A Triterpenoid and Sesquiterpenoids from the Resinous Exudates of Commiphora myrrha
A new 30(14→13)abeo‐dammarane triterpenoid, myrrhasin (1), a new 14(10→1)abeo‐eudesmane sesquiterpenoid, myrrhanolide A (2), and two new cadinane sesquiterpenoids, myrrhanolides B and C (3 and 4, resp.), as well as nine known sesquiterpenoids, 5–13, were isolated from the resinous exudates of Commip...
Gespeichert in:
Veröffentlicht in: | Helvetica chimica acta 2009-04, Vol.92 (4), p.645-652 |
---|---|
Hauptverfasser: | , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 652 |
---|---|
container_issue | 4 |
container_start_page | 645 |
container_title | Helvetica chimica acta |
container_volume | 92 |
creator | Shen, Tao Wan, Wen-Zhu Wang, Xiao-Ning Yuan, Hui-Qing Ji, Mei Lou, Hong-Xiang |
description | A new 30(14→13)abeo‐dammarane triterpenoid, myrrhasin (1), a new 14(10→1)abeo‐eudesmane sesquiterpenoid, myrrhanolide A (2), and two new cadinane sesquiterpenoids, myrrhanolides B and C (3 and 4, resp.), as well as nine known sesquiterpenoids, 5–13, were isolated from the resinous exudates of Commiphora myrrha. Their structures were determined on the basis of extensive MS and NMR spectroscopic analyses. The isolated compounds 1–6 were evaluated for their cytotoxicity against the PC3 and DU145 human prostate tumor cell lines. |
doi_str_mv | 10.1002/hlca.200800347 |
format | Article |
fullrecord | <record><control><sourceid>istex_cross</sourceid><recordid>TN_cdi_crossref_primary_10_1002_hlca_200800347</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>ark_67375_WNG_4GL57PJB_5</sourcerecordid><originalsourceid>FETCH-LOGICAL-c3277-c7036173306f882480a7124bbbb6d53af89a1e462ac601cb0b9dec15288c2a7a3</originalsourceid><addsrcrecordid>eNqFkMFKAzEQhoMoWKtXz3mBrZNkN8ke66KtsqjYit5Cms2y0W5Tky22b29LpXpzLgPDfD_8H0KXBAYEgF41c6MHFEACsFQcoR7JKE0oF9kx6gEQmQDJ307RWYzvAJDnIHpoMsTT4DoblnbhXYX1osITGz9Xv7eI6-Bb3DUWP9voFn4V8c16VenORuxrXPi2dcvGB43bTQiNPkcntZ5He_Gz--jl9mZajJPycXRXDMvEMCpEYgQwTgRjwGspaSpBC0LT2XZ4lTFdy1wTm3KqDQdiZjDLK2u2paQ0VAvN-miwzzXBxxhsrZbBtTpsFAG1U6J2StRByRbI98CXm9vNP99qXBbDv2yyZ13s7PrA6vChuGAiU68PI5WOykw83V-rjH0De991Ow</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>A Triterpenoid and Sesquiterpenoids from the Resinous Exudates of Commiphora myrrha</title><source>Wiley Online Library Journals Frontfile Complete</source><creator>Shen, Tao ; Wan, Wen-Zhu ; Wang, Xiao-Ning ; Yuan, Hui-Qing ; Ji, Mei ; Lou, Hong-Xiang</creator><creatorcontrib>Shen, Tao ; Wan, Wen-Zhu ; Wang, Xiao-Ning ; Yuan, Hui-Qing ; Ji, Mei ; Lou, Hong-Xiang</creatorcontrib><description>A new 30(14→13)abeo‐dammarane triterpenoid, myrrhasin (1), a new 14(10→1)abeo‐eudesmane sesquiterpenoid, myrrhanolide A (2), and two new cadinane sesquiterpenoids, myrrhanolides B and C (3 and 4, resp.), as well as nine known sesquiterpenoids, 5–13, were isolated from the resinous exudates of Commiphora myrrha. Their structures were determined on the basis of extensive MS and NMR spectroscopic analyses. The isolated compounds 1–6 were evaluated for their cytotoxicity against the PC3 and DU145 human prostate tumor cell lines.</description><identifier>ISSN: 0018-019X</identifier><identifier>EISSN: 1522-2675</identifier><identifier>DOI: 10.1002/hlca.200800347</identifier><language>eng</language><publisher>Zürich: WILEY-VCH Verlag</publisher><subject>Commiphora myrrha ; Cytotoxic activity ; Myrrhanolides A - C ; Myrrhasin ; Sesquiterpenoids ; Triterpenoids</subject><ispartof>Helvetica chimica acta, 2009-04, Vol.92 (4), p.645-652</ispartof><rights>Copyright © 2009 Verlag Helvetica Chimica Acta AG, Zürich, Switzerland</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3277-c7036173306f882480a7124bbbb6d53af89a1e462ac601cb0b9dec15288c2a7a3</citedby><cites>FETCH-LOGICAL-c3277-c7036173306f882480a7124bbbb6d53af89a1e462ac601cb0b9dec15288c2a7a3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fhlca.200800347$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fhlca.200800347$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,27901,27902,45550,45551</link.rule.ids></links><search><creatorcontrib>Shen, Tao</creatorcontrib><creatorcontrib>Wan, Wen-Zhu</creatorcontrib><creatorcontrib>Wang, Xiao-Ning</creatorcontrib><creatorcontrib>Yuan, Hui-Qing</creatorcontrib><creatorcontrib>Ji, Mei</creatorcontrib><creatorcontrib>Lou, Hong-Xiang</creatorcontrib><title>A Triterpenoid and Sesquiterpenoids from the Resinous Exudates of Commiphora myrrha</title><title>Helvetica chimica acta</title><addtitle>HCA</addtitle><description>A new 30(14→13)abeo‐dammarane triterpenoid, myrrhasin (1), a new 14(10→1)abeo‐eudesmane sesquiterpenoid, myrrhanolide A (2), and two new cadinane sesquiterpenoids, myrrhanolides B and C (3 and 4, resp.), as well as nine known sesquiterpenoids, 5–13, were isolated from the resinous exudates of Commiphora myrrha. Their structures were determined on the basis of extensive MS and NMR spectroscopic analyses. The isolated compounds 1–6 were evaluated for their cytotoxicity against the PC3 and DU145 human prostate tumor cell lines.</description><subject>Commiphora myrrha</subject><subject>Cytotoxic activity</subject><subject>Myrrhanolides A - C</subject><subject>Myrrhasin</subject><subject>Sesquiterpenoids</subject><subject>Triterpenoids</subject><issn>0018-019X</issn><issn>1522-2675</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2009</creationdate><recordtype>article</recordtype><recordid>eNqFkMFKAzEQhoMoWKtXz3mBrZNkN8ke66KtsqjYit5Cms2y0W5Tky22b29LpXpzLgPDfD_8H0KXBAYEgF41c6MHFEACsFQcoR7JKE0oF9kx6gEQmQDJ307RWYzvAJDnIHpoMsTT4DoblnbhXYX1osITGz9Xv7eI6-Bb3DUWP9voFn4V8c16VenORuxrXPi2dcvGB43bTQiNPkcntZ5He_Gz--jl9mZajJPycXRXDMvEMCpEYgQwTgRjwGspaSpBC0LT2XZ4lTFdy1wTm3KqDQdiZjDLK2u2paQ0VAvN-miwzzXBxxhsrZbBtTpsFAG1U6J2StRByRbI98CXm9vNP99qXBbDv2yyZ13s7PrA6vChuGAiU68PI5WOykw83V-rjH0De991Ow</recordid><startdate>200904</startdate><enddate>200904</enddate><creator>Shen, Tao</creator><creator>Wan, Wen-Zhu</creator><creator>Wang, Xiao-Ning</creator><creator>Yuan, Hui-Qing</creator><creator>Ji, Mei</creator><creator>Lou, Hong-Xiang</creator><general>WILEY-VCH Verlag</general><general>WILEY‐VCH Verlag</general><scope>BSCLL</scope><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>200904</creationdate><title>A Triterpenoid and Sesquiterpenoids from the Resinous Exudates of Commiphora myrrha</title><author>Shen, Tao ; Wan, Wen-Zhu ; Wang, Xiao-Ning ; Yuan, Hui-Qing ; Ji, Mei ; Lou, Hong-Xiang</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3277-c7036173306f882480a7124bbbb6d53af89a1e462ac601cb0b9dec15288c2a7a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2009</creationdate><topic>Commiphora myrrha</topic><topic>Cytotoxic activity</topic><topic>Myrrhanolides A - C</topic><topic>Myrrhasin</topic><topic>Sesquiterpenoids</topic><topic>Triterpenoids</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Shen, Tao</creatorcontrib><creatorcontrib>Wan, Wen-Zhu</creatorcontrib><creatorcontrib>Wang, Xiao-Ning</creatorcontrib><creatorcontrib>Yuan, Hui-Qing</creatorcontrib><creatorcontrib>Ji, Mei</creatorcontrib><creatorcontrib>Lou, Hong-Xiang</creatorcontrib><collection>Istex</collection><collection>CrossRef</collection><jtitle>Helvetica chimica acta</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Shen, Tao</au><au>Wan, Wen-Zhu</au><au>Wang, Xiao-Ning</au><au>Yuan, Hui-Qing</au><au>Ji, Mei</au><au>Lou, Hong-Xiang</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>A Triterpenoid and Sesquiterpenoids from the Resinous Exudates of Commiphora myrrha</atitle><jtitle>Helvetica chimica acta</jtitle><addtitle>HCA</addtitle><date>2009-04</date><risdate>2009</risdate><volume>92</volume><issue>4</issue><spage>645</spage><epage>652</epage><pages>645-652</pages><issn>0018-019X</issn><eissn>1522-2675</eissn><abstract>A new 30(14→13)abeo‐dammarane triterpenoid, myrrhasin (1), a new 14(10→1)abeo‐eudesmane sesquiterpenoid, myrrhanolide A (2), and two new cadinane sesquiterpenoids, myrrhanolides B and C (3 and 4, resp.), as well as nine known sesquiterpenoids, 5–13, were isolated from the resinous exudates of Commiphora myrrha. Their structures were determined on the basis of extensive MS and NMR spectroscopic analyses. The isolated compounds 1–6 were evaluated for their cytotoxicity against the PC3 and DU145 human prostate tumor cell lines.</abstract><cop>Zürich</cop><pub>WILEY-VCH Verlag</pub><doi>10.1002/hlca.200800347</doi><tpages>8</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0018-019X |
ispartof | Helvetica chimica acta, 2009-04, Vol.92 (4), p.645-652 |
issn | 0018-019X 1522-2675 |
language | eng |
recordid | cdi_crossref_primary_10_1002_hlca_200800347 |
source | Wiley Online Library Journals Frontfile Complete |
subjects | Commiphora myrrha Cytotoxic activity Myrrhanolides A - C Myrrhasin Sesquiterpenoids Triterpenoids |
title | A Triterpenoid and Sesquiterpenoids from the Resinous Exudates of Commiphora myrrha |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-30T23%3A16%3A29IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-istex_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=A%20Triterpenoid%20and%20Sesquiterpenoids%20from%20the%20Resinous%20Exudates%20of%20Commiphora%20myrrha&rft.jtitle=Helvetica%20chimica%20acta&rft.au=Shen,%20Tao&rft.date=2009-04&rft.volume=92&rft.issue=4&rft.spage=645&rft.epage=652&rft.pages=645-652&rft.issn=0018-019X&rft.eissn=1522-2675&rft_id=info:doi/10.1002/hlca.200800347&rft_dat=%3Cistex_cross%3Eark_67375_WNG_4GL57PJB_5%3C/istex_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_id=info:pmid/&rfr_iscdi=true |