AR066845A1 - Derivados de triazolopiridina e imidazopiridina una composicion farmaceutica que los comprende y su uso en la preparacion de un medicamento para el tratamiento del cancer - Google Patents
Derivados de triazolopiridina e imidazopiridina una composicion farmaceutica que los comprende y su uso en la preparacion de un medicamento para el tratamiento del cancerInfo
- Publication number
- AR066845A1 AR066845A1 ARP080102359A ARP080102359A AR066845A1 AR 066845 A1 AR066845 A1 AR 066845A1 AR P080102359 A ARP080102359 A AR P080102359A AR P080102359 A ARP080102359 A AR P080102359A AR 066845 A1 AR066845 A1 AR 066845A1
- Authority
- AR
- Argentina
- Prior art keywords
- optionally
- atom
- amino
- mono
- substituents
- Prior art date
Links
- 206010028980 Neoplasm Diseases 0.000 title 1
- 201000011510 cancer Diseases 0.000 title 1
- 229940126601 medicinal product Drugs 0.000 title 1
- 239000008194 pharmaceutical composition Substances 0.000 title 1
- 229910052799 carbon Inorganic materials 0.000 abstract 10
- 125000005843 halogen group Chemical group 0.000 abstract 8
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 abstract 8
- 229910052757 nitrogen Inorganic materials 0.000 abstract 7
- 125000001424 substituent group Chemical group 0.000 abstract 7
- 229910052717 sulfur Inorganic materials 0.000 abstract 6
- 125000003118 aryl group Chemical group 0.000 abstract 3
- 150000001875 compounds Chemical class 0.000 abstract 3
- 125000004191 (C1-C6) alkoxy group Chemical group 0.000 abstract 2
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 abstract 2
- 125000004432 carbon atom Chemical group C* 0.000 abstract 2
- 125000004122 cyclic group Chemical group 0.000 abstract 2
- 125000006517 heterocyclyl carbonyl group Chemical group 0.000 abstract 2
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 2
- 125000004433 nitrogen atom Chemical group N* 0.000 abstract 2
- 125000004430 oxygen atom Chemical group O* 0.000 abstract 2
- 125000004434 sulfur atom Chemical group 0.000 abstract 2
- 125000004916 (C1-C6) alkylcarbonyl group Chemical group 0.000 abstract 1
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 abstract 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 abstract 1
- 108091000080 Phosphotransferase Proteins 0.000 abstract 1
- 125000004457 alkyl amino carbonyl group Chemical group 0.000 abstract 1
- 239000002246 antineoplastic agent Substances 0.000 abstract 1
- 229940041181 antineoplastic drug Drugs 0.000 abstract 1
- 125000000753 cycloalkyl group Chemical group 0.000 abstract 1
- 230000002401 inhibitory effect Effects 0.000 abstract 1
- LKXGJTGMUPZNLZ-UHFFFAOYSA-N methyl N-(3-phenoxyimidazo[1,2-a]pyridin-2-yl)carbamate Chemical compound O(C1=CC=CC=C1)C1=C(N=C2N1C=CC=C2)NC(=O)OC LKXGJTGMUPZNLZ-UHFFFAOYSA-N 0.000 abstract 1
- QLSHUQAOKVFCJN-UHFFFAOYSA-N methyl n-(6-phenoxyimidazo[1,2-a]pyridin-2-yl)carbamate Chemical compound C1=CC2=NC(NC(=O)OC)=CN2C=C1OC1=CC=CC=C1 QLSHUQAOKVFCJN-UHFFFAOYSA-N 0.000 abstract 1
- ZJYIMLHKZKIPPK-UHFFFAOYSA-N methyl n-[6-(4-acetamidophenoxy)imidazo[1,2-a]pyridin-2-yl]carbamate Chemical compound C1=CC2=NC(NC(=O)OC)=CN2C=C1OC1=CC=C(NC(C)=O)C=C1 ZJYIMLHKZKIPPK-UHFFFAOYSA-N 0.000 abstract 1
- TZZZGQQJDZQFGI-UHFFFAOYSA-N methyl n-[6-(4-aminophenoxy)imidazo[1,2-a]pyridin-2-yl]carbamate Chemical compound C1=CC2=NC(NC(=O)OC)=CN2C=C1OC1=CC=C(N)C=C1 TZZZGQQJDZQFGI-UHFFFAOYSA-N 0.000 abstract 1
- RQLATXIDVPRBRQ-UHFFFAOYSA-N methyl n-[6-(4-nitrophenoxy)imidazo[1,2-a]pyridin-2-yl]carbamate Chemical compound C1=CC2=NC(NC(=O)OC)=CN2C=C1OC1=CC=C([N+]([O-])=O)C=C1 RQLATXIDVPRBRQ-UHFFFAOYSA-N 0.000 abstract 1
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 abstract 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 1
- 102000020233 phosphotransferase Human genes 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
Classifications
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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
-
- 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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P13/00—Drugs for disorders of the urinary system
- A61P13/12—Drugs for disorders of the urinary system of the kidneys
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P15/00—Drugs for genital or sexual disorders; Contraceptives
-
- 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
-
- 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
- A61P27/00—Drugs for disorders of the senses
- A61P27/02—Ophthalmic agents
-
- 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]
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
- A61P35/04—Antineoplastic agents specific for metastasis
-
- 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
-
- 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
-
- 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
- A61P9/12—Antihypertensives
-
- 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
- C07D417/12—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 linked by a chain containing hetero atoms as chain links
-
- 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
- C07D471/14—Ortho-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D513/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00
- C07D513/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00 in which the condensed system contains two hetero rings
- C07D513/04—Ortho-condensed systems
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Physical Education & Sports Medicine (AREA)
- Urology & Nephrology (AREA)
- Heart & Thoracic Surgery (AREA)
- Pulmonology (AREA)
- Rheumatology (AREA)
- Cardiology (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Ophthalmology & Optometry (AREA)
- Immunology (AREA)
- Pain & Pain Management (AREA)
- Oncology (AREA)
- Vascular Medicine (AREA)
- Endocrinology (AREA)
- Reproductive Health (AREA)
- Dermatology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Thiazole And Isothizaole Compounds (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
Abstract
Estos compuestos poseen actividad inhibidora de la quinasa. Compuesto farmacéutico que los comprende y su uso en la preparacion de medicamentos contra el cáncer. Reivindicacion 1: Un compuesto caracterizado por la formula (1), donde Z1, Z2, Z3 y Z4 muestran la siguiente combinacion: (Z1,Z2,Z3,Z4)=(CR4,N,CR5,C), (N,N,CR5,C), (N,C,CR5,N), (S,C,CR5,C) o (S,C,N,C); R1 y R2 son iguales o diferentes y cada uno es (1) un átomo de hidrogeno, (2) un átomo de halogeno, (3) un grupo unido mediante un átomo de carbono, (4) un grupo unido mediante un átomo de nitrogeno, (5) un grupo unido mediante un átomo de oxígeno o (6) un grupo unido mediante un átomo de azufre; R3 es un amino que opcionalmente tiene sustituyentes; R4 y R5 son iguales o diferentes y cada uno es (1) un átomo de hidrogeno, (2) un átomo de halogeno, (3) un grupo unido mediante un átomo de carbono, (4) un grupo unido mediante un átomo de nitrogeno, (5) un grupo unido mediante un átomo de oxígeno o (6) un grupo unido mediante un átomo de azufre; R3 y R4 forman opcionalmente un anillo que opcionalmente tiene sustituyentes; un grupo representado por la formula (2) es un grupo cíclico que opcionalmente tiene sustituyentes, con la salvedad que (1) cuando (Z1,Z2,Z3,Z4)=(S,C,CR5,C), el grupo representado por la formula (2) es un grupo representado por la formula (3) donde R6 es (1') un amino, (2') un mono-alquilamino C1-6, (3') un di-alquilamino C1-6, (4') un mono(alquil C1-6-carbonil)amino que opcionalmente tiene 1 a 3 átomos de halogeno, (5') un mono(cicloalquil C3-6-carbonil)amino, (6') un mono(cicloalquenil C3-6-carbonil)amino, (7') un mono(aril C6-10-carbonil)amino que opcionalmente tiene 1 a 3 átomos de halogeno, (8') un mono(heterociclil-carbonil monocíclico aromático de 5 o 6 miembros)amino que opcionalmente tiene 1 a 3 sustituyentes seleccionados de (a) un átomo de halogeno, (b) un alquilo C1-6 que opcionalmente tiene 1 a 3 átomos de halogeno, (c) un alcoxi C1-6 y (d) un cicloalquilo C3-6, (9') un mono(heterociclil-carbonil aromático fusionado de 8 a 12 miembros)amino que opcionalmente tiene 1 a 3 sustituyentes seleccionados de (a) un átomo de halogeno, (b) un alquilo C1-6 que opcionalmente tiene 1 a 3 átomos de halogeno, (c) un alcoxi C1-6 y (d) un cicloalquilo C3-6, (10') un mono (heterociclil-carbonil no aromático de 3 a 8 miembros)amino, (11') un monoalcoxi C1-6-carbonilamino, (12') un alquil C1-6-aminocarbonilo, (13') un di-alquil C1-6-aminocarbonilo o (14') un nitro, y el anillo B es un anillo benceno que además, opcionalmente, tiene sustituyentes, y (2) cuando (Z1,Z2,Z3,Z4)=(S,C,N,C), el grupo representado por la formula (2) es un grupo cíclico aromático que tiene sustituyentes (que excluyen 2-metoxicarbonilamino-6-(4-nitrofenoxi)imidazo[1,2-a]piridina, 2-metoxicarbonilamino-6-(fenoxi)imidazo[1,2-a]piridina, 6-(4-acetamidofenoxi)-2-metoxicarbonilaminoimidazo[1,2-a]piridina, 6-(4-aminofenoxi)-2-metoxicarbonilaminoimidazo[1,2-a]piridina y 6-(4-(2-fluoro-5-(trifluorometil) fenil)aminocarbonilamino)fenoxi-2-metoxicarbonilaminoimidazo[1,2-a]piridina), o una sal de los mismos.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2007149781 | 2007-06-05 | ||
| JP2007223284 | 2007-08-29 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| AR066845A1 true AR066845A1 (es) | 2009-09-16 |
Family
ID=39684216
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ARP080102359A AR066845A1 (es) | 2007-06-05 | 2008-06-04 | Derivados de triazolopiridina e imidazopiridina una composicion farmaceutica que los comprende y su uso en la preparacion de un medicamento para el tratamiento del cancer |
Country Status (9)
| Country | Link |
|---|---|
| US (1) | US8304557B2 (es) |
| EP (1) | EP2162445B1 (es) |
| JP (1) | JP5352476B2 (es) |
| AR (1) | AR066845A1 (es) |
| CA (1) | CA2689514C (es) |
| CL (1) | CL2008001626A1 (es) |
| PE (1) | PE20090370A1 (es) |
| TW (1) | TW200904816A (es) |
| WO (1) | WO2008150015A1 (es) |
Families Citing this family (34)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| AR066845A1 (es) | 2007-06-05 | 2009-09-16 | Takeda Pharmaceutical | Derivados de triazolopiridina e imidazopiridina una composicion farmaceutica que los comprende y su uso en la preparacion de un medicamento para el tratamiento del cancer |
| EP2181987B9 (en) | 2007-08-23 | 2014-09-03 | Takeda Pharmaceutical Company Limited | 2-Carbonylaminobenzothiazoles and their use for the prophylaxis and treatment of cancer |
| EP2184285B1 (en) * | 2007-08-29 | 2015-11-04 | Takeda Pharmaceutical Company Limited | Heterocyclic compound and use thereof |
| JPWO2009128520A1 (ja) * | 2008-04-18 | 2011-08-04 | 塩野義製薬株式会社 | Pi3k阻害活性を有する複素環化合物 |
| US8445509B2 (en) | 2008-05-08 | 2013-05-21 | Takeda Pharmaceutical Company Limited | Fused heterocyclic derivatives and use thereof |
| 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 |
| WO2010064611A1 (ja) * | 2008-12-01 | 2010-06-10 | 武田薬品工業株式会社 | 複素環化合物およびその用途 |
| JO3101B1 (ar) | 2008-12-02 | 2017-09-20 | Takeda Pharmaceuticals Co | مشتقات بنزوثيازول كعوامل مضادة للسرطان |
| CA2763900A1 (en) | 2009-06-05 | 2010-12-09 | Cephalon, Inc. | Preparation and uses of 1,2,4-triazolo [1,5a] pyridine derivatives |
| JO3030B1 (ar) | 2009-06-26 | 2016-09-05 | Galapagos Nv | مركب جديد مفيد لمعالجة الامراض التنكسية والالتهابات |
| 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 |
| CA2797533A1 (en) * | 2010-04-27 | 2011-11-10 | Calcimedica, Inc. | Compounds that modulate intracellular calcium |
| WO2011144742A1 (en) | 2010-05-21 | 2011-11-24 | Chemilia Ab | Novel pyrimidine derivatives |
| EP2423208A1 (en) | 2010-08-28 | 2012-02-29 | Lead Discovery Center GmbH | Pharmaceutically active compounds as Axl inhibitors |
| EP2688883B1 (en) | 2011-03-24 | 2016-05-18 | Noviga Research AB | Pyrimidine derivatives |
| UY34305A (es) | 2011-09-01 | 2013-04-30 | Novartis Ag | Derivados de heterociclos bicíclicos para el tratamiento de la hipertensión arterial pulmonar |
| US9023865B2 (en) * | 2011-10-27 | 2015-05-05 | Merck Sharp & Dohme Corp. | Compounds that are ERK inhibitors |
| EP2900223B1 (en) * | 2012-09-28 | 2017-10-25 | Merck Sharp & Dohme Corp. | Novel compounds that are erk inhibitors |
| JP6280554B2 (ja) | 2012-09-28 | 2018-02-14 | メルク・シャープ・アンド・ドーム・コーポレーションMerck Sharp & Dohme Corp. | Erk阻害剤である新規化合物 |
| GB201223308D0 (en) | 2012-12-21 | 2013-02-06 | Univ Sunderland | Enzyme inhibitors |
| US9073921B2 (en) | 2013-03-01 | 2015-07-07 | Novartis Ag | Salt forms of bicyclic heterocyclic derivatives |
| 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 |
| JP7269917B2 (ja) * | 2017-08-17 | 2023-05-09 | イケナ オンコロジー, インコーポレイテッド | Ahr阻害剤およびその使用 |
| GB201808575D0 (en) | 2018-05-24 | 2018-07-11 | Galapagos Nv | Methods for the treatment of psoriatic arthrits |
| WO2020097398A1 (en) | 2018-11-07 | 2020-05-14 | Dana-Farber Cancer Institute, Inc. | Benzothiazole derivatives and 7-aza-benzothiazole derivatives as janus kinase 2 inhibitors and uses thereof |
| JP7762957B2 (ja) * | 2019-04-05 | 2025-10-31 | ストーム・セラピューティクス・リミテッド | Mettl3阻害化合物 |
| CA3181537A1 (en) | 2020-05-06 | 2021-11-11 | Ajax Therapeutics, Inc. | 6-heteroaryloxy benzimidazoles and azabenzimidazoles as jak2 inhibitors |
| WO2022140527A1 (en) | 2020-12-23 | 2022-06-30 | Ajax Therapeutics, Inc. | 6-heteroaryloxy benzimidazoles and azabenzimidazoles as jak2 inhibitors |
| TW202315628A (zh) * | 2021-06-24 | 2023-04-16 | 南韓商Lg化學股份有限公司 | 作為ron抑制劑之新穎吡啶衍生物化合物 |
| WO2023009708A1 (en) * | 2021-07-29 | 2023-02-02 | Ajax Therapeutics, Inc. | Heteroaryloxy triazolo- and imidazo-azines as jak2 inhibitors |
| TW202325289A (zh) | 2021-11-09 | 2023-07-01 | 美商雅捷可斯治療公司 | Jak2抑制劑之形式及組合物 |
| CA3234638A1 (en) | 2021-11-09 | 2023-05-19 | Ajax Therapeutics, Inc. | 6-heteroaryloxy benzimidazoles and azabenzimidazoles as jak2 inhibitors |
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-
2008
- 2008-06-04 AR ARP080102359A patent/AR066845A1/es unknown
- 2008-06-04 US US12/133,063 patent/US8304557B2/en not_active Expired - Fee Related
- 2008-06-04 EP EP08765409.1A patent/EP2162445B1/en active Active
- 2008-06-04 TW TW097120686A patent/TW200904816A/zh unknown
- 2008-06-04 PE PE2008000947A patent/PE20090370A1/es not_active Application Discontinuation
- 2008-06-04 JP JP2009549311A patent/JP5352476B2/ja not_active Expired - Fee Related
- 2008-06-04 WO PCT/JP2008/060629 patent/WO2008150015A1/en not_active Ceased
- 2008-06-04 CL CL2008001626A patent/CL2008001626A1/es unknown
- 2008-06-04 CA CA2689514A patent/CA2689514C/en not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| CA2689514A1 (en) | 2008-12-11 |
| TW200904816A (en) | 2009-02-01 |
| US8304557B2 (en) | 2012-11-06 |
| US20090163488A1 (en) | 2009-06-25 |
| EP2162445A1 (en) | 2010-03-17 |
| JP5352476B2 (ja) | 2013-11-27 |
| CA2689514C (en) | 2015-09-29 |
| CL2008001626A1 (es) | 2009-06-05 |
| PE20090370A1 (es) | 2009-04-30 |
| EP2162445B1 (en) | 2013-11-27 |
| JP2010527909A (ja) | 2010-08-19 |
| WO2008150015A1 (en) | 2008-12-11 |
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