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Highly hydroxylated guaianolides of Achillea asiatica and Middle European Achillea species
From flower heads of Achillea asiatica (L.) Serg., three new guaianolides were isolated by repeated column chromatography and HPLC. The constitution and the stereochemistry of these new, labile compounds were determined by MS, one (1H, 13C, selective 1H-TOCSY and 1H-NOESY) and two-dimensional NMR ex...
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Published in: | Phytochemistry (Oxford) 2001-12, Vol.58 (8), p.1189-1194 |
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description | From flower heads of Achillea asiatica (L.) Serg., three new guaianolides were isolated by repeated column chromatography and HPLC. The constitution and the stereochemistry of these new, labile compounds were determined by MS, one (1H, 13C, selective 1H-TOCSY and 1H-NOESY) and two-dimensional NMR experiments (1H, 1H-COSY, 1H, 13C-HSQC, 1H, 13C-HMBC). The substances were identified as 8α-angeloxy-2α, 4α,10β-trihydroxy-6βH,7αH, 11βH-1(5)-guaien-12,6α-olide (1), 8α-angeloxy-1β,2β:4β,5β-diepoxy-10β-hydroxy-6βH, 7αH, 11βH-12,6α-guaianolide (2) and 8α-angeloxy-4α,10β-dihydroxy-2-oxo-6βH,7αH, 11βH-1(5)-guaien-12,6α-olide (3). They were also detected in Middle European species (Achillea collina, Achillea ceretanica (2× and 4×), Achillea roseoalba, Achillea asplenifolia) by HPLC, TLC and off line MS and have not been described before. The possibility that these compounds might be products of an oxidation process is discussed.
Three guaianolides were isolated from Achillea asiatica: 8α-angeloxy-2α,4α,10β-trihydroxy-6βH,7αH,11βH-1(5)-guaien-12,6α-olide (1), 8α-angeloxy-1β,2β: 4β,5β-diepoxy-10β-hydroxy-6βH,7αH,11βH-12,6α-guaianolide (2) and 8α-angeloxy-4α,10β-dihydroxy-2-oxo-6βH,7αH,11βH-1(5)-guaien-12,6α-olide (3). They were also detected in Middle European species (A. collina, A. ceretanica (2× and 4×), A. roseoalba, A. asplenifolia) by HPLC, TLC and offline MS and have not been described before. |
doi_str_mv | 10.1016/S0031-9422(01)00281-3 |
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Three guaianolides were isolated from Achillea asiatica: 8α-angeloxy-2α,4α,10β-trihydroxy-6βH,7αH,11βH-1(5)-guaien-12,6α-olide (1), 8α-angeloxy-1β,2β: 4β,5β-diepoxy-10β-hydroxy-6βH,7αH,11βH-12,6α-guaianolide (2) and 8α-angeloxy-4α,10β-dihydroxy-2-oxo-6βH,7αH,11βH-1(5)-guaien-12,6α-olide (3). They were also detected in Middle European species (A. collina, A. ceretanica (2× and 4×), A. roseoalba, A. asplenifolia) by HPLC, TLC and offline MS and have not been described before.</description><identifier>ISSN: 0031-9422</identifier><identifier>EISSN: 1873-3700</identifier><identifier>DOI: 10.1016/S0031-9422(01)00281-3</identifier><identifier>PMID: 11738405</identifier><language>eng</language><publisher>Amsterdam: Elsevier Ltd</publisher><subject>Achillea asiatica ; Achillea asplenifolia ; Achillea ceretanica ; Achillea collina ; Achillea roseoalba ; Asteraceae - chemistry ; Biological and medical sciences ; Chemical constitution ; Compositae ; Europe ; Fundamental and applied biological sciences. Psychology ; Guaianolides ; Hydroxylation ; Plant physiology and development ; Proazulenes ; Sesquiterpene lactones ; Sesquiterpenes - chemistry ; Sesquiterpenes - isolation & purification ; Sesquiterpenes, Guaiane</subject><ispartof>Phytochemistry (Oxford), 2001-12, Vol.58 (8), p.1189-1194</ispartof><rights>2001</rights><rights>2002 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c391t-77ea9155fc15afe2a949f3fe011b622cfeee0debb3b6fdf15494c69080ce310f3</citedby><cites>FETCH-LOGICAL-c391t-77ea9155fc15afe2a949f3fe011b622cfeee0debb3b6fdf15494c69080ce310f3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27903,27904</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=13383974$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/11738405$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Glasl, Sabine</creatorcontrib><creatorcontrib>Presser, Armin</creatorcontrib><creatorcontrib>Gunbilig, Disan</creatorcontrib><creatorcontrib>Werner, Ingrid</creatorcontrib><creatorcontrib>Narantuya, Samdan</creatorcontrib><creatorcontrib>Haslinger, Ernst</creatorcontrib><creatorcontrib>Jurenitsch, Johann</creatorcontrib><creatorcontrib>Kubelka, Wolfgang</creatorcontrib><title>Highly hydroxylated guaianolides of Achillea asiatica and Middle European Achillea species</title><title>Phytochemistry (Oxford)</title><addtitle>Phytochemistry</addtitle><description>From flower heads of Achillea asiatica (L.) Serg., three new guaianolides were isolated by repeated column chromatography and HPLC. The constitution and the stereochemistry of these new, labile compounds were determined by MS, one (1H, 13C, selective 1H-TOCSY and 1H-NOESY) and two-dimensional NMR experiments (1H, 1H-COSY, 1H, 13C-HSQC, 1H, 13C-HMBC). The substances were identified as 8α-angeloxy-2α, 4α,10β-trihydroxy-6βH,7αH, 11βH-1(5)-guaien-12,6α-olide (1), 8α-angeloxy-1β,2β:4β,5β-diepoxy-10β-hydroxy-6βH, 7αH, 11βH-12,6α-guaianolide (2) and 8α-angeloxy-4α,10β-dihydroxy-2-oxo-6βH,7αH, 11βH-1(5)-guaien-12,6α-olide (3). They were also detected in Middle European species (Achillea collina, Achillea ceretanica (2× and 4×), Achillea roseoalba, Achillea asplenifolia) by HPLC, TLC and off line MS and have not been described before. The possibility that these compounds might be products of an oxidation process is discussed.
Three guaianolides were isolated from Achillea asiatica: 8α-angeloxy-2α,4α,10β-trihydroxy-6βH,7αH,11βH-1(5)-guaien-12,6α-olide (1), 8α-angeloxy-1β,2β: 4β,5β-diepoxy-10β-hydroxy-6βH,7αH,11βH-12,6α-guaianolide (2) and 8α-angeloxy-4α,10β-dihydroxy-2-oxo-6βH,7αH,11βH-1(5)-guaien-12,6α-olide (3). They were also detected in Middle European species (A. collina, A. ceretanica (2× and 4×), A. roseoalba, A. asplenifolia) by HPLC, TLC and offline MS and have not been described before.</description><subject>Achillea asiatica</subject><subject>Achillea asplenifolia</subject><subject>Achillea ceretanica</subject><subject>Achillea collina</subject><subject>Achillea roseoalba</subject><subject>Asteraceae - chemistry</subject><subject>Biological and medical sciences</subject><subject>Chemical constitution</subject><subject>Compositae</subject><subject>Europe</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Guaianolides</subject><subject>Hydroxylation</subject><subject>Plant physiology and development</subject><subject>Proazulenes</subject><subject>Sesquiterpene lactones</subject><subject>Sesquiterpenes - chemistry</subject><subject>Sesquiterpenes - isolation & purification</subject><subject>Sesquiterpenes, Guaiane</subject><issn>0031-9422</issn><issn>1873-3700</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2001</creationdate><recordtype>article</recordtype><recordid>eNqF0D1PwzAQgGELgaAUfgIoCwiGwF2czwkhVD4kEAOwsFiOfaZGblLsBNF_T6AVHZns4bmz9TJ2gHCGgPn5EwDHuEqT5ATwFCApMeYbbIRlwWNeAGyy0R_ZYbshvANAluX5NttBLHiZQjZir7f2beoW0XShffu1cLIjHb310sqmdVZTiFoTXaqpdY5kJIOVnVXDpdHRg9XaUTTpfTsn2axVmJOyFPbYlpEu0P7qHLOX68nz1W18_3hzd3V5HyteYRcXBckKs8wozKShRFZpZbghQKzzJFGGiEBTXfM6N9pgllapyisoQRFHMHzMjpd757796Cl0YmaDIudkQ20fRJHwNC95MsBsCZVvQ_BkxNzbmfQLgSB-oorfqOKnmAAUv1EFH-YOVw_09Yz0empVcQBHKyCDks542Sgb1o7zkldFOriLpaMhx6clL8IQqlGkrSfVCd3af77yDbTflGY</recordid><startdate>20011201</startdate><enddate>20011201</enddate><creator>Glasl, Sabine</creator><creator>Presser, Armin</creator><creator>Gunbilig, Disan</creator><creator>Werner, Ingrid</creator><creator>Narantuya, Samdan</creator><creator>Haslinger, Ernst</creator><creator>Jurenitsch, Johann</creator><creator>Kubelka, Wolfgang</creator><general>Elsevier Ltd</general><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>20011201</creationdate><title>Highly hydroxylated guaianolides of Achillea asiatica and Middle European Achillea species</title><author>Glasl, Sabine ; Presser, Armin ; Gunbilig, Disan ; Werner, Ingrid ; Narantuya, Samdan ; Haslinger, Ernst ; Jurenitsch, Johann ; Kubelka, Wolfgang</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c391t-77ea9155fc15afe2a949f3fe011b622cfeee0debb3b6fdf15494c69080ce310f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2001</creationdate><topic>Achillea asiatica</topic><topic>Achillea asplenifolia</topic><topic>Achillea ceretanica</topic><topic>Achillea collina</topic><topic>Achillea roseoalba</topic><topic>Asteraceae - chemistry</topic><topic>Biological and medical sciences</topic><topic>Chemical constitution</topic><topic>Compositae</topic><topic>Europe</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Guaianolides</topic><topic>Hydroxylation</topic><topic>Plant physiology and development</topic><topic>Proazulenes</topic><topic>Sesquiterpene lactones</topic><topic>Sesquiterpenes - chemistry</topic><topic>Sesquiterpenes - isolation & purification</topic><topic>Sesquiterpenes, Guaiane</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Glasl, Sabine</creatorcontrib><creatorcontrib>Presser, Armin</creatorcontrib><creatorcontrib>Gunbilig, Disan</creatorcontrib><creatorcontrib>Werner, Ingrid</creatorcontrib><creatorcontrib>Narantuya, Samdan</creatorcontrib><creatorcontrib>Haslinger, Ernst</creatorcontrib><creatorcontrib>Jurenitsch, Johann</creatorcontrib><creatorcontrib>Kubelka, Wolfgang</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>Glasl, Sabine</au><au>Presser, Armin</au><au>Gunbilig, Disan</au><au>Werner, Ingrid</au><au>Narantuya, Samdan</au><au>Haslinger, Ernst</au><au>Jurenitsch, Johann</au><au>Kubelka, Wolfgang</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Highly hydroxylated guaianolides of Achillea asiatica and Middle European Achillea species</atitle><jtitle>Phytochemistry (Oxford)</jtitle><addtitle>Phytochemistry</addtitle><date>2001-12-01</date><risdate>2001</risdate><volume>58</volume><issue>8</issue><spage>1189</spage><epage>1194</epage><pages>1189-1194</pages><issn>0031-9422</issn><eissn>1873-3700</eissn><abstract>From flower heads of Achillea asiatica (L.) Serg., three new guaianolides were isolated by repeated column chromatography and HPLC. The constitution and the stereochemistry of these new, labile compounds were determined by MS, one (1H, 13C, selective 1H-TOCSY and 1H-NOESY) and two-dimensional NMR experiments (1H, 1H-COSY, 1H, 13C-HSQC, 1H, 13C-HMBC). The substances were identified as 8α-angeloxy-2α, 4α,10β-trihydroxy-6βH,7αH, 11βH-1(5)-guaien-12,6α-olide (1), 8α-angeloxy-1β,2β:4β,5β-diepoxy-10β-hydroxy-6βH, 7αH, 11βH-12,6α-guaianolide (2) and 8α-angeloxy-4α,10β-dihydroxy-2-oxo-6βH,7αH, 11βH-1(5)-guaien-12,6α-olide (3). They were also detected in Middle European species (Achillea collina, Achillea ceretanica (2× and 4×), Achillea roseoalba, Achillea asplenifolia) by HPLC, TLC and off line MS and have not been described before. The possibility that these compounds might be products of an oxidation process is discussed.
Three guaianolides were isolated from Achillea asiatica: 8α-angeloxy-2α,4α,10β-trihydroxy-6βH,7αH,11βH-1(5)-guaien-12,6α-olide (1), 8α-angeloxy-1β,2β: 4β,5β-diepoxy-10β-hydroxy-6βH,7αH,11βH-12,6α-guaianolide (2) and 8α-angeloxy-4α,10β-dihydroxy-2-oxo-6βH,7αH,11βH-1(5)-guaien-12,6α-olide (3). They were also detected in Middle European species (A. collina, A. ceretanica (2× and 4×), A. roseoalba, A. asplenifolia) by HPLC, TLC and offline MS and have not been described before.</abstract><cop>Amsterdam</cop><pub>Elsevier Ltd</pub><pmid>11738405</pmid><doi>10.1016/S0031-9422(01)00281-3</doi><tpages>6</tpages></addata></record> |
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subjects | Achillea asiatica Achillea asplenifolia Achillea ceretanica Achillea collina Achillea roseoalba Asteraceae - chemistry Biological and medical sciences Chemical constitution Compositae Europe Fundamental and applied biological sciences. Psychology Guaianolides Hydroxylation Plant physiology and development Proazulenes Sesquiterpene lactones Sesquiterpenes - chemistry Sesquiterpenes - isolation & purification Sesquiterpenes, Guaiane |
title | Highly hydroxylated guaianolides of Achillea asiatica and Middle European Achillea species |
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