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Antiproliferative and apoptotic sesquiterpene lactones from Carpesium faberi
Four new (1–4) and 13 known sesquiterpene lactones together with two known diterpenes were isolated from Carpesium faberi. All isolated compounds were evaluated for their antiproliferative activities against MCF-7 human breast cancer cells using the MTT assay. The sesquiterpene lactones (except tome...
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Published in: | Bioorganic & medicinal chemistry letters 2011-01, Vol.21 (1), p.366-372 |
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description | Four new (1–4) and 13 known sesquiterpene lactones together with two known diterpenes were isolated from Carpesium faberi. All isolated compounds were evaluated for their antiproliferative activities against MCF-7 human breast cancer cells using the MTT assay. The sesquiterpene lactones (except tomentosin 17) possessing an α-methylene-γ-lactone moiety were found to have significant antiproliferative activities. The cell cycle-specific inhibition and apoptosis induced by selected compounds were investigated using flow cytometry (FCM).
Four new (1–4) and 13 known (5–17) sesquiterpene lactones along with two known diterpenes (18, 19) were isolated from the whole plant of Carpesium faberi. The new structures were elucidated by means of spectroscopic techniques and some chemical transformations to be pseudoguaian-1α(H)-8α,12-olide-4β-O-β-d-glucopyranoside (1), 4β,10α-dihydroxy-5α(H)-1,11(13)-guaidien-8α,12-olide (2), 4β,10β-dihydroxy-5α(H)-1, 11(13)-guaidien-8β,12-olide (3), and (4S)-acetyloxyl-11(13)-carabren-8β,12-olide (4). All isolates were tested against MCF-7 human breast cancer cells using the MTT assay. Among them, the sesquiterpene lactones (except tomentosin 17) possessing an α-methylene-γ-lactone moiety were found to have in vitro antiproliferative activities, with IC50 values of 3.0–38.8μg/mL. The effects of four selected sesquiterpene lactones (guaianolide 2, carabranolide 4, pseudoguaianolide 9, eudesmanolide 13) on the cell cycle were examined using flow cytometry (FCM). |
doi_str_mv | 10.1016/j.bmcl.2010.10.138 |
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Four new (1–4) and 13 known (5–17) sesquiterpene lactones along with two known diterpenes (18, 19) were isolated from the whole plant of Carpesium faberi. The new structures were elucidated by means of spectroscopic techniques and some chemical transformations to be pseudoguaian-1α(H)-8α,12-olide-4β-O-β-d-glucopyranoside (1), 4β,10α-dihydroxy-5α(H)-1,11(13)-guaidien-8α,12-olide (2), 4β,10β-dihydroxy-5α(H)-1, 11(13)-guaidien-8β,12-olide (3), and (4S)-acetyloxyl-11(13)-carabren-8β,12-olide (4). All isolates were tested against MCF-7 human breast cancer cells using the MTT assay. Among them, the sesquiterpene lactones (except tomentosin 17) possessing an α-methylene-γ-lactone moiety were found to have in vitro antiproliferative activities, with IC50 values of 3.0–38.8μg/mL. The effects of four selected sesquiterpene lactones (guaianolide 2, carabranolide 4, pseudoguaianolide 9, eudesmanolide 13) on the cell cycle were examined using flow cytometry (FCM).</description><identifier>ISSN: 0960-894X</identifier><identifier>EISSN: 1464-3405</identifier><identifier>DOI: 10.1016/j.bmcl.2010.10.138</identifier><identifier>PMID: 21109433</identifier><language>eng</language><publisher>Amsterdam: Elsevier Ltd</publisher><subject>Antineoplastic Agents, Phytogenic - chemistry ; Antineoplastic Agents, Phytogenic - isolation & purification ; Antineoplastic Agents, Phytogenic - toxicity ; Antiproliferative ; Apoptosis ; Asteraceae - chemistry ; Biological and medical sciences ; breast neoplasms ; Carpesium ; Carpesium faberi ; cell cycle ; Cell Line, Tumor ; Compositae ; diterpenoids ; flow cytometry ; General pharmacology ; Humans ; inhibitory concentration 50 ; Lactones - chemistry ; Lactones - isolation & purification ; Lactones - toxicity ; Magnetic Resonance Spectroscopy ; Medical sciences ; Molecular Conformation ; Pharmacognosy. Homeopathy. Health food ; Pharmacology. Drug treatments ; Plant Extracts - chemistry ; Sesquiterpene lactones ; Sesquiterpenes - chemistry ; sesquiterpenoid lactones ; spectroscopy</subject><ispartof>Bioorganic & medicinal chemistry letters, 2011-01, Vol.21 (1), p.366-372</ispartof><rights>2010 Elsevier Ltd</rights><rights>2015 INIST-CNRS</rights><rights>Copyright © 2010 Elsevier Ltd. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c441t-fdb2bac2f8a7853fddbb58c7a301b8ae3e26dd3a270f4133661b02786f1402013</citedby><cites>FETCH-LOGICAL-c441t-fdb2bac2f8a7853fddbb58c7a301b8ae3e26dd3a270f4133661b02786f1402013</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,4024,27923,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=23726820$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/21109433$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Li, Xu-Wen</creatorcontrib><creatorcontrib>Weng, Liang</creatorcontrib><creatorcontrib>Gao, Xue</creatorcontrib><creatorcontrib>Zhao, Yun</creatorcontrib><creatorcontrib>Pang, Fei</creatorcontrib><creatorcontrib>Liu, Jian-Hui</creatorcontrib><creatorcontrib>Zhang, Hong-Feng</creatorcontrib><creatorcontrib>Hu, Jin-Feng</creatorcontrib><title>Antiproliferative and apoptotic sesquiterpene lactones from Carpesium faberi</title><title>Bioorganic & medicinal chemistry letters</title><addtitle>Bioorg Med Chem Lett</addtitle><description>Four new (1–4) and 13 known sesquiterpene lactones together with two known diterpenes were isolated from Carpesium faberi. All isolated compounds were evaluated for their antiproliferative activities against MCF-7 human breast cancer cells using the MTT assay. The sesquiterpene lactones (except tomentosin 17) possessing an α-methylene-γ-lactone moiety were found to have significant antiproliferative activities. The cell cycle-specific inhibition and apoptosis induced by selected compounds were investigated using flow cytometry (FCM).
Four new (1–4) and 13 known (5–17) sesquiterpene lactones along with two known diterpenes (18, 19) were isolated from the whole plant of Carpesium faberi. The new structures were elucidated by means of spectroscopic techniques and some chemical transformations to be pseudoguaian-1α(H)-8α,12-olide-4β-O-β-d-glucopyranoside (1), 4β,10α-dihydroxy-5α(H)-1,11(13)-guaidien-8α,12-olide (2), 4β,10β-dihydroxy-5α(H)-1, 11(13)-guaidien-8β,12-olide (3), and (4S)-acetyloxyl-11(13)-carabren-8β,12-olide (4). All isolates were tested against MCF-7 human breast cancer cells using the MTT assay. Among them, the sesquiterpene lactones (except tomentosin 17) possessing an α-methylene-γ-lactone moiety were found to have in vitro antiproliferative activities, with IC50 values of 3.0–38.8μg/mL. The effects of four selected sesquiterpene lactones (guaianolide 2, carabranolide 4, pseudoguaianolide 9, eudesmanolide 13) on the cell cycle were examined using flow cytometry (FCM).</description><subject>Antineoplastic Agents, Phytogenic - chemistry</subject><subject>Antineoplastic Agents, Phytogenic - isolation & purification</subject><subject>Antineoplastic Agents, Phytogenic - toxicity</subject><subject>Antiproliferative</subject><subject>Apoptosis</subject><subject>Asteraceae - chemistry</subject><subject>Biological and medical sciences</subject><subject>breast neoplasms</subject><subject>Carpesium</subject><subject>Carpesium faberi</subject><subject>cell cycle</subject><subject>Cell Line, Tumor</subject><subject>Compositae</subject><subject>diterpenoids</subject><subject>flow cytometry</subject><subject>General pharmacology</subject><subject>Humans</subject><subject>inhibitory concentration 50</subject><subject>Lactones - chemistry</subject><subject>Lactones - isolation & purification</subject><subject>Lactones - toxicity</subject><subject>Magnetic Resonance Spectroscopy</subject><subject>Medical sciences</subject><subject>Molecular Conformation</subject><subject>Pharmacognosy. Homeopathy. Health food</subject><subject>Pharmacology. Drug treatments</subject><subject>Plant Extracts - chemistry</subject><subject>Sesquiterpene lactones</subject><subject>Sesquiterpenes - chemistry</subject><subject>sesquiterpenoid lactones</subject><subject>spectroscopy</subject><issn>0960-894X</issn><issn>1464-3405</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><recordid>eNqFkU1v1DAQhi1ERZeFP8ABckGcsvgriVfiUq34qLRSD1CJmzWxx8irJE5tpxL_vt7uAjd6svTqmfHMM4S8YXTDKGs_Hjb9aIYNp4_Bhgn1jKyYbGUtJG2ekxXdtrRWW_nzkrxM6UApk1TKF-SSM0a3UogV2V9N2c8xDN5hhOzvsYLJVjCHOYfsTZUw3S0-Y5xxwmoAk8OEqXIxjNUOSpr8MlYOeoz-FblwMCR8fX7X5PbL5x-7b_X-5uv17mpfGylZrp3teQ-GOwWdaoSztu8bZToQlPUKUCBvrRXAO-okE6JtWU95p1pX5i_bijX5cOpbBr9bMGU9-mRwGGDCsCStlKCcN6J7miwmtqotKtaEn0gTQ0oRnZ6jHyH-1ozqo2590Efd-qj7MROqFL09t1_6Ee3fkj9-C_D-DEAyMLgIk_HpHyc63ipOC_fuxDkIGn7Fwtx-Lz815WZC8ua4yacTgUXsvceok_E4GbQ-osnaBv-_SR8ATxqnQQ</recordid><startdate>20110101</startdate><enddate>20110101</enddate><creator>Li, Xu-Wen</creator><creator>Weng, Liang</creator><creator>Gao, Xue</creator><creator>Zhao, Yun</creator><creator>Pang, Fei</creator><creator>Liu, Jian-Hui</creator><creator>Zhang, Hong-Feng</creator><creator>Hu, Jin-Feng</creator><general>Elsevier Ltd</general><general>Elsevier</general><scope>FBQ</scope><scope>IQODW</scope><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><scope>7QO</scope><scope>8FD</scope><scope>FR3</scope><scope>P64</scope></search><sort><creationdate>20110101</creationdate><title>Antiproliferative and apoptotic sesquiterpene lactones from Carpesium faberi</title><author>Li, Xu-Wen ; Weng, Liang ; Gao, Xue ; Zhao, Yun ; Pang, Fei ; Liu, Jian-Hui ; Zhang, Hong-Feng ; Hu, Jin-Feng</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c441t-fdb2bac2f8a7853fddbb58c7a301b8ae3e26dd3a270f4133661b02786f1402013</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><topic>Antineoplastic Agents, Phytogenic - chemistry</topic><topic>Antineoplastic Agents, Phytogenic - isolation & purification</topic><topic>Antineoplastic Agents, Phytogenic - toxicity</topic><topic>Antiproliferative</topic><topic>Apoptosis</topic><topic>Asteraceae - chemistry</topic><topic>Biological and medical sciences</topic><topic>breast neoplasms</topic><topic>Carpesium</topic><topic>Carpesium faberi</topic><topic>cell cycle</topic><topic>Cell Line, Tumor</topic><topic>Compositae</topic><topic>diterpenoids</topic><topic>flow cytometry</topic><topic>General pharmacology</topic><topic>Humans</topic><topic>inhibitory concentration 50</topic><topic>Lactones - chemistry</topic><topic>Lactones - isolation & purification</topic><topic>Lactones - toxicity</topic><topic>Magnetic Resonance Spectroscopy</topic><topic>Medical sciences</topic><topic>Molecular Conformation</topic><topic>Pharmacognosy. Homeopathy. Health food</topic><topic>Pharmacology. Drug treatments</topic><topic>Plant Extracts - chemistry</topic><topic>Sesquiterpene lactones</topic><topic>Sesquiterpenes - chemistry</topic><topic>sesquiterpenoid lactones</topic><topic>spectroscopy</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Li, Xu-Wen</creatorcontrib><creatorcontrib>Weng, Liang</creatorcontrib><creatorcontrib>Gao, Xue</creatorcontrib><creatorcontrib>Zhao, Yun</creatorcontrib><creatorcontrib>Pang, Fei</creatorcontrib><creatorcontrib>Liu, Jian-Hui</creatorcontrib><creatorcontrib>Zhang, Hong-Feng</creatorcontrib><creatorcontrib>Hu, Jin-Feng</creatorcontrib><collection>AGRIS</collection><collection>Pascal-Francis</collection><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><collection>Biotechnology Research Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><jtitle>Bioorganic & medicinal chemistry letters</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Li, Xu-Wen</au><au>Weng, Liang</au><au>Gao, Xue</au><au>Zhao, Yun</au><au>Pang, Fei</au><au>Liu, Jian-Hui</au><au>Zhang, Hong-Feng</au><au>Hu, Jin-Feng</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Antiproliferative and apoptotic sesquiterpene lactones from Carpesium faberi</atitle><jtitle>Bioorganic & medicinal chemistry letters</jtitle><addtitle>Bioorg Med Chem Lett</addtitle><date>2011-01-01</date><risdate>2011</risdate><volume>21</volume><issue>1</issue><spage>366</spage><epage>372</epage><pages>366-372</pages><issn>0960-894X</issn><eissn>1464-3405</eissn><abstract>Four new (1–4) and 13 known sesquiterpene lactones together with two known diterpenes were isolated from Carpesium faberi. All isolated compounds were evaluated for their antiproliferative activities against MCF-7 human breast cancer cells using the MTT assay. The sesquiterpene lactones (except tomentosin 17) possessing an α-methylene-γ-lactone moiety were found to have significant antiproliferative activities. The cell cycle-specific inhibition and apoptosis induced by selected compounds were investigated using flow cytometry (FCM).
Four new (1–4) and 13 known (5–17) sesquiterpene lactones along with two known diterpenes (18, 19) were isolated from the whole plant of Carpesium faberi. The new structures were elucidated by means of spectroscopic techniques and some chemical transformations to be pseudoguaian-1α(H)-8α,12-olide-4β-O-β-d-glucopyranoside (1), 4β,10α-dihydroxy-5α(H)-1,11(13)-guaidien-8α,12-olide (2), 4β,10β-dihydroxy-5α(H)-1, 11(13)-guaidien-8β,12-olide (3), and (4S)-acetyloxyl-11(13)-carabren-8β,12-olide (4). All isolates were tested against MCF-7 human breast cancer cells using the MTT assay. Among them, the sesquiterpene lactones (except tomentosin 17) possessing an α-methylene-γ-lactone moiety were found to have in vitro antiproliferative activities, with IC50 values of 3.0–38.8μg/mL. The effects of four selected sesquiterpene lactones (guaianolide 2, carabranolide 4, pseudoguaianolide 9, eudesmanolide 13) on the cell cycle were examined using flow cytometry (FCM).</abstract><cop>Amsterdam</cop><pub>Elsevier Ltd</pub><pmid>21109433</pmid><doi>10.1016/j.bmcl.2010.10.138</doi><tpages>7</tpages></addata></record> |
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subjects | Antineoplastic Agents, Phytogenic - chemistry Antineoplastic Agents, Phytogenic - isolation & purification Antineoplastic Agents, Phytogenic - toxicity Antiproliferative Apoptosis Asteraceae - chemistry Biological and medical sciences breast neoplasms Carpesium Carpesium faberi cell cycle Cell Line, Tumor Compositae diterpenoids flow cytometry General pharmacology Humans inhibitory concentration 50 Lactones - chemistry Lactones - isolation & purification Lactones - toxicity Magnetic Resonance Spectroscopy Medical sciences Molecular Conformation Pharmacognosy. Homeopathy. Health food Pharmacology. Drug treatments Plant Extracts - chemistry Sesquiterpene lactones Sesquiterpenes - chemistry sesquiterpenoid lactones spectroscopy |
title | Antiproliferative and apoptotic sesquiterpene lactones from Carpesium faberi |
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