Antitumorpræparater og behandlingsmetoder

This invention provides certain N-phenyl-N'-substitutedphenylsulfonylureas compounds having the formula wherein: X is halo, CH3 or CF3; X is hydrogen, halo, or CF3 with the proviso that at least one of X and X is halo; A, B, D and E are (a) independently selected from group consisting of hydrog...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Hauptverfasser: TOTH, JOHN ELDON, HOWBERT, JAMES JEFFRY, RAY, JAMES EDWARD
Format: Patent
Sprache:dan
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 TOTH, JOHN ELDON
HOWBERT, JAMES JEFFRY
RAY, JAMES EDWARD
description This invention provides certain N-phenyl-N'-substitutedphenylsulfonylureas compounds having the formula wherein: X is halo, CH3 or CF3; X is hydrogen, halo, or CF3 with the proviso that at least one of X and X is halo; A, B, D and E are (a) independently selected from group consisting of hydrogen, methyl, ethyl, chlorine, bromine and iodine with the proviso that no more than one of A, B, D or E is hydrogen, or (b) E is hydrogen and one of A, B or D is selected from the group consisting of -NH2, -NHCH3, -N(CH3)2, -N(CH3)(CH2CH3), -N(CH2CH3)2, or -OCH3 and the remaining of A, B or D are selected from (a), or (c) E is hydrogen and A and B or B and D together are -(CH2)n- or -CH=CH(CH2)n-2- wherein n is 3 or 4 or -(CH=CH)2-, or -(CH2)pO- where p is 2 or 3, or -O(CH2)qO- where q is 1 or 2 and D or A respectively is selected from (a); or pharmaceutically acceptable salt thereof, and pharmaceutical formulations employing these compounds. This invention also provides a method for treating susceptible neoplasms in mammals using these sulfonylurea compounds and processes for producing them.
format Patent
fullrecord <record><control><sourceid>epo_EVB</sourceid><recordid>TN_cdi_epo_espacenet_DK0550157TT3</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>DK0550157TT3</sourcerecordid><originalsourceid>FETCH-epo_espacenet_DK0550157TT33</originalsourceid><addsrcrecordid>eNrjZNByzCvJLCnNzS8qKDq8rCCxKLEktUghP10hKTUjMS8lJzMvvTg3tSQ_JbWIh4E1LTGnOJUXSnMzKLq5hjh76KYW5MenFhckJqfmpZbEu3gbmJoaGJqah4QYGxOjBgDo2Srx</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>patent</recordtype></control><display><type>patent</type><title>Antitumorpræparater og behandlingsmetoder</title><source>esp@cenet</source><creator>TOTH, JOHN ELDON ; HOWBERT, JAMES JEFFRY ; RAY, JAMES EDWARD</creator><creatorcontrib>TOTH, JOHN ELDON ; HOWBERT, JAMES JEFFRY ; RAY, JAMES EDWARD</creatorcontrib><description>This invention provides certain N-phenyl-N'-substitutedphenylsulfonylureas compounds having the formula wherein: X is halo, CH3 or CF3; X is hydrogen, halo, or CF3 with the proviso that at least one of X and X is halo; A, B, D and E are (a) independently selected from group consisting of hydrogen, methyl, ethyl, chlorine, bromine and iodine with the proviso that no more than one of A, B, D or E is hydrogen, or (b) E is hydrogen and one of A, B or D is selected from the group consisting of -NH2, -NHCH3, -N(CH3)2, -N(CH3)(CH2CH3), -N(CH2CH3)2, or -OCH3 and the remaining of A, B or D are selected from (a), or (c) E is hydrogen and A and B or B and D together are -(CH2)n- or -CH=CH(CH2)n-2- wherein n is 3 or 4 or -(CH=CH)2-, or -(CH2)pO- where p is 2 or 3, or -O(CH2)qO- where q is 1 or 2 and D or A respectively is selected from (a); or pharmaceutically acceptable salt thereof, and pharmaceutical formulations employing these compounds. This invention also provides a method for treating susceptible neoplasms in mammals using these sulfonylurea compounds and processes for producing them.</description><edition>6</edition><language>dan</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>1997</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=19971201&amp;DB=EPODOC&amp;CC=DK&amp;NR=0550157T3$$EHTML$$P50$$Gepo$$Hfree_for_read</linktohtml><link.rule.ids>230,308,776,881,25542,76290</link.rule.ids><linktorsrc>$$Uhttps://worldwide.espacenet.com/publicationDetails/biblio?FT=D&amp;date=19971201&amp;DB=EPODOC&amp;CC=DK&amp;NR=0550157T3$$EView_record_in_European_Patent_Office$$FView_record_in_$$GEuropean_Patent_Office$$Hfree_for_read</linktorsrc></links><search><creatorcontrib>TOTH, JOHN ELDON</creatorcontrib><creatorcontrib>HOWBERT, JAMES JEFFRY</creatorcontrib><creatorcontrib>RAY, JAMES EDWARD</creatorcontrib><title>Antitumorpræparater og behandlingsmetoder</title><description>This invention provides certain N-phenyl-N'-substitutedphenylsulfonylureas compounds having the formula wherein: X is halo, CH3 or CF3; X is hydrogen, halo, or CF3 with the proviso that at least one of X and X is halo; A, B, D and E are (a) independently selected from group consisting of hydrogen, methyl, ethyl, chlorine, bromine and iodine with the proviso that no more than one of A, B, D or E is hydrogen, or (b) E is hydrogen and one of A, B or D is selected from the group consisting of -NH2, -NHCH3, -N(CH3)2, -N(CH3)(CH2CH3), -N(CH2CH3)2, or -OCH3 and the remaining of A, B or D are selected from (a), or (c) E is hydrogen and A and B or B and D together are -(CH2)n- or -CH=CH(CH2)n-2- wherein n is 3 or 4 or -(CH=CH)2-, or -(CH2)pO- where p is 2 or 3, or -O(CH2)qO- where q is 1 or 2 and D or A respectively is selected from (a); or pharmaceutically acceptable salt thereof, and pharmaceutical formulations employing these compounds. This invention also provides a method for treating susceptible neoplasms in mammals using these sulfonylurea compounds and processes for producing them.</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>1997</creationdate><recordtype>patent</recordtype><sourceid>EVB</sourceid><recordid>eNrjZNByzCvJLCnNzS8qKDq8rCCxKLEktUghP10hKTUjMS8lJzMvvTg3tSQ_JbWIh4E1LTGnOJUXSnMzKLq5hjh76KYW5MenFhckJqfmpZbEu3gbmJoaGJqah4QYGxOjBgDo2Srx</recordid><startdate>19971201</startdate><enddate>19971201</enddate><creator>TOTH, JOHN ELDON</creator><creator>HOWBERT, JAMES JEFFRY</creator><creator>RAY, JAMES EDWARD</creator><scope>EVB</scope></search><sort><creationdate>19971201</creationdate><title>Antitumorpræparater og behandlingsmetoder</title><author>TOTH, JOHN ELDON ; HOWBERT, JAMES JEFFRY ; RAY, JAMES EDWARD</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-epo_espacenet_DK0550157TT33</frbrgroupid><rsrctype>patents</rsrctype><prefilter>patents</prefilter><language>dan</language><creationdate>1997</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>TOTH, JOHN ELDON</creatorcontrib><creatorcontrib>HOWBERT, JAMES JEFFRY</creatorcontrib><creatorcontrib>RAY, JAMES EDWARD</creatorcontrib><collection>esp@cenet</collection></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext_linktorsrc</fulltext></delivery><addata><au>TOTH, JOHN ELDON</au><au>HOWBERT, JAMES JEFFRY</au><au>RAY, JAMES EDWARD</au><format>patent</format><genre>patent</genre><ristype>GEN</ristype><title>Antitumorpræparater og behandlingsmetoder</title><date>1997-12-01</date><risdate>1997</risdate><abstract>This invention provides certain N-phenyl-N'-substitutedphenylsulfonylureas compounds having the formula wherein: X is halo, CH3 or CF3; X is hydrogen, halo, or CF3 with the proviso that at least one of X and X is halo; A, B, D and E are (a) independently selected from group consisting of hydrogen, methyl, ethyl, chlorine, bromine and iodine with the proviso that no more than one of A, B, D or E is hydrogen, or (b) E is hydrogen and one of A, B or D is selected from the group consisting of -NH2, -NHCH3, -N(CH3)2, -N(CH3)(CH2CH3), -N(CH2CH3)2, or -OCH3 and the remaining of A, B or D are selected from (a), or (c) E is hydrogen and A and B or B and D together are -(CH2)n- or -CH=CH(CH2)n-2- wherein n is 3 or 4 or -(CH=CH)2-, or -(CH2)pO- where p is 2 or 3, or -O(CH2)qO- where q is 1 or 2 and D or A respectively is selected from (a); or pharmaceutically acceptable salt thereof, and pharmaceutical formulations employing these compounds. This invention also provides a method for treating susceptible neoplasms in mammals using these sulfonylurea compounds and processes for producing them.</abstract><edition>6</edition><oa>free_for_read</oa></addata></record>
fulltext fulltext_linktorsrc
identifier
ispartof
issn
language dan
recordid cdi_epo_espacenet_DK0550157TT3
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 Antitumorpræparater og behandlingsmetoder
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-04T01%3A41%3A26IST&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=TOTH,%20JOHN%20ELDON&rft.date=1997-12-01&rft_id=info:doi/&rft_dat=%3Cepo_EVB%3EDK0550157TT3%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