BRPI0407479A - Compostos heterocìclicos úteis como ativadores de nurr-1 - Google Patents

Compostos heterocìclicos úteis como ativadores de nurr-1

Info

Publication number
BRPI0407479A
BRPI0407479A BR0407479-3A BRPI0407479A BRPI0407479A BR PI0407479 A BRPI0407479 A BR PI0407479A BR PI0407479 A BRPI0407479 A BR PI0407479A BR PI0407479 A BRPI0407479 A BR PI0407479A
Authority
BR
Brazil
Prior art keywords
alkoxy
alkylamino
alkyl
hydroxy
nurr
Prior art date
Application number
BR0407479-3A
Other languages
English (en)
Inventor
Samuel Hintermann
Bastian Hengerer
Boris Schmidt
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 BRPI0407479A publication Critical patent/BRPI0407479A/pt

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

"COMPOSTOS HETEROCìCLICOS úTEIS COMO ATIVADORES DE NURR-1". A presente invenção refere-se a um composto da fórmula I; na qual R~ 1~, é hidróxi, C~ 1-4~ alcóxi, amina, C~ 1-4~ alquil - amino, di C~ 1-4~ alquilamino, benzilóxi ou C~ 2-7~ alcanoíla; R~ 2~ é C~ 1-4~ alquila, C~ 1-4~ alcóxi, C~ 1-4~ alcóxi C~ 1-4~ alcóxi, CF~ 3~, halogênio, C~ 1-4~ alquilamino, di- C~ 1-4~ alquilamino, di- C~ 1-4~ alquilamino di- C~ 1-4~ alcóxi, ou N-C~ 1-4~ alcóxi C~ 1-4~ alquil-N-C~ 1-4~ alquilamino, N-C~ 1-4~ alquil-piperazinila, morfolinila, pirrolidinil- C~ 1-4~ alcóxi, em que os radicais C~ 1-4~ alquila em R~ 2~ são ainda substituídos de modo opcional por C~ 1-4~ alquila, halogênio, ciano, amino, alcóxi ou alquiltio; X é N ou O; Yé N, O ou CH; Z é N ou CH, e W é N ou CH; contanto que (a) R~ 1~, não seja hidróxi ou C~ 1-4~ alcóxi quando R~ 2~ for CF~ 3~, X seja O, Y seja CH, Z seja N e W seja CH; (b) R~ 1~ não seja hidróxi ou C~ 1-4~ alcóxi quando R~ 2~ for CF~ 3~, ou cloro, X for N, Y for O, Z for CH e W for CH; (c) R~ 1~ não seja hidróxi, quando R~ 2~ for CF~ 3~, X for O, Y for N, Z for CH e W for CH e (d) X e Y não sejam ao mesmo tempo O; os sais dos mesmos, as preparações dos mesmos, o uso dos mesmos e composições farmacêuticas que contêm os mesmos.
BR0407479-3A 2003-02-14 2004-02-13 Compostos heterocìclicos úteis como ativadores de nurr-1 BRPI0407479A (pt)

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
BRPI0407479A true BRPI0407479A (pt) 2006-02-07

Family

ID=9953078

Family Applications (1)

Application Number Title Priority Date Filing Date
BR0407479-3A BRPI0407479A (pt) 2003-02-14 2004-02-13 Compostos heterocìclicos úteis como ativadores de nurr-1

Country Status (14)

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

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ZA200508298B (en) 2003-04-11 2007-01-31 Ptc Therapeutics Inc 1,2,4-oxadiazole benzoic acid compounds
EP1799659A1 (en) * 2004-10-13 2007-06-27 PTC Therapeutics, Inc. Compounds for nonsense suppression, and methods for their use
US8716321B2 (en) 2005-04-08 2014-05-06 Ptc Therapeutics, Inc. Methods for dosing an orally active 1,2,4-oxadiazole
AU2006239418A1 (en) 2005-04-26 2006-11-02 Neurosearch A/S Novel oxadiazole derivatives and their medical use
MX2008012515A (es) 2006-03-30 2008-11-19 Ptc Therapeutics Inc Metodos para la produccion de proteina funcional a partir de adn que tiene una mutacion sin sentido y el tratamiento de trastornos asociados con la misma.
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
FR2903108B1 (fr) * 2006-07-03 2008-08-29 Sanofi Aventis Sa Utilisation de derives d'imidazo[1,2-a] pyridine-2-carboxamides en therapeutique.
NZ598012A (en) 2006-09-08 2013-08-30 Ptc Therapeutics Inc Processes for the preparation of 1,2,4-oxadiazole benzoic acids
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
CL2007002743A1 (es) 2006-09-25 2008-07-11 Pct Therapeutics Inc Soc Organ Forma cristalina del acido 3-[5-(2-fluorofenil)-[1,2,4]oxadiazol-3-il]-benzoico; composicion farmaceutica que comprende a dicha forma cristalina; y su uso para modular la terminacion prematura de traslado o decaimiento de marn, tales como carcicoma.
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
SI2073805T1 (sl) * 2006-10-12 2015-10-30 Ptc Therapeutics, Inc. Postopki za odmerjanje peroralno aktivnega 1,2,4-oksadiazola za zdravljenje supresije nesmiselnih mutacij
WO2009029632A1 (en) 2007-08-27 2009-03-05 Helicon Therapeutics, Inc. Therapeutic isoxazole compounds
PT2307381T (pt) 2008-06-09 2021-03-15 Univ Muenchen Ludwig Maximilians Novas drogas para inibir a agregação de proteínas envolvidas em doenças relacionadas com a agregação de proteínas e/ou doenças neurodegenerativas
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
KR101829086B1 (ko) * 2010-10-14 2018-02-13 다이이찌 산쿄 가부시키가이샤 아실벤젠 유도체
AR098311A1 (es) 2013-11-05 2016-05-26 Bayer Cropscience Ag Compuestos para el control de artrópodos
TWI695717B (zh) 2014-03-06 2020-06-11 美商 Ptc 治療公司 1,2,4-二唑苯甲酸之鹽及醫藥組合物
JP2018531975A (ja) 2015-10-30 2018-11-01 ピーティーシー セラピューティクス,インコーポレーテッド てんかんの治療方法
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

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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
WO1997003967A1 (en) * 1995-07-22 1997-02-06 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
WO2000001679A1 (fr) * 1998-07-01 2000-01-13 Takeda Chemical Industries, Ltd. Regulateurs du recepteur associe aux retinoides
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
ATE257827T1 (de) * 1999-07-21 2004-01-15 Hoffmann La Roche Triazolderivate
BR0013427A (pt) * 1999-08-19 2002-07-30 Nps Pharma Inc Compostos heteropolicìclicos e seus usos como antagonistas no receptor de glutamato metabotrópico
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
JP2006517564A (ja) 2006-07-27
WO2004072050A1 (en) 2004-08-26
TW200502225A (en) 2005-01-16
AU2004212151B2 (en) 2008-09-04
GB0303503D0 (en) 2003-03-19
US7432293B2 (en) 2008-10-07
AR043168A1 (es) 2005-07-20
US20060089365A1 (en) 2006-04-27
CN100475795C (zh) 2009-04-08
AU2004212151A1 (en) 2004-08-26
MXPA05008584A (es) 2005-11-04
EP1597243A1 (en) 2005-11-23
CA2515847A1 (en) 2004-08-26
PE20050193A1 (es) 2005-04-11
CN101665469A (zh) 2010-03-10
CN1747942A (zh) 2006-03-15
PL376754A1 (pl) 2006-01-09

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Legal Events

Date Code Title Description
B06F Objections, documents and/or translations needed after an examination request according [chapter 6.6 patent gazette]
B08F Application fees: application dismissed [chapter 8.6 patent gazette]

Free format text: REFERENTE A 8A ANUIDADE.

B08K Patent lapsed as no evidence of payment of the annual fee has been furnished to inpi [chapter 8.11 patent gazette]

Free format text: REFERENTE AO DESPACHO 8.6 PUBLICADO NA RPI 2159 DE 22/05/2012.