AR058006A1 - Mimeticos de glucocorticoides, composiciones farmaceiticas y usos de los mismos - Google Patents
Mimeticos de glucocorticoides, composiciones farmaceiticas y usos de los mismosInfo
- Publication number
- AR058006A1 AR058006A1 ARP060102414A ARP060102414A AR058006A1 AR 058006 A1 AR058006 A1 AR 058006A1 AR P060102414 A ARP060102414 A AR P060102414A AR P060102414 A ARP060102414 A AR P060102414A AR 058006 A1 AR058006 A1 AR 058006A1
- Authority
- AR
- Argentina
- Prior art keywords
- alkyl
- independently
- atom
- optionally
- heteroaryl
- Prior art date
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- 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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- A61P17/02—Drugs for dermatological disorders for treating wounds, ulcers, burns, scars, keloids, or the like
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- A61P19/00—Drugs for skeletal disorders
- A61P19/02—Drugs for skeletal disorders for joint disorders, e.g. arthritis, arthrosis
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- A—HUMAN NECESSITIES
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- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/04—Centrally acting analgesics, e.g. opioids
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
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- A61P27/02—Ophthalmic agents
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- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
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- A61P3/04—Anorexiants; Antiobesity agents
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- A61P3/08—Drugs for disorders of the metabolism for glucose homeostasis
- A61P3/10—Drugs for disorders of the metabolism for glucose homeostasis for hyperglycaemia, e.g. antidiabetics
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- A61P37/02—Immunomodulators
- A61P37/06—Immunosuppressants, e.g. drugs for graft rejection
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- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
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- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/12—Antihypertensives
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- C07D209/02—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
- C07D209/04—Indoles; Hydrogenated indoles
- C07D209/08—Indoles; Hydrogenated indoles with only hydrogen atoms or radicals containing only hydrogen and carbon atoms, directly attached to carbon atoms of the hetero ring
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- C07D209/02—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
- C07D209/04—Indoles; Hydrogenated indoles
- C07D209/10—Indoles; Hydrogenated indoles with substituted hydrocarbon radicals attached to carbon atoms of the hetero ring
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
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- C07D231/54—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings condensed with carbocyclic rings or ring systems
- C07D231/56—Benzopyrazoles; Hydrogenated benzopyrazoles
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- C07D235/04—Benzimidazoles; Hydrogenated benzimidazoles
- C07D235/06—Benzimidazoles; Hydrogenated benzimidazoles with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached in position 2
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- C07D235/02—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings condensed with carbocyclic rings or ring systems
- C07D235/04—Benzimidazoles; Hydrogenated benzimidazoles
- C07D235/06—Benzimidazoles; Hydrogenated benzimidazoles with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached in position 2
- C07D235/12—Radicals substituted by oxygen atoms
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- C07D249/00—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms
- C07D249/16—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms condensed with carbocyclic rings or ring systems
- C07D249/18—Benzotriazoles
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- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/06—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
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- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
- C07D403/06—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
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- C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
- C07D405/06—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
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- C07D405/14—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing three or more hetero rings
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- C07D413/06—Heterocyclic 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 linked by a carbon chain containing only aliphatic carbon atoms
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- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Pharmacology & Pharmacy (AREA)
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- Bioinformatics & Cheminformatics (AREA)
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- Immunology (AREA)
- Diabetes (AREA)
- Pulmonology (AREA)
- Dermatology (AREA)
- Cardiology (AREA)
- Heart & Thoracic Surgery (AREA)
- Ophthalmology & Optometry (AREA)
- Hematology (AREA)
- Vascular Medicine (AREA)
- Otolaryngology (AREA)
- Obesity (AREA)
- Endocrinology (AREA)
- Pain & Pain Management (AREA)
- Rheumatology (AREA)
- Biomedical Technology (AREA)
- Neurology (AREA)
- Neurosurgery (AREA)
- Urology & Nephrology (AREA)
- Communicable Diseases (AREA)
- Oncology (AREA)
- Child & Adolescent Psychology (AREA)
- Gastroenterology & Hepatology (AREA)
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Abstract
Composiciones farmacéuticas que contienen dichos compuestos. Reivindicacion 1: Un compuesto de formula (1) en la que R1 es arilo, heteroarilo o cicloalquilo C3-7 cada uno opcionalmente sustituido independientemente con 1 a 3 grupos sustituyentes seleccionados entre alquilo C1-3, hidroxi, halogeno, oxo, metoxi, amino donde el átomo de N está opcionalmente mono- o disustituido independientemente con un grupo metilo; o tiometilo donde el átomo de S está opcionalmente oxidado en un sulfoxido o sulfona; R2 es H o un halogeno; cada uno de A y B es independientemente CH o N; cada uno de C y E es independientemente un enlace o a -CH2-; D es -CR4R5-, donde R4 es -CF3 y R5 es -OH; y R3 es alquilo C1-6, cicloalquilo, cicloalquenilo, arilo, heteroarilo, heterociclilo, NR6R7, OR8 o SR9, cada uno opcionalmente sustituido independientemente con 1 a 3 grupos sustituyentes, donde cada grupo sustituyente de R3 es independientemente arilo, heteroarilo, heterociclilo, alquilo C1-5, alquenilo C1-5, cicloalquilo, cicloalquenilo, acilo, alcoxicarbonilo, alcanoiloxi C1-5, alcanoílo C1-5, aroílo, alcanoilamino C1-5, alquilaminocarbonilo, dialquilaminocarbonilo, aminocarboniloxi, alquilaminocarboniloxi C1-5, dialquilaminocarboniloxi C1-5, alcanoilamino C1-5, alcoxicarbonilamino C1-5, alquilsulfonilamino C1-5, aminosulfonilo, alquilaminosulfonilo C1-5, dialquilaminosulfonilo C1-5, alquiloxi C1-5, ariloxi, halogeno, hidroxi, oxo, ciano, trifluorometilo, nitro, carboxilo, aminocarbonilo, amino donde el átomo de N está opcionalmente mono- o disustituido independientemente con un alquilo C1-5 o alquiltio C1-5 donde el átomo de S está opcionalmente oxidado en un sulfoxido o sulfona; donde cada grupo sustituyente de R3 está opcionalmente sustituido independientemente con 1 a 3 sustituyentes seleccionados entre arilo, heteroarilo, heterociclilo, acilo, alquilo C1-5, alcanoiloxi C1-5, alcanoilo C1-5, alcanoilamino C1-5, alquilaminocarbonilo, dialquilaminocarbonilo, alquilsulfonilamino C1-5, aminosulfonilo, alquilaminosulfonilo C1-5, dialquilaminosulfonilo C1-5, alquiloxi C1-5, cicloalquilo C1-5, ariloxi, halogeno, hidroxi, oxo, ciano, trifluorometilo, nitro, aminocarbonilo, amino donde el átomo de N está opcionalmente mono- o disustituido independientemente con un alquilo C1-5 o alquiltio C1-5 donde el átomo de S está opcionalmente oxidado en un sulfoxido o sulfona; donde R6 es un H o alquilo C1-3, y cada uno de R7, R8 y R9 es independientemente alquilo C1-5, alquenilo C1-5, cicloalquilo, cicloalquenilo, arilo, heteroarilo o heterociclilo opcionalmente sustituido independientemente con 1 a 3 grupos sustituyentes, donde cada grupo sustituyente de R7, R8 y R9 es independientemente heteroarilo, heterociclilo, alquilo C1- 5, cicloalquilo, cicloalquenilo, acilo, alcoxicarbonilo, alcanoiloxi C1-5, alcanoílo C1-5, aroílo, alcanoilamino C1-5, alquilaminocarbonilo, dialquilaminocarbonilo, aminocarboniloxi, alquilaminocarboniloxi C1- 5, dialquilaminocarboniloxi C1-5, alcanoilamino C1-5, alcoxicarbonilamino C1-5, alquilsulfonilamino C1-5, aminosulfonilo, alquilaminosulfonilo C1-5, dialquilaminosulfonilo C1-5, alquiloxi C1-5, ariloxi, halogeno, hidroxi, oxo, ciano, trifluorometilo, nitro, aminocarbonilo, amino donde el átomo de N está opcionalmente mono- o disustituido independientemente con un alquilo C1-5 o alquiltio C1-5 donde el átomo de S está opcionalmente oxidado en un sulfoxido o sulfona; donde cada grupo sustituyente de R7, R8 y R9 está opcionalmente sustituido independientemente con 1 a 3 grupos sustituyentes seleccionados entre heteroarilo, heterociclilo, acilo, alquilo C1-5, alcanoilamino C1-5, alquilaminocarbonilo, dialquilaminocarbonilo, alquilsulfonilamino C1-5, aminosulfonilo, alquilaminosulfonilo C1-5, dialquilaminosulfonilo C1-5, alquiloxi C1-5, ariloxi, halogeno, hidroxi, oxo, ciano, trifluorometilo, nitro, aminocarbonilo, amino donde el átomo de N está opcionalmente mono- o disustituido independientemente con un alquilo C1-5 o alquiltio C1-5 donde el átomo de S está opcionalmente oxidado en un sulfoxido o sulfona; o un tautomero, profármaco, solvato o sal del mismo.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
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US68941205P | 2005-06-10 | 2005-06-10 |
Publications (1)
Publication Number | Publication Date |
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AR058006A1 true AR058006A1 (es) | 2008-01-23 |
Family
ID=37057165
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
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ARP060102414A AR058006A1 (es) | 2005-06-10 | 2006-06-09 | Mimeticos de glucocorticoides, composiciones farmaceiticas y usos de los mismos |
Country Status (17)
Country | Link |
---|---|
US (1) | US7622594B2 (es) |
EP (1) | EP1893588A1 (es) |
JP (1) | JP2008543780A (es) |
KR (1) | KR20080027828A (es) |
CN (1) | CN101193869B (es) |
AR (1) | AR058006A1 (es) |
AU (1) | AU2006257861A1 (es) |
BR (1) | BRPI0611620A2 (es) |
CA (1) | CA2610588A1 (es) |
IL (1) | IL187976A0 (es) |
MX (1) | MX2007014811A (es) |
NZ (1) | NZ564696A (es) |
PE (1) | PE20070112A1 (es) |
RU (1) | RU2007148225A (es) |
TW (1) | TW200716573A (es) |
WO (1) | WO2006135826A1 (es) |
ZA (1) | ZA200709430B (es) |
Families Citing this family (38)
Publication number | Priority date | Publication date | Assignee | Title |
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DE19856475A1 (de) | 1998-11-27 | 2000-05-31 | Schering Ag | Nichtsteroidale Entzündungshemmer |
US6960581B2 (en) * | 2002-01-14 | 2005-11-01 | Boehringer Ingelheim Pharmaceuticals, Inc. | Glucocorticoid mimetics, methods of making them, pharmaceutical formulations, and uses thereof |
PT1490062E (pt) | 2002-03-26 | 2008-01-30 | Boehringer Ingelheim Pharma | Miméticos de glucocorticóides, métodos para a sua preparação, composições farmacêuticas e suas utilizações |
CA2477764A1 (en) * | 2002-03-26 | 2003-10-09 | Boehringer Ingelheim Pharmaceuticals, Inc. | Glucocorticoid mimetics, methods of making them, pharmaceutical compositions, and uses thereof |
CA2512257A1 (en) * | 2003-01-03 | 2004-07-29 | Boehringer Ingelheim Pharmaceuticals, Inc. | 1-propanol and 1-propylamine derivatives and their use as glucocorticoid ligands |
UY28526A1 (es) * | 2003-09-24 | 2005-04-29 | Boehringer Ingelheim Pharma | Miméticos de glucocorticoides, métodos de preparación composiciones farmacéuticas y usos de los mismos |
TW200523503A (en) * | 2003-09-29 | 2005-07-16 | Sony Corp | Backlight, light guiding plate, method for manufacturing diffusion plate and light guiding plate, and liquid crystal display device |
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2006
- 2006-06-08 RU RU2007148225/04A patent/RU2007148225A/ru not_active Application Discontinuation
- 2006-06-08 BR BRPI0611620-5A patent/BRPI0611620A2/pt not_active IP Right Cessation
- 2006-06-08 KR KR1020087000662A patent/KR20080027828A/ko not_active Application Discontinuation
- 2006-06-08 PE PE2006000643A patent/PE20070112A1/es not_active Application Discontinuation
- 2006-06-08 WO PCT/US2006/022651 patent/WO2006135826A1/en active Application Filing
- 2006-06-08 AU AU2006257861A patent/AU2006257861A1/en not_active Abandoned
- 2006-06-08 US US11/449,231 patent/US7622594B2/en active Active
- 2006-06-08 MX MX2007014811A patent/MX2007014811A/es active IP Right Grant
- 2006-06-08 EP EP06772813A patent/EP1893588A1/en not_active Withdrawn
- 2006-06-08 NZ NZ564696A patent/NZ564696A/xx unknown
- 2006-06-08 CA CA002610588A patent/CA2610588A1/en not_active Abandoned
- 2006-06-08 CN CN2006800205382A patent/CN101193869B/zh not_active Expired - Fee Related
- 2006-06-08 JP JP2008515997A patent/JP2008543780A/ja active Pending
- 2006-06-09 TW TW095120658A patent/TW200716573A/zh unknown
- 2006-06-09 AR ARP060102414A patent/AR058006A1/es not_active Application Discontinuation
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2007
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EP1893588A1 (en) | 2008-03-05 |
WO2006135826A1 (en) | 2006-12-21 |
KR20080027828A (ko) | 2008-03-28 |
NZ564696A (en) | 2011-05-27 |
US7622594B2 (en) | 2009-11-24 |
BRPI0611620A2 (pt) | 2009-01-13 |
RU2007148225A (ru) | 2009-07-20 |
AU2006257861A1 (en) | 2006-12-21 |
CA2610588A1 (en) | 2006-12-21 |
PE20070112A1 (es) | 2007-03-08 |
US20070060633A1 (en) | 2007-03-15 |
CN101193869A (zh) | 2008-06-04 |
MX2007014811A (es) | 2008-02-14 |
TW200716573A (en) | 2007-05-01 |
IL187976A0 (en) | 2008-03-20 |
JP2008543780A (ja) | 2008-12-04 |
ZA200709430B (en) | 2008-11-26 |
CN101193869B (zh) | 2011-03-02 |
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