AR092530A1 - Compuesto de amino-quinolina, composicion farmaceutica que lo comprende y uso de dicho compuesto para la preparacion de un medicamento - Google Patents
Compuesto de amino-quinolina, composicion farmaceutica que lo comprende y uso de dicho compuesto para la preparacion de un medicamentoInfo
- Publication number
- AR092530A1 AR092530A1 ARP130103248A ARP130103248A AR092530A1 AR 092530 A1 AR092530 A1 AR 092530A1 AR P130103248 A ARP130103248 A AR P130103248A AR P130103248 A ARP130103248 A AR P130103248A AR 092530 A1 AR092530 A1 AR 092530A1
- Authority
- AR
- Argentina
- Prior art keywords
- alkoxy
- alkyl
- pyrazol
- dimethyl
- amine
- Prior art date
Links
- 150000001875 compounds Chemical class 0.000 title abstract 2
- GCMNJUJAKQGROZ-UHFFFAOYSA-N 1,2-Dihydroquinolin-2-imine Chemical compound C1=CC=CC2=NC(N)=CC=C21 GCMNJUJAKQGROZ-UHFFFAOYSA-N 0.000 title 1
- 239000002131 composite material Substances 0.000 title 1
- 229940126601 medicinal product Drugs 0.000 title 1
- 239000008194 pharmaceutical composition Substances 0.000 title 1
- -1 amino-quinoline compound Chemical class 0.000 abstract 11
- 125000000592 heterocycloalkyl group Chemical group 0.000 abstract 6
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 abstract 5
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 5
- 125000004191 (C1-C6) alkoxy group Chemical group 0.000 abstract 4
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 abstract 4
- FQYRLEXKXQRZDH-UHFFFAOYSA-N 4-aminoquinoline Chemical compound C1=CC=C2C(N)=CC=NC2=C1 FQYRLEXKXQRZDH-UHFFFAOYSA-N 0.000 abstract 4
- 125000003545 alkoxy group Chemical group 0.000 abstract 4
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 abstract 3
- 125000000229 (C1-C4)alkoxy group Chemical group 0.000 abstract 3
- 125000000472 sulfonyl group Chemical group *S(*)(=O)=O 0.000 abstract 3
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 abstract 3
- 125000004093 cyano group Chemical group *C#N 0.000 abstract 2
- 125000001153 fluoro group Chemical group F* 0.000 abstract 2
- 229910052736 halogen Inorganic materials 0.000 abstract 2
- 125000005843 halogen group Chemical group 0.000 abstract 2
- 150000002367 halogens Chemical class 0.000 abstract 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 abstract 2
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 abstract 2
- 150000003839 salts Chemical class 0.000 abstract 2
- 125000006273 (C1-C3) alkyl group Chemical group 0.000 abstract 1
- PMZDQRJGMBOQBF-UHFFFAOYSA-N 1H-quinolin-4-one Natural products C1=CC=C2C(O)=CC=NC2=C1 PMZDQRJGMBOQBF-UHFFFAOYSA-N 0.000 abstract 1
- HZDJLSITORIPGT-UHFFFAOYSA-N 2-[4-[(4,5-dimethyl-1h-pyrazol-3-yl)amino]-7-methoxyquinolin-6-yl]sulfonyl-2-methylpropan-1-ol Chemical compound C=12C=C(S(=O)(=O)C(C)(C)CO)C(OC)=CC2=NC=CC=1NC1=NNC(C)=C1C HZDJLSITORIPGT-UHFFFAOYSA-N 0.000 abstract 1
- HRBKEPLXBIHJME-UHFFFAOYSA-N 2-[6-tert-butylsulfonyl-4-[(4,5-dimethyl-1h-pyrazol-3-yl)amino]quinolin-7-yl]oxyethanol Chemical compound CC1=C(C)NN=C1NC1=CC=NC2=CC(OCCO)=C(S(=O)(=O)C(C)(C)C)C=C12 HRBKEPLXBIHJME-UHFFFAOYSA-N 0.000 abstract 1
- OVPZGUMHWDAVSH-UHFFFAOYSA-N 6-(2,2-dimethyloxan-4-yl)sulfonyl-n-(4,5-dimethyl-1h-pyrazol-3-yl)-7-methoxyquinolin-4-amine Chemical compound C=12C=C(S(=O)(=O)C3CC(C)(C)OCC3)C(OC)=CC2=NC=CC=1NC1=NNC(C)=C1C OVPZGUMHWDAVSH-UHFFFAOYSA-N 0.000 abstract 1
- QWECBUNTPLWDBL-UHFFFAOYSA-N 6-tert-butylsulfonyl-4-[(4,5-dimethyl-1H-pyrazol-3-yl)amino]quinolin-7-ol Chemical compound CC1=C(C)NN=C1NC1=CC=NC2=CC(O)=C(S(=O)(=O)C(C)(C)C)C=C12 QWECBUNTPLWDBL-UHFFFAOYSA-N 0.000 abstract 1
- DPILGXGHKJEOAS-UHFFFAOYSA-N 6-tert-butylsulfonyl-7-(difluoromethoxy)-n-(4,5-dimethyl-1h-pyrazol-3-yl)quinolin-4-amine Chemical compound CC1=C(C)NN=C1NC1=CC=NC2=CC(OC(F)F)=C(S(=O)(=O)C(C)(C)C)C=C12 DPILGXGHKJEOAS-UHFFFAOYSA-N 0.000 abstract 1
- UVCJVWDOTPZNJM-UHFFFAOYSA-N 6-tert-butylsulfonyl-n-(4,5-dimethyl-1h-pyrazol-3-yl)-7-ethoxyquinolin-4-amine Chemical compound C=12C=C(S(=O)(=O)C(C)(C)C)C(OCC)=CC2=NC=CC=1NC1=NNC(C)=C1C UVCJVWDOTPZNJM-UHFFFAOYSA-N 0.000 abstract 1
- LHPFRDAGGDMRMZ-UHFFFAOYSA-N 6-tert-butylsulfonyl-n-(4,5-dimethyl-1h-pyrazol-3-yl)-7-methoxyquinolin-4-amine Chemical compound C=12C=C(S(=O)(=O)C(C)(C)C)C(OC)=CC2=NC=CC=1NC1=NNC(C)=C1C LHPFRDAGGDMRMZ-UHFFFAOYSA-N 0.000 abstract 1
- SVARURAGDUBTCW-UHFFFAOYSA-N 7-(difluoromethoxy)-n-(4,5-dimethyl-1h-pyrazol-3-yl)-6-(oxan-4-ylsulfonyl)quinolin-4-amine Chemical compound CC1=C(C)NN=C1NC1=CC=NC2=CC(OC(F)F)=C(S(=O)(=O)C3CCOCC3)C=C12 SVARURAGDUBTCW-UHFFFAOYSA-N 0.000 abstract 1
- GMWIWJMSCHALJV-UHFFFAOYSA-N 7-methoxy-n-[4-methyl-5-(trifluoromethyl)-1h-pyrazol-3-yl]-6-(oxan-4-ylsulfonyl)quinolin-4-amine Chemical compound C=12C=C(S(=O)(=O)C3CCOCC3)C(OC)=CC2=NC=CC=1NC1=NNC(C(F)(F)F)=C1C GMWIWJMSCHALJV-UHFFFAOYSA-N 0.000 abstract 1
- LHUXIXHXMCIUBN-UHFFFAOYSA-N 7-methoxy-n-[4-methyl-5-(trifluoromethyl)-1h-pyrazol-3-yl]-6-propan-2-ylsulfonylquinolin-4-amine Chemical compound C=12C=C(S(=O)(=O)C(C)C)C(OC)=CC2=NC=CC=1NC1=NNC(C(F)(F)F)=C1C LHUXIXHXMCIUBN-UHFFFAOYSA-N 0.000 abstract 1
- 125000004183 alkoxy alkyl group Chemical group 0.000 abstract 1
- 125000000217 alkyl group Chemical group 0.000 abstract 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 abstract 1
- 125000004438 haloalkoxy group Chemical group 0.000 abstract 1
- GRVDJDISBSALJP-UHFFFAOYSA-N methyloxidanyl Chemical group [O]C GRVDJDISBSALJP-UHFFFAOYSA-N 0.000 abstract 1
- UTGFZERHPKWOOY-UHFFFAOYSA-N n-(4,5-dimethyl-1h-pyrazol-3-yl)-7-methoxy-6-(2-methoxyethylsulfonyl)quinolin-4-amine Chemical compound C1=CN=C2C=C(OC)C(S(=O)(=O)CCOC)=CC2=C1NC1=NNC(C)=C1C UTGFZERHPKWOOY-UHFFFAOYSA-N 0.000 abstract 1
- GTRTXSSFSXXYFL-UHFFFAOYSA-N n-(4,5-dimethyl-1h-pyrazol-3-yl)-7-methoxy-6-(4-methyloxan-4-yl)sulfonylquinolin-4-amine Chemical compound C=12C=C(S(=O)(=O)C3(C)CCOCC3)C(OC)=CC2=NC=CC=1NC1=NNC(C)=C1C GTRTXSSFSXXYFL-UHFFFAOYSA-N 0.000 abstract 1
- CXRQMMOWWNSBTM-UHFFFAOYSA-N n-(4,5-dimethyl-1h-pyrazol-3-yl)-7-methoxy-6-(oxan-4-ylsulfonyl)quinolin-4-amine Chemical compound C=12C=C(S(=O)(=O)C3CCOCC3)C(OC)=CC2=NC=CC=1NC1=NNC(C)=C1C CXRQMMOWWNSBTM-UHFFFAOYSA-N 0.000 abstract 1
- YZBBCCBLKFNURH-UHFFFAOYSA-N n-(4,5-dimethyl-1h-pyrazol-3-yl)-7-methoxy-6-propan-2-ylsulfonylquinolin-4-amine Chemical compound C=12C=C(S(=O)(=O)C(C)C)C(OC)=CC2=NC=CC=1NC1=NNC(C)=C1C YZBBCCBLKFNURH-UHFFFAOYSA-N 0.000 abstract 1
- VSGPVHSTVTXREH-UHFFFAOYSA-N quinolin-4-one Chemical compound C1=CC=C[C]2C(=O)C=CN=C21 VSGPVHSTVTXREH-UHFFFAOYSA-N 0.000 abstract 1
Classifications
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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
- C07D401/02—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
- C07D401/12—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 chain containing hetero atoms as chain links
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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
- A61P1/04—Drugs for disorders of the alimentary tract or the digestive system for ulcers, gastritis or reflux esophagitis, e.g. antacids, inhibitors of acid secretion, mucosal protectants
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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
- A61P1/16—Drugs for disorders of the alimentary tract or the digestive system for liver or gallbladder disorders, e.g. hepatoprotective agents, cholagogues, litholytics
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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
-
- 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
- A61P17/00—Drugs for dermatological disorders
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P19/00—Drugs for skeletal disorders
-
- A—HUMAN NECESSITIES
- 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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P21/00—Drugs for disorders of the muscular or neuromuscular 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
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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
- A61P3/00—Drugs for disorders of the metabolism
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- 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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- 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
- A61P37/02—Immunomodulators
- A61P37/06—Immunosuppressants, e.g. drugs for graft rejection
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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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- A—HUMAN NECESSITIES
- 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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- Engineering & Computer Science (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Immunology (AREA)
- Diabetes (AREA)
- Pulmonology (AREA)
- Physical Education & Sports Medicine (AREA)
- Rheumatology (AREA)
- Hematology (AREA)
- Obesity (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Neurology (AREA)
- Endocrinology (AREA)
- Heart & Thoracic Surgery (AREA)
- Ophthalmology & Optometry (AREA)
- Pain & Pain Management (AREA)
- Cardiology (AREA)
- Vascular Medicine (AREA)
- Gastroenterology & Hepatology (AREA)
- Biomedical Technology (AREA)
- Urology & Nephrology (AREA)
- Neurosurgery (AREA)
- Transplantation (AREA)
- Emergency Medicine (AREA)
- Dermatology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
Abstract
Reivindicación 1: Un compuesto de amino-quinolina caracterizado porque es de la fórmula (1), en la que: R¹ es alquilo C₁₋₆, halo-alquilo C₁₋₆, cicloalquilo C₃₋₆ o heterocicloalquilo de 4 - 6 miembros, en donde: dicho alquilo C₁₋₆ está opcionalmente sustituido con un grupo seleccionado del grupo que consiste en ciano, hidroxilo, alcoxi C₁₋₆, alcoxi C₁₋₆alcoxi C₂₋₆, -CO₂H, -CO₂-alquilo C₁₋₄, -SO₂-alquilo C₁₋₄, cicloalquilo C₃₋₆ y heterocicloalquilo de 4 - 6 miembros, en donde dicho cicloalquilo C₃₋₆ o heterocicloalquilo de 4 - 6 miembros está opcionalmente sustituido con 1 ó 2 grupos cada uno seleccionado independientemente del grupo que consiste en halógeno, -CF₃, hidroxilo, amino, alquil C₁₋₄-amino-, alquil C₁₋₄-alquil C₁₋₄-amino-, alquilo C₁₋₄, hidroxi-alquilo C₁₋₄ y alcoxi C₁₋₄, dicho cicloalquilo C₃₋₆ o heterocicloalquilo de 4 - 6 miembros está opcionalmente sustituido con 1 - 3 grupos seleccionados cada uno independientemente del grupo que consiste en halógeno, -CF₃, hidroxilo, ciano, amino, alquil C₁₋₄-amino-, alquil C₁₋₄-alquil C₁₋₄amino-, alquilo C₁₋₄, hidroxi-alquilo C₁₋₄-, oxo y alcoxi C₁₋₄ y R² es fluoro, hidroxi, alcoxi C₁₋₆-, halo-alcoxi C₁₋₆-, alcoxi C₁₋₄alcoxi C₂₋₆, halo-alcoxi C₁₋₄alcoxi C₂₋₆-, hidroxi-alcoxi C₂₋₆-, cicloalquil C₃₋₆-alcoxi C₁₋₄-, cicloalquil C₃₋₆-oxi-, heterocicloalquil (de 4 - 6 miembros)-alcoxi C₁₋₄ o heterocicloalquil (de 4 - 6 miembros)-oxi-, en donde el resto halo-alquilo C₁₋₆ del halo-alcoxi C₁₋₆- y el resto haloalquilo C₁₋₄ de los grupos halo-alcoxi C₁₋₄alcoxi C₂₋₆- contienen 1, 2 ó 3 átomos de fluoro, en donde el resto cicloalquilo C₃₋₆ del cicloalquil C₃₋₆-alcoxi C₁₋₄- o el cicloalcoxi C₃₋₆- está opcionalmente sustituido con un grupo seleccionado del grupo que consiste en ciano, halo, hidroxilo, alcoxi C₁₋₆ y alcoxi C₁₋₄alcoxi C₂₋₆, y en donde el resto heterocicloalquilo de 4 - 6 miembros del heterocicloalquil (de 4 - 6 miembros)-alcoxi C₁₋₄- o heterocicloalquil (de 4 - 6 miembros)-oxi- está opcionalmente sustituido con un grupo seleccionado del grupo que consiste en ciano, halo, hidroxilo, alcoxi C₁₋₆ y alcoxi C₁₋₄alcoxi C₂₋₆; R³ es H, metilo; R⁴ es H, metilo o trifluorometilo; y R⁵ es H o alquilo C₁₋₃; o una de sus sales; con la condición de que el compuesto no sea: 6-(terc-butilsulfonil)-N-(4,5-dimetil-1H-pirazol-3-il)-7-metoxiquinolin-4-amina, 2-((4-((4,5-dimetil-1H-pirazol-3-il)amino)-7-metoxiquinolin-6-il)sulfonil)-2-metilpropan-1-ol, N-(4,5-dimetil-1H-pirazol-3-il)-7-metoxi-6-((tetrahidro-2H-piran-4-il)sulfonil)quinolin-4-amina, N-(4,5-dimetil-1H-pirazol-3-il)-6-((2,2-dimetiltetrahidro-2H-piran-4-il)sulfonil)-7-metoxiquinolin-4-amina, N-(4,5-dimetil-1H-pirazol-3-il)-7-metoxi-6-((4-metiltetrahidro-2H-piran-4-il)sulfonil)quinolin-4-amina, N-(4,5-dimetil-1H-pirazol-3-il)-7-metoxi-6-((2-metoxietil)sulfonil)quinolin-4-amina, N-(4,5-dimetil-1H-pirazol-3-il)-7-metoxi-6-(((3R,4R)-3-metiltetrahidro-2H-piran-4-il)sulfonil)quinolin-4-amina, N-(4,5-dimetil-1H-pirazol-3-il)-6-(((2R,6S)-2,6-dimetiltetrahidro-2H-piran-4-il)sulfonil)-7-metoxiquinolin-4-amina, 6-(terc-butilsulfonil)-4-((4,5-dimetil-1H-pirazol-3-il)amino)quinolin-7-ol, 2-{[4-[(4,5-dimetil-1H-pirazol-3-il)amino]-7-(metiloxi)-6-quinolinil]sulfonil}etanol, N-(4,5-dimetil-1H-pirazol-3-il)-6-[(1-metiletil)sulfonil]-7-(metiloxi)-4-quinolinamina, 6-(isopropil-sulfonil)-7-metoxi-N-(4-metil-5-(trifluorometil)-1H-pirazol-3-il)quinolin-4-amina, 6-(terc-butilsulfonil)-7-metoxi-N-(4-metil-5-(trifluorometil)-1H-pirazol-3-il)quinolin-4-amina, 6-(terc-butilsulfonil)-N-(4,5-dimetil-1H-pirazol-3-il)-7-etoxiquinolin-4-amina, 7-metoxi-N-(4-metil-5-(trifluorometil)-1H-pirazol-3-il)-6-((tetrahidro-2H-piran-4-il)sulfonil)quinolin-4-amina, 2-((6-(terc-butilsulfonil)-4-((4,5-dimetil-1H-pirazol-3-il)amino)quinolin-7-il)oxi)etanol, 6-(terc-butilsulfonil)-7-(difluorometoxi)-N-(4,5-dimetil-1H-pirazol-3-il)quinolin-4-amina, o 7-(difluorometoxi)-N-(4,5-dimetil-1H-pirazol-3-il)-6-((tetrahidro-2H-piran-4-il)sulfonil)quinolin-4-amina, o una de sus sales.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201261700536P | 2012-09-13 | 2012-09-13 | |
| US201361767378P | 2013-02-21 | 2013-02-21 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| AR092530A1 true AR092530A1 (es) | 2015-04-22 |
Family
ID=50278701
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ARP130103248A AR092530A1 (es) | 2012-09-13 | 2013-09-11 | Compuesto de amino-quinolina, composicion farmaceutica que lo comprende y uso de dicho compuesto para la preparacion de un medicamento |
Country Status (21)
| Country | Link |
|---|---|
| US (1) | US9216965B2 (es) |
| EP (1) | EP2895167B1 (es) |
| JP (1) | JP6258331B2 (es) |
| KR (1) | KR20150053920A (es) |
| CN (1) | CN104602692B (es) |
| AR (1) | AR092530A1 (es) |
| AU (1) | AU2013315387B2 (es) |
| BR (1) | BR112015004967A2 (es) |
| CA (1) | CA2883155A1 (es) |
| CL (1) | CL2015000615A1 (es) |
| CR (1) | CR20150133A (es) |
| DO (1) | DOP2015000059A (es) |
| EA (1) | EA027984B1 (es) |
| ES (1) | ES2713172T3 (es) |
| IL (1) | IL237158A0 (es) |
| MX (1) | MX2015003275A (es) |
| PE (1) | PE20150774A1 (es) |
| PH (1) | PH12015500345A1 (es) |
| SG (1) | SG11201500973WA (es) |
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| UY33549A (es) * | 2010-08-10 | 2012-01-31 | Glaxo Group Ltd | Quinolil aminas como agentes inhibidores de las quinasas |
| BR112013022307A2 (pt) | 2011-03-04 | 2020-09-24 | Glaxosmithkline Intellectual Property (No. 2) Limited | aminoquinolinas como inibidores de quinase |
| TWI547494B (zh) | 2011-08-18 | 2016-09-01 | 葛蘭素史克智慧財產發展有限公司 | 作為激酶抑制劑之胺基喹唑啉類 |
| AR092530A1 (es) | 2012-09-13 | 2015-04-22 | Glaxosmithkline Llc | Compuesto de amino-quinolina, composicion farmaceutica que lo comprende y uso de dicho compuesto para la preparacion de un medicamento |
| AR092529A1 (es) | 2012-09-13 | 2015-04-22 | Glaxosmithkline Llc | Compuesto de aminoquinazolina, composicion farmaceutica que lo comprende y uso de dicho compuesto para la preparacion de un medicamento |
| TWI630203B (zh) | 2013-02-21 | 2018-07-21 | 葛蘭素史克智慧財產發展有限公司 | 做為激酶抑制劑的喹唑啉類 |
| GB201506872D0 (en) | 2015-04-22 | 2015-06-03 | Ge Oil & Gas Uk Ltd | Novel compounds |
| GB201516243D0 (en) | 2015-09-14 | 2015-10-28 | Glaxosmithkline Ip Dev Ltd | Novel compounds |
| AU2016333987A1 (en) | 2015-10-05 | 2018-05-10 | Ny State Psychiatric Institute | Activators of autophagic flux and phospholipase D and clearance of protein aggregates including tau and treatment of proteinopathies |
| CN107158385B (zh) * | 2016-03-14 | 2020-07-14 | 苏州大学 | Rip3抑制剂在制备抗血小板血栓药物中的用途 |
| EP3445759A1 (en) | 2016-04-20 | 2019-02-27 | GlaxoSmithKline Intellectual Property Development Ltd | Conjugates comprising ripk2 inhibitors |
| WO2020094613A1 (en) | 2018-11-06 | 2020-05-14 | INSERM (Institut National de la Santé et de la Recherche Médicale) | Nod2 inhibitors for the treatment of hereditary periodic fevers |
| CN114014890A (zh) * | 2021-03-12 | 2022-02-08 | 爱科诺生物医药(香港)有限公司 | 具有rip2激酶抑制活性的化合物，包含其的药物组合物，及其应用 |
| WO2025078493A1 (en) | 2023-10-11 | 2025-04-17 | Institut National de la Santé et de la Recherche Médicale | Local administration of ripk2 inhibitors for the curative treatment of allergic asthma |
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- 2013-09-13 CN CN201380045559.XA patent/CN104602692B/zh not_active Expired - Fee Related
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- 2013-09-13 KR KR1020157006177A patent/KR20150053920A/ko not_active Withdrawn
- 2013-09-13 EA EA201590552A patent/EA027984B1/ru not_active IP Right Cessation
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- 2013-09-13 BR BR112015004967A patent/BR112015004967A2/pt active Search and Examination
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Also Published As
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| TW201425307A (zh) | 2014-07-01 |
| EP2895167B1 (en) | 2018-12-05 |
| ES2713172T3 (es) | 2019-05-20 |
| JP2015528508A (ja) | 2015-09-28 |
| CA2883155A1 (en) | 2014-03-20 |
| CR20150133A (es) | 2015-05-04 |
| MX2015003275A (es) | 2015-07-06 |
| SG11201500973WA (en) | 2015-04-29 |
| EA027984B1 (ru) | 2017-09-29 |
| IL237158A0 (en) | 2015-04-30 |
| JP6258331B2 (ja) | 2018-01-10 |
| BR112015004967A2 (pt) | 2020-04-22 |
| EP2895167A1 (en) | 2015-07-22 |
| EP2895167A4 (en) | 2016-03-16 |
| CN104602692A (zh) | 2015-05-06 |
| EA201590552A1 (ru) | 2015-06-30 |
| AU2013315387B2 (en) | 2016-09-08 |
| PH12015500345A1 (en) | 2015-04-20 |
| US20150094333A1 (en) | 2015-04-02 |
| CN104602692B (zh) | 2017-06-23 |
| WO2014043437A1 (en) | 2014-03-20 |
| US9216965B2 (en) | 2015-12-22 |
| DOP2015000059A (es) | 2015-05-15 |
| CL2015000615A1 (es) | 2015-08-28 |
| PE20150774A1 (es) | 2015-05-28 |
| AU2013315387A1 (en) | 2015-02-26 |
| KR20150053920A (ko) | 2015-05-19 |
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