ForeName>Ji-Kai</ForeName>
<Initials>JK</Initials>
<Identifier Source="ORCID">0000-0001-6279-7893</Identifier>
<AffiliationInfo><Affiliation>School of Pharmaceutical Sciences , South-Central University for Nationalities , Wuhan 430074 , China.</Affiliation>
</AffiliationInfo>
</Author>
</AuthorList>
<Language>eng</Language>
<PublicationTypeList><PublicationType UI="D016428">Journal Article</PublicationType>
<PublicationType UI="D013485">Research Support, Non-U.S. Gov't</PublicationType>
</PublicationTypeList>
<ArticleDate DateType="Electronic"><Year>2018</Year>
<Month>12</Month>
<Day>12</Day>
</ArticleDate>
</Article>
<MedlineJournalInfo><Country>United States</Country>
<MedlineTA>Org Lett</MedlineTA>
<NlmUniqueID>100890393</NlmUniqueID>
<ISSNLinking>1523-7052</ISSNLinking>
</MedlineJournalInfo>
<ChemicalList><Chemical><RegistryNumber>0</RegistryNumber>
<NameOfSubstance UI="D000935">Antifungal Agents</NameOfSubstance>
</Chemical>
<Chemical><RegistryNumber>0</RegistryNumber>
<NameOfSubstance UI="D005659">Fungicides, Industrial</NameOfSubstance>
</Chemical>
</ChemicalList>
<CitationSubset>IM</CitationSubset>
<MeshHeadingList><MeshHeading><DescriptorName UI="D000528" MajorTopicYN="N">Alternaria</DescriptorName>
<QualifierName UI="Q000187" MajorTopicYN="N">drug effects</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D000935" MajorTopicYN="N">Antifungal Agents</DescriptorName>
<QualifierName UI="Q000737" MajorTopicYN="N">chemistry</QualifierName>
<QualifierName UI="Q000302" MajorTopicYN="N">isolation & purification</QualifierName>
<QualifierName UI="Q000494" MajorTopicYN="Y">pharmacology</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D001203" MajorTopicYN="N">Ascomycota</DescriptorName>
<QualifierName UI="Q000737" MajorTopicYN="Y">chemistry</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D004305" MajorTopicYN="N">Dose-Response Relationship, Drug</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D005659" MajorTopicYN="N">Fungicides, Industrial</DescriptorName>
<QualifierName UI="Q000737" MajorTopicYN="N">chemistry</QualifierName>
<QualifierName UI="Q000302" MajorTopicYN="N">isolation & purification</QualifierName>
<QualifierName UI="Q000494" MajorTopicYN="Y">pharmacology</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D005670" MajorTopicYN="N">Fusarium</DescriptorName>
<QualifierName UI="Q000187" MajorTopicYN="N">drug effects</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D008826" MajorTopicYN="N">Microbial Sensitivity Tests</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D008968" MajorTopicYN="N">Molecular Conformation</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D055750" MajorTopicYN="N">Phytophthora infestans</DescriptorName>
<QualifierName UI="Q000187" MajorTopicYN="N">drug effects</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D012232" MajorTopicYN="N">Rhizoctonia</DescriptorName>
<QualifierName UI="Q000187" MajorTopicYN="N">drug effects</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D013329" MajorTopicYN="N">Structure-Activity Relationship</DescriptorName>
</MeshHeading>
</MeshHeadingList>
</MedlineCitation>
<PubmedData><History><PubMedPubDate PubStatus="pubmed"><Year>2018</Year>
<Month>12</Month>
<Day>13</Day>
<Hour>6</Hour>
<Minute>0</Minute>
</PubMedPubDate>
<PubMedPubDate PubStatus="medline"><Year>2019</Year>
<Month>7</Month>
<Day>16</Day>
<Hour>6</Hour>
<Minute>0</Minute>
</PubMedPubDate>
<PubMedPubDate PubStatus="entrez"><Year>2018</Year>
<Month>12</Month>
<Day>13</Day>
<Hour>6</Hour>
<Minute>0</Minute>
</PubMedPubDate>
</History>
<PublicationStatus>ppublish</PublicationStatus>
<ArticleIdList><ArticleId IdType="pubmed">30540193</ArticleId>
<ArticleId IdType="doi">10.1021/acs.orglett.8b03735</ArticleId>
</ArticleIdList>
</PubmedData>
</pubmed>
<affiliations><list><country><li>République populaire de Chine</li>
</country>
</list>
<tree><country name="République populaire de Chine"><noRegion><name sortKey="Yang, Hui Xiang" sort="Yang, Hui Xiang" uniqKey="Yang H" first="Hui-Xiang" last="Yang">Hui-Xiang Yang</name>
</noRegion>
<name sortKey="Ai, Hong Lian" sort="Ai, Hong Lian" uniqKey="Ai H" first="Hong-Lian" last="Ai">Hong-Lian Ai</name>
<name sortKey="Feng, Tao" sort="Feng, Tao" uniqKey="Feng T" first="Tao" last="Feng">Tao Feng</name>
<name sortKey="He, Juan" sort="He, Juan" uniqKey="He J" first="Juan" last="He">Juan He</name>
<name sortKey="Li, Zheng Hui" sort="Li, Zheng Hui" uniqKey="Li Z" first="Zheng-Hui" last="Li">Zheng-Hui Li</name>
<name sortKey="Liu, Ji Kai" sort="Liu, Ji Kai" uniqKey="Liu J" first="Ji-Kai" last="Liu">Ji-Kai Liu</name>
<name sortKey="Sun, Huan" sort="Sun, Huan" uniqKey="Sun H" first="Huan" last="Sun">Huan Sun</name>
<name sortKey="Wang, Wen Xuan" sort="Wang, Wen Xuan" uniqKey="Wang W" first="Wen-Xuan" last="Wang">Wen-Xuan Wang</name>
<name sortKey="Wu, Bin" sort="Wu, Bin" uniqKey="Wu B" first="Bin" last="Wu">Bin Wu</name>
<name sortKey="Zheng, Yong Sheng" sort="Zheng, Yong Sheng" uniqKey="Zheng Y" first="Yong-Sheng" last="Zheng">Yong-Sheng Zheng</name>
</country>
</tree>
</affiliations>
</record>
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