IN2014CN03250A - - Google Patents
Download PDFInfo
- Publication number
- IN2014CN03250A IN2014CN03250A IN3250CHN2014A IN2014CN03250A IN 2014CN03250 A IN2014CN03250 A IN 2014CN03250A IN 3250CHN2014 A IN3250CHN2014 A IN 3250CHN2014A IN 2014CN03250 A IN2014CN03250 A IN 2014CN03250A
- Authority
- IN
- India
- Prior art keywords
- formula
- pyridone
- compounds
- btk kinase
- disorders
- Prior art date
Links
Classifications
-
- 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
- C07D487/12—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 three hetero rings
- C07D487/14—Ortho-condensed systems
-
- 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
- A61K31/495—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
-
- 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
- A61K31/495—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
- A61K31/495—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
- A61K31/4965—Non-condensed pyrazines
- A61K31/497—Non-condensed pyrazines 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
- A61K31/495—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
- A61K31/4985—Pyrazines or piperazines ortho- or peri-condensed with heterocyclic ring systems
-
- 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
- A61K31/495—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
- A61K31/4995—Pyrazines or piperazines forming part of bridged ring systems
-
- 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
- A61K31/495—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
- A61K31/50—Pyridazines; Hydrogenated pyridazines
- A61K31/501—Pyridazines; Hydrogenated pyridazines not 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
- A61K31/495—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
- A61K31/50—Pyridazines; Hydrogenated pyridazines
- A61K31/5025—Pyridazines; Hydrogenated pyridazines ortho- or peri-condensed with heterocyclic ring systems
-
- 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
- A61K31/495—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
- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
- A61K31/506—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim not 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
- A61K31/53—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with three nitrogens as the only ring hetero atoms, e.g. chlorazanil, melamine
-
- 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
-
- 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
- A61K31/5383—1,4-Oxazines, e.g. morpholine ortho- or peri-condensed with heterocyclic ring systems
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K45/00—Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
- A61K45/06—Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/20—Pills, tablets, discs, rods
-
- 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
- A61P37/00—Drugs for immunological or allergic disorders
-
- 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
- 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
- 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
- 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
- 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
-
- 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
- C07D487/08—Bridged systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D495/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms
- C07D495/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
- C07D495/04—Ortho-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D495/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms
- C07D495/12—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms in which the condensed system contains three hetero rings
- C07D495/14—Ortho-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D498/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D498/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
- C07D498/04—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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D519/00—Heterocyclic compounds containing more than one system of two or more relevant hetero rings condensed among themselves or condensed with a common carbocyclic ring system not provided for in groups C07D453/00 or C07D455/00
-
- 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
- C07F7/00—Compounds containing elements of Groups 4 or 14 of the Periodic Table
- C07F7/02—Silicon compounds
- C07F7/08—Compounds having one or more C—Si linkages
- C07F7/18—Compounds having one or more C—Si linkages as well as one or more C—O—Si linkages
- C07F7/1804—Compounds having Si-O-C linkages
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Organic Chemistry (AREA)
- Veterinary Medicine (AREA)
- Pharmacology & Pharmacy (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Epidemiology (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Immunology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Plural Heterocyclic Compounds (AREA)
Abstract
123 in vitro in situ in vivoHeteroaryl pyridone and aza pyridone compounds of Formula I are provided where one or two of X X and Xare N and including stereoisomers tautomers and pharmaceutically acceptable salts thereof useful for inhibiting Btk kinase and for treating immune disorders such as inflammation mediated by Btk kinase. Methods of using compounds of Formula I for and diagnosis and treatment of such disorders in mammalian cells or associated pathological conditions are disclosed.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201161555393P | 2011-11-03 | 2011-11-03 | |
| PCT/US2012/063194 WO2013067274A1 (en) | 2011-11-03 | 2012-11-02 | Heteroaryl pyridone and aza-pyridone compounds as inhibitors of btk activity |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| IN2014CN03250A true IN2014CN03250A (en) | 2015-07-03 |
Family
ID=47146779
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| IN3250CHN2014 IN2014CN03250A (en) | 2011-11-03 | 2012-11-02 |
Country Status (34)
| Country | Link |
|---|---|
| US (11) | US8716274B2 (en) |
| EP (5) | EP4019508A1 (en) |
| JP (5) | JP5976827B2 (en) |
| KR (2) | KR101659193B1 (en) |
| CN (2) | CN104125959B (en) |
| AR (2) | AR088641A1 (en) |
| AU (5) | AU2012332365B2 (en) |
| CA (1) | CA2853975C (en) |
| CL (1) | CL2014001103A1 (en) |
| CO (1) | CO6950472A2 (en) |
| CR (1) | CR20140194A (en) |
| CY (1) | CY1117097T1 (en) |
| DK (2) | DK3002284T3 (en) |
| EA (1) | EA023263B1 (en) |
| ES (3) | ES2738329T3 (en) |
| HR (2) | HRP20151442T1 (en) |
| HU (2) | HUE044959T2 (en) |
| IL (1) | IL232060A (en) |
| IN (1) | IN2014CN03250A (en) |
| LT (1) | LT3002284T (en) |
| MA (1) | MA35819B1 (en) |
| MX (2) | MX2014005331A (en) |
| PE (1) | PE20141586A1 (en) |
| PH (1) | PH12014500936A1 (en) |
| PL (3) | PL3521288T3 (en) |
| PT (2) | PT2773638E (en) |
| RS (2) | RS59016B1 (en) |
| SG (1) | SG11201401992YA (en) |
| SI (2) | SI3002284T1 (en) |
| TR (1) | TR201909849T4 (en) |
| TW (4) | TWI609868B (en) |
| UA (1) | UA111756C2 (en) |
| WO (1) | WO2013067274A1 (en) |
| ZA (1) | ZA201804727B (en) |
Families Citing this family (77)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| UA111756C2 (en) * | 2011-11-03 | 2016-06-10 | Ф. Хоффманн-Ля Рош Аг | HETEROARYLPYRIDONE AND AZAPIRIDONE COMPOUNDS AS BRUTON TYROSINKINASE INHIBITORS |
| EP2773639B1 (en) * | 2011-11-03 | 2017-04-26 | F. Hoffmann-La Roche AG | Alkylated piperazine compounds as inhibitors of btk activity |
| WO2015000949A1 (en) | 2013-07-03 | 2015-01-08 | F. Hoffmann-La Roche Ag | Heteroaryl pyridone and aza-pyridone amide compounds |
| WO2015050703A1 (en) * | 2013-10-04 | 2015-04-09 | Yi Chen | Inhibitors of bruton's tyrosine kinase |
| WO2015082583A1 (en) | 2013-12-05 | 2015-06-11 | F. Hoffmann-La Roche Ag | Heteroaryl pyridone and aza-pyridone compounds with electrophilic functionality |
| CN106922146B (en) | 2014-10-02 | 2020-05-26 | 豪夫迈·罗氏有限公司 | Pyrazole carboxamide compounds for the treatment of diseases mediated by Bruton's Tyrosine Kinase (BTK) |
| JP6368043B2 (en) | 2014-10-27 | 2018-08-01 | エフ.ホフマン−ラ ロシュ アーゲーF. Hoffmann−La Roche Aktiengesellschaft | Method for producing tricyclic lactam compound |
| CN106188063A (en) * | 2015-05-08 | 2016-12-07 | 中国科学院上海药物研究所 | Bicyclic compound used as Lp-PLA2 inhibitor, its preparation method and medical application |
| JP6532599B2 (en) | 2015-09-02 | 2019-06-19 | グラクソスミスクライン、インテレクチュアル、プロパティー、(ナンバー2)、リミテッドGlaxosmithkline Intellectual Property (No.2) Limited | Pyridinone dicarboxamides for use as bromo domain inhibitors |
| US10208024B2 (en) | 2015-10-23 | 2019-02-19 | Array Biopharma Inc. | 2-aryl- and 2-heteroaryl-substituted 2-pyridazin-3(2H)-one compounds as inhibitors of FGFR tyrosine kinases |
| US20200270265A1 (en) * | 2016-02-19 | 2020-08-27 | Novartis Ag | Tetracyclic pyridone compounds as antivirals |
| WO2017148837A1 (en) * | 2016-02-29 | 2017-09-08 | F. Hoffmann-La Roche Ag | Dosage form compositions comprising an inhibitor of bruton's tyrosine kinase |
| JP6983813B2 (en) * | 2016-04-28 | 2021-12-17 | エフ.ホフマン−ラ ロシュ アーゲーF. Hoffmann−La Roche Aktiengesellschaft | Process for the preparation of 2-pyrazolo [1,5-a] pyrazine-2-ylpyrido [1,2-a] pyrimidin-4-one |
| CN108101905A (en) * | 2016-11-24 | 2018-06-01 | 中国科学院上海药物研究所 | Pyrimido [5,4-b] indolizine or pyrimido [5,4-b] pyrrole biopterin compound, preparation method and the usage |
| CA3045339A1 (en) | 2016-12-03 | 2018-06-07 | Juno Therapeutics, Inc. | Methods and compositions for use of therapeutic t cells in combination with kinase inhibitors |
| KR20190112263A (en) | 2016-12-12 | 2019-10-04 | 멀티비르 인코포레이티드 | Methods and compositions comprising viral gene therapy and immune checkpoint inhibitors for the treatment and prevention of cancer and infectious diseases |
| WO2018109050A1 (en) * | 2016-12-15 | 2018-06-21 | F. Hoffmann-La Roche Ag | Process for preparing btk inhibitors |
| WO2018113771A1 (en) | 2016-12-22 | 2018-06-28 | Betta Pharmaceuticals Co., Ltd | Benzimidazole derivatives, preparation methods and uses theirof |
| CN110709702A (en) * | 2017-03-24 | 2020-01-17 | 豪夫迈·罗氏有限公司 | Methods of treating autoimmune and inflammatory diseases |
| CN107445981B (en) * | 2017-08-25 | 2018-06-22 | 牡丹江医学院 | A kind of reactive compound for anti-treating cervicitis |
| KR102613433B1 (en) | 2017-10-11 | 2023-12-13 | 주식회사 대웅제약 | Novel phenyl pyridine derivatives and pharmaceutical composition comprising the same |
| CN111386272B (en) | 2017-10-27 | 2023-01-06 | 费森尤斯卡比肿瘤学有限公司 | Improved preparation method of Riboxib and salt thereof |
| KR102861971B1 (en) | 2018-02-19 | 2025-09-19 | 광조우 루펭 파마슈티칼 컴퍼니 엘티디. | Inhibitors of BTK and its mutants |
| TWI801517B (en) | 2018-03-12 | 2023-05-11 | 加拿大商愛彼特生物製藥公司 | Substituted 2-pyridone tricyclic compounds, analogues thereof, and methods using same |
| WO2019208805A1 (en) | 2018-04-27 | 2019-10-31 | 小野薬品工業株式会社 | PREVENTIVE AND/OR THERAPEUTIC AGENT FOR AUTOIMMUNE DISEASE COMPRISING COMPOUND HAVING Btk INHIBITORY ACTIVITY AS ACTIVE INGREDIENT |
| CN112839648B (en) | 2018-06-07 | 2025-04-04 | 达萨玛治疗公司 | SARM1 inhibitors |
| KR20210038877A (en) | 2018-07-25 | 2021-04-08 | 노파르티스 아게 | NLRP3 inplasmasome inhibitor |
| KR102328682B1 (en) * | 2018-08-27 | 2021-11-18 | 주식회사 대웅제약 | Novel heterocyclicamine derivatives and pharmaceutical composition comprising the same |
| CA3111126A1 (en) | 2018-08-31 | 2020-03-05 | Stichting Katholieke Universiteit | Synergistic combinations of amino acid depletion agent sensitizers (aadas) and amino acid depletion agents (aada), and therapeutic methods of use thereof |
| MX2021004191A (en) | 2018-10-15 | 2021-05-27 | Nurix Therapeutics Inc | BIFUNCTIONAL COMPOUNDS TO DEGRADE BRUTON'S TYROSINE KINASE (BTK) THROUGH THE PROTEOSOME UBIQUITIN PATHWAY. |
| EP3898626A1 (en) | 2018-12-19 | 2021-10-27 | Array Biopharma, Inc. | Substituted pyrazolo[1,5-a]pyridine compounds as inhibitors of fgfr tyrosine kinases |
| EP3897670A4 (en) | 2018-12-19 | 2022-09-07 | Disarm Therapeutics, Inc. | Inhibitors of sarm1 in combination with neuroprotective agents |
| US12351571B2 (en) | 2018-12-19 | 2025-07-08 | Array Biopharma Inc. | Substituted quinoxaline compounds as inhibitors of FGFR tyrosine kinases |
| TW202033523A (en) * | 2019-01-17 | 2020-09-16 | 美商愛彼特生物製藥股份有限公司 | Substituted polycyclic carboxylic acids, analogues thereof, and methods using same |
| TW202042815A (en) | 2019-01-22 | 2020-12-01 | 美商建南德克公司 | Methods of treating rheumatoid arthritis, chronic spontaneous urticaria, and systemic lupus erythematosis using an inhibitor of bruton's tyrosine kinase |
| US12582722B2 (en) | 2019-02-13 | 2026-03-24 | Nurix Therapeutics, Inc. | Bifunctional compounds for degrading BTK via ubiquitin proteosome pathway |
| WO2020176403A1 (en) | 2019-02-25 | 2020-09-03 | Newave Pharmaceutical Inc. | Inhibitor of btk and mutants thereof |
| EA202192575A1 (en) | 2019-03-21 | 2022-01-14 | Онксео | DBAIT COMPOUNDS IN COMBINATION WITH KINASE INHIBITORS FOR CANCER TREATMENT |
| CA3136348A1 (en) | 2019-04-09 | 2020-10-15 | Nurix Therapeutics, Inc. | 3-substituted piperidine compounds for cbl-b inhibition, and use of a cbl-b inhibitor in combination with a cancer vaccine and/or oncolytic virus |
| AR119731A1 (en) | 2019-05-17 | 2022-01-05 | Novartis Ag | NLRP3 INFLAMASOME INHIBITORS |
| AU2020278592B2 (en) | 2019-05-17 | 2024-10-10 | Nurix Therapeutics, Inc. | Cyano cyclobutyl compounds for Cbl-b inhibition and uses thereof |
| MX2021015675A (en) | 2019-06-26 | 2022-02-03 | Nurix Therapeutics Inc | SUBSTITUTED BENCYL-TRIAZOLE COMPOUNDS FOR THE INHIBITION OF CBL-B AND OTHER USES THEREOF. |
| EP4034140A1 (en) | 2019-09-24 | 2022-08-03 | Nurix Therapeutics, Inc. | Cbl inhibitors and compositions for use in adoptive cell therapy |
| US20220363689A1 (en) | 2019-10-05 | 2022-11-17 | Newave Pharmaceutical Inc. | Inhibitor of btk and mutants thereof |
| US20230024442A1 (en) * | 2019-11-08 | 2023-01-26 | Nurix Therapeutics, Inc. | Bifunctional compounds for grading btk via ubiquitin proteosome pathway |
| CN114761006A (en) | 2019-11-08 | 2022-07-15 | Inserm(法国国家健康医学研究院) | Methods of treating cancer resistant to kinase inhibitors |
| WO2021113557A1 (en) | 2019-12-04 | 2021-06-10 | Nurix Therapeutics, Inc. | Bifunctional compounds for degrading btk via ubiquitin proteosome pathway |
| WO2021148581A1 (en) | 2020-01-22 | 2021-07-29 | Onxeo | Novel dbait molecule and its use |
| IL295589A (en) | 2020-02-20 | 2022-10-01 | Hutchison Medipharma Ltd | Heteroaryl heterocyclic compounds and uses thereof |
| WO2021173740A1 (en) | 2020-02-28 | 2021-09-02 | Genentech, Inc. | Methods of treating primary progressive multiple sclerosis using an inhibitor of bruton's tyrosine kinase |
| BR112022019846A2 (en) | 2020-04-03 | 2022-11-22 | Genentech Inc | METHOD OF TREATMENT OF RECURRENT MULTIPLE SCLEROSIS (RMS), METHODS TO REDUCED THE ANUALIZED RECURRENCE RATE (ARR), REDUCE THE RISK OF EXPERIENCE CCDP12 AND INCREASE TIME TO START OF CCDP12 AND COMPOUNDS |
| CN115715291B (en) * | 2020-06-18 | 2025-04-29 | 上海华汇拓医药科技有限公司 | Bruton's tyrosine kinase inhibitor and preparation method thereof |
| US20230295109A1 (en) * | 2020-08-04 | 2023-09-21 | Hoffmann-La Roche Inc. | Pyridinone compounds for the treatment of autoimmune disease |
| AU2021326530A1 (en) * | 2020-08-14 | 2023-04-20 | Guangzhou Lupeng Pharmaceutical Company Ltd. | Dosage form compositions comprising an inhibitor of btk and mutants thereof |
| JP7545570B2 (en) | 2020-08-14 | 2024-09-04 | ノバルティス アーゲー | Heteroaryl-substituted spiro piperidinyl derivatives and pharmaceutical uses thereof |
| CN121226379A (en) | 2020-09-21 | 2025-12-30 | 和记黄埔医药(上海)有限公司 | Heteroaryl heterocyclic compounds and their uses |
| WO2022094172A2 (en) | 2020-10-30 | 2022-05-05 | Newave Pharmaceutical Inc. | Inhibitors of btk |
| US20240058457A1 (en) | 2020-12-20 | 2024-02-22 | Newave Pharmaceutical Inc. | Btk degrader |
| EP4313023A1 (en) | 2021-04-02 | 2024-02-07 | Biogen MA Inc. | Combination treatment methods of multiple sclerosis |
| WO2022217123A2 (en) | 2021-04-08 | 2022-10-13 | Nurix Therapeutics, Inc. | Combination therapies with cbl-b inhibitor compounds |
| EP4545537A3 (en) | 2021-05-05 | 2025-07-16 | F. Hoffmann-La Roche AG | Process for preparing btk inhibitors |
| CN113603685A (en) * | 2021-07-23 | 2021-11-05 | 都创(上海)医药开发有限公司 | Crystal form of Fenebbrutinib compound, preparation method and application thereof |
| CA3236073A1 (en) | 2021-10-26 | 2023-05-04 | Robert J. Brown | Piperidinylpyrazine-carboxamide compounds for treating and preventing cancer and for degrading btk |
| KR20240157639A (en) | 2021-12-14 | 2024-11-01 | 크로스파이어 온콜로지 홀딩 비.브이. | Macrocyclic BTK inhibitor |
| US20250136620A1 (en) * | 2022-01-17 | 2025-05-01 | Newave Pharmaceutical Inc. | Btk degrader |
| TW202346276A (en) | 2022-01-27 | 2023-12-01 | 日商田邊三菱製藥股份有限公司 | Novel b0at1 inhibitor |
| WO2023143491A1 (en) | 2022-01-28 | 2023-08-03 | 和记黄埔医药(上海)有限公司 | Synthesis method for 7,8-dihydro-2h-cyclopentapyrrolopyrazinone compound |
| UY40374A (en) | 2022-08-03 | 2024-02-15 | Novartis Ag | NLRP3 INFLAMASOME INHIBITORS |
| JPWO2024210198A1 (en) | 2023-04-06 | 2024-10-10 | ||
| TW202508592A (en) | 2023-05-16 | 2025-03-01 | 美商建南德克公司 | Methods of treating relapsing multiple sclerosis using an inhibitor of bruton's tyrosine kinase |
| WO2024246287A1 (en) | 2023-06-02 | 2024-12-05 | Crossfire Oncology Holding B.V. | Medical use of a macrocyclic 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 |
| 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 |
| WO2024256568A1 (en) | 2023-06-13 | 2024-12-19 | Crossfire Oncology Holding B.V. | Salt and crystal forms of a macrocyclic btk inhibitor |
| WO2024256574A1 (en) | 2023-06-13 | 2024-12-19 | Crossfire Oncology Holding B.V. | Process for preparing macrocyclic btk inhibitors |
| WO2025031344A1 (en) * | 2023-08-07 | 2025-02-13 | 广州麓鹏制药有限公司 | Crystal form vi of acrylamide compound, and preparation method therefor and use thereof |
| WO2026017823A1 (en) | 2024-07-18 | 2026-01-22 | F. Hoffmann-La Roche Ag | Process for preparing btk inhibitor intermediates |
Family Cites Families (43)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3773919A (en) | 1969-10-23 | 1973-11-20 | Du Pont | Polylactide-drug mixtures |
| US5583024A (en) | 1985-12-02 | 1996-12-10 | The Regents Of The University Of California | Recombinant expression of Coleoptera luciferase |
| US5543523A (en) | 1994-11-15 | 1996-08-06 | Regents Of The University Of Minnesota | Method and intermediates for the synthesis of korupensamines |
| JPH08336393A (en) | 1995-04-13 | 1996-12-24 | Mitsubishi Chem Corp | Process for producing optically active γ-substituted-β-hydroxybutyric acid ester |
| US6602677B1 (en) | 1997-09-19 | 2003-08-05 | Promega Corporation | Thermostable luciferases and methods of production |
| KR20040024564A (en) | 2001-07-12 | 2004-03-20 | 아베시아 리미티드 | Microencapsulated catalyst, methods of preparation and methods of use thereof |
| US7405295B2 (en) | 2003-06-04 | 2008-07-29 | Cgi Pharmaceuticals, Inc. | Certain imidazo[1,2-a]pyrazin-8-ylamines and method of inhibition of Bruton's tyrosine kinase by such compounds |
| WO2005005429A1 (en) | 2003-06-30 | 2005-01-20 | Cellular Genomics, Inc. | Certain heterocyclic substituted imidazo[1,2-a]pyrazin-8-ylamines and methods of inhibition of bruton’s tyrosine kinase by such compounds |
| CA2573644A1 (en) | 2004-07-12 | 2006-02-16 | Idun Pharmaceuticals, Inc. | Tetrapeptide analogs |
| AU2005304473A1 (en) | 2004-11-10 | 2006-05-18 | Cgi Pharmaceuticals, Inc. | Imidazo[1 , 2-a] pyrazin-8-ylamines useful as modulators of kinase activity |
| MX2007011041A (en) | 2005-03-10 | 2008-02-22 | Cgi Pharmaceuticals Inc | Certain substituted amides, method of making, and method of use thereof. |
| SI1934174T1 (en) | 2005-10-07 | 2011-08-31 | Exelixis Inc | Azetidines as mek inhibitors for the treatment of proliferative diseases |
| US7838523B2 (en) | 2006-09-11 | 2010-11-23 | Cgi Pharmaceuticals, Inc. | Certain substituted amides, method of making, and method of use thereof |
| AR063946A1 (en) | 2006-09-11 | 2009-03-04 | Cgi Pharmaceuticals Inc | CERTAIN REPLACED PIRIMIDINS, THE USE OF THE SAME FOR THE TREATMENT OF DISEASES MEDIATED BY THE INHIBITION OF THE ACTIVITY OF BTK AND PHARMACEUTICAL COMPOSITIONS THAT UNDERSTAND THEM. |
| AR063706A1 (en) | 2006-09-11 | 2009-02-11 | Cgi Pharmaceuticals Inc | CERTAIN AMIDAS REPLACED, THE USE OF THE SAME FOR THE TREATMENT OF DISEASES MEDIATED BY THE INHIBITION OF THE ACTIVITY OF BTK AND PHARMACEUTICAL COMPOSITIONS THAT UNDERSTAND THEM. |
| DK2526933T3 (en) * | 2006-09-22 | 2015-05-18 | Pharmacyclics Inc | Inhibitors of Bruton's tyrosine kinase |
| CL2008002793A1 (en) * | 2007-09-20 | 2009-09-04 | Cgi Pharmaceuticals Inc | Compounds derived from substituted amides, inhibitors of btk activity; pharmaceutical composition comprising them; Useful in the treatment of cancer, bone disorders, autoimmune diseases, among others |
| CN101835755B (en) * | 2007-10-23 | 2013-12-11 | 霍夫曼-拉罗奇有限公司 | Novel kinase inhibitors |
| US8426441B2 (en) | 2007-12-14 | 2013-04-23 | Roche Palo Alto Llc | Inhibitors of bruton's tyrosine kinase |
| US7683064B2 (en) | 2008-02-05 | 2010-03-23 | Roche Palo Alto Llc | Inhibitors of Bruton's tyrosine kinase |
| PL2242749T3 (en) * | 2008-02-05 | 2013-09-30 | Hoffmann La Roche | Novel pyridinones and pyridazinones |
| CA2723237A1 (en) | 2008-05-06 | 2009-11-12 | Peter A. Blomgren | Substituted amides, method of making, and use as btk inhibitors |
| PH12012502374A1 (en) * | 2008-06-24 | 2014-11-12 | Hoffmann La Roche | Novel substituted pyridin-2-ones and pyridazin-3-ones |
| PE20110164A1 (en) | 2008-07-02 | 2011-03-28 | Hoffmann La Roche | NEW PHENYLpyRAZINONES AS KINASE INHIBITORS |
| CA2636807A1 (en) | 2008-07-04 | 2010-01-04 | Steven Splinter | Methods for obtaining cyclopamine |
| WO2010006947A1 (en) | 2008-07-15 | 2010-01-21 | F. Hoffmann-La Roche Ag | Novel phenyl-imidazopyridines and pyridazines |
| US8598174B2 (en) | 2008-11-12 | 2013-12-03 | Genetech, Inc. | Pyridazinones, method of making, and method of use thereof |
| US8299077B2 (en) * | 2009-03-02 | 2012-10-30 | Roche Palo Alto Llc | Inhibitors of Bruton's tyrosine kinase |
| WO2010122038A1 (en) * | 2009-04-24 | 2010-10-28 | F. Hoffmann-La Roche Ag | Inhibitors of bruton's tyrosine kinase |
| US8765754B2 (en) * | 2009-04-29 | 2014-07-01 | Locus Pharmaceuticals, Inc. | Pyrrolotriazine compounds |
| NZ598985A (en) * | 2009-09-04 | 2013-07-26 | Biogen Idec Inc | Bruton's tyrosine kinase inhibitors |
| EP2566869B1 (en) * | 2010-05-07 | 2016-03-02 | Gilead Connecticut, Inc. | Pyridone and aza-pyridone compounds and methods of use |
| AR082590A1 (en) * | 2010-08-12 | 2012-12-19 | Hoffmann La Roche | INHIBITORS OF THE TIROSINA-QUINASA DE BRUTON |
| US8975260B2 (en) | 2010-09-01 | 2015-03-10 | Genetech, Inc | Pyridazinones, method of making, and method of use thereof |
| CA2809836C (en) | 2010-09-01 | 2019-01-15 | Gilead Connecticut, Inc. | Pyridinones/pyrazinones, method of making, and method of use thereof for the treatment of disorders mediated by bruton's tyrosine kinase |
| AU2012257802A1 (en) | 2011-05-17 | 2013-10-31 | F. Hoffmann-La Roche Ag | Inhibitors of Bruton's tyrosine kinase |
| CA2841801A1 (en) | 2011-08-17 | 2013-02-21 | F.Hoffmann-La Roche Ag | Inhibitors of bruton's tyrosine kinase |
| EP2773639B1 (en) * | 2011-11-03 | 2017-04-26 | F. Hoffmann-La Roche AG | Alkylated piperazine compounds as inhibitors of btk activity |
| UA111756C2 (en) * | 2011-11-03 | 2016-06-10 | Ф. Хоффманн-Ля Рош Аг | HETEROARYLPYRIDONE AND AZAPIRIDONE COMPOUNDS AS BRUTON TYROSINKINASE INHIBITORS |
| MX2014005282A (en) * | 2011-11-03 | 2014-05-30 | Hoffmann La Roche | 8-fluorophthalazin-1 (2h) - one compounds as inhibitors of btk activity. |
| WO2015000949A1 (en) * | 2013-07-03 | 2015-01-08 | F. Hoffmann-La Roche Ag | Heteroaryl pyridone and aza-pyridone amide compounds |
| WO2015082583A1 (en) * | 2013-12-05 | 2015-06-11 | F. Hoffmann-La Roche Ag | Heteroaryl pyridone and aza-pyridone compounds with electrophilic functionality |
| WO2017148837A1 (en) * | 2016-02-29 | 2017-09-08 | F. Hoffmann-La Roche Ag | Dosage form compositions comprising an inhibitor of bruton's tyrosine kinase |
-
2012
- 2012-02-11 UA UAA201405799A patent/UA111756C2/en unknown
- 2012-11-02 MX MX2014005331A patent/MX2014005331A/en active IP Right Grant
- 2012-11-02 TW TW101140919A patent/TWI609868B/en active
- 2012-11-02 MX MX2015003514A patent/MX361807B/en unknown
- 2012-11-02 KR KR1020147014661A patent/KR101659193B1/en active Active
- 2012-11-02 EP EP21171114.8A patent/EP4019508A1/en active Pending
- 2012-11-02 SI SI201231643T patent/SI3002284T1/en unknown
- 2012-11-02 EP EP19152979.1A patent/EP3521288B1/en active Active
- 2012-11-02 PT PT127838373T patent/PT2773638E/en unknown
- 2012-11-02 CN CN201280065965.8A patent/CN104125959B/en active Active
- 2012-11-02 SG SG11201401992YA patent/SG11201401992YA/en unknown
- 2012-11-02 JP JP2014541114A patent/JP5976827B2/en active Active
- 2012-11-02 HR HRP20151442TT patent/HRP20151442T1/en unknown
- 2012-11-02 EP EP12783837.3A patent/EP2773638B1/en active Active
- 2012-11-02 DK DK15188086.1T patent/DK3002284T3/en active
- 2012-11-02 HU HUE15188086A patent/HUE044959T2/en unknown
- 2012-11-02 ES ES15188086T patent/ES2738329T3/en active Active
- 2012-11-02 DK DK12783837.3T patent/DK2773638T3/en active
- 2012-11-02 CN CN201710227680.4A patent/CN107011348B/en active Active
- 2012-11-02 PL PL19152979T patent/PL3521288T3/en unknown
- 2012-11-02 TW TW109129648A patent/TW202124384A/en unknown
- 2012-11-02 LT LTEP15188086.1T patent/LT3002284T/en unknown
- 2012-11-02 HU HUE12783837A patent/HUE028019T2/en unknown
- 2012-11-02 EA EA201490858A patent/EA023263B1/en unknown
- 2012-11-02 TW TW107141781A patent/TWI701250B/en active
- 2012-11-02 IN IN3250CHN2014 patent/IN2014CN03250A/en unknown
- 2012-11-02 RS RS20190888A patent/RS59016B1/en unknown
- 2012-11-02 PH PH1/2014/500936A patent/PH12014500936A1/en unknown
- 2012-11-02 WO PCT/US2012/063194 patent/WO2013067274A1/en not_active Ceased
- 2012-11-02 US US13/667,133 patent/US8716274B2/en not_active Ceased
- 2012-11-02 PE PE2014000638A patent/PE20141586A1/en active IP Right Grant
- 2012-11-02 AR ARP120104128A patent/AR088641A1/en active IP Right Grant
- 2012-11-02 AU AU2012332365A patent/AU2012332365B2/en active Active
- 2012-11-02 PT PT15188086T patent/PT3002284T/en unknown
- 2012-11-02 SI SI201230367T patent/SI2773638T1/en unknown
- 2012-11-02 EP EP15188086.1A patent/EP3002284B1/en active Active
- 2012-11-02 TR TR2019/09849T patent/TR201909849T4/en unknown
- 2012-11-02 PL PL12783837T patent/PL2773638T3/en unknown
- 2012-11-02 ES ES19152979T patent/ES2898938T3/en active Active
- 2012-11-02 KR KR1020157036122A patent/KR20160003328A/en not_active Withdrawn
- 2012-11-02 TW TW106130019A patent/TWI652270B/en active
- 2012-11-02 EP EP22157147.4A patent/EP4050012A1/en active Pending
- 2012-11-02 RS RS20160001A patent/RS54505B1/en unknown
- 2012-11-02 PL PL15188086T patent/PL3002284T3/en unknown
- 2012-11-02 CA CA2853975A patent/CA2853975C/en active Active
- 2012-11-02 ES ES12783837.3T patent/ES2555168T3/en active Active
-
2014
- 2014-03-13 US US14/207,966 patent/US8921353B2/en active Active
- 2014-04-10 IL IL232060A patent/IL232060A/en active IP Right Grant
- 2014-04-28 CR CR20140194A patent/CR20140194A/en unknown
- 2014-04-28 CO CO14090476A patent/CO6950472A2/en active IP Right Grant
- 2014-04-29 CL CL2014001103A patent/CL2014001103A1/en unknown
- 2014-05-27 MA MA37075A patent/MA35819B1/en unknown
- 2014-09-08 US US14/479,529 patent/US9238655B2/en active Active
-
2015
- 2015-08-24 JP JP2015165300A patent/JP2016028046A/en not_active Withdrawn
- 2015-11-17 US US14/943,552 patent/US9782405B2/en active Active
-
2016
- 2016-01-04 CY CY20161100003T patent/CY1117097T1/en unknown
- 2016-12-15 AU AU2016273930A patent/AU2016273930B2/en active Active
-
2017
- 2017-08-31 US US15/693,022 patent/US10045983B2/en active Active
-
2018
- 2018-01-04 JP JP2018000309A patent/JP6571215B2/en active Active
- 2018-03-05 AU AU2018201557A patent/AU2018201557B2/en active Active
- 2018-06-27 US US16/020,270 patent/US20190194203A1/en not_active Abandoned
- 2018-07-16 ZA ZA2018/04727A patent/ZA201804727B/en unknown
- 2018-10-30 US US16/175,278 patent/USRE48239E1/en active Active
-
2019
- 2019-02-14 JP JP2019024668A patent/JP2019108342A/en not_active Withdrawn
- 2019-07-18 HR HRP20191307TT patent/HRP20191307T1/en unknown
- 2019-08-16 AU AU2019216728A patent/AU2019216728B2/en active Active
- 2019-10-31 US US16/670,898 patent/US20200062769A1/en not_active Abandoned
- 2019-12-23 AR ARP190103844A patent/AR117501A2/en unknown
-
2020
- 2020-04-22 AU AU2020202707A patent/AU2020202707B2/en active Active
- 2020-07-02 JP JP2020114594A patent/JP2020183397A/en not_active Withdrawn
- 2020-08-24 US US17/001,205 patent/US20210079002A1/en not_active Abandoned
-
2022
- 2022-12-20 US US18/069,099 patent/US20230279012A1/en not_active Abandoned
-
2023
- 2023-11-29 US US18/523,284 patent/US20240270747A1/en active Pending
Also Published As
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| IN2014CN03250A (en) | ||
| MY160349A (en) | Pyridone and aza-pyridone compounds and methods of use | |
| IN2014CN03265A (en) | ||
| MX2014005285A (en) | Bicyclic piperazine compounds. | |
| MX2014005282A (en) | 8-fluorophthalazin-1 (2h) - one compounds as inhibitors of btk activity. | |
| MX2016007171A (en) | Heteroaryl pyridone and aza-pyridone compounds with electrophilic functionality. | |
| MX2015018038A (en) | Heteroaryl pyridone and aza-pyridone amide compounds. | |
| MX355852B (en) | PYRAZOLO[3,4-c]PYRIDINE COMPOUNDS AND METHODS OF USE. | |
| MX2014014828A (en) | 5-azaindazole compounds and methods of use. | |
| PH12015500488A1 (en) | Cyclic ether pyrazol-4-yl-heterocyclyl-carboxamide compounds and methods of use | |
| MX340013B (en) | Benzoxazepin compounds selective for pi3k p110 delta and methods of use. | |
| PH12012501864A1 (en) | Pyrazol-4-yl-heterocyclyl-carboxamide compounds and methods of use | |
| BR112013020329A2 (en) | heterocyclic compounds as pi3 kinase inhibitors | |
| PH12013502445A1 (en) | Pyridin-2 (1h) -one derivatives useful as medicaments for the treatment of myeloproliferative disorders, transplant rejection, immune-mediated and inflammatory diseases | |
| MX350112B (en) | Furo [3, 2 - b] - and thieno [3, 2 - b] pyridine derivatives as tbk1 and ikk inhibitors. | |
| PH12014501829A1 (en) | Bicyclic pyrazinone derivatives | |
| SG10201805392YA (en) | 1,2,4-triazine-6-carboxamide kinase inhibitors | |
| MX362855B (en) | Quinazolinone derivatives as parp inhibitors. | |
| MX2013012977A (en) | Thiazole derivatives. | |
| PH12015500063A1 (en) | Azaindole derivatives which act as pi3k inhibitors | |
| IN2014CN04065A (en) | ||
| MY166463A (en) | Positive allosteric modulators of nicotinic acetylcholine receptor | |
| MX2016012007A (en) | Oxepan-2-yl-pyrazol-4-yl-heterocyclyl-carboxamide compounds and methods of use. | |
| NZ620928A (en) | Pyrazol-4-yl-heterocyclyl-carboxamide compounds and methods of use | |
| MA42864A1 (en) | Cyclic ether-pyrazol-4-yl-heterocyclyl-carboxamide compounds and methods of use |