EPI-EPIBATIDINDERIVATI
EPI-EPIBATIDINDERIVATI - Jedinjenja opšte formule XVII gde je R je niži alkil, niži alkenil, niži alkinil, ili cikloaikil, aril, heteroaril, aril-niži alkil ili heteroaril-mži alkil gde pomenute grupe mogu biti supstituisane sa jednim ili više supstituenata odabranih iz grupe koju Cine niži alkil, n...
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creator | TEMES-VARI, E MANDI, A GYERTYAN, I BLASKO, G FEKETE, M LAX, G DRABANT, S SZEMEREDI, K SZANTAY, C SIMIG, G LADY, B MOLDVAI, I CSORGB, M GIGLER, G SOMOGYI, M ZALLAST, T BALOGH, Z |
description | EPI-EPIBATIDINDERIVATI - Jedinjenja opšte formule XVII gde je R je niži alkil, niži alkenil, niži alkinil, ili cikloaikil, aril, heteroaril, aril-niži alkil ili heteroaril-mži alkil gde pomenute grupe mogu biti supstituisane sa jednim ili više supstituenata odabranih iz grupe koju Cine niži alkil, niži alkenil, niži alkinil, niži cikloaikil, aril, hetroaril, aril-niži alkil, hetroaril-niži alkil, hidroksi, niži alkoksi fenoksi, halogeno, halogeno-niži alkil, amino-, mono- ili disupstituisan amino-amido i/ili sulВfonamide; i R' je R' je vodonik, niži alkil, niži alkenil, niži alkinil, niži cikloaikil, niži cikloalkenil, niži cikloalkinil, aril-niži alkil, aril, heteroaril, halogeno-niži alkil, hidroksi-niži alkil ili acil; i njihove farmaceutski prihvatljive, aidicione soli kisleina koja pokazuju jak analgeziski efekat.Jedinjenja forВmule XVII su, nova jedinjenja sem kada R je 6-hloro-3-piridil a R' je vodonik.
The subject-matter of the invention are epi-epibatidine derivatives of general formula wherein R stands for a C1-4-alkyl, C2-4-alkenyl, C2-4-alkinyl, C3-7-cycloalkyl, aryl, heteroaryl, aryl-C1-4-alkyl or heteroaryl-C1-4-alkyl group, said groups optionally being substituted by 1 or more C1-4-alkyl, C2-4-alkenyl, C2-4-alkinyl, C3-7-cycloalkyl, aryl, heteroaryl, aryl-C1-4-alkyl, heteroaryl-C1-4-alkyl, hydroxy, C1-4-alkoxy, phenoxy, halogen, halogeno-C1-4-alkyl and/or amino, amido and/or sulfonamido substituent(s), optionally mono- or di-C1-4-alkyl-, -C2-4-alkenyl- and/or -C2-4-alkinyl substituted, and R' represents hydrogen or a C1-4-alkyl, C2-4-alkenyl, C2-4-alkinyl, C3-7-cycloalkyl, C3-7-cycloalkenyl, C3-7-cycloalkinyl, aryl-C1-4-alkyl, aryl, hetero-aryl, halogeno-C1-4-alkyl, hydroxy-C1-4-alkyl or, preferably C1-4-aliphatic; aromatic or heterocyclic, acyl group with the proviso that, if R' stands for hydrogen, R is different from 6-(chloro)-pyrid-3-yl as well as optically active forms and acid addition salts thereof. Further aspects of the invention are concerned with a process and intermediates for preparing these compounds as well as medicaments containing them and their use. |
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fullrecord | <record><control><sourceid>epo_EVB</sourceid><recordid>TN_cdi_epo_espacenet_YU71994A</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>YU71994A</sourcerecordid><originalsourceid>FETCH-epo_espacenet_YU71994A3</originalsourceid><addsrcrecordid>eNrjZBBzDfDUBWInxxBPF08_F9cgzzAgk4eBNS0xpziVF0pzM8i6uYY4e-imFuTHpxYXJCan5qWWxEeGmhtaWpo4GhOSBwDa1B3n</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>patent</recordtype></control><display><type>patent</type><title>EPI-EPIBATIDINDERIVATI</title><source>esp@cenet</source><creator>TEMES-VARI, E ; MANDI, A ; GYERTYAN, I ; BLASKO, G ; FEKETE, M ; LAX, G ; DRABANT, S ; SZEMEREDI, K ; SZANTAY, C ; SIMIG, G ; LADY, B ; MOLDVAI, I ; CSORGB, M ; GIGLER, G ; SOMOGYI, M ; ZALLAST, T ; BALOGH, Z</creator><creatorcontrib>TEMES-VARI, E ; MANDI, A ; GYERTYAN, I ; BLASKO, G ; FEKETE, M ; LAX, G ; DRABANT, S ; SZEMEREDI, K ; SZANTAY, C ; SIMIG, G ; LADY, B ; MOLDVAI, I ; CSORGB, M ; GIGLER, G ; SOMOGYI, M ; ZALLAST, T ; BALOGH, Z</creatorcontrib><description>EPI-EPIBATIDINDERIVATI - Jedinjenja opšte formule XVII gde je R je niži alkil, niži alkenil, niži alkinil, ili cikloaikil, aril, heteroaril, aril-niži alkil ili heteroaril-mži alkil gde pomenute grupe mogu biti supstituisane sa jednim ili više supstituenata odabranih iz grupe koju Cine niži alkil, niži alkenil, niži alkinil, niži cikloaikil, aril, hetroaril, aril-niži alkil, hetroaril-niži alkil, hidroksi, niži alkoksi fenoksi, halogeno, halogeno-niži alkil, amino-, mono- ili disupstituisan amino-amido i/ili sulВfonamide; i R' je R' je vodonik, niži alkil, niži alkenil, niži alkinil, niži cikloaikil, niži cikloalkenil, niži cikloalkinil, aril-niži alkil, aril, heteroaril, halogeno-niži alkil, hidroksi-niži alkil ili acil; i njihove farmaceutski prihvatljive, aidicione soli kisleina koja pokazuju jak analgeziski efekat.Jedinjenja forВmule XVII su, nova jedinjenja sem kada R je 6-hloro-3-piridil a R' je vodonik.
The subject-matter of the invention are epi-epibatidine derivatives of general formula wherein R stands for a C1-4-alkyl, C2-4-alkenyl, C2-4-alkinyl, C3-7-cycloalkyl, aryl, heteroaryl, aryl-C1-4-alkyl or heteroaryl-C1-4-alkyl group, said groups optionally being substituted by 1 or more C1-4-alkyl, C2-4-alkenyl, C2-4-alkinyl, C3-7-cycloalkyl, aryl, heteroaryl, aryl-C1-4-alkyl, heteroaryl-C1-4-alkyl, hydroxy, C1-4-alkoxy, phenoxy, halogen, halogeno-C1-4-alkyl and/or amino, amido and/or sulfonamido substituent(s), optionally mono- or di-C1-4-alkyl-, -C2-4-alkenyl- and/or -C2-4-alkinyl substituted, and R' represents hydrogen or a C1-4-alkyl, C2-4-alkenyl, C2-4-alkinyl, C3-7-cycloalkyl, C3-7-cycloalkenyl, C3-7-cycloalkinyl, aryl-C1-4-alkyl, aryl, hetero-aryl, halogeno-C1-4-alkyl, hydroxy-C1-4-alkyl or, preferably C1-4-aliphatic; aromatic or heterocyclic, acyl group with the proviso that, if R' stands for hydrogen, R is different from 6-(chloro)-pyrid-3-yl as well as optically active forms and acid addition salts thereof. Further aspects of the invention are concerned with a process and intermediates for preparing these compounds as well as medicaments containing them and their use.</description><language>eng</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>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&date=19971205&DB=EPODOC&CC=YU&NR=71994A$$EHTML$$P50$$Gepo$$Hfree_for_read</linktohtml><link.rule.ids>230,308,777,882,25545,76296</link.rule.ids><linktorsrc>$$Uhttps://worldwide.espacenet.com/publicationDetails/biblio?FT=D&date=19971205&DB=EPODOC&CC=YU&NR=71994A$$EView_record_in_European_Patent_Office$$FView_record_in_$$GEuropean_Patent_Office$$Hfree_for_read</linktorsrc></links><search><creatorcontrib>TEMES-VARI, E</creatorcontrib><creatorcontrib>MANDI, A</creatorcontrib><creatorcontrib>GYERTYAN, I</creatorcontrib><creatorcontrib>BLASKO, G</creatorcontrib><creatorcontrib>FEKETE, M</creatorcontrib><creatorcontrib>LAX, G</creatorcontrib><creatorcontrib>DRABANT, S</creatorcontrib><creatorcontrib>SZEMEREDI, K</creatorcontrib><creatorcontrib>SZANTAY, C</creatorcontrib><creatorcontrib>SIMIG, G</creatorcontrib><creatorcontrib>LADY, B</creatorcontrib><creatorcontrib>MOLDVAI, I</creatorcontrib><creatorcontrib>CSORGB, M</creatorcontrib><creatorcontrib>GIGLER, G</creatorcontrib><creatorcontrib>SOMOGYI, M</creatorcontrib><creatorcontrib>ZALLAST, T</creatorcontrib><creatorcontrib>BALOGH, Z</creatorcontrib><title>EPI-EPIBATIDINDERIVATI</title><description>EPI-EPIBATIDINDERIVATI - Jedinjenja opšte formule XVII gde je R je niži alkil, niži alkenil, niži alkinil, ili cikloaikil, aril, heteroaril, aril-niži alkil ili heteroaril-mži alkil gde pomenute grupe mogu biti supstituisane sa jednim ili više supstituenata odabranih iz grupe koju Cine niži alkil, niži alkenil, niži alkinil, niži cikloaikil, aril, hetroaril, aril-niži alkil, hetroaril-niži alkil, hidroksi, niži alkoksi fenoksi, halogeno, halogeno-niži alkil, amino-, mono- ili disupstituisan amino-amido i/ili sulВfonamide; i R' je R' je vodonik, niži alkil, niži alkenil, niži alkinil, niži cikloaikil, niži cikloalkenil, niži cikloalkinil, aril-niži alkil, aril, heteroaril, halogeno-niži alkil, hidroksi-niži alkil ili acil; i njihove farmaceutski prihvatljive, aidicione soli kisleina koja pokazuju jak analgeziski efekat.Jedinjenja forВmule XVII su, nova jedinjenja sem kada R je 6-hloro-3-piridil a R' je vodonik.
The subject-matter of the invention are epi-epibatidine derivatives of general formula wherein R stands for a C1-4-alkyl, C2-4-alkenyl, C2-4-alkinyl, C3-7-cycloalkyl, aryl, heteroaryl, aryl-C1-4-alkyl or heteroaryl-C1-4-alkyl group, said groups optionally being substituted by 1 or more C1-4-alkyl, C2-4-alkenyl, C2-4-alkinyl, C3-7-cycloalkyl, aryl, heteroaryl, aryl-C1-4-alkyl, heteroaryl-C1-4-alkyl, hydroxy, C1-4-alkoxy, phenoxy, halogen, halogeno-C1-4-alkyl and/or amino, amido and/or sulfonamido substituent(s), optionally mono- or di-C1-4-alkyl-, -C2-4-alkenyl- and/or -C2-4-alkinyl substituted, and R' represents hydrogen or a C1-4-alkyl, C2-4-alkenyl, C2-4-alkinyl, C3-7-cycloalkyl, C3-7-cycloalkenyl, C3-7-cycloalkinyl, aryl-C1-4-alkyl, aryl, hetero-aryl, halogeno-C1-4-alkyl, hydroxy-C1-4-alkyl or, preferably C1-4-aliphatic; aromatic or heterocyclic, acyl group with the proviso that, if R' stands for hydrogen, R is different from 6-(chloro)-pyrid-3-yl as well as optically active forms and acid addition salts thereof. Further aspects of the invention are concerned with a process and intermediates for preparing these compounds as well as medicaments containing them and their use.</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>1997</creationdate><recordtype>patent</recordtype><sourceid>EVB</sourceid><recordid>eNrjZBBzDfDUBWInxxBPF08_F9cgzzAgk4eBNS0xpziVF0pzM8i6uYY4e-imFuTHpxYXJCan5qWWxEeGmhtaWpo4GhOSBwDa1B3n</recordid><startdate>19971205</startdate><enddate>19971205</enddate><creator>TEMES-VARI, E</creator><creator>MANDI, A</creator><creator>GYERTYAN, I</creator><creator>BLASKO, G</creator><creator>FEKETE, M</creator><creator>LAX, G</creator><creator>DRABANT, S</creator><creator>SZEMEREDI, K</creator><creator>SZANTAY, C</creator><creator>SIMIG, G</creator><creator>LADY, B</creator><creator>MOLDVAI, I</creator><creator>CSORGB, M</creator><creator>GIGLER, G</creator><creator>SOMOGYI, M</creator><creator>ZALLAST, T</creator><creator>BALOGH, Z</creator><scope>EVB</scope></search><sort><creationdate>19971205</creationdate><title>EPI-EPIBATIDINDERIVATI</title><author>TEMES-VARI, E ; MANDI, A ; GYERTYAN, I ; BLASKO, G ; FEKETE, M ; LAX, G ; DRABANT, S ; SZEMEREDI, K ; SZANTAY, C ; SIMIG, G ; LADY, B ; MOLDVAI, I ; CSORGB, M ; GIGLER, G ; SOMOGYI, M ; ZALLAST, T ; BALOGH, Z</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-epo_espacenet_YU71994A3</frbrgroupid><rsrctype>patents</rsrctype><prefilter>patents</prefilter><language>eng</language><creationdate>1997</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>TEMES-VARI, E</creatorcontrib><creatorcontrib>MANDI, A</creatorcontrib><creatorcontrib>GYERTYAN, I</creatorcontrib><creatorcontrib>BLASKO, G</creatorcontrib><creatorcontrib>FEKETE, M</creatorcontrib><creatorcontrib>LAX, G</creatorcontrib><creatorcontrib>DRABANT, S</creatorcontrib><creatorcontrib>SZEMEREDI, K</creatorcontrib><creatorcontrib>SZANTAY, C</creatorcontrib><creatorcontrib>SIMIG, G</creatorcontrib><creatorcontrib>LADY, B</creatorcontrib><creatorcontrib>MOLDVAI, I</creatorcontrib><creatorcontrib>CSORGB, M</creatorcontrib><creatorcontrib>GIGLER, G</creatorcontrib><creatorcontrib>SOMOGYI, M</creatorcontrib><creatorcontrib>ZALLAST, T</creatorcontrib><creatorcontrib>BALOGH, Z</creatorcontrib><collection>esp@cenet</collection></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext_linktorsrc</fulltext></delivery><addata><au>TEMES-VARI, E</au><au>MANDI, A</au><au>GYERTYAN, I</au><au>BLASKO, G</au><au>FEKETE, M</au><au>LAX, G</au><au>DRABANT, S</au><au>SZEMEREDI, K</au><au>SZANTAY, C</au><au>SIMIG, G</au><au>LADY, B</au><au>MOLDVAI, I</au><au>CSORGB, M</au><au>GIGLER, G</au><au>SOMOGYI, M</au><au>ZALLAST, T</au><au>BALOGH, Z</au><format>patent</format><genre>patent</genre><ristype>GEN</ristype><title>EPI-EPIBATIDINDERIVATI</title><date>1997-12-05</date><risdate>1997</risdate><abstract>EPI-EPIBATIDINDERIVATI - Jedinjenja opšte formule XVII gde je R je niži alkil, niži alkenil, niži alkinil, ili cikloaikil, aril, heteroaril, aril-niži alkil ili heteroaril-mži alkil gde pomenute grupe mogu biti supstituisane sa jednim ili više supstituenata odabranih iz grupe koju Cine niži alkil, niži alkenil, niži alkinil, niži cikloaikil, aril, hetroaril, aril-niži alkil, hetroaril-niži alkil, hidroksi, niži alkoksi fenoksi, halogeno, halogeno-niži alkil, amino-, mono- ili disupstituisan amino-amido i/ili sulВfonamide; i R' je R' je vodonik, niži alkil, niži alkenil, niži alkinil, niži cikloaikil, niži cikloalkenil, niži cikloalkinil, aril-niži alkil, aril, heteroaril, halogeno-niži alkil, hidroksi-niži alkil ili acil; i njihove farmaceutski prihvatljive, aidicione soli kisleina koja pokazuju jak analgeziski efekat.Jedinjenja forВmule XVII su, nova jedinjenja sem kada R je 6-hloro-3-piridil a R' je vodonik.
The subject-matter of the invention are epi-epibatidine derivatives of general formula wherein R stands for a C1-4-alkyl, C2-4-alkenyl, C2-4-alkinyl, C3-7-cycloalkyl, aryl, heteroaryl, aryl-C1-4-alkyl or heteroaryl-C1-4-alkyl group, said groups optionally being substituted by 1 or more C1-4-alkyl, C2-4-alkenyl, C2-4-alkinyl, C3-7-cycloalkyl, aryl, heteroaryl, aryl-C1-4-alkyl, heteroaryl-C1-4-alkyl, hydroxy, C1-4-alkoxy, phenoxy, halogen, halogeno-C1-4-alkyl and/or amino, amido and/or sulfonamido substituent(s), optionally mono- or di-C1-4-alkyl-, -C2-4-alkenyl- and/or -C2-4-alkinyl substituted, and R' represents hydrogen or a C1-4-alkyl, C2-4-alkenyl, C2-4-alkinyl, C3-7-cycloalkyl, C3-7-cycloalkenyl, C3-7-cycloalkinyl, aryl-C1-4-alkyl, aryl, hetero-aryl, halogeno-C1-4-alkyl, hydroxy-C1-4-alkyl or, preferably C1-4-aliphatic; aromatic or heterocyclic, acyl group with the proviso that, if R' stands for hydrogen, R is different from 6-(chloro)-pyrid-3-yl as well as optically active forms and acid addition salts thereof. Further aspects of the invention are concerned with a process and intermediates for preparing these compounds as well as medicaments containing them and their use.</abstract><oa>free_for_read</oa></addata></record> |
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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 | EPI-EPIBATIDINDERIVATI |
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