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A new 1,4-benzoxazine derivative produced by endophytic Colletotrichum gloeosporioides B-142
Colletotrin A (1), a new 1,4-benzoxazine derivative, and eight known compounds, including two alkaloids (2-3), one acylamide (4), one benzaldehyde (5), and four sterols (6-9) were obtained from endophytic fungus Colletotrichum gloeosporioides B-142, which was isolated from Dracaena cochinchinensis....
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Published in: | Natural product research 2024-04, Vol.38 (8), p.1341-1346 |
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creator | Zhang, Bing Huang, Zhi-pu Si, Yu Zhang, Ke-tao Xu, Xiao-rong Chen, Jian-hong Zhao, Qing Zhang, Xiao-mei |
description | Colletotrin A (1), a new 1,4-benzoxazine derivative, and eight known compounds, including two alkaloids (2-3), one acylamide (4), one benzaldehyde (5), and four sterols (6-9) were obtained from endophytic fungus Colletotrichum gloeosporioides B-142, which was isolated from Dracaena cochinchinensis. Among them, 1,2,3,4-tetrahydroquinoline-4,8-diol (2) was reported for the first time as natural product. The structure of compound 1 was elucidated with help of spectroscopic data including IR, UV, electronic circular dichroism (ECD) calculation, HRESIMS, 1D and 2D NMR (COSY, HSQC and HMBC). The antimicrobial activities were evaluated by disc diffusion method. |
doi_str_mv | 10.1080/14786419.2022.2141735 |
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Among them, 1,2,3,4-tetrahydroquinoline-4,8-diol (2) was reported for the first time as natural product. The structure of compound 1 was elucidated with help of spectroscopic data including IR, UV, electronic circular dichroism (ECD) calculation, HRESIMS, 1D and 2D NMR (COSY, HSQC and HMBC). The antimicrobial activities were evaluated by disc diffusion method.</description><identifier>ISSN: 1478-6419</identifier><identifier>EISSN: 1478-6427</identifier><identifier>DOI: 10.1080/14786419.2022.2141735</identifier><identifier>PMID: 36323318</identifier><language>eng</language><publisher>England: Taylor & Francis</publisher><subject>antimicrobial activities ; Benzaldehyde ; Benzoxazine ; Benzoxazines ; Circular dichroism ; Colletotrichum gloeosporioides ; colletotrin A ; Dichroism ; endophyte ; Endophytes ; Natural products ; NMR ; Nuclear magnetic resonance ; Sterols</subject><ispartof>Natural product research, 2024-04, Vol.38 (8), p.1341-1346</ispartof><rights>2022 Informa UK Limited, trading as Taylor & Francis Group 2022</rights><rights>2022 Informa UK Limited, trading as Taylor & Francis Group</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c441t-ce1dd108f10130aba46c6c275d1998d3d22d8e8575163b37c45ad2c1ecb913553</citedby><cites>FETCH-LOGICAL-c441t-ce1dd108f10130aba46c6c275d1998d3d22d8e8575163b37c45ad2c1ecb913553</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/36323318$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Zhang, Bing</creatorcontrib><creatorcontrib>Huang, Zhi-pu</creatorcontrib><creatorcontrib>Si, Yu</creatorcontrib><creatorcontrib>Zhang, Ke-tao</creatorcontrib><creatorcontrib>Xu, Xiao-rong</creatorcontrib><creatorcontrib>Chen, Jian-hong</creatorcontrib><creatorcontrib>Zhao, Qing</creatorcontrib><creatorcontrib>Zhang, Xiao-mei</creatorcontrib><title>A new 1,4-benzoxazine derivative produced by endophytic Colletotrichum gloeosporioides B-142</title><title>Natural product research</title><addtitle>Nat Prod Res</addtitle><description>Colletotrin A (1), a new 1,4-benzoxazine derivative, and eight known compounds, including two alkaloids (2-3), one acylamide (4), one benzaldehyde (5), and four sterols (6-9) were obtained from endophytic fungus Colletotrichum gloeosporioides B-142, which was isolated from Dracaena cochinchinensis. Among them, 1,2,3,4-tetrahydroquinoline-4,8-diol (2) was reported for the first time as natural product. The structure of compound 1 was elucidated with help of spectroscopic data including IR, UV, electronic circular dichroism (ECD) calculation, HRESIMS, 1D and 2D NMR (COSY, HSQC and HMBC). The antimicrobial activities were evaluated by disc diffusion method.</description><subject>antimicrobial activities</subject><subject>Benzaldehyde</subject><subject>Benzoxazine</subject><subject>Benzoxazines</subject><subject>Circular dichroism</subject><subject>Colletotrichum gloeosporioides</subject><subject>colletotrin A</subject><subject>Dichroism</subject><subject>endophyte</subject><subject>Endophytes</subject><subject>Natural products</subject><subject>NMR</subject><subject>Nuclear magnetic resonance</subject><subject>Sterols</subject><issn>1478-6419</issn><issn>1478-6427</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><recordid>eNp9kEtP3DAQgC1UVB7tT6Cy1AsHsvX4ESc3YEUfElIvcKtkOfakGCXxYifA8uvJahcOPfQ0o9E3r4-QE2ALYBX7BlJXpYR6wRnnCw4StFB75HBTL0rJ9Yf3HOoDcpTzPWMclFIfyYEoBRcCqkPy54IO-EThTBYNDi_x2b6EAanHFB7tGB6RrlL0k0NPmzXFwcfV3XoMji5j1-EYxxTc3dTTv13EmFcxhRg8ZnpZgOSfyH5ru4yfd_GY3H6_uln-LK5___i1vLgunJQwFg7B-_mpFhgIZhsrS1c6rpWHuq688Jz7CiulFZSiEdpJZT13gK6pQSgljsnpdu5868OEeTR9yA67zg4Yp2y4FqChLks-o1__Qe_jlIb5OsNrLSrgADBTaku5FHNO2JpVCr1NawPMbPSbN_1mo9_s9M99X3bTp6ZH_9715nsGzrdAGNqYevsUU-fNaNddTG2ygwvZiP_veAWiMpKu</recordid><startdate>20240417</startdate><enddate>20240417</enddate><creator>Zhang, Bing</creator><creator>Huang, Zhi-pu</creator><creator>Si, Yu</creator><creator>Zhang, Ke-tao</creator><creator>Xu, Xiao-rong</creator><creator>Chen, Jian-hong</creator><creator>Zhao, Qing</creator><creator>Zhang, Xiao-mei</creator><general>Taylor & Francis</general><general>Taylor & Francis Ltd</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QL</scope><scope>7QO</scope><scope>7QP</scope><scope>7QR</scope><scope>7T7</scope><scope>7TK</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>M7N</scope><scope>P64</scope><scope>7X8</scope></search><sort><creationdate>20240417</creationdate><title>A new 1,4-benzoxazine derivative produced by endophytic Colletotrichum gloeosporioides B-142</title><author>Zhang, Bing ; Huang, Zhi-pu ; Si, Yu ; Zhang, Ke-tao ; Xu, Xiao-rong ; Chen, Jian-hong ; Zhao, Qing ; Zhang, Xiao-mei</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c441t-ce1dd108f10130aba46c6c275d1998d3d22d8e8575163b37c45ad2c1ecb913553</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>antimicrobial activities</topic><topic>Benzaldehyde</topic><topic>Benzoxazine</topic><topic>Benzoxazines</topic><topic>Circular dichroism</topic><topic>Colletotrichum gloeosporioides</topic><topic>colletotrin A</topic><topic>Dichroism</topic><topic>endophyte</topic><topic>Endophytes</topic><topic>Natural products</topic><topic>NMR</topic><topic>Nuclear magnetic resonance</topic><topic>Sterols</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Zhang, Bing</creatorcontrib><creatorcontrib>Huang, Zhi-pu</creatorcontrib><creatorcontrib>Si, Yu</creatorcontrib><creatorcontrib>Zhang, Ke-tao</creatorcontrib><creatorcontrib>Xu, Xiao-rong</creatorcontrib><creatorcontrib>Chen, Jian-hong</creatorcontrib><creatorcontrib>Zhao, Qing</creatorcontrib><creatorcontrib>Zhang, Xiao-mei</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Biotechnology Research Abstracts</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Chemoreception Abstracts</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Neurosciences Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Natural product research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Zhang, Bing</au><au>Huang, Zhi-pu</au><au>Si, Yu</au><au>Zhang, Ke-tao</au><au>Xu, Xiao-rong</au><au>Chen, Jian-hong</au><au>Zhao, Qing</au><au>Zhang, Xiao-mei</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>A new 1,4-benzoxazine derivative produced by endophytic Colletotrichum gloeosporioides B-142</atitle><jtitle>Natural product research</jtitle><addtitle>Nat Prod Res</addtitle><date>2024-04-17</date><risdate>2024</risdate><volume>38</volume><issue>8</issue><spage>1341</spage><epage>1346</epage><pages>1341-1346</pages><issn>1478-6419</issn><eissn>1478-6427</eissn><abstract>Colletotrin A (1), a new 1,4-benzoxazine derivative, and eight known compounds, including two alkaloids (2-3), one acylamide (4), one benzaldehyde (5), and four sterols (6-9) were obtained from endophytic fungus Colletotrichum gloeosporioides B-142, which was isolated from Dracaena cochinchinensis. 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subjects | antimicrobial activities Benzaldehyde Benzoxazine Benzoxazines Circular dichroism Colletotrichum gloeosporioides colletotrin A Dichroism endophyte Endophytes Natural products NMR Nuclear magnetic resonance Sterols |
title | A new 1,4-benzoxazine derivative produced by endophytic Colletotrichum gloeosporioides B-142 |
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