Bioactive aporphine alkaloids from the stems of Dasymaschalon rostratum
[Display omitted] •Compound 1 is a nitro aporphine alkaloid and its absolute configuration was defined based on negative specific rotation and single-crystal X-ray diffraction.•Compound 2 represents the first example of oxoaporphine alkaloid N-oxide.•Compound 1 exhibited significant inhibition again...
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Veröffentlicht in: | Bioorganic chemistry 2019-09, Vol.90, p.103069-103069, Article 103069 |
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creator | Yu, Zhangxin Han, Changri Song, Xiaoping Chen, Guangying Chen, Jinxiong |
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•Compound 1 is a nitro aporphine alkaloid and its absolute configuration was defined based on negative specific rotation and single-crystal X-ray diffraction.•Compound 2 represents the first example of oxoaporphine alkaloid N-oxide.•Compound 1 exhibited significant inhibition against Escherichia coli and Saphylococcus aureus with MIC values of 1.2 and 2.5 μM, respectively.
Three undescribed aporphine alkaloids dasymaroine A (1), 3-methoxyoxoputerine N-oxide (2), and dasymaroine B (3), along with nine known analogues (4–12) were isolated from the stems of Dasymaschalon rostratum Merr. The structures were elucidated using spectroscopic methods and by comparison with published NMR spectroscopic data. Compound 1 is a rarely reported nitro aporphine alkaloid and its absolute configuration was defined based on negative specific rotation and single-crystal X-ray diffraction. Compound 2 represents the first example of oxoaporphine alkaloid N-oxide. All compounds were evaluated for their activities of six pathogenic bacteria, 1 exhibited significant inhibition against Escherichia coli and Saphylococcus aureus with MIC values of 1.2 and 2.5 μM, respectively. As well as compounds 1–5, 7, 10, 12 were evaluated for their anti-HIV activities with EC50 ranged from 1.93 to 9.70 μM. |
doi_str_mv | 10.1016/j.bioorg.2019.103069 |
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•Compound 1 is a nitro aporphine alkaloid and its absolute configuration was defined based on negative specific rotation and single-crystal X-ray diffraction.•Compound 2 represents the first example of oxoaporphine alkaloid N-oxide.•Compound 1 exhibited significant inhibition against Escherichia coli and Saphylococcus aureus with MIC values of 1.2 and 2.5 μM, respectively.
Three undescribed aporphine alkaloids dasymaroine A (1), 3-methoxyoxoputerine N-oxide (2), and dasymaroine B (3), along with nine known analogues (4–12) were isolated from the stems of Dasymaschalon rostratum Merr. The structures were elucidated using spectroscopic methods and by comparison with published NMR spectroscopic data. Compound 1 is a rarely reported nitro aporphine alkaloid and its absolute configuration was defined based on negative specific rotation and single-crystal X-ray diffraction. Compound 2 represents the first example of oxoaporphine alkaloid N-oxide. All compounds were evaluated for their activities of six pathogenic bacteria, 1 exhibited significant inhibition against Escherichia coli and Saphylococcus aureus with MIC values of 1.2 and 2.5 μM, respectively. As well as compounds 1–5, 7, 10, 12 were evaluated for their anti-HIV activities with EC50 ranged from 1.93 to 9.70 μM.</description><identifier>ISSN: 0045-2068</identifier><identifier>EISSN: 1090-2120</identifier><identifier>DOI: 10.1016/j.bioorg.2019.103069</identifier><identifier>PMID: 31271945</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Anti-HIV ; Dasymaschalon rostratum ; Nitro aporphine alkaloid ; Oxoaporphine N-oxide</subject><ispartof>Bioorganic chemistry, 2019-09, Vol.90, p.103069-103069, Article 103069</ispartof><rights>2019 Elsevier Inc.</rights><rights>Copyright © 2019 Elsevier Inc. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c362t-380a2035799b56739212e2693376f62ee94b2493745734bd7570f2432d7b95cb3</citedby><cites>FETCH-LOGICAL-c362t-380a2035799b56739212e2693376f62ee94b2493745734bd7570f2432d7b95cb3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0045206819303463$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/31271945$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Yu, Zhangxin</creatorcontrib><creatorcontrib>Han, Changri</creatorcontrib><creatorcontrib>Song, Xiaoping</creatorcontrib><creatorcontrib>Chen, Guangying</creatorcontrib><creatorcontrib>Chen, Jinxiong</creatorcontrib><title>Bioactive aporphine alkaloids from the stems of Dasymaschalon rostratum</title><title>Bioorganic chemistry</title><addtitle>Bioorg Chem</addtitle><description>[Display omitted]
•Compound 1 is a nitro aporphine alkaloid and its absolute configuration was defined based on negative specific rotation and single-crystal X-ray diffraction.•Compound 2 represents the first example of oxoaporphine alkaloid N-oxide.•Compound 1 exhibited significant inhibition against Escherichia coli and Saphylococcus aureus with MIC values of 1.2 and 2.5 μM, respectively.
Three undescribed aporphine alkaloids dasymaroine A (1), 3-methoxyoxoputerine N-oxide (2), and dasymaroine B (3), along with nine known analogues (4–12) were isolated from the stems of Dasymaschalon rostratum Merr. The structures were elucidated using spectroscopic methods and by comparison with published NMR spectroscopic data. Compound 1 is a rarely reported nitro aporphine alkaloid and its absolute configuration was defined based on negative specific rotation and single-crystal X-ray diffraction. Compound 2 represents the first example of oxoaporphine alkaloid N-oxide. All compounds were evaluated for their activities of six pathogenic bacteria, 1 exhibited significant inhibition against Escherichia coli and Saphylococcus aureus with MIC values of 1.2 and 2.5 μM, respectively. As well as compounds 1–5, 7, 10, 12 were evaluated for their anti-HIV activities with EC50 ranged from 1.93 to 9.70 μM.</description><subject>Anti-HIV</subject><subject>Dasymaschalon rostratum</subject><subject>Nitro aporphine alkaloid</subject><subject>Oxoaporphine N-oxide</subject><issn>0045-2068</issn><issn>1090-2120</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><recordid>eNp9kDtPwzAQgC0EoqXwDxDKyJLiV-x6QYICBakSC8yW41yoS1IXO6nUf49RCiPTnU7fvT6ELgmeEkzEzXpaOu_Dx5RiolKJYaGO0JhghXNKKD5GY4x5kVMsZiN0FuMaY0K4FKdoxAiVRPFijBb3zhvbuR1kZuvDduU2KWs-TeNdFbM6-DbrVpDFDtqY-Tp7MHHfmmhXidhkwccumK5vz9FJbZoIF4c4Qe9Pj2_z53z5uniZ3y1zywTtcjbDhmJWSKXKQkim0qVAhWJMilpQAMVLyhWTvJCMl5UsJK4pZ7SSpSpsySboepi7Df6rh9jp1kULTWM24PuoKS0YI0mFTCgfUJuujAFqvQ2uNWGvCdY_CvVaDwr1j0I9KExtV4cNfdlC9df06ywBtwMA6c-dg6CjdbCxULkAttOVd_9v-AawAIJW</recordid><startdate>201909</startdate><enddate>201909</enddate><creator>Yu, Zhangxin</creator><creator>Han, Changri</creator><creator>Song, Xiaoping</creator><creator>Chen, Guangying</creator><creator>Chen, Jinxiong</creator><general>Elsevier Inc</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>201909</creationdate><title>Bioactive aporphine alkaloids from the stems of Dasymaschalon rostratum</title><author>Yu, Zhangxin ; Han, Changri ; Song, Xiaoping ; Chen, Guangying ; Chen, Jinxiong</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c362t-380a2035799b56739212e2693376f62ee94b2493745734bd7570f2432d7b95cb3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Anti-HIV</topic><topic>Dasymaschalon rostratum</topic><topic>Nitro aporphine alkaloid</topic><topic>Oxoaporphine N-oxide</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Yu, Zhangxin</creatorcontrib><creatorcontrib>Han, Changri</creatorcontrib><creatorcontrib>Song, Xiaoping</creatorcontrib><creatorcontrib>Chen, Guangying</creatorcontrib><creatorcontrib>Chen, Jinxiong</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Bioorganic chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Yu, Zhangxin</au><au>Han, Changri</au><au>Song, Xiaoping</au><au>Chen, Guangying</au><au>Chen, Jinxiong</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Bioactive aporphine alkaloids from the stems of Dasymaschalon rostratum</atitle><jtitle>Bioorganic chemistry</jtitle><addtitle>Bioorg Chem</addtitle><date>2019-09</date><risdate>2019</risdate><volume>90</volume><spage>103069</spage><epage>103069</epage><pages>103069-103069</pages><artnum>103069</artnum><issn>0045-2068</issn><eissn>1090-2120</eissn><abstract>[Display omitted]
•Compound 1 is a nitro aporphine alkaloid and its absolute configuration was defined based on negative specific rotation and single-crystal X-ray diffraction.•Compound 2 represents the first example of oxoaporphine alkaloid N-oxide.•Compound 1 exhibited significant inhibition against Escherichia coli and Saphylococcus aureus with MIC values of 1.2 and 2.5 μM, respectively.
Three undescribed aporphine alkaloids dasymaroine A (1), 3-methoxyoxoputerine N-oxide (2), and dasymaroine B (3), along with nine known analogues (4–12) were isolated from the stems of Dasymaschalon rostratum Merr. The structures were elucidated using spectroscopic methods and by comparison with published NMR spectroscopic data. Compound 1 is a rarely reported nitro aporphine alkaloid and its absolute configuration was defined based on negative specific rotation and single-crystal X-ray diffraction. Compound 2 represents the first example of oxoaporphine alkaloid N-oxide. All compounds were evaluated for their activities of six pathogenic bacteria, 1 exhibited significant inhibition against Escherichia coli and Saphylococcus aureus with MIC values of 1.2 and 2.5 μM, respectively. As well as compounds 1–5, 7, 10, 12 were evaluated for their anti-HIV activities with EC50 ranged from 1.93 to 9.70 μM.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>31271945</pmid><doi>10.1016/j.bioorg.2019.103069</doi><tpages>1</tpages></addata></record> |
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subjects | Anti-HIV Dasymaschalon rostratum Nitro aporphine alkaloid Oxoaporphine N-oxide |
title | Bioactive aporphine alkaloids from the stems of Dasymaschalon rostratum |
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