SUBSTITUIERTE 4-HYDROXYPHENYLALKANSAURE-DERIVATE MIT AGONISTISCHER WIRKUNG AUF PPAR-GAMMA

A compound having formula (I), wherein A is selected from the group consisting of: (i) phenyl, wherein said phenyl is optionally substituted by one or more halogen atoms, C1-6alkyl, C1-3alkoxy, C1-3fluoroalkoxy, nitrile, or -NR7R8 where R7 and R8 are independently hydrogen or C1-3alkyl; (ii) a 5- or...

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Hauptverfasser: MOOK, ROBERT, ANTHONY, JR, DEATON, DAVID, NORMAN, DRIVE, COLLINS, JON, LOREN, HENKE, BRAD, RICHARD, WILLSON, TIMOTHY, MARK, COBB, JEFFREY, EDMOND, SHARP, MATTHEW, JUDE, KALDOR, ISTVAN, ERICKSON, GREG, ALAN, BOSWELL, GRADY, EVAN, BRACKEEN, MARCUS, O'CALLAGHAN, JOHN, MARK
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creator MOOK, ROBERT, ANTHONY, JR
DEATON, DAVID, NORMAN
DRIVE
COLLINS, JON, LOREN
HENKE, BRAD, RICHARD
WILLSON, TIMOTHY, MARK
COBB, JEFFREY, EDMOND
SHARP, MATTHEW, JUDE
KALDOR, ISTVAN
ERICKSON, GREG, ALAN
BOSWELL, GRADY, EVAN
BRACKEEN, MARCUS
O'CALLAGHAN, JOHN, MARK
description A compound having formula (I), wherein A is selected from the group consisting of: (i) phenyl, wherein said phenyl is optionally substituted by one or more halogen atoms, C1-6alkyl, C1-3alkoxy, C1-3fluoroalkoxy, nitrile, or -NR7R8 where R7 and R8 are independently hydrogen or C1-3alkyl; (ii) a 5- or 6-membered hetrocyclic group containing at least one heteroatom selected from oxygen, nitrogen and sulfur; and (iii) a fused bicyclic ring (a), wherein ring C represents a heterocyclic group as defined in point (ii) above, which bicyclic ring is attached to group B via a ring atom of ring C; B is selected from the group consisting of: (iv) C1-6alkylene; (v) -MC1-6alkylene or C1-6alkyleneMC1-6alkylene, wherein M is O, S, or -NR2 wherein R2 represents hydrogen or C1-3alkyl; (vi) a 5- or 6-membered heterocyclic group containing at least one nitrogen heteroatom and optionally at least one further heteroatom selected from oxygen, nitrogen and sulfur and optionally substituted by C1-3alkyl; and (vii) Het-C1-6alkylene, wherein Het represents a heterocyclic group as defined in point (vi) above; Alk represents C1-3alkylene; R1 represents hydrogen or C1-3alkyl; Z is selected from the group consisting of: (viii) -(C1-3alkylene) phenyl, which phenyl is optionally substituted by one or more halogen atoms; and (ix) -NR3R4, wherein R3 represents hydrogen or C1-3alkyl, and R4 represents -Y-(C=O)-T-R5, or -Y-(CH(OH))-T-R5.
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BOSWELL, GRADY, EVAN ; BRACKEEN, MARCUS ; O'CALLAGHAN, JOHN, MARK</creator><creatorcontrib>MOOK, ROBERT, ANTHONY, JR ; DEATON, DAVID, NORMAN ; DRIVE ; COLLINS, JON, LOREN ; HENKE, BRAD, RICHARD ; WILLSON, TIMOTHY, MARK ; COBB, JEFFREY, EDMOND ; SHARP, MATTHEW, JUDE ; KALDOR, ISTVAN ; ERICKSON, GREG, ALAN ; BOSWELL, GRADY, EVAN ; BRACKEEN, MARCUS ; O'CALLAGHAN, JOHN, MARK</creatorcontrib><description>A compound having formula (I), wherein A is selected from the group consisting of: (i) phenyl, wherein said phenyl is optionally substituted by one or more halogen atoms, C1-6alkyl, C1-3alkoxy, C1-3fluoroalkoxy, nitrile, or -NR7R8 where R7 and R8 are independently hydrogen or C1-3alkyl; (ii) a 5- or 6-membered hetrocyclic group containing at least one heteroatom selected from oxygen, nitrogen and sulfur; and (iii) a fused bicyclic ring (a), wherein ring C represents a heterocyclic group as defined in point (ii) above, which bicyclic ring is attached to group B via a ring atom of ring C; B is selected from the group consisting of: (iv) C1-6alkylene; (v) -MC1-6alkylene or C1-6alkyleneMC1-6alkylene, wherein M is O, S, or -NR2 wherein R2 represents hydrogen or C1-3alkyl; (vi) a 5- or 6-membered heterocyclic group containing at least one nitrogen heteroatom and optionally at least one further heteroatom selected from oxygen, nitrogen and sulfur and optionally substituted by C1-3alkyl; and (vii) Het-C1-6alkylene, wherein Het represents a heterocyclic group as defined in point (vi) above; Alk represents C1-3alkylene; R1 represents hydrogen or C1-3alkyl; Z is selected from the group consisting of: (viii) -(C1-3alkylene) phenyl, which phenyl is optionally substituted by one or more halogen atoms; and (ix) -NR3R4, wherein R3 represents hydrogen or C1-3alkyl, and R4 represents -Y-(C=O)-T-R5, or -Y-(CH(OH))-T-R5.</description><edition>7</edition><language>ger</language><subject>ACYCLIC OR CARBOCYCLIC COMPOUNDS ; 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&amp;date=20010915&amp;DB=EPODOC&amp;CC=AT&amp;NR=E205485T1$$EHTML$$P50$$Gepo$$Hfree_for_read</linktohtml><link.rule.ids>230,308,778,883,25547,76298</link.rule.ids><linktorsrc>$$Uhttps://worldwide.espacenet.com/publicationDetails/biblio?FT=D&amp;date=20010915&amp;DB=EPODOC&amp;CC=AT&amp;NR=E205485T1$$EView_record_in_European_Patent_Office$$FView_record_in_$$GEuropean_Patent_Office$$Hfree_for_read</linktorsrc></links><search><creatorcontrib>MOOK, ROBERT, ANTHONY, JR</creatorcontrib><creatorcontrib>DEATON, DAVID, NORMAN</creatorcontrib><creatorcontrib>DRIVE</creatorcontrib><creatorcontrib>COLLINS, JON, LOREN</creatorcontrib><creatorcontrib>HENKE, BRAD, RICHARD</creatorcontrib><creatorcontrib>WILLSON, TIMOTHY, MARK</creatorcontrib><creatorcontrib>COBB, JEFFREY, EDMOND</creatorcontrib><creatorcontrib>SHARP, MATTHEW, JUDE</creatorcontrib><creatorcontrib>KALDOR, ISTVAN</creatorcontrib><creatorcontrib>ERICKSON, GREG, ALAN</creatorcontrib><creatorcontrib>BOSWELL, GRADY, EVAN</creatorcontrib><creatorcontrib>BRACKEEN, MARCUS</creatorcontrib><creatorcontrib>O'CALLAGHAN, JOHN, MARK</creatorcontrib><title>SUBSTITUIERTE 4-HYDROXYPHENYLALKANSAURE-DERIVATE MIT AGONISTISCHER WIRKUNG AUF PPAR-GAMMA</title><description>A compound having formula (I), wherein A is selected from the group consisting of: (i) phenyl, wherein said phenyl is optionally substituted by one or more halogen atoms, C1-6alkyl, C1-3alkoxy, C1-3fluoroalkoxy, nitrile, or -NR7R8 where R7 and R8 are independently hydrogen or C1-3alkyl; (ii) a 5- or 6-membered hetrocyclic group containing at least one heteroatom selected from oxygen, nitrogen and sulfur; and (iii) a fused bicyclic ring (a), wherein ring C represents a heterocyclic group as defined in point (ii) above, which bicyclic ring is attached to group B via a ring atom of ring C; B is selected from the group consisting of: (iv) C1-6alkylene; (v) -MC1-6alkylene or C1-6alkyleneMC1-6alkylene, wherein M is O, S, or -NR2 wherein R2 represents hydrogen or C1-3alkyl; (vi) a 5- or 6-membered heterocyclic group containing at least one nitrogen heteroatom and optionally at least one further heteroatom selected from oxygen, nitrogen and sulfur and optionally substituted by C1-3alkyl; and (vii) Het-C1-6alkylene, wherein Het represents a heterocyclic group as defined in point (vi) above; Alk represents C1-3alkylene; R1 represents hydrogen or C1-3alkyl; Z is selected from the group consisting of: (viii) -(C1-3alkylene) phenyl, which phenyl is optionally substituted by one or more halogen atoms; 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DEATON, DAVID, NORMAN ; DRIVE ; COLLINS, JON, LOREN ; HENKE, BRAD, RICHARD ; WILLSON, TIMOTHY, MARK ; COBB, JEFFREY, EDMOND ; SHARP, MATTHEW, JUDE ; KALDOR, ISTVAN ; ERICKSON, GREG, ALAN ; BOSWELL, GRADY, EVAN ; BRACKEEN, MARCUS ; O'CALLAGHAN, JOHN, MARK</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-epo_espacenet_ATE205485TT13</frbrgroupid><rsrctype>patents</rsrctype><prefilter>patents</prefilter><language>ger</language><creationdate>2001</creationdate><topic>ACYCLIC OR CARBOCYCLIC COMPOUNDS</topic><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>MOOK, ROBERT, ANTHONY, JR</creatorcontrib><creatorcontrib>DEATON, DAVID, NORMAN</creatorcontrib><creatorcontrib>DRIVE</creatorcontrib><creatorcontrib>COLLINS, JON, LOREN</creatorcontrib><creatorcontrib>HENKE, BRAD, RICHARD</creatorcontrib><creatorcontrib>WILLSON, TIMOTHY, MARK</creatorcontrib><creatorcontrib>COBB, JEFFREY, EDMOND</creatorcontrib><creatorcontrib>SHARP, MATTHEW, JUDE</creatorcontrib><creatorcontrib>KALDOR, ISTVAN</creatorcontrib><creatorcontrib>ERICKSON, GREG, ALAN</creatorcontrib><creatorcontrib>BOSWELL, GRADY, EVAN</creatorcontrib><creatorcontrib>BRACKEEN, MARCUS</creatorcontrib><creatorcontrib>O'CALLAGHAN, JOHN, MARK</creatorcontrib><collection>esp@cenet</collection></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext_linktorsrc</fulltext></delivery><addata><au>MOOK, ROBERT, ANTHONY, JR</au><au>DEATON, DAVID, NORMAN</au><au>DRIVE</au><au>COLLINS, JON, LOREN</au><au>HENKE, BRAD, RICHARD</au><au>WILLSON, TIMOTHY, MARK</au><au>COBB, JEFFREY, EDMOND</au><au>SHARP, MATTHEW, JUDE</au><au>KALDOR, ISTVAN</au><au>ERICKSON, GREG, ALAN</au><au>BOSWELL, GRADY, EVAN</au><au>BRACKEEN, MARCUS</au><au>O'CALLAGHAN, JOHN, MARK</au><format>patent</format><genre>patent</genre><ristype>GEN</ristype><title>SUBSTITUIERTE 4-HYDROXYPHENYLALKANSAURE-DERIVATE MIT AGONISTISCHER WIRKUNG AUF PPAR-GAMMA</title><date>2001-09-15</date><risdate>2001</risdate><abstract>A compound having formula (I), wherein A is selected from the group consisting of: (i) phenyl, wherein said phenyl is optionally substituted by one or more halogen atoms, C1-6alkyl, C1-3alkoxy, C1-3fluoroalkoxy, nitrile, or -NR7R8 where R7 and R8 are independently hydrogen or C1-3alkyl; (ii) a 5- or 6-membered hetrocyclic group containing at least one heteroatom selected from oxygen, nitrogen and sulfur; and (iii) a fused bicyclic ring (a), wherein ring C represents a heterocyclic group as defined in point (ii) above, which bicyclic ring is attached to group B via a ring atom of ring C; B is selected from the group consisting of: (iv) C1-6alkylene; (v) -MC1-6alkylene or C1-6alkyleneMC1-6alkylene, wherein M is O, S, or -NR2 wherein R2 represents hydrogen or C1-3alkyl; (vi) a 5- or 6-membered heterocyclic group containing at least one nitrogen heteroatom and optionally at least one further heteroatom selected from oxygen, nitrogen and sulfur and optionally substituted by C1-3alkyl; and (vii) Het-C1-6alkylene, wherein Het represents a heterocyclic group as defined in point (vi) above; Alk represents C1-3alkylene; R1 represents hydrogen or C1-3alkyl; Z is selected from the group consisting of: (viii) -(C1-3alkylene) phenyl, which phenyl is optionally substituted by one or more halogen atoms; and (ix) -NR3R4, wherein R3 represents hydrogen or C1-3alkyl, and R4 represents -Y-(C=O)-T-R5, or -Y-(CH(OH))-T-R5.</abstract><edition>7</edition><oa>free_for_read</oa></addata></record>
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subjects ACYCLIC OR CARBOCYCLIC COMPOUNDS
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 SUBSTITUIERTE 4-HYDROXYPHENYLALKANSAURE-DERIVATE MIT AGONISTISCHER WIRKUNG AUF PPAR-GAMMA
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