Loading…
A new sesquiterpene lactone from Sarcandra glabra
A new eudesmanolide sesquiterpene, atractylenolide IV (1), together with seven known compounds were isolated from the 70% aqueous acetonic extract of the whole plant of Sarcandra glabra (Chloranthaceae). Their structures were established by spectral analysis, mainly UV, IR, HRESI-MS, 1D and 2D-NMR e...
Saved in:
Published in: | Natural product research 2013-07, Vol.27 (13), p.1197-1201 |
---|---|
Main Authors: | , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
cited_by | cdi_FETCH-LOGICAL-c363t-ee70c556975aa0c545b371f4ba0923eb955009dc02462c1535c6800dcbe29dc33 |
---|---|
cites | cdi_FETCH-LOGICAL-c363t-ee70c556975aa0c545b371f4ba0923eb955009dc02462c1535c6800dcbe29dc33 |
container_end_page | 1201 |
container_issue | 13 |
container_start_page | 1197 |
container_title | Natural product research |
container_volume | 27 |
creator | Hu, Xiao-Ru Wu, Hai-Feng Zhang, Xiao-Po Yang, Jun-Shan Dai, Zhong Lin, Rui-Chao Xu, Xu-Dong |
description | A new eudesmanolide sesquiterpene, atractylenolide IV (1), together with seven known compounds were isolated from the 70% aqueous acetonic extract of the whole plant of Sarcandra glabra (Chloranthaceae). Their structures were established by spectral analysis, mainly UV, IR, HRESI-MS, 1D and 2D-NMR experiments (HSQC, HMBC and NOESY). Compounds 1-4 showed no remarkable cytotoxic activity against Hela, HCT-8 and MCF-7 cancer cell lines with IC
50
> 50 µg mL
−1
. |
doi_str_mv | 10.1080/14786419.2012.722084 |
format | article |
fullrecord | <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_proquest_miscellaneous_1399504852</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>1399504852</sourcerecordid><originalsourceid>FETCH-LOGICAL-c363t-ee70c556975aa0c545b371f4ba0923eb955009dc02462c1535c6800dcbe29dc33</originalsourceid><addsrcrecordid>eNp9kEtLw0AUhQdRbK3-A5Es3aTeeSWZlZRSH1Bwoa6HyeRGIkmmnUko_fempO3S1T0czrkHPkLuKcwpZPBERZolgqo5A8rmKWOQiQsyPdhxIlh6edZUTchNCL8AjEopr8mEMSUSmaVTQhdRi7soYNj2VYd-gy1GtbGdG27pXRN9Gm9NW3gT_dQm9-aWXJWmDnh3vDPy_bL6Wr7F64_X9-ViHVue8C5GTMFKmahUGjMoIXOe0lLkBhTjmCspAVRhgYmEWSq5tEkGUNgc2WBzPiOP49-Nd9seQ6ebKlisa9Oi64OmXCkJIpNsiIoxar0LwWOpN75qjN9rCvoAS59g6QMsPcIaag_HhT5vsDiXTnSGwPMYqNrS-cbsnK8L3Zl97XzpTWuroPm_E3_CBXbA</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1399504852</pqid></control><display><type>article</type><title>A new sesquiterpene lactone from Sarcandra glabra</title><source>Taylor and Francis Science and Technology Collection</source><creator>Hu, Xiao-Ru ; Wu, Hai-Feng ; Zhang, Xiao-Po ; Yang, Jun-Shan ; Dai, Zhong ; Lin, Rui-Chao ; Xu, Xu-Dong</creator><creatorcontrib>Hu, Xiao-Ru ; Wu, Hai-Feng ; Zhang, Xiao-Po ; Yang, Jun-Shan ; Dai, Zhong ; Lin, Rui-Chao ; Xu, Xu-Dong</creatorcontrib><description>A new eudesmanolide sesquiterpene, atractylenolide IV (1), together with seven known compounds were isolated from the 70% aqueous acetonic extract of the whole plant of Sarcandra glabra (Chloranthaceae). Their structures were established by spectral analysis, mainly UV, IR, HRESI-MS, 1D and 2D-NMR experiments (HSQC, HMBC and NOESY). Compounds 1-4 showed no remarkable cytotoxic activity against Hela, HCT-8 and MCF-7 cancer cell lines with IC
50
> 50 µg mL
−1
.</description><identifier>ISSN: 1478-6419</identifier><identifier>EISSN: 1478-6427</identifier><identifier>DOI: 10.1080/14786419.2012.722084</identifier><identifier>PMID: 22946587</identifier><language>eng</language><publisher>England: Taylor & Francis Group</publisher><subject>atractylenolide IV ; chloranthaceae ; cytotoxic activity ; Lactones - chemistry ; Magnoliopsida - chemistry ; Sarcandra glabra ; sesquiterpene ; Sesquiterpenes - chemistry</subject><ispartof>Natural product research, 2013-07, Vol.27 (13), p.1197-1201</ispartof><rights>Copyright Taylor & Francis Group, LLC 2013</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c363t-ee70c556975aa0c545b371f4ba0923eb955009dc02462c1535c6800dcbe29dc33</citedby><cites>FETCH-LOGICAL-c363t-ee70c556975aa0c545b371f4ba0923eb955009dc02462c1535c6800dcbe29dc33</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/22946587$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Hu, Xiao-Ru</creatorcontrib><creatorcontrib>Wu, Hai-Feng</creatorcontrib><creatorcontrib>Zhang, Xiao-Po</creatorcontrib><creatorcontrib>Yang, Jun-Shan</creatorcontrib><creatorcontrib>Dai, Zhong</creatorcontrib><creatorcontrib>Lin, Rui-Chao</creatorcontrib><creatorcontrib>Xu, Xu-Dong</creatorcontrib><title>A new sesquiterpene lactone from Sarcandra glabra</title><title>Natural product research</title><addtitle>Nat Prod Res</addtitle><description>A new eudesmanolide sesquiterpene, atractylenolide IV (1), together with seven known compounds were isolated from the 70% aqueous acetonic extract of the whole plant of Sarcandra glabra (Chloranthaceae). Their structures were established by spectral analysis, mainly UV, IR, HRESI-MS, 1D and 2D-NMR experiments (HSQC, HMBC and NOESY). Compounds 1-4 showed no remarkable cytotoxic activity against Hela, HCT-8 and MCF-7 cancer cell lines with IC
50
> 50 µg mL
−1
.</description><subject>atractylenolide IV</subject><subject>chloranthaceae</subject><subject>cytotoxic activity</subject><subject>Lactones - chemistry</subject><subject>Magnoliopsida - chemistry</subject><subject>Sarcandra glabra</subject><subject>sesquiterpene</subject><subject>Sesquiterpenes - chemistry</subject><issn>1478-6419</issn><issn>1478-6427</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><recordid>eNp9kEtLw0AUhQdRbK3-A5Es3aTeeSWZlZRSH1Bwoa6HyeRGIkmmnUko_fempO3S1T0czrkHPkLuKcwpZPBERZolgqo5A8rmKWOQiQsyPdhxIlh6edZUTchNCL8AjEopr8mEMSUSmaVTQhdRi7soYNj2VYd-gy1GtbGdG27pXRN9Gm9NW3gT_dQm9-aWXJWmDnh3vDPy_bL6Wr7F64_X9-ViHVue8C5GTMFKmahUGjMoIXOe0lLkBhTjmCspAVRhgYmEWSq5tEkGUNgc2WBzPiOP49-Nd9seQ6ebKlisa9Oi64OmXCkJIpNsiIoxar0LwWOpN75qjN9rCvoAS59g6QMsPcIaag_HhT5vsDiXTnSGwPMYqNrS-cbsnK8L3Zl97XzpTWuroPm_E3_CBXbA</recordid><startdate>20130701</startdate><enddate>20130701</enddate><creator>Hu, Xiao-Ru</creator><creator>Wu, Hai-Feng</creator><creator>Zhang, Xiao-Po</creator><creator>Yang, Jun-Shan</creator><creator>Dai, Zhong</creator><creator>Lin, Rui-Chao</creator><creator>Xu, Xu-Dong</creator><general>Taylor & Francis Group</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></search><sort><creationdate>20130701</creationdate><title>A new sesquiterpene lactone from Sarcandra glabra</title><author>Hu, Xiao-Ru ; Wu, Hai-Feng ; Zhang, Xiao-Po ; Yang, Jun-Shan ; Dai, Zhong ; Lin, Rui-Chao ; Xu, Xu-Dong</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c363t-ee70c556975aa0c545b371f4ba0923eb955009dc02462c1535c6800dcbe29dc33</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>atractylenolide IV</topic><topic>chloranthaceae</topic><topic>cytotoxic activity</topic><topic>Lactones - chemistry</topic><topic>Magnoliopsida - chemistry</topic><topic>Sarcandra glabra</topic><topic>sesquiterpene</topic><topic>Sesquiterpenes - chemistry</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Hu, Xiao-Ru</creatorcontrib><creatorcontrib>Wu, Hai-Feng</creatorcontrib><creatorcontrib>Zhang, Xiao-Po</creatorcontrib><creatorcontrib>Yang, Jun-Shan</creatorcontrib><creatorcontrib>Dai, Zhong</creatorcontrib><creatorcontrib>Lin, Rui-Chao</creatorcontrib><creatorcontrib>Xu, Xu-Dong</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><jtitle>Natural product research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Hu, Xiao-Ru</au><au>Wu, Hai-Feng</au><au>Zhang, Xiao-Po</au><au>Yang, Jun-Shan</au><au>Dai, Zhong</au><au>Lin, Rui-Chao</au><au>Xu, Xu-Dong</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>A new sesquiterpene lactone from Sarcandra glabra</atitle><jtitle>Natural product research</jtitle><addtitle>Nat Prod Res</addtitle><date>2013-07-01</date><risdate>2013</risdate><volume>27</volume><issue>13</issue><spage>1197</spage><epage>1201</epage><pages>1197-1201</pages><issn>1478-6419</issn><eissn>1478-6427</eissn><abstract>A new eudesmanolide sesquiterpene, atractylenolide IV (1), together with seven known compounds were isolated from the 70% aqueous acetonic extract of the whole plant of Sarcandra glabra (Chloranthaceae). Their structures were established by spectral analysis, mainly UV, IR, HRESI-MS, 1D and 2D-NMR experiments (HSQC, HMBC and NOESY). Compounds 1-4 showed no remarkable cytotoxic activity against Hela, HCT-8 and MCF-7 cancer cell lines with IC
50
> 50 µg mL
−1
.</abstract><cop>England</cop><pub>Taylor & Francis Group</pub><pmid>22946587</pmid><doi>10.1080/14786419.2012.722084</doi><tpages>5</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1478-6419 |
ispartof | Natural product research, 2013-07, Vol.27 (13), p.1197-1201 |
issn | 1478-6419 1478-6427 |
language | eng |
recordid | cdi_proquest_miscellaneous_1399504852 |
source | Taylor and Francis Science and Technology Collection |
subjects | atractylenolide IV chloranthaceae cytotoxic activity Lactones - chemistry Magnoliopsida - chemistry Sarcandra glabra sesquiterpene Sesquiterpenes - chemistry |
title | A new sesquiterpene lactone from Sarcandra glabra |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-01T12%3A45%3A58IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=A%20new%20sesquiterpene%20lactone%20from%20Sarcandra%20glabra&rft.jtitle=Natural%20product%20research&rft.au=Hu,%20Xiao-Ru&rft.date=2013-07-01&rft.volume=27&rft.issue=13&rft.spage=1197&rft.epage=1201&rft.pages=1197-1201&rft.issn=1478-6419&rft.eissn=1478-6427&rft_id=info:doi/10.1080/14786419.2012.722084&rft_dat=%3Cproquest_pubme%3E1399504852%3C/proquest_pubme%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c363t-ee70c556975aa0c545b371f4ba0923eb955009dc02462c1535c6800dcbe29dc33%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=1399504852&rft_id=info:pmid/22946587&rfr_iscdi=true |