Antimicrobial biflavonoids from the aerial part of Ouratea sulcata

Investigation of the aerial parts of Ouratea sulcata led to the isolation of a biflavonoid named sulcatone A, together with the known compounds, 3-hydroxy-2,3-dihydroapigenyl-[I-4′,O,II-3′]-dihydrokaempferol, amentoflavone, lophirone A, agathisflavone, stigmasterol and stigmasteryl-3-O-β-d-glucopyra...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Phytochemistry (Oxford) 2005-08, Vol.66 (16), p.1922-1926
Hauptverfasser: Pegnyemb, D.E., Mbing, J.N., Atchadé, A.T., Ghogomu, R., Sondengam, A., Blond, Alain, Bodo, Bernard
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 1926
container_issue 16
container_start_page 1922
container_title Phytochemistry (Oxford)
container_volume 66
creator Pegnyemb, D.E.
Mbing, J.N.
Atchadé, A.T.
Ghogomu, R.
Sondengam, A.
Blond, Alain
Bodo, Bernard
description Investigation of the aerial parts of Ouratea sulcata led to the isolation of a biflavonoid named sulcatone A, together with the known compounds, 3-hydroxy-2,3-dihydroapigenyl-[I-4′,O,II-3′]-dihydrokaempferol, amentoflavone, lophirone A, agathisflavone, stigmasterol and stigmasteryl-3-O-β-d-glucopyranoside. The structure of the compound was assigned as apigenyl-[I-4′,O,II-3′]-dihydrokaempferol, by means of spectroscopic analysis. Sulcatone A and 3-hydroxy-2,3-dihydroapigenyl-[I-4′,O,II-3′]-dihydrokaempferol exhibited significant in vitro antimicrobial activities against a range of microorganisms.
doi_str_mv 10.1016/j.phytochem.2005.06.017
format Article
fullrecord <record><control><sourceid>hal</sourceid><recordid>TN_cdi_hal_primary_oai_HAL_hal_00086260v1</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>oai_HAL_hal_00086260v1</sourcerecordid><originalsourceid>FETCH-hal_primary_oai_HAL_hal_00086260v13</originalsourceid><addsrcrecordid>eNqVjb0KwjAURjMoWH-ewawOxpvURh2rKA6Ci3u5rSlNSZuSpAXfXgVfwOnAdz44hCw5MA5cbmrWVa9gi0o1TAAkDCQDvhuRCCDm68NWiAmZel_DRyZSRuSYtkE3unA212horkuDg22tfnpaOtvQUCmKyn1lhy5QW9J77zAopL43BQack3GJxqvFjzOyupwfp-u6QpN1TjfoXplFnV3TW_bdPvG9FBIGHv_zfQM7uEWI</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>Antimicrobial biflavonoids from the aerial part of Ouratea sulcata</title><source>ScienceDirect Journals (5 years ago - present)</source><creator>Pegnyemb, D.E. ; Mbing, J.N. ; Atchadé, A.T. ; Ghogomu, R. ; Sondengam, A. ; Blond, Alain ; Bodo, Bernard</creator><creatorcontrib>Pegnyemb, D.E. ; Mbing, J.N. ; Atchadé, A.T. ; Ghogomu, R. ; Sondengam, A. ; Blond, Alain ; Bodo, Bernard</creatorcontrib><description>Investigation of the aerial parts of Ouratea sulcata led to the isolation of a biflavonoid named sulcatone A, together with the known compounds, 3-hydroxy-2,3-dihydroapigenyl-[I-4′,O,II-3′]-dihydrokaempferol, amentoflavone, lophirone A, agathisflavone, stigmasterol and stigmasteryl-3-O-β-d-glucopyranoside. The structure of the compound was assigned as apigenyl-[I-4′,O,II-3′]-dihydrokaempferol, by means of spectroscopic analysis. Sulcatone A and 3-hydroxy-2,3-dihydroapigenyl-[I-4′,O,II-3′]-dihydrokaempferol exhibited significant in vitro antimicrobial activities against a range of microorganisms.</description><identifier>ISSN: 0031-9422</identifier><identifier>DOI: 10.1016/j.phytochem.2005.06.017</identifier><language>eng</language><publisher>Elsevier</publisher><subject>Biochemistry ; Biochemistry, Molecular Biology ; Chemical Sciences ; Life Sciences ; Organic chemistry</subject><ispartof>Phytochemistry (Oxford), 2005-08, Vol.66 (16), p.1922-1926</ispartof><rights>Distributed under a Creative Commons Attribution 4.0 International License</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,780,784,885,27923,27924</link.rule.ids><backlink>$$Uhttps://hal.science/hal-00086260$$DView record in HAL$$Hfree_for_read</backlink></links><search><creatorcontrib>Pegnyemb, D.E.</creatorcontrib><creatorcontrib>Mbing, J.N.</creatorcontrib><creatorcontrib>Atchadé, A.T.</creatorcontrib><creatorcontrib>Ghogomu, R.</creatorcontrib><creatorcontrib>Sondengam, A.</creatorcontrib><creatorcontrib>Blond, Alain</creatorcontrib><creatorcontrib>Bodo, Bernard</creatorcontrib><title>Antimicrobial biflavonoids from the aerial part of Ouratea sulcata</title><title>Phytochemistry (Oxford)</title><description>Investigation of the aerial parts of Ouratea sulcata led to the isolation of a biflavonoid named sulcatone A, together with the known compounds, 3-hydroxy-2,3-dihydroapigenyl-[I-4′,O,II-3′]-dihydrokaempferol, amentoflavone, lophirone A, agathisflavone, stigmasterol and stigmasteryl-3-O-β-d-glucopyranoside. The structure of the compound was assigned as apigenyl-[I-4′,O,II-3′]-dihydrokaempferol, by means of spectroscopic analysis. Sulcatone A and 3-hydroxy-2,3-dihydroapigenyl-[I-4′,O,II-3′]-dihydrokaempferol exhibited significant in vitro antimicrobial activities against a range of microorganisms.</description><subject>Biochemistry</subject><subject>Biochemistry, Molecular Biology</subject><subject>Chemical Sciences</subject><subject>Life Sciences</subject><subject>Organic chemistry</subject><issn>0031-9422</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2005</creationdate><recordtype>article</recordtype><recordid>eNqVjb0KwjAURjMoWH-ewawOxpvURh2rKA6Ci3u5rSlNSZuSpAXfXgVfwOnAdz44hCw5MA5cbmrWVa9gi0o1TAAkDCQDvhuRCCDm68NWiAmZel_DRyZSRuSYtkE3unA212horkuDg22tfnpaOtvQUCmKyn1lhy5QW9J77zAopL43BQack3GJxqvFjzOyupwfp-u6QpN1TjfoXplFnV3TW_bdPvG9FBIGHv_zfQM7uEWI</recordid><startdate>200508</startdate><enddate>200508</enddate><creator>Pegnyemb, D.E.</creator><creator>Mbing, J.N.</creator><creator>Atchadé, A.T.</creator><creator>Ghogomu, R.</creator><creator>Sondengam, A.</creator><creator>Blond, Alain</creator><creator>Bodo, Bernard</creator><general>Elsevier</general><scope>1XC</scope></search><sort><creationdate>200508</creationdate><title>Antimicrobial biflavonoids from the aerial part of Ouratea sulcata</title><author>Pegnyemb, D.E. ; Mbing, J.N. ; Atchadé, A.T. ; Ghogomu, R. ; Sondengam, A. ; Blond, Alain ; Bodo, Bernard</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-hal_primary_oai_HAL_hal_00086260v13</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2005</creationdate><topic>Biochemistry</topic><topic>Biochemistry, Molecular Biology</topic><topic>Chemical Sciences</topic><topic>Life Sciences</topic><topic>Organic chemistry</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Pegnyemb, D.E.</creatorcontrib><creatorcontrib>Mbing, J.N.</creatorcontrib><creatorcontrib>Atchadé, A.T.</creatorcontrib><creatorcontrib>Ghogomu, R.</creatorcontrib><creatorcontrib>Sondengam, A.</creatorcontrib><creatorcontrib>Blond, Alain</creatorcontrib><creatorcontrib>Bodo, Bernard</creatorcontrib><collection>Hyper Article en Ligne (HAL)</collection><jtitle>Phytochemistry (Oxford)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Pegnyemb, D.E.</au><au>Mbing, J.N.</au><au>Atchadé, A.T.</au><au>Ghogomu, R.</au><au>Sondengam, A.</au><au>Blond, Alain</au><au>Bodo, Bernard</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Antimicrobial biflavonoids from the aerial part of Ouratea sulcata</atitle><jtitle>Phytochemistry (Oxford)</jtitle><date>2005-08</date><risdate>2005</risdate><volume>66</volume><issue>16</issue><spage>1922</spage><epage>1926</epage><pages>1922-1926</pages><issn>0031-9422</issn><abstract>Investigation of the aerial parts of Ouratea sulcata led to the isolation of a biflavonoid named sulcatone A, together with the known compounds, 3-hydroxy-2,3-dihydroapigenyl-[I-4′,O,II-3′]-dihydrokaempferol, amentoflavone, lophirone A, agathisflavone, stigmasterol and stigmasteryl-3-O-β-d-glucopyranoside. The structure of the compound was assigned as apigenyl-[I-4′,O,II-3′]-dihydrokaempferol, by means of spectroscopic analysis. Sulcatone A and 3-hydroxy-2,3-dihydroapigenyl-[I-4′,O,II-3′]-dihydrokaempferol exhibited significant in vitro antimicrobial activities against a range of microorganisms.</abstract><pub>Elsevier</pub><doi>10.1016/j.phytochem.2005.06.017</doi></addata></record>
fulltext fulltext
identifier ISSN: 0031-9422
ispartof Phytochemistry (Oxford), 2005-08, Vol.66 (16), p.1922-1926
issn 0031-9422
language eng
recordid cdi_hal_primary_oai_HAL_hal_00086260v1
source ScienceDirect Journals (5 years ago - present)
subjects Biochemistry
Biochemistry, Molecular Biology
Chemical Sciences
Life Sciences
Organic chemistry
title Antimicrobial biflavonoids from the aerial part of Ouratea sulcata
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-11T14%3A28%3A02IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-hal&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Antimicrobial%20biflavonoids%20from%20the%20aerial%20part%20of%20Ouratea%20sulcata&rft.jtitle=Phytochemistry%20(Oxford)&rft.au=Pegnyemb,%20D.E.&rft.date=2005-08&rft.volume=66&rft.issue=16&rft.spage=1922&rft.epage=1926&rft.pages=1922-1926&rft.issn=0031-9422&rft_id=info:doi/10.1016/j.phytochem.2005.06.017&rft_dat=%3Chal%3Eoai_HAL_hal_00086260v1%3C/hal%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_id=info:pmid/&rfr_iscdi=true