N-(3-BENZOFURANYL)UREA DERIVATIVES, MIXTURE OF THEIR ISOMERS OR INDIVIDUAL ISOMERS AND THEIR SALTS
organic synthesis. SUBSTANCE: invention provides novel derivatives of N-(3-benzofuranyl)urea having general formula I: (I), where A and D, identical or different, denote hydrogen, linear or branched C1-C6-acyl, linear or branched alkoxycarbonyl with 1-6 carbon atoms in its alkoxy moiety, halogen, OR...
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creator | MEHRI F. FITSDZHERAL'D GABRIEHLE BROJNLIKH KARL-KHAJNTS SHLEMMER GREHKHEHM STARTON ROL'F KHENNING RJUDIGER FISHER STEFEN TUDKHOP UL'RIKH NIL'SH TRIVOR S. EHBREM MATSEN EHS-SAJED MIKHAEHL' SHPERTSEL' |
description | organic synthesis. SUBSTANCE: invention provides novel derivatives of N-(3-benzofuranyl)urea having general formula I: (I), where A and D, identical or different, denote hydrogen, linear or branched C1-C6-acyl, linear or branched alkoxycarbonyl with 1-6 carbon atoms in its alkoxy moiety, halogen, OR4 group, wherein R4 is hydrogen, linear or branched C1-C8-alkyl, alkoxycarbonyl with 1-6 carbon atoms in its alkoxy moiety, benzyl, group, wherein R5 is , linear or branched C1-C4-alkyl, or group , wherein R6 is phenyl; L is oxygen or sulfur atom; R1 and R2, identical or different, denote hydrogen, cycloalkyl with up to 6 carbon atoms, linear or branched C1-C8-alkyl, C1-C8-alkoxycarbonyl, C2-C8-alkenyl, or benzoyl, or yet R1 and R2 in common with nitrogen atom form 5-7-membered saturated heterocycle; R3 is phenyl optionally substituted by 1 to 3 identical or different substituents from group including halogen, nitro, C1-C8-alkyl or C1-C8-alkoxy; in the form of isomer mixtures or individual isomers or their salts. Compounds I are biologically active. In particular, they inhibit lipoxygenase and can be useful in treatment of acute or chronic inflammatory conditions. EFFECT: extended choice of antiinflammatory agents. 14 cl, 11 tbl, 21 ex |
format | Patent |
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EHBREM ; MATSEN EHS-SAJED ; MIKHAEHL' SHPERTSEL'</creator><creatorcontrib>MEHRI F. FITSDZHERAL'D ; GABRIEHLE BROJNLIKH ; KARL-KHAJNTS SHLEMMER ; GREHKHEHM STARTON ; ROL'F KHENNING ; RJUDIGER FISHER ; STEFEN TUDKHOP ; UL'RIKH NIL'SH ; TRIVOR S. EHBREM ; MATSEN EHS-SAJED ; MIKHAEHL' SHPERTSEL'</creatorcontrib><description>organic synthesis. SUBSTANCE: invention provides novel derivatives of N-(3-benzofuranyl)urea having general formula I: (I), where A and D, identical or different, denote hydrogen, linear or branched C1-C6-acyl, linear or branched alkoxycarbonyl with 1-6 carbon atoms in its alkoxy moiety, halogen, OR4 group, wherein R4 is hydrogen, linear or branched C1-C8-alkyl, alkoxycarbonyl with 1-6 carbon atoms in its alkoxy moiety, benzyl, group, wherein R5 is , linear or branched C1-C4-alkyl, or group , wherein R6 is phenyl; L is oxygen or sulfur atom; R1 and R2, identical or different, denote hydrogen, cycloalkyl with up to 6 carbon atoms, linear or branched C1-C8-alkyl, C1-C8-alkoxycarbonyl, C2-C8-alkenyl, or benzoyl, or yet R1 and R2 in common with nitrogen atom form 5-7-membered saturated heterocycle; R3 is phenyl optionally substituted by 1 to 3 identical or different substituents from group including halogen, nitro, C1-C8-alkyl or C1-C8-alkoxy; in the form of isomer mixtures or individual isomers or their salts. Compounds I are biologically active. In particular, they inhibit lipoxygenase and can be useful in treatment of acute or chronic inflammatory conditions. EFFECT: extended choice of antiinflammatory agents. 14 cl, 11 tbl, 21 ex</description><edition>7</edition><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>2001</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=20010210&DB=EPODOC&CC=RU&NR=2162845C2$$EHTML$$P50$$Gepo$$Hfree_for_read</linktohtml><link.rule.ids>230,308,776,881,25542,76289</link.rule.ids><linktorsrc>$$Uhttps://worldwide.espacenet.com/publicationDetails/biblio?FT=D&date=20010210&DB=EPODOC&CC=RU&NR=2162845C2$$EView_record_in_European_Patent_Office$$FView_record_in_$$GEuropean_Patent_Office$$Hfree_for_read</linktorsrc></links><search><creatorcontrib>MEHRI F. FITSDZHERAL'D</creatorcontrib><creatorcontrib>GABRIEHLE BROJNLIKH</creatorcontrib><creatorcontrib>KARL-KHAJNTS SHLEMMER</creatorcontrib><creatorcontrib>GREHKHEHM STARTON</creatorcontrib><creatorcontrib>ROL'F KHENNING</creatorcontrib><creatorcontrib>RJUDIGER FISHER</creatorcontrib><creatorcontrib>STEFEN TUDKHOP</creatorcontrib><creatorcontrib>UL'RIKH NIL'SH</creatorcontrib><creatorcontrib>TRIVOR S. EHBREM</creatorcontrib><creatorcontrib>MATSEN EHS-SAJED</creatorcontrib><creatorcontrib>MIKHAEHL' SHPERTSEL'</creatorcontrib><title>N-(3-BENZOFURANYL)UREA DERIVATIVES, MIXTURE OF THEIR ISOMERS OR INDIVIDUAL ISOMERS AND THEIR SALTS</title><description>organic synthesis. SUBSTANCE: invention provides novel derivatives of N-(3-benzofuranyl)urea having general formula I: (I), where A and D, identical or different, denote hydrogen, linear or branched C1-C6-acyl, linear or branched alkoxycarbonyl with 1-6 carbon atoms in its alkoxy moiety, halogen, OR4 group, wherein R4 is hydrogen, linear or branched C1-C8-alkyl, alkoxycarbonyl with 1-6 carbon atoms in its alkoxy moiety, benzyl, group, wherein R5 is , linear or branched C1-C4-alkyl, or group , wherein R6 is phenyl; L is oxygen or sulfur atom; R1 and R2, identical or different, denote hydrogen, cycloalkyl with up to 6 carbon atoms, linear or branched C1-C8-alkyl, C1-C8-alkoxycarbonyl, C2-C8-alkenyl, or benzoyl, or yet R1 and R2 in common with nitrogen atom form 5-7-membered saturated heterocycle; R3 is phenyl optionally substituted by 1 to 3 identical or different substituents from group including halogen, nitro, C1-C8-alkyl or C1-C8-alkoxy; in the form of isomer mixtures or individual isomers or their salts. Compounds I are biologically active. In particular, they inhibit lipoxygenase and can be useful in treatment of acute or chronic inflammatory conditions. EFFECT: extended choice of antiinflammatory agents. 14 cl, 11 tbl, 21 ex</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>2001</creationdate><recordtype>patent</recordtype><sourceid>EVB</sourceid><recordid>eNrjZEjy09Uw1nVy9YvydwsNcvSL9NEMDXJ1VHBxDfIMcwzxDHMN1lHw9YwIAYoq-LsphHi4egYpeAb7-7oGBSv4A5l-Lp5hni6hjj5wUUc_F6i6YEefkGAeBta0xJziVF4ozc2g4OYa4uyhm1qQH59aXJCYnJqXWhIfFGpkaGZkYWLqbGRMhBIAgfYzwA</recordid><startdate>20010210</startdate><enddate>20010210</enddate><creator>MEHRI F. FITSDZHERAL'D</creator><creator>GABRIEHLE BROJNLIKH</creator><creator>KARL-KHAJNTS SHLEMMER</creator><creator>GREHKHEHM STARTON</creator><creator>ROL'F KHENNING</creator><creator>RJUDIGER FISHER</creator><creator>STEFEN TUDKHOP</creator><creator>UL'RIKH NIL'SH</creator><creator>TRIVOR S. EHBREM</creator><creator>MATSEN EHS-SAJED</creator><creator>MIKHAEHL' SHPERTSEL'</creator><scope>EVB</scope></search><sort><creationdate>20010210</creationdate><title>N-(3-BENZOFURANYL)UREA DERIVATIVES, MIXTURE OF THEIR ISOMERS OR INDIVIDUAL ISOMERS AND THEIR SALTS</title><author>MEHRI F. FITSDZHERAL'D ; GABRIEHLE BROJNLIKH ; KARL-KHAJNTS SHLEMMER ; GREHKHEHM STARTON ; ROL'F KHENNING ; RJUDIGER FISHER ; STEFEN TUDKHOP ; UL'RIKH NIL'SH ; TRIVOR S. EHBREM ; MATSEN EHS-SAJED ; MIKHAEHL' SHPERTSEL'</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-epo_espacenet_RU2162845C23</frbrgroupid><rsrctype>patents</rsrctype><prefilter>patents</prefilter><language>eng</language><creationdate>2001</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>MEHRI F. FITSDZHERAL'D</creatorcontrib><creatorcontrib>GABRIEHLE BROJNLIKH</creatorcontrib><creatorcontrib>KARL-KHAJNTS SHLEMMER</creatorcontrib><creatorcontrib>GREHKHEHM STARTON</creatorcontrib><creatorcontrib>ROL'F KHENNING</creatorcontrib><creatorcontrib>RJUDIGER FISHER</creatorcontrib><creatorcontrib>STEFEN TUDKHOP</creatorcontrib><creatorcontrib>UL'RIKH NIL'SH</creatorcontrib><creatorcontrib>TRIVOR S. EHBREM</creatorcontrib><creatorcontrib>MATSEN EHS-SAJED</creatorcontrib><creatorcontrib>MIKHAEHL' SHPERTSEL'</creatorcontrib><collection>esp@cenet</collection></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext_linktorsrc</fulltext></delivery><addata><au>MEHRI F. FITSDZHERAL'D</au><au>GABRIEHLE BROJNLIKH</au><au>KARL-KHAJNTS SHLEMMER</au><au>GREHKHEHM STARTON</au><au>ROL'F KHENNING</au><au>RJUDIGER FISHER</au><au>STEFEN TUDKHOP</au><au>UL'RIKH NIL'SH</au><au>TRIVOR S. EHBREM</au><au>MATSEN EHS-SAJED</au><au>MIKHAEHL' SHPERTSEL'</au><format>patent</format><genre>patent</genre><ristype>GEN</ristype><title>N-(3-BENZOFURANYL)UREA DERIVATIVES, MIXTURE OF THEIR ISOMERS OR INDIVIDUAL ISOMERS AND THEIR SALTS</title><date>2001-02-10</date><risdate>2001</risdate><abstract>organic synthesis. SUBSTANCE: invention provides novel derivatives of N-(3-benzofuranyl)urea having general formula I: (I), where A and D, identical or different, denote hydrogen, linear or branched C1-C6-acyl, linear or branched alkoxycarbonyl with 1-6 carbon atoms in its alkoxy moiety, halogen, OR4 group, wherein R4 is hydrogen, linear or branched C1-C8-alkyl, alkoxycarbonyl with 1-6 carbon atoms in its alkoxy moiety, benzyl, group, wherein R5 is , linear or branched C1-C4-alkyl, or group , wherein R6 is phenyl; L is oxygen or sulfur atom; R1 and R2, identical or different, denote hydrogen, cycloalkyl with up to 6 carbon atoms, linear or branched C1-C8-alkyl, C1-C8-alkoxycarbonyl, C2-C8-alkenyl, or benzoyl, or yet R1 and R2 in common with nitrogen atom form 5-7-membered saturated heterocycle; R3 is phenyl optionally substituted by 1 to 3 identical or different substituents from group including halogen, nitro, C1-C8-alkyl or C1-C8-alkoxy; in the form of isomer mixtures or individual isomers or their salts. Compounds I are biologically active. In particular, they inhibit lipoxygenase and can be useful in treatment of acute or chronic inflammatory conditions. EFFECT: extended choice of antiinflammatory agents. 14 cl, 11 tbl, 21 ex</abstract><edition>7</edition><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 | N-(3-BENZOFURANYL)UREA DERIVATIVES, MIXTURE OF THEIR ISOMERS OR INDIVIDUAL ISOMERS AND THEIR SALTS |
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