Loading…

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...

Full description

Saved in:
Bibliographic Details
Published in:Phytochemistry (Oxford) 2001-12, Vol.58 (8), p.1189-1194
Main Authors: Glasl, Sabine, Presser, Armin, Gunbilig, Disan, Werner, Ingrid, Narantuya, Samdan, Haslinger, Ernst, Jurenitsch, Johann, Kubelka, Wolfgang
Format: Article
Language:English
Subjects:
Citations: Items that this one cites
Items that cite this one
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
cited_by cdi_FETCH-LOGICAL-c391t-77ea9155fc15afe2a949f3fe011b622cfeee0debb3b6fdf15494c69080ce310f3
cites cdi_FETCH-LOGICAL-c391t-77ea9155fc15afe2a949f3fe011b622cfeee0debb3b6fdf15494c69080ce310f3
container_end_page 1194
container_issue 8
container_start_page 1189
container_title Phytochemistry (Oxford)
container_volume 58
creator Glasl, Sabine
Presser, Armin
Gunbilig, Disan
Werner, Ingrid
Narantuya, Samdan
Haslinger, Ernst
Jurenitsch, Johann
Kubelka, Wolfgang
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
format article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_72346832</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S0031942201002813</els_id><sourcerecordid>72346832</sourcerecordid><originalsourceid>FETCH-LOGICAL-c391t-77ea9155fc15afe2a949f3fe011b622cfeee0debb3b6fdf15494c69080ce310f3</originalsourceid><addsrcrecordid>eNqF0D1PwzAQgGELgaAUfgIoCwiGwF2czwkhVD4kEAOwsFiOfaZGblLsBNF_T6AVHZns4bmz9TJ2gHCGgPn5EwDHuEqT5ATwFCApMeYbbIRlwWNeAGyy0R_ZYbshvANAluX5NttBLHiZQjZir7f2beoW0XShffu1cLIjHb310sqmdVZTiFoTXaqpdY5kJIOVnVXDpdHRg9XaUTTpfTsn2axVmJOyFPbYlpEu0P7qHLOX68nz1W18_3hzd3V5HyteYRcXBckKs8wozKShRFZpZbghQKzzJFGGiEBTXfM6N9pgllapyisoQRFHMHzMjpd757796Cl0YmaDIudkQ20fRJHwNC95MsBsCZVvQ_BkxNzbmfQLgSB-oorfqOKnmAAUv1EFH-YOVw_09Yz0empVcQBHKyCDks542Sgb1o7zkldFOriLpaMhx6clL8IQqlGkrSfVCd3af77yDbTflGY</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>72346832</pqid></control><display><type>article</type><title>Highly hydroxylated guaianolides of Achillea asiatica and Middle European Achillea species</title><source>ScienceDirect Freedom Collection</source><creator>Glasl, Sabine ; Presser, Armin ; Gunbilig, Disan ; Werner, Ingrid ; Narantuya, Samdan ; Haslinger, Ernst ; Jurenitsch, Johann ; Kubelka, Wolfgang</creator><creatorcontrib>Glasl, Sabine ; Presser, Armin ; Gunbilig, Disan ; Werner, Ingrid ; Narantuya, Samdan ; Haslinger, Ernst ; Jurenitsch, Johann ; Kubelka, Wolfgang</creatorcontrib><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><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 &amp; 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&amp;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 &amp; 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 &amp; 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>
fulltext fulltext
identifier ISSN: 0031-9422
ispartof Phytochemistry (Oxford), 2001-12, Vol.58 (8), p.1189-1194
issn 0031-9422
1873-3700
language eng
recordid cdi_proquest_miscellaneous_72346832
source ScienceDirect Freedom Collection
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
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-27T17%3A28%3A53IST&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=Highly%20hydroxylated%20guaianolides%20of%20Achillea%20asiatica%20and%20Middle%20European%20Achillea%20species&rft.jtitle=Phytochemistry%20(Oxford)&rft.au=Glasl,%20Sabine&rft.date=2001-12-01&rft.volume=58&rft.issue=8&rft.spage=1189&rft.epage=1194&rft.pages=1189-1194&rft.issn=0031-9422&rft.eissn=1873-3700&rft_id=info:doi/10.1016/S0031-9422(01)00281-3&rft_dat=%3Cproquest_cross%3E72346832%3C/proquest_cross%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c391t-77ea9155fc15afe2a949f3fe011b622cfeee0debb3b6fdf15494c69080ce310f3%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=72346832&rft_id=info:pmid/11738405&rfr_iscdi=true