Loading…
Plant coumarins. IX. Phenolic compounds of Ferulopsis hystrix growing in Mongolia. Cytotoxic activity of 8,9-dihydrofurocoumarins
It was shown that plants of the genus Ferulopsis are valuable sources of coumarins. Nine angular 8-substituted and 8,9-disubstituted 8,9-dihydrofurocoumarins were isolated. The cytotoxicity of these compounds was studied on models of human CEM-13, MT-4, and U-937 tumor cells. X-ray structure data we...
Saved in:
Published in: | Chemistry of natural compounds 2012-05, Vol.48 (2), p.211-217 |
---|---|
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-c595t-25e683ea5244db1d191e414a2a5b1429315c0c89a743657e0fd5ec66b4352693 |
---|---|
cites | cdi_FETCH-LOGICAL-c595t-25e683ea5244db1d191e414a2a5b1429315c0c89a743657e0fd5ec66b4352693 |
container_end_page | 217 |
container_issue | 2 |
container_start_page | 211 |
container_title | Chemistry of natural compounds |
container_volume | 48 |
creator | Shulˈts, E. E. Ganbaatar, Zh Petrova, T. N. Shakirov, M. M. Bagryanskaya, I. Yu Taraskin, V. V. Radnaeva, L. D. Otgonsuren, D. Pokrovskii, A. G. Tolstikov, G. A. |
description | It was shown that plants of the genus
Ferulopsis
are valuable sources of coumarins. Nine angular 8-substituted and 8,9-disubstituted 8,9-dihydrofurocoumarins were isolated. The cytotoxicity of these compounds was studied on models of human CEM-13, MT-4, and U-937 tumor cells. X-ray structure data were obtained for peucenidin. |
doi_str_mv | 10.1007/s10600-012-0207-3 |
format | article |
fullrecord | <record><control><sourceid>gale_cross</sourceid><recordid>TN_cdi_gale_infotracmisc_A357034755</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><galeid>A357034755</galeid><sourcerecordid>A357034755</sourcerecordid><originalsourceid>FETCH-LOGICAL-c595t-25e683ea5244db1d191e414a2a5b1429315c0c89a743657e0fd5ec66b4352693</originalsourceid><addsrcrecordid>eNp9kU1LJDEQhoO44Oj6A7wFPC2YttLp9MdRhnUdUFZ2PewtZNLpnkhPMiRpnT7uPzfDiDAgkkOR4nmqoF6ELihkFKC6DhRKAAI0J5BDRdgRmlFeMVKzuj5GMwBoCKMMTtBpCM_pW5dlPUP_HwdpI1ZuXEtvbMjw4l-GH1fausGo1F9v3GjbgF2Hb7UfB7cJJuDVFKI3W9x792psj43FD872yZEZnk_RRbdNulTRvJg47ez6qiGtWU2td93o3cfG7-hbJ4egz9_rGXq6_fk0vyP3v38t5jf3RPGGR5JzXdZMS54XRbukLW2oLmghc8mXtMgbRrkCVTeyKljJKw1dy7Uqy2XBeF427Axd7sf2ctDC2M5FL9XaBCVuGK-AFRXnico-odJr9dooZ3VnUv9A-HEgJCbqbezlGIJY_P1zyNI9q7wLwetObLxJR5gEBbFLUexTFClFsUtRsOTkeyck1vbai2c3epsO9YX0Bm2TnqU</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>Plant coumarins. IX. Phenolic compounds of Ferulopsis hystrix growing in Mongolia. Cytotoxic activity of 8,9-dihydrofurocoumarins</title><source>Springer Nature</source><creator>Shulˈts, E. E. ; Ganbaatar, Zh ; Petrova, T. N. ; Shakirov, M. M. ; Bagryanskaya, I. Yu ; Taraskin, V. V. ; Radnaeva, L. D. ; Otgonsuren, D. ; Pokrovskii, A. G. ; Tolstikov, G. A.</creator><creatorcontrib>Shulˈts, E. E. ; Ganbaatar, Zh ; Petrova, T. N. ; Shakirov, M. M. ; Bagryanskaya, I. Yu ; Taraskin, V. V. ; Radnaeva, L. D. ; Otgonsuren, D. ; Pokrovskii, A. G. ; Tolstikov, G. A.</creatorcontrib><description>It was shown that plants of the genus
Ferulopsis
are valuable sources of coumarins. Nine angular 8-substituted and 8,9-disubstituted 8,9-dihydrofurocoumarins were isolated. The cytotoxicity of these compounds was studied on models of human CEM-13, MT-4, and U-937 tumor cells. X-ray structure data were obtained for peucenidin.</description><identifier>ISSN: 0009-3130</identifier><identifier>EISSN: 1573-8388</identifier><identifier>DOI: 10.1007/s10600-012-0207-3</identifier><language>eng</language><publisher>Boston: Springer US</publisher><subject>Coumarins ; Medicine ; Organic Chemistry ; Pharmacy ; Plant Sciences</subject><ispartof>Chemistry of natural compounds, 2012-05, Vol.48 (2), p.211-217</ispartof><rights>Springer Science+Business Media, Inc. 2012</rights><rights>COPYRIGHT 2012 Springer</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c595t-25e683ea5244db1d191e414a2a5b1429315c0c89a743657e0fd5ec66b4352693</citedby><cites>FETCH-LOGICAL-c595t-25e683ea5244db1d191e414a2a5b1429315c0c89a743657e0fd5ec66b4352693</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></links><search><creatorcontrib>Shulˈts, E. E.</creatorcontrib><creatorcontrib>Ganbaatar, Zh</creatorcontrib><creatorcontrib>Petrova, T. N.</creatorcontrib><creatorcontrib>Shakirov, M. M.</creatorcontrib><creatorcontrib>Bagryanskaya, I. Yu</creatorcontrib><creatorcontrib>Taraskin, V. V.</creatorcontrib><creatorcontrib>Radnaeva, L. D.</creatorcontrib><creatorcontrib>Otgonsuren, D.</creatorcontrib><creatorcontrib>Pokrovskii, A. G.</creatorcontrib><creatorcontrib>Tolstikov, G. A.</creatorcontrib><title>Plant coumarins. IX. Phenolic compounds of Ferulopsis hystrix growing in Mongolia. Cytotoxic activity of 8,9-dihydrofurocoumarins</title><title>Chemistry of natural compounds</title><addtitle>Chem Nat Compd</addtitle><description>It was shown that plants of the genus
Ferulopsis
are valuable sources of coumarins. Nine angular 8-substituted and 8,9-disubstituted 8,9-dihydrofurocoumarins were isolated. The cytotoxicity of these compounds was studied on models of human CEM-13, MT-4, and U-937 tumor cells. X-ray structure data were obtained for peucenidin.</description><subject>Coumarins</subject><subject>Medicine</subject><subject>Organic Chemistry</subject><subject>Pharmacy</subject><subject>Plant Sciences</subject><issn>0009-3130</issn><issn>1573-8388</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><recordid>eNp9kU1LJDEQhoO44Oj6A7wFPC2YttLp9MdRhnUdUFZ2PewtZNLpnkhPMiRpnT7uPzfDiDAgkkOR4nmqoF6ELihkFKC6DhRKAAI0J5BDRdgRmlFeMVKzuj5GMwBoCKMMTtBpCM_pW5dlPUP_HwdpI1ZuXEtvbMjw4l-GH1fausGo1F9v3GjbgF2Hb7UfB7cJJuDVFKI3W9x792psj43FD872yZEZnk_RRbdNulTRvJg47ez6qiGtWU2td93o3cfG7-hbJ4egz9_rGXq6_fk0vyP3v38t5jf3RPGGR5JzXdZMS54XRbukLW2oLmghc8mXtMgbRrkCVTeyKljJKw1dy7Uqy2XBeF427Axd7sf2ctDC2M5FL9XaBCVuGK-AFRXnico-odJr9dooZ3VnUv9A-HEgJCbqbezlGIJY_P1zyNI9q7wLwetObLxJR5gEBbFLUexTFClFsUtRsOTkeyck1vbai2c3epsO9YX0Bm2TnqU</recordid><startdate>20120501</startdate><enddate>20120501</enddate><creator>Shulˈts, E. E.</creator><creator>Ganbaatar, Zh</creator><creator>Petrova, T. N.</creator><creator>Shakirov, M. M.</creator><creator>Bagryanskaya, I. Yu</creator><creator>Taraskin, V. V.</creator><creator>Radnaeva, L. D.</creator><creator>Otgonsuren, D.</creator><creator>Pokrovskii, A. G.</creator><creator>Tolstikov, G. A.</creator><general>Springer US</general><general>Springer</general><scope>AAYXX</scope><scope>CITATION</scope><scope>ISR</scope></search><sort><creationdate>20120501</creationdate><title>Plant coumarins. IX. Phenolic compounds of Ferulopsis hystrix growing in Mongolia. Cytotoxic activity of 8,9-dihydrofurocoumarins</title><author>Shulˈts, E. E. ; Ganbaatar, Zh ; Petrova, T. N. ; Shakirov, M. M. ; Bagryanskaya, I. Yu ; Taraskin, V. V. ; Radnaeva, L. D. ; Otgonsuren, D. ; Pokrovskii, A. G. ; Tolstikov, G. A.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c595t-25e683ea5244db1d191e414a2a5b1429315c0c89a743657e0fd5ec66b4352693</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2012</creationdate><topic>Coumarins</topic><topic>Medicine</topic><topic>Organic Chemistry</topic><topic>Pharmacy</topic><topic>Plant Sciences</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Shulˈts, E. E.</creatorcontrib><creatorcontrib>Ganbaatar, Zh</creatorcontrib><creatorcontrib>Petrova, T. N.</creatorcontrib><creatorcontrib>Shakirov, M. M.</creatorcontrib><creatorcontrib>Bagryanskaya, I. Yu</creatorcontrib><creatorcontrib>Taraskin, V. V.</creatorcontrib><creatorcontrib>Radnaeva, L. D.</creatorcontrib><creatorcontrib>Otgonsuren, D.</creatorcontrib><creatorcontrib>Pokrovskii, A. G.</creatorcontrib><creatorcontrib>Tolstikov, G. A.</creatorcontrib><collection>CrossRef</collection><collection>Science (Gale in Context)</collection><jtitle>Chemistry of natural compounds</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Shulˈts, E. E.</au><au>Ganbaatar, Zh</au><au>Petrova, T. N.</au><au>Shakirov, M. M.</au><au>Bagryanskaya, I. Yu</au><au>Taraskin, V. V.</au><au>Radnaeva, L. D.</au><au>Otgonsuren, D.</au><au>Pokrovskii, A. G.</au><au>Tolstikov, G. A.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Plant coumarins. IX. Phenolic compounds of Ferulopsis hystrix growing in Mongolia. Cytotoxic activity of 8,9-dihydrofurocoumarins</atitle><jtitle>Chemistry of natural compounds</jtitle><stitle>Chem Nat Compd</stitle><date>2012-05-01</date><risdate>2012</risdate><volume>48</volume><issue>2</issue><spage>211</spage><epage>217</epage><pages>211-217</pages><issn>0009-3130</issn><eissn>1573-8388</eissn><abstract>It was shown that plants of the genus
Ferulopsis
are valuable sources of coumarins. Nine angular 8-substituted and 8,9-disubstituted 8,9-dihydrofurocoumarins were isolated. The cytotoxicity of these compounds was studied on models of human CEM-13, MT-4, and U-937 tumor cells. X-ray structure data were obtained for peucenidin.</abstract><cop>Boston</cop><pub>Springer US</pub><doi>10.1007/s10600-012-0207-3</doi><tpages>7</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0009-3130 |
ispartof | Chemistry of natural compounds, 2012-05, Vol.48 (2), p.211-217 |
issn | 0009-3130 1573-8388 |
language | eng |
recordid | cdi_gale_infotracmisc_A357034755 |
source | Springer Nature |
subjects | Coumarins Medicine Organic Chemistry Pharmacy Plant Sciences |
title | Plant coumarins. IX. Phenolic compounds of Ferulopsis hystrix growing in Mongolia. Cytotoxic activity of 8,9-dihydrofurocoumarins |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-07T14%3A52%3A00IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-gale_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Plant%20coumarins.%20IX.%20Phenolic%20compounds%20of%20Ferulopsis%20hystrix%20growing%20in%20Mongolia.%20Cytotoxic%20activity%20of%208,9-dihydrofurocoumarins&rft.jtitle=Chemistry%20of%20natural%20compounds&rft.au=Shul%CB%88ts,%20E.%20E.&rft.date=2012-05-01&rft.volume=48&rft.issue=2&rft.spage=211&rft.epage=217&rft.pages=211-217&rft.issn=0009-3130&rft.eissn=1573-8388&rft_id=info:doi/10.1007/s10600-012-0207-3&rft_dat=%3Cgale_cross%3EA357034755%3C/gale_cross%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c595t-25e683ea5244db1d191e414a2a5b1429315c0c89a743657e0fd5ec66b4352693%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_id=info:pmid/&rft_galeid=A357034755&rfr_iscdi=true |