Antibacterial Biphenanthrenes from the Fibrous Roots of Bletilla striata
Four new 9′,10′-dihydro-biphenanthrenes, including an unprecedented 1,2′-linked biphenanthrene, 4,7,3′,5′-tetramethoxy-9′,10′-dihydro(1,2′-biphenanthrene)-2,7′-diol (1), a new 1,3′-linked biphenanthrene, 4,7,7′-trimethoxy-9′,10′-dihydro(1,3′-biphenanthrene)-2,2′,5′-triol (2), and two new 1,1′-link...
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Veröffentlicht in: | Journal of natural products (Washington, D.C.) D.C.), 2015-04, Vol.78 (4), p.939-943 |
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creator | Qian, Chao-Dong Jiang, Fu-Sheng Yu, Hang-Su Shen, Yong Fu, Yu-Hang Cheng, Dong-Qing Gan, Li-She Ding, Zhi-Shan |
description | Four new 9′,10′-dihydro-biphenanthrenes, including an unprecedented 1,2′-linked biphenanthrene, 4,7,3′,5′-tetramethoxy-9′,10′-dihydro(1,2′-biphenanthrene)-2,7′-diol (1), a new 1,3′-linked biphenanthrene, 4,7,7′-trimethoxy-9′,10′-dihydro(1,3′-biphenanthrene)-2,2′,5′-triol (2), and two new 1,1′-linked biphenanthrenes, 4,7,4′-trimethoxy-9′,10′-dihydro(1,1′-biphenanthrene)-2,2′,7′-triol (3) and 4,7,3′,5′-tetramethoxy-9′,10′-dihydro(1,1′-biphenanthrene)-2,2′,7′-triol (4), as well as two known biphenanthrenes (5, 6), were isolated from a 95% ethanol extract of the fibrous roots of Bletilla striata. Their structures were determined by spectroscopic and spectrometric methods. Atropisomerism of these compounds was considered based on their chiral optical properties and potential energy surface scans at the ab initio HF/3-21G level, which revealed their racemic mixture form. Compounds 2–6 showed potent antibacterial activities against six Gram-positive bacterial strains. |
doi_str_mv | 10.1021/np501012n |
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Their structures were determined by spectroscopic and spectrometric methods. Atropisomerism of these compounds was considered based on their chiral optical properties and potential energy surface scans at the ab initio HF/3-21G level, which revealed their racemic mixture form. Compounds 2–6 showed potent antibacterial activities against six Gram-positive bacterial strains.</description><identifier>ISSN: 0163-3864</identifier><identifier>EISSN: 1520-6025</identifier><identifier>DOI: 10.1021/np501012n</identifier><identifier>PMID: 25760525</identifier><language>eng</language><publisher>United States: American Chemical Society and American Society of Pharmacognosy</publisher><subject>Anti-Bacterial Agents - chemistry ; Anti-Bacterial Agents - isolation & purification ; Anti-Bacterial Agents - pharmacology ; Drugs, Chinese Herbal - chemistry ; Drugs, Chinese Herbal - isolation & purification ; Drugs, Chinese Herbal - pharmacology ; Gram-Positive Bacteria - drug effects ; Microbial Sensitivity Tests ; Molecular Structure ; Nuclear Magnetic Resonance, Biomolecular ; Orchidaceae - chemistry ; Phenanthrenes - chemistry ; Phenanthrenes - isolation & purification ; Phenanthrenes - pharmacology ; Rhizome - chemistry</subject><ispartof>Journal of natural products (Washington, D.C.), 2015-04, Vol.78 (4), p.939-943</ispartof><rights>Copyright © American Chemical Society and American Society of Pharmacognosy</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-a348t-7774be83305630ea5b8c8f59128c3f95c2b8bc3cefa9e94ea8e225626eb1e83e3</citedby><cites>FETCH-LOGICAL-a348t-7774be83305630ea5b8c8f59128c3f95c2b8bc3cefa9e94ea8e225626eb1e83e3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://pubs.acs.org/doi/pdf/10.1021/np501012n$$EPDF$$P50$$Gacs$$H</linktopdf><linktohtml>$$Uhttps://pubs.acs.org/doi/10.1021/np501012n$$EHTML$$P50$$Gacs$$H</linktohtml><link.rule.ids>314,776,780,2752,27055,27903,27904,56716,56766</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/25760525$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Qian, Chao-Dong</creatorcontrib><creatorcontrib>Jiang, Fu-Sheng</creatorcontrib><creatorcontrib>Yu, Hang-Su</creatorcontrib><creatorcontrib>Shen, Yong</creatorcontrib><creatorcontrib>Fu, Yu-Hang</creatorcontrib><creatorcontrib>Cheng, Dong-Qing</creatorcontrib><creatorcontrib>Gan, Li-She</creatorcontrib><creatorcontrib>Ding, Zhi-Shan</creatorcontrib><title>Antibacterial Biphenanthrenes from the Fibrous Roots of Bletilla striata</title><title>Journal of natural products (Washington, D.C.)</title><addtitle>J. Nat. Prod</addtitle><description>Four new 9′,10′-dihydro-biphenanthrenes, including an unprecedented 1,2′-linked biphenanthrene, 4,7,3′,5′-tetramethoxy-9′,10′-dihydro(1,2′-biphenanthrene)-2,7′-diol (1), a new 1,3′-linked biphenanthrene, 4,7,7′-trimethoxy-9′,10′-dihydro(1,3′-biphenanthrene)-2,2′,5′-triol (2), and two new 1,1′-linked biphenanthrenes, 4,7,4′-trimethoxy-9′,10′-dihydro(1,1′-biphenanthrene)-2,2′,7′-triol (3) and 4,7,3′,5′-tetramethoxy-9′,10′-dihydro(1,1′-biphenanthrene)-2,2′,7′-triol (4), as well as two known biphenanthrenes (5, 6), were isolated from a 95% ethanol extract of the fibrous roots of Bletilla striata. Their structures were determined by spectroscopic and spectrometric methods. Atropisomerism of these compounds was considered based on their chiral optical properties and potential energy surface scans at the ab initio HF/3-21G level, which revealed their racemic mixture form. Compounds 2–6 showed potent antibacterial activities against six Gram-positive bacterial strains.</description><subject>Anti-Bacterial Agents - chemistry</subject><subject>Anti-Bacterial Agents - isolation & purification</subject><subject>Anti-Bacterial Agents - pharmacology</subject><subject>Drugs, Chinese Herbal - chemistry</subject><subject>Drugs, Chinese Herbal - isolation & purification</subject><subject>Drugs, Chinese Herbal - pharmacology</subject><subject>Gram-Positive Bacteria - drug effects</subject><subject>Microbial Sensitivity Tests</subject><subject>Molecular Structure</subject><subject>Nuclear Magnetic Resonance, Biomolecular</subject><subject>Orchidaceae - chemistry</subject><subject>Phenanthrenes - chemistry</subject><subject>Phenanthrenes - isolation & purification</subject><subject>Phenanthrenes - pharmacology</subject><subject>Rhizome - chemistry</subject><issn>0163-3864</issn><issn>1520-6025</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkE1LAzEQhoMotlYP_gHJRdDDaj422eRoi7VCQRA9L9k4S7fsZtcke_DfG2ntyYMwMJfnfZl5ELqk5I4SRu_dIAgllLkjNKWCkUwSJo7RlFDJM65kPkFnIWwJIZxocYomTBSSCCamaPXgYlMZG8E3psXzZtiAMy5uPDgIuPZ9h-MG8LKpfD8G_Nr3MeC-xvMWYtO2BoeYktGco5PatAEu9nuG3pePb4tVtn55el48rDPDcxWzoijyChTnREhOwIhKWVULTZmyvNbCskpVlluojQadg1HAmJBMQkVTDPgM3ex6B99_jhBi2TXBQrrEQTqwpFLnOn1XyH-ghVCF5mlm6HaHWt-H4KEuB990xn-VlJQ_jsuD48Re7WvHqoOPA_krNQHXO8DYUG770bsk5I-ib-Wlgjc</recordid><startdate>20150424</startdate><enddate>20150424</enddate><creator>Qian, Chao-Dong</creator><creator>Jiang, Fu-Sheng</creator><creator>Yu, Hang-Su</creator><creator>Shen, Yong</creator><creator>Fu, Yu-Hang</creator><creator>Cheng, Dong-Qing</creator><creator>Gan, Li-She</creator><creator>Ding, Zhi-Shan</creator><general>American Chemical Society and American Society of Pharmacognosy</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>7QL</scope><scope>7T7</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>P64</scope></search><sort><creationdate>20150424</creationdate><title>Antibacterial Biphenanthrenes from the Fibrous Roots of Bletilla striata</title><author>Qian, Chao-Dong ; Jiang, Fu-Sheng ; Yu, Hang-Su ; Shen, Yong ; Fu, Yu-Hang ; Cheng, Dong-Qing ; Gan, Li-She ; Ding, Zhi-Shan</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a348t-7774be83305630ea5b8c8f59128c3f95c2b8bc3cefa9e94ea8e225626eb1e83e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Anti-Bacterial Agents - chemistry</topic><topic>Anti-Bacterial Agents - isolation & purification</topic><topic>Anti-Bacterial Agents - pharmacology</topic><topic>Drugs, Chinese Herbal - chemistry</topic><topic>Drugs, Chinese Herbal - isolation & purification</topic><topic>Drugs, Chinese Herbal - pharmacology</topic><topic>Gram-Positive Bacteria - drug effects</topic><topic>Microbial Sensitivity Tests</topic><topic>Molecular Structure</topic><topic>Nuclear Magnetic Resonance, Biomolecular</topic><topic>Orchidaceae - chemistry</topic><topic>Phenanthrenes - chemistry</topic><topic>Phenanthrenes - isolation & purification</topic><topic>Phenanthrenes - pharmacology</topic><topic>Rhizome - chemistry</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Qian, Chao-Dong</creatorcontrib><creatorcontrib>Jiang, Fu-Sheng</creatorcontrib><creatorcontrib>Yu, Hang-Su</creatorcontrib><creatorcontrib>Shen, Yong</creatorcontrib><creatorcontrib>Fu, Yu-Hang</creatorcontrib><creatorcontrib>Cheng, Dong-Qing</creatorcontrib><creatorcontrib>Gan, Li-She</creatorcontrib><creatorcontrib>Ding, Zhi-Shan</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><jtitle>Journal of natural products (Washington, D.C.)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Qian, Chao-Dong</au><au>Jiang, Fu-Sheng</au><au>Yu, Hang-Su</au><au>Shen, Yong</au><au>Fu, Yu-Hang</au><au>Cheng, Dong-Qing</au><au>Gan, Li-She</au><au>Ding, Zhi-Shan</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Antibacterial Biphenanthrenes from the Fibrous Roots of Bletilla striata</atitle><jtitle>Journal of natural products (Washington, D.C.)</jtitle><addtitle>J. Nat. Prod</addtitle><date>2015-04-24</date><risdate>2015</risdate><volume>78</volume><issue>4</issue><spage>939</spage><epage>943</epage><pages>939-943</pages><issn>0163-3864</issn><eissn>1520-6025</eissn><abstract>Four new 9′,10′-dihydro-biphenanthrenes, including an unprecedented 1,2′-linked biphenanthrene, 4,7,3′,5′-tetramethoxy-9′,10′-dihydro(1,2′-biphenanthrene)-2,7′-diol (1), a new 1,3′-linked biphenanthrene, 4,7,7′-trimethoxy-9′,10′-dihydro(1,3′-biphenanthrene)-2,2′,5′-triol (2), and two new 1,1′-linked biphenanthrenes, 4,7,4′-trimethoxy-9′,10′-dihydro(1,1′-biphenanthrene)-2,2′,7′-triol (3) and 4,7,3′,5′-tetramethoxy-9′,10′-dihydro(1,1′-biphenanthrene)-2,2′,7′-triol (4), as well as two known biphenanthrenes (5, 6), were isolated from a 95% ethanol extract of the fibrous roots of Bletilla striata. Their structures were determined by spectroscopic and spectrometric methods. 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subjects | Anti-Bacterial Agents - chemistry Anti-Bacterial Agents - isolation & purification Anti-Bacterial Agents - pharmacology Drugs, Chinese Herbal - chemistry Drugs, Chinese Herbal - isolation & purification Drugs, Chinese Herbal - pharmacology Gram-Positive Bacteria - drug effects Microbial Sensitivity Tests Molecular Structure Nuclear Magnetic Resonance, Biomolecular Orchidaceae - chemistry Phenanthrenes - chemistry Phenanthrenes - isolation & purification Phenanthrenes - pharmacology Rhizome - chemistry |
title | Antibacterial Biphenanthrenes from the Fibrous Roots of Bletilla striata |
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