Macrocyclic diterpenes from Euphorbia nivulia
The latex of Euphorbia nivulia afforded two ingol diterpenes 3,12-diacetyl-8-benzoylingol (4) and 3,12-diacetyl-7-benzoyl-8-nicotinylingol (5) along with three known ingol diterpenes 1, 2,and 3, and two known triterpenes cycloart-25-en-3beta-ol and cyclonivulinol. Their structures have been assigned...
Gespeichert in:
| Veröffentlicht in: | Phytochemistry (Oxford) 2002-02, Vol.59 (3), p.331-335 |
|---|---|
| Hauptverfasser: | , , , , , |
| Format: | Artikel |
| Sprache: | eng |
| Schlagworte: | |
| Online-Zugang: | Volltext |
| Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
| container_end_page | 335 |
|---|---|
| container_issue | 3 |
| container_start_page | 331 |
| container_title | Phytochemistry (Oxford) |
| container_volume | 59 |
| creator | RAVIKANTH, V NIRANJAN REDDY, V. L PRABHAKAR RAO, T DIWAN, P. V RAMAKRISHNA, S VENKATESWARLU, Y |
| description | The latex of Euphorbia nivulia afforded two ingol diterpenes 3,12-diacetyl-8-benzoylingol (4) and 3,12-diacetyl-7-benzoyl-8-nicotinylingol (5) along with three known ingol diterpenes 1, 2,and 3, and two known triterpenes cycloart-25-en-3beta-ol and cyclonivulinol. Their structures have been assigned on the basis of their structural data as well as their acetylated products. The diterpenes 1-5 were tested for the LPS induced PGE(2) inhibition activity. |
| doi_str_mv | 10.1016/S0031-9422(01)00461-7 |
| format | Article |
| fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_71490481</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>71490481</sourcerecordid><originalsourceid>FETCH-LOGICAL-c335t-c0eba09b0cfad1399f534c340eb83864ee1a6f164cd1a541211dd8e03f12dba43</originalsourceid><addsrcrecordid>eNpFkE1Lw0AQhhdRbK3-BCUXRQ_Rmewm2RxLqR9Q8aCel81-4Eq-3G2E_nvTNtjTwPC88zIPIZcI9wiYPbwDUIwLliS3gHcALMM4PyJT5DmNaQ5wTKb_yISchfANAGmaZadkgsgpIEumJH6VyrdqoyqnIu3WxnemMSGyvq2jZd99tb50Mmrcb185eU5OrKyCuRjnjHw-Lj8Wz_Hq7ellMV_FitJ0HSswpYSiBGWlRloUNqVMUTasOeUZMwZlZjFjSqNMGSaIWnMD1GKiS8nojNzs73a-_elNWIvaBWWqSjam7YPIkRXAOA5gugeHJ0LwxorOu1r6jUAQW09i50lsJQhAsfMk8iF3NRb0ZW30ITWKGYDrEZBBycp62SgXDhwd2jln9A_PGm90</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>71490481</pqid></control><display><type>article</type><title>Macrocyclic diterpenes from Euphorbia nivulia</title><source>MEDLINE</source><source>Elsevier ScienceDirect Journals Complete</source><creator>RAVIKANTH, V ; NIRANJAN REDDY, V. L ; PRABHAKAR RAO, T ; DIWAN, P. V ; RAMAKRISHNA, S ; VENKATESWARLU, Y</creator><creatorcontrib>RAVIKANTH, V ; NIRANJAN REDDY, V. L ; PRABHAKAR RAO, T ; DIWAN, P. V ; RAMAKRISHNA, S ; VENKATESWARLU, Y</creatorcontrib><description>The latex of Euphorbia nivulia afforded two ingol diterpenes 3,12-diacetyl-8-benzoylingol (4) and 3,12-diacetyl-7-benzoyl-8-nicotinylingol (5) along with three known ingol diterpenes 1, 2,and 3, and two known triterpenes cycloart-25-en-3beta-ol and cyclonivulinol. Their structures have been assigned on the basis of their structural data as well as their acetylated products. The diterpenes 1-5 were tested for the LPS induced PGE(2) inhibition activity.</description><identifier>ISSN: 0031-9422</identifier><identifier>EISSN: 1873-3700</identifier><identifier>DOI: 10.1016/S0031-9422(01)00461-7</identifier><identifier>PMID: 11830142</identifier><language>eng</language><publisher>Amsterdam: Elsevier</publisher><subject>Biological and medical sciences ; Chemical constitution ; Dinoprostone - antagonists & inhibitors ; Diterpenes - chemistry ; Diterpenes - isolation & purification ; Diterpenes - pharmacology ; Euphorbia - chemistry ; Fundamental and applied biological sciences. Psychology ; General pharmacology ; Humans ; Magnetic Resonance Spectroscopy ; Medical sciences ; Pharmacognosy. Homeopathy. Health food ; Pharmacology. Drug treatments ; Plant physiology and development ; Triterpenes - chemistry ; Triterpenes - isolation & purification</subject><ispartof>Phytochemistry (Oxford), 2002-02, Vol.59 (3), p.331-335</ispartof><rights>2002 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c335t-c0eba09b0cfad1399f534c340eb83864ee1a6f164cd1a541211dd8e03f12dba43</citedby><cites>FETCH-LOGICAL-c335t-c0eba09b0cfad1399f534c340eb83864ee1a6f164cd1a541211dd8e03f12dba43</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=13481884$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/11830142$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>RAVIKANTH, V</creatorcontrib><creatorcontrib>NIRANJAN REDDY, V. L</creatorcontrib><creatorcontrib>PRABHAKAR RAO, T</creatorcontrib><creatorcontrib>DIWAN, P. V</creatorcontrib><creatorcontrib>RAMAKRISHNA, S</creatorcontrib><creatorcontrib>VENKATESWARLU, Y</creatorcontrib><title>Macrocyclic diterpenes from Euphorbia nivulia</title><title>Phytochemistry (Oxford)</title><addtitle>Phytochemistry</addtitle><description>The latex of Euphorbia nivulia afforded two ingol diterpenes 3,12-diacetyl-8-benzoylingol (4) and 3,12-diacetyl-7-benzoyl-8-nicotinylingol (5) along with three known ingol diterpenes 1, 2,and 3, and two known triterpenes cycloart-25-en-3beta-ol and cyclonivulinol. Their structures have been assigned on the basis of their structural data as well as their acetylated products. The diterpenes 1-5 were tested for the LPS induced PGE(2) inhibition activity.</description><subject>Biological and medical sciences</subject><subject>Chemical constitution</subject><subject>Dinoprostone - antagonists & inhibitors</subject><subject>Diterpenes - chemistry</subject><subject>Diterpenes - isolation & purification</subject><subject>Diterpenes - pharmacology</subject><subject>Euphorbia - chemistry</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>General pharmacology</subject><subject>Humans</subject><subject>Magnetic Resonance Spectroscopy</subject><subject>Medical sciences</subject><subject>Pharmacognosy. Homeopathy. Health food</subject><subject>Pharmacology. Drug treatments</subject><subject>Plant physiology and development</subject><subject>Triterpenes - chemistry</subject><subject>Triterpenes - isolation & purification</subject><issn>0031-9422</issn><issn>1873-3700</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2002</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpFkE1Lw0AQhhdRbK3-BCUXRQ_Rmewm2RxLqR9Q8aCel81-4Eq-3G2E_nvTNtjTwPC88zIPIZcI9wiYPbwDUIwLliS3gHcALMM4PyJT5DmNaQ5wTKb_yISchfANAGmaZadkgsgpIEumJH6VyrdqoyqnIu3WxnemMSGyvq2jZd99tb50Mmrcb185eU5OrKyCuRjnjHw-Lj8Wz_Hq7ellMV_FitJ0HSswpYSiBGWlRloUNqVMUTasOeUZMwZlZjFjSqNMGSaIWnMD1GKiS8nojNzs73a-_elNWIvaBWWqSjam7YPIkRXAOA5gugeHJ0LwxorOu1r6jUAQW09i50lsJQhAsfMk8iF3NRb0ZW30ITWKGYDrEZBBycp62SgXDhwd2jln9A_PGm90</recordid><startdate>20020201</startdate><enddate>20020201</enddate><creator>RAVIKANTH, V</creator><creator>NIRANJAN REDDY, V. L</creator><creator>PRABHAKAR RAO, T</creator><creator>DIWAN, P. V</creator><creator>RAMAKRISHNA, S</creator><creator>VENKATESWARLU, Y</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>20020201</creationdate><title>Macrocyclic diterpenes from Euphorbia nivulia</title><author>RAVIKANTH, V ; NIRANJAN REDDY, V. L ; PRABHAKAR RAO, T ; DIWAN, P. V ; RAMAKRISHNA, S ; VENKATESWARLU, Y</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c335t-c0eba09b0cfad1399f534c340eb83864ee1a6f164cd1a541211dd8e03f12dba43</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2002</creationdate><topic>Biological and medical sciences</topic><topic>Chemical constitution</topic><topic>Dinoprostone - antagonists & inhibitors</topic><topic>Diterpenes - chemistry</topic><topic>Diterpenes - isolation & purification</topic><topic>Diterpenes - pharmacology</topic><topic>Euphorbia - chemistry</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>General pharmacology</topic><topic>Humans</topic><topic>Magnetic Resonance Spectroscopy</topic><topic>Medical sciences</topic><topic>Pharmacognosy. Homeopathy. Health food</topic><topic>Pharmacology. Drug treatments</topic><topic>Plant physiology and development</topic><topic>Triterpenes - chemistry</topic><topic>Triterpenes - isolation & purification</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>RAVIKANTH, V</creatorcontrib><creatorcontrib>NIRANJAN REDDY, V. L</creatorcontrib><creatorcontrib>PRABHAKAR RAO, T</creatorcontrib><creatorcontrib>DIWAN, P. V</creatorcontrib><creatorcontrib>RAMAKRISHNA, S</creatorcontrib><creatorcontrib>VENKATESWARLU, Y</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>RAVIKANTH, V</au><au>NIRANJAN REDDY, V. L</au><au>PRABHAKAR RAO, T</au><au>DIWAN, P. V</au><au>RAMAKRISHNA, S</au><au>VENKATESWARLU, Y</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Macrocyclic diterpenes from Euphorbia nivulia</atitle><jtitle>Phytochemistry (Oxford)</jtitle><addtitle>Phytochemistry</addtitle><date>2002-02-01</date><risdate>2002</risdate><volume>59</volume><issue>3</issue><spage>331</spage><epage>335</epage><pages>331-335</pages><issn>0031-9422</issn><eissn>1873-3700</eissn><abstract>The latex of Euphorbia nivulia afforded two ingol diterpenes 3,12-diacetyl-8-benzoylingol (4) and 3,12-diacetyl-7-benzoyl-8-nicotinylingol (5) along with three known ingol diterpenes 1, 2,and 3, and two known triterpenes cycloart-25-en-3beta-ol and cyclonivulinol. Their structures have been assigned on the basis of their structural data as well as their acetylated products. The diterpenes 1-5 were tested for the LPS induced PGE(2) inhibition activity.</abstract><cop>Amsterdam</cop><pub>Elsevier</pub><pmid>11830142</pmid><doi>10.1016/S0031-9422(01)00461-7</doi><tpages>5</tpages></addata></record> |
| fulltext | fulltext |
| identifier | ISSN: 0031-9422 |
| ispartof | Phytochemistry (Oxford), 2002-02, Vol.59 (3), p.331-335 |
| issn | 0031-9422 1873-3700 |
| language | eng |
| recordid | cdi_proquest_miscellaneous_71490481 |
| source | MEDLINE; Elsevier ScienceDirect Journals Complete |
| subjects | Biological and medical sciences Chemical constitution Dinoprostone - antagonists & inhibitors Diterpenes - chemistry Diterpenes - isolation & purification Diterpenes - pharmacology Euphorbia - chemistry Fundamental and applied biological sciences. Psychology General pharmacology Humans Magnetic Resonance Spectroscopy Medical sciences Pharmacognosy. Homeopathy. Health food Pharmacology. Drug treatments Plant physiology and development Triterpenes - chemistry Triterpenes - isolation & purification |
| title | Macrocyclic diterpenes from Euphorbia nivulia |
| url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-05T13%3A04%3A12IST&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=Macrocyclic%20diterpenes%20from%20Euphorbia%20nivulia&rft.jtitle=Phytochemistry%20(Oxford)&rft.au=RAVIKANTH,%20V&rft.date=2002-02-01&rft.volume=59&rft.issue=3&rft.spage=331&rft.epage=335&rft.pages=331-335&rft.issn=0031-9422&rft.eissn=1873-3700&rft_id=info:doi/10.1016/S0031-9422(01)00461-7&rft_dat=%3Cproquest_cross%3E71490481%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=71490481&rft_id=info:pmid/11830142&rfr_iscdi=true |