Benzopyranones from the endophytic fungus Hyalodendriella sp. Ponipodef12 and their bioactivities.
Identifieur interne : 002B87 ( Main/Exploration ); précédent : 002B86; suivant : 002B88Benzopyranones from the endophytic fungus Hyalodendriella sp. Ponipodef12 and their bioactivities.
Auteurs : Xiangjie Meng [République populaire de Chine] ; Ziling Mao ; Jingfeng Lou ; Liang Xu ; Lingyun Zhong ; Youliang Peng ; Ligang Zhou ; Mingan WangSource :
- Molecules (Basel, Switzerland) [ 1420-3049 ] ; 2012.
Descripteurs français
- KwdFr :
- Animaux (MeSH), Anti-infectieux (composition chimique), Anti-infectieux (pharmacologie), Anticholinestérasiques (pharmacologie), Antihelminthiques antinématodes (pharmacologie), Ascomycota (composition chimique), Benzopyranes (composition chimique), Benzopyranes (pharmacologie), Caenorhabditis elegans (effets des médicaments et des substances chimiques), Concentration inhibitrice 50 (MeSH), Tests de sensibilité microbienne (MeSH).
- MESH :
- composition chimique : Anti-infectieux, Ascomycota, Benzopyranes.
- effets des médicaments et des substances chimiques : Caenorhabditis elegans.
- pharmacologie : Anti-infectieux, Anticholinestérasiques, Antihelminthiques antinématodes, Benzopyranes.
- Animaux, Concentration inhibitrice 50, Tests de sensibilité microbienne.
English descriptors
- KwdEn :
- Animals (MeSH), Anti-Infective Agents (chemistry), Anti-Infective Agents (pharmacology), Antinematodal Agents (pharmacology), Ascomycota (chemistry), Benzopyrans (chemistry), Benzopyrans (pharmacology), Caenorhabditis elegans (drug effects), Cholinesterase Inhibitors (pharmacology), Inhibitory Concentration 50 (MeSH), Microbial Sensitivity Tests (MeSH).
- MESH :
- chemical , chemistry : Anti-Infective Agents, Benzopyrans.
- chemical , pharmacology : Anti-Infective Agents, Antinematodal Agents, Benzopyrans, Cholinesterase Inhibitors.
- chemistry : Ascomycota.
- drug effects : Caenorhabditis elegans.
- Animals, Inhibitory Concentration 50, Microbial Sensitivity Tests.
Abstract
The endophytic fungus Hyalodendriella sp. Ponipodef12 was isolated from the hybrid 'Neva' of Populus deltoides Marsh × P. nigra L. In this study, four benzopyranones were isolated from the ethyl acetate extract of Hyalodendriella sp. Ponipodef12, and identified as palmariol B (1), 4-hydroxymellein (2), alternariol 9-methyl ether (3), and botrallin (4) by means of physicochemical and spectroscopic analysis. All the compounds were evaluated for their antibacterial, antifungal, antinematodal and acetylcholinesterase inhibitory activities. 4-Hydroxymellein (2) exhibited stronger antibacterial activity than the other compounds. Palmariol B (1) showed stronger antimicrobial, antinematodal and acetylcholinesterase inhibitory activities than alternariol 9-methyl ether (3) which indicated that the chlorine substitution at position 2 may contribute to its bioactivity. The results indicate the potential of this endophytic fungus as a source of bioactive benzopyranones.
DOI: 10.3390/molecules171011303
PubMed: 23011274
PubMed Central: PMC6268909
Affiliations:
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Ponipodef12 and their bioactivities.</title><author><name sortKey="Meng, Xiangjie" sort="Meng, Xiangjie" uniqKey="Meng X" first="Xiangjie" last="Meng">Xiangjie Meng</name><affiliation wicri:level="1"><nlm:affiliation>College of Agronomy and Biotechnology, China Agricultural University, Beijing 100193, China. lgzhou@cau.edu.cn.</nlm:affiliation><country xml:lang="fr">République populaire de Chine</country><wicri:regionArea>College of Agronomy and Biotechnology, China Agricultural University, Beijing 100193</wicri:regionArea><placeName><settlement type="city">Pékin</settlement></placeName></affiliation></author><author><name sortKey="Mao, Ziling" sort="Mao, Ziling" uniqKey="Mao Z" first="Ziling" last="Mao">Ziling Mao</name></author><author><name sortKey="Lou, Jingfeng" sort="Lou, Jingfeng" uniqKey="Lou J" first="Jingfeng" last="Lou">Jingfeng Lou</name></author><author><name sortKey="Xu, Liang" sort="Xu, Liang" uniqKey="Xu L" first="Liang" last="Xu">Liang Xu</name></author><author><name sortKey="Zhong, Lingyun" sort="Zhong, Lingyun" uniqKey="Zhong L" first="Lingyun" last="Zhong">Lingyun Zhong</name></author><author><name sortKey="Peng, Youliang" sort="Peng, Youliang" uniqKey="Peng Y" first="Youliang" last="Peng">Youliang Peng</name></author><author><name sortKey="Zhou, Ligang" sort="Zhou, Ligang" uniqKey="Zhou L" first="Ligang" last="Zhou">Ligang Zhou</name></author><author><name sortKey="Wang, Mingan" sort="Wang, Mingan" uniqKey="Wang M" first="Mingan" last="Wang">Mingan Wang</name></author></analytic><series><title level="j">Molecules (Basel, Switzerland)</title><idno type="eISSN">1420-3049</idno><imprint><date when="2012" type="published">2012</date></imprint></series></biblStruct></sourceDesc></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Animals (MeSH)</term><term>Anti-Infective Agents (chemistry)</term><term>Anti-Infective Agents (pharmacology)</term><term>Antinematodal Agents (pharmacology)</term><term>Ascomycota (chemistry)</term><term>Benzopyrans (chemistry)</term><term>Benzopyrans (pharmacology)</term><term>Caenorhabditis elegans (drug effects)</term><term>Cholinesterase Inhibitors (pharmacology)</term><term>Inhibitory Concentration 50 (MeSH)</term><term>Microbial Sensitivity Tests (MeSH)</term></keywords><keywords scheme="KwdFr" xml:lang="fr"><term>Animaux (MeSH)</term><term>Anti-infectieux (composition chimique)</term><term>Anti-infectieux (pharmacologie)</term><term>Anticholinestérasiques (pharmacologie)</term><term>Antihelminthiques antinématodes (pharmacologie)</term><term>Ascomycota (composition chimique)</term><term>Benzopyranes (composition chimique)</term><term>Benzopyranes (pharmacologie)</term><term>Caenorhabditis elegans (effets des médicaments et des substances chimiques)</term><term>Concentration inhibitrice 50 (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>Benzopyrans</term></keywords><keywords scheme="MESH" type="chemical" qualifier="pharmacology" xml:lang="en"><term>Anti-Infective Agents</term><term>Antinematodal Agents</term><term>Benzopyrans</term><term>Cholinesterase Inhibitors</term></keywords><keywords scheme="MESH" qualifier="chemistry" xml:lang="en"><term>Ascomycota</term></keywords><keywords scheme="MESH" qualifier="composition chimique" xml:lang="fr"><term>Anti-infectieux</term><term>Ascomycota</term><term>Benzopyranes</term></keywords><keywords scheme="MESH" qualifier="drug effects" xml:lang="en"><term>Caenorhabditis elegans</term></keywords><keywords scheme="MESH" qualifier="effets des médicaments et des substances chimiques" xml:lang="fr"><term>Caenorhabditis elegans</term></keywords><keywords scheme="MESH" qualifier="pharmacologie" xml:lang="fr"><term>Anti-infectieux</term><term>Anticholinestérasiques</term><term>Antihelminthiques antinématodes</term><term>Benzopyranes</term></keywords><keywords scheme="MESH" xml:lang="en"><term>Animals</term><term>Inhibitory Concentration 50</term><term>Microbial Sensitivity Tests</term></keywords><keywords scheme="MESH" xml:lang="fr"><term>Animaux</term><term>Concentration inhibitrice 50</term><term>Tests de sensibilité microbienne</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">The endophytic fungus Hyalodendriella sp. Ponipodef12 was isolated from the hybrid 'Neva' of Populus deltoides Marsh × P. nigra L. In this study, four benzopyranones were isolated from the ethyl acetate extract of Hyalodendriella sp. Ponipodef12, and identified as palmariol B (1), 4-hydroxymellein (2), alternariol 9-methyl ether (3), and botrallin (4) by means of physicochemical and spectroscopic analysis. All the compounds were evaluated for their antibacterial, antifungal, antinematodal and acetylcholinesterase inhibitory activities. 4-Hydroxymellein (2) exhibited stronger antibacterial activity than the other compounds. Palmariol B (1) showed stronger antimicrobial, antinematodal and acetylcholinesterase inhibitory activities than alternariol 9-methyl ether (3) which indicated that the chlorine substitution at position 2 may contribute to its bioactivity. The results indicate the potential of this endophytic fungus as a source of bioactive benzopyranones.</div></front></TEI><pubmed><MedlineCitation Status="MEDLINE" Owner="NLM"><PMID Version="1">23011274</PMID><DateCompleted><Year>2013</Year><Month>03</Month><Day>21</Day></DateCompleted><DateRevised><Year>2018</Year><Month>12</Month><Day>17</Day></DateRevised><Article PubModel="Electronic"><Journal><ISSN IssnType="Electronic">1420-3049</ISSN><JournalIssue CitedMedium="Internet"><Volume>17</Volume><Issue>10</Issue><PubDate><Year>2012</Year><Month>Sep</Month><Day>25</Day></PubDate></JournalIssue><Title>Molecules (Basel, Switzerland)</Title><ISOAbbreviation>Molecules</ISOAbbreviation></Journal><ArticleTitle>Benzopyranones from the endophytic fungus Hyalodendriella sp. Ponipodef12 and their bioactivities.</ArticleTitle><Pagination><MedlinePgn>11303-14</MedlinePgn></Pagination><Abstract><AbstractText>The endophytic fungus Hyalodendriella sp. Ponipodef12 was isolated from the hybrid 'Neva' of Populus deltoides Marsh × P. nigra L. In this study, four benzopyranones were isolated from the ethyl acetate extract of Hyalodendriella sp. Ponipodef12, and identified as palmariol B (1), 4-hydroxymellein (2), alternariol 9-methyl ether (3), and botrallin (4) by means of physicochemical and spectroscopic analysis. All the compounds were evaluated for their antibacterial, antifungal, antinematodal and acetylcholinesterase inhibitory activities. 4-Hydroxymellein (2) exhibited stronger antibacterial activity than the other compounds. Palmariol B (1) showed stronger antimicrobial, antinematodal and acetylcholinesterase inhibitory activities than alternariol 9-methyl ether (3) which indicated that the chlorine substitution at position 2 may contribute to its bioactivity. The results indicate the potential of this endophytic fungus as a source of bioactive benzopyranones.</AbstractText></Abstract><AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Meng</LastName><ForeName>Xiangjie</ForeName><Initials>X</Initials><AffiliationInfo><Affiliation>College of Agronomy and Biotechnology, China Agricultural University, Beijing 100193, China. lgzhou@cau.edu.cn.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Mao</LastName><ForeName>Ziling</ForeName><Initials>Z</Initials></Author><Author ValidYN="Y"><LastName>Lou</LastName><ForeName>Jingfeng</ForeName><Initials>J</Initials></Author><Author ValidYN="Y"><LastName>Xu</LastName><ForeName>Liang</ForeName><Initials>L</Initials></Author><Author ValidYN="Y"><LastName>Zhong</LastName><ForeName>Lingyun</ForeName><Initials>L</Initials></Author><Author ValidYN="Y"><LastName>Peng</LastName><ForeName>Youliang</ForeName><Initials>Y</Initials></Author><Author ValidYN="Y"><LastName>Zhou</LastName><ForeName>Ligang</ForeName><Initials>L</Initials></Author><Author ValidYN="Y"><LastName>Wang</LastName><ForeName>Mingan</ForeName><Initials>M</Initials></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>2012</Year><Month>09</Month><Day>25</Day></ArticleDate></Article><MedlineJournalInfo><Country>Switzerland</Country><MedlineTA>Molecules</MedlineTA><NlmUniqueID>100964009</NlmUniqueID><ISSNLinking>1420-3049</ISSNLinking></MedlineJournalInfo><ChemicalList><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance UI="D000890">Anti-Infective Agents</NameOfSubstance></Chemical><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance UI="D000969">Antinematodal 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Lingyun" uniqKey="Zhong L" first="Lingyun" last="Zhong">Lingyun Zhong</name><name sortKey="Zhou, Ligang" sort="Zhou, Ligang" uniqKey="Zhou L" first="Ligang" last="Zhou">Ligang Zhou</name></noCountry><country name="République populaire de Chine"><noRegion><name sortKey="Meng, Xiangjie" sort="Meng, Xiangjie" uniqKey="Meng X" first="Xiangjie" last="Meng">Xiangjie Meng</name></noRegion></country></tree></affiliations></record>Pour manipuler ce document sous Unix (Dilib)
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