PYRAZOLO 3,4-B PYRIDINVERBINDUNGEN UND IHRE VERWENDUNG ALS PHOSPHODIESTERASE INHIBITOREN
The invention relates to a compound of formula (I) or a salt thereof: wherein: R1 is C1-4alkyl, C1-3fluoroalkyl or -(CH2)2OH; R2 is a hydrogen atom (H), methyl or C1fluoroalkyl; R3a is a hydrogen atom (H) or C1-3alkyl; R3 is optionally substituted branched C3-6alkyl, optionally substituted C3-8cyclo...
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creator | COOK, CAROLINE MARY EDLIN, CHRISTOPHER ALLEN, DAVID GEORGE COOPER, ANTHONY WILLIAM JAMES HAMBLIN, JULIE NICOLE JOHNSON ,MARTIN, REDPATH COE, DIANE MARY REDGRAVE, ALISON DOWLE, MICHAEL DENNIS MITCHELL, CHARLOTTE JONES, PAUL SPENCER LINDVALL, MIKA |
description | The invention relates to a compound of formula (I) or a salt thereof: wherein: R1 is C1-4alkyl, C1-3fluoroalkyl or -(CH2)2OH; R2 is a hydrogen atom (H), methyl or C1fluoroalkyl; R3a is a hydrogen atom (H) or C1-3alkyl; R3 is optionally substituted branched C3-6alkyl, optionally substituted C3-8cycloalkyl, optionally substituted mono-unsaturated-C5-7cycloalkenyl, optionally substituted phenyl, or an optionally substituted heterocyclic group of sub-formula (aa), (bb) or (cc): in which n1 and n2 independently are 1 or 2; and Y is O, S, SO2, or NR4; and wherein Het is of sub-formula (i), (ii), (iii), (iv) or (v): The compounds are phosphodiesterase (PDE) inhibitors, in particular PDE4 inhibitors. Also provided is the use of a compound of formula (I), or a pharmaceutically acceptable salt thereof, in the manufacture of a medicament for the treatment and/or prophylaxis of an inflammatory and/or allergic disease in a mammal such as a human, for example chronic obstructive pulmonary disease (COPD), asthma, or allergic rhinitis. |
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Also provided is the use of a compound of formula (I), or a pharmaceutically acceptable salt thereof, in the manufacture of a medicament for the treatment and/or prophylaxis of an inflammatory and/or allergic disease in a mammal such as a human, for example chronic obstructive pulmonary disease (COPD), asthma, or allergic rhinitis.</description><language>ger</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>2010</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=20100515&DB=EPODOC&CC=AT&NR=E466012T1$$EHTML$$P50$$Gepo$$Hfree_for_read</linktohtml><link.rule.ids>230,308,780,885,25563,76418</link.rule.ids><linktorsrc>$$Uhttps://worldwide.espacenet.com/publicationDetails/biblio?FT=D&date=20100515&DB=EPODOC&CC=AT&NR=E466012T1$$EView_record_in_European_Patent_Office$$FView_record_in_$$GEuropean_Patent_Office$$Hfree_for_read</linktorsrc></links><search><creatorcontrib>COOK, CAROLINE MARY</creatorcontrib><creatorcontrib>EDLIN, CHRISTOPHER</creatorcontrib><creatorcontrib>ALLEN, DAVID GEORGE</creatorcontrib><creatorcontrib>COOPER, ANTHONY WILLIAM JAMES</creatorcontrib><creatorcontrib>HAMBLIN, JULIE NICOLE</creatorcontrib><creatorcontrib>JOHNSON ,MARTIN, REDPATH</creatorcontrib><creatorcontrib>COE, DIANE MARY</creatorcontrib><creatorcontrib>REDGRAVE, ALISON</creatorcontrib><creatorcontrib>DOWLE, MICHAEL DENNIS</creatorcontrib><creatorcontrib>MITCHELL, CHARLOTTE</creatorcontrib><creatorcontrib>JONES, PAUL SPENCER</creatorcontrib><creatorcontrib>LINDVALL, MIKA</creatorcontrib><title>PYRAZOLO 3,4-B PYRIDINVERBINDUNGEN UND IHRE VERWENDUNG ALS PHOSPHODIESTERASE INHIBITOREN</title><description>The invention relates to a compound of formula (I) or a salt thereof: wherein: R1 is C1-4alkyl, C1-3fluoroalkyl or -(CH2)2OH; R2 is a hydrogen atom (H), methyl or C1fluoroalkyl; R3a is a hydrogen atom (H) or C1-3alkyl; R3 is optionally substituted branched C3-6alkyl, optionally substituted C3-8cycloalkyl, optionally substituted mono-unsaturated-C5-7cycloalkenyl, optionally substituted phenyl, or an optionally substituted heterocyclic group of sub-formula (aa), (bb) or (cc): in which n1 and n2 independently are 1 or 2; and Y is O, S, SO2, or NR4; and wherein Het is of sub-formula (i), (ii), (iii), (iv) or (v): The compounds are phosphodiesterase (PDE) inhibitors, in particular PDE4 inhibitors. Also provided is the use of a compound of formula (I), or a pharmaceutically acceptable salt thereof, in the manufacture of a medicament for the treatment and/or prophylaxis of an inflammatory and/or allergic disease in a mammal such as a human, for example chronic obstructive pulmonary disease (COPD), asthma, or allergic rhinitis.</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>2010</creationdate><recordtype>patent</recordtype><sourceid>EVB</sourceid><recordid>eNrjZIgIiAxyjPL38Vcw1jHRdVIAcj1dPP3CXIOcPP1cQv3cXf0UQv1cFDw9glwVgKLhrmBRBUefYIUAD_9gIHbxdA0OcQ1yDHZV8PTz8HTyDPEPcvXjYWBNS8wpTuWF0twMim6uIc4euqkF-fGpxQWJyal5qSXxjiGuJmZmBoZGISGGxsSoAQAnPTIo</recordid><startdate>20100515</startdate><enddate>20100515</enddate><creator>COOK, CAROLINE MARY</creator><creator>EDLIN, CHRISTOPHER</creator><creator>ALLEN, DAVID GEORGE</creator><creator>COOPER, ANTHONY WILLIAM JAMES</creator><creator>HAMBLIN, JULIE NICOLE</creator><creator>JOHNSON ,MARTIN, REDPATH</creator><creator>COE, DIANE MARY</creator><creator>REDGRAVE, ALISON</creator><creator>DOWLE, MICHAEL DENNIS</creator><creator>MITCHELL, CHARLOTTE</creator><creator>JONES, PAUL SPENCER</creator><creator>LINDVALL, MIKA</creator><scope>EVB</scope></search><sort><creationdate>20100515</creationdate><title>PYRAZOLO 3,4-B PYRIDINVERBINDUNGEN UND IHRE VERWENDUNG ALS PHOSPHODIESTERASE INHIBITOREN</title><author>COOK, CAROLINE MARY ; EDLIN, CHRISTOPHER ; ALLEN, DAVID GEORGE ; COOPER, ANTHONY WILLIAM JAMES ; HAMBLIN, JULIE NICOLE ; JOHNSON ,MARTIN, REDPATH ; COE, DIANE MARY ; REDGRAVE, ALISON ; DOWLE, MICHAEL DENNIS ; MITCHELL, CHARLOTTE ; JONES, PAUL SPENCER ; LINDVALL, MIKA</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-epo_espacenet_ATE466012TT13</frbrgroupid><rsrctype>patents</rsrctype><prefilter>patents</prefilter><language>ger</language><creationdate>2010</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>COOK, CAROLINE MARY</creatorcontrib><creatorcontrib>EDLIN, CHRISTOPHER</creatorcontrib><creatorcontrib>ALLEN, DAVID GEORGE</creatorcontrib><creatorcontrib>COOPER, ANTHONY WILLIAM JAMES</creatorcontrib><creatorcontrib>HAMBLIN, JULIE NICOLE</creatorcontrib><creatorcontrib>JOHNSON ,MARTIN, REDPATH</creatorcontrib><creatorcontrib>COE, DIANE MARY</creatorcontrib><creatorcontrib>REDGRAVE, ALISON</creatorcontrib><creatorcontrib>DOWLE, MICHAEL DENNIS</creatorcontrib><creatorcontrib>MITCHELL, CHARLOTTE</creatorcontrib><creatorcontrib>JONES, PAUL SPENCER</creatorcontrib><creatorcontrib>LINDVALL, MIKA</creatorcontrib><collection>esp@cenet</collection></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext_linktorsrc</fulltext></delivery><addata><au>COOK, CAROLINE MARY</au><au>EDLIN, CHRISTOPHER</au><au>ALLEN, DAVID GEORGE</au><au>COOPER, ANTHONY WILLIAM JAMES</au><au>HAMBLIN, JULIE NICOLE</au><au>JOHNSON ,MARTIN, REDPATH</au><au>COE, DIANE MARY</au><au>REDGRAVE, ALISON</au><au>DOWLE, MICHAEL DENNIS</au><au>MITCHELL, CHARLOTTE</au><au>JONES, PAUL SPENCER</au><au>LINDVALL, MIKA</au><format>patent</format><genre>patent</genre><ristype>GEN</ristype><title>PYRAZOLO 3,4-B PYRIDINVERBINDUNGEN UND IHRE VERWENDUNG ALS PHOSPHODIESTERASE INHIBITOREN</title><date>2010-05-15</date><risdate>2010</risdate><abstract>The invention relates to a compound of formula (I) or a salt thereof: wherein: R1 is C1-4alkyl, C1-3fluoroalkyl or -(CH2)2OH; R2 is a hydrogen atom (H), methyl or C1fluoroalkyl; R3a is a hydrogen atom (H) or C1-3alkyl; R3 is optionally substituted branched C3-6alkyl, optionally substituted C3-8cycloalkyl, optionally substituted mono-unsaturated-C5-7cycloalkenyl, optionally substituted phenyl, or an optionally substituted heterocyclic group of sub-formula (aa), (bb) or (cc): in which n1 and n2 independently are 1 or 2; and Y is O, S, SO2, or NR4; and wherein Het is of sub-formula (i), (ii), (iii), (iv) or (v): The compounds are phosphodiesterase (PDE) inhibitors, in particular PDE4 inhibitors. Also provided is the use of a compound of formula (I), or a pharmaceutically acceptable salt thereof, in the manufacture of a medicament for the treatment and/or prophylaxis of an inflammatory and/or allergic disease in a mammal such as a human, for example chronic obstructive pulmonary disease (COPD), asthma, or allergic rhinitis.</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 | PYRAZOLO 3,4-B PYRIDINVERBINDUNGEN UND IHRE VERWENDUNG ALS PHOSPHODIESTERASE INHIBITOREN |
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