INDOLE OR BENZIMIDAZOLE DERIVATIVES FOR MODULATING IkappaB KINASE

Pronalazak se odnosi na sjedinjenja formule I. http://www.wipo.int/patentscope/search/en/docservice_fpimage/WOEP2003008629 false Jedinjenja formule I su pogodna za proizvodnju ljekova za profilaksu i liječenje oboljenja na čiji tok utiče povećana aktivnost IκB-kinaze. Substituted indole and benzimid...

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description Pronalazak se odnosi na sjedinjenja formule I. http://www.wipo.int/patentscope/search/en/docservice_fpimage/WOEP2003008629 false Jedinjenja formule I su pogodna za proizvodnju ljekova za profilaksu i liječenje oboljenja na čiji tok utiče povećana aktivnost IκB-kinaze. Substituted indole and benzimidazole derivatives (I), their stereoisomers and/or salts are new. Substituted indole and benzimidazole derivatives of formula (I), their stereoisomers and/or salts are new. [Image] X and M : nitrogen or CH; R1 and R11 : hydrogen, fluoro, chloro, bromo, iodo, 1-4C alkyl, cyano, trifluoromethyl, OR5, NR5R6, COR5 or S(O) xR5; x : 0-2; R5 and R6 : hydrogen or 1-4C alkyl; R2 : 3-hydroxypyrro-2,4-dione, imidazole, imidazol(id)ine, indazole, isothiazole, isothiazolidine, isoxazole, 2-isoxazolidine, isoxazolone, (thio)morpholine, oxazole, 1,3,4-oxadiazole, oxadiazolidinedione, oxadiazolone, 1,2,3,5-oxathiadiazole-2-oxide, 5-oxo-4,5-dihydro[1,3,4]oxadiazole, 5-oxo-1,2,4-thiadiazole, piperazine, pyrazine, pyrazole, pyrazoline, pyrazolidine, pyridazine, pyrimidine, tetrazole, thiadiazole, thiazole, triazole or triazolone (all optionally substituted by 1-3 of COR5, 1-4C alkyl, OR5, NR5R6, halo or keto), COR5, COOR5, or CONR7R8; R7 and R8 : hydrogen or 1-4C (hydroxy)alkyl or alkoxy; R3 : hydrogen or 1-4C alkyl; R4 : pyrrole, furan, thiophene, imidazole, pyrazole, oxazole, isoxazole, (iso)thiazole, tetrazole, 1,2,3,5-oxathiadiazole-2-oxide, triazolone, oxadiazolone, isoxazolone, oxadiazolidinedione, triazole, 3-hydroxypyrro-2,4-dione, 5-oxo-1,2,4-thiadiazole, pyridine, pyrazine, pyrimidine, (iso)indole, indazole, phthalazine, (iso)quinoline, quinoxaline, quinazoline, cinnoline, beta -carboline, all optionally benzo-fused or as cyclopenta- or cyclohexa-derivatives, or phenyl, 1- or 2-naphthyl, 2-, 3- or 4-biphenylyl, anthryl or fluorenyl, all optionally substituted by 1-3 1-5C alkyl or alkoxy, halo, nitro, amino, trifluoromethyl, hydroxy, 1-4C hydroxyalkyl, (m)ethylenedioxy, formyl, acetyl, cyano, carboxy, aminocarbonyl or 1-4C alkoxycarbonyl. An independent claim is also included for a method for preparing (I). ACTIVITY : Antiarthritic; Antirheumatic; Osteopathic; Antidiabetic; Antiinflammatory; Immunomodulator; Neuroprotective; Antiarteriosclerotic; Vasotropic; Antiulcer; Nootropic; Cytostatic; Cardiant; Antigout; Immunosuppressive; Antibacterial; Virucide; Hepatotropic; Anti-HIV; Protozoacide; Fungicide; Antiasthmatic; Antipsoriatic. MECHANISM OF ACTION : Inhibition of Ikapp
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Substituted indole and benzimidazole derivatives (I), their stereoisomers and/or salts are new. Substituted indole and benzimidazole derivatives of formula (I), their stereoisomers and/or salts are new. [Image] X and M : nitrogen or CH; R1 and R11 : hydrogen, fluoro, chloro, bromo, iodo, 1-4C alkyl, cyano, trifluoromethyl, OR5, NR5R6, COR5 or S(O) xR5; x : 0-2; R5 and R6 : hydrogen or 1-4C alkyl; R2 : 3-hydroxypyrro-2,4-dione, imidazole, imidazol(id)ine, indazole, isothiazole, isothiazolidine, isoxazole, 2-isoxazolidine, isoxazolone, (thio)morpholine, oxazole, 1,3,4-oxadiazole, oxadiazolidinedione, oxadiazolone, 1,2,3,5-oxathiadiazole-2-oxide, 5-oxo-4,5-dihydro[1,3,4]oxadiazole, 5-oxo-1,2,4-thiadiazole, piperazine, pyrazine, pyrazole, pyrazoline, pyrazolidine, pyridazine, pyrimidine, tetrazole, thiadiazole, thiazole, triazole or triazolone (all optionally substituted by 1-3 of COR5, 1-4C alkyl, OR5, NR5R6, halo or keto), COR5, COOR5, or CONR7R8; R7 and R8 : hydrogen or 1-4C (hydroxy)alkyl or alkoxy; R3 : hydrogen or 1-4C alkyl; R4 : pyrrole, furan, thiophene, imidazole, pyrazole, oxazole, isoxazole, (iso)thiazole, tetrazole, 1,2,3,5-oxathiadiazole-2-oxide, triazolone, oxadiazolone, isoxazolone, oxadiazolidinedione, triazole, 3-hydroxypyrro-2,4-dione, 5-oxo-1,2,4-thiadiazole, pyridine, pyrazine, pyrimidine, (iso)indole, indazole, phthalazine, (iso)quinoline, quinoxaline, quinazoline, cinnoline, beta -carboline, all optionally benzo-fused or as cyclopenta- or cyclohexa-derivatives, or phenyl, 1- or 2-naphthyl, 2-, 3- or 4-biphenylyl, anthryl or fluorenyl, all optionally substituted by 1-3 1-5C alkyl or alkoxy, halo, nitro, amino, trifluoromethyl, hydroxy, 1-4C hydroxyalkyl, (m)ethylenedioxy, formyl, acetyl, cyano, carboxy, aminocarbonyl or 1-4C alkoxycarbonyl. An independent claim is also included for a method for preparing (I). ACTIVITY : Antiarthritic; Antirheumatic; Osteopathic; Antidiabetic; Antiinflammatory; Immunomodulator; Neuroprotective; Antiarteriosclerotic; Vasotropic; Antiulcer; Nootropic; Cytostatic; Cardiant; Antigout; Immunosuppressive; Antibacterial; Virucide; Hepatotropic; Anti-HIV; Protozoacide; Fungicide; Antiasthmatic; Antipsoriatic. MECHANISM OF ACTION : Inhibition of IkappaB kinase. 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Substituted indole and benzimidazole derivatives (I), their stereoisomers and/or salts are new. Substituted indole and benzimidazole derivatives of formula (I), their stereoisomers and/or salts are new. [Image] X and M : nitrogen or CH; R1 and R11 : hydrogen, fluoro, chloro, bromo, iodo, 1-4C alkyl, cyano, trifluoromethyl, OR5, NR5R6, COR5 or S(O) xR5; x : 0-2; R5 and R6 : hydrogen or 1-4C alkyl; R2 : 3-hydroxypyrro-2,4-dione, imidazole, imidazol(id)ine, indazole, isothiazole, isothiazolidine, isoxazole, 2-isoxazolidine, isoxazolone, (thio)morpholine, oxazole, 1,3,4-oxadiazole, oxadiazolidinedione, oxadiazolone, 1,2,3,5-oxathiadiazole-2-oxide, 5-oxo-4,5-dihydro[1,3,4]oxadiazole, 5-oxo-1,2,4-thiadiazole, piperazine, pyrazine, pyrazole, pyrazoline, pyrazolidine, pyridazine, pyrimidine, tetrazole, thiadiazole, thiazole, triazole or triazolone (all optionally substituted by 1-3 of COR5, 1-4C alkyl, OR5, NR5R6, halo or keto), COR5, COOR5, or CONR7R8; R7 and R8 : hydrogen or 1-4C (hydroxy)alkyl or alkoxy; R3 : hydrogen or 1-4C alkyl; R4 : pyrrole, furan, thiophene, imidazole, pyrazole, oxazole, isoxazole, (iso)thiazole, tetrazole, 1,2,3,5-oxathiadiazole-2-oxide, triazolone, oxadiazolone, isoxazolone, oxadiazolidinedione, triazole, 3-hydroxypyrro-2,4-dione, 5-oxo-1,2,4-thiadiazole, pyridine, pyrazine, pyrimidine, (iso)indole, indazole, phthalazine, (iso)quinoline, quinoxaline, quinazoline, cinnoline, beta -carboline, all optionally benzo-fused or as cyclopenta- or cyclohexa-derivatives, or phenyl, 1- or 2-naphthyl, 2-, 3- or 4-biphenylyl, anthryl or fluorenyl, all optionally substituted by 1-3 1-5C alkyl or alkoxy, halo, nitro, amino, trifluoromethyl, hydroxy, 1-4C hydroxyalkyl, (m)ethylenedioxy, formyl, acetyl, cyano, carboxy, aminocarbonyl or 1-4C alkoxycarbonyl. An independent claim is also included for a method for preparing (I). ACTIVITY : Antiarthritic; Antirheumatic; Osteopathic; Antidiabetic; Antiinflammatory; Immunomodulator; Neuroprotective; Antiarteriosclerotic; Vasotropic; Antiulcer; Nootropic; Cytostatic; Cardiant; Antigout; Immunosuppressive; Antibacterial; Virucide; Hepatotropic; Anti-HIV; Protozoacide; Fungicide; Antiasthmatic; Antipsoriatic. MECHANISM OF ACTION : Inhibition of IkappaB kinase. The compound 2-(2-methylaminopyrimidin-4-yl)-1H-indol-5-carboxylic acid [(S)-2-diphenylamino-1-(5-oxo-4,5-dihydro[1,3,4]oxadiazol-2-yl)ethyl]amide (Ia) has IC50 against IkappaB 0.050 mu M.</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>2011</creationdate><recordtype>patent</recordtype><sourceid>EVB</sourceid><recordid>eNrjZHD09HPx93FV8A9ScHL1i_L09XRxjAIJuLgGeYY5hniGuQYruAFlff1dQn2AfD93Bc_sxIKCRCcFb08_x2BXHgbWtMSc4lReKM3NIOfmGuLsoZtakB-fWlyQmJyal1oS7-saYGZgZmDhaExQAQAtWyqp</recordid><startdate>20110510</startdate><enddate>20110510</enddate><creator>RITZELER, OLAF</creator><creator>JAEHNE, GERHARD</creator><scope>EVB</scope></search><sort><creationdate>20110510</creationdate><title>INDOLE OR BENZIMIDAZOLE DERIVATIVES FOR MODULATING IkappaB KINASE</title><author>RITZELER, OLAF ; JAEHNE, GERHARD</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-epo_espacenet_MEP60608A3</frbrgroupid><rsrctype>patents</rsrctype><prefilter>patents</prefilter><language>hrv ; eng</language><creationdate>2011</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>RITZELER, OLAF</creatorcontrib><creatorcontrib>JAEHNE, GERHARD</creatorcontrib><collection>esp@cenet</collection></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext_linktorsrc</fulltext></delivery><addata><au>RITZELER, OLAF</au><au>JAEHNE, GERHARD</au><format>patent</format><genre>patent</genre><ristype>GEN</ristype><title>INDOLE OR BENZIMIDAZOLE DERIVATIVES FOR MODULATING IkappaB KINASE</title><date>2011-05-10</date><risdate>2011</risdate><abstract>Pronalazak se odnosi na sjedinjenja formule I. http://www.wipo.int/patentscope/search/en/docservice_fpimage/WOEP2003008629 false Jedinjenja formule I su pogodna za proizvodnju ljekova za profilaksu i liječenje oboljenja na čiji tok utiče povećana aktivnost IκB-kinaze. Substituted indole and benzimidazole derivatives (I), their stereoisomers and/or salts are new. Substituted indole and benzimidazole derivatives of formula (I), their stereoisomers and/or salts are new. [Image] X and M : nitrogen or CH; R1 and R11 : hydrogen, fluoro, chloro, bromo, iodo, 1-4C alkyl, cyano, trifluoromethyl, OR5, NR5R6, COR5 or S(O) xR5; x : 0-2; R5 and R6 : hydrogen or 1-4C alkyl; R2 : 3-hydroxypyrro-2,4-dione, imidazole, imidazol(id)ine, indazole, isothiazole, isothiazolidine, isoxazole, 2-isoxazolidine, isoxazolone, (thio)morpholine, oxazole, 1,3,4-oxadiazole, oxadiazolidinedione, oxadiazolone, 1,2,3,5-oxathiadiazole-2-oxide, 5-oxo-4,5-dihydro[1,3,4]oxadiazole, 5-oxo-1,2,4-thiadiazole, piperazine, pyrazine, pyrazole, pyrazoline, pyrazolidine, pyridazine, pyrimidine, tetrazole, thiadiazole, thiazole, triazole or triazolone (all optionally substituted by 1-3 of COR5, 1-4C alkyl, OR5, NR5R6, halo or keto), COR5, COOR5, or CONR7R8; R7 and R8 : hydrogen or 1-4C (hydroxy)alkyl or alkoxy; R3 : hydrogen or 1-4C alkyl; R4 : pyrrole, furan, thiophene, imidazole, pyrazole, oxazole, isoxazole, (iso)thiazole, tetrazole, 1,2,3,5-oxathiadiazole-2-oxide, triazolone, oxadiazolone, isoxazolone, oxadiazolidinedione, triazole, 3-hydroxypyrro-2,4-dione, 5-oxo-1,2,4-thiadiazole, pyridine, pyrazine, pyrimidine, (iso)indole, indazole, phthalazine, (iso)quinoline, quinoxaline, quinazoline, cinnoline, beta -carboline, all optionally benzo-fused or as cyclopenta- or cyclohexa-derivatives, or phenyl, 1- or 2-naphthyl, 2-, 3- or 4-biphenylyl, anthryl or fluorenyl, all optionally substituted by 1-3 1-5C alkyl or alkoxy, halo, nitro, amino, trifluoromethyl, hydroxy, 1-4C hydroxyalkyl, (m)ethylenedioxy, formyl, acetyl, cyano, carboxy, aminocarbonyl or 1-4C alkoxycarbonyl. An independent claim is also included for a method for preparing (I). ACTIVITY : Antiarthritic; Antirheumatic; Osteopathic; Antidiabetic; Antiinflammatory; Immunomodulator; Neuroprotective; Antiarteriosclerotic; Vasotropic; Antiulcer; Nootropic; Cytostatic; Cardiant; Antigout; Immunosuppressive; Antibacterial; Virucide; Hepatotropic; Anti-HIV; Protozoacide; Fungicide; Antiasthmatic; Antipsoriatic. MECHANISM OF ACTION : Inhibition of IkappaB kinase. The compound 2-(2-methylaminopyrimidin-4-yl)-1H-indol-5-carboxylic acid [(S)-2-diphenylamino-1-(5-oxo-4,5-dihydro[1,3,4]oxadiazol-2-yl)ethyl]amide (Ia) has IC50 against IkappaB 0.050 mu M.</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 INDOLE OR BENZIMIDAZOLE DERIVATIVES FOR MODULATING IkappaB KINASE
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