AR036152A1 - Compuestos antiinflamatorios de triazolopiridinas, uso en la preparacion de medicamentos y composicion farmaceutica - Google Patents
Compuestos antiinflamatorios de triazolopiridinas, uso en la preparacion de medicamentos y composicion farmaceuticaInfo
- Publication number
- AR036152A1 AR036152A1 ARP020100826A ARP020100826A AR036152A1 AR 036152 A1 AR036152 A1 AR 036152A1 AR P020100826 A ARP020100826 A AR P020100826A AR P020100826 A ARP020100826 A AR P020100826A AR 036152 A1 AR036152 A1 AR 036152A1
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- Prior art keywords
- alkyl
- phenyl
- heterocyclyl
- cycloalkyl
- heteroaryl
- Prior art date
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- 230000003110 anti-inflammatory effect Effects 0.000 title 1
- 150000001875 compounds Chemical class 0.000 title 1
- 239000003814 drug Substances 0.000 title 1
- 239000008194 pharmaceutical composition Substances 0.000 title 1
- 125000000217 alkyl group Chemical group 0.000 abstract 37
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 abstract 31
- 125000000623 heterocyclic group Chemical group 0.000 abstract 25
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 24
- 125000001072 heteroaryl group Chemical group 0.000 abstract 21
- 125000006376 (C3-C10) cycloalkyl group Chemical group 0.000 abstract 14
- -1 C1-6 perhaloalkyl Chemical group 0.000 abstract 11
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 abstract 11
- 125000004191 (C1-C6) alkoxy group Chemical group 0.000 abstract 9
- 229910052739 hydrogen Inorganic materials 0.000 abstract 9
- 239000001257 hydrogen Substances 0.000 abstract 9
- 125000004435 hydrogen atom Chemical class [H]* 0.000 abstract 9
- 125000005843 halogen group Chemical group 0.000 abstract 8
- 125000001424 substituent group Chemical group 0.000 abstract 8
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 abstract 7
- 125000003601 C2-C6 alkynyl group Chemical group 0.000 abstract 6
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 6
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 abstract 6
- GOJUJUVQIVIZAV-UHFFFAOYSA-N 2-amino-4,6-dichloropyrimidine-5-carbaldehyde Chemical group NC1=NC(Cl)=C(C=O)C(Cl)=N1 GOJUJUVQIVIZAV-UHFFFAOYSA-N 0.000 abstract 5
- 125000000753 cycloalkyl group Chemical group 0.000 abstract 5
- JCXJVPUVTGWSNB-UHFFFAOYSA-N Nitrogen dioxide Chemical compound O=[N]=O JCXJVPUVTGWSNB-UHFFFAOYSA-N 0.000 abstract 3
- 125000002837 carbocyclic group Chemical group 0.000 abstract 3
- 229910052799 carbon Inorganic materials 0.000 abstract 3
- 125000004432 carbon atom Chemical group C* 0.000 abstract 3
- 125000004093 cyano group Chemical group *C#N 0.000 abstract 3
- 125000004890 (C1-C6) alkylamino group Chemical group 0.000 abstract 2
- 101001043818 Mus musculus Interleukin-31 receptor subunit alpha Proteins 0.000 abstract 2
- 125000002485 formyl group Chemical group [H]C(*)=O 0.000 abstract 2
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 abstract 2
- 125000006163 5-membered heteroaryl group Chemical group 0.000 abstract 1
- 101100495911 Arabidopsis thaliana CHR10 gene Proteins 0.000 abstract 1
- 229920001774 Perfluoroether Polymers 0.000 abstract 1
- 125000000304 alkynyl group Chemical group 0.000 abstract 1
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 abstract 1
- 125000005842 heteroatom Chemical group 0.000 abstract 1
- 229910052757 nitrogen Inorganic materials 0.000 abstract 1
- 125000004433 nitrogen atom Chemical group N* 0.000 abstract 1
- 125000005010 perfluoroalkyl group Chemical group 0.000 abstract 1
- 150000008523 triazolopyridines Chemical class 0.000 abstract 1
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- 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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- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
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- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P13/00—Drugs for disorders of the urinary system
- A61P13/02—Drugs for disorders of the urinary system of urine or of the urinary tract, e.g. urine acidifiers
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- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P19/00—Drugs for skeletal disorders
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- A61P19/10—Drugs for skeletal disorders for bone diseases, e.g. rachitism, Paget's disease for osteoporosis
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- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
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- A61P21/00—Drugs for disorders of the muscular or neuromuscular system
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- A61P25/00—Drugs for disorders of the nervous system
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- 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
- A61P25/14—Drugs for disorders of the nervous system for treating abnormal movements, e.g. chorea, dyskinesia
- A61P25/16—Anti-Parkinson drugs
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- A—HUMAN NECESSITIES
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- A61P25/00—Drugs for disorders of the nervous system
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- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- 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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- A61P3/00—Drugs for disorders of the metabolism
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Abstract
Triazolopiridinas de la fórmula (1) en la que Het es un heteroarilo de 5 miembros opcionalmente sustituido que, tomado conjuntamente con (R3)s-fenilo, se selecciona del grupo de fórmulas (2); cada R1 se selecciona independientemente de hidrógeno, alquilo C1-6, fenilo, heteroarilo C1-10, heterociclilo C1-10 y cicloalquilo C3-10; pudiendo estar opcionalmente sustituido cada uno de los anteriormente citados sustituyentes R1 alquilo C1-6, fenilo, heteroarilo C1-10, heterociclilo C1-10 y cicloalquilo C3-10 con uno a cuatro restos seleccionados independientemente del grupo constituido por halo, alquilo C1-6, alquenilo C2-6, alquinilo C2-6, perhaloalquilo C1-6, fenilo, heteroarilo C1-10, heterociclilo C1-10, cicloalquilo C3-10, hidroxi, alcoxi C1-6, perhaloalcoxi C1-6, fenoxi, heteroaril C1-10-O-, heterociclil C1-10-O-, cicloalquil C3-10-O-, alquil C1-6-S-, alquil C1-6-SO2-, alquil C1-6-NH-SO2, -NO2, amino, alquil C1-6-amino, [alquil C1-6]2-amino, alquil C1-6-SO2-NH, alquil C1-6-(C=O)-NH-, alquil C1-6-(C=O)-[alquil C1-6-N]-, fenil-(C=O)-NH-, fenil-(C=O)-[alquil C1-6-N]-, -CN, alquil C1-6-(C=O)-, fenil-(C=O)-, heteroaril C1-10-(C=O)-, heterociclil C1-10-(C=O)-, cicloalquil C3-10-(C=O)-, HO-(C=O)-, alquil C1-6-O-(C=O)-, H2N(C=O)-, alquil C1-6-NH-(C=O)-, [alquil C1-6]2-N-(C=O)-, fenil-NH-(C=O)-, fenil-[alquil C1-6-N]-(C=O)-, heteroaril C1-10-NH-(C=O)-, heterociclil C1-10-NH-(C=O)-, cicloalquil C3-10-NH-(C=O)-, alquil C1-6-(C=O)-O- y fenil-(C=O)-; pudiendo tomarse dos grupos R1 alquilo C1-6 conjuntamente con el átomo de nitrógeno al que están unidos para formar un anillo heterocíclico o heteroarílico de cinco a seis miembros; R2 se selecciona del grupo constituido por hidrógeno, -CN, alquilo C1-6, alquenilo C2-6, alquinilo C2-6, cicloalquilo C3-10, fenilo, heteroarilo C1-10, heterociclilo C1-10 y (R1)2-N-; pudiendo estar opcionalmente sustituido cada uno de los sustituyentes anteriormente citados alquilo C1-6, cicloalquilo C3-10, fenilo, heteroarilo C1-10 y heterociclilo C1-10 de forma independiente con uno a cuatro restos independientemente seleccionados del grupo constituido por halo, alquilo C1-6, alquenilo C2-6, alquinilo C2-6, perhaloalquilo C1-6, fenilo, cicloalquilo C3-10, heteroarilo C1-10, heterociclilo C1-10, formilo, -CN, alquil C1-6-(C=O)-, fenil-(C=O)-, HO-(C=O)-, alquil C1-6-O-(C=O)-, alquil C1-6-NH-(C=O)-, [alquil C1-6]2-N-(C=O)-, fenil-NH-(C=O)-, fenil-[alquil C1-6-N]-(C=O)-, NO2, amino, alquil C1-6-amino, [alquil C1-6]2-amino, alquil C1-6-(C=O)-NH-, alquil C1-6-(C=O)-[alquil C1-6-N]-, fenil-(C=O)-NH-, fenil-(C=O)-[alquil C1-6-N]-, H2N-(C=O)-NH-, alquil C1-6-HN-(C=O)-NH-, [alquil C1-6]2-N-(C=O)-NH-, alquil C1-6-NH-(C=O)-[alquil C1-6-N]-, [alquil C1-6]2-N-(C=O)-[alquil C1-6-N]-, fenil-NH-(C=O)-NH-, (fenil)2-N-(C=O)-NH-, fenil-NH-(C=O)-[alquil C1-6-N], (fenil)2-NH-(C=O)-[alquil C1-6-N]-, alquil C1-6-O-(C=O)-NH-, alquil C1-6-O-(C=O)-[alquil C1-6-N]-, fenil-O-(C=O)-NH-, fenil-O-(C=O)-[alquil C1-6-N]-, alquil C1-6-SO2-NH-, fenil-SO2NH-, alquil C1-6-SO2-, fenil-SO2-, hidroxi, alcoxi C1-6, perhaloalcoxi C1-6, fenoxi, alquil C1-6-(C=O)-O-, fenil-(C=O)-O-, H2N(C=O)-O, alquil C1-6-HN-(C=O)-O-, [alquil C1-6]2-N-(C=O)-O-, fenil-NH-(C=O)-O-, (fenil)2-N-(C=O)-O-; pudiendo, cuando el citado R2 fenilo contiene dos sustituyentes adyacentes, tomarse opcionalmente dichos sustituyentes conjuntamente con el átomo de carbono al que están unidos para formar un anillo carbocíclico o heterocíclico de cinco a seis miembros; pudiendo estar opcionalmente sustituido cada uno de los citados restos que contienen un fenilo alternativo con uno o dos radicales seleccionados independientemente del grupo constituido por alquilo C1-6, halo, alcoxi C1-6, perhaloalquilo C1-6 y perhaloalcoxi C1-6; cada R3 se selecciona independientemente del grupo constituido por halo, alquilo C1-6, alquenilo C2-6, alquinilo C2-6, perhaloalquilo C1-6, fenilo, heteroarilo C1-10, heterociclilo C1-10, cicloalquilo C3-10, hidroxi, alcoxi C1-6, perhaloalcoxi C1-6, fenoxi, heteroaril C1-10-O-, heterociclil C1-10-O-, cicloalquil C3-10-O-, alquil C1-6-S-, alquil C1-6-SO2-, alquil C1-6-NH-SO2, -NO2, amino, alquil C1-6-amino, [alquil C1-6]2-amino, alquil C1-6-SO2-NH, alquil C1-6-(C=O)-NH-, alquil C1-6-(C=O)-[alquil C1-6-N]-, fenil-(C=O)-NH-, fenil-(C=O)-[alquil C1-6-N]-, -CN, alquil C1-6-(C=O)-, fenil-(C=O)-, heteroaril C1-10-(C=O)-, heterociclil C1-10-(C=O)-, cicloalquil C3-10-(C=O)-, HO-(C=O)-, alquil C1-6-O-(C=O)-, H2N(C=O)-, alquil C1-6-NH-(C=O)-, [alquil C1-6]2-N-(C=O)-, fenil-NH-(C=O)-, fenil-[alquil C1-6-N]-(C=O)-, heteroaril C1-10-NH-(C=O)-, heterociclil C1-10-NH-(C=O)-, cicloalquil C3-10-NH-(C=O)- y alquil C1-6-(C=O)-O-; pudiendo tomarse opcionalmente dos sustituyentes R3 adyacentes, conjuntamente con los átomos de carbono a los que están unidos, para formar un anillo carbocíclico o heterocíclico de cinco a seis miembros; s es un número entero de cero a cinco; R4 y R6 se seleccionan cada uno independientemente del grupo constituido por hidrógeno, halo o R9-B-(CH2)n-; n es un número entero de cero a seis; cada B es independientemente un enlace, -(CHR10)-, -O-, -S-, -(SO2)-, -(C=O)-, -O-(C=O)-, -(C=O)-O-, -(C=O)-NR10-, -(R10-N)-, -(R10-N)-SO2-, -(R10-N)-(C=O)-, -SO2-(NR10)-, -(R10N)-(C=O)-(NR11)-, -(O)-(C=O)-(NR10)- ó -(R10N)-(C=O)-O-; R5 y R7 se seleccionan cada uno independientemente del grupo constituido por hidrógeno, R14-(CR15H)p-, fenilo, heteroarilo C1-10, heterociclilo C1-10, cicloalquilo C3-10, alquil C1-6-(SO2)-, fenil-(SO2)-, H2N-(SO2)-, alquil C1-6-NH-(SO2)-, [alquil C1-6]2N-(SO2)-, fenil-NH-(SO2)-, (fenil)2N-(SO2)-, R16-alquil C1-6-(C=O)-, fenil-(C=O)-, heteroaril C1-10-(C=O)-, heterociclil C1-10-(C=O)-, cicloalquil C3-10-(C=O)-, alquil C1-6-O-(C=O)-, heterociclil C1-10-O-(C=O)-, cicloalquil C3-10-O-(C=O)-, H2N-(C=O)-, alquil C1-6-NH-(C=O)-, fenil-NH-(C=O)-, heteroaril C1-10-NH-(C=O)-, heterociclil C1-10-NH-(C=O)-, cicloalquil C3-10-NH-(C=O)-, [alquil C1-6]2N-(C=O)-, (fenil)2N-(C=O)-, fenil-[alquil C1-6-N]-(C=O)-, heteroaril C1-10-[alquil C1-6-N]-(C=O)-, heterociclil C1-10-[alquil C1-6-N]-(C=O)- y cicloalquil C3-10-[alquil C1-6-N]-(C=O)-; pudiendo estar cada uno de los anteriormente citados sustituyentes R5 y R7 fenilo, heterociclilo, heteroarilo o cicloalquilo opcionalmente sustituido de forma independiente con uno a cuatro restos seleccionados independientemente del grupo constituido por halo, R16-alquilo C1-6, alquenilo C2-6, alquinilo C2-6, perhaloalquilo C1-6, cicloalquilo C3-10, fenilo, bencilo, heterociclilo C1-10, heteroarilo C1-10, alquil C1-6-SO2-, formilo, -CN, alquil C1-6-(C=O)-, cicloalquil C3-10-(C=O)-, fenil-(C=O)-, heterociclil C1-10-(C=O)-, heteroaril C1-10-(C=O)-, HO-(C=O)-, alquil C1-6-O-(C=O)-, cicloalquil C3-10-O-(C=O)-, heterociclil C1-10-O-(C=O)-, alquil C1-6-NH-(C=O)-, cicloalquil C3-10-NH-(C=O)-, fenil-NH-(C=O)-, heterociclil C1-10-NH-(C=O)-, heteroaril C1-10-NH-(C=O)-, [alquil C1-6]2-N-(C=O)-, fenil-[alquil C1-6-N]-(C=O)-, hidroxi, alcoxi C1-6, perhaloalcoxi C1-6, cicloalquil C3-10-O-, fenoxi, heterociclil C1-10-O-, heteroaril C1-10-O-, alquil C1-6-(C=O)-O-, cicloalquil C3-10-(C=O)-O-, fenil-(C=O)-O-, heterociclil C1-10-(C=O)-O-, heteroaril C1-10-(C=O)-O-, NO2, amino, alquil C1-6-amino, [alquil C1-6]2-amino, formamidilo, alquil C1-6-(C=O)-NH-, cicloalquil C3-10-(C=O)-NH-, fenil-(C=O)-NH-, heterociclil C1-10-(C=O)-NH-, heteroaril C1-10-(C=O)-NH-, alquil C1-6-(C=O)-[alquil C1-6-N]-, fenil-(C=O)-[alquil C1-6-N]-, alquil C1-6-SO2-NH-, cicloalquil C3-10-SO2-NH-, fenil-SO2NH-, heterociclil C1-10-SO2NH- y heteroaril C1-10-SO2NH-; pudiendo estar opcionalmente sustituidos cada uno de los citados restos fenilo y heteroarilo con uno o dos radicales seleccionados independientemente de halo, alquilo C1-6, alcoxi C1-6, perfluoroalquilo C1-6 y perfluoroalcoxi C1-6; p es un número entero de uno a seis; R9 se selecciona del grupo constituido por hidrógeno, -CF3, -CN, R13-(R12CH)m-, fenilo, heterociclilo C1-10, heteroarilo C1-10 y cicloalquilo C3-10; pudiendo estar opcionalmente sustituidos cada uno de los anteriormente citados sustituyentes R9 fenilo, heteroarilo C1-10, heterociclilo C1-10 y cicloalquilo C3-10 con uno a cuatro restos seleccionados independientemente del grupo constituido por halo, alquilo C1-6, alquenilo C2-6, alquinilo C2-6, perhaloalquilo C1-6, fenilo, heteroarilo C1-10, heterociclilo C1-10, cicloalquilo C3-10, hidroxi, alcoxi C1-6, perhaloalcoxi C1-6, fenoxi, heteroaril C1-10-O-, heterociclil C1-10-O-, cicloalquil C3-10-O-, alquil C1-6-S-, alquil C1-6-SO2-, alquil C1-6-NH-SO2-, NO2, amino, alquil C1-6-amino, [alquil C1-6]2-amino, alquil C1-6-SO2-NH-, alquil C1-6-(C=O)-NH-, alquil C1-6-(C=O)-[alquil C1-6-N]-, fenil-(C=O)-NH-, fenil-(C=O)-[alquil C1-6-N]-, -CN, alquil C1-6-(C=O)-, fenil-(C=O)-, heteroaril C1-10-(C=O)-, heterociclil C1-10-(C=O)-, cicloalquil C3-10-(C=O)-, HO-(C=O)-, alquil C1-6-O-(C=O)-, H2N(C=O)-, alquil C1-6-NH-(C=O)-, [alquil C1-6]2-N-(C=O)-, fenil-NH-(C=O)-, fenil-[alquil C1-6-N]-(C=O)-, heteroaril C1-10-NH-(C=O)-, heterociclil C1-10-NH-(C=O)-, cicloalquil C3-10-NH-(C=O)-, alquil C1-6-(C=O)-O- y fenil-(C=O)-O-; pudiendo tomarse opcionalmente dos sustituyentes R9 adyacentes de los citados fenilo, heteroarilo C1-10, heterociclilo C1-10 y cicloalquilo C3-10, conjuntamente con el átomo de carbono o heteroátomo al que están unidos, para formar un anillo carbocíclico o heterocíclico de cinco o seis miembros; m es un número entero de uno a seis; R10 es hidrógeno, alquil C1-6-SO2- ó alquilo C1-6; R11 es hidrógeno o alquilo C1-6; cada R12 se selecciona independientemente del grupo constituido por hidrógeno, amino, alcoxi C1-6 y alquilo C1-6; R13 se selecciona del grupo constituido por hidrógeno, alquilo C1-6, alquenilo C2-6, alquinilo C2-6, fenilo, heteroarilo C1-10, heterociclilo C1-10, cicloalquilo C3-10, hidroxi, alcoxi C1-6, perhaloalcoxi C1-6, fenoxi, heteroaril C1-10-O-, heterociclil C1-10-O-, cicloalquil C3-10-O-, alquil C1-6-S-, alquil C1-6-SO2-, alquil C1-6-NH-SO2-, NO2, amino, alquil C1-6-amino, [alquil
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Families Citing this family (79)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6372206B1 (en) * | 1989-03-02 | 2002-04-16 | University Of Florida | Orally-administered interferon-TAU compositions and methods |
| US20040077605A1 (en) * | 2001-06-20 | 2004-04-22 | Salvati Mark E. | Fused heterocyclic succinimide compounds and analogs thereof, modulators of nuclear hormone receptor function |
| EP1854798A3 (en) * | 2000-09-19 | 2007-11-28 | Bristol-Myers Squibb Company | Fused heterocyclic succinimide compounds and analogs thereof, modulators of nuclear hormone receptor function |
| US20040087548A1 (en) | 2001-02-27 | 2004-05-06 | Salvati Mark E. | Fused cyclic succinimide compounds and analogs thereof, modulators of nuclear hormone receptor function |
| GB0124941D0 (en) * | 2001-10-17 | 2001-12-05 | Glaxo Group Ltd | Chemical compounds |
| GB0124936D0 (en) * | 2001-10-17 | 2001-12-05 | Glaxo Group Ltd | Chemical compounds |
| GB0124939D0 (en) * | 2001-10-17 | 2001-12-05 | Glaxo Group Ltd | Chemical compounds |
| GB0124934D0 (en) | 2001-10-17 | 2001-12-05 | Glaxo Group Ltd | Chemical compounds |
| GB0124933D0 (en) * | 2001-10-17 | 2001-12-05 | Glaxo Group Ltd | Chemical compounds |
| GB0124938D0 (en) * | 2001-10-17 | 2001-12-05 | Glaxo Group Ltd | Chemical compounds |
| GB0124931D0 (en) * | 2001-10-17 | 2001-12-05 | Glaxo Group Ltd | Chemical compounds |
| AU2002364082A1 (en) * | 2001-12-19 | 2003-07-09 | Bristol-Myers Squibb Company | Fused heterocyclic compounds and analogs thereof: modulators of nuclear hormone receptor function |
| KR101058292B1 (ko) * | 2002-02-12 | 2011-08-22 | 글락소스미스클라인 엘엘씨 | P38 억제제로 유용한 니코틴아미드 유도체 |
| GB0217757D0 (en) | 2002-07-31 | 2002-09-11 | Glaxo Group Ltd | Novel compounds |
| PA8579601A1 (es) * | 2002-08-30 | 2004-05-07 | Pfizer Prod Inc | Compuestos antiinflamatorios de di y trifloruro-triazolo-piridinas |
| US7005523B2 (en) | 2002-08-30 | 2006-02-28 | Pfizer Inc. | Cycloalkyl-[4-(trifluorophenyl)-oxazol-5yl]-triazolo-pyridines |
| US7037923B2 (en) | 2002-08-30 | 2006-05-02 | Pfizer, Inc. | Alkyl-[4-(trifluorophenyl)-oxazol-5-yl]-triazolo-pyridines |
| US20040092547A1 (en) * | 2002-08-30 | 2004-05-13 | Pfizer Inc | Alkyl-[4-(difluorophenyl)-oxazol-5-yl]-triazolo-pyridines |
| MXPA05002123A (es) * | 2002-08-30 | 2005-06-06 | Pfizer Prod Inc | Nuevos procedimientos e intermedios para preparar triazolo-piridinas. |
| US6949652B2 (en) | 2002-08-30 | 2005-09-27 | Pfizer, Inc. | Crystalline forms of 3-isopropyl-6-[4-(2,5-difluoro-phenyl)-oxazol-5-yl]-[1,2,4]triazolo-[4,3-A]pyridine |
| US7012143B2 (en) | 2002-08-30 | 2006-03-14 | Dombroski Mark A | Cycloalkyl-[4-(difluorophenyl)-oxazol-5-yl]-triazolo-pyridines |
| BRPI0407384A (pt) * | 2003-02-14 | 2006-02-21 | Pfizer Prod Inc | piridinas-triazóis como compostos antiinflamatórios |
| JP4617299B2 (ja) | 2003-03-03 | 2011-01-19 | アレイ バイオファーマ、インコーポレイテッド | p38阻害剤及びその使用法 |
| US7135575B2 (en) * | 2003-03-03 | 2006-11-14 | Array Biopharma, Inc. | P38 inhibitors and methods of use thereof |
| PA8595001A1 (es) * | 2003-03-04 | 2004-09-28 | Pfizer Prod Inc | Nuevos compuestos heteroaromaticos condensados que son inhibidores del factor de crecimiento transforante (tgf) |
| GB0308201D0 (en) * | 2003-04-09 | 2003-05-14 | Smithkline Beecham Corp | Novel compounds |
| GB0308185D0 (en) * | 2003-04-09 | 2003-05-14 | Smithkline Beecham Corp | Novel compounds |
| GB0308186D0 (en) * | 2003-04-09 | 2003-05-14 | Smithkline Beecham Corp | Novel compounds |
| BRPI0417674A (pt) * | 2003-12-18 | 2007-03-20 | Pfizer Prod Inc | método para tratar a inflamação aguda em animais, com inibidores de quinase map p38 |
| GB0402143D0 (en) * | 2004-01-30 | 2004-03-03 | Smithkline Beecham Corp | Novel compounds |
| TWI332003B (en) | 2004-01-30 | 2010-10-21 | Lilly Co Eli | Kinase inhibitors |
| AU2005260031B2 (en) * | 2004-06-25 | 2008-10-09 | Amgen Inc. | Condensed triazoles and indazoles useful in treating citokines mediated diseases and other diseases |
| PL1778686T3 (pl) * | 2004-08-12 | 2009-04-30 | Pfizer | Pochodne triazolopirydynylosulfanylowe jako inhibitory kinazy MAP P38 |
| KR100871535B1 (ko) | 2004-08-12 | 2008-12-05 | 화이자 인코포레이티드 | P38 map 키나아제 억제제로서의트리아졸로피리딘일설판일 유도체 |
| US20090215817A1 (en) * | 2004-08-18 | 2009-08-27 | Pfizer Inc | Novel Triazolopyridine Compounds for the Treatment of Inflammation |
| WO2006018735A2 (en) * | 2004-08-18 | 2006-02-23 | Pharmacia & Upjohn Company Llc | Triazolopyridine compounds |
| US20080051416A1 (en) * | 2004-10-05 | 2008-02-28 | Smithkline Beecham Corporation | Novel Compounds |
| US7572807B2 (en) * | 2005-06-09 | 2009-08-11 | Bristol-Myers Squibb Company | Heteroaryl 11-beta-hydroxysteroid dehydrogenase type I inhibitors |
| US7579360B2 (en) * | 2005-06-09 | 2009-08-25 | Bristol-Myers Squibb Company | Triazolopyridine 11-beta hydroxysteroid dehydrogenase type I inhibitors |
| GB0512429D0 (en) * | 2005-06-17 | 2005-07-27 | Smithkline Beecham Corp | Novel compound |
| PE20070182A1 (es) | 2005-07-29 | 2007-03-06 | Wyeth Corp | Derivados cianopirrol-fenil amida como moduladores del receptor de progesterona |
| PE20070404A1 (es) * | 2005-07-29 | 2007-05-10 | Wyeth Corp | Compuestos derivados de cianopirrol-sulfonamida como moduladores del receptor de progesterona |
| PE20070341A1 (es) * | 2005-07-29 | 2007-04-13 | Wyeth Corp | Derivados de pirrol como moduladores del receptor de progesterona |
| WO2007089646A1 (en) | 2006-01-31 | 2007-08-09 | Array Biopharma Inc. | Kinase inhibitors and methods of use thereof |
| JP2010500365A (ja) | 2006-08-07 | 2010-01-07 | インサイト・コーポレイション | キナーゼ阻害剤としてのトリアゾロトリアジン |
| ES2301380B1 (es) | 2006-08-09 | 2009-06-08 | Laboratorios Almirall S.A. | Nuevos derivados de 1,7-naftiridina. |
| EP2068869A4 (en) | 2006-10-06 | 2011-05-25 | Abbott Lab | NEW IMIDAZOTHIAZOLE AND IMIDAZOXAZOLE |
| JP5572388B2 (ja) | 2006-11-22 | 2014-08-13 | インサイト・コーポレイション | キナーゼ阻害剤としてのイミダゾトリアジンおよびイミダゾピリミジン |
| ES2320955B1 (es) | 2007-03-02 | 2010-03-16 | Laboratorios Almirall S.A. | Nuevos derivados de 3-((1,2,4)triazolo(4,3-a)piridin-7-il)benzamida. |
| ES2329639B1 (es) | 2007-04-26 | 2010-09-23 | Laboratorios Almirall S.A. | Nuevos derivados de 4,8-difenilpoliazanaftaleno. |
| US8188083B2 (en) * | 2007-06-28 | 2012-05-29 | Abbott Laboratories | Triazolopyridazines |
| MX2010002312A (es) | 2007-08-31 | 2010-03-18 | Merck Serono Sa | Compuestos de triazolopiridina y su uso como inhibidores de cinasa reguladora de señal de apoptosis. |
| US8119658B2 (en) | 2007-10-01 | 2012-02-21 | Bristol-Myers Squibb Company | Triazolopyridine 11-beta hydroxysteroid dehydrogenase type I inhibitors |
| EP2108641A1 (en) | 2008-04-11 | 2009-10-14 | Laboratorios Almirall, S.A. | New substituted spiro[cycloalkyl-1,3'-indo]-2'(1'H)-one derivatives and their use as p38 mitogen-activated kinase inhibitors |
| EP2113503A1 (en) | 2008-04-28 | 2009-11-04 | Laboratorios Almirall, S.A. | New substituted indolin-2-one derivatives and their use as p39 mitogen-activated kinase inhibitors |
| JP6022158B2 (ja) | 2008-05-21 | 2016-11-09 | インサイト・ホールディングス・コーポレイションIncyte Holdings Corporation | 2−フルオロ−N−メチル−4−[7−(キノリン−6−イル−メチル)−イミダゾ[1,2−b][1,2,4]トリアジン−2−イル]ベンズアミドの塩及びそれを調製することに関する方法 |
| TWI496779B (zh) | 2008-08-19 | 2015-08-21 | Array Biopharma Inc | 作為pim激酶抑制劑之三唑吡啶化合物 |
| US8557809B2 (en) | 2008-08-19 | 2013-10-15 | Array Biopharma Inc. | Triazolopyridine compounds as PIM kinase inhibitors |
| US8987251B2 (en) | 2008-08-19 | 2015-03-24 | Array Biopharma Inc. | Triazolopyridine compounds as PIM kinase inhibitors |
| US8895550B2 (en) | 2008-08-19 | 2014-11-25 | Array Biopharma Inc. | Triazolopyridine compounds as PIM kinase inhibitors |
| EA025824B1 (ru) | 2009-07-27 | 2017-02-28 | Джилид Сайэнс, Инк. | Конденсированные гетероциклические соединения в качестве модуляторов ионных каналов |
| EP2322176A1 (en) | 2009-11-11 | 2011-05-18 | Almirall, S.A. | New 7-phenyl-[1,2,4]triazolo[4,3-a]pyridin-3(2H)-one derivatives |
| ES2608329T3 (es) | 2010-02-03 | 2017-04-07 | Incyte Holdings Corporation | Imidazo[1,2-b][1,2,4]triazinas como inhibidores de c-Met |
| ES2529119T3 (es) | 2010-07-02 | 2015-02-17 | Gilead Sciences, Inc. | Compuestos heterocíclicos condensados como moduladores de canales iónicos |
| WO2012065297A1 (en) * | 2010-11-16 | 2012-05-24 | Impact Therapeutics, Inc. | 3-ARYL-6-ARYL-[1,2,4]TRIAZOLO[4,3-a]PYRIDINES AS INHIBITORS OF CELL PROLIFERATION AND THE USE THEREOF |
| CN103370316B (zh) * | 2010-11-16 | 2015-06-24 | 南京英派药业有限公司 | 作为细胞增殖抑制剂的3-芳基-6-芳基-[1,2,4]三唑并[4,3-a]吡啶及其应用 |
| UA111075C2 (uk) | 2011-02-25 | 2016-03-25 | Еррей Біофарма Інк. | Триазолопіридинові сполуки як інгібітори кінази рім |
| KR20140033377A (ko) | 2011-05-10 | 2014-03-18 | 길리애드 사이언시즈, 인코포레이티드 | 나트륨 채널 조절제로서의 융합된 헤테로시클릭 화합물 |
| NO3175985T3 (es) | 2011-07-01 | 2018-04-28 | ||
| TW201837023A (zh) | 2011-07-01 | 2018-10-16 | 美商基利科學股份有限公司 | 作為離子通道調節劑之稠合雜環化合物 |
| JP6096370B2 (ja) * | 2013-03-14 | 2017-03-15 | ジェネンテック, インコーポレイテッド | 置換トリアゾロピリジンとその使用方法 |
| GB201321742D0 (en) * | 2013-12-09 | 2014-01-22 | Ucb Pharma Sa | Therapeutic agents |
| WO2015157955A1 (en) | 2014-04-17 | 2015-10-22 | Abbvie Inc. | Heterocyclic btk inhibit ors |
| GB201511382D0 (en) | 2015-06-29 | 2015-08-12 | Imp Innovations Ltd | Novel compounds and their use in therapy |
| US20190060286A1 (en) | 2016-02-29 | 2019-02-28 | University Of Florida Research Foundation, Incorpo | Chemotherapeutic Methods |
| RS63581B1 (sr) | 2017-10-05 | 2022-10-31 | Fulcrum Therapeutics Inc | Inhibitori p38 kinaze smanjuju ekspresiju dux4 i nizvodnih gena u cilju lečenja fshd |
| US10342786B2 (en) | 2017-10-05 | 2019-07-09 | Fulcrum Therapeutics, Inc. | P38 kinase inhibitors reduce DUX4 and downstream gene expression for the treatment of FSHD |
| CN116514801B (zh) * | 2022-01-20 | 2024-11-08 | 四川大学 | 2-苯基-[1,2,4]三唑并[1,5-a]吡啶类化合物、其氮氧化物及用途 |
| CN114504636B (zh) * | 2022-01-27 | 2023-09-26 | 华南理工大学 | 一种杏仁油烫伤膏及其制备方法与应用 |
Family Cites Families (15)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US576499A (en) * | 1897-02-02 | Gas apparatus | ||
| US5716972A (en) * | 1993-01-13 | 1998-02-10 | Smithkline Beecham Corporation | Pyridyl substituted imidazoles |
| CN1048731C (zh) | 1993-09-17 | 2000-01-26 | 史密丝克莱恩比彻姆公司 | 编码细胞因子抑制性抗炎药物结合蛋白质的多核苷酸 |
| IT1269176B (it) * | 1994-01-11 | 1997-03-21 | Isagro Srl | Eterobicicli ad attivita' fungicida |
| US5717100A (en) | 1995-10-06 | 1998-02-10 | Merck & Co., Inc. | Substituted imidazoles having anti-cancer and cytokine inhibitory activity |
| TR199801361T2 (xx) | 1996-01-11 | 1998-10-21 | Smithkline Beecham Corporation | Yeni ikameli imidazol bile�imleri. |
| ZA97175B (en) * | 1996-01-11 | 1997-11-04 | Smithkline Beecham Corp | Novel substituted imidazole compounds. |
| GB9713726D0 (en) | 1997-06-30 | 1997-09-03 | Ciba Geigy Ag | Organic compounds |
| CA2333157A1 (en) | 1998-05-26 | 1999-12-02 | Smithkline Beecham Corporation | Novel substituted imidazole compounds |
| US6207687B1 (en) * | 1998-07-31 | 2001-03-27 | Merck & Co., Inc. | Substituted imidazoles having cytokine inhibitory activity |
| US6350744B1 (en) | 1998-11-20 | 2002-02-26 | Merck & Co., Inc. | Compounds having cytokine inhibitory activity |
| DE69903976T2 (de) | 1998-12-16 | 2003-07-24 | Aventis Pharma Ltd | Heteroaryl-zyklische acetale |
| EP1140083A4 (en) | 1999-01-08 | 2004-01-02 | Smithkline Beecham Corp | NEW CONNECTIONS |
| HK1042251B (en) | 1999-01-13 | 2012-07-20 | Bayer Healthcare Llc | Omega-carboxy aryl substituted diphenyl ureas as p38 kinase inhibitors |
| CO5170501A1 (es) | 1999-04-14 | 2002-06-27 | Novartis Ag | AZOLES SUSTITUIDOS UTILES PARA EL TRATAMIENTO DE ENFERMEDADES MEDIADAS POR TNFa eIL-1 Y ENFERMEDADES DEL METABOLISMO OSEO |
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- 2002-02-08 CN CNA028062825A patent/CN1496366A/zh active Pending
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