SULPHONYL AMIDINES

Novel substituted benzenesulfonamides are disclosed in which the sulfonamido nitrogen is substituted with various amino or alkoxy alkylene groups. The compounds are active anthelmintic agents and are particularly active against mature and immature fasciola. Processes for their preparation utilizing...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
1. Verfasser: HELMUT HUGO MROZIK
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 HELMUT HUGO MROZIK
description Novel substituted benzenesulfonamides are disclosed in which the sulfonamido nitrogen is substituted with various amino or alkoxy alkylene groups. The compounds are active anthelmintic agents and are particularly active against mature and immature fasciola. Processes for their preparation utilizing novel intermediates as well as compositions and methods for the treatment of helminthiasis are also disclosed.
format Patent
fullrecord <record><control><sourceid>epo_EVB</sourceid><recordid>TN_cdi_epo_espacenet_AU1204576A</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>AU1204576A</sourcerecordid><originalsourceid>FETCH-epo_espacenet_AU1204576A3</originalsourceid><addsrcrecordid>eNrjZBAKDvUJ8PD3i_RRcPT1dPH0cw3mYWBNS8wpTuWF0twM8m6uIc4euqkF-fGpxQWJyal5qSXxjqGGRgYmpuZmjsaEVQAA26odaQ</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>patent</recordtype></control><display><type>patent</type><title>SULPHONYL AMIDINES</title><source>esp@cenet</source><creator>HELMUT HUGO MROZIK</creator><creatorcontrib>HELMUT HUGO MROZIK</creatorcontrib><description>Novel substituted benzenesulfonamides are disclosed in which the sulfonamido nitrogen is substituted with various amino or alkoxy alkylene groups. The compounds are active anthelmintic agents and are particularly active against mature and immature fasciola. Processes for their preparation utilizing novel intermediates as well as compositions and methods for the treatment of helminthiasis are also disclosed.</description><language>eng</language><subject>CHEMISTRY ; HETEROCYCLIC COMPOUNDS ; METALLURGY ; ORGANIC CHEMISTRY</subject><creationdate>1977</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=19770922&amp;DB=EPODOC&amp;CC=AU&amp;NR=1204576A$$EHTML$$P50$$Gepo$$Hfree_for_read</linktohtml><link.rule.ids>230,308,776,881,25542,76289</link.rule.ids><linktorsrc>$$Uhttps://worldwide.espacenet.com/publicationDetails/biblio?FT=D&amp;date=19770922&amp;DB=EPODOC&amp;CC=AU&amp;NR=1204576A$$EView_record_in_European_Patent_Office$$FView_record_in_$$GEuropean_Patent_Office$$Hfree_for_read</linktorsrc></links><search><creatorcontrib>HELMUT HUGO MROZIK</creatorcontrib><title>SULPHONYL AMIDINES</title><description>Novel substituted benzenesulfonamides are disclosed in which the sulfonamido nitrogen is substituted with various amino or alkoxy alkylene groups. The compounds are active anthelmintic agents and are particularly active against mature and immature fasciola. Processes for their preparation utilizing novel intermediates as well as compositions and methods for the treatment of helminthiasis are also disclosed.</description><subject>CHEMISTRY</subject><subject>HETEROCYCLIC COMPOUNDS</subject><subject>METALLURGY</subject><subject>ORGANIC CHEMISTRY</subject><fulltext>true</fulltext><rsrctype>patent</rsrctype><creationdate>1977</creationdate><recordtype>patent</recordtype><sourceid>EVB</sourceid><recordid>eNrjZBAKDvUJ8PD3i_RRcPT1dPH0cw3mYWBNS8wpTuWF0twM8m6uIc4euqkF-fGpxQWJyal5qSXxjqGGRgYmpuZmjsaEVQAA26odaQ</recordid><startdate>19770922</startdate><enddate>19770922</enddate><creator>HELMUT HUGO MROZIK</creator><scope>EVB</scope></search><sort><creationdate>19770922</creationdate><title>SULPHONYL AMIDINES</title><author>HELMUT HUGO MROZIK</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-epo_espacenet_AU1204576A3</frbrgroupid><rsrctype>patents</rsrctype><prefilter>patents</prefilter><language>eng</language><creationdate>1977</creationdate><topic>CHEMISTRY</topic><topic>HETEROCYCLIC COMPOUNDS</topic><topic>METALLURGY</topic><topic>ORGANIC CHEMISTRY</topic><toplevel>online_resources</toplevel><creatorcontrib>HELMUT HUGO MROZIK</creatorcontrib><collection>esp@cenet</collection></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext_linktorsrc</fulltext></delivery><addata><au>HELMUT HUGO MROZIK</au><format>patent</format><genre>patent</genre><ristype>GEN</ristype><title>SULPHONYL AMIDINES</title><date>1977-09-22</date><risdate>1977</risdate><abstract>Novel substituted benzenesulfonamides are disclosed in which the sulfonamido nitrogen is substituted with various amino or alkoxy alkylene groups. The compounds are active anthelmintic agents and are particularly active against mature and immature fasciola. Processes for their preparation utilizing novel intermediates as well as compositions and methods for the treatment of helminthiasis are also disclosed.</abstract><oa>free_for_read</oa></addata></record>
fulltext fulltext_linktorsrc
identifier
ispartof
issn
language eng
recordid cdi_epo_espacenet_AU1204576A
source esp@cenet
subjects CHEMISTRY
HETEROCYCLIC COMPOUNDS
METALLURGY
ORGANIC CHEMISTRY
title SULPHONYL AMIDINES
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-11T04%3A01%3A16IST&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=HELMUT%20HUGO%20MROZIK&rft.date=1977-09-22&rft_id=info:doi/&rft_dat=%3Cepo_EVB%3EAU1204576A%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