PE20061348A1 - DERIVADOS DEL ACIDO PIRMIDINCARBOXILICO COMO MODULADORES DE PPAR-alfa - Google Patents

DERIVADOS DEL ACIDO PIRMIDINCARBOXILICO COMO MODULADORES DE PPAR-alfa

Info

Publication number
PE20061348A1
PE20061348A1 PE2006000274A PE2006000274A PE20061348A1 PE 20061348 A1 PE20061348 A1 PE 20061348A1 PE 2006000274 A PE2006000274 A PE 2006000274A PE 2006000274 A PE2006000274 A PE 2006000274A PE 20061348 A1 PE20061348 A1 PE 20061348A1
Authority
PE
Peru
Prior art keywords
acid
halogen
alkyl
phenylpyrimidin
ppar
Prior art date
Application number
PE2006000274A
Other languages
English (en)
Inventor
Elisabeth Woltering
Arounarith Tuch
Axel Kretschmer
Marcus Bauser
Klemens Lustig
Olaf Weber
Elisabeth Pook
Peter Ellinghaus
Lars Barfacker
Elke Dittrich-Wengeroth
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 PE20061348A1 publication Critical patent/PE20061348A1/es

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    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
    • C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
    • C07D239/24—Heterocyclic 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
    • C07D239/28—Heterocyclic 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
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/495—Heterocyclic 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
    • A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
    • A61P1/04—Drugs for disorders of the alimentary tract or the digestive system for ulcers, gastritis or reflux esophagitis, e.g. antacids, inhibitors of acid secretion, mucosal protectants
    • A—HUMAN NECESSITIES
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    • A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
    • A61P1/18—Drugs for disorders of the alimentary tract or the digestive system for pancreatic disorders, e.g. pancreatic enzymes
    • A—HUMAN NECESSITIES
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    • A61P11/06—Antiasthmatics
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    • A61P9/08—Vasodilators for multiple indications
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    • A61P9/12—Antihypertensives
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00—Drugs for disorders of the cardiovascular system
    • A61P9/14—Vasoprotectives; Antihaemorrhoidals; Drugs for varicose therapy; Capillary stabilisers
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
    • C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
    • C07D239/24—Heterocyclic 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
    • C07D239/28—Heterocyclic 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
    • C07D239/32—One oxygen, sulfur or nitrogen atom
    • C07D239/34—One oxygen atom

Abstract

SE REFIERE A COMPUESTOS DERIVADOS DE ACIDO PIRIMIDINCARBOXILICO, DE FORMULA (I) EN DONDE A ES CH2 U O; R1 ES HALOGENO, CIANO O ALQUILO(C1-C4); R2 ES HALOGENO, CIANO, ALQUILO(C1-C6) Y ALCOXI(C1-C6) OPCIONALMENTE SUSTITUIDOS CON UNO O MAS VECES CON FLUOR, -NR7- ENTRE OTROS; n ES DE 0 A 3; R3 ES H, FLUOR O CLORO; R4 ES H, HALOGENO, NITRO, CN, ENTRE OTROS; R5 Y R6 SON H, HALOGENO, CN, NITRO, ALQUILO(C1-C6) O ALCOXI OPCIONALMENTE SUSTITUIDOS, HETEROCICLO DE 4 A 7 MIEMBROS, ENTRE OTROS; Z ES H O ALQUILO(C1-C4). SON COMPUESTOS PREFERIDOS: ESTER ETILICO DEL ACIDO 4-(2-CLOROFENOXI)-2-FENILPIRIMIDIN-5-CARBOXILICO, ACIDO 4-(2-METILFENOXI)-2-FENILPIRIMIDIN-5-CARBOXILICO, ACIDO 4-(2-CLORO-4-METOXIFENOXI)-2-FENILPIRIMIDIN-5-CARBOXILICO, ENTRE OTROS. SE REFIERE TAMBIEN A UN PROCEDIMIENTO DE PREPARACION Y A UNA COMPOSICION FARMACEUTICA. DICHOS COMPUESTOS SON MODULADORES DE LOS RECEPTORES ACTIVADOS POR EL PROLIFERADOR DE PEROXISOMAS (PPAR)-ALFA SIENDO UTILES EN EL TRATAMIENTO DE ENFERMEDADES CARDIOVASCULARES TALES COMO DISLIPIDEMIAS Y ARTERIOESCLEROSIS
PE2006000274A 2005-03-12 2006-03-10 DERIVADOS DEL ACIDO PIRMIDINCARBOXILICO COMO MODULADORES DE PPAR-alfa PE20061348A1 (es)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
DE102005011447 2005-03-12
DE102005027150A DE102005027150A1 (de) 2005-03-12 2005-06-11 Pyrimidincarbonsäure-Derivate und ihre Verwendung

Publications (1)

Publication Number Publication Date
PE20061348A1 true PE20061348A1 (es) 2007-01-28

Family

ID=36218368

Family Applications (1)

Application Number Title Priority Date Filing Date
PE2006000274A PE20061348A1 (es) 2005-03-12 2006-03-10 DERIVADOS DEL ACIDO PIRMIDINCARBOXILICO COMO MODULADORES DE PPAR-alfa

Country Status (17)

Country Link
US (1) US20080194598A1 (es)
EP (1) EP1866289A1 (es)
JP (1) JP2008533063A (es)
KR (1) KR20070116876A (es)
AR (1) AR055744A1 (es)
AU (1) AU2006224812A1 (es)
BR (1) BRPI0609207A2 (es)
CA (1) CA2600681A1 (es)
DE (1) DE102005027150A1 (es)
DO (1) DOP2006000062A (es)
GT (1) GT200600109A (es)
IL (1) IL185895A0 (es)
MX (1) MX2007011070A (es)
PE (1) PE20061348A1 (es)
TW (1) TW200724532A (es)
UY (1) UY29416A1 (es)
WO (1) WO2006097220A1 (es)

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WO2006121648A2 (en) 2005-05-06 2006-11-16 E. I. Du Pont De Nemours And Company Method for preparation of optionally 2-substituted 1,6-dihydro-6-oxo-4-pyrimidinecarboxylic acids
DE102006043520A1 (de) * 2006-09-12 2008-03-27 Bayer Healthcare Ag 2-Phenoxynikotinsäure-Derivate und ihre Verwendung
DE102006043519A1 (de) * 2006-09-12 2008-03-27 Bayer Healthcare Ag 4-Phenoxynikotinsäure-Derivate und ihre Verwendung
AU2008239659B2 (en) * 2007-04-13 2013-09-05 Millennium Pharmaceuticals, Inc. Combination anticoagulant therapy with a compound that acts as a factor Xa inhibitor
DE102007042754A1 (de) * 2007-09-07 2009-03-12 Bayer Healthcare Ag Substituierte 6-Phenylnikotinsäuren und ihre Verwendung
DE102007061756A1 (de) * 2007-12-20 2009-06-25 Bayer Healthcare Ag Substituierte 4-Aminopyrimidin-5-carbonsäuren und ihre Verwendung
DE102007061757A1 (de) 2007-12-20 2009-06-25 Bayer Healthcare Ag Substituierte 2-Phenylpyrimidin-5-carbonsäuren und ihre Verwendung
WO2011150286A2 (en) 2010-05-26 2011-12-01 Satiogen Pharmaceuticals,Inc. Bile acid recycling inhibitors and satiogens for treatment of diabetes, obesity, and inflammatory gastrointestinal conditions
AU2011296737A1 (en) 2010-08-31 2013-04-11 Snu R&Db Foundation Use of the fetal reprogramming of a PPAR delta agonist
KR20210131431A (ko) 2011-10-28 2021-11-02 샤이어 휴먼 지네틱 테라피즈 인크. 고담혈증 및 담즙 정체성 간 질환 치료용 담즙산 재순환 억제제
US20130109671A1 (en) 2011-10-28 2013-05-02 Lumena Pharmaceuticals, Inc. Bile Acid Recycling Inhibitors for Treatment of Pediatric Cholestatic Liver Diseases
WO2014144650A2 (en) 2013-03-15 2014-09-18 Lumena Pharmaceuticals, Inc. Bile acid recycling inhibitors for treatment of primary sclerosing cholangitis and inflammatory bowel disease
RU2015139732A (ru) 2013-03-15 2017-04-24 ЛУМЕНА ФАРМАСЬЮТИКАЛС ЭлЭлСи Ингибиторы рециркуляции желчных кислот для лечения пищевода барретта и гастроэзофагеальной рефлюксной болезни
WO2020167964A1 (en) 2019-02-12 2020-08-20 Mirum Pharmaceuticals, Inc. Genotype and dose-dependent response to an asbti in patients with bile salt export pump deficiency

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IL145922A0 (en) * 1999-04-28 2002-07-25 Aventis Pharma Gmbh Di-aryl acid derivatives as ppar receptor ligands
YU39503A (sh) * 2000-11-22 2006-05-25 F. Hoffmann-La Roche Ag. Derivati pirimidina

Also Published As

Publication number Publication date
GT200600109A (es) 2007-02-14
JP2008533063A (ja) 2008-08-21
UY29416A1 (es) 2006-10-31
WO2006097220A1 (de) 2006-09-21
DOP2006000062A (es) 2006-12-15
DE102005027150A1 (de) 2006-09-28
TW200724532A (en) 2007-07-01
AU2006224812A1 (en) 2006-09-21
CA2600681A1 (en) 2006-09-21
AR055744A1 (es) 2007-09-05
IL185895A0 (en) 2008-01-06
EP1866289A1 (de) 2007-12-19
KR20070116876A (ko) 2007-12-11
BRPI0609207A2 (pt) 2010-03-02
US20080194598A1 (en) 2008-08-14
MX2007011070A (es) 2007-11-07

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