AR054514A1 - Derivados de pirazolopiridina como inhibidores del receptor beta-adrenergico cinasa 1 - Google Patents
Derivados de pirazolopiridina como inhibidores del receptor beta-adrenergico cinasa 1Info
- Publication number
- AR054514A1 AR054514A1 ARP060102721A ARP060102721A AR054514A1 AR 054514 A1 AR054514 A1 AR 054514A1 AR P060102721 A ARP060102721 A AR P060102721A AR P060102721 A ARP060102721 A AR P060102721A AR 054514 A1 AR054514 A1 AR 054514A1
- Authority
- AR
- Argentina
- Prior art keywords
- alkyl
- alkylene
- substituted
- heterocyclyl
- halogen
- Prior art date
Links
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic 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
- C07D471/02—Heterocyclic 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
- C07D471/04—Ortho-condensed systems
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- 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
- A61K31/435—Heterocyclic 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
- A61K31/4353—Heterocyclic 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
- A61K31/437—Heterocyclic 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
-
- 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
- A61P1/16—Drugs for disorders of the alimentary tract or the digestive system for liver or gallbladder disorders, e.g. hepatoprotective agents, cholagogues, litholytics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/30—Drugs for disorders of the nervous system for treating abuse or dependence
- A61P25/36—Opioid-abuse
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/12—Antivirals
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- 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
-
- 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
- A61P9/04—Inotropic agents, i.e. stimulants of cardiac contraction; Drugs for heart failure
-
- 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
- A61P9/10—Drugs 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
-
- 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
- A61P9/12—Antihypertensives
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Veterinary Medicine (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Cardiology (AREA)
- Heart & Thoracic Surgery (AREA)
- Addiction (AREA)
- Biomedical Technology (AREA)
- Neurosurgery (AREA)
- Neurology (AREA)
- Communicable Diseases (AREA)
- Oncology (AREA)
- Urology & Nephrology (AREA)
- Psychiatry (AREA)
- Vascular Medicine (AREA)
- Virology (AREA)
- Hospice & Palliative Care (AREA)
- Gastroenterology & Hepatology (AREA)
- Epidemiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
Abstract
Las composiciones que contienen dichos compuestos y a su utilizacion para el tratamiento y prevencion de la insuficiencia cardíaca cronica, la hipertension, isquemia de miocardio y de las infecciones por el virus de la hepatitis C (HCV) y para la prevencion de la adicion a los opioides. Reivindicacion 1: Un compuesto de formula (1), en la que: R1 es H o alquilo C1-6, en el que el grupo alquilo C1-6 está sustituido o sustituido por uno o más grupos OH, halogeno o NH2; y R2 es fenilo, cicloalquilo C3-10 o un grupo heterociclilo C4-10 que están insustituidos o sustituidos por 1, 2 o 3 restos independientemente seleccionados de: alquilo C1-6; alquenilo C2-6; alquinilo C2-6; alquilenoC1-6-COOH; alquilenoC1-6-C(O)O- alquiloC1-6; alquilenoC1-6-C(O)NH2; alquilenoC1-6-C(O)NH-alquiloC1-6; alquilenoC1-6 -O-alquiloC1-6; alquilenoC1-6-OH; alquilenoC1-6-NH2; alquilenoC1-6-NH-alquiloC1-6; alquilenoC1-6-N[alquiloC1-6]2; CN; COOH; alquiloC1-6C(O)O; C(O)NH2; alquiloC1-6C(O)NH; C(O)N(alquiloC1-6) 2; alquiloC1-6C(O); halogeno; -NH2; alquiloC1-6NH; N(alquiloC1-6)2; alquiloC1-6NH-C(O); OH; alquiloC1-6O; alqueniloC2-6O; alquiniloC2-6O; aquilenoC1-6O-C(O)OH; alquilenoC1-6-C(O)O-alquiloC1-6; alquilenoC1-6O-C(O)NH2; alquilenoC1-6O- C(O)NH-alquiloC1-6; alquilenoC1-6-OH; alquilenoC1-6O-O-alquiloC1-6; alquilenjoC1-6O-NH2; alquilenoC1-6O-NH-alquiloC1-6; alquiloC1-6O-C(O); alquiloC1-6-S; alquiloC1-4S(O)2; ariloaC6-10; heterociclilo C4-10; alquilenoC1-6-ariloC6-10; alquilenoC1-6- heteterocicliloC4-10; alquilenoC1-6-O-ariloC6-10; alquilenoC1-6-O- heterocicliloC4-10; arilo C6-10; heterocicliloC4-10O; alquilenoC1-6O-ariloC6-10; alquilenoC1-6-O-heterocicliloC4-10; en la que los grupos arilo C6-10 y heterociclilo C4-10 en los restos 40 a 49 están insustituidos o sustituidos por 1, 2 o 3 restos independientemente seleccionados de OH, halogeno, NH2, O-alquiloC1-6, alquilo C1-6, S(O)2-alquiloC1-4 o cicloalquilo C3-10; y/o están sustituidos en las proximidades por un resto de formula -O-(CH2)n-O-, en la que n es 1, 2 o 3 y en la que uno o más átomos de hidrogeno pueden estar sustituidos por átomos de halogeno; y R3 es H; alquilo C1-6 o O-alquiloC1-6, en la que el grupo alquilo C1-6 está insustituido o sustituido por OH, halogeno, NH2, alquiloC1-6NH o N(alquiloC1-6)2; o cicloalquilo C3-10, en la que el cicloalquilo C3-10 está sustituido o sustituido por uno o más átomos de fluor; o una de sus sales fisiologicamente aceptables.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP05013774 | 2005-06-27 |
Publications (1)
Publication Number | Publication Date |
---|---|
AR054514A1 true AR054514A1 (es) | 2007-06-27 |
Family
ID=35395578
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
ARP060102721A AR054514A1 (es) | 2005-06-27 | 2006-06-23 | Derivados de pirazolopiridina como inhibidores del receptor beta-adrenergico 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 (7)
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 |
JPWO2009107391A1 (ja) * | 2008-02-27 | 2011-06-30 | 武田薬品工業株式会社 | 6員芳香環含有化合物 |
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 |
US20210403468A1 (en) * | 2018-10-24 | 2021-12-30 | Bristol-Myers Squibb Company | Substituted indole and indazole compounds |
Family Cites Families (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CA2314355A1 (en) * | 1997-12-13 | 1999-06-24 | Bristol-Myers Squibb Company | Use of pyrazolo ¢3,4-b! pyridine as cyclin dependent kinase inhibitors |
JP2002020386A (ja) * | 2000-07-07 | 2002-01-23 | Ono Pharmaceut Co Ltd | ピラゾロピリジン誘導体 |
AU2003245700A1 (en) * | 2002-02-12 | 2003-09-04 | Glaxo Group Limited | Pyrazolopyridine derivatives |
BR0313262A (pt) * | 2002-08-07 | 2005-07-12 | Mitsubishi Pharma Corp | Compostos de dihidropirazolpiridina |
EP1611131B1 (en) * | 2003-02-27 | 2010-09-15 | Palau Pharma, S.A. | Pyrazolopyridine derivates |
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2006
- 2006-06-13 DE DE602006005242T patent/DE602006005242D1/de active Active
- 2006-06-13 WO PCT/EP2006/005649 patent/WO2007000241A1/en active Application Filing
- 2006-06-13 AU AU2006264044A patent/AU2006264044A1/en not_active Abandoned
- 2006-06-13 PT PT06754324T patent/PT1899333E/pt unknown
- 2006-06-13 MX MX2007015829A patent/MX2007015829A/es active IP Right Grant
- 2006-06-13 ES ES06754324T patent/ES2322197T3/es active Active
- 2006-06-13 EP EP06754324A patent/EP1899333B1/en active Active
- 2006-06-13 RS RSP-2009/0165A patent/RS50821B/sr unknown
- 2006-06-13 JP JP2008518660A patent/JP5010594B2/ja not_active Expired - Fee Related
- 2006-06-13 BR BRPI0612320-1A patent/BRPI0612320A2/pt not_active IP Right Cessation
- 2006-06-13 CA CA002611296A patent/CA2611296A1/en not_active Abandoned
- 2006-06-13 RU RU2008102970/04A patent/RU2415855C2/ru not_active IP Right Cessation
- 2006-06-13 AT AT06754324T patent/ATE423118T1/de not_active IP Right Cessation
- 2006-06-13 SI SI200630284T patent/SI1899333T1/sl unknown
- 2006-06-13 KR KR1020077030289A patent/KR20080020638A/ko not_active Application Discontinuation
- 2006-06-13 PL PL06754324T patent/PL1899333T3/pl unknown
- 2006-06-13 DK DK06754324T patent/DK1899333T3/da active
- 2006-06-13 CN CN200680023397XA patent/CN101208340B/zh not_active Expired - Fee Related
- 2006-06-13 NZ NZ564757A patent/NZ564757A/en not_active IP Right Cessation
- 2006-06-23 AR ARP060102721A patent/AR054514A1/es not_active Application Discontinuation
- 2006-06-23 TW TW095122584A patent/TW200800982A/zh unknown
- 2006-06-26 MY MYPI20063009A patent/MY139016A/en unknown
- 2006-06-27 UY UY29632A patent/UY29632A1/es not_active Application Discontinuation
-
2007
- 2007-11-15 ZA ZA200709853A patent/ZA200709853B/xx unknown
- 2007-11-30 MA MA30441A patent/MA29498B1/fr unknown
- 2007-12-20 US US11/961,282 patent/US7910602B2/en not_active Expired - Fee Related
- 2007-12-24 IL IL188381A patent/IL188381A0/en unknown
-
2008
- 2008-01-21 NO NO20080392A patent/NO20080392L/no not_active Application Discontinuation
-
2009
- 2009-04-24 HR HR20090244T patent/HRP20090244T2/xx unknown
- 2009-05-11 CY CY20091100501T patent/CY1110464T1/el unknown
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Legal Events
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FA | Abandonment or withdrawal |