Secondary metabolites from Senecio burtonii (Compositae)
A cacalolide derivative named 4α-[2′-hydroxymethylacryloxy]-1β-hydroxy-14-(5-6)abeo eremophilan-12,8-olide and a shikimic acid derivative named (3′ E)-(1α)-3-hydroxymethyl-4β, 5α-dimethoxycyclohex-2-enyloctadec-3′-enoate together with three known compounds were isolated from Senecio burtonii. A caca...
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| Veröffentlicht in: | Phytochemistry (Oxford) 2006-04, Vol.67 (8), p.838-842 |
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| creator | Ndom, J.C. Mbafor, J.T. Azebaze, A.G.B. Vardamides, J.C. Kakam, Z. Kamdem, A.F.W. Deville, A. Ngando, T.M. Fomum, Z.T. |
| description | A cacalolide derivative named 4α-[2′-hydroxymethylacryloxy]-1β-hydroxy-14-(5-6)abeo eremophilan-12,8-olide and a shikimic acid derivative named (3′
E)-(1α)-3-hydroxymethyl-4β, 5α-dimethoxycyclohex-2-enyloctadec-3′-enoate together with three known compounds were isolated from
Senecio burtonii.
A cacalolide derivative named 4α-[2′-hydroxymethylacryloxy]-1β-hydroxy-14-(5
→
6) abeo eremophilan-12,8-olide and a shikimic acid derivative named (3′
E)-(1α)-3-hydroxymethyl-4β,5α-dimethoxycyclohex-2-enyloctadec-3′-enoate along with three known compounds, octacosan-1-ol, 3β-hydroxyolean-12-en-28-oic acid and 3β-acetoxyolean-12-en-28-oic acid were isolated from
Senecio burtonii. Their structures and relative configurations were established on the basis of spectroscopic analysis. |
| doi_str_mv | 10.1016/j.phytochem.2006.02.010 |
| format | Article |
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E)-(1α)-3-hydroxymethyl-4β, 5α-dimethoxycyclohex-2-enyloctadec-3′-enoate together with three known compounds were isolated from
Senecio burtonii.
A cacalolide derivative named 4α-[2′-hydroxymethylacryloxy]-1β-hydroxy-14-(5
→
6) abeo eremophilan-12,8-olide and a shikimic acid derivative named (3′
E)-(1α)-3-hydroxymethyl-4β,5α-dimethoxycyclohex-2-enyloctadec-3′-enoate along with three known compounds, octacosan-1-ol, 3β-hydroxyolean-12-en-28-oic acid and 3β-acetoxyolean-12-en-28-oic acid were isolated from
Senecio burtonii. Their structures and relative configurations were established on the basis of spectroscopic analysis.</description><identifier>ISSN: 0031-9422</identifier><identifier>EISSN: 1873-3700</identifier><identifier>DOI: 10.1016/j.phytochem.2006.02.010</identifier><identifier>PMID: 16580035</identifier><language>eng</language><publisher>Amsterdam: Elsevier Ltd</publisher><subject>Asteraceae ; Biological and medical sciences ; Cacalolide ; Chemical constitution ; chemical structure ; Compositae ; Fundamental and applied biological sciences. Psychology ; medicinal plants ; Molecular Structure ; Naphthalenes - chemistry ; Naphthalenes - isolation & purification ; phytochemicals ; Plant physiology and development ; Plant Structures - chemistry ; secondary metabolites ; Senecio ; Senecio - chemistry ; Senecio burtonii ; Shikimic ; shikimic acid ; Shikimic Acid - analogs & derivatives ; Shikimic Acid - chemistry ; Shikimic Acid - isolation & purification ; spectral analysis</subject><ispartof>Phytochemistry (Oxford), 2006-04, Vol.67 (8), p.838-842</ispartof><rights>2006 Elsevier Ltd</rights><rights>2006 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c423t-3a420d7f900a3b182932b27bafd1bf3ee3be7a93c78a1fb41df8f60a7016885b3</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.phytochem.2006.02.010$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>315,781,785,3551,27926,27927,45997</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=17712841$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/16580035$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Ndom, J.C.</creatorcontrib><creatorcontrib>Mbafor, J.T.</creatorcontrib><creatorcontrib>Azebaze, A.G.B.</creatorcontrib><creatorcontrib>Vardamides, J.C.</creatorcontrib><creatorcontrib>Kakam, Z.</creatorcontrib><creatorcontrib>Kamdem, A.F.W.</creatorcontrib><creatorcontrib>Deville, A.</creatorcontrib><creatorcontrib>Ngando, T.M.</creatorcontrib><creatorcontrib>Fomum, Z.T.</creatorcontrib><title>Secondary metabolites from Senecio burtonii (Compositae)</title><title>Phytochemistry (Oxford)</title><addtitle>Phytochemistry</addtitle><description>A cacalolide derivative named 4α-[2′-hydroxymethylacryloxy]-1β-hydroxy-14-(5-6)abeo eremophilan-12,8-olide and a shikimic acid derivative named (3′
E)-(1α)-3-hydroxymethyl-4β, 5α-dimethoxycyclohex-2-enyloctadec-3′-enoate together with three known compounds were isolated from
Senecio burtonii.
A cacalolide derivative named 4α-[2′-hydroxymethylacryloxy]-1β-hydroxy-14-(5
→
6) abeo eremophilan-12,8-olide and a shikimic acid derivative named (3′
E)-(1α)-3-hydroxymethyl-4β,5α-dimethoxycyclohex-2-enyloctadec-3′-enoate along with three known compounds, octacosan-1-ol, 3β-hydroxyolean-12-en-28-oic acid and 3β-acetoxyolean-12-en-28-oic acid were isolated from
Senecio burtonii. Their structures and relative configurations were established on the basis of spectroscopic analysis.</description><subject>Asteraceae</subject><subject>Biological and medical sciences</subject><subject>Cacalolide</subject><subject>Chemical constitution</subject><subject>chemical structure</subject><subject>Compositae</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>medicinal plants</subject><subject>Molecular Structure</subject><subject>Naphthalenes - chemistry</subject><subject>Naphthalenes - isolation & purification</subject><subject>phytochemicals</subject><subject>Plant physiology and development</subject><subject>Plant Structures - chemistry</subject><subject>secondary metabolites</subject><subject>Senecio</subject><subject>Senecio - chemistry</subject><subject>Senecio burtonii</subject><subject>Shikimic</subject><subject>shikimic acid</subject><subject>Shikimic Acid - analogs & derivatives</subject><subject>Shikimic Acid - chemistry</subject><subject>Shikimic Acid - isolation & purification</subject><subject>spectral analysis</subject><issn>0031-9422</issn><issn>1873-3700</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2006</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkD1v2zAQQImiQeyk-Qu1lgbtIPVISiI1BkaaBgiQwclMkNSxpiGJLikXyL8vAxv12FtuuHdfj5AVhYoCbb_vqv32bQ52i2PFANoKWAUUPpAllYKXXAB8JEsATsuuZmxBrlLaAUDTtO0lWdC2kbnYLIncoA1Tr-NbMeKsTRj8jKlwMYzFBie0PhTmEOcweV98XYdxH5KfNX77RC6cHhLenPI1ef1x_7L-WT49Pzyu755KWzM-l1zXDHrhOgDNDZWs48wwYbTrqXEckRsUuuNWSE2dqWnvpGtBi_yllI3h1-T2OHcfw-8DplmNPlkcBj1hOCTVCilkJyCD4gjaGFKK6NQ--jE_piiod2lqp_5JU-_SFDCVpeXOz6cVBzNif-47WcrAlxOgk9WDi3qyPp05ISiTNc3c6sg5HZT-FTPzumFAOdAcjeCZuDsSmJX98RhVsh4ni72PaGfVB__fc_8C6dOXxA</recordid><startdate>20060401</startdate><enddate>20060401</enddate><creator>Ndom, J.C.</creator><creator>Mbafor, J.T.</creator><creator>Azebaze, A.G.B.</creator><creator>Vardamides, J.C.</creator><creator>Kakam, Z.</creator><creator>Kamdem, A.F.W.</creator><creator>Deville, A.</creator><creator>Ngando, T.M.</creator><creator>Fomum, Z.T.</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></search><sort><creationdate>20060401</creationdate><title>Secondary metabolites from Senecio burtonii (Compositae)</title><author>Ndom, J.C. ; Mbafor, J.T. ; Azebaze, A.G.B. ; Vardamides, J.C. ; Kakam, Z. ; Kamdem, A.F.W. ; Deville, A. ; Ngando, T.M. ; Fomum, Z.T.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c423t-3a420d7f900a3b182932b27bafd1bf3ee3be7a93c78a1fb41df8f60a7016885b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2006</creationdate><topic>Asteraceae</topic><topic>Biological and medical sciences</topic><topic>Cacalolide</topic><topic>Chemical constitution</topic><topic>chemical structure</topic><topic>Compositae</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>medicinal plants</topic><topic>Molecular Structure</topic><topic>Naphthalenes - chemistry</topic><topic>Naphthalenes - isolation & purification</topic><topic>phytochemicals</topic><topic>Plant physiology and development</topic><topic>Plant Structures - chemistry</topic><topic>secondary metabolites</topic><topic>Senecio</topic><topic>Senecio - chemistry</topic><topic>Senecio burtonii</topic><topic>Shikimic</topic><topic>shikimic acid</topic><topic>Shikimic Acid - analogs & derivatives</topic><topic>Shikimic Acid - chemistry</topic><topic>Shikimic Acid - isolation & purification</topic><topic>spectral analysis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ndom, J.C.</creatorcontrib><creatorcontrib>Mbafor, J.T.</creatorcontrib><creatorcontrib>Azebaze, A.G.B.</creatorcontrib><creatorcontrib>Vardamides, J.C.</creatorcontrib><creatorcontrib>Kakam, Z.</creatorcontrib><creatorcontrib>Kamdem, A.F.W.</creatorcontrib><creatorcontrib>Deville, A.</creatorcontrib><creatorcontrib>Ngando, T.M.</creatorcontrib><creatorcontrib>Fomum, Z.T.</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><jtitle>Phytochemistry (Oxford)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ndom, J.C.</au><au>Mbafor, J.T.</au><au>Azebaze, A.G.B.</au><au>Vardamides, J.C.</au><au>Kakam, Z.</au><au>Kamdem, A.F.W.</au><au>Deville, A.</au><au>Ngando, T.M.</au><au>Fomum, Z.T.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Secondary metabolites from Senecio burtonii (Compositae)</atitle><jtitle>Phytochemistry (Oxford)</jtitle><addtitle>Phytochemistry</addtitle><date>2006-04-01</date><risdate>2006</risdate><volume>67</volume><issue>8</issue><spage>838</spage><epage>842</epage><pages>838-842</pages><issn>0031-9422</issn><eissn>1873-3700</eissn><abstract>A cacalolide derivative named 4α-[2′-hydroxymethylacryloxy]-1β-hydroxy-14-(5-6)abeo eremophilan-12,8-olide and a shikimic acid derivative named (3′
E)-(1α)-3-hydroxymethyl-4β, 5α-dimethoxycyclohex-2-enyloctadec-3′-enoate together with three known compounds were isolated from
Senecio burtonii.
A cacalolide derivative named 4α-[2′-hydroxymethylacryloxy]-1β-hydroxy-14-(5
→
6) abeo eremophilan-12,8-olide and a shikimic acid derivative named (3′
E)-(1α)-3-hydroxymethyl-4β,5α-dimethoxycyclohex-2-enyloctadec-3′-enoate along with three known compounds, octacosan-1-ol, 3β-hydroxyolean-12-en-28-oic acid and 3β-acetoxyolean-12-en-28-oic acid were isolated from
Senecio burtonii. Their structures and relative configurations were established on the basis of spectroscopic analysis.</abstract><cop>Amsterdam</cop><pub>Elsevier Ltd</pub><pmid>16580035</pmid><doi>10.1016/j.phytochem.2006.02.010</doi><tpages>5</tpages></addata></record> |
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| subjects | Asteraceae Biological and medical sciences Cacalolide Chemical constitution chemical structure Compositae Fundamental and applied biological sciences. Psychology medicinal plants Molecular Structure Naphthalenes - chemistry Naphthalenes - isolation & purification phytochemicals Plant physiology and development Plant Structures - chemistry secondary metabolites Senecio Senecio - chemistry Senecio burtonii Shikimic shikimic acid Shikimic Acid - analogs & derivatives Shikimic Acid - chemistry Shikimic Acid - isolation & purification spectral analysis |
| title | Secondary metabolites from Senecio burtonii (Compositae) |
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