AR069637A1 - Derivados de pirazinas - Google Patents
Derivados de pirazinasInfo
- Publication number
- AR069637A1 AR069637A1 ARP080105334A AR069637A1 AR 069637 A1 AR069637 A1 AR 069637A1 AR P080105334 A ARP080105334 A AR P080105334A AR 069637 A1 AR069637 A1 AR 069637A1
- Authority
- AR
- Argentina
- Prior art keywords
- carbon atoms
- groups
- optionally substituted
- alkyl
- heterocyclic group
- Prior art date
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D519/00—Heterocyclic compounds containing more than one system of two or more relevant hetero rings condensed among themselves or condensed with a common carbocyclic ring system not provided for in groups C07D453/00 or C07D455/00
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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
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/4965—Non-condensed pyrazines
- A61K31/497—Non-condensed pyrazines containing further heterocyclic rings
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- 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
- A61P1/02—Stomatological preparations, e.g. drugs for caries, aphtae, periodontitis
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
- A61P11/06—Antiasthmatics
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
- A61P11/08—Bronchodilators
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P27/00—Drugs for disorders of the senses
- A61P27/02—Ophthalmic agents
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- A—HUMAN NECESSITIES
- 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
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/08—Antiallergic agents
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- 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
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- 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
- C07D403/12—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 chain containing hetero atoms as chain links
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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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- 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
- C07D471/10—Spiro-condensed systems
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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
- C07D471/12—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 three hetero rings
- C07D471/20—Spiro-condensed systems
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D473/00—Heterocyclic compounds containing purine ring systems
- C07D473/26—Heterocyclic compounds containing purine ring systems with an oxygen, sulphur, or nitrogen atom directly attached in position 2 or 6, but not in both
- C07D473/32—Nitrogen atom
- C07D473/34—Nitrogen atom attached in position 6, e.g. adenine
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- 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
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Pulmonology (AREA)
- Epidemiology (AREA)
- Immunology (AREA)
- Oncology (AREA)
- Pain & Pain Management (AREA)
- Rheumatology (AREA)
- Ophthalmology & Optometry (AREA)
- Communicable Diseases (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Plural Heterocyclic Compounds (AREA)
- Hydrogenated Pyridines (AREA)
- Pyridine Compounds (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
- Image Processing (AREA)
- Processing Or Creating Images (AREA)
- Image Analysis (AREA)
Abstract
Compuestos utiles para el tratamiento de enfermedades que respondan al bloqueo del canal de sodio epitelial. También se describen composiciones farmacéuticas que contienen los compuestos, y procesos para la preparacion de los compuestos. Reivindicacion 1: Un compuesto de la formula (1), o solvatos, hidratos o sales farmacéuticamente aceptables del mismo, en donde R1 es H, halogeno, alquilo de 1 a 8 átomos de carbono, halo-alquilo de 1 a 8 átomos de carbono, halo-alcoxilo de 1 a 8 átomos de carbono, grupo carbocíclico de 3 a 15 átomos de carbono, nitro, ciano, un grupo carbocíclico aromático de 6 a 15 miembros, o un alquilo de 1 a 8 átomos de carbono sustituido por un grupo carbocíclico aromático de 6 a 15 miembros; R2, R3, R4 y R5 se seleccionan cada uno independientemente a partir de H y alquilo de 1 a 6 átomos de carbono; R6, R7, R8, R9, R10 y R11 se seleccionan cada uno independientemente a partir de H; SO2R16; arilo opcionalmente sustituido por uno o más grupos Z; un grupo carbocíclico de 3 a 10 átomos de carbono opcionalmente sustituido por uno o más grupos Z; un grupo heterocíclico de 3 a 14 átomos de carbono opcionalmente sustituido por uno o más grupos Z; alquilo de 1 a 8 átomos de carbono opcionalmente sustituido por un grupo arilo que está opcionalmente sustituido por uno o más grupos Z, un grupo carbocíclico de 3 a 10 átomos de carbono opcionalmente sustituido por uno o más grupos Z, o un grupo heterocíclico de 3 a 14 átomos de carbono opcionalmente sustituido por uno o más grupos Z; o está representado por la formula (2): -(alquileno de 0 a 6 átomos de carbono)-A(alquileno de 0 a 6 átomos de carbono)-B-(X-R12)q-R22 (2); en donde los grupos alquileno están opcionalmente sustituidos por uno o más grupos Z; o R6 y R7, junto con los átomos con los que están unidos, forman un grupo heterocíclico de 3 a 10 miembros, incluyendo el grupo heterocíclico uno o más heteroátomos adicionales seleccionados a partir de N, O y S, y estando el grupo heterocíclico opcionalmente sustituido por uno o más grupos Z; SO2R16 grupo carbocíclico aromático de 6 a 15 átomos de carbono opcionalmente sustituido por uno o más grupos Z; un grupo carbocíclico de 3 a 10 átomos de carbono; un grupo heterocíclico de 3 a 14 átomos de carbono opcionalmente sustituido por uno o más grupos Z; o un grupo representado por la formula (2); o R7 y R8, junto con el átomo de carbono con el que están unidos, forman un grupo carbocíclico o heterocíclico de 3 a 10 miembros, incluyendo el grupo heterocíclico uno o más heteroátomos seleccionados a partir de N, O y S, y estando los grupos carbocíclico y heterocíclico opcionalmente sustituidos por uno o más grupos Z; SO2R16; grupo carbocíclico aromático de 6 a 15 átomos de carbono opcionalmente sustituido por uno o más grupos Z; un grupo carbocíclico de 3 a 10 átomos de carbono; un grupo heterocíclico de 3 a 14 átomos de carbono opcionalmente sustituido por uno o más grupos Z; o un grupo representado por la formula 2; o R9 y R10, junto con el átomo de carbono con el que están unidos, forman un grupo carbocíclico o heterocíclico de 3 a 10 miembros, incluyendo el grupo heterocíclico uno o más heteroátomos seleccionados a partir de N, O y S, y estando los grupos carbocíclico y heterocíclico opcionalmente sustituidos por uno o más grupos Z; SO2R16; grupo carbocíclico aromático de 6 a 15 átomos de carbono opcionalmente sustituido por uno o más grupos Z; un grupo carbocíclico de 3 a 10 átomos de carbono; un grupo heterocíclico de 3 a 14 átomos de carbono opcionalmente sustituido por uno o más grupos Z; o un grupo representado por la formula 2; o R8 y R9, junto con los átomos de carbono con los que están unidos, forman un cicloalquilo de 3 a 10 miembros, o un grupo heterocíclico de 3 a 10 miembros, incluyendo el grupo heterocíclico uno o más heteroátomos seleccionados a partir de N, O y S, y estando los grupos carbocíclico y heterocíclico opcionalmente sustituidos por uno o más grupos Z; SO2R16; grupo carbocíclico aromático de 6 a 15 átomos de carbono opcionalmente sustituido por uno o más grupos Z; un grupo carbocíclico de 3 a 10 átomos de carbono; un grupo heterocíclico de 3 a 14 átomos de carbono opcionalmente sustituido por uno o más grupos Z; o un grupo representado por la formula (2); o R10 y R11, junto con los átomos con los que están unidos, forman un grupo heterocíclico de 3 a 10 miembros, incluyendo el grupo heterocíclico uno o más heteroátomos adicionales seleccionados a partir de N, O y S, y estando el grupo heterocíclico opcionalmente sustituido por uno o más grupos Z; SO2R16; grupo carbocíclico aromático de 6 a 15 átomos de carbono opcionalmente sustituido por uno o más grupos Z; un grupo carbocíclico de 3 a 10 átomos de carbono; un grupo heterocíclico de 3 a 14 átomos de carbono opcionalmente sustituido por uno o más grupos Z; o un grupo representado por la formula (2); A se selecciona a partir de un enlace, -NR13(SO2)-, -(SO2)NR13-, -(SO2)-, -NR13C(O)-, -C(O)NR13-, -NR13C(O)NR14-, -NR13C(O)O-, -NR13-, C(O)O, OC(O), C(O), O y S; B se selecciona a partir de un enlace, -(grupo alquenilo de 2 a 4 átomos de carbono)-, -(grupo alquinilo de 2 a 4 átomos de carbono)-, -NH-, arilo, O-arilo, NH-arilo, un grupo carbocíclico de 3 a 14 átomos de carbono, y un grupo heterocíclico de 3 a 14 miembros, incluyendo el grupo heterocíclico uno o más heteroátomos seleccionados a partir de N, O y S, en donde los grupos arilo, carbocíclico y heterocíclico están cada uno opcionalmente sustituidos por uno o más grupos Z; X se selecciona a partir de un enlace, -NR15(SO2)-, -(SO2)NR15-, -(SO2)-, -NR15C(O)-, -C(O)NR15-, -NR15C(O)NR17-, -NR15C(O)O-, -NR15-, C(O)O, CO(O), C(O), O y S; R12 se selecciona a partir de alquileno de 1 a 8 átomos de carbono, alquenileno de 1 a 8 átomos de carbono, -cicloalquilo de 3 a 8 átomos de carbono-, -alquileno de 1 a 8 átomos de carbono, -cicloalquilo de 3 a 8 átomos de carbono-, y -arilo-, en donde los grupos alquileno, cicloalquilo y arilo están opcionalmente sustituidos por uno o más grupos Z; R13, R14, R15 y R17 se seleccionan cada uno independientemente a partir de H y alquilo de 1 a 6 átomos de carbono; R16 se selecciona a partir de alquilo de 1 a 8 átomos de carbono, arilo, y un grupo heterocíclico de 3 a 14 miembros, incluyendo el grupo heterocíclico uno o más heteroátomos seleccionados a partir de N, O, y S; Z se selecciona independientemente a partir de OH, arilo, O-arilo, aralquilo de 7 a 14 átomos de carbono, O-aralquilo de 7 a 14 átomos de carbono, alquilo de 1 a 6 átomos de carbono, alcoxilo de 1 a 6 átomos de carbono, NR19(SO2)R21, (SO2)NR19R21, (SO2)R20, NR19C(O)R20, C(O)NR19R20. NR19C(O)NR20R18. NR19C(O)OR20, NR19R21, C(O)OR10, C(O)R19, SR19, OR19, oxo, CN, NO2, y halogeno, en donde los grupos alquilo. alcoxilo, aralquilo y arilo están cada uno opcionalmente sustituidos por uno o más sustituyentes seleccionados a partir de OH, halogeno, halo-alquilo de 1 a 4 átomos de carbono y alcoxilo de 1 a 4 átomos de carbono; R18 y R20 se seleccionan cada uno independientemente a partir de H y alquilo de 1 a 6 átomos de carbono; R19 y R21 se seleccionan cada uno independientemente a partir de H; alquilo de 1 a 8 átomos de carbono; cicloalquilo de 3 a 8 átomos de carbono; alcoxilo de 1 a 4 átomos de carbono-alquilo de 1 a 4 átomos de carbono; (alquilo de 0 a 4 átomos de carbono)-arilo opcionalmente sustituido por uno o más grupos seleccionados a partir de alquilo de 1 a 6 átomos de carbono, alcoxilo de 1 a 6 átomos de carbono y halogeno; (alquilo de 0 a 4 átomos de carbono)-grupo heterocíclico de 3 a 14 miembros, incluyendo el grupo heterocíclico uno o más heteroátomos seleccionados a partir de N, O y S, opcionalmente sustituido por uno o más grupos seleccionados a partir de halogeno, oxo, alquilo de 1 a 6 átomos de carbono y C(O)alquilo de 1 a 6 átomos de carbono; (alquilo de 0 a 4 átomos de carbono)-O-arilo opcionalmente sustituido por uno o más grupos seleccionados a partir de alquilo de 1 a 6 átomos de carbono, alcoxilo de 1 a 6 átomos de carbono y halogeno; y (alquilo de 0 a 4 átomos de carbono)-O-grupo heterocíclico de 3 a 14 miembros, incluyendo el grupo heterocíclico uno o más heteroátomos seleccionados a partir de N, O y S, opcionalmente sustituido por uno o más grupos seleccionados a partir de halogeno, alquilo de 1 a 6 átomos de carbono y C(O)-alquilo de 1 a 6 átomos de carbono; en donde los grupos alquilo y alcoxilo están opcionalmente sustituidos por uno o más átomos de halogeno, alcoxilo de 1 a 4 átomos de carbono, C(O)NH2, C(O)NH-alquilo de 1 a 6 átomos de carbono o C(O)N(alquilo de 1 a 6 átomos de carbono)2 ; o R19 y R20, junto con el átomo de nitrogeno con el que están unidos, forman un grupo heterocíclico de 5 a 10 miembros, incluyendo el grupo heterocíclico uno o más heteroátomos adicionales seleccionados a partir de N, O y S, estando el grupo heterocíclico opcionalmente sustituido por uno o más sustituyentes seleccionados a partir de OH; halogeno; arilo; grupo heterocíclico de 5 a 10 miembros que incluye uno o más heteroátomos seleccionados a partir de N, O, y S; S(O)2-arilo; S(O)2-alquilo de 1 a 6 átomos de carbono; alquilo de 1 a 6 átomos de carbono opcionalmente sustituido por uno o más átomos de halogeno; alcoxilo de 1 a 6 átomos de carbono opcionalmente sustituido por uno o más grupos OH, o alcoxilo de 1 a 4 átomos de carbono; y C(O)O-alquilo de 1 a 6 átomos de carbono, en donde los grupos sustituyentes de arilo y heterocíclicos están ellos mismos opcionalmente sustituidos por alquilo de 1 a 6 átomos de carbono, halo-alquilo de 1 a 6 átomos de carbono o alcoxilo de 1 a 6 átomos de carbono; R22 se selecciona a partir de H, halogeno, alquilo de 1 a 8 átomos de carbono, alcoxilo de 1 a 8 átomos de carbono. arilo, O-arilo, S(O)2-arilo, S(O)2-alquilo de 1 a 6 átomos de carbono, S(O)2NR23R24, NHS(O)2NR23R24, un grupo carbocíclico de 3 a 14 átomos de carbono, un grupo heterocíclico de 3 a 14 miembros, incluyendo el grupo heterocíclico uno o más heteroátomos selecciona
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
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EP07122739 | 2007-12-10 |
Publications (1)
Publication Number | Publication Date |
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AR069637A1 true AR069637A1 (es) | 2010-02-10 |
Family
ID=39322745
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
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ARP080105334 AR069637A1 (es) | 2007-12-10 | 2008-12-09 | Derivados de pirazinas |
Country Status (30)
Country | Link |
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US (5) | US8039472B2 (es) |
EP (3) | EP2444120B1 (es) |
JP (1) | JP5455922B2 (es) |
KR (1) | KR101578235B1 (es) |
CN (1) | CN101939054B (es) |
AR (1) | AR069637A1 (es) |
AU (1) | AU2008334629B2 (es) |
BR (1) | BRPI0820669A2 (es) |
CA (1) | CA2707857C (es) |
CL (1) | CL2008003651A1 (es) |
CO (1) | CO6310968A2 (es) |
CR (1) | CR11470A (es) |
CU (1) | CU23967B1 (es) |
EA (1) | EA017919B1 (es) |
EC (1) | ECSP10010242A (es) |
ES (2) | ES2602331T3 (es) |
HN (1) | HN2010001165A (es) |
IL (1) | IL206165A0 (es) |
MA (1) | MA31894B1 (es) |
MX (1) | MX2010006421A (es) |
MY (1) | MY152955A (es) |
NZ (1) | NZ585789A (es) |
PE (1) | PE20091096A1 (es) |
PL (1) | PL2444120T3 (es) |
PT (1) | PT2444120T (es) |
TN (1) | TN2010000256A1 (es) |
TW (1) | TWI439462B (es) |
UA (1) | UA104997C2 (es) |
WO (1) | WO2009074575A2 (es) |
ZA (1) | ZA201003837B (es) |
Families Citing this family (89)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6858615B2 (en) | 2002-02-19 | 2005-02-22 | Parion Sciences, Inc. | Phenyl guanidine sodium channel blockers |
US8354427B2 (en) | 2004-06-24 | 2013-01-15 | Vertex Pharmaceutical Incorporated | Modulators of ATP-binding cassette transporters |
PT2444120T (pt) | 2007-12-10 | 2018-01-03 | Novartis Ag | Análogos da amilorida espirocíclicos como bloqueadores de enac |
ES2485642T3 (es) | 2008-02-26 | 2014-08-14 | Parion Sciences, Inc. | Bloqueantes poli-aromáticos de los canales de sodio |
UA103198C2 (en) | 2008-08-04 | 2013-09-25 | Новартис Аг | Squaramide derivatives as cxcr2 antagonists |
WO2010039260A2 (en) * | 2008-10-02 | 2010-04-08 | The Johns Hopkins University | Spiperone derivatives and methods of treating disorders |
EA018891B1 (ru) | 2008-10-23 | 2013-11-29 | Вертекс Фармасьютикалз, Инкорпорейтед | Модуляторы регулятора трансмембранной проводимости при муковисцидозе |
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