New Acyclic 12-Hydroxygeranylgeraniol-Derived Diterpenoids from the Seeds of Carpesium triste
Five new acyclic 12‐hydroxygeranylgeraniol‐derived diterpenoids, i.e., 1–5, were isolated from the seeds of Carpesium triste. The structures including the absolute configurations of the new compounds were elucidated by spectroscopic methods. All the compounds, except for 2, were evaluated for their...
Gespeichert in:
Veröffentlicht in: | Helvetica chimica acta 2008-10, Vol.91 (10), p.1934-1939 |
---|---|
Hauptverfasser: | , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 1939 |
---|---|
container_issue | 10 |
container_start_page | 1934 |
container_title | Helvetica chimica acta |
container_volume | 91 |
creator | Gao, Xue Zhang, Zhan-Xin Jia, Zhong-Jian |
description | Five new acyclic 12‐hydroxygeranylgeraniol‐derived diterpenoids, i.e., 1–5, were isolated from the seeds of Carpesium triste. The structures including the absolute configurations of the new compounds were elucidated by spectroscopic methods. All the compounds, except for 2, were evaluated for their in vitro cytotoxic activity against cultured SMMC‐7721 (human hepatoma), HL‐60 (human promyelocytic leukemia), and L02 (human hepatocyte) cells. |
doi_str_mv | 10.1002/hlca.200890206 |
format | Article |
fullrecord | <record><control><sourceid>istex_cross</sourceid><recordid>TN_cdi_crossref_primary_10_1002_hlca_200890206</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>ark_67375_WNG_DMSK81NV_V</sourcerecordid><originalsourceid>FETCH-LOGICAL-c3276-33934841170d63610401793b4e8546413c6c574e7f0a4e6be5f89ee52b291b413</originalsourceid><addsrcrecordid>eNqFkM1PwkAQxTdGExG9eu4_UJz96G73SIqCEfGAohez6cdUVgsluyj0v7eIId48vcy8-U3yHiGXFHoUgF3NqzztMYBYAwN5RDo0YixkUkXHpANA4xCofjklZ96_A4DWoDrkdYKboJ83eWXzgLJw1BSu3jZv6NJlU_2IratwgM5-YREM7BrdCpe1LXxQunoRrOcYTBHbsS6DJG1Nbz_btbN-jefkpEwrjxe_2iVPN9ePySgcPwxvk_44zDlTMuRccxELShUUkksKAqjSPBMYR0IKynOZR0qgKiEVKDOMylgjRixjmmat3yW9_d_c1d47LM3K2UXqGkPB7Moxu3LMoZwW0HtgYyts_rk2o3HS_8uGe3aXcHtgU_dhpOIqMs-ToRncT-9iOpmZGf8GmW13pw</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>New Acyclic 12-Hydroxygeranylgeraniol-Derived Diterpenoids from the Seeds of Carpesium triste</title><source>Wiley Online Library Journals Frontfile Complete</source><creator>Gao, Xue ; Zhang, Zhan-Xin ; Jia, Zhong-Jian</creator><creatorcontrib>Gao, Xue ; Zhang, Zhan-Xin ; Jia, Zhong-Jian</creatorcontrib><description>Five new acyclic 12‐hydroxygeranylgeraniol‐derived diterpenoids, i.e., 1–5, were isolated from the seeds of Carpesium triste. The structures including the absolute configurations of the new compounds were elucidated by spectroscopic methods. All the compounds, except for 2, were evaluated for their in vitro cytotoxic activity against cultured SMMC‐7721 (human hepatoma), HL‐60 (human promyelocytic leukemia), and L02 (human hepatocyte) cells.</description><identifier>ISSN: 0018-019X</identifier><identifier>EISSN: 1522-2675</identifier><identifier>DOI: 10.1002/hlca.200890206</identifier><language>eng</language><publisher>Zürich: WILEY-VCH Verlag</publisher><subject>Carpesium triste ; Cytotoxic activity ; Diterpenoids</subject><ispartof>Helvetica chimica acta, 2008-10, Vol.91 (10), p.1934-1939</ispartof><rights>Copyright © 2008 Verlag Helvetica Chimica Acta AG, Zürich, Switzerland</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3276-33934841170d63610401793b4e8546413c6c574e7f0a4e6be5f89ee52b291b413</citedby><cites>FETCH-LOGICAL-c3276-33934841170d63610401793b4e8546413c6c574e7f0a4e6be5f89ee52b291b413</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.200890206$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fhlca.200890206$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,27903,27904,45553,45554</link.rule.ids></links><search><creatorcontrib>Gao, Xue</creatorcontrib><creatorcontrib>Zhang, Zhan-Xin</creatorcontrib><creatorcontrib>Jia, Zhong-Jian</creatorcontrib><title>New Acyclic 12-Hydroxygeranylgeraniol-Derived Diterpenoids from the Seeds of Carpesium triste</title><title>Helvetica chimica acta</title><addtitle>HCA</addtitle><description>Five new acyclic 12‐hydroxygeranylgeraniol‐derived diterpenoids, i.e., 1–5, were isolated from the seeds of Carpesium triste. The structures including the absolute configurations of the new compounds were elucidated by spectroscopic methods. All the compounds, except for 2, were evaluated for their in vitro cytotoxic activity against cultured SMMC‐7721 (human hepatoma), HL‐60 (human promyelocytic leukemia), and L02 (human hepatocyte) cells.</description><subject>Carpesium triste</subject><subject>Cytotoxic activity</subject><subject>Diterpenoids</subject><issn>0018-019X</issn><issn>1522-2675</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2008</creationdate><recordtype>article</recordtype><recordid>eNqFkM1PwkAQxTdGExG9eu4_UJz96G73SIqCEfGAohez6cdUVgsluyj0v7eIId48vcy8-U3yHiGXFHoUgF3NqzztMYBYAwN5RDo0YixkUkXHpANA4xCofjklZ96_A4DWoDrkdYKboJ83eWXzgLJw1BSu3jZv6NJlU_2IratwgM5-YREM7BrdCpe1LXxQunoRrOcYTBHbsS6DJG1Nbz_btbN-jefkpEwrjxe_2iVPN9ePySgcPwxvk_44zDlTMuRccxELShUUkksKAqjSPBMYR0IKynOZR0qgKiEVKDOMylgjRixjmmat3yW9_d_c1d47LM3K2UXqGkPB7Moxu3LMoZwW0HtgYyts_rk2o3HS_8uGe3aXcHtgU_dhpOIqMs-ToRncT-9iOpmZGf8GmW13pw</recordid><startdate>200810</startdate><enddate>200810</enddate><creator>Gao, Xue</creator><creator>Zhang, Zhan-Xin</creator><creator>Jia, Zhong-Jian</creator><general>WILEY-VCH Verlag</general><general>WILEY‐VCH Verlag</general><scope>BSCLL</scope><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>200810</creationdate><title>New Acyclic 12-Hydroxygeranylgeraniol-Derived Diterpenoids from the Seeds of Carpesium triste</title><author>Gao, Xue ; Zhang, Zhan-Xin ; Jia, Zhong-Jian</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3276-33934841170d63610401793b4e8546413c6c574e7f0a4e6be5f89ee52b291b413</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2008</creationdate><topic>Carpesium triste</topic><topic>Cytotoxic activity</topic><topic>Diterpenoids</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Gao, Xue</creatorcontrib><creatorcontrib>Zhang, Zhan-Xin</creatorcontrib><creatorcontrib>Jia, Zhong-Jian</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>Gao, Xue</au><au>Zhang, Zhan-Xin</au><au>Jia, Zhong-Jian</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>New Acyclic 12-Hydroxygeranylgeraniol-Derived Diterpenoids from the Seeds of Carpesium triste</atitle><jtitle>Helvetica chimica acta</jtitle><addtitle>HCA</addtitle><date>2008-10</date><risdate>2008</risdate><volume>91</volume><issue>10</issue><spage>1934</spage><epage>1939</epage><pages>1934-1939</pages><issn>0018-019X</issn><eissn>1522-2675</eissn><abstract>Five new acyclic 12‐hydroxygeranylgeraniol‐derived diterpenoids, i.e., 1–5, were isolated from the seeds of Carpesium triste. The structures including the absolute configurations of the new compounds were elucidated by spectroscopic methods. All the compounds, except for 2, were evaluated for their in vitro cytotoxic activity against cultured SMMC‐7721 (human hepatoma), HL‐60 (human promyelocytic leukemia), and L02 (human hepatocyte) cells.</abstract><cop>Zürich</cop><pub>WILEY-VCH Verlag</pub><doi>10.1002/hlca.200890206</doi><tpages>6</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0018-019X |
ispartof | Helvetica chimica acta, 2008-10, Vol.91 (10), p.1934-1939 |
issn | 0018-019X 1522-2675 |
language | eng |
recordid | cdi_crossref_primary_10_1002_hlca_200890206 |
source | Wiley Online Library Journals Frontfile Complete |
subjects | Carpesium triste Cytotoxic activity Diterpenoids |
title | New Acyclic 12-Hydroxygeranylgeraniol-Derived Diterpenoids from the Seeds of Carpesium triste |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-25T00%3A43%3A34IST&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=New%20Acyclic%2012-Hydroxygeranylgeraniol-Derived%20Diterpenoids%20from%20the%20Seeds%20of%20Carpesium%20triste&rft.jtitle=Helvetica%20chimica%20acta&rft.au=Gao,%20Xue&rft.date=2008-10&rft.volume=91&rft.issue=10&rft.spage=1934&rft.epage=1939&rft.pages=1934-1939&rft.issn=0018-019X&rft.eissn=1522-2675&rft_id=info:doi/10.1002/hlca.200890206&rft_dat=%3Cistex_cross%3Eark_67375_WNG_DMSK81NV_V%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 |