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Chemistry and tumor cell growth inhibitory activity of 11,20-epoxy-3Z,5(6)E-diene briaranes from the South China Sea gorgonian Dichotella gemmacea
Eighteen new 11,20-epoxy-3Z,5E-dien briaranes, gemmacolides AA-AR (1-18), were isolated together with three known analogs, dichotellides F (19) and I (20), and juncenolide C (21), from the South China Sea gorgonian Dichotella gemmacea. The structures of the compounds were elucidated by detailed spec...
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Published in: | Marine drugs 2013-05, Vol.11 (5), p.1565-1582 |
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description | Eighteen new 11,20-epoxy-3Z,5E-dien briaranes, gemmacolides AA-AR (1-18), were isolated together with three known analogs, dichotellides F (19) and I (20), and juncenolide C (21), from the South China Sea gorgonian Dichotella gemmacea. The structures of the compounds were elucidated by detailed spectroscopic analysis and comparison with reported data. The absolute configuration was determined based on the ECD experiment. In the in vitro bioassay, compounds 1-3, 5, 6, 8-12, and 14-19 exhibited different levels of growth inhibition activity against A549 and MG63 cell lines. Preliminary structure-activity analysis suggests that 12-O-isovalerate may increase the activity whereas 13- or 14-O-isovalerate may decrease the activity. Contribution of substitutions at C-2 and C-16 remains uncertain. |
doi_str_mv | 10.3390/md11051565 |
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The structures of the compounds were elucidated by detailed spectroscopic analysis and comparison with reported data. The absolute configuration was determined based on the ECD experiment. In the in vitro bioassay, compounds 1-3, 5, 6, 8-12, and 14-19 exhibited different levels of growth inhibition activity against A549 and MG63 cell lines. Preliminary structure-activity analysis suggests that 12-O-isovalerate may increase the activity whereas 13- or 14-O-isovalerate may decrease the activity. Contribution of substitutions at C-2 and C-16 remains uncertain.</description><identifier>ISSN: 1660-3397</identifier><identifier>EISSN: 1660-3397</identifier><identifier>DOI: 10.3390/md11051565</identifier><identifier>PMID: 23697947</identifier><language>eng</language><publisher>Switzerland: MDPI AG</publisher><subject>Animals ; Anthozoa - chemistry ; Antineoplastic Agents - chemistry ; Antineoplastic Agents - isolation & purification ; Antineoplastic Agents - pharmacology ; biological activity ; briarane diterpenoids ; Cell Line, Tumor ; China ; Dichotella gemmacea ; Diterpenes - chemistry ; Diterpenes - isolation & purification ; Diterpenes - pharmacology ; Drug Screening Assays, Antitumor ; gorgonian ; Humans ; Neoplasms - drug therapy ; Neoplasms - pathology ; Oceans and Seas ; Spectrum Analysis ; Structure-Activity Relationship</subject><ispartof>Marine drugs, 2013-05, Vol.11 (5), p.1565-1582</ispartof><rights>Copyright MDPI AG 2013</rights><rights>2013 by the authors; licensee MDPI, Basel, Switzerland. 2013</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c472t-c73fcab50f19654e6126c4451355b8c62f3291fafe95331ffcbef8e8fd6724b93</citedby><cites>FETCH-LOGICAL-c472t-c73fcab50f19654e6126c4451355b8c62f3291fafe95331ffcbef8e8fd6724b93</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/1535653172/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/1535653172?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,25752,27923,27924,37011,37012,44589,53790,53792,74897</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/23697947$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Li, Cui</creatorcontrib><creatorcontrib>Jiang, Mei</creatorcontrib><creatorcontrib>La, Ming-Ping</creatorcontrib><creatorcontrib>Li, Tie-Jun</creatorcontrib><creatorcontrib>Tang, Hua</creatorcontrib><creatorcontrib>Sun, Peng</creatorcontrib><creatorcontrib>Liu, Bao-Shu</creatorcontrib><creatorcontrib>Yi, Yang-Hua</creatorcontrib><creatorcontrib>Liu, Zhiyong</creatorcontrib><creatorcontrib>Zhang, Wen</creatorcontrib><title>Chemistry and tumor cell growth inhibitory activity of 11,20-epoxy-3Z,5(6)E-diene briaranes from the South China Sea gorgonian Dichotella gemmacea</title><title>Marine drugs</title><addtitle>Mar Drugs</addtitle><description>Eighteen new 11,20-epoxy-3Z,5E-dien briaranes, gemmacolides AA-AR (1-18), were isolated together with three known analogs, dichotellides F (19) and I (20), and juncenolide C (21), from the South China Sea gorgonian Dichotella gemmacea. The structures of the compounds were elucidated by detailed spectroscopic analysis and comparison with reported data. The absolute configuration was determined based on the ECD experiment. In the in vitro bioassay, compounds 1-3, 5, 6, 8-12, and 14-19 exhibited different levels of growth inhibition activity against A549 and MG63 cell lines. Preliminary structure-activity analysis suggests that 12-O-isovalerate may increase the activity whereas 13- or 14-O-isovalerate may decrease the activity. Contribution of substitutions at C-2 and C-16 remains uncertain.</description><subject>Animals</subject><subject>Anthozoa - chemistry</subject><subject>Antineoplastic Agents - chemistry</subject><subject>Antineoplastic Agents - isolation & purification</subject><subject>Antineoplastic Agents - pharmacology</subject><subject>biological activity</subject><subject>briarane diterpenoids</subject><subject>Cell Line, Tumor</subject><subject>China</subject><subject>Dichotella gemmacea</subject><subject>Diterpenes - chemistry</subject><subject>Diterpenes - isolation & purification</subject><subject>Diterpenes - pharmacology</subject><subject>Drug Screening Assays, Antitumor</subject><subject>gorgonian</subject><subject>Humans</subject><subject>Neoplasms - drug therapy</subject><subject>Neoplasms - pathology</subject><subject>Oceans and Seas</subject><subject>Spectrum Analysis</subject><subject>Structure-Activity Relationship</subject><issn>1660-3397</issn><issn>1660-3397</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNpdkk1v1DAQhiMEoh9w4QcgS1xa1IC_nVyQ0FKgUiUOhQsXy3HGG6-SeOs4hf0b_GIctpQWX8Yav3pmPPMWxQuC3zBW47dDSwgWREjxqDgkUuIyp9Xje_eD4miaNhgzUdX8aXFAmaxVzdVh8WvVweCnFHfIjC1K8xAistD3aB3Dj9QhP3a-8SksApv8jU87FBwi5IziErbh565k38_EiTw9L1sPI6AmehPNCBNyMQwodYCuwpxRq86PBl2BQesQ12H0ZkQfvO1CyvVyEobBWDDPiifO9BM8v43HxbeP519Xn8vLL58uVu8vS8sVTaVVzFnTCOxILQUHSai0nAvChGgqK6ljtCbOOKgFY8Q524CroHKtVJQ3NTsuLvbcNpiN3kY_mLjTwXj9J5Fb1CYmb3vQrmJUMmoxzyeXrSrRtKqljjKRI8-sd3vWdm4GaC2MKZr-AfThy-g7vQ43mimsiKQZcHILiOF6hinpvJVlD3mQYZ708iuuFOYqS1_9J92EOY55VJoIll3AiFqAr_cqG8M0RXB3zRCsF9vof7bJ4pf327-T_vUJ-w04Ib1r</recordid><startdate>20130515</startdate><enddate>20130515</enddate><creator>Li, Cui</creator><creator>Jiang, Mei</creator><creator>La, Ming-Ping</creator><creator>Li, Tie-Jun</creator><creator>Tang, Hua</creator><creator>Sun, Peng</creator><creator>Liu, Bao-Shu</creator><creator>Yi, Yang-Hua</creator><creator>Liu, Zhiyong</creator><creator>Zhang, Wen</creator><general>MDPI AG</general><general>MDPI</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>3V.</scope><scope>7T7</scope><scope>7TN</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FD</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AEUYN</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>BKSAR</scope><scope>C1K</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>F1W</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>H95</scope><scope>H99</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>L.F</scope><scope>L.G</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M7P</scope><scope>P64</scope><scope>PCBAR</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope></search><sort><creationdate>20130515</creationdate><title>Chemistry and tumor cell growth inhibitory activity of 11,20-epoxy-3Z,5(6)E-diene briaranes from the South China Sea gorgonian Dichotella gemmacea</title><author>Li, Cui ; Jiang, Mei ; La, Ming-Ping ; Li, Tie-Jun ; Tang, Hua ; Sun, Peng ; Liu, Bao-Shu ; Yi, Yang-Hua ; Liu, Zhiyong ; Zhang, Wen</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c472t-c73fcab50f19654e6126c4451355b8c62f3291fafe95331ffcbef8e8fd6724b93</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>Animals</topic><topic>Anthozoa - 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Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJÂ Directory of Open Access Journals</collection><jtitle>Marine drugs</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Li, Cui</au><au>Jiang, Mei</au><au>La, Ming-Ping</au><au>Li, Tie-Jun</au><au>Tang, Hua</au><au>Sun, Peng</au><au>Liu, Bao-Shu</au><au>Yi, Yang-Hua</au><au>Liu, Zhiyong</au><au>Zhang, Wen</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Chemistry and tumor cell growth inhibitory activity of 11,20-epoxy-3Z,5(6)E-diene briaranes from the South China Sea gorgonian Dichotella gemmacea</atitle><jtitle>Marine drugs</jtitle><addtitle>Mar Drugs</addtitle><date>2013-05-15</date><risdate>2013</risdate><volume>11</volume><issue>5</issue><spage>1565</spage><epage>1582</epage><pages>1565-1582</pages><issn>1660-3397</issn><eissn>1660-3397</eissn><abstract>Eighteen new 11,20-epoxy-3Z,5E-dien briaranes, gemmacolides AA-AR (1-18), were isolated together with three known analogs, dichotellides F (19) and I (20), and juncenolide C (21), from the South China Sea gorgonian Dichotella gemmacea. The structures of the compounds were elucidated by detailed spectroscopic analysis and comparison with reported data. The absolute configuration was determined based on the ECD experiment. In the in vitro bioassay, compounds 1-3, 5, 6, 8-12, and 14-19 exhibited different levels of growth inhibition activity against A549 and MG63 cell lines. Preliminary structure-activity analysis suggests that 12-O-isovalerate may increase the activity whereas 13- or 14-O-isovalerate may decrease the activity. Contribution of substitutions at C-2 and C-16 remains uncertain.</abstract><cop>Switzerland</cop><pub>MDPI AG</pub><pmid>23697947</pmid><doi>10.3390/md11051565</doi><tpages>18</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Animals Anthozoa - chemistry Antineoplastic Agents - chemistry Antineoplastic Agents - isolation & purification Antineoplastic Agents - pharmacology biological activity briarane diterpenoids Cell Line, Tumor China Dichotella gemmacea Diterpenes - chemistry Diterpenes - isolation & purification Diterpenes - pharmacology Drug Screening Assays, Antitumor gorgonian Humans Neoplasms - drug therapy Neoplasms - pathology Oceans and Seas Spectrum Analysis Structure-Activity Relationship |
title | Chemistry and tumor cell growth inhibitory activity of 11,20-epoxy-3Z,5(6)E-diene briaranes from the South China Sea gorgonian Dichotella gemmacea |
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