AR129632A2 - Agentes inhibidores de la tirosina quinasa de bruton - Google Patents
Agentes inhibidores de la tirosina quinasa de brutonInfo
- Publication number
- AR129632A2 AR129632A2 ARP230101541A ARP230101541A AR129632A2 AR 129632 A2 AR129632 A2 AR 129632A2 AR P230101541 A ARP230101541 A AR P230101541A AR P230101541 A ARP230101541 A AR P230101541A AR 129632 A2 AR129632 A2 AR 129632A2
- Authority
- AR
- Argentina
- Prior art keywords
- membered monocyclic
- alkyl
- alkynyl
- alkenyl
- carbocyclyl
- Prior art date
Links
Classifications
-
- 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
- C07D403/12—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 chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing three or more hetero 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
- A61K31/55—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole
-
- 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
-
- 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
-
- 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
-
- 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
-
- 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
-
- 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
-
- 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
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/14—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing three or more hetero rings
-
- 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
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F5/00—Compounds containing elements of Groups 3 or 13 of the Periodic Table
- C07F5/02—Boron compounds
- C07F5/025—Boronic and borinic acid compounds
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07B—GENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
- C07B2200/00—Indexing scheme relating to specific properties of organic compounds
- C07B2200/13—Crystalline forms, e.g. polymorphs
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (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)
- Gastroenterology & Hepatology (AREA)
- Epidemiology (AREA)
- Neurology (AREA)
- Neurosurgery (AREA)
- Biomedical Technology (AREA)
- Transplantation (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Hospice & Palliative Care (AREA)
- Psychiatry (AREA)
- Preparation Of Compounds By Using Micro-Organisms (AREA)
Abstract
Reivindicación 1: Un compuesto de fórmula (1) o una sal farmacéuticamente aceptable, en donde: El anillo A es un heteroarilo monocíclico de 5 miembros que contiene 3 heteroátomos seleccionados independientemente entre N, O y S, en donde dicho heteroarilo monocíclico de 5 miembros está opcionalmente sustituido con uno o más R¹; Q¹, Q² y Q³ son cada uno, independientemente, seleccionados de O, N(R²) y CH-R³, en donde al menos dos de Q¹, Q² y Q³ son C-R³; W se selecciona de CH y N; Y se selecciona de CH y N; R¹ en cada caso se selecciona independientemente de alquilo C₁₋₆ y carbociclilo de 3 a 5 miembros, en donde dicho alquilo C₁₋₆ y carbociclilo de 3 a 5 miembros están opcionalmente sustituidos con uno o más R¹⁰; R¹⁰ en cada caso se selecciona independientemente de halo, -CN, alquilo C₁₋₆ y carbociclilo de 3 a 5 miembros; R² se selecciona de H, alquilo C₁₋₆, alquenilo C₂₋₆, alquinilo C₂₋₆, carbociclilo monocíclico de 4 a 6 miembros, heterociclilo monocíclico de 4 a 6 miembros, -CN, -C(O)R²ᵃ, -C(O)₂R²ᵃ, -C(O)N(R²ᵃ)₂, -S(O)₂R²ᵃ, y -S(O)₂N(R²ᵃ)₂, en donde dicho alquilo C₁₋₆, alquenilo C₂₋₆, alquinilo C₂₋₆, carbociclilo monocíclico de 4 a 6 miembros, y heterociclilo monocíclico de 4 a 6 miembros están opcionalmente sustituidos con uno o más R²⁰; R²ᵃ en cada aparición se selecciona independientemente de H, alquilo C₁₋₆, alquenilo C₂₋₆, alquinilo C₂₋₆, carbociclilo monocíclico de 4 a 6 miembros, y heterociclilo monocíclico de 4 a 6 miembros, en donde dicho alquilo C₁₋₆, alquenilo C₂₋₆, alquinilo C₂₋₆, carbociclilo monocíclico de 4 a 6 miembros, y heterociclilo monocíclico de 4 a 6 miembros en cada aparición están opcionalmente e independientemente sustituidos con uno o más R²⁰; R²⁰ en cada aparición se selecciona independientemente de alquilo C₁₋₆, alquenilo C₂₋₆, alquinilo C₂₋₆, carbociclilo monocíclico de 4 a 6 miembros, heterociclilo monocíclico de 4 a 6 miembros, halo, -CN, -C(O)R²⁰ᵃ, -C(O)₂R²⁰ᵃ, -C(O)N(R²⁰ᵃ)₂, -N(R²⁰ᵃ)₂, -N(R²⁰ᵃ)C(O)R²⁰ᵃ, -N(R²⁰ᵃ)C(O)₂R²⁰ᵃ, -N(R²⁰ᵃ)C(O)N(R²⁰ᵃ)₂, -N(R²⁰ᵃ)S(O)₂R²⁰ᵃ, -OR²⁰ᵃ, -OC(O)R²⁰ᵃ, -OC(O)N(R²⁰ᵃ)₂, -SR²⁰ᵃ, -S(O)R²⁰ᵃ, -S(O)₂R²⁰ᵃ, -S(O)N(R²⁰ᵃ)₂, y -S(O)₂N(R²⁰ᵃ)₂; R²⁰ᵃ en cada aparición se selecciona independientemente de H, alquilo C₁₋₆, alquenilo C₂₋₆, alquinilo C₂₋₆, carbociclilo monocíclico de 4 a 6 miembros y heterociclilo monocíclico de 4 a 6 miembros; R³ se selecciona de H, alquilo C₁₋₆, alquenilo C₂₋₆, alquinilo C₂₋₆, carbociclilo monocíclico de 4 a 6 miembros, heterociclilo monocíclico de 4 a 6 miembros, halo, -CN, -C(O)R³ᵃ, -C(O)₂R³ᵃ, -C(O)N(R³ᵃ)₂, -N(R³ᵃ)₂, -N(R³ᵃ)C(O)R³ᵃ, -N(R³ᵃ)C(O)₂R³ᵃ, -N(R³ᵃ)C(O)N(R³ᵃ)₂, -N(R³ᵃ)S(O)₂R³ᵃ, -OR³ᵃ, -OC(O)R³ᵃ, -OC(O)N(R³ᵃ)₂, -SR³ᵃ, -S(O)R³ᵃ, -S(O)₂R³ᵃ, -S(O)N(R³ᵃ)₂, y -S(O)₂N(R³ᵃ)₂, en donde dicho alquilo C₁₋₆, alquenilo C₂₋₆, alquinilo C₂₋₆, carbociclilo monocíclico de 4 a 6 miembros, y heterociclilo monocíclico de 4 a 6 miembros están opcionalmente sustituidos con uno o más R³⁰; R³ᵃ en cada aparición se selecciona independientemente de H, alquilo C₁₋₆, alquenilo C₂₋₆, alquinilo C₂₋₆, carbociclilo monocíclico de 4 a 6 miembros, y heterociclilo monocíclico de 4 a 6 miembros, en donde dicho alquilo C₁₋₆, alquenilo C₂₋₆, alquinilo C₂₋₆, carbociclilo monocíclico de 4 a 6 miembros y heterociclilo monocíclico de 4 a 6 miembros en cada aparición están opcional e independientemente sustituidos con uno o más R³⁰; R³⁰ en cada aparición se selecciona independientemente de alquilo C₁₋₆, alquenilo C₂₋₆, alquinilo C₂₋₆, carbociclilo monocíclico de 4 a 6 miembros, heterociclilo monocíclico de 4 a 6 miembros, halo, -CN, -C(O)R³⁰ᵃ, -C(O)₂R³⁰ᵃ, -C(O)N(R³⁰ᵃ)₂, -N(R³⁰ᵃ)₂, -N(R³⁰ᵃ)C(O)R³⁰ᵃ, -N(R³⁰ᵃ)C(O)₂R³⁰ᵃ, -N(R³⁰ᵃ)C(O)N(R³⁰ᵃ)₂, -N(R³⁰ᵃ)S(O)₂R³⁰ᵃ, -OR³⁰ᵃ, -OC(O)R³⁰ᵃ, -OC(O)N(R³⁰ᵃ)₂, -SR³⁰ᵃ, -S(O)R³⁰ᵃ, -S(O)₂R³⁰ᵃ, -S(O)N(R³⁰ᵃ)₂, y -S(O)₂N(R³⁰ᵃ)₂; R³⁰ᵃ en cada aparición se selecciona independientemente de H, alquilo C₁₋₆, alquenilo C₂₋₆, alquinilo C₂₋₆, carbociclilo monocíclico de 4 a 6 miembros y heterociclilo monocíclico de 4 a 6 miembros; R⁴ se selecciona de H y alquilo C₁₋₆, en donde dicho alquilo C₁₋₆ está opcionalmente sustituido con uno o más halo; R⁵ se selecciona de H y alquilo C₁₋₆ en donde dicho alquilo C₁₋₆ está opcionalmente sustituido con uno o más halo; R⁶ se selecciona de H y alquilo C₁₋₆, en donde dicho alquilo C₁₋₆ está opcionalmente sustituido con uno o más halo; o R⁵ y R⁶, junto con los átomos a los que están unidos, forman un anillo que contiene uno o dos heteroátomos seleccionados de O, N y S, en donde el anillo está opcionalmente sustituido con uno o más R⁵⁰; y R⁵⁰ es alquilo C₁₋₆. Reivindicación 38: La forma A cristalina de (R)-1-(terc-butil)-N-(8-(2-((1-metil-1H-pirazol-4-il)amino)pirimidin-4-il)-2-(oxetan-3-il)-2,3,4,5-tetrahidro-1H-benzo[c]azepin-5-il)-1H-1,2,3-triazol-4-carboxamida. Reivindicación 48: La Forma G cristalina de (R)-1-(terc-butil)-N-(8-(2-((1-metil-1H-pirazol-4-il)amino)pirimidin-4-il)-2-(oxetan-3-il)-2,3,4,5-tetrahidro-1H-benzo[c]azepin-5-il)-1H-1,2,3-triazol-4-carboxamida.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201762485745P | 2017-04-14 | 2017-04-14 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| AR129632A2 true AR129632A2 (es) | 2024-09-11 |
Family
ID=62092333
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ARP180100935A AR111594A1 (es) | 2017-04-14 | 2018-04-13 | Agentes inhibidores de la tirosina quinasa de bruton |
| ARP230101541A AR129632A2 (es) | 2017-04-14 | 2023-06-15 | Agentes inhibidores de la tirosina quinasa de bruton |
Family Applications Before (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ARP180100935A AR111594A1 (es) | 2017-04-14 | 2018-04-13 | Agentes inhibidores de la tirosina quinasa de bruton |
Country Status (36)
| Country | Link |
|---|---|
| US (5) | US10227341B2 (es) |
| EP (2) | EP4249071A3 (es) |
| JP (3) | JP7145874B2 (es) |
| KR (3) | KR102862996B1 (es) |
| CN (2) | CN110621670B (es) |
| AR (2) | AR111594A1 (es) |
| AU (3) | AU2018253209B2 (es) |
| CA (1) | CA3058774A1 (es) |
| CL (1) | CL2019002900A1 (es) |
| CO (1) | CO2019012571A2 (es) |
| CR (2) | CR20190517A (es) |
| DK (1) | DK3609886T3 (es) |
| EA (1) | EA201992354A1 (es) |
| ES (1) | ES2975769T3 (es) |
| FI (1) | FI3609886T3 (es) |
| HR (1) | HRP20240361T1 (es) |
| HU (1) | HUE066253T2 (es) |
| IL (3) | IL294175B2 (es) |
| JO (1) | JOP20190233B1 (es) |
| LT (1) | LT3609886T (es) |
| MA (1) | MA50013B1 (es) |
| MD (1) | MD3609886T2 (es) |
| MX (1) | MX2023000812A (es) |
| PE (2) | PE20240930A1 (es) |
| PH (1) | PH12019502334A1 (es) |
| PL (1) | PL3609886T3 (es) |
| PT (1) | PT3609886T (es) |
| RS (1) | RS65386B1 (es) |
| SA (1) | SA519410292B1 (es) |
| SG (1) | SG11201909224QA (es) |
| SI (1) | SI3609886T1 (es) |
| SM (1) | SMT202400166T1 (es) |
| TW (2) | TWI790227B (es) |
| UA (1) | UA127347C2 (es) |
| WO (1) | WO2018191577A1 (es) |
| ZA (1) | ZA202306172B (es) |
Families Citing this family (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP3080103B9 (en) | 2013-12-11 | 2018-09-19 | Biogen MA Inc. | Biaryl compounds useful for the treatment of human diseases in oncology, neurology and immunology |
| JP7145874B2 (ja) | 2017-04-14 | 2022-10-03 | バイオジェン・エムエイ・インコーポレイテッド | ブルトン型チロシンキナーゼの阻害剤としてのベンゾアゼピン類似体 |
| EP3866926A1 (en) * | 2018-10-15 | 2021-08-25 | Biogen MA Inc. | Crystalline polymorphs of bruton's tyrosine kinase inhibitors |
| WO2020232330A1 (en) * | 2019-05-15 | 2020-11-19 | Biogen Ma Inc. | Inhibiting agents for bruton's tyrosine kinase |
| US20240100172A1 (en) | 2020-12-21 | 2024-03-28 | Hangzhou Jijing Pharmaceutical Technology Limited | Methods and compounds for targeted autophagy |
| US20240216330A1 (en) * | 2021-04-02 | 2024-07-04 | Biogen Ma Inc. | Combination treatment methods of multiple sclerosis |
| EP4429770A1 (en) | 2021-11-10 | 2024-09-18 | Biogen MA Inc. | Btk inhibitors |
| AU2022424178A1 (en) | 2021-12-30 | 2024-07-11 | Beone Medicines I Gmbh | Degradation of bruton's tyrosine kinase (btk) by conjugation of btk inhibitors with e3 ligase ligand and methods of use |
| JP7805983B2 (ja) | 2022-03-22 | 2026-01-26 | アッヴィ・インコーポレイテッド | ブルトン型チロシンキナーゼを分解するためのピリミジン |
| WO2024245577A1 (en) | 2023-06-02 | 2024-12-05 | Netherlands Translational Research Center Holding B.V. | Therapeutic combinations of an irreversible btk inhibitor and a reversible btk inhibitor |
| WO2024245578A1 (en) | 2023-06-02 | 2024-12-05 | Netherlands Translational Research Center Holding B.V. | Therapeutic combinations of an irreversible btk inhibitor and a macrocyclic reversible btk inhibitor |
Family Cites Families (15)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4938949A (en) | 1988-09-12 | 1990-07-03 | University Of New York | Treatment of damaged bone marrow and dosage units therefor |
| EP2125819B1 (en) | 2007-03-21 | 2014-10-22 | Bristol-Myers Squibb Company | Fused heterocyclic compounds useful for the treatment of proliferative, allergic, autoimmune or inflammatory diseases |
| BRPI0817503B8 (pt) | 2007-10-05 | 2021-05-25 | Sstarbio Pte Ltd | derivados de purina substituídos por pirimidina, composição farmacêutica compreendendo ditos compostos e uso dos mesmos para a prevenção ou tratamento de uma condição proliferativa |
| US20110009421A1 (en) | 2008-02-27 | 2011-01-13 | Takeda Pharmaceutical Company Limited | Compound having 6-membered aromatic ring |
| US8338439B2 (en) | 2008-06-27 | 2012-12-25 | Celgene Avilomics Research, Inc. | 2,4-disubstituted pyrimidines useful as kinase inhibitors |
| TWI546290B (zh) | 2008-06-27 | 2016-08-21 | 賽基艾維洛米斯研究股份有限公司 | 雜芳基化合物及其用途 |
| PT2473049T (pt) * | 2009-09-04 | 2019-03-04 | Sunesis Pharmaceuticals Inc | Inibidores de tirosina quinase de bruton |
| US8334292B1 (en) | 2010-06-14 | 2012-12-18 | Cystic Fibrosis Foundation Therapeutics, Inc. | Pyrimidine compounds and methods of making and using same |
| BR112014001255B1 (pt) | 2011-07-19 | 2019-07-02 | Merck Sharp & Dohme B.V. | Composto, uso de um composto, combinação, composição farmacêutica, e, sal farmaceuticamente aceitável de um composto |
| TWI648274B (zh) * | 2013-02-15 | 2019-01-21 | 英商葛蘭素史克智慧財產發展有限公司 | 作為激酶抑制劑之雜環醯胺類 （二） |
| WO2014130856A2 (en) | 2013-02-21 | 2014-08-28 | Wayne Rothbaum | Treatment of skeletal-related disorders |
| BR112016008632A8 (pt) | 2013-10-21 | 2020-03-17 | Merck Patent Gmbh | compostos de heteroarila como inibidores de btk, seus usos, e composição farmacêutica |
| EP3080103B9 (en) | 2013-12-11 | 2018-09-19 | Biogen MA Inc. | Biaryl compounds useful for the treatment of human diseases in oncology, neurology and immunology |
| ES2907622T3 (es) * | 2014-10-06 | 2022-04-25 | Merck Patent Gmbh | Compuestos de heteroarilo como inhibidores de BTK y usos de estos |
| JP7145874B2 (ja) | 2017-04-14 | 2022-10-03 | バイオジェン・エムエイ・インコーポレイテッド | ブルトン型チロシンキナーゼの阻害剤としてのベンゾアゼピン類似体 |
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2018
- 2018-04-13 JP JP2019555961A patent/JP7145874B2/ja active Active
- 2018-04-13 KR KR1020237040706A patent/KR102862996B1/ko active Active
- 2018-04-13 IL IL294175A patent/IL294175B2/en unknown
- 2018-04-13 PE PE2024000228A patent/PE20240930A1/es unknown
- 2018-04-13 MD MDE20200193T patent/MD3609886T2/ro unknown
- 2018-04-13 FI FIEP18721632.0T patent/FI3609886T3/fi active
- 2018-04-13 RS RS20240419A patent/RS65386B1/sr unknown
- 2018-04-13 CR CR20190517A patent/CR20190517A/es unknown
- 2018-04-13 EP EP23187919.8A patent/EP4249071A3/en active Pending
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