SUBSTITUIERTE (CHINOLIN-2-YL-METHOXY)PHENYL-CARBONYLHARNSTOFFE

Substituted (quinolin-2-ylmethoxy)phenylcarbonylureas can be prepared by reaction of substituted (quinolin-2-ylmethoxy)anilines with isocyanates and, if appropriate, subsequent alkylation. The substituted (quinolin-2-ylmethoxy)phenylcarbonylureas can be employed as active substances in medicaments,...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Hauptverfasser: RADDATZ, SIEGFRIED. DR., 5000 KOELN, DE, KOHLSDORFER, CHRISTIAN-BIOL. DR., 5042 ERFTSTADT, DE, FRUCHTMANN, ROMANIS-BIOL., 5000 KOELN, DE, MUELLER-PEDDINGHAUS, REINER, THEISEN, PIA-OEC.TROPH. DR., 5060 BERGISCH GLADBACH, DE, MOHRS, KLAUS. DR., 5600 WUPPERTAL, DE, FUGMANN, BURKHARD. DR., 5603 WUELFRATH, DE
Format: Patent
Sprache:ger
Schlagworte:
Online-Zugang:Volltext bestellen
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page
container_issue
container_start_page
container_title
container_volume
creator RADDATZ, SIEGFRIED. DR., 5000 KOELN, DE
KOHLSDORFER, CHRISTIAN-BIOL. DR., 5042 ERFTSTADT, DE
FRUCHTMANN, ROMANIS-BIOL., 5000 KOELN, DE
MUELLER-PEDDINGHAUS, REINER
THEISEN, PIA-OEC.TROPH. DR., 5060 BERGISCH GLADBACH, DE
MOHRS, KLAUS. DR., 5600 WUPPERTAL, DE
FUGMANN, BURKHARD. DR., 5603 WUELFRATH, DE
description Substituted (quinolin-2-ylmethoxy)phenylcarbonylureas can be prepared by reaction of substituted (quinolin-2-ylmethoxy)anilines with isocyanates and, if appropriate, subsequent alkylation. The substituted (quinolin-2-ylmethoxy)phenylcarbonylureas can be employed as active substances in medicaments, in particular for the inhibition of enzymatic reactions in the context of arachidonic acid metabolism.
format Patent
fullrecord <record><control><sourceid>epo_EVB</sourceid><recordid>TN_cdi_epo_espacenet_DE3935491A1</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>DE3935491A1</sourcerecordid><originalsourceid>FETCH-epo_espacenet_DE3935491A13</originalsourceid><addsrcrecordid>eNrjZLALDnUKDvEMCfV0DQpxVdBw9vD08_fx9NM10o300fV1DfHwj4jUDPBw9QNynR2DnPyBDA_HIL_gEH83N1ceBta0xJziVF4ozc2g4OYa4uyhm1qQH59aXJCYnJqXWhLv4mpsaWxqYmnoaGhMhBIATXgqTQ</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>patent</recordtype></control><display><type>patent</type><title>SUBSTITUIERTE (CHINOLIN-2-YL-METHOXY)PHENYL-CARBONYLHARNSTOFFE</title><source>esp@cenet</source><creator>RADDATZ, SIEGFRIED. DR., 5000 KOELN, DE ; KOHLSDORFER, CHRISTIAN-BIOL. DR., 5042 ERFTSTADT, DE ; FRUCHTMANN, ROMANIS-BIOL., 5000 KOELN, DE ; MUELLER-PEDDINGHAUS, REINER ; THEISEN, PIA-OEC.TROPH. DR., 5060 BERGISCH GLADBACH, DE ; MOHRS, KLAUS. DR., 5600 WUPPERTAL, DE ; FUGMANN, BURKHARD. DR., 5603 WUELFRATH, DE</creator><creatorcontrib>RADDATZ, SIEGFRIED. DR., 5000 KOELN, DE ; KOHLSDORFER, CHRISTIAN-BIOL. DR., 5042 ERFTSTADT, DE ; FRUCHTMANN, ROMANIS-BIOL., 5000 KOELN, DE ; MUELLER-PEDDINGHAUS, REINER ; THEISEN, PIA-OEC.TROPH. DR., 5060 BERGISCH GLADBACH, DE ; MOHRS, KLAUS. DR., 5600 WUPPERTAL, DE ; FUGMANN, BURKHARD. DR., 5603 WUELFRATH, DE</creatorcontrib><description>Substituted (quinolin-2-ylmethoxy)phenylcarbonylureas can be prepared by reaction of substituted (quinolin-2-ylmethoxy)anilines with isocyanates and, if appropriate, subsequent alkylation. The substituted (quinolin-2-ylmethoxy)phenylcarbonylureas can be employed as active substances in medicaments, in particular for the inhibition of enzymatic reactions in the context of arachidonic acid metabolism.</description><language>ger</language><subject>CHEMISTRY ; HETEROCYCLIC COMPOUNDS ; HUMAN NECESSITIES ; HYGIENE ; MEDICAL OR VETERINARY SCIENCE ; METALLURGY ; ORGANIC CHEMISTRY ; PREPARATIONS FOR MEDICAL, DENTAL, OR TOILET PURPOSES ; SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS ORMEDICINAL PREPARATIONS</subject><creationdate>1991</creationdate><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://worldwide.espacenet.com/publicationDetails/biblio?FT=D&amp;date=19910502&amp;DB=EPODOC&amp;CC=DE&amp;NR=3935491A1$$EHTML$$P50$$Gepo$$Hfree_for_read</linktohtml><link.rule.ids>230,308,780,885,25564,76547</link.rule.ids><linktorsrc>$$Uhttps://worldwide.espacenet.com/publicationDetails/biblio?FT=D&amp;date=19910502&amp;DB=EPODOC&amp;CC=DE&amp;NR=3935491A1$$EView_record_in_European_Patent_Office$$FView_record_in_$$GEuropean_Patent_Office$$Hfree_for_read</linktorsrc></links><search><creatorcontrib>RADDATZ, SIEGFRIED. DR., 5000 KOELN, DE</creatorcontrib><creatorcontrib>KOHLSDORFER, CHRISTIAN-BIOL. DR., 5042 ERFTSTADT, DE</creatorcontrib><creatorcontrib>FRUCHTMANN, ROMANIS-BIOL., 5000 KOELN, DE</creatorcontrib><creatorcontrib>MUELLER-PEDDINGHAUS, REINER</creatorcontrib><creatorcontrib>THEISEN, PIA-OEC.TROPH. DR., 5060 BERGISCH GLADBACH, DE</creatorcontrib><creatorcontrib>MOHRS, KLAUS. DR., 5600 WUPPERTAL, DE</creatorcontrib><creatorcontrib>FUGMANN, BURKHARD. DR., 5603 WUELFRATH, DE</creatorcontrib><title>SUBSTITUIERTE (CHINOLIN-2-YL-METHOXY)PHENYL-CARBONYLHARNSTOFFE</title><description>Substituted (quinolin-2-ylmethoxy)phenylcarbonylureas can be prepared by reaction of substituted (quinolin-2-ylmethoxy)anilines with isocyanates and, if appropriate, subsequent alkylation. The substituted (quinolin-2-ylmethoxy)phenylcarbonylureas can be employed as active substances in medicaments, in particular for the inhibition of enzymatic reactions in the context of arachidonic acid metabolism.</description><subject>CHEMISTRY</subject><subject>HETEROCYCLIC COMPOUNDS</subject><subject>HUMAN NECESSITIES</subject><subject>HYGIENE</subject><subject>MEDICAL OR VETERINARY SCIENCE</subject><subject>METALLURGY</subject><subject>ORGANIC CHEMISTRY</subject><subject>PREPARATIONS FOR MEDICAL, DENTAL, OR TOILET PURPOSES</subject><subject>SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS ORMEDICINAL PREPARATIONS</subject><fulltext>true</fulltext><rsrctype>patent</rsrctype><creationdate>1991</creationdate><recordtype>patent</recordtype><sourceid>EVB</sourceid><recordid>eNrjZLALDnUKDvEMCfV0DQpxVdBw9vD08_fx9NM10o300fV1DfHwj4jUDPBw9QNynR2DnPyBDA_HIL_gEH83N1ceBta0xJziVF4ozc2g4OYa4uyhm1qQH59aXJCYnJqXWhLv4mpsaWxqYmnoaGhMhBIATXgqTQ</recordid><startdate>19910502</startdate><enddate>19910502</enddate><creator>RADDATZ, SIEGFRIED. DR., 5000 KOELN, DE</creator><creator>KOHLSDORFER, CHRISTIAN-BIOL. DR., 5042 ERFTSTADT, DE</creator><creator>FRUCHTMANN, ROMANIS-BIOL., 5000 KOELN, DE</creator><creator>MUELLER-PEDDINGHAUS, REINER</creator><creator>THEISEN, PIA-OEC.TROPH. DR., 5060 BERGISCH GLADBACH, DE</creator><creator>MOHRS, KLAUS. DR., 5600 WUPPERTAL, DE</creator><creator>FUGMANN, BURKHARD. DR., 5603 WUELFRATH, DE</creator><scope>EVB</scope></search><sort><creationdate>19910502</creationdate><title>SUBSTITUIERTE (CHINOLIN-2-YL-METHOXY)PHENYL-CARBONYLHARNSTOFFE</title><author>RADDATZ, SIEGFRIED. DR., 5000 KOELN, DE ; KOHLSDORFER, CHRISTIAN-BIOL. DR., 5042 ERFTSTADT, DE ; FRUCHTMANN, ROMANIS-BIOL., 5000 KOELN, DE ; MUELLER-PEDDINGHAUS, REINER ; THEISEN, PIA-OEC.TROPH. DR., 5060 BERGISCH GLADBACH, DE ; MOHRS, KLAUS. DR., 5600 WUPPERTAL, DE ; FUGMANN, BURKHARD. DR., 5603 WUELFRATH, DE</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-epo_espacenet_DE3935491A13</frbrgroupid><rsrctype>patents</rsrctype><prefilter>patents</prefilter><language>ger</language><creationdate>1991</creationdate><topic>CHEMISTRY</topic><topic>HETEROCYCLIC COMPOUNDS</topic><topic>HUMAN NECESSITIES</topic><topic>HYGIENE</topic><topic>MEDICAL OR VETERINARY SCIENCE</topic><topic>METALLURGY</topic><topic>ORGANIC CHEMISTRY</topic><topic>PREPARATIONS FOR MEDICAL, DENTAL, OR TOILET PURPOSES</topic><topic>SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS ORMEDICINAL PREPARATIONS</topic><toplevel>online_resources</toplevel><creatorcontrib>RADDATZ, SIEGFRIED. DR., 5000 KOELN, DE</creatorcontrib><creatorcontrib>KOHLSDORFER, CHRISTIAN-BIOL. DR., 5042 ERFTSTADT, DE</creatorcontrib><creatorcontrib>FRUCHTMANN, ROMANIS-BIOL., 5000 KOELN, DE</creatorcontrib><creatorcontrib>MUELLER-PEDDINGHAUS, REINER</creatorcontrib><creatorcontrib>THEISEN, PIA-OEC.TROPH. DR., 5060 BERGISCH GLADBACH, DE</creatorcontrib><creatorcontrib>MOHRS, KLAUS. DR., 5600 WUPPERTAL, DE</creatorcontrib><creatorcontrib>FUGMANN, BURKHARD. DR., 5603 WUELFRATH, DE</creatorcontrib><collection>esp@cenet</collection></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext_linktorsrc</fulltext></delivery><addata><au>RADDATZ, SIEGFRIED. DR., 5000 KOELN, DE</au><au>KOHLSDORFER, CHRISTIAN-BIOL. DR., 5042 ERFTSTADT, DE</au><au>FRUCHTMANN, ROMANIS-BIOL., 5000 KOELN, DE</au><au>MUELLER-PEDDINGHAUS, REINER</au><au>THEISEN, PIA-OEC.TROPH. DR., 5060 BERGISCH GLADBACH, DE</au><au>MOHRS, KLAUS. DR., 5600 WUPPERTAL, DE</au><au>FUGMANN, BURKHARD. DR., 5603 WUELFRATH, DE</au><format>patent</format><genre>patent</genre><ristype>GEN</ristype><title>SUBSTITUIERTE (CHINOLIN-2-YL-METHOXY)PHENYL-CARBONYLHARNSTOFFE</title><date>1991-05-02</date><risdate>1991</risdate><abstract>Substituted (quinolin-2-ylmethoxy)phenylcarbonylureas can be prepared by reaction of substituted (quinolin-2-ylmethoxy)anilines with isocyanates and, if appropriate, subsequent alkylation. The substituted (quinolin-2-ylmethoxy)phenylcarbonylureas can be employed as active substances in medicaments, in particular for the inhibition of enzymatic reactions in the context of arachidonic acid metabolism.</abstract><oa>free_for_read</oa></addata></record>
fulltext fulltext_linktorsrc
identifier
ispartof
issn
language ger
recordid cdi_epo_espacenet_DE3935491A1
source esp@cenet
subjects CHEMISTRY
HETEROCYCLIC COMPOUNDS
HUMAN NECESSITIES
HYGIENE
MEDICAL OR VETERINARY SCIENCE
METALLURGY
ORGANIC CHEMISTRY
PREPARATIONS FOR MEDICAL, DENTAL, OR TOILET PURPOSES
SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS ORMEDICINAL PREPARATIONS
title SUBSTITUIERTE (CHINOLIN-2-YL-METHOXY)PHENYL-CARBONYLHARNSTOFFE
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-02T21%3A04%3A54IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-epo_EVB&rft_val_fmt=info:ofi/fmt:kev:mtx:patent&rft.genre=patent&rft.au=RADDATZ,%20SIEGFRIED.%20DR.,%205000%20KOELN,%20DE&rft.date=1991-05-02&rft_id=info:doi/&rft_dat=%3Cepo_EVB%3EDE3935491A1%3C/epo_EVB%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