A 2-Arylbenzofuran Derivative from Hopea Mengarawan
A new 2-arylbenzofuran derivative (diptoindonesin G) (1), along with nine known oligostilbenes, have been isolated and identified from the acetone extract of the tree bark of Hopea mengarawan. The structures of these compounds were determined based on spectroscopic data, including 2D NMR and HREIMS...
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Veröffentlicht in: | Natural product communications 2009-07, Vol.4 (7), p.947-950 |
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creator | Juliawaty, Lia D. Sahidin Hakim, Euis H. Achmad, Sjamsul A. Syah, Yana M. Latip, Jalifah Said, Ikram M. |
description | A new 2-arylbenzofuran derivative (diptoindonesin G) (1), along with nine known oligostilbenes, have been isolated and identified from the acetone extract of the tree bark of Hopea mengarawan. The structures of these compounds were determined based on spectroscopic data, including 2D NMR and HREIMS spectra. On cytotoxic evaluation of the isolated compounds against murin leukemia P-388 cells, compound 1 was the strongest in inhibiting the growth of the cells. |
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The structures of these compounds were determined based on spectroscopic data, including 2D NMR and HREIMS spectra. On cytotoxic evaluation of the isolated compounds against murin leukemia P-388 cells, compound 1 was the strongest in inhibiting the growth of the cells.</description><identifier>ISSN: 1934-578X</identifier><identifier>EISSN: 1555-9475</identifier><identifier>DOI: 10.1177/1934578X0900400715</identifier><identifier>PMID: 19731600</identifier><language>eng</language><publisher>Los Angeles, CA: SAGE Publications</publisher><subject>Animals ; Antineoplastic Agents, Phytogenic - chemistry ; Antineoplastic Agents, Phytogenic - isolation & purification ; Antineoplastic Agents, Phytogenic - pharmacology ; Benzofurans - chemistry ; Benzofurans - isolation & purification ; Benzofurans - pharmacology ; Cell Line, Tumor ; Dipterocarpaceae - chemistry ; Drug Screening Assays, Antitumor ; Leukemia P388 - drug therapy ; Magnetic Resonance Spectroscopy ; Mice ; Plant Bark - chemistry ; Solvents ; Spectrometry, Mass, Electrospray Ionization ; Spectrophotometry, Infrared ; Spectrophotometry, Ultraviolet ; Spectroscopy, Fourier Transform Infrared</subject><ispartof>Natural product communications, 2009-07, Vol.4 (7), p.947-950</ispartof><rights>2009 SAGE Publications Inc.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c385t-17231f4902c0371ee611015b51c6bb5306ccb12e3e5bf8d4461adbd6276d558f3</citedby><cites>FETCH-LOGICAL-c385t-17231f4902c0371ee611015b51c6bb5306ccb12e3e5bf8d4461adbd6276d558f3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://journals.sagepub.com/doi/pdf/10.1177/1934578X0900400715$$EPDF$$P50$$Gsage$$H</linktopdf><linktohtml>$$Uhttps://journals.sagepub.com/doi/10.1177/1934578X0900400715$$EHTML$$P50$$Gsage$$H</linktohtml><link.rule.ids>314,777,781,21947,27834,27905,27906,44926,45314</link.rule.ids><linktorsrc>$$Uhttps://journals.sagepub.com/doi/full/10.1177/1934578X0900400715?utm_source=summon&utm_medium=discovery-provider$$EView_record_in_SAGE_Publications$$FView_record_in_$$GSAGE_Publications</linktorsrc><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/19731600$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Juliawaty, Lia D.</creatorcontrib><creatorcontrib>Sahidin</creatorcontrib><creatorcontrib>Hakim, Euis H.</creatorcontrib><creatorcontrib>Achmad, Sjamsul A.</creatorcontrib><creatorcontrib>Syah, Yana M.</creatorcontrib><creatorcontrib>Latip, Jalifah</creatorcontrib><creatorcontrib>Said, Ikram M.</creatorcontrib><title>A 2-Arylbenzofuran Derivative from Hopea Mengarawan</title><title>Natural product communications</title><addtitle>Nat Prod Commun</addtitle><description>A new 2-arylbenzofuran derivative (diptoindonesin G) (1), along with nine known oligostilbenes, have been isolated and identified from the acetone extract of the tree bark of Hopea mengarawan. The structures of these compounds were determined based on spectroscopic data, including 2D NMR and HREIMS spectra. On cytotoxic evaluation of the isolated compounds against murin leukemia P-388 cells, compound 1 was the strongest in inhibiting the growth of the cells.</description><subject>Animals</subject><subject>Antineoplastic Agents, Phytogenic - chemistry</subject><subject>Antineoplastic Agents, Phytogenic - isolation & purification</subject><subject>Antineoplastic Agents, Phytogenic - pharmacology</subject><subject>Benzofurans - chemistry</subject><subject>Benzofurans - isolation & purification</subject><subject>Benzofurans - pharmacology</subject><subject>Cell Line, Tumor</subject><subject>Dipterocarpaceae - chemistry</subject><subject>Drug Screening Assays, Antitumor</subject><subject>Leukemia P388 - drug therapy</subject><subject>Magnetic Resonance Spectroscopy</subject><subject>Mice</subject><subject>Plant Bark - chemistry</subject><subject>Solvents</subject><subject>Spectrometry, Mass, Electrospray Ionization</subject><subject>Spectrophotometry, Infrared</subject><subject>Spectrophotometry, Ultraviolet</subject><subject>Spectroscopy, Fourier Transform Infrared</subject><issn>1934-578X</issn><issn>1555-9475</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2009</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kE1Lw0AQhhdRbKn9Ax4kJ2-xM9mv5FjqR4WKFwVvYTeZlJQ0qbtNpf56t7TgQXAuM4fnfWEexq4R7hC1nmDGhdTpB2QAAkCjPGNDlFLGmdDyPNwBiA_EgI29X0GYNBUgsks2wExzVABDxqdREk_dvrHUfndV70wb3ZOrd2Zb7yiqXLeO5t2GTPRC7dI482XaK3ZRmcbT-LRH7P3x4W02jxevT8-z6SIueCq3MeqEYyUySArgGokUIqC0EgtlreSgisJiQpykrdJSCIWmtKVKtCqlTCs-YrfH3o3rPnvy23xd-4KaxrTU9T5XWvFA8wAmR7BwnfeOqnzj6rVx-xwhP9jK_9oKoZtTe2_XVP5GTm4CMDkC3iwpX3W9a8O3_1X-AM2bcDM</recordid><startdate>20090701</startdate><enddate>20090701</enddate><creator>Juliawaty, Lia D.</creator><creator>Sahidin</creator><creator>Hakim, Euis H.</creator><creator>Achmad, Sjamsul A.</creator><creator>Syah, Yana M.</creator><creator>Latip, Jalifah</creator><creator>Said, Ikram M.</creator><general>SAGE Publications</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>20090701</creationdate><title>A 2-Arylbenzofuran Derivative from Hopea Mengarawan</title><author>Juliawaty, Lia D. ; 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subjects | Animals Antineoplastic Agents, Phytogenic - chemistry Antineoplastic Agents, Phytogenic - isolation & purification Antineoplastic Agents, Phytogenic - pharmacology Benzofurans - chemistry Benzofurans - isolation & purification Benzofurans - pharmacology Cell Line, Tumor Dipterocarpaceae - chemistry Drug Screening Assays, Antitumor Leukemia P388 - drug therapy Magnetic Resonance Spectroscopy Mice Plant Bark - chemistry Solvents Spectrometry, Mass, Electrospray Ionization Spectrophotometry, Infrared Spectrophotometry, Ultraviolet Spectroscopy, Fourier Transform Infrared |
title | A 2-Arylbenzofuran Derivative from Hopea Mengarawan |
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