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MXPA05008584A - Compuestos heterociclicos utiles como activadores de nurr-1. - Google Patents

Compuestos heterociclicos utiles como activadores de nurr-1.

Info

Publication number
MXPA05008584A
MXPA05008584A MXPA05008584A MXPA05008584A MXPA05008584A MX PA05008584 A MXPA05008584 A MX PA05008584A MX PA05008584 A MXPA05008584 A MX PA05008584A MX PA05008584 A MXPA05008584 A MX PA05008584A MX PA05008584 A MXPA05008584 A MX PA05008584A
Authority
MX
Mexico
Prior art keywords
alkoxy
alkyl
hydroxy
nurr
activators
Prior art date
Application number
MXPA05008584A
Other languages
English (en)
Inventor
Schmidt Boris
Original Assignee
Novartis 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 Novartis Ag filed Critical Novartis Ag
Publication of MXPA05008584A publication Critical patent/MXPA05008584A/es

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D271/00Heterocyclic compounds containing five-membered rings having two nitrogen atoms and one oxygen atom as the only ring hetero atoms
    • C07D271/02Heterocyclic compounds containing five-membered rings having two nitrogen atoms and one oxygen atom as the only ring hetero atoms not condensed with other rings
    • C07D271/061,2,4-Oxadiazoles; Hydrogenated 1,2,4-oxadiazoles
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/14Drugs for disorders of the nervous system for treating abnormal movements, e.g. chorea, dyskinesia
    • A61P25/16Anti-Parkinson drugs
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D261/00Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings
    • C07D261/02Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings
    • C07D261/06Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings having two or more double bonds between ring members or between ring members and non-ring members
    • C07D261/08Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings having two or more double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D263/00Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings
    • C07D263/02Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings
    • C07D263/30Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
    • C07D263/32Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D413/00Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D413/02Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
    • C07D413/04Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings directly linked by a ring-member-to-ring-member bond

Landscapes

  • Organic Chemistry (AREA)
  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Engineering & Computer Science (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Medicinal Chemistry (AREA)
  • Biomedical Technology (AREA)
  • Neurology (AREA)
  • Neurosurgery (AREA)
  • Psychology (AREA)
  • Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)

Abstract

La presente invencion se refiere a compuestos de la formula I: en donde: R1 es hidroxi, alcoxi de C1-4, amino, alquilamino de C1-4, dialquilamino de C1-4, benciloxi o alcanoilo de C2-7, R2 es alquilo de C1-4, alcoxi de C1-4, alcoxi de C1-4-alcoxi de C1-4, CF3, halogeno, alquilamino de C1-4, dialquilamino de C1-4, dialquilamino de C1-4-alcoxi de C1-4 o N-alcoxi de C1-4-alquilo de C1-4-N-alquilamino de C1-4, N-alquilpiperazinilo de C1-4, morfolinilo, pirrolidinilalcoxi de C1-4, en donde los radicales alquilo de C1-4, en R2 ademas estan opcionalmente substituidos por alquilo de C1-4, halogeno, ciano, amino, alcoxi o alquiltio, X es N u O, Y es N, O u CH, Z es N o CH, y W es N o CH, siempre que (a) R1 no sea hidroxi o alcoxi de C1-4 cuando R2 sea CF3, X sea O, Y sea CH, Z sea N y W sea CH, (b) R1 no sea hidroxi o alcoxi de C1-4 cuando R2 es CF3 o cloro, X es N, Y es O, Z es CH y W es CH, (c) R1 no sea hidroxi cuando R2 sea CF3, X sea O, Y sea N, Z sea CH y W sea CH y (d) X e Y simultaneamente no sean O, sus sales; su preparacion, su uso y composiciones farmaceuticas que lo contienen (ver formula I).
MXPA05008584A 2003-02-14 2004-02-13 Compuestos heterociclicos utiles como activadores de nurr-1. MXPA05008584A (es)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
GBGB0303503.7A GB0303503D0 (en) 2003-02-14 2003-02-14 Organic compounds
PCT/EP2004/001372 WO2004072050A1 (en) 2003-02-14 2004-02-13 Heterocyclic compounds useful as nurr-1 activators

Publications (1)

Publication Number Publication Date
MXPA05008584A true MXPA05008584A (es) 2005-11-04

Family

ID=9953078

Family Applications (1)

Application Number Title Priority Date Filing Date
MXPA05008584A MXPA05008584A (es) 2003-02-14 2004-02-13 Compuestos heterociclicos utiles como activadores de nurr-1.

Country Status (14)

Country Link
US (1) US7432293B2 (es)
EP (1) EP1597243A1 (es)
JP (1) JP2006517564A (es)
CN (2) CN101665469A (es)
AR (1) AR043168A1 (es)
AU (1) AU2004212151B2 (es)
BR (1) BRPI0407479A (es)
CA (1) CA2515847A1 (es)
GB (1) GB0303503D0 (es)
MX (1) MXPA05008584A (es)
PE (1) PE20050193A1 (es)
PL (1) PL376754A1 (es)
TW (1) TW200502225A (es)
WO (1) WO2004072050A1 (es)

Families Citing this family (25)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6992096B2 (en) 2003-04-11 2006-01-31 Ptc Therapeutics, Inc. 1,2,4-oxadiazole benzoic acid compounds and their use for nonsense suppression and the treatment of disease
WO2006044456A1 (en) * 2004-10-13 2006-04-27 Ptc Therapeutics, Inc. Compounds for nonsense suppression, and methods for their use
PT1874306E (pt) 2005-04-08 2012-10-11 Ptc Therapeutics Inc Composições de um 1,2,4-oxadiazole oralmente activo para terapia de supressão de mutações sem sentido (ou nonsense)
AU2006239418A1 (en) 2005-04-26 2006-11-02 Neurosearch A/S Novel oxadiazole derivatives and their medical use
SG170819A1 (en) 2006-03-30 2011-05-30 Ptc Therapeutics Inc Methods for the production of functional protein from dna having a nonsense mutation and the treatment of disorders associated therewith
FR2903108B1 (fr) * 2006-07-03 2008-08-29 Sanofi Aventis Sa Utilisation de derives d'imidazo[1,2-a] pyridine-2-carboxamides en therapeutique.
FR2903105A1 (fr) 2006-07-03 2008-01-04 Sanofi Aventis Sa Derives de 2-benzoyl-imidazopyridines, leur preparation et leur application en therapeutique
FR2903107B1 (fr) 2006-07-03 2008-08-22 Sanofi Aventis Sa Derives d'imidazopyridine-2-carboxamides, leur preparation et leur application en therapeutique
CN101535284B (zh) 2006-09-08 2014-12-10 Ptc医疗公司 制备1,2,4-噁二唑苯甲酸的方法
FR2906250B1 (fr) * 2006-09-22 2008-10-31 Sanofi Aventis Sa Derives de 2-aryl-6phenyl-imidazo(1,2-a) pyridines, leur preparation et leur application en therapeutique
DK2076501T3 (da) 2006-09-25 2016-02-29 Ptc Therapeutics Inc Krystallinske former af 3-[5-(2-fluorphenyl)-[1,2,4]oxadiazol-3-yl]-benzoesyre
WO2008130370A1 (en) 2006-09-25 2008-10-30 Ptc Therapeutics, Inc. Hydroxylated 1,2,4-oxadiazole benzoic acid compounds, compositions thereof and the use for nonsense suppression
EP2073805B1 (en) * 2006-10-12 2015-03-04 PTC Therapeutics, Inc. Methods for dosing an orally active 1,2,4-oxadiazole for nonsense mutation suppression therapy
EP2182809B1 (en) * 2007-08-27 2018-01-17 Dart Neuroscience (Cayman) Ltd Therapeutic isoxazole compounds
DK2307381T3 (da) 2008-06-09 2021-03-15 Univ Muenchen Ludwig Maximilians Nye lægemidler til inhibering af aggregering af proteiner involveret i sygdomme forbundet med proteinaggregering og/eller neurodegenerative sygdomme
CN102076670B (zh) * 2008-06-24 2013-05-22 Irm责任有限公司 调节g蛋白偶联受体的化合物和方法
FR2933609B1 (fr) 2008-07-10 2010-08-27 Fournier Lab Sa Utilisation de derives d'indole comme activateurs de nurr-1, pour le traitement de la maladie de parkinson.
WO2011009484A1 (en) * 2009-07-22 2011-01-27 Novartis Ag Arylpyrazoles and arylisoxazoles and their use as pkd modulators
FR2950053B1 (fr) 2009-09-11 2014-08-01 Fournier Lab Sa Utilisation de derives d'indole benzoique comme activateurs de nurr-1, pour le traitement de la maladie de parkinson
FR2955110A1 (fr) * 2010-01-08 2011-07-15 Fournier Lab Sa Nouveaux derives de type pyrrolopyridine benzoique
DK2628733T3 (en) * 2010-10-14 2015-03-30 Daiichi Sankyo Co Ltd Acylbenzenderivat
KR20160078974A (ko) * 2013-11-05 2016-07-05 바이엘 크롭사이언스 악티엔게젤샤프트 절지동물 방제용 신규 화합물
US9873677B2 (en) 2014-03-06 2018-01-23 Ptc Therapeutics, Inc. Pharmaceutical compositions and salts of a 1,2,4-oxadiazole benzoic acid
MX2018005361A (es) 2015-10-30 2018-06-07 Ptc Therapeutics Inc Metodos para tratar epilepsia.
AU2018265584B2 (en) 2017-05-12 2023-09-28 Ludwig-Maximilians-Universität München Phenyl-heterocycle-phenyl derivatives for use in the treatment or prevention of melanoma

Family Cites Families (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH04295470A (ja) * 1991-03-22 1992-10-20 Wakamoto Pharmaceut Co Ltd モノアミンオキシダーゼ−b酵素阻害活性を有する1,2,4−オキサジアゾール誘導体及びその製造法
AU6526896A (en) * 1995-07-22 1997-02-18 Rhone-Poulenc Rorer Limited Substituted aromatic compounds and their pharmaceutical use
DE19620041A1 (de) * 1996-05-17 1998-01-29 Merck Patent Gmbh Adhäsionsrezeptor-Antagonisten
DE19643037A1 (de) * 1996-10-18 1998-04-23 Boehringer Ingelheim Kg Neue Oxadiazole, Verfahren zu ihrer Herstellung sowie deren Verwendung als Arzneimittel
IT1300055B1 (it) 1998-04-17 2000-04-05 Boehringer Ingelheim Italia Eterocicli con anello a 5 termini difenil-sostituiti loro procedimento di preparazione e loro impiego come farmici
US6545009B1 (en) * 1998-07-01 2003-04-08 Takeda Chemical Industries, Ltd. Retinoid-related receptor function regulating agent
JP2000080086A (ja) * 1998-07-01 2000-03-21 Takeda Chem Ind Ltd レチノイド関連受容体機能調節剤
DK1070708T3 (da) * 1999-07-21 2004-05-10 Hoffmann La Roche Triazolderivater
CZ2002599A3 (cs) * 1999-08-19 2002-06-12 Nps Pharmaceuticals Inc. Heteropolycyklické sloučeniny a jejich pouľití jako antagonistů metabotropního receptoru glutamátu
PL369598A1 (en) * 2001-02-21 2005-05-02 Nps Pharmaceuticals, Inc. Heteropolycyclic compounds and their use as metabotropic glutamate receptor antagonists
US7223791B2 (en) * 2001-06-26 2007-05-29 Takeda Pharmaceutical Company Limited Function regulator for retinoid relative receptor

Also Published As

Publication number Publication date
CN1747942A (zh) 2006-03-15
JP2006517564A (ja) 2006-07-27
PL376754A1 (pl) 2006-01-09
CN100475795C (zh) 2009-04-08
GB0303503D0 (en) 2003-03-19
TW200502225A (en) 2005-01-16
WO2004072050A1 (en) 2004-08-26
BRPI0407479A (pt) 2006-02-07
US7432293B2 (en) 2008-10-07
AU2004212151B2 (en) 2008-09-04
AU2004212151A1 (en) 2004-08-26
CN101665469A (zh) 2010-03-10
US20060089365A1 (en) 2006-04-27
AR043168A1 (es) 2005-07-20
PE20050193A1 (es) 2005-04-11
CA2515847A1 (en) 2004-08-26
EP1597243A1 (en) 2005-11-23

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