Cytotoxic labdane diterpenoids from Croton oblongifolius
Three labdane diterpenoids, 2-acetoxy-3-hydroxy-labda-8(17),12(E)-14-triene, 3-acetoxy-2-hydroxy-labda-8(17),12(E)-14-triene, and 2,3-dihydroxy-labda-8(17),12(E),14-triene were isolated from stem bark of Croton oblongifolius. Their structures were established by spectroscopic data, and each was also...
Gespeichert in:
Veröffentlicht in: | Phytochemistry (Oxford) 2001-01, Vol.56 (1), p.103-107 |
---|---|
Hauptverfasser: | , , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 107 |
---|---|
container_issue | 1 |
container_start_page | 103 |
container_title | Phytochemistry (Oxford) |
container_volume | 56 |
creator | ROENGSUMRAN, Sophon PETSOM, Amorn KUPTIYANUWAT, Narupat VILAIVAN, Tirayut NGAMROJNAVANICH, Nattaya CHAICHANTIPYUTH, Chaiyo PHUTHONG, Songchan |
description | Three labdane diterpenoids, 2-acetoxy-3-hydroxy-labda-8(17),12(E)-14-triene, 3-acetoxy-2-hydroxy-labda-8(17),12(E)-14-triene, and 2,3-dihydroxy-labda-8(17),12(E),14-triene were isolated from stem bark of Croton oblongifolius. Their structures were established by spectroscopic data, and each was also tested for cytotoxicity against various human tumor cell lines. The latter compound showed non-specific, moderate, cytotoxicities against all the cell lines; whereas the first two compounds were less active. |
doi_str_mv | 10.1016/S0031-9422(00)00358-7 |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_70586679</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>70586679</sourcerecordid><originalsourceid>FETCH-LOGICAL-c333t-58b46d0ab1c5345f8271d0f2ba61302704f758ba7c54a84ef4071c27fbf26b7c3</originalsourceid><addsrcrecordid>eNpF0F1LwzAUgOEgipvTn6AUBNGL6knSfOxSil8w8EK9DkmaSKVtZtKC-_d2s8yrEHjOSXgROsdwiwHzuzcAivNlQcg1wM14YTIXB2iOpaA5FQCHaL4nM3SS0hcAMMb5MZphjJdSYj5Hstz0oQ8_tc0abSrduayqexfXrgt1lTIfQ5uVcSRdFkwTus_ah6Ye0ik68rpJ7mw6F-jj8eG9fM5Xr08v5f0qt5TSPmfSFLwCbbBltGBeEoEr8MRojikQAYUXo9HCskLLwvkCBLZEeOMJN8LSBbr627uO4XtwqVdtnaxrmvGrYUhKAJOci-UI2R-0MaQUnVfrWLc6bhQGtU2mdsnUtocCULtkSoxzF9MDg2ld9T81NRrB5QR0srrxUXe2TnsnGQZG6C-4NnMJ</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>70586679</pqid></control><display><type>article</type><title>Cytotoxic labdane diterpenoids from Croton oblongifolius</title><source>MEDLINE</source><source>Elsevier ScienceDirect Journals Complete</source><creator>ROENGSUMRAN, Sophon ; PETSOM, Amorn ; KUPTIYANUWAT, Narupat ; VILAIVAN, Tirayut ; NGAMROJNAVANICH, Nattaya ; CHAICHANTIPYUTH, Chaiyo ; PHUTHONG, Songchan</creator><creatorcontrib>ROENGSUMRAN, Sophon ; PETSOM, Amorn ; KUPTIYANUWAT, Narupat ; VILAIVAN, Tirayut ; NGAMROJNAVANICH, Nattaya ; CHAICHANTIPYUTH, Chaiyo ; PHUTHONG, Songchan</creatorcontrib><description>Three labdane diterpenoids, 2-acetoxy-3-hydroxy-labda-8(17),12(E)-14-triene, 3-acetoxy-2-hydroxy-labda-8(17),12(E)-14-triene, and 2,3-dihydroxy-labda-8(17),12(E),14-triene were isolated from stem bark of Croton oblongifolius. Their structures were established by spectroscopic data, and each was also tested for cytotoxicity against various human tumor cell lines. The latter compound showed non-specific, moderate, cytotoxicities against all the cell lines; whereas the first two compounds were less active.</description><identifier>ISSN: 0031-9422</identifier><identifier>EISSN: 1873-3700</identifier><identifier>DOI: 10.1016/S0031-9422(00)00358-7</identifier><identifier>PMID: 11198816</identifier><language>eng</language><publisher>Amsterdam: Elsevier</publisher><subject>Antineoplastic Agents, Phytogenic - chemistry ; Antineoplastic Agents, Phytogenic - isolation & purification ; Antineoplastic Agents, Phytogenic - pharmacology ; Biological and medical sciences ; Chemical constitution ; Diterpenes - chemistry ; Diterpenes - isolation & purification ; Diterpenes - pharmacology ; Drug Screening Assays, Antitumor ; Fundamental and applied biological sciences. Psychology ; General pharmacology ; Humans ; Medical sciences ; Naphthols - chemistry ; Pharmacognosy. Homeopathy. Health food ; Pharmacology. Drug treatments ; Plant physiology and development ; Rosales - chemistry ; Spectrum Analysis ; Tumor Cells, Cultured</subject><ispartof>Phytochemistry (Oxford), 2001-01, Vol.56 (1), p.103-107</ispartof><rights>2001 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c333t-58b46d0ab1c5345f8271d0f2ba61302704f758ba7c54a84ef4071c27fbf26b7c3</citedby><cites>FETCH-LOGICAL-c333t-58b46d0ab1c5345f8271d0f2ba61302704f758ba7c54a84ef4071c27fbf26b7c3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=851052$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/11198816$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>ROENGSUMRAN, Sophon</creatorcontrib><creatorcontrib>PETSOM, Amorn</creatorcontrib><creatorcontrib>KUPTIYANUWAT, Narupat</creatorcontrib><creatorcontrib>VILAIVAN, Tirayut</creatorcontrib><creatorcontrib>NGAMROJNAVANICH, Nattaya</creatorcontrib><creatorcontrib>CHAICHANTIPYUTH, Chaiyo</creatorcontrib><creatorcontrib>PHUTHONG, Songchan</creatorcontrib><title>Cytotoxic labdane diterpenoids from Croton oblongifolius</title><title>Phytochemistry (Oxford)</title><addtitle>Phytochemistry</addtitle><description>Three labdane diterpenoids, 2-acetoxy-3-hydroxy-labda-8(17),12(E)-14-triene, 3-acetoxy-2-hydroxy-labda-8(17),12(E)-14-triene, and 2,3-dihydroxy-labda-8(17),12(E),14-triene were isolated from stem bark of Croton oblongifolius. Their structures were established by spectroscopic data, and each was also tested for cytotoxicity against various human tumor cell lines. The latter compound showed non-specific, moderate, cytotoxicities against all the cell lines; whereas the first two compounds were less active.</description><subject>Antineoplastic Agents, Phytogenic - chemistry</subject><subject>Antineoplastic Agents, Phytogenic - isolation & purification</subject><subject>Antineoplastic Agents, Phytogenic - pharmacology</subject><subject>Biological and medical sciences</subject><subject>Chemical constitution</subject><subject>Diterpenes - chemistry</subject><subject>Diterpenes - isolation & purification</subject><subject>Diterpenes - pharmacology</subject><subject>Drug Screening Assays, Antitumor</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>General pharmacology</subject><subject>Humans</subject><subject>Medical sciences</subject><subject>Naphthols - chemistry</subject><subject>Pharmacognosy. Homeopathy. Health food</subject><subject>Pharmacology. Drug treatments</subject><subject>Plant physiology and development</subject><subject>Rosales - chemistry</subject><subject>Spectrum Analysis</subject><subject>Tumor Cells, Cultured</subject><issn>0031-9422</issn><issn>1873-3700</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2001</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpF0F1LwzAUgOEgipvTn6AUBNGL6knSfOxSil8w8EK9DkmaSKVtZtKC-_d2s8yrEHjOSXgROsdwiwHzuzcAivNlQcg1wM14YTIXB2iOpaA5FQCHaL4nM3SS0hcAMMb5MZphjJdSYj5Hstz0oQ8_tc0abSrduayqexfXrgt1lTIfQ5uVcSRdFkwTus_ah6Ye0ik68rpJ7mw6F-jj8eG9fM5Xr08v5f0qt5TSPmfSFLwCbbBltGBeEoEr8MRojikQAYUXo9HCskLLwvkCBLZEeOMJN8LSBbr627uO4XtwqVdtnaxrmvGrYUhKAJOci-UI2R-0MaQUnVfrWLc6bhQGtU2mdsnUtocCULtkSoxzF9MDg2ld9T81NRrB5QR0srrxUXe2TnsnGQZG6C-4NnMJ</recordid><startdate>20010101</startdate><enddate>20010101</enddate><creator>ROENGSUMRAN, Sophon</creator><creator>PETSOM, Amorn</creator><creator>KUPTIYANUWAT, Narupat</creator><creator>VILAIVAN, Tirayut</creator><creator>NGAMROJNAVANICH, Nattaya</creator><creator>CHAICHANTIPYUTH, Chaiyo</creator><creator>PHUTHONG, Songchan</creator><general>Elsevier</general><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></search><sort><creationdate>20010101</creationdate><title>Cytotoxic labdane diterpenoids from Croton oblongifolius</title><author>ROENGSUMRAN, Sophon ; PETSOM, Amorn ; KUPTIYANUWAT, Narupat ; VILAIVAN, Tirayut ; NGAMROJNAVANICH, Nattaya ; CHAICHANTIPYUTH, Chaiyo ; PHUTHONG, Songchan</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c333t-58b46d0ab1c5345f8271d0f2ba61302704f758ba7c54a84ef4071c27fbf26b7c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2001</creationdate><topic>Antineoplastic Agents, Phytogenic - chemistry</topic><topic>Antineoplastic Agents, Phytogenic - isolation & purification</topic><topic>Antineoplastic Agents, Phytogenic - pharmacology</topic><topic>Biological and medical sciences</topic><topic>Chemical constitution</topic><topic>Diterpenes - chemistry</topic><topic>Diterpenes - isolation & purification</topic><topic>Diterpenes - pharmacology</topic><topic>Drug Screening Assays, Antitumor</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>General pharmacology</topic><topic>Humans</topic><topic>Medical sciences</topic><topic>Naphthols - chemistry</topic><topic>Pharmacognosy. Homeopathy. Health food</topic><topic>Pharmacology. Drug treatments</topic><topic>Plant physiology and development</topic><topic>Rosales - chemistry</topic><topic>Spectrum Analysis</topic><topic>Tumor Cells, Cultured</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>ROENGSUMRAN, Sophon</creatorcontrib><creatorcontrib>PETSOM, Amorn</creatorcontrib><creatorcontrib>KUPTIYANUWAT, Narupat</creatorcontrib><creatorcontrib>VILAIVAN, Tirayut</creatorcontrib><creatorcontrib>NGAMROJNAVANICH, Nattaya</creatorcontrib><creatorcontrib>CHAICHANTIPYUTH, Chaiyo</creatorcontrib><creatorcontrib>PHUTHONG, Songchan</creatorcontrib><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><jtitle>Phytochemistry (Oxford)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>ROENGSUMRAN, Sophon</au><au>PETSOM, Amorn</au><au>KUPTIYANUWAT, Narupat</au><au>VILAIVAN, Tirayut</au><au>NGAMROJNAVANICH, Nattaya</au><au>CHAICHANTIPYUTH, Chaiyo</au><au>PHUTHONG, Songchan</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Cytotoxic labdane diterpenoids from Croton oblongifolius</atitle><jtitle>Phytochemistry (Oxford)</jtitle><addtitle>Phytochemistry</addtitle><date>2001-01-01</date><risdate>2001</risdate><volume>56</volume><issue>1</issue><spage>103</spage><epage>107</epage><pages>103-107</pages><issn>0031-9422</issn><eissn>1873-3700</eissn><abstract>Three labdane diterpenoids, 2-acetoxy-3-hydroxy-labda-8(17),12(E)-14-triene, 3-acetoxy-2-hydroxy-labda-8(17),12(E)-14-triene, and 2,3-dihydroxy-labda-8(17),12(E),14-triene were isolated from stem bark of Croton oblongifolius. Their structures were established by spectroscopic data, and each was also tested for cytotoxicity against various human tumor cell lines. The latter compound showed non-specific, moderate, cytotoxicities against all the cell lines; whereas the first two compounds were less active.</abstract><cop>Amsterdam</cop><pub>Elsevier</pub><pmid>11198816</pmid><doi>10.1016/S0031-9422(00)00358-7</doi><tpages>5</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0031-9422 |
ispartof | Phytochemistry (Oxford), 2001-01, Vol.56 (1), p.103-107 |
issn | 0031-9422 1873-3700 |
language | eng |
recordid | cdi_proquest_miscellaneous_70586679 |
source | MEDLINE; Elsevier ScienceDirect Journals Complete |
subjects | Antineoplastic Agents, Phytogenic - chemistry Antineoplastic Agents, Phytogenic - isolation & purification Antineoplastic Agents, Phytogenic - pharmacology Biological and medical sciences Chemical constitution Diterpenes - chemistry Diterpenes - isolation & purification Diterpenes - pharmacology Drug Screening Assays, Antitumor Fundamental and applied biological sciences. Psychology General pharmacology Humans Medical sciences Naphthols - chemistry Pharmacognosy. Homeopathy. Health food Pharmacology. Drug treatments Plant physiology and development Rosales - chemistry Spectrum Analysis Tumor Cells, Cultured |
title | Cytotoxic labdane diterpenoids from Croton oblongifolius |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-05T14%3A19%3A13IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Cytotoxic%20labdane%20diterpenoids%20from%20Croton%20oblongifolius&rft.jtitle=Phytochemistry%20(Oxford)&rft.au=ROENGSUMRAN,%20Sophon&rft.date=2001-01-01&rft.volume=56&rft.issue=1&rft.spage=103&rft.epage=107&rft.pages=103-107&rft.issn=0031-9422&rft.eissn=1873-3700&rft_id=info:doi/10.1016/S0031-9422(00)00358-7&rft_dat=%3Cproquest_cross%3E70586679%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=70586679&rft_id=info:pmid/11198816&rfr_iscdi=true |