PE20060657A1 - Derivados de pirimidina como moduladores de ppar-alfa - Google Patents

Derivados de pirimidina como moduladores de ppar-alfa

Info

Publication number
PE20060657A1
PE20060657A1 PE2005001101A PE2005001101A PE20060657A1 PE 20060657 A1 PE20060657 A1 PE 20060657A1 PE 2005001101 A PE2005001101 A PE 2005001101A PE 2005001101 A PE2005001101 A PE 2005001101A PE 20060657 A1 PE20060657 A1 PE 20060657A1
Authority
PE
Peru
Prior art keywords
alkyl
methyl
phenyl
ppar
acid
Prior art date
Application number
PE2005001101A
Other languages
English (en)
Inventor
Elke Dittrich-Wengenroth
Lars Barfacker
Claudia Hirth-Dietrich
Martin Raabe
Christian Pilger
Stephan Bartel
Armin Kern
Marcus Bauser
Dieter Lang
Klemens Lustig
Ulrich Rosentreter
Hilmar Bischoff
Peter Ellinghaus
Axel Kretschmer
Original Assignee
Bayer Healthcare Ag
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Bayer Healthcare Ag filed Critical Bayer Healthcare Ag
Publication of PE20060657A1 publication Critical patent/PE20060657A1/es

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D239/00Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
    • C07D239/02Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
    • C07D239/24Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
    • C07D239/28Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to ring carbon atoms
    • C07D239/32One oxygen, sulfur or nitrogen atom
    • C07D239/42One nitrogen atom
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/495Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
    • A61K31/505Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P3/00Drugs for disorders of the metabolism
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P3/00Drugs for disorders of the metabolism
    • A61P3/06Antihyperlipidemics
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P7/00Drugs for disorders of the blood or the extracellular fluid
    • A61P7/02Antithrombotic agents; Anticoagulants; Platelet aggregation inhibitors
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00Drugs for disorders of the cardiovascular system
    • A61P9/04Inotropic agents, i.e. stimulants of cardiac contraction; Drugs for heart failure
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00Drugs for disorders of the cardiovascular system
    • A61P9/10Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D239/00Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
    • C07D239/02Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
    • C07D239/24Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
    • C07D239/28Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to ring carbon atoms
    • C07D239/46Two or more oxygen, sulphur or nitrogen atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D403/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
    • C07D403/02Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
    • C07D403/12Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D405/00Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
    • C07D405/02Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
    • C07D405/12Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a chain containing hetero atoms as chain links

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Pharmacology & Pharmacy (AREA)
  • General Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • Medicinal Chemistry (AREA)
  • Animal Behavior & Ethology (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Cardiology (AREA)
  • Diabetes (AREA)
  • Hematology (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Obesity (AREA)
  • Hospice & Palliative Care (AREA)
  • Urology & Nephrology (AREA)
  • Vascular Medicine (AREA)
  • Epidemiology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)

Abstract

REFERIDA A UN COMPUESTO DERIVADO DE PIRIMIDINA DE FORMULA I, DONDE A ES O O S; UNO DE LOS MIEMBROS DE ANILLO D Y E REPRESENTA N Y EL OTRO CH; Z ES (CH2)m, O O N-R9; m ES 0, 1 O 2; R9 ES H O ALQUILO C1-C6; n ES 0, 1 O 2; R1 ES ARILO C6-C10 O HETEROARILO DE 5 A 10 MIEMBROS QUE PUEDE ESTAR SUSTITUIDO POR HALOGENO, CIANO, ALQUILO C1-C6, ENTRE OTROS; R10 ES H, ALQUILO C1-C6, FENILO, ENTRE OTROS; R11 ES H, ALQUILO C1-C6, FENILO, ENTRE OTROS; R2 ES H, ARILO C6-C10, ALQUENILO C2-C6, ENTRE OTROS; R3 Y R4 SON H, ALQUILO C1-C6, ALQUENILO C2-C6, ENTRE OTROS; R5 Y R6 SON H, ALQUILO C1-C6, FENOXI, ENTRE OTROS; R7 ES -NHR16 U -OR17; R16 ES H O ALQUILO C1-C4; R17 ES H O UN GRUPO HIDROLIZABLE, QUE PUEDE SER TRANSFORMADO EN EL ACIDO CARBOXILICO CORRESPONDIENTE; R8 ES H O METILO. SON COMPUESTOS PREFERIDOS: ACIDO 2-({4-[((2-FURILMETIL){[6-(4-METILFENIL)-PIRIMIDIN-4-IL]-METIL}-AMINO)METIL]-FENIL}-TIO)-2-METILPROPANOICO, CLORHIDRATO DE ACIDO 2-({4-[((2-FURILMETIL){[6-(3-TRIFLUOROMETILFENIL)PIRIMIDIN-4-IL]METIL}AMINO)METIL]FENIL}TIO)-2-METILPROPANOICO, ENTRE OTROS. TAMBIEN ESTA REFERIDA A UN PROCEDIMIENTO DE PREPARACION . DICHOS COMPUESTOS SON MODULADORES DEL RECEPTOR ALFA ACTIVADO POR INDUCTORES DE LA PRODUCCION DE PEROXISOMAS (PPAR-ALFA) Y SON UTILES PARA EL TRATAMIENTO Y/O PREVENCION DE ENFERMEDADES CARDIOVASCULARES, PARTICULARMENTE DISLIPIDEMIAS, ARTERIOSCLEROSIS, INSUFICIENCIA CARDIACA, TROMBOSIS Y TRASTORNOS METABOLICOS
PE2005001101A 2004-09-25 2005-09-23 Derivados de pirimidina como moduladores de ppar-alfa PE20060657A1 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DE102004046623A DE102004046623A1 (de) 2004-09-25 2004-09-25 Neue Pyrimidin-Derivate und ihre Verwendung

Publications (1)

Publication Number Publication Date
PE20060657A1 true PE20060657A1 (es) 2006-08-12

Family

ID=35063041

Family Applications (1)

Application Number Title Priority Date Filing Date
PE2005001101A PE20060657A1 (es) 2004-09-25 2005-09-23 Derivados de pirimidina como moduladores de ppar-alfa

Country Status (22)

Country Link
US (1) US20080261990A1 (es)
EP (1) EP1797045A1 (es)
JP (1) JP2008514559A (es)
KR (1) KR20070055621A (es)
CN (1) CN101065364A (es)
AR (1) AR051295A1 (es)
AU (1) AU2005287589A1 (es)
BR (1) BRPI0517327A (es)
CA (1) CA2582492A1 (es)
DE (1) DE102004046623A1 (es)
EC (1) ECSP077340A (es)
GT (1) GT200500266A (es)
IL (1) IL182136A0 (es)
MA (1) MA28882B1 (es)
MX (1) MX2007003428A (es)
NO (1) NO20072051L (es)
PE (1) PE20060657A1 (es)
RU (1) RU2007115215A (es)
SV (1) SV2007002235A (es)
TW (1) TW200628451A (es)
UY (1) UY29127A1 (es)
WO (1) WO2006032384A1 (es)

Families Citing this family (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
MX2009010953A (es) * 2007-04-13 2009-10-29 Millenium Pharmaceuticals Inc Terapia anticoagulante en combinacion, con un compuesto que actua como un inhibidor del factor xa.
KR100813387B1 (ko) * 2007-06-26 2008-03-12 신명곤 부형제 첨가없이 인삼농축액으로 유동성 및 저장성이우수한 인삼농축액환 제조 방법
EP3593802A3 (en) 2010-05-26 2020-03-25 Satiogen Pharmaceuticals, Inc. Bile acid recycling inhibitors and satiogens for treatment of diabetes, obesity, and inflammatory gastrointestinal conditions
US20130197043A1 (en) 2010-08-31 2013-08-01 Snu R&Db Foundation Use of the fetal reprogramming of a ppar agonist
SG10201406155QA (en) 2011-10-28 2014-11-27 Lumena Pharmaceuticals Inc Bile Acid Recycling Inhibitors For Treatment Of Pediatric Cholestatic Liver Diseases
MX369466B (es) 2011-10-28 2019-11-08 Lumena Pharmaceuticals Inc Inhibidores de la recirculación de ácidos biliares para el tratamiento de enfermedades hepáticas colestásicas pediátricas.
CN103130732A (zh) * 2011-11-22 2013-06-05 上海博康精细化工有限公司 3,5-二甲基-4-氯甲基异噁唑的制备方法
MX2015013193A (es) 2013-03-15 2016-04-15 Lumena Pharmaceuticals Inc Inhibidores del reciclaje de acidos biliares para el tratamiento de colangitis esclerosante primaria y enfermedad inflamatoria intestinal.
WO2014144485A1 (en) 2013-03-15 2014-09-18 Lumena Pharmaceuticals, Inc. Bile acid recycling inhibitors for treatment of barrett's esophagus and gastroesophageal reflux disease
WO2017190050A1 (en) * 2016-04-28 2017-11-02 Cornell University Inhibitors of soluble adenylyl cyclase
US20220152022A1 (en) 2019-02-12 2022-05-19 Mirum Pharmaceuticals, Inc. Methods for increasing growth in pediatric subjects having cholestatic liver disease
CN115598267B (zh) * 2022-12-13 2023-05-09 山东省食品药品检验研究院 一种格列齐特中潜在遗传毒性杂质的分析方法

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
YU72201A (sh) * 1999-04-28 2005-07-19 Aventis Pharma Deutschland Gmbh. Derivati di-aril kiseline kao ppar receptorski ligandi
GB0214254D0 (en) * 2002-06-20 2002-07-31 Glaxo Group Ltd Chemical compounds

Also Published As

Publication number Publication date
BRPI0517327A (pt) 2008-10-07
NO20072051L (no) 2007-06-07
WO2006032384A1 (de) 2006-03-30
SV2007002235A (es) 2007-03-20
US20080261990A1 (en) 2008-10-23
AU2005287589A1 (en) 2006-03-30
MA28882B1 (fr) 2007-09-03
CN101065364A (zh) 2007-10-31
CA2582492A1 (en) 2006-03-30
IL182136A0 (en) 2007-07-24
UY29127A1 (es) 2006-04-28
DE102004046623A1 (de) 2006-03-30
KR20070055621A (ko) 2007-05-30
GT200500266A (es) 2006-05-11
ECSP077340A (es) 2007-04-26
RU2007115215A (ru) 2008-11-10
EP1797045A1 (de) 2007-06-20
MX2007003428A (es) 2008-03-13
JP2008514559A (ja) 2008-05-08
AR051295A1 (es) 2007-01-03
TW200628451A (en) 2006-08-16

Similar Documents

Publication Publication Date Title
PE20060657A1 (es) Derivados de pirimidina como moduladores de ppar-alfa
AR038419A1 (es) Derivados de piridina y quinolina
PE20061353A1 (es) Compuestos de sulfonamida-tiazolopiridina como activadores de glucocinasa
PE20120399A1 (es) Derivados del l-(piperidin-4-il)-pirazol como moduladores de gpr 119
PE20060336A1 (es) Compuestos derivados de 1-amino-ftalazina como moduladores de mch1
PE20091376A1 (es) Derivados de fenilamino como moduladores de beta-amiloide
PE20061490A1 (es) Derivados de ciclohexanosulfonilo como inhibidores del transportador de glicina glyt1
PE20021152A1 (es) Derivados de oxazol como agonistas de receptores activados por proliferacion de peroxisoma
AR061644A1 (es) Derivados de benzofurano
PE20081845A1 (es) Nuevos derivados de aminopirimidina como inhibidores de plk1
AR064459A1 (es) Derivados de sulfonamida
PE20050132A1 (es) Piperazinas heterociclicas sustituidas
PE20080772A1 (es) Nuevos derivados de bipiridina sustituidos y su uso
CO5690643A2 (es) Derivados de triaza-espiropiperidina para usarlos como inhibidores de glyt-1 en el tratamiento de desordenes neurologicos y neuropsiquiatricos
PE20060357A1 (es) Compuestos y composiciones como moduladores de receptor activado de proliferador de peroxisoma (ppar)
DE602006006850D1 (de) Als modulatoren von dopamin-d3-rezeptoren geeignete azabicyclo-(3,1,0)-hexan-derivate
PE20130155A1 (es) Derivados de ariletinilo
PE20061348A1 (es) DERIVADOS DEL ACIDO PIRMIDINCARBOXILICO COMO MODULADORES DE PPAR-alfa
PE20080843A1 (es) Inhibidores de renina y metodo para su utilizacion
NO20050429L (no) Substituert kinolin-CCR5-reseptorantagonister
PE20080091A1 (es) Derivados de cicloalquilamino como agentes moduladores de s1p
PE20110196A1 (es) 5-alquinil-pirimidinas
AR062409A1 (es) Compuesto y composicion farmaceutica, utiles como agentes terapeuticos en el tratamiento, prevencion o mejoramiento de enfermedad o trastorno caracterizado por depositos o niveles de b-amiloide elevados o para inhibir o elucidar la enzima b-secretasa, y proceso para la preparacion del compuesto
PE20070550A1 (es) Derivados de la 1-amino-ftalazina sustituida afines al receptor mch1 y su preparacion
PE20060881A1 (es) Sulfonamido-macrociclos y sus sales como inhibidores de tie2 y composiciones farmaceuticas que comprenden estos compuestos

Legal Events

Date Code Title Description
FC Refusal