MX370010B - Inhibidores de tirosina cinasa de bruton. - Google Patents
Inhibidores de tirosina cinasa de bruton.Info
- Publication number
- MX370010B MX370010B MX2016006763A MX2016006763A MX370010B MX 370010 B MX370010 B MX 370010B MX 2016006763 A MX2016006763 A MX 2016006763A MX 2016006763 A MX2016006763 A MX 2016006763A MX 370010 B MX370010 B MX 370010B
- Authority
- MX
- Mexico
- Prior art keywords
- compounds
- btk
- bruton
- inhibitors
- tyrosine kinase
- Prior art date
Links
- 102000001714 Agammaglobulinaemia Tyrosine Kinase Human genes 0.000 title 1
- 108010029445 Agammaglobulinaemia Tyrosine Kinase Proteins 0.000 title 1
- 239000003112 inhibitor Substances 0.000 title 1
- 150000001875 compounds Chemical class 0.000 abstract 4
- 230000000694 effects Effects 0.000 abstract 2
- 208000023275 Autoimmune disease Diseases 0.000 abstract 1
- 230000003844 B-cell-activation Effects 0.000 abstract 1
- 230000001594 aberrant effect Effects 0.000 abstract 1
- 230000001363 autoimmune Effects 0.000 abstract 1
- 239000003085 diluting agent Substances 0.000 abstract 1
- 201000010099 disease Diseases 0.000 abstract 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 abstract 1
- 208000027866 inflammatory disease Diseases 0.000 abstract 1
- 239000000203 mixture Substances 0.000 abstract 1
- 230000000771 oncological effect Effects 0.000 abstract 1
- 239000000546 pharmaceutical excipient Substances 0.000 abstract 1
Classifications
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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
- C07D403/06—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 carbon chain containing only aliphatic carbon atoms
-
- 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
- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
- A61K31/415—1,2-Diazoles
- A61K31/4155—1,2-Diazoles non condensed and containing further heterocyclic rings
-
- 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
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/4427—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
- A61K31/4439—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. omeprazole
-
- A—HUMAN NECESSITIES
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- 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
- A61K31/496—Non-condensed piperazines containing further heterocyclic rings, e.g. rifampin, thiothixene or sparfloxacin
-
- 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
- A61K31/535—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one oxygen as the ring hetero atoms, e.g. 1,2-oxazines
- A61K31/5375—1,4-Oxazines, e.g. morpholine
- A61K31/5377—1,4-Oxazines, e.g. morpholine not condensed and containing further heterocyclic rings, e.g. timolol
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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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- 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
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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
-
- 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
- C07D401/14—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 three or more hetero rings
-
- 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
- C07D403/14—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 three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
- C07D409/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing three or more hetero rings
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Medicinal Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- Public Health (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Immunology (AREA)
- Neurology (AREA)
- Epidemiology (AREA)
- Neurosurgery (AREA)
- Biomedical Technology (AREA)
- Diabetes (AREA)
- Physical Education & Sports Medicine (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Pulmonology (AREA)
- Urology & Nephrology (AREA)
- Dermatology (AREA)
- Cardiology (AREA)
- Heart & Thoracic Surgery (AREA)
- Rheumatology (AREA)
- Hematology (AREA)
- Endocrinology (AREA)
- Emergency Medicine (AREA)
- Psychiatry (AREA)
- Hospice & Palliative Care (AREA)
- Obesity (AREA)
- Pain & Pain Management (AREA)
- Communicable Diseases (AREA)
- Oncology (AREA)
- Vascular Medicine (AREA)
- Transplantation (AREA)
Abstract
Esta invención describe compuestos de acuerdo con la fórmula genérica (I): (ver Fórmula) en la que todas las variables se definen como se describe en la presente, que inhiben Btk. Los compuestos descritos en la presente son útiles para modular la actividad de Btk y tratar enfermedades asociadas con exceso de actividad Btk. Los compuestos son útiles para el tratamiento de enfermedades oncológicas, autoinmunes, e inflamatorias causadas por la activación aberrante de células B. También se describen composiciones que contienen compuestos de la Fórmula (I) y al menos un portador, diluyente o excipiente.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201361915576P | 2013-12-13 | 2013-12-13 | |
| PCT/EP2014/077113 WO2015086635A1 (en) | 2013-12-13 | 2014-12-10 | Inhibitors of bruton's tyrosine kinase |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| MX2016006763A MX2016006763A (es) | 2016-09-06 |
| MX370010B true MX370010B (es) | 2019-11-28 |
Family
ID=52016582
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| MX2016006763A MX370010B (es) | 2013-12-13 | 2014-12-10 | Inhibidores de tirosina cinasa de bruton. |
Country Status (11)
| Country | Link |
|---|---|
| US (5) | US9624201B2 (es) |
| EP (1) | EP3080097B1 (es) |
| JP (1) | JP6263626B2 (es) |
| KR (1) | KR101824346B1 (es) |
| CN (1) | CN105814035B (es) |
| BR (1) | BR112016013540B1 (es) |
| CA (1) | CA2929747C (es) |
| MX (1) | MX370010B (es) |
| RU (1) | RU2653504C2 (es) |
| TW (1) | TWI531568B (es) |
| WO (1) | WO2015086635A1 (es) |
Families Citing this family (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| TW201609093A (zh) | 2013-12-27 | 2016-03-16 | Chugai Pharmaceutical Co Ltd | Fgfr門控蛋白變異基因及以其爲標的之醫藥 |
| WO2016204261A1 (ja) * | 2015-06-17 | 2016-12-22 | 中外製薬株式会社 | アミノピラゾール誘導体 |
| EP3339305B1 (en) * | 2015-08-20 | 2022-05-04 | Zhejiang Hisun Pharmaceutical Co., Ltd | Indole derivative, preparation method thereof, and use thereof in pharmaceutical drug |
| KR102543382B1 (ko) | 2016-06-30 | 2023-06-13 | 엘지디스플레이 주식회사 | 구동 방법, 터치 센싱 회로, 표시패널 및 터치 표시 장치 |
| US20240100172A1 (en) | 2020-12-21 | 2024-03-28 | Hangzhou Jijing Pharmaceutical Technology Limited | Methods and compounds for targeted autophagy |
| KR20220099825A (ko) | 2021-01-07 | 2022-07-14 | 주식회사 온코빅스 | 브루톤 타이로신 키나제 억제용 화합물 및 이들의 의약 용도 |
Family Cites Families (23)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5072023A (en) | 1990-02-15 | 1991-12-10 | E. R. Squibb & Sons, Inc. | Process for preparing highly substituted phenyls |
| US6316466B1 (en) | 1998-05-05 | 2001-11-13 | Syntex (U.S.A.) Llc | Pyrazole derivatives P-38 MAP kinase inhibitors |
| GB9820113D0 (en) | 1998-09-15 | 1998-11-11 | Merck Sharp & Dohme | Therapeutic agents |
| US20030236288A1 (en) | 2002-02-28 | 2003-12-25 | Karl Schoenafinger | Use of substituted 3-phenyl-5-alkoxy-3H-(1,3,4)-oxadizol-2-ones for inhibiting pancreatic lipase |
| BRPI0411859A (pt) | 2003-06-24 | 2006-08-29 | Uniroyal Chem Co Inc | composto de fenóxi fenil hidrazina |
| WO2005009973A1 (en) | 2003-06-26 | 2005-02-03 | Novartis Ag | 5-membered heterocycle-based p38 kinase inhibitors |
| DK1703909T3 (da) | 2003-09-09 | 2009-06-22 | Hoffmann La Roche | 1-benzoyl-piperazinderivater som glycinoptagelsesinhibitorer til behandling af psykoser |
| WO2007061694A2 (en) | 2005-11-18 | 2007-05-31 | Merck & Co., Inc. | Spirohydantoin tricyclic cgrp receptor antagonists |
| CN101460466B (zh) | 2006-04-11 | 2012-06-13 | 沃泰克斯药物股份有限公司 | 适用作蛋白激酶抑制剂的噻唑类、咪唑类和吡唑类 |
| TW200920369A (en) | 2007-10-26 | 2009-05-16 | Amira Pharmaceuticals Inc | 5-lipoxygenase activating protein (flap) inhibitor |
| US8124762B2 (en) | 2008-09-05 | 2012-02-28 | Korea Institute Of Science & Technology | Diphenyl amine derivatives having luminescence property |
| WO2010087430A1 (ja) | 2009-01-30 | 2010-08-05 | 富山化学工業株式会社 | N-アシルアントラニル酸誘導体またはその塩 |
| PT2471786E (pt) | 2009-08-07 | 2016-03-04 | Hoffmann La Roche | Derivado de aminopirazol |
| CN102574788A (zh) | 2009-09-24 | 2012-07-11 | 弗·哈夫曼-拉罗切有限公司 | 作为crac调节剂的吲哚衍生物 |
| AU2010303670A1 (en) | 2009-10-06 | 2012-03-29 | Bristol-Myers Squibb Company | Pyrrolidine GPR40 modulators |
| US7741330B1 (en) | 2009-10-12 | 2010-06-22 | Pharmacyclics, Inc. | Pyrazolo-pyrimidine inhibitors of Bruton's tyrosine kinase |
| BR112012023935A2 (pt) | 2010-03-23 | 2015-09-15 | Basf Se | piridazina substituída da fórmula i, composto para fórmula i, composição e método para o controle de vegetação indesejada |
| US8563593B2 (en) | 2010-06-08 | 2013-10-22 | Vertex Pharmaceuticals Incorporated | Formulations of (R)-1-(2,2-difluorobenzo[D] [1,3] dioxol-5-yl)-N-(1-(2,3-dihydroxypropyl)-6-fluoro-2-(1-hydroxy-2-methylpropan-2-yl)-1H-indol-5-yl)cyclopropanecarboxamide |
| WO2012078859A2 (en) | 2010-12-09 | 2012-06-14 | University Of Pittsburgh - Of The Commonwealth System Of Higher Education | Protein kinase d inhibitors |
| AU2012257802A1 (en) | 2011-05-17 | 2013-10-31 | F. Hoffmann-La Roche Ag | Inhibitors of Bruton's tyrosine kinase |
| JP6131272B2 (ja) | 2012-01-09 | 2017-05-17 | エックス−アールエックス,インコーポレーテッド | キナーゼ阻害活性を有するベンズヒドロール−ピラゾール誘導体及びその使用 |
| US9802920B2 (en) | 2013-12-13 | 2017-10-31 | Hoffman-La Roche Inc. | Inhibitors of bruton's tyrosine kinase |
| JP6219523B2 (ja) * | 2013-12-13 | 2017-10-25 | エフ.ホフマン−ラ ロシュ アーゲーF. Hoffmann−La Roche Aktiengesellschaft | ブルトンチロシンキナーゼの阻害剤 |
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2014
- 2014-12-10 JP JP2016539186A patent/JP6263626B2/ja not_active Expired - Fee Related
- 2014-12-10 RU RU2016126178A patent/RU2653504C2/ru active
- 2014-12-10 CN CN201480067564.5A patent/CN105814035B/zh not_active Expired - Fee Related
- 2014-12-10 KR KR1020167015416A patent/KR101824346B1/ko not_active Expired - Fee Related
- 2014-12-10 WO PCT/EP2014/077113 patent/WO2015086635A1/en not_active Ceased
- 2014-12-10 CA CA2929747A patent/CA2929747C/en active Active
- 2014-12-10 US US15/102,315 patent/US9624201B2/en not_active Expired - Fee Related
- 2014-12-10 BR BR112016013540-7A patent/BR112016013540B1/pt not_active IP Right Cessation
- 2014-12-10 MX MX2016006763A patent/MX370010B/es active IP Right Grant
- 2014-12-10 EP EP14809642.3A patent/EP3080097B1/en active Active
- 2014-12-10 US US16/815,443 patent/US11104668B2/en not_active Expired - Fee Related
- 2014-12-11 TW TW103143354A patent/TWI531568B/zh not_active IP Right Cessation
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2017
- 2017-03-09 US US15/454,452 patent/US10093657B2/en active Active
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2018
- 2018-06-26 US US16/018,683 patent/US10640491B2/en not_active Expired - Fee Related
-
2020
- 2020-03-11 US US16/815,443 patent/US20200207741A1/en active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| EP3080097B1 (en) | 2018-04-18 |
| TWI531568B (zh) | 2016-05-01 |
| US20160318907A1 (en) | 2016-11-03 |
| US11104668B2 (en) | 2021-08-31 |
| CN105814035A (zh) | 2016-07-27 |
| US20170183327A1 (en) | 2017-06-29 |
| WO2015086635A1 (en) | 2015-06-18 |
| US10093657B2 (en) | 2018-10-09 |
| US20180305340A1 (en) | 2018-10-25 |
| JP6263626B2 (ja) | 2018-01-17 |
| KR101824346B1 (ko) | 2018-01-31 |
| CA2929747A1 (en) | 2015-06-18 |
| US10640491B2 (en) | 2020-05-05 |
| BR112016013540B1 (pt) | 2021-03-02 |
| EP3080097A1 (en) | 2016-10-19 |
| US9624201B2 (en) | 2017-04-18 |
| MX2016006763A (es) | 2016-09-06 |
| TW201534599A (zh) | 2015-09-16 |
| JP2016540788A (ja) | 2016-12-28 |
| KR20160083114A (ko) | 2016-07-11 |
| CA2929747C (en) | 2018-01-23 |
| RU2653504C2 (ru) | 2018-05-10 |
| CN105814035B (zh) | 2018-02-02 |
| US20200207741A1 (en) | 2020-07-02 |
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