AR048315A1 - Compuestos heterociclicos inhibidores de la produccion de citocinas; composiciones farmaceuticas que los contienen y su uso en el tratamiento de enfermedades inflamatorias y oncologicas. - Google Patents
Compuestos heterociclicos inhibidores de la produccion de citocinas; composiciones farmaceuticas que los contienen y su uso en el tratamiento de enfermedades inflamatorias y oncologicas.Info
- Publication number
- AR048315A1 AR048315A1 ARP050100899A ARP050100899A AR048315A1 AR 048315 A1 AR048315 A1 AR 048315A1 AR P050100899 A ARP050100899 A AR P050100899A AR P050100899 A ARP050100899 A AR P050100899A AR 048315 A1 AR048315 A1 AR 048315A1
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- Prior art keywords
- alkyl
- optionally
- alkoxy
- substituted
- cr7r8
- Prior art date
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- C07D417/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
- C07D417/04—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings directly linked by a ring-member-to-ring-member bond
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- A61P11/06—Antiasthmatics
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- A61P13/00—Drugs for disorders of the urinary system
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- A61P17/00—Drugs for dermatological disorders
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- A61P17/00—Drugs for dermatological disorders
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- A61P19/00—Drugs for skeletal disorders
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- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- 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
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- 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
- A61P25/02—Drugs for disorders of the nervous system for peripheral neuropathies
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- 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
- A61P25/28—Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
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- A—HUMAN NECESSITIES
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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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- A—HUMAN NECESSITIES
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- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
- 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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- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/04—Antibacterial agents
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- A61P35/00—Antineoplastic agents
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- A61P37/00—Drugs for immunological or allergic disorders
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- A61P37/02—Immunomodulators
- A61P37/06—Immunosuppressants, e.g. drugs for graft rejection
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- A61P39/02—Antidotes
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- A61P9/00—Drugs for disorders of the cardiovascular system
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- 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
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- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- 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
- C07D401/04—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 directly linked by a ring-member-to-ring-member bond
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- 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
- C07D401/14—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 three or more hetero rings
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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
- C07D403/04—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 directly linked by a ring-member-to-ring-member bond
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- C07D405/00—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
- 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
- C07D405/04—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 directly linked by a ring-member-to-ring-member bond
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- 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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- C07—ORGANIC CHEMISTRY
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- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
- C07D487/04—Ortho-condensed systems
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- C07—ORGANIC CHEMISTRY
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- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
- C07D487/10—Spiro-condensed systems
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- C07D513/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00 in which the condensed system contains two hetero rings
- C07D513/04—Ortho-condensed systems
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Abstract
Compuestos descriptos de la formula (1), que inhiben la produccion de citocinas implicadas en procesos inflamatorios y que, por lo tanto, son utiles para tratar enfermedades y afecciones patologicas que implican inflamacion, como la enfermedad inflamatoria cronica. También se describen composiciones farmacéuticas que comprenden estos compuestos utilizables para el tratamiento de enfermedades oncologicas además de las ya mencionadas. Reivindicacion 1: Un compuesto de la formula (1), en el que: Ar1 se selecciona entre i), ii) y iii) a continuacion: i) un carbociclo sustituido con R1, R2 y Rx; ii) una formula (2), en el que uno de E o F es nitrogeno y el otro es carbono, R1 está covalentemente unido o bien a E o F y, cuando nitrogeno es N-R1, no está presente el enlace doble entre E y F; iii) una formula (3) en el que c es un anillo benzo condensado al anillo d que es un anillo heterocíclico de 5-7 miembros opcionalmente sustituido con un grupo oxo (=O), y uno a dos grupos R, siendo cada uno independientemente H o alquilo C1-3; R1 se selecciona entre hidrogeno, NO2, -N(Rc)2, J-C(O)-N(Rc)-, J-S(O)m-N(Rc)-, alquiloC1-6S(O)m-; o R1 se selecciona entre alquilo C1-6, cicloalquilo C3-7, alcoxilo C1-5 o cicloalcoxilo C3-7, alquiltiol C1-5 o cicicloalquiltiol C3-7, acilo C1-5, alcoxicarbonilo C1-5, aciloxi C1-5, acilamino C1-5, alquenilo C2-5, alquinilo C2-5, heterociclo, heterocicloalquilo C1-6, heteroarilo, heteroarilalquilo C1-6 y nitrilo; cada uno de los anteriormente mencionados, cuando es posible, está opcionalmente parcial o totalmente halogenado o está opcionalmente sustituido además con alquilsulfonilamino, aminocarboxilo, alcoxilo, amino, alquilamino, dialquilamino, hidroxilo, oxo, nitro o nitrilo; R2 se selecciona entre: hidrogeno, halogeno, nitrilo, alquiloC1-5S(O)m-, ariloS(O)m, J-O-C(O)-O-, N(Rc)2-C(O)-(CH2)n-, acetilo C1-6, aroilo, alcoxicarbonilo C1-6, alquilo C1-6, cicloalquilo C3-7, alcoxi C1-6, cicloalcoxi C3-5, alquilo C1- 5alcoxiC1-5, hidroxi, hidroxialquilo C1-5 y amino opcionalmente mono o di-sustituido C1-5, arilo o arilalquilo C1-5; cada uno de los ya mencionados, cuando es posible, está opcionalmente parcial o totalmente halogenado u opcionalmente también sustituido con alquilo C1-3, alquilsulfonilamino, alcoxilo, amino, alquilamino, dialquilamino, hidroxilo, oxo, nitro o nitrilo; cada Rx se selecciona entre alquilo C1-6 o cicloalquilo C3-7, estando cada uno opcionalmente sustituido con alquilo C1-3 y opcionalmente parcial o totalmente halogenado, acilo C1-4, aroilo, alcoxi C1-4, alquiloC1-5S(O)m-, en los que cada uno puede estar opcionalmente parcial o totalmente halogenado, halogeno, alcoxicarbonilo C1-6, carbociclosulfonilo; cada Rc es indepedientemente hidrogeno o alquilo C1-5; D, A y B del resto de formula (4) de la formula (1) se seleccionan cada uno independientemente entre N o CH, en los que el átomo de hidrogeno está opcionalmente reemplazado con R6; Het es un anillo de heteroarilo o heterocíclico, en el que Het está opcionalmente sustituido con uno a tres R5; m es 0, 1 o 2; J se selecciona entre alquilo C1-10 y cicloalquilo C3-7, cada uno opcionalmente sustituido con Rb; R3, R4, R6, R7 y R8 se seleccionan cada uno independientemente entre hidrogeno, halogeno, alquilo C1-5, alcoxi C1-5, alquiloC1-5alcoxiC1-5, hidroxi, hidroxialquilo C1-5 o amino opcionalmente mono o di-sustituido con alquilo C1-5, arilo o arilalquilo C1-5; R5 es: Ra, -O-Ra, -S(O)m-Ra, -N(Ra)2, -C(O)-Ra, -NH(CR7R8)n-Ra, N(Ra)2-(CH2)1-2-, -(CR7R8)n-Ra, -O(CR7R8)n-Ra, -C(O)-O(CR7R8)n-Ra, -C(O)(CR7R8)n-Ra, -C(O)C(O)Ra, -C(O)C(O)ORa, -C(O)NHRa o -C(O)NH(CR7R8)n-, cada uno opcionalmente sustituido con alquilo C1-3, halogeno o hidroxi; en los que n es 1-5; o R5 es arilo, heteroarilo o heterociclilo, cada uno opcionalmente sustituido con Ra; Ra y Rb se seleccionan cada uno independientemente entre hidrogeno, alquilo C1-6, hidroxialquilo C1-5, alquenilo C2-5, alquinilo C2-5, carbociclo, carbocicloalquilo C0-2, arilo, heterociclo, heteroarilo, alcoxi C1-5, alquiltio C1-5, amino, alquilamino C1-5, dialquilamino C1-5, arilamino, arilalquilamino C1-5, diarilamino, acilo C1-5, alcoxicarbonilo C1-5, aciloxi C1-5, acilamino C1-5, en los que cada uno de los ya mencionados está opcionalmente parcial o totalmente halogenado, o Ra y Rb se seleccionan entre alquilsulfonilamino C1-5, hidroxi, oxo, halogeno, CF3, -CH2-CF3, nitro y nitrilo, en los que cada carbociclo, heterociclo o heteroarilo C1-3, halogeno o hidroxi; y X es O o S; o sus sales farmacéuticamente aceptables.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US55144504P | 2004-03-09 | 2004-03-09 |
Publications (1)
Publication Number | Publication Date |
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AR048315A1 true AR048315A1 (es) | 2006-04-19 |
Family
ID=34962594
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
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ARP050100899A Pending AR048315A1 (es) | 2004-03-09 | 2005-03-09 | Compuestos heterociclicos inhibidores de la produccion de citocinas; composiciones farmaceuticas que los contienen y su uso en el tratamiento de enfermedades inflamatorias y oncologicas. |
Country Status (30)
Country | Link |
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US (2) | US7214802B2 (es) |
EP (2) | EP1887003A1 (es) |
JP (1) | JP4850824B2 (es) |
KR (1) | KR20060129077A (es) |
CN (1) | CN1930144A (es) |
AR (1) | AR048315A1 (es) |
AT (1) | ATE432273T1 (es) |
AU (1) | AU2005223738B2 (es) |
BR (1) | BRPI0508561A (es) |
CA (1) | CA2557856C (es) |
CY (1) | CY1109333T1 (es) |
DE (1) | DE602005014621D1 (es) |
DK (1) | DK1725544T3 (es) |
EA (1) | EA011634B1 (es) |
EC (1) | ECSP066833A (es) |
ES (1) | ES2327940T3 (es) |
HR (1) | HRP20090334T1 (es) |
IL (1) | IL177937A0 (es) |
MY (1) | MY143000A (es) |
NO (1) | NO20064120L (es) |
NZ (1) | NZ550148A (es) |
PE (1) | PE20051146A1 (es) |
PL (1) | PL1725544T3 (es) |
PT (1) | PT1725544E (es) |
RS (1) | RS50796B (es) |
SI (1) | SI1725544T1 (es) |
TW (1) | TW200602313A (es) |
UA (1) | UA85702C2 (es) |
WO (1) | WO2005090333A1 (es) |
ZA (1) | ZA200606177B (es) |
Families Citing this family (55)
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US7858804B2 (en) | 2006-04-18 | 2010-12-28 | Boehringer Ingelheim International Gmbh | Process for making cytokine inhibiting compounds containing 4- and 5-imidazolyl rings and the intermediates thereof |
EP2041116A1 (de) * | 2006-07-07 | 2009-04-01 | Boehringer Ingelheim International GmbH | Phenyl substituierte heteroaryl-derivate und deren verwendung als antitumormittel |
EP2090570B1 (en) | 2006-09-05 | 2011-11-09 | Kyowa Hakko Kirin Co., Ltd. | Imidazole derivative |
WO2009003998A2 (en) * | 2007-07-02 | 2009-01-08 | Boehringer Ingelheim International Gmbh | Antiproliferative compounds based on 5-membered heterocycles |
CL2008001943A1 (es) * | 2007-07-02 | 2009-09-11 | Boehringer Ingelheim Int | Compuestos derivados de fenil-triazol, inhibidores de enzimas de señales especificas que participan del control de la proliferacion celular; composicion farmaceutica que comprende a dichos compuestos; y su uso para tratar cancer, infecciones, enfermedades inflamatorias y autoinmunes. |
US8278340B2 (en) | 2007-11-27 | 2012-10-02 | North Carolina State University | Inhibition of biofilms in plants with imidazole derivatives |
US9005643B2 (en) | 2008-04-04 | 2015-04-14 | North Carolina State University | Inhibition of bacterial biofilms with imidazole-phenyl derivatives |
WO2009131654A2 (en) | 2008-04-21 | 2009-10-29 | North Carolina State University | Inhibition and dispersion of bacterial biofilms with imidazole-triazole derivatives |
EP2324007B1 (en) * | 2008-09-02 | 2012-08-15 | NeuroSearch A/S | Triazole derivatives and their use as nicotinic acetylcholine receptor modulators |
TW201014860A (en) | 2008-09-08 | 2010-04-16 | Boehringer Ingelheim Int | New chemical compounds |
EA201100564A1 (ru) * | 2008-09-29 | 2011-12-30 | Бёрингер Ингельхайм Интернациональ Гмбх | Антипролиферативные соединения |
US9625475B2 (en) | 2008-09-29 | 2017-04-18 | Abbvie Inc. | Indole and indoline derivatives and methods of use thereof |
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