PE20091225A1 - Derivados de quinolina como antagonistas del receptor p2x7 - Google Patents
Derivados de quinolina como antagonistas del receptor p2x7Info
- Publication number
- PE20091225A1 PE20091225A1 PE2008000516A PE2008000516A PE20091225A1 PE 20091225 A1 PE20091225 A1 PE 20091225A1 PE 2008000516 A PE2008000516 A PE 2008000516A PE 2008000516 A PE2008000516 A PE 2008000516A PE 20091225 A1 PE20091225 A1 PE 20091225A1
- Authority
- PE
- Peru
- Prior art keywords
- methyl
- hydroxy
- quinolin
- carboxamide
- quinoline derivatives
- Prior art date
Links
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
- C07D401/04—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
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- 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
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/47—Quinolines; Isoquinolines
- A61K31/4709—Non-condensed quinolines and 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
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- 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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- A61P1/12—Antidiarrhoeals
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- 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
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- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
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- 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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- A61P11/14—Antitussive agents
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
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- 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
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- A61P15/00—Drugs for genital or sexual disorders; Contraceptives
- A61P15/02—Drugs for genital or sexual disorders; Contraceptives for disorders of the vagina
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- A61P25/02—Drugs for disorders of the nervous system for peripheral neuropathies
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- A61P3/10—Drugs for disorders of the metabolism for glucose homeostasis for hyperglycaemia, e.g. antidiabetics
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- A61P7/02—Antithrombotic agents; Anticoagulants; Platelet aggregation inhibitors
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- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
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- 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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- 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
- C07D403/04—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings directly linked by a ring-member-to-ring-member bond
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- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (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)
- Engineering & Computer Science (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Neurology (AREA)
- Physical Education & Sports Medicine (AREA)
- Neurosurgery (AREA)
- Diabetes (AREA)
- Immunology (AREA)
- Pulmonology (AREA)
- Biomedical Technology (AREA)
- Endocrinology (AREA)
- Dermatology (AREA)
- Urology & Nephrology (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Rheumatology (AREA)
- Reproductive Health (AREA)
- Pain & Pain Management (AREA)
- Gynecology & Obstetrics (AREA)
- Cardiology (AREA)
- Hematology (AREA)
- Heart & Thoracic Surgery (AREA)
- Virology (AREA)
- Molecular Biology (AREA)
- Psychiatry (AREA)
- Communicable Diseases (AREA)
- Oncology (AREA)
- Ophthalmology & Optometry (AREA)
- AIDS & HIV (AREA)
Abstract
SE REFIERE A DERIVADOS DE QUINOLINA DE FORMULA (I), DONDE n ES 0 O 1; CUANDO n ES 0, R1 ES H O METILO, R2 ES OXHIDRILO Y R3 ES H; Y CUANDO n ES 1, R1 ES H Y UNO DE R2 Y R3 ES OXHIDRILO Y EL OTRO R2 Y R3 ES H. SON COMPUESTOS PREFERIDOS: 6-CLORO-N-{[(1S,3S)-1-HIDROXI-3-METILCICLOHEXIL]METIL}-2-[(3S)-3-HIDROXIPIRROLIDIN-1-IL]QUINOLIN-5-CARBOXAMIDA, 6-CLORO-N-{[(1S,3S)-1-HIDROXI-3-METILCICLOHEXIL]METIL}-2-(4-HIDROXIPIRIDIN-1-IL)QUINOLIN-5-CARBOXAMIDA, 6-CLORO-N-{[(1S,3S)-1-HIDROXI-3-METILCICLOHEXIL]METIL}-2-(3-HIDROXI-3-METILPIRROLIDIN-1-IL)QUINOLIN-5-CARBOXAMIDA, ENTRE OTROS. TAMBIEN SE REFIERE A UN METODO DE PREPARACION PARA UN COMPOSICION FARMACEUTICA. DICHO COMPUESTO ES ANTAGONISTA DE P2X7, SIENDO DE UTILIDAD EN EL TRATAMIENTO DE ENFERMEDADES OBSTRUCTIVAS DE LAS VIAS RESPIRATORIAS, ARTRITIS ASOCIADAS CON OSTEOARTRITIS/OSTEOARTROSIS, PSORIASIS, DERMATITIS ATOPICA, TRASTORNOS INFLAMATORIOS, ENFERMEDADES CARDIOVASCULARES, ENTRE OTROS
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US89629807P | 2007-03-22 | 2007-03-22 |
Publications (1)
Publication Number | Publication Date |
---|---|
PE20091225A1 true PE20091225A1 (es) | 2009-09-16 |
Family
ID=39471999
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PE2008000516A PE20091225A1 (es) | 2007-03-22 | 2008-03-19 | Derivados de quinolina como antagonistas del receptor p2x7 |
Country Status (18)
Country | Link |
---|---|
US (1) | US7964616B2 (es) |
EP (1) | EP2139879B1 (es) |
JP (1) | JP2010522227A (es) |
KR (1) | KR20090122396A (es) |
CN (1) | CN101679350B (es) |
AR (1) | AR065806A1 (es) |
AU (1) | AU2008228067B2 (es) |
BR (1) | BRPI0809106A2 (es) |
CA (1) | CA2680761A1 (es) |
CL (1) | CL2008000825A1 (es) |
ES (1) | ES2388454T3 (es) |
HK (1) | HK1138850A1 (es) |
MX (1) | MX2009010059A (es) |
PE (1) | PE20091225A1 (es) |
RU (1) | RU2460727C2 (es) |
TW (1) | TW200904427A (es) |
UY (1) | UY30976A1 (es) |
WO (1) | WO2008114002A1 (es) |
Families Citing this family (30)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
AR065806A1 (es) | 2007-03-22 | 2009-07-01 | Astrazeneca Ab | Derivados de quinolina, procesos para su preparacion, composiciones farmaceuticas que los contienen y usos para el tratamiento de la artritis reumatoidea. |
US8106073B2 (en) * | 2007-11-30 | 2012-01-31 | Astrazeneca Ab | Quinoline derivatives 057 |
AR087274A1 (es) | 2011-07-22 | 2014-03-12 | Actelion Pharmaceuticals Ltd | Derivados de amidas heterociclicas como antagonistas de receptores p2x7 |
EP2804865B1 (en) | 2012-01-20 | 2015-12-23 | Actelion Pharmaceuticals Ltd. | Heterocyclic amide derivatives as p2x7 receptor antagonists |
JP6295269B2 (ja) | 2012-12-12 | 2018-03-14 | イドーシア ファーマシューティカルズ リミテッドIdorsia Pharmaceuticals Ltd | P2x7受容体アンタゴニストとしてのインドールカルボキサミド誘導体 |
TW201427945A (zh) | 2012-12-18 | 2014-07-16 | Actelion Pharmaceuticals Ltd | 作爲p2x7受體拮抗劑之吲哚羧醯胺衍生物 |
CN104918946B (zh) | 2013-01-22 | 2017-03-29 | 埃科特莱茵药品有限公司 | 作为p2x7受体拮抗剂的杂环酰胺衍生物 |
JP6282016B2 (ja) | 2013-01-22 | 2018-02-21 | イドーシア ファーマシューティカルズ リミテッドIdorsia Pharmaceuticals Ltd | P2x7受容体アンタゴニストとしての複素環アミド誘導体 |
RS59911B1 (sr) | 2013-10-14 | 2020-03-31 | Eisai R&D Man Co Ltd | Selektivno supstituisana jedinjenja hinolina |
JP6692759B2 (ja) * | 2014-06-05 | 2020-05-13 | メルク パテント ゲゼルシャフト ミット ベシュレンクテル ハフツングMerck Patent Gesellschaft mit beschraenkter Haftung | 新規キノリン誘導体及び神経変性疾患におけるそれらの使用 |
TW201718581A (zh) | 2015-10-19 | 2017-06-01 | 英塞特公司 | 作為免疫調節劑之雜環化合物 |
TWI763641B (zh) | 2015-11-19 | 2022-05-11 | 美商英塞特公司 | 作為免疫調節劑之雜環化合物 |
MX2018007774A (es) | 2015-12-22 | 2018-11-09 | Incyte Corp | Compuestos heterociclicos como inmunomoduladores. |
AR108396A1 (es) | 2016-05-06 | 2018-08-15 | Incyte Corp | Compuestos heterocíclicos como inmunomoduladores |
US20170342060A1 (en) | 2016-05-26 | 2017-11-30 | Incyte Corporation | Heterocyclic compounds as immunomodulators |
LT3472167T (lt) | 2016-06-20 | 2022-11-10 | Incyte Corporation | Heterocikliniai junginiai kaip imunomoduliatoriai |
US20180016260A1 (en) | 2016-07-14 | 2018-01-18 | Incyte Corporation | Heterocyclic compounds as immunomodulators |
MA46045A (fr) | 2016-08-29 | 2021-04-28 | Incyte Corp | Composés hétérocycliques utilisés comme immunomodulateurs |
EP3558989B1 (en) | 2016-12-22 | 2021-04-14 | Incyte Corporation | Triazolo[1,5-a]pyridine derivatives as immunomodulators |
WO2018119221A1 (en) | 2016-12-22 | 2018-06-28 | Incyte Corporation | Pyridine derivatives as immunomodulators |
ES2934230T3 (es) | 2016-12-22 | 2023-02-20 | Incyte Corp | Derivados de benzooxazol como inmunomoduladores |
EP4212529A1 (en) | 2018-03-30 | 2023-07-19 | Incyte Corporation | Heterocyclic compounds as immunomodulators |
CN112752756A (zh) | 2018-05-11 | 2021-05-04 | 因赛特公司 | 作为PD-L1免疫调节剂的四氢-咪唑并[4,5-c]吡啶衍生物 |
MA55805A (fr) | 2019-05-03 | 2022-03-09 | Flagship Pioneering Innovations V Inc | Métodes de modulation de l'activité immunitaire |
US11753406B2 (en) | 2019-08-09 | 2023-09-12 | Incyte Corporation | Salts of a PD-1/PD-L1 inhibitor |
BR112022005826A2 (pt) | 2019-09-30 | 2022-06-21 | Incyte Corp | Compostos de pirido[3,2-d]pirimidina como imunomoduladores |
BR112022009031A2 (pt) | 2019-11-11 | 2022-10-11 | Incyte Corp | Sais e formas cristalinas de um inibidor de pd-1/pd-l1 |
AR124001A1 (es) | 2020-11-06 | 2023-02-01 | Incyte Corp | Proceso para fabricar un inhibidor pd-1 / pd-l1 y sales y formas cristalinas del mismo |
US11760756B2 (en) | 2020-11-06 | 2023-09-19 | Incyte Corporation | Crystalline form of a PD-1/PD-L1 inhibitor |
WO2022099018A1 (en) | 2020-11-06 | 2022-05-12 | Incyte Corporation | Process of preparing a pd-1/pd-l1 inhibitor |
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-
2008
- 2008-03-19 AR ARP080101169A patent/AR065806A1/es unknown
- 2008-03-19 CN CN200880017135.1A patent/CN101679350B/zh not_active Expired - Fee Related
- 2008-03-19 EP EP08718785A patent/EP2139879B1/en not_active Not-in-force
- 2008-03-19 MX MX2009010059A patent/MX2009010059A/es active IP Right Grant
- 2008-03-19 WO PCT/GB2008/000946 patent/WO2008114002A1/en active Application Filing
- 2008-03-19 JP JP2010500344A patent/JP2010522227A/ja active Pending
- 2008-03-19 ES ES08718785T patent/ES2388454T3/es active Active
- 2008-03-19 CA CA002680761A patent/CA2680761A1/en not_active Abandoned
- 2008-03-19 BR BRPI0809106-4A patent/BRPI0809106A2/pt not_active IP Right Cessation
- 2008-03-19 RU RU2009135621/04A patent/RU2460727C2/ru not_active IP Right Cessation
- 2008-03-19 PE PE2008000516A patent/PE20091225A1/es not_active Application Discontinuation
- 2008-03-19 KR KR1020097021940A patent/KR20090122396A/ko not_active Application Discontinuation
- 2008-03-19 AU AU2008228067A patent/AU2008228067B2/en not_active Ceased
- 2008-03-20 CL CL2008000825A patent/CL2008000825A1/es unknown
- 2008-03-21 US US12/052,908 patent/US7964616B2/en not_active Expired - Fee Related
- 2008-03-21 TW TW097110021A patent/TW200904427A/zh unknown
- 2008-03-24 UY UY30976A patent/UY30976A1/es unknown
-
2010
- 2010-06-10 HK HK10105772.1A patent/HK1138850A1/xx not_active IP Right Cessation
Also Published As
Publication number | Publication date |
---|---|
AR065806A1 (es) | 2009-07-01 |
RU2460727C2 (ru) | 2012-09-10 |
CN101679350B (zh) | 2014-03-12 |
CL2008000825A1 (es) | 2008-11-03 |
CN101679350A (zh) | 2010-03-24 |
RU2009135621A (ru) | 2011-04-27 |
UY30976A1 (es) | 2008-10-31 |
WO2008114002A1 (en) | 2008-09-25 |
EP2139879A1 (en) | 2010-01-06 |
BRPI0809106A2 (pt) | 2014-08-26 |
TW200904427A (en) | 2009-02-01 |
EP2139879B1 (en) | 2012-07-11 |
US7964616B2 (en) | 2011-06-21 |
AU2008228067A1 (en) | 2008-09-25 |
HK1138850A1 (en) | 2010-09-03 |
CA2680761A1 (en) | 2008-09-25 |
MX2009010059A (es) | 2009-10-12 |
US20080234319A1 (en) | 2008-09-25 |
ES2388454T3 (es) | 2012-10-15 |
JP2010522227A (ja) | 2010-07-01 |
AU2008228067B2 (en) | 2011-12-08 |
KR20090122396A (ko) | 2009-11-27 |
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