UY29632A1 - Derivados de pirazolopiridina como inhibidores del receptor b(beta)-adrenérgico cinasa 1 - Google Patents

Derivados de pirazolopiridina como inhibidores del receptor b(beta)-adrenérgico cinasa 1

Info

Publication number
UY29632A1
UY29632A1 UY29632A UY29632A UY29632A1 UY 29632 A1 UY29632 A1 UY 29632A1 UY 29632 A UY29632 A UY 29632A UY 29632 A UY29632 A UY 29632A UY 29632 A1 UY29632 A1 UY 29632A1
Authority
UY
Uruguay
Prior art keywords
inhibitors
beta
derivatives
pirazolopiridine
adrenérgico
Prior art date
Application number
UY29632A
Other languages
English (en)
Inventor
Dr Kurt Ritter
Dr Henning Steinhagen
Dr Jochen Huber
Dr Bernard Pirard
Dr Kirsten Bjergarde
Dr Marcel Patek
Drr Martin Smrcina
Dr Linli Wei
Original Assignee
Sanofi Aventis Deutschland
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 Sanofi Aventis Deutschland filed Critical Sanofi Aventis Deutschland
Publication of UY29632A1 publication Critical patent/UY29632A1/es

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D471/00Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
    • C07D471/02Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
    • C07D471/04Ortho-condensed systems
    • 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
    • A61K31/435Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/4353Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems
    • A61K31/437Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems the heterocyclic ring system containing a five-membered ring having nitrogen as a ring hetero atom, e.g. indolizine, beta-carboline
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P1/00Drugs for disorders of the alimentary tract or the digestive system
    • A61P1/16Drugs for disorders of the alimentary tract or the digestive system for liver or gallbladder disorders, e.g. hepatoprotective agents, cholagogues, litholytics
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/30Drugs for disorders of the nervous system for treating abuse or dependence
    • A61P25/36Opioid-abuse
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/12Antivirals
    • 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
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00Drugs for disorders of the cardiovascular system
    • 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
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00Drugs for disorders of the cardiovascular system
    • A61P9/12Antihypertensives

Landscapes

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • Medicinal Chemistry (AREA)
  • General Health & Medical Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Cardiology (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Addiction (AREA)
  • Neurosurgery (AREA)
  • Neurology (AREA)
  • Biomedical Technology (AREA)
  • Hospice & Palliative Care (AREA)
  • Communicable Diseases (AREA)
  • Vascular Medicine (AREA)
  • Urology & Nephrology (AREA)
  • Oncology (AREA)
  • Virology (AREA)
  • Psychiatry (AREA)
  • Gastroenterology & Hepatology (AREA)
  • Epidemiology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)

Abstract

La invención se refiere a los derivados 6-amido sustituidos de pirazolopiridina de fórmula (I) útiles como inhibidores del receptor beta-adrenérgico cinasa 1 (BARK-1), a las composiciones que contienen dichos compuestos y a su utilización para el tratamietno y prevención de la insuficiencia cardíaca crónica, la hipertensión, isquemia de miocardio y de las infecciones por el virus de la hepatitis C (HCV) y para le prevención de la adicción a los opioides.
UY29632A 2005-06-27 2006-06-27 Derivados de pirazolopiridina como inhibidores del receptor b(beta)-adrenérgico cinasa 1 UY29632A1 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
EP05013774 2005-06-27

Publications (1)

Publication Number Publication Date
UY29632A1 true UY29632A1 (es) 2007-01-31

Family

ID=35395578

Family Applications (1)

Application Number Title Priority Date Filing Date
UY29632A UY29632A1 (es) 2005-06-27 2006-06-27 Derivados de pirazolopiridina como inhibidores del receptor b(beta)-adrenérgico cinasa 1

Country Status (30)

Country Link
US (1) US7910602B2 (es)
EP (1) EP1899333B1 (es)
JP (1) JP5010594B2 (es)
KR (1) KR20080020638A (es)
CN (1) CN101208340B (es)
AR (1) AR054514A1 (es)
AT (1) ATE423118T1 (es)
AU (1) AU2006264044A1 (es)
BR (1) BRPI0612320A2 (es)
CA (1) CA2611296A1 (es)
CY (1) CY1110464T1 (es)
DE (1) DE602006005242D1 (es)
DK (1) DK1899333T3 (es)
ES (1) ES2322197T3 (es)
HR (1) HRP20090244T2 (es)
IL (1) IL188381A0 (es)
MA (1) MA29498B1 (es)
MX (1) MX2007015829A (es)
MY (1) MY139016A (es)
NO (1) NO20080392L (es)
NZ (1) NZ564757A (es)
PL (1) PL1899333T3 (es)
PT (1) PT1899333E (es)
RS (1) RS50821B (es)
RU (1) RU2415855C2 (es)
SI (1) SI1899333T1 (es)
TW (1) TW200800982A (es)
UY (1) UY29632A1 (es)
WO (1) WO2007000241A1 (es)
ZA (1) ZA200709853B (es)

Families Citing this family (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
TW200815438A (en) * 2006-06-13 2008-04-01 Bayer Schering Pharma Ag Substituted pyrazolopyridines and salts thereof, pharmaceutical compositions comprising same, methods of preparing same and uses of same
EP2253618A1 (en) * 2008-02-27 2010-11-24 Takeda Pharmaceutical Company Limited Compound having 6-membered aromatic ring
US9321787B2 (en) * 2011-07-07 2016-04-26 Sanofi Carboxylic acid derivatives having an oxazolo[5,4-d]pyrimidine ring
US8889730B2 (en) 2012-04-10 2014-11-18 Pfizer Inc. Indole and indazole compounds that activate AMPK
CA2905242C (en) 2013-03-15 2016-11-29 Pfizer Inc. Indole compounds that activate ampk
GB201410815D0 (en) * 2014-06-17 2014-07-30 Ucb Biopharma Sprl And Katholieke Universiteit Leuven Therapeutic agents
WO2020086503A1 (en) * 2018-10-24 2020-04-30 Bristol-Myers Squibb Company Substituted indole and indazole compounds
EP3870589B1 (en) 2018-10-24 2023-09-06 Bristol-Myers Squibb Company Substituted indole dimer compounds
WO2024137671A1 (en) * 2022-12-20 2024-06-27 Exelixis, Inc. Compounds that inhibit pkmyt1

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
ATE355841T1 (de) * 1997-12-13 2007-03-15 Bristol Myers Squibb Co Verwendung von pyrazolo ( 3,4-b) pyridin als cyclin-abhängige kinase hemmer
JP2002020386A (ja) * 2000-07-07 2002-01-23 Ono Pharmaceut Co Ltd ピラゾロピリジン誘導体
WO2003068773A1 (en) * 2002-02-12 2003-08-21 Glaxo Group Limited Pyrazolopyridine derivatives
EA200500322A1 (ru) * 2002-08-07 2005-08-25 Мицубиси Фарма Корпорейшн Соединения дигидропиразолопиридина
WO2004076450A1 (en) * 2003-02-27 2004-09-10 J. Uriach Y Compañia S.A. Pyrazolopyridine derivates

Also Published As

Publication number Publication date
NZ564757A (en) 2009-12-24
MY139016A (en) 2009-08-28
AU2006264044A1 (en) 2007-01-04
CN101208340A (zh) 2008-06-25
EP1899333A1 (en) 2008-03-19
RS50821B (sr) 2010-08-31
MA29498B1 (fr) 2008-05-02
JP5010594B2 (ja) 2012-08-29
ATE423118T1 (de) 2009-03-15
DE602006005242D1 (de) 2009-04-02
DK1899333T3 (da) 2009-06-15
RU2415855C2 (ru) 2011-04-10
MX2007015829A (es) 2008-02-22
JP2008543957A (ja) 2008-12-04
AR054514A1 (es) 2007-06-27
US20080227777A1 (en) 2008-09-18
IL188381A0 (en) 2008-04-13
RU2008102970A (ru) 2009-08-10
CN101208340B (zh) 2010-12-22
WO2007000241A1 (en) 2007-01-04
ES2322197T3 (es) 2009-06-17
KR20080020638A (ko) 2008-03-05
PT1899333E (pt) 2009-04-23
ZA200709853B (en) 2008-12-31
US7910602B2 (en) 2011-03-22
BRPI0612320A2 (pt) 2010-11-09
CY1110464T1 (el) 2015-04-29
PL1899333T3 (pl) 2009-07-31
CA2611296A1 (en) 2007-01-04
EP1899333B1 (en) 2009-02-18
HRP20090244T1 (en) 2009-06-30
TW200800982A (en) 2008-01-01
SI1899333T1 (sl) 2009-08-31
HRP20090244T2 (en) 2009-07-31
NO20080392L (no) 2008-02-28

Similar Documents

Publication Publication Date Title
UY29632A1 (es) Derivados de pirazolopiridina como inhibidores del receptor b(beta)-adrenérgico cinasa 1
PE20221629A1 (es) Analogos novedosos de nucleosidos sustituidos en el anillo aromatico biciclico 6-6 para su uso como inhibidores de prmt5
NI200700102A (es) Derivados de indol tetraciclicos como agentes antiviricos
DOP2009000133A (es) Derivados de indol como agonistas de los receptores s1p1
GT200600165A (es) Derivados dihidrobenzofuranos y usos de los mismos
CL2008003431A1 (es) Compuestos derivados de nucleosidos 2',4' sustituidos; proceso de preparacion de dichos compuestos; composicion farmaceutica que los comprende; su metodo de preparacion; y su uso para el tratamiento y/o la prevencion de cualquier condicion resultante de una infeccion por vhb, vhc o vih.
UY29184A1 (es) Derivados de sulfonilbencimidazol
ECSP055640A (es) Composiciones de pirazol útiles como inhibidores de gsk-3
DOP2010000064A (es) 2-anilinopurin 8-onas como inhibidores de ttk/mps1 para el tratamiento de trastornos proliferativos
UY32462A (es) Derivados de bifenilo novedosos para el tratamiento de infección por virus de hepatitis c 644
PE20070832A1 (es) Derivados de piridazinona como inhibidores de la tirosina quinasa
UY28766A1 (es) Compuestos heteropolicíclicos adicionales y su uso como antagonistas del receptor de glutamato metabotrópico
EA201100580A1 (ru) Имидазопиридазинкарбонитрилы, используемые в качестве ингибиторов киназы
ATE483707T1 (de) 2-cyclopropylthiazolderivate
MA32812B1 (fr) Composition pharmaceutique d'un inhibiteur puissant du vhc pour une administration orale
ECSP055762A (es) 4-amino-1-(piridilmetil)piperidina sustituida como antagonistas de receptores muscarinicos
CL2011001364A1 (es) Compuestos derivados de nucleotidos de uracil ciclopropilicos, inhibidores de la polimerasa del virus de la hepatitis c; composiciones farmaceuticas; y uso del compuesto para el tratamiento de hepatitis c (hcv).
GT200600081A (es) Derivados de acetilenno
CL2008000959A1 (es) Compuestos derivados de 1,2,4-tiadiazina o 1,4-tiazina; composiciones farmaceuticas que los contienen; y su uso para la prevencion y/o tratamiento de infecciones producidas por el virus de la hepatitis c.
ECSP078062A (es) Heterociclos de 1,4-dihidropiridina-condensados, procesos para preparar los mismos, uso y composiciones que los contienen
UY28821A1 (es) Hidrocloruro de (4-(5-aminometil-2-fluoro-fenil)-piperidin-1-il)-(4-bromo-3-metil-5-propoxi-tiofen-2-il)-metanona como un inhibidor de la triptasa de mastocitos.
GT200500292A (es) Derivados de 2-amido-4-feniltiazol, su preparacion y su aplicacion en terapeutica
ECSP109900A (es) Derivados de pirimidina utiles para el tratamiento de condiciones inflamatorias o alergicas
ECSP10010303A (es) (dihidro)pirrolo[2,1-a]isoquinolinas
AR073769A1 (es) Inhibidores de la integrasa del vih derivados de azepina y oxazepinas condensadas, composiciones farmaceuticas que los contienen y uso de los mismos para el tratamiento de infecciones por vih.

Legal Events

Date Code Title Description
109 Application deemed to be withdrawn

Effective date: 20130128