AR067562A1 - Compuestos heterociclicos inhibidores de kinasa - Google Patents
Compuestos heterociclicos inhibidores de kinasaInfo
- Publication number
- AR067562A1 AR067562A1 ARP080103052A ARP080103052A AR067562A1 AR 067562 A1 AR067562 A1 AR 067562A1 AR P080103052 A ARP080103052 A AR P080103052A AR P080103052 A ARP080103052 A AR P080103052A AR 067562 A1 AR067562 A1 AR 067562A1
- Authority
- AR
- Argentina
- Prior art keywords
- substituted
- amino
- aryl
- hetero
- aryloxy
- Prior art date
Links
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
- C07D417/04—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 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
- 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
- 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
- A61P17/00—Drugs for dermatological disorders
- A61P17/06—Antipsoriatics
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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
- A61P19/02—Drugs for skeletal disorders for joint disorders, e.g. arthritis, arthrosis
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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
- A61P3/04—Anorexiants; Antiobesity agents
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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
- 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
- A61P37/02—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
- A61P9/00—Drugs for disorders of the cardiovascular system
-
- 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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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing three or more hetero rings
-
- 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
-
- 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
Landscapes
- Health & Medical Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Veterinary Medicine (AREA)
- Animal Behavior & Ethology (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Immunology (AREA)
- Diabetes (AREA)
- Rheumatology (AREA)
- Obesity (AREA)
- Cardiology (AREA)
- Heart & Thoracic Surgery (AREA)
- Hematology (AREA)
- Vascular Medicine (AREA)
- Child & Adolescent Psychology (AREA)
- Urology & Nephrology (AREA)
- Emergency Medicine (AREA)
- Endocrinology (AREA)
- Communicable Diseases (AREA)
- Oncology (AREA)
- Pain & Pain Management (AREA)
- Transplantation (AREA)
- Dermatology (AREA)
- Pulmonology (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Physical Education & Sports Medicine (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
Abstract
Reivindicacion 1: Un compuesto de la formula (A): en donde: el anillo AD es un anillo heterocíclico aromático 5,6-bicíclico, en donde A es un anillo heterocíclico aromático de 5 miembros que contiene uno o mas átomos de O, S y N del anillo fusionado con el anillo D, el cual es un anillo de fenilo o un anillo heterocíclico aromático de 6 miembros que contiene uno, dos o tres átomos de nitrogeno del anillo, en donde el anillo AD esta sustituido por R2, R3, R4, y R5; E es un arilo de 6 a 10 átomos de carbono, un hetero-arilo de 5 a 10 miembros, o halogeno, en donde los anillos están opcionalmente sustituidos por R6, R7 y R8; Q es O o S; R1 se selecciona a partir del grupo que consiste en hidrogeno, alquilo, alquilo sustituido, alquenilo, alquenilo sustituido, alquinilo, alquinilo sustituido alcoxilo, alcoxilo sustituido amino, amino sustituido, arilo, arilo sustituido, hetero-arilo, hetero-arilo sustituido, heterociclilo, cicloalquilo, cicloalquilo sustituido, heterociclilo sustituido, ariloxilo, ariloxilo sustituido, hetero-ariloxilo, hetero-ariloxilo sustituido, heterocicliloxilo, heterocicliloxilo sustituido, cicloalquiloxilo, cicloalquiloxilo sustituido, y alquil-amino; R2 Y R3 se seleccionan independientemente a partir del grupo que consiste en hidrogeno, alquilo, alquilo sustituido, alquenilo, alquenilo sustituido, alquinilo, alquinilo sustituido, alcoxilo, alcoxilo sustituido, arilo, arilo sustituido, hetero-arilo, hetero-arilo sustituido, heterociclilo, cicloalquilo, cicloalquilo sustituido, heterociclilo sustituido, ariloxilo, ariloxilo sustituido, hetero-ariloxilo, hetero-ariloxilo sustituido, heterocicliloxilo, heterocicliloxilo sustituido, cicloalquiloxilo, cicloalquiloxilo sustituido, acilo, acilamino, aciloxilo, amino, amino sustituido, amino-carbonilo, amino-tiocarbonilo, amino-carbonil-amino, amino-tiocarbonil-amino, amino-carboniloxilo, amino-sulfonilo, amino-sulfoniloxilo, amino-sulfonil-amino, amidino, carboxilo, carboxil-éster, (carboxil-éster)-amino, (carboxil-éster)-oxilo, ciano, halogeno, hidroxilo, nitro, SO3H, sulfonilo, sulfonilo sustituido, sulfoniloxilo, tioacilo, tiol, tioalquilo, y tioalquilo sustituido; R4 y R5 se seleccionan independientemente a partir del grupo que consiste en hidrogeno, halogeno, ciano, nitro, amino, amino sustituido, alcoxilo, alcoxilo sustituido, alquilo, y alquilo sustituido; R6 se selecciona a partir del grupo que consiste en hidrogeno, halogeno, ciano, nitro, alcoxilo, alcoxilo sustituido, alquilo, y alquilo sustituido; y R7 y R8 se seleccionan independientemente a partir del grupo que consiste en hidrogeno, alquilo, alquilo sustituido, alquenilo, alquenilo sustituido, alquinilo, alquinilo sustituido, alcoxilo, alcoxilo sustituido, arilo, arilo sustituido, hetero-arilo, hetero-arilo sustituido, heterociclilo, cicloalquilo, cicloalquilo sustituido, heterociclilo sustituido, ariloxilo, ariloxilo sustituido, hetero-ariloxilo, hetero-ariloxilo sustituido, heterocicliloxilo, heterocicliloxilo sustituido, cicloalquiloxilo, cicloalquiloxilo sustituido, acilo, aciloxilo, amino-carbonilo, amino-tiocarbonilo, amino-tiocarbonil-amino, amino-carboniloxilo, amino-sulfonilo, amino-sulfoniloxilo, amino-sulfonil-amino, amidino, carboxilo, carboxil-éster, (carboxil-éster)-oxilo, ciano, halogeno, hidroxilo, nitro, SO3H, sulfonilo, sulfonilo sustituido, sulfoniloxilo, tioacilo, tiol, tioalquilo, y tioalquilo sustituido; o R7 y R8 junto con los átomos del anillo con los que están unidos, forman un grupo carbocíclico o heterocíclico de 5 a 8 miembros. Compuestos inhibidores de cinasa de fosíatidil-inositol (Pl)-3, sus sales farmacéuticamente aceptables, y pro-fármacos de los mismos; composiciones de los nuevos compuestos, ya sea solos o bien en combinacion con cuando menos un agente terapéutico adicional, con un vehículo farmacéuticamente aceptable y utilizacion de los compuestos, ya sea solos o bien en combinacion con cuando menos un agente terapéutico adicional, en la profilaxis o el tratamiento de enfermedades proliferativas caracterizadas por la actividad anormal de los factores de crecimiento, las cinasas de proteína serina/treonina, y las cinasas de fosfolípidos.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP07112688 | 2007-07-18 |
Publications (1)
Publication Number | Publication Date |
---|---|
AR067562A1 true AR067562A1 (es) | 2009-10-14 |
Family
ID=38800784
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
ARP080103052A AR067562A1 (es) | 2007-07-18 | 2008-07-16 | Compuestos heterociclicos inhibidores de kinasa |
Country Status (15)
Country | Link |
---|---|
US (1) | US8053574B2 (es) |
EP (1) | EP2178868A1 (es) |
JP (1) | JP2010533680A (es) |
KR (1) | KR20100049073A (es) |
CN (1) | CN101801966A (es) |
AR (1) | AR067562A1 (es) |
AU (1) | AU2008277628B2 (es) |
BR (1) | BRPI0813831A2 (es) |
CA (1) | CA2693232A1 (es) |
CL (1) | CL2008002097A1 (es) |
EA (1) | EA201000130A1 (es) |
MX (1) | MX2010000716A (es) |
PE (1) | PE20090492A1 (es) |
TW (1) | TW200908969A (es) |
WO (1) | WO2009010530A1 (es) |
Families Citing this family (77)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US7723477B2 (en) | 2005-10-31 | 2010-05-25 | Oncomed Pharmaceuticals, Inc. | Compositions and methods for inhibiting Wnt-dependent solid tumor cell growth |
US8883820B2 (en) | 2006-08-30 | 2014-11-11 | Cellzome Ltd. | Triazole derivatives as kinase inhibitors |
ES2401557T3 (es) | 2007-08-02 | 2013-04-22 | Amgen, Inc | Moduladores de Pl3 cinasas y métodos de uso |
WO2009068482A1 (en) | 2007-11-27 | 2009-06-04 | Cellzome Limited | Amino triazoles as pi3k inhibitors |
JP5520831B2 (ja) * | 2007-12-19 | 2014-06-11 | アムジエン・インコーポレーテツド | Pi3キナーゼの阻害薬 |
EP2283013A1 (en) * | 2008-04-16 | 2011-02-16 | Vertex Pharmaceuticals Incorporated | Inhibitors of phosphatidylinositol 3-kinase |
EP2444403A1 (en) | 2008-04-18 | 2012-04-25 | Shionogi Co., Ltd. | Heterocyclic compound having inhibitory activity on PI3K |
US8415376B2 (en) | 2008-05-30 | 2013-04-09 | Amgen Inc. | Inhibitors of PI3 kinase |
WO2010010188A1 (en) * | 2008-07-25 | 2010-01-28 | Galapagos Nv | Novel compounds useful for the treatment of degenerative and inflammatory diseases. |
WO2010010186A1 (en) * | 2008-07-25 | 2010-01-28 | Galapagos Nv | Novel compounds useful for the treatment of degenerative and inflammatory diseases |
JO3041B1 (ar) * | 2008-07-25 | 2016-09-05 | Galapagos Nv | مركبات جديدة مفيدة لمعالجة الأمراض التنكسية والالتهابية |
ES2663536T3 (es) | 2008-09-26 | 2018-04-13 | Oncomed Pharmaceuticals, Inc. | Agentes que se unen a receptores frizzled y usos de los mismos |
WO2010074089A1 (ja) | 2008-12-24 | 2010-07-01 | 第一三共株式会社 | インダニル化合物 |
BRPI0923654A2 (pt) | 2008-12-24 | 2018-10-16 | Daiichi Sankyo Company, Limited | composto, uso de um composto, e , composição farmacêutica. |
WO2010092015A1 (en) * | 2009-02-10 | 2010-08-19 | Cellzome Limited | Urea triazololo [1, 5-a] pyridine derivatives as pi3k inhibitors |
JP2012521354A (ja) | 2009-03-20 | 2012-09-13 | アムジエン・インコーポレーテツド | Pi3キナーゼの阻害薬 |
WO2010125799A1 (ja) | 2009-04-27 | 2010-11-04 | 塩野義製薬株式会社 | Pi3k阻害活性を有するウレア誘導体 |
EP2432782A1 (en) | 2009-05-20 | 2012-03-28 | Cellzome Ag | Methods for the identification of phosphatidylinositol kinase interacting molecules and for the purification of phosphatidylinositol kinase proteins |
US8501936B2 (en) | 2009-06-05 | 2013-08-06 | Cephalon, Inc. | Preparation and uses of 1,2,4-triazolo [1,5a] pyridine derivatives |
TWI462920B (zh) | 2009-06-26 | 2014-12-01 | 葛萊伯格有限公司 | 用於治療退化性及發炎疾病之新穎化合物 |
JO3030B1 (ar) | 2009-06-26 | 2016-09-05 | Galapagos Nv | مركب جديد مفيد لمعالجة الامراض التنكسية والالتهابات |
EP2448946B1 (en) * | 2009-07-02 | 2013-07-24 | Novartis AG | 2-carboxamide cycloamino ureas useful as pi3k inhibitors |
EP2343297A1 (en) * | 2009-11-30 | 2011-07-13 | Bayer Schering Pharma AG | Triazolopyridines |
EP2343294A1 (en) * | 2009-11-30 | 2011-07-13 | Bayer Schering Pharma AG | Substituted triazolopyridines |
EP2343295A1 (en) * | 2009-11-30 | 2011-07-13 | Bayer Schering Pharma AG | Triazolopyridine derivates |
TWI535445B (zh) | 2010-01-12 | 2016-06-01 | 安可美德藥物股份有限公司 | Wnt拮抗劑及治療和篩選方法 |
WO2011107494A1 (de) | 2010-03-03 | 2011-09-09 | Sanofi | Neue aromatische glykosidderivate, diese verbindungen enthaltende arzneimittel und deren verwendung |
EP2576544A4 (en) * | 2010-06-01 | 2013-09-11 | Angion Biomedica Corp | INHIBITORS OF CYTOCHROMES P450 AND USES THEREOF |
UY33452A (es) | 2010-06-16 | 2012-01-31 | Bayer Schering Pharma Ag | Triazolopiridinas sustituidas |
US8530413B2 (en) | 2010-06-21 | 2013-09-10 | Sanofi | Heterocyclically substituted methoxyphenyl derivatives with an oxo group, processes for preparation thereof and use thereof as medicaments |
TW201215388A (en) | 2010-07-05 | 2012-04-16 | Sanofi Sa | (2-aryloxyacetylamino)phenylpropionic acid derivatives, processes for preparation thereof and use thereof as medicaments |
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TW201221505A (en) | 2010-07-05 | 2012-06-01 | Sanofi Sa | Aryloxyalkylene-substituted hydroxyphenylhexynoic acids, process for preparation thereof and use thereof as a medicament |
PL2699575T3 (pl) | 2011-04-21 | 2015-08-31 | Bayer Ip Gmbh | Triazolopirydyny |
WO2012160029A1 (en) | 2011-05-23 | 2012-11-29 | Bayer Intellectual Property Gmbh | Substituted triazolopyridines |
WO2013037390A1 (en) | 2011-09-12 | 2013-03-21 | Sanofi | 6-(4-hydroxy-phenyl)-3-styryl-1h-pyrazolo[3,4-b]pyridine-4-carboxylic acid amide derivatives as kinase inhibitors |
WO2013045413A1 (en) | 2011-09-27 | 2013-04-04 | Sanofi | 6-(4-hydroxy-phenyl)-3-alkyl-1h-pyrazolo[3,4-b]pyridine-4-carboxylic acid amide derivatives as kinase inhibitors |
US20150132301A1 (en) * | 2011-12-09 | 2015-05-14 | Oncomed Pharmaceuticals, Inc. | Combination Therapy for Treatment of Cancer |
UA112096C2 (uk) | 2011-12-12 | 2016-07-25 | Байєр Інтеллектуал Проперті Гмбх | Заміщені триазолопіридини та їх застосування як інгібіторів ttk |
US9512126B2 (en) | 2012-03-14 | 2016-12-06 | Bayer Intellectual Property Gmbh | Substituted imidazopyridazines |
AP3778A (en) | 2012-07-10 | 2016-08-31 | Bayer Pharma AG | Method for preparing substituted triazolopyridines |
WO2014020043A1 (en) | 2012-08-02 | 2014-02-06 | Bayer Pharma Aktiengesellschaft | Combinations for the treatment of cancer |
EP2914260A1 (en) | 2012-10-31 | 2015-09-09 | INSERM (Institut National de la Santé et de la Recherche Médicale) | Methods for preventing antiphospholipid syndrome (aps) |
CN104870017B (zh) | 2012-11-08 | 2020-08-14 | 理森制药股份公司 | 含有PDE4抑制剂和PI3δ或双重PI3δ-γ激酶抑制剂的药物组合物 |
JP2016510411A (ja) | 2013-02-04 | 2016-04-07 | オンコメッド ファーマシューティカルズ インコーポレイテッド | Wnt経路インヒビターによる処置の方法およびモニタリング |
LT3008062T (lt) | 2013-06-11 | 2017-06-12 | Bayer Pharma Aktiengesellschaft | Pakeistųjų triazolpiridinų provaistų dariniai |
WO2015039333A1 (en) * | 2013-09-22 | 2015-03-26 | Merck Sharp & Dohme Corp. | TrkA KINASE INHIBITORS, COMPOSITIONS AND METHODS THEREOF |
GB201402071D0 (en) | 2014-02-07 | 2014-03-26 | Galapagos Nv | Novel salts and pharmaceutical compositions thereof for the treatment of inflammatory disorders |
GB201402070D0 (en) | 2014-02-07 | 2014-03-26 | Galapagos Nv | Pharmaceutical compositions for the treatment of inflammatory disorders |
US9527835B2 (en) | 2014-02-13 | 2016-12-27 | Incyte Corporation | Cyclopropylamines as LSD1 inhibitors |
SG10201806846RA (en) | 2014-02-13 | 2018-09-27 | Incyte Corp | Cyclopropylamines as lsd1 inhibitors |
EP3392244A1 (en) | 2014-02-13 | 2018-10-24 | Incyte Corporation | Cyclopropylamines as lsd1 inhibitors |
PH12020552066A1 (en) | 2014-02-13 | 2022-05-11 | Incyte Corp | Cyclopropylamines as lsd1 inhibitors |
US9598424B2 (en) | 2014-03-06 | 2017-03-21 | Takeda Pharmaceutical Company Limited | Heteroarylamide inhibitors of TBK1 |
WO2016007727A1 (en) | 2014-07-10 | 2016-01-14 | Incyte Corporation | Triazolopyridines and triazolopyrazines as lsd1 inhibitors |
US9695168B2 (en) | 2014-07-10 | 2017-07-04 | Incyte Corporation | Substituted imidazo[1,5-α]pyridines and imidazo[1,5-α]pyrazines as LSD1 inhibitors |
TW201613925A (en) | 2014-07-10 | 2016-04-16 | Incyte Corp | Imidazopyrazines as LSD1 inhibitors |
WO2016007722A1 (en) | 2014-07-10 | 2016-01-14 | Incyte Corporation | Triazolopyridines and triazolopyrazines as lsd1 inhibitors |
WO2016059220A1 (en) | 2014-10-16 | 2016-04-21 | INSERM (Institut National de la Santé et de la Recherche Médicale) | Tcr-activating agents for use in the treatment of t-all |
PH12017501817B1 (en) | 2015-04-03 | 2023-06-16 | Incyte Holdings Corp | Heterocyclic compounds as lsd1 inhibitors |
TWI765860B (zh) | 2015-08-12 | 2022-06-01 | 美商英塞特公司 | Lsd1抑制劑之鹽 |
US10722484B2 (en) | 2016-03-09 | 2020-07-28 | K-Gen, Inc. | Methods of cancer treatment |
CN109414410B (zh) | 2016-04-22 | 2022-08-12 | 因赛特公司 | Lsd1抑制剂的制剂 |
BR112019010511A2 (pt) | 2016-11-23 | 2019-09-17 | Bayer Ag | derivados de heterociclo bicíclico fundido como pesticidas |
MA46888A (fr) * | 2016-11-28 | 2021-06-02 | Bristol Myers Squibb Co | Inhibiteurs de gsk-3 |
CA3078173A1 (en) | 2017-10-02 | 2019-04-11 | 1ST Biotherapeutics, Inc. | Benzothiazol compounds and methods using the same for treating neurodegenerative disorders |
KR20200139153A (ko) | 2018-02-27 | 2020-12-11 | 인사이트 코포레이션 | A2a / a2b 억제제로서의 이미다조피리미딘 및 트리아졸로피리미딘 |
CA3100731A1 (en) | 2018-05-18 | 2019-11-21 | Incyte Corporation | Fused pyrimidine derivatives as a2a / a2b inhibitors |
GEP20237560B (en) | 2018-07-05 | 2023-10-25 | Incyte Corp | Fused pyrazine derivatives as a2a / a2b inhibitors |
WO2020047198A1 (en) | 2018-08-31 | 2020-03-05 | Incyte Corporation | Salts of an lsd1 inhibitor and processes for preparing the same |
TWI829857B (zh) | 2019-01-29 | 2024-01-21 | 美商英塞特公司 | 作為a2a / a2b抑制劑之吡唑并吡啶及三唑并吡啶 |
US11098044B2 (en) | 2019-02-22 | 2021-08-24 | 1ST Biotherapeutics, Inc. | Imidazopyridinyl compounds and use thereof for treatment of neurodegenerative disorders |
WO2020178795A1 (en) * | 2019-03-07 | 2020-09-10 | 1ST Biotherapeutics, Inc. | [ 18f]-labeled benzothiazole derivative as pet radiotracer |
US10385046B1 (en) | 2019-03-19 | 2019-08-20 | 1ST Biotherapeutics, Inc. | Processes for preparing benzothiazol compounds and methods of using the same for treating neurodegenerative disorders |
CN111116580B (zh) * | 2019-12-27 | 2022-08-23 | 上海应用技术大学 | 一种尼麦角林的改进制备方法 |
KR20240168991A (ko) * | 2022-03-25 | 2024-12-02 | 주식회사 퍼스트바이오테라퓨틱스 | 조혈 전구체 키나제 1(hpk1) 억제제로서의 인다졸 및 이를 사용하는 방법 |
CN118239953A (zh) * | 2022-12-23 | 2024-06-25 | 中国科学院合肥物质科学研究院 | 用于治疗PI3Kγ介导的疾病的化合物及其用途 |
Family Cites Families (8)
Publication number | Priority date | Publication date | Assignee | Title |
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EP0261459A3 (de) | 1986-09-09 | 1988-05-11 | Nihon Tokushu Noyaku Seizo K.K. | Neue N-Benzothiazolylamide |
SK286450B6 (sk) | 1999-10-08 | 2008-10-07 | Grnenthal Gmbh | Bicyklické imidazo-3-yl-amíny, spôsob ich výroby,ich použitie a liečivá obsahujúce tieto látky |
HUP0300359A2 (hu) * | 2000-02-07 | 2003-06-28 | Abbott Gmbh & Co. Kg. | 2-Benzotiazolil-karbamid-származékok és protein kináz inhibitorként történő felhasználásuk és ezeket tartalmazó gyógyszerkészítmények |
BRPI0507653A (pt) | 2004-03-19 | 2007-07-10 | Warner Lambert Co | derivados de imidazopiridina e imidazopiridina formulação farmacêutica compreendendo os mesmos e uso |
JP2008500284A (ja) | 2004-05-12 | 2008-01-10 | ブリストル−マイヤーズ スクイブ カンパニー | 血栓症の治療に有用なp2y1レセプターのウレアアンタゴニスト |
US7636348B2 (en) | 2004-06-30 | 2009-12-22 | Bettis Sonny R | Distributed IP architecture for telecommunications system with video mail |
MX2007004179A (es) * | 2004-10-07 | 2007-06-07 | Warner Lambert Co | Derivados de triazolpiridina como agentes antibacterianos. |
US7576090B2 (en) * | 2004-12-27 | 2009-08-18 | 4Sc Ag | Benzazole analogues and uses thereof |
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2008
- 2008-07-16 CA CA2693232A patent/CA2693232A1/en not_active Abandoned
- 2008-07-16 EP EP08775120A patent/EP2178868A1/en not_active Withdrawn
- 2008-07-16 AR ARP080103052A patent/AR067562A1/es not_active Application Discontinuation
- 2008-07-16 AU AU2008277628A patent/AU2008277628B2/en not_active Expired - Fee Related
- 2008-07-16 EA EA201000130A patent/EA201000130A1/ru unknown
- 2008-07-16 KR KR1020107003426A patent/KR20100049073A/ko not_active Application Discontinuation
- 2008-07-16 JP JP2010516500A patent/JP2010533680A/ja not_active Withdrawn
- 2008-07-16 PE PE2008001205A patent/PE20090492A1/es not_active Application Discontinuation
- 2008-07-16 US US12/669,536 patent/US8053574B2/en not_active Expired - Fee Related
- 2008-07-16 MX MX2010000716A patent/MX2010000716A/es not_active Application Discontinuation
- 2008-07-16 WO PCT/EP2008/059298 patent/WO2009010530A1/en active Application Filing
- 2008-07-16 CN CN200880107620A patent/CN101801966A/zh active Pending
- 2008-07-16 BR BRPI0813831-1A2A patent/BRPI0813831A2/pt not_active IP Right Cessation
- 2008-07-17 CL CL2008002097A patent/CL2008002097A1/es unknown
- 2008-07-17 TW TW097127181A patent/TW200908969A/zh unknown
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CL2008002097A1 (es) | 2009-02-20 |
AU2008277628A1 (en) | 2009-01-22 |
US8053574B2 (en) | 2011-11-08 |
US20100197682A1 (en) | 2010-08-05 |
MX2010000716A (es) | 2010-03-26 |
JP2010533680A (ja) | 2010-10-28 |
TW200908969A (en) | 2009-03-01 |
CA2693232A1 (en) | 2009-01-22 |
CN101801966A (zh) | 2010-08-11 |
AU2008277628B2 (en) | 2012-03-15 |
WO2009010530A1 (en) | 2009-01-22 |
EA201000130A1 (ru) | 2010-08-30 |
KR20100049073A (ko) | 2010-05-11 |
EP2178868A1 (en) | 2010-04-28 |
PE20090492A1 (es) | 2009-05-27 |
BRPI0813831A2 (pt) | 2015-01-06 |
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