Synthesis of sulfonate derivatives of maltol and their biological activity against Phytophthora capsici and Bursaphelenchus xylophilus in vitro.
Identifieur interne : 000039 ( Main/Exploration ); précédent : 000038; suivant : 000040Synthesis of sulfonate derivatives of maltol and their biological activity against Phytophthora capsici and Bursaphelenchus xylophilus in vitro.
Auteurs : Yue-E Tian [République populaire de Chine] ; Di Sun [République populaire de Chine] ; Jin-Ming Yang [République populaire de Chine] ; Zhi-Ping Che [République populaire de Chine] ; Sheng-Ming Liu [République populaire de Chine] ; Xiao-Min Lin [République populaire de Chine] ; Jia Jiang [République populaire de Chine] ; Gen-Qiang Chen [République populaire de Chine]Source :
- Journal of Asian natural products research [ 1477-2213 ] ; 2020.
Descripteurs français
- KwdFr :
- MESH :
English descriptors
- KwdEn :
- MESH :
- chemical : Antinematodal Agents, Pyrones.
- Molecular Structure, Phytophthora.
Abstract
Sixteen sulfonate derivatives of maltol were synthesized and screened in vitro for their anti-oomycete and nematicidal activity against Phytophthora capsici and Bursaphelenchus xylophilus, respectively. Among all the compounds, 3e, 3m, and 3p exhibited the most promising and pronounced anti-oomycete activity against P. capsici than zoxamide, and the EC50 values of 25.42, 18.44, 23.69, and 27.99 mg/L, respectively; compounds 3e, 3m, 3n, and 3p exhibited potent nematicidal activity with LC50 values ranging from 1 to 2 mg/L, especially 3m and 3n showed the best promising and pronounced nematicidal activity, with LC50 values of 1.1762 and 1.2384 mg/L, respectively. [Formula: see text].
DOI: 10.1080/10286020.2019.1608958
PubMed: 31046458
Affiliations:
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471003</wicri:noRegion></affiliation></author><author><name sortKey="Chen, Gen Qiang" sort="Chen, Gen Qiang" uniqKey="Chen G" first="Gen-Qiang" last="Chen">Gen-Qiang Chen</name><affiliation wicri:level="1"><nlm:affiliation>Laboratory of Pharmaceutical Design and Synthesis, Department of Plant Protection, College of Forestry, Henan University of Science and Technology, Luoyang 471003, China.</nlm:affiliation><country xml:lang="fr">République populaire de Chine</country><wicri:regionArea>Laboratory of Pharmaceutical Design and Synthesis, Department of Plant Protection, College of Forestry, Henan University of Science and Technology, Luoyang 471003</wicri:regionArea><wicri:noRegion>Luoyang 471003</wicri:noRegion></affiliation></author></titleStmt><publicationStmt><idno type="wicri:source">PubMed</idno><date when="2020">2020</date><idno type="RBID">pubmed:31046458</idno><idno type="pmid">31046458</idno><idno type="doi">10.1080/10286020.2019.1608958</idno><idno 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Chine</country><wicri:regionArea>Laboratory of Pharmaceutical Design and Synthesis, Department of Plant Protection, College of Forestry, Henan University of Science and Technology, Luoyang 471003</wicri:regionArea><wicri:noRegion>Luoyang 471003</wicri:noRegion></affiliation></author><author><name sortKey="Sun, Di" sort="Sun, Di" uniqKey="Sun D" first="Di" last="Sun">Di Sun</name><affiliation wicri:level="1"><nlm:affiliation>Laboratory of Pharmaceutical Design and Synthesis, Department of Plant Protection, College of Forestry, Henan University of Science and Technology, Luoyang 471003, China.</nlm:affiliation><country xml:lang="fr">République populaire de Chine</country><wicri:regionArea>Laboratory of Pharmaceutical Design and Synthesis, Department of Plant Protection, College of Forestry, Henan University of Science and Technology, Luoyang 471003</wicri:regionArea><wicri:noRegion>Luoyang 471003</wicri:noRegion></affiliation></author><author><name sortKey="Yang, Jin Ming" sort="Yang, Jin Ming" uniqKey="Yang J" first="Jin-Ming" last="Yang">Jin-Ming Yang</name><affiliation wicri:level="1"><nlm:affiliation>Laboratory of Pharmaceutical Design and Synthesis, Department of Plant Protection, College of Forestry, Henan University of Science and Technology, Luoyang 471003, China.</nlm:affiliation><country xml:lang="fr">République populaire de Chine</country><wicri:regionArea>Laboratory of Pharmaceutical Design and Synthesis, Department of Plant Protection, College of Forestry, Henan University of Science and Technology, Luoyang 471003</wicri:regionArea><wicri:noRegion>Luoyang 471003</wicri:noRegion></affiliation></author><author><name sortKey="Che, Zhi Ping" sort="Che, Zhi Ping" uniqKey="Che Z" first="Zhi-Ping" last="Che">Zhi-Ping Che</name><affiliation wicri:level="1"><nlm:affiliation>Laboratory of Pharmaceutical Design and Synthesis, Department of Plant Protection, College of Forestry, Henan University of Science and Technology, Luoyang 471003, China.</nlm:affiliation><country xml:lang="fr">République populaire de Chine</country><wicri:regionArea>Laboratory of Pharmaceutical Design and Synthesis, Department of Plant Protection, College of Forestry, Henan University of Science and Technology, Luoyang 471003</wicri:regionArea><wicri:noRegion>Luoyang 471003</wicri:noRegion></affiliation></author><author><name sortKey="Liu, Sheng Ming" sort="Liu, Sheng Ming" uniqKey="Liu S" first="Sheng-Ming" last="Liu">Sheng-Ming Liu</name><affiliation wicri:level="1"><nlm:affiliation>Laboratory of Pharmaceutical Design and Synthesis, Department of Plant Protection, College of Forestry, Henan University of Science and Technology, Luoyang 471003, China.</nlm:affiliation><country xml:lang="fr">République populaire de Chine</country><wicri:regionArea>Laboratory of Pharmaceutical Design and Synthesis, Department of Plant Protection, College of Forestry, Henan University of Science and Technology, Luoyang 471003</wicri:regionArea><wicri:noRegion>Luoyang 471003</wicri:noRegion></affiliation></author><author><name sortKey="Lin, Xiao Min" sort="Lin, Xiao Min" uniqKey="Lin X" first="Xiao-Min" last="Lin">Xiao-Min Lin</name><affiliation wicri:level="1"><nlm:affiliation>Laboratory of Pharmaceutical Design and Synthesis, Department of Plant Protection, College of Forestry, Henan University of Science and Technology, Luoyang 471003, China.</nlm:affiliation><country xml:lang="fr">République populaire de Chine</country><wicri:regionArea>Laboratory of Pharmaceutical Design and Synthesis, Department of Plant Protection, College of Forestry, Henan University of Science and Technology, Luoyang 471003</wicri:regionArea><wicri:noRegion>Luoyang 471003</wicri:noRegion></affiliation></author><author><name sortKey="Jiang, Jia" sort="Jiang, Jia" uniqKey="Jiang J" first="Jia" last="Jiang">Jia Jiang</name><affiliation wicri:level="1"><nlm:affiliation>Laboratory of Pharmaceutical Design and Synthesis, Department of Plant Protection, College of Forestry, Henan University of Science and Technology, Luoyang 471003, China.</nlm:affiliation><country xml:lang="fr">République populaire de Chine</country><wicri:regionArea>Laboratory of Pharmaceutical Design and Synthesis, Department of Plant Protection, College of Forestry, Henan University of Science and Technology, Luoyang 471003</wicri:regionArea><wicri:noRegion>Luoyang 471003</wicri:noRegion></affiliation></author><author><name sortKey="Chen, Gen Qiang" sort="Chen, Gen Qiang" uniqKey="Chen G" first="Gen-Qiang" last="Chen">Gen-Qiang Chen</name><affiliation wicri:level="1"><nlm:affiliation>Laboratory of Pharmaceutical Design and Synthesis, Department of Plant Protection, College of Forestry, Henan University of Science and Technology, Luoyang 471003, China.</nlm:affiliation><country xml:lang="fr">République populaire de Chine</country><wicri:regionArea>Laboratory of Pharmaceutical Design and Synthesis, Department of Plant Protection, College of Forestry, Henan University of Science and Technology, Luoyang 471003</wicri:regionArea><wicri:noRegion>Luoyang 471003</wicri:noRegion></affiliation></author></analytic><series><title level="j">Journal of Asian natural products research</title><idno type="eISSN">1477-2213</idno><imprint><date when="2020" type="published">2020</date></imprint></series></biblStruct></sourceDesc></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Antinematodal Agents (MeSH)</term><term>Molecular Structure (MeSH)</term><term>Phytophthora (MeSH)</term><term>Pyrones (MeSH)</term></keywords><keywords scheme="KwdFr" xml:lang="fr"><term>Antihelminthiques antinématodes (MeSH)</term><term>Phytophthora (MeSH)</term><term>Pyrones (MeSH)</term><term>Structure moléculaire (MeSH)</term></keywords><keywords scheme="MESH" type="chemical" xml:lang="en"><term>Antinematodal Agents</term><term>Pyrones</term></keywords><keywords scheme="MESH" xml:lang="en"><term>Molecular Structure</term><term>Phytophthora</term></keywords><keywords scheme="MESH" xml:lang="fr"><term>Antihelminthiques antinématodes</term><term>Phytophthora</term><term>Pyrones</term><term>Structure moléculaire</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">Sixteen sulfonate derivatives of maltol were synthesized and screened <i>in vitro</i> for their anti-oomycete and nematicidal activity against <i>Phytophthora capsici</i> and <i>Bursaphelenchus xylophilus</i>, respectively. Among all the compounds, <b>3e</b>, <b>3m</b>, and <b>3p</b> exhibited the most promising and pronounced anti-oomycete activity against <i>P. capsici</i> than zoxamide, and the EC<sub>50</sub> values of 25.42, 18.44, 23.69, and 27.99 mg/L, respectively; compounds <b>3e</b>, <b>3m</b>, <b>3n</b>, and <b>3p</b> exhibited potent nematicidal activity with LC<sub>50</sub> values ranging from 1 to 2 mg/L, especially <b>3m</b> and <b>3n</b> showed the best promising and pronounced nematicidal activity, with LC<sub>50</sub> values of 1.1762 and 1.2384 mg/L, respectively. [Formula: see text].</div></front></TEI><pubmed><MedlineCitation Status="MEDLINE" IndexingMethod="Automated" Owner="NLM"><PMID Version="1">31046458</PMID><DateCompleted><Year>2020</Year><Month>04</Month><Day>28</Day></DateCompleted><DateRevised><Year>2020</Year><Month>04</Month><Day>28</Day></DateRevised><Article PubModel="Print-Electronic"><Journal><ISSN IssnType="Electronic">1477-2213</ISSN><JournalIssue CitedMedium="Internet"><Volume>22</Volume><Issue>6</Issue><PubDate><Year>2020</Year><Month>Jun</Month></PubDate></JournalIssue><Title>Journal of Asian natural products research</Title><ISOAbbreviation>J Asian Nat Prod Res</ISOAbbreviation></Journal><ArticleTitle>Synthesis of sulfonate derivatives of maltol and their biological activity against <i>Phytophthora capsici</i> and <i>Bursaphelenchus xylophilus in vitro</i>.</ArticleTitle><Pagination><MedlinePgn>578-587</MedlinePgn></Pagination><ELocationID EIdType="doi" ValidYN="Y">10.1080/10286020.2019.1608958</ELocationID><Abstract><AbstractText>Sixteen sulfonate derivatives of maltol were synthesized and screened <i>in vitro</i> for their anti-oomycete and nematicidal activity against <i>Phytophthora capsici</i> and <i>Bursaphelenchus xylophilus</i>, respectively. Among all the compounds, <b>3e</b>, <b>3m</b>, and <b>3p</b> exhibited the most promising and pronounced anti-oomycete activity against <i>P. capsici</i> than zoxamide, and the EC<sub>50</sub> values of 25.42, 18.44, 23.69, and 27.99 mg/L, respectively; compounds <b>3e</b>, <b>3m</b>, <b>3n</b>, and <b>3p</b> exhibited potent nematicidal activity with LC<sub>50</sub> values ranging from 1 to 2 mg/L, especially <b>3m</b> and <b>3n</b> showed the best promising and pronounced nematicidal activity, with LC<sub>50</sub> values of 1.1762 and 1.2384 mg/L, respectively. [Formula: see text].</AbstractText></Abstract><AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Tian</LastName><ForeName>Yue-E</ForeName><Initials>YE</Initials><AffiliationInfo><Affiliation>Laboratory of Pharmaceutical Design and Synthesis, Department of Plant Protection, College of Forestry, Henan University of Science and Technology, Luoyang 471003, China.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Sun</LastName><ForeName>Di</ForeName><Initials>D</Initials><AffiliationInfo><Affiliation>Laboratory of Pharmaceutical Design and Synthesis, Department of Plant Protection, College of Forestry, Henan University of Science and Technology, Luoyang 471003, China.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Yang</LastName><ForeName>Jin-Ming</ForeName><Initials>JM</Initials><AffiliationInfo><Affiliation>Laboratory of Pharmaceutical Design and Synthesis, Department of Plant Protection, College of Forestry, Henan University of Science and Technology, Luoyang 471003, China.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Che</LastName><ForeName>Zhi-Ping</ForeName><Initials>ZP</Initials><AffiliationInfo><Affiliation>Laboratory of Pharmaceutical Design and Synthesis, Department of Plant Protection, College of Forestry, Henan University of Science and Technology, Luoyang 471003, China.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Liu</LastName><ForeName>Sheng-Ming</ForeName><Initials>SM</Initials><AffiliationInfo><Affiliation>Laboratory of Pharmaceutical Design and Synthesis, Department of Plant Protection, College of Forestry, Henan University of Science and Technology, Luoyang 471003, China.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Lin</LastName><ForeName>Xiao-Min</ForeName><Initials>XM</Initials><AffiliationInfo><Affiliation>Laboratory of Pharmaceutical Design and Synthesis, Department of Plant Protection, College of Forestry, Henan University of Science and Technology, Luoyang 471003, China.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Jiang</LastName><ForeName>Jia</ForeName><Initials>J</Initials><AffiliationInfo><Affiliation>Laboratory of Pharmaceutical Design and Synthesis, Department of Plant Protection, College of Forestry, Henan University of Science and Technology, Luoyang 471003, China.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Chen</LastName><ForeName>Gen-Qiang</ForeName><Initials>GQ</Initials><AffiliationInfo><Affiliation>Laboratory of Pharmaceutical Design and Synthesis, Department of Plant Protection, College of Forestry, Henan University of Science and Technology, Luoyang 471003, China.</Affiliation></AffiliationInfo></Author></AuthorList><Language>eng</Language><PublicationTypeList><PublicationType UI="D016428">Journal Article</PublicationType></PublicationTypeList><ArticleDate DateType="Electronic"><Year>2019</Year><Month>05</Month><Day>03</Day></ArticleDate></Article><MedlineJournalInfo><Country>England</Country><MedlineTA>J Asian Nat Prod Res</MedlineTA><NlmUniqueID>100888334</NlmUniqueID><ISSNLinking>1028-6020</ISSNLinking></MedlineJournalInfo><ChemicalList><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance UI="D000969">Antinematodal Agents</NameOfSubstance></Chemical><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance UI="D011753">Pyrones</NameOfSubstance></Chemical><Chemical><RegistryNumber>3A9RD92BS4</RegistryNumber><NameOfSubstance UI="C008316">maltol</NameOfSubstance></Chemical></ChemicalList><CitationSubset>IM</CitationSubset><MeshHeadingList><MeshHeading><DescriptorName UI="D000969" MajorTopicYN="N">Antinematodal Agents</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D015394" MajorTopicYN="N">Molecular Structure</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D010838" MajorTopicYN="Y">Phytophthora</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D011753" MajorTopicYN="N">Pyrones</DescriptorName></MeshHeading></MeshHeadingList><KeywordList Owner="NOTNLM"><Keyword MajorTopicYN="N"> anti-oomycete activity</Keyword><Keyword MajorTopicYN="N">Maltol</Keyword><Keyword MajorTopicYN="N">nematicidal activity</Keyword><Keyword MajorTopicYN="N">semisynthesis</Keyword><Keyword MajorTopicYN="N">sulfonate</Keyword></KeywordList></MedlineCitation><PubmedData><History><PubMedPubDate PubStatus="pubmed"><Year>2019</Year><Month>5</Month><Day>3</Day><Hour>6</Hour><Minute>0</Minute></PubMedPubDate><PubMedPubDate PubStatus="medline"><Year>2020</Year><Month>4</Month><Day>29</Day><Hour>6</Hour><Minute>0</Minute></PubMedPubDate><PubMedPubDate PubStatus="entrez"><Year>2019</Year><Month>5</Month><Day>4</Day><Hour>6</Hour><Minute>0</Minute></PubMedPubDate></History><PublicationStatus>ppublish</PublicationStatus><ArticleIdList><ArticleId IdType="pubmed">31046458</ArticleId><ArticleId IdType="doi">10.1080/10286020.2019.1608958</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="Tian, Yue E" sort="Tian, Yue E" uniqKey="Tian Y" first="Yue-E" last="Tian">Yue-E Tian</name></noRegion><name sortKey="Che, Zhi Ping" sort="Che, Zhi Ping" uniqKey="Che Z" first="Zhi-Ping" last="Che">Zhi-Ping Che</name><name sortKey="Chen, Gen Qiang" sort="Chen, Gen Qiang" uniqKey="Chen G" first="Gen-Qiang" last="Chen">Gen-Qiang Chen</name><name sortKey="Jiang, Jia" sort="Jiang, Jia" uniqKey="Jiang J" first="Jia" last="Jiang">Jia Jiang</name><name sortKey="Lin, Xiao Min" sort="Lin, Xiao Min" uniqKey="Lin X" first="Xiao-Min" last="Lin">Xiao-Min Lin</name><name sortKey="Liu, Sheng Ming" sort="Liu, Sheng Ming" uniqKey="Liu S" first="Sheng-Ming" last="Liu">Sheng-Ming Liu</name><name sortKey="Sun, Di" sort="Sun, Di" uniqKey="Sun D" first="Di" last="Sun">Di Sun</name><name sortKey="Yang, Jin Ming" sort="Yang, Jin Ming" uniqKey="Yang J" first="Jin-Ming" last="Yang">Jin-Ming Yang</name></country></tree></affiliations></record>Pour manipuler ce document sous Unix (Dilib)
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