Amide des Cysteins als Inhibitoren der Farnesyltransferase
The invention relates to compounds of formula (I) which have inhibitory effects on farnesyl transferase. Some of these compounds present in vitro inhibition of farnesyl transferase at concentrations < 1 mu M. The compounds provided for in the invention have the general formula (I), in which n is...
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creator | THIERICKE, RALF SATTLER, ISABEL GRABLEY, SUSANNE SCHLITZER, MARTIN SAKOWSKI, JACEK |
description | The invention relates to compounds of formula (I) which have inhibitory effects on farnesyl transferase. Some of these compounds present in vitro inhibition of farnesyl transferase at concentrations < 1 mu M. The compounds provided for in the invention have the general formula (I), in which n is between 0 and 3; R , R are H, alkyl, aryl, heteroaryl, acyl; R is H, halogen, alkyl, aryl, heteroaryl, arylalkyl, acyl, CN, NO2, R -X-; R is H, alkyl, aryl, heteroaryl, aralkyl, acyl; X is NH, O, S, SO2, NHSO2, OSO2; and A, B, C are organic rests.
Die Erfindung betrifft Verbindungen der Formel I mit inhibitorischen Wirkungen auf die Farnesyltransferase. Einige Verbindungen zeigen eine in vitro Hemmung der Farnesyltransferase bei Konzentrationen < 1 muM. DOLLAR A Die erfindungsgemäßen Verbindungen haben die allgemeine Formel (I) DOLLAR F1 worin DOLLAR A n = 0-3; R·1·, R·2· = H, Alkyl, Aryl, Heteroaryl, Acyl; R·3· = H, Halogen, Alkyl, Aryl, Heteroaryl, Arylalkyl, Acyl, CN, NO¶2¶, R·4·-X-; R·4· = H, Alkyl, Aryl, Heteroaryl, Aralkyl, Acyl; X = NH, O, S, SO¶2¶, NHSO¶2¶, OSO¶2¶ und A, B, C = organische Reste sind. |
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Die Erfindung betrifft Verbindungen der Formel I mit inhibitorischen Wirkungen auf die Farnesyltransferase. Einige Verbindungen zeigen eine in vitro Hemmung der Farnesyltransferase bei Konzentrationen < 1 muM. DOLLAR A Die erfindungsgemäßen Verbindungen haben die allgemeine Formel (I) DOLLAR F1 worin DOLLAR A n = 0-3; R·1·, R·2· = H, Alkyl, Aryl, Heteroaryl, Acyl; R·3· = H, Halogen, Alkyl, Aryl, Heteroaryl, Arylalkyl, Acyl, CN, NO¶2¶, R·4·-X-; R·4· = H, Alkyl, Aryl, Heteroaryl, Aralkyl, Acyl; X = NH, O, S, SO¶2¶, NHSO¶2¶, OSO¶2¶ und A, B, C = organische Reste sind.</description><edition>7</edition><language>ger</language><subject>ACYCLIC OR CARBOCYCLIC COMPOUNDS ; CHEMISTRY ; METALLURGY ; ORGANIC CHEMISTRY</subject><creationdate>2000</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&date=20000511&DB=EPODOC&CC=DE&NR=19851714A1$$EHTML$$P50$$Gepo$$Hfree_for_read</linktohtml><link.rule.ids>230,309,781,886,25569,76552</link.rule.ids><linktorsrc>$$Uhttps://worldwide.espacenet.com/publicationDetails/biblio?FT=D&date=20000511&DB=EPODOC&CC=DE&NR=19851714A1$$EView_record_in_European_Patent_Office$$FView_record_in_$$GEuropean_Patent_Office$$Hfree_for_read</linktorsrc></links><search><creatorcontrib>THIERICKE, RALF</creatorcontrib><creatorcontrib>SATTLER, ISABEL</creatorcontrib><creatorcontrib>GRABLEY, SUSANNE</creatorcontrib><creatorcontrib>SCHLITZER, MARTIN</creatorcontrib><creatorcontrib>SAKOWSKI, JACEK</creatorcontrib><title>Amide des Cysteins als Inhibitoren der Farnesyltransferase</title><description>The invention relates to compounds of formula (I) which have inhibitory effects on farnesyl transferase. Some of these compounds present in vitro inhibition of farnesyl transferase at concentrations < 1 mu M. The compounds provided for in the invention have the general formula (I), in which n is between 0 and 3; R , R are H, alkyl, aryl, heteroaryl, acyl; R is H, halogen, alkyl, aryl, heteroaryl, arylalkyl, acyl, CN, NO2, R -X-; R is H, alkyl, aryl, heteroaryl, aralkyl, acyl; X is NH, O, S, SO2, NHSO2, OSO2; and A, B, C are organic rests.
Die Erfindung betrifft Verbindungen der Formel I mit inhibitorischen Wirkungen auf die Farnesyltransferase. Einige Verbindungen zeigen eine in vitro Hemmung der Farnesyltransferase bei Konzentrationen < 1 muM. DOLLAR A Die erfindungsgemäßen Verbindungen haben die allgemeine Formel (I) DOLLAR F1 worin DOLLAR A n = 0-3; R·1·, R·2· = H, Alkyl, Aryl, Heteroaryl, Acyl; R·3· = H, Halogen, Alkyl, Aryl, Heteroaryl, Arylalkyl, Acyl, CN, NO¶2¶, R·4·-X-; R·4· = H, Alkyl, Aryl, Heteroaryl, Aralkyl, Acyl; X = NH, O, S, SO¶2¶, NHSO¶2¶, OSO¶2¶ und A, B, C = organische Reste sind.</description><subject>ACYCLIC OR CARBOCYCLIC COMPOUNDS</subject><subject>CHEMISTRY</subject><subject>METALLURGY</subject><subject>ORGANIC CHEMISTRY</subject><fulltext>true</fulltext><rsrctype>patent</rsrctype><creationdate>2000</creationdate><recordtype>patent</recordtype><sourceid>EVB</sourceid><recordid>eNrjZLByzM1MSVVISS1WcK4sLknNzCtWSMwpVvDMy8hMyizJL0rNA0oWKbglFuWlFlfmlBQl5hWnpRYlFqfyMLCmAZWm8kJpbgZFN9cQZw_d1IL8-NTigsTk1LzUkngXV0NLC1NDc0MTR0NjYtQAAHEHLyE</recordid><startdate>20000511</startdate><enddate>20000511</enddate><creator>THIERICKE, RALF</creator><creator>SATTLER, ISABEL</creator><creator>GRABLEY, SUSANNE</creator><creator>SCHLITZER, MARTIN</creator><creator>SAKOWSKI, JACEK</creator><scope>EVB</scope></search><sort><creationdate>20000511</creationdate><title>Amide des Cysteins als Inhibitoren der Farnesyltransferase</title><author>THIERICKE, RALF ; SATTLER, ISABEL ; GRABLEY, SUSANNE ; SCHLITZER, MARTIN ; SAKOWSKI, JACEK</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-epo_espacenet_DE19851714A13</frbrgroupid><rsrctype>patents</rsrctype><prefilter>patents</prefilter><language>ger</language><creationdate>2000</creationdate><topic>ACYCLIC OR CARBOCYCLIC COMPOUNDS</topic><topic>CHEMISTRY</topic><topic>METALLURGY</topic><topic>ORGANIC CHEMISTRY</topic><toplevel>online_resources</toplevel><creatorcontrib>THIERICKE, RALF</creatorcontrib><creatorcontrib>SATTLER, ISABEL</creatorcontrib><creatorcontrib>GRABLEY, SUSANNE</creatorcontrib><creatorcontrib>SCHLITZER, MARTIN</creatorcontrib><creatorcontrib>SAKOWSKI, JACEK</creatorcontrib><collection>esp@cenet</collection></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext_linktorsrc</fulltext></delivery><addata><au>THIERICKE, RALF</au><au>SATTLER, ISABEL</au><au>GRABLEY, SUSANNE</au><au>SCHLITZER, MARTIN</au><au>SAKOWSKI, JACEK</au><format>patent</format><genre>patent</genre><ristype>GEN</ristype><title>Amide des Cysteins als Inhibitoren der Farnesyltransferase</title><date>2000-05-11</date><risdate>2000</risdate><abstract>The invention relates to compounds of formula (I) which have inhibitory effects on farnesyl transferase. Some of these compounds present in vitro inhibition of farnesyl transferase at concentrations < 1 mu M. The compounds provided for in the invention have the general formula (I), in which n is between 0 and 3; R , R are H, alkyl, aryl, heteroaryl, acyl; R is H, halogen, alkyl, aryl, heteroaryl, arylalkyl, acyl, CN, NO2, R -X-; R is H, alkyl, aryl, heteroaryl, aralkyl, acyl; X is NH, O, S, SO2, NHSO2, OSO2; and A, B, C are organic rests.
Die Erfindung betrifft Verbindungen der Formel I mit inhibitorischen Wirkungen auf die Farnesyltransferase. Einige Verbindungen zeigen eine in vitro Hemmung der Farnesyltransferase bei Konzentrationen < 1 muM. DOLLAR A Die erfindungsgemäßen Verbindungen haben die allgemeine Formel (I) DOLLAR F1 worin DOLLAR A n = 0-3; R·1·, R·2· = H, Alkyl, Aryl, Heteroaryl, Acyl; R·3· = H, Halogen, Alkyl, Aryl, Heteroaryl, Arylalkyl, Acyl, CN, NO¶2¶, R·4·-X-; R·4· = H, Alkyl, Aryl, Heteroaryl, Aralkyl, Acyl; X = NH, O, S, SO¶2¶, NHSO¶2¶, OSO¶2¶ und A, B, C = organische Reste sind.</abstract><edition>7</edition><oa>free_for_read</oa></addata></record> |
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subjects | ACYCLIC OR CARBOCYCLIC COMPOUNDS CHEMISTRY METALLURGY ORGANIC CHEMISTRY |
title | Amide des Cysteins als Inhibitoren der Farnesyltransferase |
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