JPS6352625B

The invention provides sulphonamides of the formula (I) wherein R is a hydrogen atom or a lower alkyl radical; R1 is alkyl, aryl, aralkyl or aralkenyl, the aryl moiety of which in each case can be optionally substituted one or more times by hydroxyl, halogen, trifluoromethyl, lower alkyl or alkoxy o...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Hauptverfasser: HANSU PEETAA UORUFU, EEGON RESHU, KAARUHAINTSU SHUTEEKUMAIAA, ERUNSUTOOKURISUCHIAN UITSUCHI
Format: Patent
Sprache:eng
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 HANSU PEETAA UORUFU
EEGON RESHU
KAARUHAINTSU SHUTEEKUMAIAA
ERUNSUTOOKURISUCHIAN UITSUCHI
description The invention provides sulphonamides of the formula (I) wherein R is a hydrogen atom or a lower alkyl radical; R1 is alkyl, aryl, aralkyl or aralkenyl, the aryl moiety of which in each case can be optionally substituted one or more times by hydroxyl, halogen, trifluoromethyl, lower alkyl or alkoxy or by acyl, carboxy or alkoxycarbonyl; n is 1, 2 or 3; and W is a valence bond or a divalent aliphatic hydrocarbon linkage and the physiologically acceptable salts, esters and amides of such compound. These compounds have excellent pharmacological lipid depressing activity and inhibit thrombocyte aggregation.
format Patent
fullrecord <record><control><sourceid>epo_EVB</sourceid><recordid>TN_cdi_epo_espacenet_JPS6352625BB2</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>JPS6352625BB2</sourcerecordid><originalsourceid>FETCH-epo_espacenet_JPS6352625BB23</originalsourceid><addsrcrecordid>eNrjZOD2Cgg2MzY1MjMydeJhYE1LzClO5YXS3AxKbq4hzh66qQX58anFBYnJqXmpJfFIOpyMjIlSBACD9Bxs</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>patent</recordtype></control><display><type>patent</type><title>JPS6352625B</title><source>esp@cenet</source><creator>HANSU PEETAA UORUFU ; EEGON RESHU ; KAARUHAINTSU SHUTEEKUMAIAA ; ERUNSUTOOKURISUCHIAN UITSUCHI</creator><creatorcontrib>HANSU PEETAA UORUFU ; EEGON RESHU ; KAARUHAINTSU SHUTEEKUMAIAA ; ERUNSUTOOKURISUCHIAN UITSUCHI</creatorcontrib><description>The invention provides sulphonamides of the formula (I) wherein R is a hydrogen atom or a lower alkyl radical; R1 is alkyl, aryl, aralkyl or aralkenyl, the aryl moiety of which in each case can be optionally substituted one or more times by hydroxyl, halogen, trifluoromethyl, lower alkyl or alkoxy or by acyl, carboxy or alkoxycarbonyl; n is 1, 2 or 3; and W is a valence bond or a divalent aliphatic hydrocarbon linkage and the physiologically acceptable salts, esters and amides of such compound. These compounds have excellent pharmacological lipid depressing activity and inhibit thrombocyte aggregation.</description><language>eng</language><subject>ACYCLIC OR CARBOCYCLIC COMPOUNDS ; CHEMISTRY ; 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>1988</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=19881019&amp;DB=EPODOC&amp;CC=JP&amp;NR=S6352625B2$$EHTML$$P50$$Gepo$$Hfree_for_read</linktohtml><link.rule.ids>230,308,776,881,25542,76289</link.rule.ids><linktorsrc>$$Uhttps://worldwide.espacenet.com/publicationDetails/biblio?FT=D&amp;date=19881019&amp;DB=EPODOC&amp;CC=JP&amp;NR=S6352625B2$$EView_record_in_European_Patent_Office$$FView_record_in_$$GEuropean_Patent_Office$$Hfree_for_read</linktorsrc></links><search><creatorcontrib>HANSU PEETAA UORUFU</creatorcontrib><creatorcontrib>EEGON RESHU</creatorcontrib><creatorcontrib>KAARUHAINTSU SHUTEEKUMAIAA</creatorcontrib><creatorcontrib>ERUNSUTOOKURISUCHIAN UITSUCHI</creatorcontrib><title>JPS6352625B</title><description>The invention provides sulphonamides of the formula (I) wherein R is a hydrogen atom or a lower alkyl radical; R1 is alkyl, aryl, aralkyl or aralkenyl, the aryl moiety of which in each case can be optionally substituted one or more times by hydroxyl, halogen, trifluoromethyl, lower alkyl or alkoxy or by acyl, carboxy or alkoxycarbonyl; n is 1, 2 or 3; and W is a valence bond or a divalent aliphatic hydrocarbon linkage and the physiologically acceptable salts, esters and amides of such compound. These compounds have excellent pharmacological lipid depressing activity and inhibit thrombocyte aggregation.</description><subject>ACYCLIC OR CARBOCYCLIC COMPOUNDS</subject><subject>CHEMISTRY</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>1988</creationdate><recordtype>patent</recordtype><sourceid>EVB</sourceid><recordid>eNrjZOD2Cgg2MzY1MjMydeJhYE1LzClO5YXS3AxKbq4hzh66qQX58anFBYnJqXmpJfFIOpyMjIlSBACD9Bxs</recordid><startdate>19881019</startdate><enddate>19881019</enddate><creator>HANSU PEETAA UORUFU</creator><creator>EEGON RESHU</creator><creator>KAARUHAINTSU SHUTEEKUMAIAA</creator><creator>ERUNSUTOOKURISUCHIAN UITSUCHI</creator><scope>EVB</scope></search><sort><creationdate>19881019</creationdate><title>JPS6352625B</title><author>HANSU PEETAA UORUFU ; EEGON RESHU ; KAARUHAINTSU SHUTEEKUMAIAA ; ERUNSUTOOKURISUCHIAN UITSUCHI</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-epo_espacenet_JPS6352625BB23</frbrgroupid><rsrctype>patents</rsrctype><prefilter>patents</prefilter><language>eng</language><creationdate>1988</creationdate><topic>ACYCLIC OR CARBOCYCLIC COMPOUNDS</topic><topic>CHEMISTRY</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>HANSU PEETAA UORUFU</creatorcontrib><creatorcontrib>EEGON RESHU</creatorcontrib><creatorcontrib>KAARUHAINTSU SHUTEEKUMAIAA</creatorcontrib><creatorcontrib>ERUNSUTOOKURISUCHIAN UITSUCHI</creatorcontrib><collection>esp@cenet</collection></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext_linktorsrc</fulltext></delivery><addata><au>HANSU PEETAA UORUFU</au><au>EEGON RESHU</au><au>KAARUHAINTSU SHUTEEKUMAIAA</au><au>ERUNSUTOOKURISUCHIAN UITSUCHI</au><format>patent</format><genre>patent</genre><ristype>GEN</ristype><title>JPS6352625B</title><date>1988-10-19</date><risdate>1988</risdate><abstract>The invention provides sulphonamides of the formula (I) wherein R is a hydrogen atom or a lower alkyl radical; R1 is alkyl, aryl, aralkyl or aralkenyl, the aryl moiety of which in each case can be optionally substituted one or more times by hydroxyl, halogen, trifluoromethyl, lower alkyl or alkoxy or by acyl, carboxy or alkoxycarbonyl; n is 1, 2 or 3; and W is a valence bond or a divalent aliphatic hydrocarbon linkage and the physiologically acceptable salts, esters and amides of such compound. These compounds have excellent pharmacological lipid depressing activity and inhibit thrombocyte aggregation.</abstract><oa>free_for_read</oa></addata></record>
fulltext fulltext_linktorsrc
identifier
ispartof
issn
language eng
recordid cdi_epo_espacenet_JPS6352625BB2
source esp@cenet
subjects ACYCLIC OR CARBOCYCLIC COMPOUNDS
CHEMISTRY
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 JPS6352625B
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-04T15%3A00%3A42IST&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=HANSU%20PEETAA%20UORUFU&rft.date=1988-10-19&rft_id=info:doi/&rft_dat=%3Cepo_EVB%3EJPS6352625BB2%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