AR040400A1 - Tratamiento de enfermedades mediadas por quimiocinas - Google Patents
Tratamiento de enfermedades mediadas por quimiocinasInfo
- Publication number
- AR040400A1 AR040400A1 AR20030100943A ARP030100943A AR040400A1 AR 040400 A1 AR040400 A1 AR 040400A1 AR 20030100943 A AR20030100943 A AR 20030100943A AR P030100943 A ARP030100943 A AR P030100943A AR 040400 A1 AR040400 A1 AR 040400A1
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- Argentina
- Prior art keywords
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- substituted
- unsubstituted
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- Prior art date
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- 201000010099 disease Diseases 0.000 title abstract 4
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 title abstract 4
- 230000001404 mediated effect Effects 0.000 title abstract 4
- 125000001424 substituent group Chemical group 0.000 abstract 25
- 125000000217 alkyl group Chemical group 0.000 abstract 17
- 125000001072 heteroaryl group Chemical group 0.000 abstract 13
- 229910052736 halogen Inorganic materials 0.000 abstract 8
- 150000002367 halogens Chemical class 0.000 abstract 8
- 125000003107 substituted aryl group Chemical group 0.000 abstract 8
- 125000000753 cycloalkyl group Chemical group 0.000 abstract 7
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 abstract 7
- 125000003710 aryl alkyl group Chemical group 0.000 abstract 6
- 125000003118 aryl group Chemical group 0.000 abstract 6
- 125000004093 cyano group Chemical group *C#N 0.000 abstract 6
- 125000001316 cycloalkyl alkyl group Chemical group 0.000 abstract 6
- 229910052739 hydrogen Inorganic materials 0.000 abstract 6
- 150000001875 compounds Chemical class 0.000 abstract 5
- 125000004446 heteroarylalkyl group Chemical group 0.000 abstract 5
- 125000000623 heterocyclic group Chemical group 0.000 abstract 5
- 239000001257 hydrogen Substances 0.000 abstract 5
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 abstract 5
- 125000003545 alkoxy group Chemical group 0.000 abstract 4
- 239000003814 drug Substances 0.000 abstract 4
- 229940079593 drug Drugs 0.000 abstract 4
- 150000002431 hydrogen Chemical group 0.000 abstract 4
- 125000003709 fluoroalkyl group Chemical group 0.000 abstract 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Substances N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 abstract 3
- 125000000547 substituted alkyl group Chemical group 0.000 abstract 3
- 125000005346 substituted cycloalkyl group Chemical group 0.000 abstract 3
- 230000001225 therapeutic effect Effects 0.000 abstract 3
- 125000000876 trifluoromethoxy group Chemical group FC(F)(F)O* 0.000 abstract 3
- 102000019034 Chemokines Human genes 0.000 abstract 2
- 108010012236 Chemokines Proteins 0.000 abstract 2
- 239000002253 acid Substances 0.000 abstract 2
- 239000003795 chemical substances by application Substances 0.000 abstract 2
- 125000000524 functional group Chemical group 0.000 abstract 2
- 238000002483 medication Methods 0.000 abstract 2
- 229910052757 nitrogen Inorganic materials 0.000 abstract 2
- 229910052760 oxygen Inorganic materials 0.000 abstract 2
- -1 -OH Chemical group 0.000 abstract 1
- 125000003341 7 membered heterocyclic group Chemical group 0.000 abstract 1
- 108050006947 CXC Chemokine Proteins 0.000 abstract 1
- 102000019388 CXC chemokine Human genes 0.000 abstract 1
- 229940123907 Disease modifying antirheumatic drug Drugs 0.000 abstract 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract 1
- 125000003342 alkenyl group Chemical group 0.000 abstract 1
- 125000004183 alkoxy alkyl group Chemical group 0.000 abstract 1
- 125000000304 alkynyl group Chemical group 0.000 abstract 1
- 239000002260 anti-inflammatory agent Substances 0.000 abstract 1
- 229940121363 anti-inflammatory agent Drugs 0.000 abstract 1
- 230000008512 biological response Effects 0.000 abstract 1
- 229940111134 coxibs Drugs 0.000 abstract 1
- 125000004122 cyclic group Chemical group 0.000 abstract 1
- 125000000392 cycloalkenyl group Chemical group 0.000 abstract 1
- 239000003260 cyclooxygenase 1 inhibitor Substances 0.000 abstract 1
- 239000003255 cyclooxygenase 2 inhibitor Substances 0.000 abstract 1
- 239000002988 disease modifying antirheumatic drug Substances 0.000 abstract 1
- 125000005842 heteroatom Chemical group 0.000 abstract 1
- 125000004366 heterocycloalkenyl group Chemical group 0.000 abstract 1
- 125000005885 heterocycloalkylalkyl group Chemical group 0.000 abstract 1
- 125000004356 hydroxy functional group Chemical group O* 0.000 abstract 1
- 125000002768 hydroxyalkyl group Chemical group 0.000 abstract 1
- 229960003444 immunosuppressant agent Drugs 0.000 abstract 1
- 230000001861 immunosuppressant effect Effects 0.000 abstract 1
- 239000003018 immunosuppressive agent Substances 0.000 abstract 1
- 238000004519 manufacturing process Methods 0.000 abstract 1
- 239000003607 modifier Substances 0.000 abstract 1
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 abstract 1
- 239000000041 non-steroidal anti-inflammatory agent Substances 0.000 abstract 1
- 229940021182 non-steroidal anti-inflammatory drug Drugs 0.000 abstract 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 229920006395 saturated elastomer Polymers 0.000 abstract 1
- 239000012453 solvate Substances 0.000 abstract 1
- 150000003431 steroids Chemical class 0.000 abstract 1
- 229910052717 sulfur Inorganic materials 0.000 abstract 1
Classifications
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Landscapes
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Veterinary Medicine (AREA)
- Pharmacology & Pharmacy (AREA)
- Chemical & Material Sciences (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Physical Education & Sports Medicine (AREA)
- Pulmonology (AREA)
- Virology (AREA)
- Neurology (AREA)
- Rheumatology (AREA)
- Immunology (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Communicable Diseases (AREA)
- Oncology (AREA)
- Neurosurgery (AREA)
- Biomedical Technology (AREA)
- Hematology (AREA)
- Diabetes (AREA)
- Dermatology (AREA)
- Tropical Medicine & Parasitology (AREA)
- Epidemiology (AREA)
- Pain & Pain Management (AREA)
- Molecular Biology (AREA)
- Cardiology (AREA)
- Heart & Thoracic Surgery (AREA)
- Urology & Nephrology (AREA)
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- Ophthalmology & Optometry (AREA)
- Obesity (AREA)
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Abstract
Reivindicación 1: Un uso de uno o más compuestos de formula (1), o una de sus sales o solvatos aceptables para uso farmacéutico; para la fabricación de uno o más medicamentos para tratar una enfermedad mediada por la quimiocina CXC, en la cual el tratamiento comprende administrar a un paciente: (a) uno o más de dichos medicamentos; en combinación con (b) uno o más fármacos, agentes o productos terapéuticos útiles para el tratamiento de enfermedades mediadas por quimiocinas; donde para dichos compuestos de formula (1), A se selecciona de un resto del grupo de fórmulas (2), donde los anillos de dichos grupos A están substituidos con 1 a 6 substituyentes seleccionados cada uno en forma independiente del grupo formado por grupos R9; y radicales del grupo de fórmulas (3); en donde uno o ambos de los anillos de dichos grupos A están substituidos con 1 a 6 substituyentes cada uno seleccionados en forma independiente del grupo formado por grupos R9; y las fórmulas (a), y (b) del grupo (2) donde los grupos fenilo de dichos grupos A están substituidos con 1 a 3 substituyentes seleccionados cada uno en forma independiente del grupo formado por grupos R9; y restos del grupo de fórmulas (4); B se selecciona del grupo de fórmulas (5); n es 0 a 6; p es 1 a 5; X es O, NH, o S; Z es 1 a 3; R2 se selecciona del grupo formado por hidrógeno, OH, -C(O)OH, -SH, -NHSO2NR13R14, -NHC(O)R13, -NHSO2R13R14, -NHSO2R13, -NR13R14, -C(O)NR13R14, -C(O)NHOR13, -C(O)NR13OH, -S(O2)OH, -OC(O)R13, un grupo funcional ácido heterocíclico no substituido, y un grupo funcional ácido heterocíclico substituido; donde hay 1 a 6 substituyentes en donde cada substituyente se selecciona del grupo formado por R9; cada R3 y R4 son seleccionados en forma independiente del grupo formado por hidrógeno, ciano, halógeno, alquilo, alcoxi, -OH, -CF3, -OCF3, -NO2, -C(O)R13, -C(O)OR13, -C(O)NHR17, -C(O)NR13R14, -SO(t)NR13R14, -SO(t)R13, -C(O)NR13OR14, arilo no substituido o substituido, heteroarilo no substituido o substituido, o restos del grupo de fórmulas (6); donde hay 1 a 6 substituyentes en dicho grupo arilo substituido y cada substituyente se selecciona del grupo formado por grupos R9; y donde hay 1 a 6 substituyentes en dicho grupo heteroarilo substituido y cada substituyente se selecciona del grupo formado por grupos R9; cada R5 y R6 son iguales o diferentes y se seleccionan en forma independiente del grupo formado por hidrógeno, halógeno, alquilo, alcoxi, -CF3, -OCF3, -NO2, -C(O)R13, -C(O)OR13, -C(O)NR13R14, -SO(t)NR13R14, -C(O)NR13OR14, ciano, arilo no substituido o substituido, y heteroarilo no substituido o substituido; donde hay 1 a 6 substituyentes en dicho grupo arilo substituido y cada substituyente se selecciona en forma independiente del grupo formado por grupos R9; y donde hay 1 a 6 substituyentes en dicho grupo heteroarilo substituido y cada substituyente se selecciona en forma independiente del grupo formado por grupos R9; cada R7 y R8 se seleccionan en forma independiente del grupo formado por H, alquilo no substituido o substituido, arilo no substituido o substituido, heteroarilo no substituido o substituido, arilalquilo no substituido o substituido, heteroarilalquilo no substituido o substituido, cicloalquilo no substituido o substituido, cicloalquilalquilo no substituido o substituido, -CO2R13, -CONR13R14, alquinilo, alquenilo, y cicloalquenilo ; y donde hay uno o más substituyentes en dichos grupos R7 y R8 substituidos, donde cada substituyente se selecciona del grupo formado por: a) halógeno, b) -CF3, c) -COR13, d) -OR13, e) -NR13R14 f) -NO2, g) -CN, h) -SO2OR13, i) -Si(alquilo)3, donde cada alquilo se selecciona en forma independiente, j) -Si(aril)3, donde cada alquilo se selecciona en forma independiente, k) -(R13)2R14Si, donde cada R13 se selecciona en forma independiente, I) -CO2R13, m) -C(O)NR13R14, n)-SO2NR13R14, o) -SO2R13, p) -OC(O)R13, q) -OC(O)NR13R14, r) -NR13C(O)R14, y s) -NR13CO2R14; R8a se selecciona del grupo formado por: hidrógeno, alquilo, cicloalquilo y cicloalquilalquilo; cada R9 se selecciona en forma independiente del grupo formado por: a) -R13 b) halógeno, c) -CF3, d) -COR13, e) -OR13, f) -NR13R14 g)-NO2, h) -CN, i) -SO2R13, j) -SO2NR13R14, k) -NR13COR14, l) -CONR13R14, m) -NR13CO2R14, n) -CO2R13, o) un compuesto de fórmula (7), p) alquilo substituido con uno o más grupos -OH, q) alquilo substituido con uno o más grupos -NR13R14, y r) -N(R13)SO2R14 ; cada R10 y R11 se selecciona en forma independiente del grupo formado por: R13, halógeno, -CF3, -OCF3, -NR13R14, -NR13C(O)NR13R14, -OH, -C(O)OR13, -SH, - SO(t)NR13R14, -SO2R13, -NHC(O)R13, -NHSO2NR13R14, -NHSO2R13, -C(O)NR13R14, -C(O)NR13OR14, -OC(O)R13 y ciano ; R12 se selecciona en forma independiente del grupo formado por: hidrógeno, -C(O)OR13, arilo no substituido o substituido, heteroarilo no substituido o substituido, arilalquilo no substituido o substituido, cicloalquilo no substituido o substituido, alquilo no substituido o substituido, cicloalquilalquilo no substituido o substituido, y heteroarilalquilo no substituido o substituido; donde hay 1 a 6 substituyentes en los grupos R12 substituidos y cada substituyente se selecciona en forma independiente del grupo formado por: grupos R9; cada R13 y R14 se selecciona en forma independiente del grupo formado por: H, alquilo no substituido o substituido, arilo no substituido o substituido, heteroarilo no substituido o substituido, arilalquilo no substituido o substituido, heteroarilalquilo no substituido o substituido, cicloalquilo no substituido o substituido, cicloalquilalquilo no substituido o substituido, heterocíclico no substituido o substituido, fluoroalquilo no substituido o substituido, y heterocicloalquilalquilo no substituido o substituido (donde "heterociloalquilo" significa heterocíclico); donde hay 1 a 6 substituyentes en dichos grupos R13 y R14 substituidos y cada substituyente se selecciona en forma independiente del grupo formado por: alquilo, -CF3, -OH, alcoxi, arilo, arilalquilo, fluoroalquilo, cicloalquilo, cicloalquilalquilo, heteroarilo, heteroarilalquilo, -N(R40)2, -C(O)OR15, -C(O)NR15R16, -S(O)tNR15R16, -C(O)R15, -SO2R15 siempre que R15 no sea H, halógeno, y -NHC(O)NR15R16; o R13 y R14 tomados junto con el nitrógeno al cual están unidos en los grupos -C(O)NR13R14 y -SO2NR13R14 forman un anillo heterocíclico saturado no substituido o substituido (con preferencia un anillo heterocíclico de 3 a 7 miembros), dicho anillo contiene en forma opcional un heteroátomo adicional seleccionado del grupo formado por: O, S y NR18; donde hay 1 a 3 substituyentes en los grupos R13 y R14 ciclizados substituidos (es decir, hay 1 a 3 substituyentes en el anillo formado cuando los grupos R13 y R14 se toman junto con el nitrógeno al cual están unidos) y cada substituyente se selecciona en forma independiente del grupo formado por: alquilo, arilo, hidroxi, hidroxialquilo, alcoxi, alcoxialquilo, arilalquilo, fluoroalquilo, cicloalquilo, cicloalquilalquilo, heteroarilo, heteroarilalquilo, amino, -C(O)OR, -C(O)NR15R16, -SOtNR15R16, -C(O)R15, -SO2R15 siempre que R15 no sea H, -NHC(O)NR15R16, -NHC(O)OR15, halógeno, y un grupo heterocicloalquenilo; cada R15 y R16 se selecciona en forma independiente del grupo formado por: H, alquilo, arilo, arilalquilo, cicloalquilo y heteroarilo; R17 se selecciona del grupo formado por: -SO2alquilo, -SO2arilo, - SO2cicloalquilo, y -SO2heteroarilo; R18 se selecciona del grupo formado por: H, alquilo, arilo, heteroarilo, -C(O)R19, -SO2R19 y -C(O)NR19R20; cada R19 y R20 se selecciona en forma independiente del grupo formado por: alquilo, arilo y heteroarilo; R30 se selecciona del grupo formado por: alquilo, cicloalquilo, -CN, -NO2, o -SO2R15 siempre que R15 no sea H; cada R31 se selecciona en forma independiente del grupo formado por: alquilo no substituido, arilo no substituido o substituido, heteroarilo no substituido o substituido y cicloalquilo no substituido o substituido; donde hay 1 a 6 substituyentes en dichos grupos R31 substituidos y cada substituyente se selecciona en forma independiente del grupo formado por: alquilo, halógeno y -CF3; cada R40 se selecciona en forma independiente del grupo formado por: H, alquilo y cicloalquilo; g es 1 ó 2; y t es 0, 1 ó 2. Reivindicación 2: El uso de la reivindicación 1 en el cual B se selecciona de un compuesto de fórmula (a) del grupo (5) y R3 para este grupo B se selecciona del grupo formado por: -C(O)NR13R14, y las fórmulas del grupo (6) y todos los otros substituyentes son como se los definió en la reivindicación 1. Reivindicación 42: El uso de la reivindicación 1 en el cual dicho fármaco, agente o producto terapéutico usado en combinación con dichos compuestos de fórmula (1) se selecciona del grupo formado por: (a) un fármaco anti-reumático modificador de la enfermedad; (b) un fármaco antiinflamatorio no esteroide; (c) un inhibidor selectivo de COX-2; (d) un inhibidor de COX-1; (e) un inmunosupresor; (f) un esteroide; (g) un modificador de la respuesta biológica y (h) otros agentes antiinflamatorios o productos terapéuticos útiles para el tratamiento de enfermedades mediadas por quimiocinas.
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| EP1551818B1 (en) | 2002-10-09 | 2009-02-04 | Schering Corporation | Thiadiazoledioxides and thiadiazoleoxides as cxc- and cc-chemokine receptor ligands |
-
2003
- 2003-03-17 WO PCT/US2003/008287 patent/WO2003080053A1/en not_active Ceased
- 2003-03-17 US US10/390,078 patent/US20040053953A1/en not_active Abandoned
- 2003-03-17 JP JP2003577881A patent/JP4733350B2/ja not_active Expired - Fee Related
- 2003-03-17 MX MXPA04009127A patent/MXPA04009127A/es unknown
- 2003-03-17 NZ NZ535314A patent/NZ535314A/en not_active IP Right Cessation
- 2003-03-17 AU AU2003220384A patent/AU2003220384B2/en not_active Ceased
- 2003-03-17 BR BR0308739-5A patent/BR0308739A/pt not_active IP Right Cessation
- 2003-03-17 CN CNB038106183A patent/CN100444839C/zh not_active Expired - Fee Related
- 2003-03-17 EP EP03716685.7A patent/EP1485089B1/en not_active Expired - Lifetime
- 2003-03-17 CA CA2479126A patent/CA2479126C/en not_active Expired - Fee Related
- 2003-03-18 AR AR20030100943A patent/AR040400A1/es not_active Application Discontinuation
- 2003-03-18 TW TW096114061A patent/TW200808314A/zh unknown
- 2003-03-18 TW TW092105892A patent/TW200304811A/zh unknown
-
2004
- 2004-09-13 ZA ZA200407339A patent/ZA200407339B/en unknown
- 2004-10-15 NO NO20044402A patent/NO20044402L/no not_active Application Discontinuation
-
2007
- 2007-02-14 US US11/705,929 patent/US7960433B2/en not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| US20040053953A1 (en) | 2004-03-18 |
| AU2003220384A1 (en) | 2003-10-08 |
| US7960433B2 (en) | 2011-06-14 |
| ZA200407339B (en) | 2005-10-06 |
| US20070155756A1 (en) | 2007-07-05 |
| BR0308739A (pt) | 2005-01-11 |
| MXPA04009127A (es) | 2005-01-25 |
| EP1485089B1 (en) | 2013-04-17 |
| JP4733350B2 (ja) | 2011-07-27 |
| WO2003080053A1 (en) | 2003-10-02 |
| CN100444839C (zh) | 2008-12-24 |
| NZ535314A (en) | 2007-08-31 |
| AU2003220384B2 (en) | 2007-05-10 |
| TW200304811A (en) | 2003-10-16 |
| JP2005533005A (ja) | 2005-11-04 |
| CA2479126A1 (en) | 2003-10-02 |
| EP1485089A1 (en) | 2004-12-15 |
| TW200808314A (en) | 2008-02-16 |
| NO20044402L (no) | 2004-12-17 |
| CA2479126C (en) | 2011-11-15 |
| CN1652779A (zh) | 2005-08-10 |
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