(+)-10 alpha-Hydroxy-4-muurolen-3-one, a new inhibitor of leukotriene biosynthesis from a Favolaschia species. Comparison with other sesquiterpenes

A new inhibitor of leukotriene biosynthesis, (+)-10 alpha-hydroxy-4-muurolen-3-one (1), was isolated from fermentations of Favolaschia sp. 87129. Its structure was established by spectroscopic methods. The compound exhibited no antifungal or antibacterial activities. The effects of 1 on leukotriene...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Zeitschrift für Naturforschung C. A journal of biosciences 1996-07, Vol.51 (7-8), p.487
Hauptverfasser: Zapf, S, Wunder, A, Anke, T, Klostermeyer, D, Steglich, W, Shan, R, Sterner, O, Scheuer, W
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page
container_issue 7-8
container_start_page 487
container_title Zeitschrift für Naturforschung C. A journal of biosciences
container_volume 51
creator Zapf, S
Wunder, A
Anke, T
Klostermeyer, D
Steglich, W
Shan, R
Sterner, O
Scheuer, W
description A new inhibitor of leukotriene biosynthesis, (+)-10 alpha-hydroxy-4-muurolen-3-one (1), was isolated from fermentations of Favolaschia sp. 87129. Its structure was established by spectroscopic methods. The compound exhibited no antifungal or antibacterial activities. The effects of 1 on leukotriene biosynthesis were compared with (+)-T-cadinol, (-)-3-oxo-T-cadinol, and (+)-3 alpha-hydroxy-T-cadinol, three related sesquiterpenes.
format Article
fullrecord <record><control><sourceid>pubmed</sourceid><recordid>TN_cdi_pubmed_primary_8810091</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>8810091</sourcerecordid><originalsourceid>FETCH-LOGICAL-p138t-10ccfea019b6fe3fa040cefbc7f8dc2ff226fddbd4d8b6a57e0af13b7e1220e03</originalsourceid><addsrcrecordid>eNotkLtOwzAYRj2ASik8ApJHEBjZcXMbUUQpUiUWmCtffiuGxDZ2Qslz9IWJRKdvOkdH3xla0prXJKdlfoEuU_qklBd5mS_QoqoYpTVbouPt_R1hFIsutIJsJx3970TWpB_H6DtwhBPv4AEL7OCArWuttIOP2Bvcwfjlh2jBAZbWp8kNLSSbsIm-n4GN-PGdSKq1AqcAykJ6xI3vg4g2eYcPdmixn5mIE6Tv0Q4QwyxLV-jciC7B9WlX6GPz_N5sye7t5bV52pHAeDXM1UoZEJTVsjDAjaBrqsBIVZpKq8yYLCuM1lKvdSULkZdAhWFclsCyjALlK3Tz7w2j7EHvQ7S9iNP-dA7_A4PCY4w</addsrcrecordid><sourcetype>Index Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>(+)-10 alpha-Hydroxy-4-muurolen-3-one, a new inhibitor of leukotriene biosynthesis from a Favolaschia species. Comparison with other sesquiterpenes</title><source>MEDLINE</source><source>Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals</source><creator>Zapf, S ; Wunder, A ; Anke, T ; Klostermeyer, D ; Steglich, W ; Shan, R ; Sterner, O ; Scheuer, W</creator><creatorcontrib>Zapf, S ; Wunder, A ; Anke, T ; Klostermeyer, D ; Steglich, W ; Shan, R ; Sterner, O ; Scheuer, W</creatorcontrib><description>A new inhibitor of leukotriene biosynthesis, (+)-10 alpha-hydroxy-4-muurolen-3-one (1), was isolated from fermentations of Favolaschia sp. 87129. Its structure was established by spectroscopic methods. The compound exhibited no antifungal or antibacterial activities. The effects of 1 on leukotriene biosynthesis were compared with (+)-T-cadinol, (-)-3-oxo-T-cadinol, and (+)-3 alpha-hydroxy-T-cadinol, three related sesquiterpenes.</description><identifier>ISSN: 0939-5075</identifier><identifier>PMID: 8810091</identifier><language>eng</language><publisher>Germany</publisher><subject>Animals ; Antineoplastic Agents, Phytogenic - chemistry ; Antineoplastic Agents, Phytogenic - isolation &amp; purification ; Antineoplastic Agents, Phytogenic - toxicity ; Calcium - pharmacology ; Cell Line ; Cell Survival - drug effects ; Dinoprostone - biosynthesis ; Dinoprostone - blood ; Fermentation ; HeLa Cells ; HL-60 Cells ; Humans ; In Vitro Techniques ; Leukemia L1210 ; Leukocytes - drug effects ; Leukocytes - metabolism ; Leukotriene Antagonists ; Leukotriene C4 - biosynthesis ; Leukotriene C4 - blood ; Leukotrienes - biosynthesis ; Mice ; Molecular Conformation ; Molecular Structure ; Polyporaceae ; Rats ; Sesquiterpenes - chemistry ; Sesquiterpenes - isolation &amp; purification ; Sesquiterpenes - pharmacology</subject><ispartof>Zeitschrift für Naturforschung C. A journal of biosciences, 1996-07, Vol.51 (7-8), p.487</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/8810091$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Zapf, S</creatorcontrib><creatorcontrib>Wunder, A</creatorcontrib><creatorcontrib>Anke, T</creatorcontrib><creatorcontrib>Klostermeyer, D</creatorcontrib><creatorcontrib>Steglich, W</creatorcontrib><creatorcontrib>Shan, R</creatorcontrib><creatorcontrib>Sterner, O</creatorcontrib><creatorcontrib>Scheuer, W</creatorcontrib><title>(+)-10 alpha-Hydroxy-4-muurolen-3-one, a new inhibitor of leukotriene biosynthesis from a Favolaschia species. Comparison with other sesquiterpenes</title><title>Zeitschrift für Naturforschung C. A journal of biosciences</title><addtitle>Z Naturforsch C</addtitle><description>A new inhibitor of leukotriene biosynthesis, (+)-10 alpha-hydroxy-4-muurolen-3-one (1), was isolated from fermentations of Favolaschia sp. 87129. Its structure was established by spectroscopic methods. The compound exhibited no antifungal or antibacterial activities. The effects of 1 on leukotriene biosynthesis were compared with (+)-T-cadinol, (-)-3-oxo-T-cadinol, and (+)-3 alpha-hydroxy-T-cadinol, three related sesquiterpenes.</description><subject>Animals</subject><subject>Antineoplastic Agents, Phytogenic - chemistry</subject><subject>Antineoplastic Agents, Phytogenic - isolation &amp; purification</subject><subject>Antineoplastic Agents, Phytogenic - toxicity</subject><subject>Calcium - pharmacology</subject><subject>Cell Line</subject><subject>Cell Survival - drug effects</subject><subject>Dinoprostone - biosynthesis</subject><subject>Dinoprostone - blood</subject><subject>Fermentation</subject><subject>HeLa Cells</subject><subject>HL-60 Cells</subject><subject>Humans</subject><subject>In Vitro Techniques</subject><subject>Leukemia L1210</subject><subject>Leukocytes - drug effects</subject><subject>Leukocytes - metabolism</subject><subject>Leukotriene Antagonists</subject><subject>Leukotriene C4 - biosynthesis</subject><subject>Leukotriene C4 - blood</subject><subject>Leukotrienes - biosynthesis</subject><subject>Mice</subject><subject>Molecular Conformation</subject><subject>Molecular Structure</subject><subject>Polyporaceae</subject><subject>Rats</subject><subject>Sesquiterpenes - chemistry</subject><subject>Sesquiterpenes - isolation &amp; purification</subject><subject>Sesquiterpenes - pharmacology</subject><issn>0939-5075</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1996</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNotkLtOwzAYRj2ASik8ApJHEBjZcXMbUUQpUiUWmCtffiuGxDZ2Qslz9IWJRKdvOkdH3xla0prXJKdlfoEuU_qklBd5mS_QoqoYpTVbouPt_R1hFIsutIJsJx3970TWpB_H6DtwhBPv4AEL7OCArWuttIOP2Bvcwfjlh2jBAZbWp8kNLSSbsIm-n4GN-PGdSKq1AqcAykJ6xI3vg4g2eYcPdmixn5mIE6Tv0Q4QwyxLV-jciC7B9WlX6GPz_N5sye7t5bV52pHAeDXM1UoZEJTVsjDAjaBrqsBIVZpKq8yYLCuM1lKvdSULkZdAhWFclsCyjALlK3Tz7w2j7EHvQ7S9iNP-dA7_A4PCY4w</recordid><startdate>199607</startdate><enddate>199607</enddate><creator>Zapf, S</creator><creator>Wunder, A</creator><creator>Anke, T</creator><creator>Klostermeyer, D</creator><creator>Steglich, W</creator><creator>Shan, R</creator><creator>Sterner, O</creator><creator>Scheuer, W</creator><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope></search><sort><creationdate>199607</creationdate><title>(+)-10 alpha-Hydroxy-4-muurolen-3-one, a new inhibitor of leukotriene biosynthesis from a Favolaschia species. Comparison with other sesquiterpenes</title><author>Zapf, S ; Wunder, A ; Anke, T ; Klostermeyer, D ; Steglich, W ; Shan, R ; Sterner, O ; Scheuer, W</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-p138t-10ccfea019b6fe3fa040cefbc7f8dc2ff226fddbd4d8b6a57e0af13b7e1220e03</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1996</creationdate><topic>Animals</topic><topic>Antineoplastic Agents, Phytogenic - chemistry</topic><topic>Antineoplastic Agents, Phytogenic - isolation &amp; purification</topic><topic>Antineoplastic Agents, Phytogenic - toxicity</topic><topic>Calcium - pharmacology</topic><topic>Cell Line</topic><topic>Cell Survival - drug effects</topic><topic>Dinoprostone - biosynthesis</topic><topic>Dinoprostone - blood</topic><topic>Fermentation</topic><topic>HeLa Cells</topic><topic>HL-60 Cells</topic><topic>Humans</topic><topic>In Vitro Techniques</topic><topic>Leukemia L1210</topic><topic>Leukocytes - drug effects</topic><topic>Leukocytes - metabolism</topic><topic>Leukotriene Antagonists</topic><topic>Leukotriene C4 - biosynthesis</topic><topic>Leukotriene C4 - blood</topic><topic>Leukotrienes - biosynthesis</topic><topic>Mice</topic><topic>Molecular Conformation</topic><topic>Molecular Structure</topic><topic>Polyporaceae</topic><topic>Rats</topic><topic>Sesquiterpenes - chemistry</topic><topic>Sesquiterpenes - isolation &amp; purification</topic><topic>Sesquiterpenes - pharmacology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Zapf, S</creatorcontrib><creatorcontrib>Wunder, A</creatorcontrib><creatorcontrib>Anke, T</creatorcontrib><creatorcontrib>Klostermeyer, D</creatorcontrib><creatorcontrib>Steglich, W</creatorcontrib><creatorcontrib>Shan, R</creatorcontrib><creatorcontrib>Sterner, O</creatorcontrib><creatorcontrib>Scheuer, W</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><jtitle>Zeitschrift für Naturforschung C. A journal of biosciences</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Zapf, S</au><au>Wunder, A</au><au>Anke, T</au><au>Klostermeyer, D</au><au>Steglich, W</au><au>Shan, R</au><au>Sterner, O</au><au>Scheuer, W</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>(+)-10 alpha-Hydroxy-4-muurolen-3-one, a new inhibitor of leukotriene biosynthesis from a Favolaschia species. Comparison with other sesquiterpenes</atitle><jtitle>Zeitschrift für Naturforschung C. A journal of biosciences</jtitle><addtitle>Z Naturforsch C</addtitle><date>1996-07</date><risdate>1996</risdate><volume>51</volume><issue>7-8</issue><spage>487</spage><pages>487-</pages><issn>0939-5075</issn><abstract>A new inhibitor of leukotriene biosynthesis, (+)-10 alpha-hydroxy-4-muurolen-3-one (1), was isolated from fermentations of Favolaschia sp. 87129. Its structure was established by spectroscopic methods. The compound exhibited no antifungal or antibacterial activities. The effects of 1 on leukotriene biosynthesis were compared with (+)-T-cadinol, (-)-3-oxo-T-cadinol, and (+)-3 alpha-hydroxy-T-cadinol, three related sesquiterpenes.</abstract><cop>Germany</cop><pmid>8810091</pmid></addata></record>
fulltext fulltext
identifier ISSN: 0939-5075
ispartof Zeitschrift für Naturforschung C. A journal of biosciences, 1996-07, Vol.51 (7-8), p.487
issn 0939-5075
language eng
recordid cdi_pubmed_primary_8810091
source MEDLINE; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals
subjects Animals
Antineoplastic Agents, Phytogenic - chemistry
Antineoplastic Agents, Phytogenic - isolation & purification
Antineoplastic Agents, Phytogenic - toxicity
Calcium - pharmacology
Cell Line
Cell Survival - drug effects
Dinoprostone - biosynthesis
Dinoprostone - blood
Fermentation
HeLa Cells
HL-60 Cells
Humans
In Vitro Techniques
Leukemia L1210
Leukocytes - drug effects
Leukocytes - metabolism
Leukotriene Antagonists
Leukotriene C4 - biosynthesis
Leukotriene C4 - blood
Leukotrienes - biosynthesis
Mice
Molecular Conformation
Molecular Structure
Polyporaceae
Rats
Sesquiterpenes - chemistry
Sesquiterpenes - isolation & purification
Sesquiterpenes - pharmacology
title (+)-10 alpha-Hydroxy-4-muurolen-3-one, a new inhibitor of leukotriene biosynthesis from a Favolaschia species. Comparison with other sesquiterpenes
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-25T07%3A49%3A21IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-pubmed&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=(+)-10%20alpha-Hydroxy-4-muurolen-3-one,%20a%20new%20inhibitor%20of%20leukotriene%20biosynthesis%20from%20a%20Favolaschia%20species.%20Comparison%20with%20other%20sesquiterpenes&rft.jtitle=Zeitschrift%20f%C3%BCr%20Naturforschung%20C.%20A%20journal%20of%20biosciences&rft.au=Zapf,%20S&rft.date=1996-07&rft.volume=51&rft.issue=7-8&rft.spage=487&rft.pages=487-&rft.issn=0939-5075&rft_id=info:doi/&rft_dat=%3Cpubmed%3E8810091%3C/pubmed%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_id=info:pmid/8810091&rfr_iscdi=true