IN2012DN00755A - - Google Patents
Download PDFInfo
- Publication number
- IN2012DN00755A IN2012DN00755A IN755DEN2012A IN2012DN00755A IN 2012DN00755 A IN2012DN00755 A IN 2012DN00755A IN 755DEN2012 A IN755DEN2012 A IN 755DEN2012A IN 2012DN00755 A IN2012DN00755 A IN 2012DN00755A
- Authority
- IN
- India
- Prior art keywords
- compound
- formula
- pharmaceutically acceptable
- janus
- diasteriomers
- Prior art date
Links
- 102000015617 Janus Kinases Human genes 0.000 abstract 2
- 108010024121 Janus Kinases Proteins 0.000 abstract 2
- 150000001875 compounds Chemical class 0.000 abstract 2
- HBAQYPYDRFILMT-UHFFFAOYSA-N 8-[3-(1-cyclopropylpyrazol-4-yl)-1H-pyrazolo[4,3-d]pyrimidin-5-yl]-3-methyl-3,8-diazabicyclo[3.2.1]octan-2-one Chemical class C1(CC1)N1N=CC(=C1)C1=NNC2=C1N=C(N=C2)N1C2C(N(CC1CC2)C)=O HBAQYPYDRFILMT-UHFFFAOYSA-N 0.000 abstract 1
- 239000002671 adjuvant Substances 0.000 abstract 1
- 201000010099 disease Diseases 0.000 abstract 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 abstract 1
- 239000003937 drug carrier Substances 0.000 abstract 1
- 239000003112 inhibitor Substances 0.000 abstract 1
- 230000005764 inhibitory process Effects 0.000 abstract 1
- 239000008194 pharmaceutical composition Substances 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 239000003981 vehicle Substances 0.000 abstract 1
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
- C07D487/02—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
-
- 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
- A61K31/4353—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 ortho- or peri-condensed with heterocyclic ring systems
- A61K31/437—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 ortho- or peri-condensed with heterocyclic ring systems the heterocyclic ring system containing a five-membered ring having nitrogen as a ring hetero atom, e.g. indolizine, beta-carboline
-
- 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
- A61K31/445—Non condensed piperidines, e.g. piperocaine
-
- 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
- A61K31/519—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
-
- 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
- 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
- A61P35/02—Antineoplastic agents specific for leukemia
-
- 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
- C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
- C07D413/06—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Epidemiology (AREA)
- Oncology (AREA)
- Hematology (AREA)
- Pain & Pain Management (AREA)
- Rheumatology (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Dermatology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
Abstract
A compound of Formula I, enantiomers, diasteriomers, tautomers or pharmaceutically acceptable salts thereof, wherein R1, R2 and R3 are defined herein, are useful as inhibitors of one or more Janus kinases. A pharmaceutical composition that includes a compound of Formula 1 and a pharmaceutically acceptable carrier, adjuvant or vehicle, and methods of treating or lessening the severity of a disease or condition responsive to the inhibition of a Janus kinase activity in a patient are disclosed.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US22291809P | 2009-07-02 | 2009-07-02 | |
| PCT/US2010/040906 WO2011003065A2 (en) | 2009-07-02 | 2010-07-02 | Pyrazolopyrimidine jak inhibitor compounds and methods |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| IN2012DN00755A true IN2012DN00755A (en) | 2015-06-19 |
Family
ID=43411778
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| IN755DEN2012 IN2012DN00755A (en) | 2009-07-02 | 2010-07-02 |
Country Status (35)
| Country | Link |
|---|---|
| US (6) | US8999998B2 (en) |
| EP (3) | EP3333169B1 (en) |
| JP (4) | JP5769261B2 (en) |
| KR (3) | KR101903305B1 (en) |
| CN (2) | CN102482284B (en) |
| AU (1) | AU2010266188B2 (en) |
| BR (1) | BRPI1010197A2 (en) |
| CA (1) | CA2767097A1 (en) |
| CL (1) | CL2012000001A1 (en) |
| CO (1) | CO6491081A2 (en) |
| CR (2) | CR20170115A (en) |
| DK (1) | DK2448941T3 (en) |
| EC (1) | ECSP12011645A (en) |
| ES (1) | ES2657839T3 (en) |
| HR (1) | HRP20180157T1 (en) |
| HU (1) | HUE035537T2 (en) |
| IL (3) | IL217224B (en) |
| IN (1) | IN2012DN00755A (en) |
| LT (1) | LT2448941T (en) |
| MA (1) | MA33502B1 (en) |
| MX (1) | MX2012000169A (en) |
| MY (1) | MY160156A (en) |
| NO (1) | NO2448941T3 (en) |
| NZ (4) | NZ738778A (en) |
| PE (2) | PE20120575A1 (en) |
| PH (1) | PH12015500666A1 (en) |
| PL (1) | PL2448941T3 (en) |
| PT (1) | PT2448941T (en) |
| RS (1) | RS56671B1 (en) |
| RU (2) | RU2675857C2 (en) |
| SG (2) | SG10201509607XA (en) |
| SI (1) | SI2448941T1 (en) |
| UA (1) | UA110324C2 (en) |
| WO (1) | WO2011003065A2 (en) |
| ZA (2) | ZA201200490B (en) |
Families Citing this family (127)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| PT2455382T (en) | 2005-12-13 | 2017-01-31 | Incyte Holdings Corp | PYRIDOLES [2,3-B] PYRIDINES AND PYRROLE [2,3-B] PYRIMIDINES SUBSTITUTED BY HETEROARYLO AS JANUS KINASES INHIBITORS |
| ES2903444T3 (en) | 2007-06-13 | 2022-04-01 | Incyte Holdings Corp | Use of Janus(R)-3-(4-(7H-pyrrolo[2,3-d]pyrimidin-4-yl)-1H-pyrazol-1-yl)-3-cyclopentylpropanenitrile kinase inhibitor salts |
| EP2962566A1 (en) | 2008-10-31 | 2016-01-06 | Genentech, Inc. | Pyrazolopyrimidine jak inhibitor compounds and methods |
| WO2010135621A1 (en) | 2009-05-22 | 2010-11-25 | Incyte Corporation | 3-[4-(7h-pyrrolo[2,3-d]pyrimidin-4-yl)-1h-pyrazol-1-yl]octane- or heptane-nitrile as jak inhibitors |
| UA110324C2 (en) | 2009-07-02 | 2015-12-25 | Genentech Inc | Jak inhibitory compounds based on pyrazolo pyrimidine |
| TWI592413B (en) | 2010-03-10 | 2017-07-21 | 英塞特公司 | Piperidin-4-yl azetidine derivatives as jak1 inhibitors |
| SG184475A1 (en) | 2010-04-07 | 2012-11-29 | Hoffmann La Roche | Pyrazol-4-yl-heterocyclyl-carboxamide compounds and methods of use |
| UA111588C2 (en) | 2010-05-21 | 2016-05-25 | Інсайт Холдінгс Корпорейшн | JAK INHIBITOR COMPOSITION FOR LOCAL APPLICATION |
| KR101995013B1 (en) * | 2010-07-13 | 2019-07-02 | 에프. 호프만-라 로슈 아게 | Pyrazolo[1,5a]pyrimidine and thieno[3,2b]pyrimidine derivatives as irak4 modulators |
| ES2775125T3 (en) | 2010-11-03 | 2020-07-23 | Dow Agrosciences Llc | Pesticide compositions and related procedures |
| WO2012067822A1 (en) * | 2010-11-16 | 2012-05-24 | Abbott Laboratories | Pyrazolo [1, 5 -a] pyrimidin potassium channel modulators |
| WO2012068450A1 (en) | 2010-11-19 | 2012-05-24 | Incyte Corporation | Cyclobutyl substituted pyrrolopyridine and pyrrolopyrimidine derivatives as jak inhibitors |
| EP2688872A4 (en) * | 2011-03-22 | 2014-08-27 | Merck Sharp & Dohme | KINASE INHIBITORS ASSOCIATED WITH AMIDOPYRAZOLE-BASED INTERLEUKIN RECEPTORS |
| US8859549B2 (en) | 2011-05-13 | 2014-10-14 | Abbvie, Inc. | Potassium channel modulators |
| AU2012273164B2 (en) | 2011-06-20 | 2015-05-28 | Incyte Holdings Corporation | Azetidinyl phenyl, pyridyl or pyrazinyl carboxamide derivatives as JAK inhibitors |
| EP2723746A1 (en) | 2011-06-22 | 2014-04-30 | Vertex Pharmaceuticals Inc. | Compounds useful as inhibitors of atr kinase |
| UA111854C2 (en) | 2011-09-07 | 2016-06-24 | Інсайт Холдінгс Корпорейшн | METHODS AND INTERMEDIATE COMPOUNDS FOR JAK INHIBITORS |
| BR112014007203A2 (en) | 2011-09-27 | 2017-06-13 | F.Hoffmann-La Roche Ag | compound, pharmaceutical composition, method of treatment, use of a compound, assembly and invention |
| US9090630B2 (en) | 2011-09-30 | 2015-07-28 | Oncodesign S.A. | Macrocyclic FLT3 kinase inhibitors |
| CA2852688C (en) | 2011-10-26 | 2021-06-29 | Dow Agrosciences Llc | Pesticidal compositions and processes related thereto |
| US9012443B2 (en) | 2011-12-07 | 2015-04-21 | Amgen Inc. | Bicyclic aryl and heteroaryl sodium channel inhibitors |
| PH12017500997A1 (en) | 2012-04-04 | 2018-02-19 | Samumed Llc | Indazole inhibitors of the wnt signal pathway and therapeutic uses thereof |
| US8940742B2 (en) | 2012-04-10 | 2015-01-27 | Infinity Pharmaceuticals, Inc. | Heterocyclic compounds and uses thereof |
| US9708288B2 (en) | 2012-04-27 | 2017-07-18 | Dow Agrosciences Llc | Pesticidal compositions and processes related thereto |
| CA2870090A1 (en) | 2012-04-27 | 2013-10-31 | Dow Agrosciences Llc | Pesticidal compositions and processes related thereto |
| US9282739B2 (en) | 2012-04-27 | 2016-03-15 | Dow Agrosciences Llc | Pesticidal compositions and processes related thereto |
| HK1212344A1 (en) * | 2012-08-10 | 2016-06-10 | F. Hoffmann-La Roche Ag | Pyrazole carboxamide compounds, compositions and methods of use |
| CN103073549A (en) * | 2012-09-07 | 2013-05-01 | 苏州康润医药有限公司 | 3-bromopyrazol[1,5-alpha]pyrimidine-2-formic acid synthesis process |
| WO2014064134A1 (en) | 2012-10-26 | 2014-05-01 | F. Hoffmann-La Roche Ag | 3,4-disubstituted 1 h-pyrazole and 4,5-disubstituted thiazole inhibitors of syk |
| ES2880814T3 (en) | 2012-11-15 | 2021-11-25 | Incyte Holdings Corp | Ruxolitinib Sustained Release Dosage Forms |
| CN104903325B (en) | 2012-12-07 | 2017-10-20 | 沃泰克斯药物股份有限公司 | Compounds useful as ATR kinase inhibitors |
| EP2951590A1 (en) | 2013-02-04 | 2015-12-09 | INSERM (Institut National de la Santé et de la Recherche Médicale) | Methods for assaying jak2 activity in red blood cells and uses thereof |
| CR20190518A (en) | 2013-03-06 | 2020-01-10 | Incyte Corp | Processes and intermediates for making a jak inhibitor |
| WO2014143241A1 (en) * | 2013-03-15 | 2014-09-18 | Vertex Pharmaceuticals Incorporated | Compounds useful as inhibitors of atr kinase |
| JP2016512815A (en) * | 2013-03-15 | 2016-05-09 | バーテックス ファーマシューティカルズ インコーポレイテッドVertex Pharmaceuticals Incorporated | Condensed pyrazolopyrimidine derivatives useful as inhibitors of ATR kinase |
| JP2016512816A (en) * | 2013-03-15 | 2016-05-09 | バーテックス ファーマシューティカルズ インコーポレイテッドVertex Pharmaceuticals Incorporated | Compounds useful as inhibitors of ATR kinase |
| KR20160045081A (en) | 2013-08-07 | 2016-04-26 | 인사이트 코포레이션 | Sustained release dosage forms for a jak1 inhibitor |
| PH12016500582B1 (en) | 2013-10-04 | 2023-06-30 | Infinity Pharmaceuticals Inc | Heterocyclic compounds and uses thereof |
| CN105636442B (en) | 2013-10-17 | 2018-04-27 | 美国陶氏益农公司 | The method for preparing Pesticidal compound |
| CN105636445B (en) | 2013-10-17 | 2018-12-07 | 美国陶氏益农公司 | Process for preparing pesticidal compounds |
| MX2016004946A (en) | 2013-10-17 | 2016-06-28 | Dow Agrosciences Llc | Processes for the preparation of pesticidal compounds. |
| CA2925873A1 (en) | 2013-10-17 | 2015-04-23 | Dow Agrosciences Llc | Processes for the preparation of pesticidal compounds |
| CA2926095A1 (en) | 2013-10-17 | 2015-04-23 | Dow Agrosciences Llc | Processes for the preparation of pesticidal compounds |
| EP3057427B1 (en) | 2013-10-17 | 2018-07-18 | Dow AgroSciences LLC | Processes for the preparation of pesticidal compounds |
| CA2925595A1 (en) | 2013-10-17 | 2015-04-23 | Dow Agrosciences Llc | Processes for the preparation of pesticidal compounds |
| TW201519772A (en) | 2013-10-22 | 2015-06-01 | Dow Agrosciences Llc | Synergistic pesticidal compositions and related methods |
| CA2927195A1 (en) | 2013-10-22 | 2015-04-30 | Dow Agrosciences Llc | Synergistic pesticidal compositions and related methods |
| TW201519783A (en) | 2013-10-22 | 2015-06-01 | Dow Agrosciences Llc | Pesticidal compositions and related methods |
| AU2014340437B2 (en) | 2013-10-22 | 2017-09-07 | Dow Agrosciences Llc | Synergistic pesticidal compositions and related methods |
| AR098099A1 (en) | 2013-10-22 | 2016-05-04 | Dow Agrosciences Llc | SYNERGIC PESTICIDE COMPOSITIONS AND RELATED METHODS |
| MX2016005304A (en) | 2013-10-22 | 2017-03-01 | Dow Agrosciences Llc | Synergistic pesticidal compositions and related methods. |
| AR098105A1 (en) | 2013-10-22 | 2016-05-04 | Dow Agrosciences Llc | PESTICIATED COMPOSITIONS AND RELATED METHODS |
| US9149040B2 (en) | 2013-10-22 | 2015-10-06 | Dow Agrosciences Llc | Synergistic pesticidal compositions and related methods |
| AR098102A1 (en) | 2013-10-22 | 2016-05-04 | Dow Agrosciences Llc | PESTICIATED COMPOSITIONS AND RELATED METHODS |
| AR098088A1 (en) | 2013-10-22 | 2016-05-04 | Dow Agrosciences Llc | SYNERGIC PESTICIATED COMPOSITIONS AND RELATED METHODS |
| EP3060051A4 (en) | 2013-10-22 | 2017-04-05 | Dow AgroSciences LLC | Synergistic pesticidal compositions and related methods |
| JP2016535025A (en) | 2013-10-22 | 2016-11-10 | ダウ アグロサイエンシィズ エルエルシー | Synergistic pest control compositions and related methods |
| AR098101A1 (en) | 2013-10-22 | 2016-05-04 | Dow Agrosciences Llc | PESTICIATED COMPOSITIONS AND RELATED METHODS |
| CA2926345A1 (en) | 2013-10-22 | 2015-04-30 | Dow Agrosciences Llc | Synergistic pesticidal compositions and related methods |
| EP3060046A4 (en) | 2013-10-22 | 2017-07-26 | Dow AgroSciences LLC | Pesticidal compositions and related methods |
| WO2015061151A1 (en) | 2013-10-22 | 2015-04-30 | Dow Agrosciences Llc | Pesticidal compositions and related methods |
| RU2016119368A (en) | 2013-10-22 | 2017-11-28 | ДАУ АГРОСАЙЕНСИЗ ЭлЭлСи | SYNERGETIC PESTICIDAL COMPOSITIONS AND RELATED WAYS |
| TW201605847A (en) * | 2013-11-08 | 2016-02-16 | 武田藥品工業股份有限公司 | Heterocyclic compound |
| CN104650092B (en) * | 2013-11-16 | 2017-11-10 | 广东东阳光药业有限公司 | Substituted heteroaryl compound and combinations thereof and purposes |
| MD4649C1 (en) | 2013-12-05 | 2020-04-30 | Pfizer Inc. | Pyrrolo[2,3-d]pyrimidinyl, pyrrolo[2,3-b]pyrazinyl and pyrrolo[2,3-d]pyridinyl acrylamides |
| SI3077397T1 (en) * | 2013-12-06 | 2020-02-28 | Vertex Pharmaceuticals Inc. | 2-amino-6-fluoro-n-(5-fluoro-pyridin-3-yl)pyrazolo(1,5-a)pyrimidin-3-carboxamide compound useful as atr kinase inhibitor, its preparation, different solid forms and radiolabelled derivatives thereof |
| EP3077393A1 (en) * | 2013-12-06 | 2016-10-12 | Vertex Pharmaceuticals Incorporated | Compounds useful as inhibitors of atr kinase |
| TW201620911A (en) * | 2014-03-17 | 2016-06-16 | 雷西肯製藥股份有限公司 | Inhibitors of adapter associated kinase 1, compositions comprising them, and methods of their use |
| CN113616656B (en) | 2014-03-19 | 2023-02-17 | 无限药品股份有限公司 | Heterocyclic compounds for the treatment of PI 3K-gamma mediated disorders |
| US9493439B1 (en) | 2014-04-07 | 2016-11-15 | University Of Kentucky Research Foundation | Proteasome inhibitors |
| UA119767C2 (en) * | 2014-04-08 | 2019-08-12 | Інсайт Корпорейшн | Treatment of b-cell malignancies by a combination jak and pi3k inhibitor |
| WO2015177326A1 (en) * | 2014-05-23 | 2015-11-26 | F. Hoffmann-La Roche Ag | 5-chloro-2-difluoromethoxyphenyl pyrazolopyrimidine compounds which are jak inhibitors |
| US9498467B2 (en) | 2014-05-30 | 2016-11-22 | Incyte Corporation | Treatment of chronic neutrophilic leukemia (CNL) and atypical chronic myeloid leukemia (aCML) by inhibitors of JAK1 |
| AU2015271030B2 (en) * | 2014-06-05 | 2019-05-16 | Vertex Pharmaceuticals Incorporated | Radiolabelled derivatives of a 2-amino-6-fluoro-n-[5-fluoro-pyridin-3-yl]- pyrazolo [1,5-a] pyrimidin-3-carboxamide compound useful as ATR kinase inhibitor, the preparation of said compound and different solid forms thereof |
| RU2736219C2 (en) | 2014-06-17 | 2020-11-12 | Вертекс Фармасьютикалз Инкорпорейтед | Method of treating cancer using a combination of chk1 and atr inhibitors |
| KR20170039121A (en) | 2014-07-31 | 2017-04-10 | 다우 아그로사이언시즈 엘엘씨 | Process for the preparation of 3-(3-chloro-1h-pyrazol-1-yl)pyridine |
| JP2017523168A (en) | 2014-07-31 | 2017-08-17 | ダウ アグロサイエンシィズ エルエルシー | Method for producing 3- (3-chloro-1H-pyrazol-1-yl) pyridine |
| WO2016018442A1 (en) | 2014-07-31 | 2016-02-04 | Dow Agrosciences Llc | Process for the preparation of 3-(3-chloro-1h-pyrazol-1-yl)pyridine |
| US9024031B1 (en) | 2014-08-19 | 2015-05-05 | Dow Agrosciences Llc | Process for the preparation of 3-(3-chloro-1H-pyrazol-1-yl)pyridine |
| US9085552B1 (en) | 2014-09-12 | 2015-07-21 | Dow Agrosciences Llc | Process for the preparation of 3-(3-chloro-1H-pyrazol-1-yl)pyridine |
| WO2016054491A1 (en) | 2014-10-03 | 2016-04-07 | Infinity Pharmaceuticals, Inc. | Heterocyclic compounds and uses thereof |
| WO2016202898A1 (en) * | 2015-06-19 | 2016-12-22 | Bayer Pharma Aktiengesellschaft | Glucose transport inhibitors |
| JP6980649B2 (en) | 2015-09-14 | 2021-12-15 | インフィニティー ファーマシューティカルズ, インコーポレイテッド | The solid form of the isoquinolinone derivative, the method for producing it, the composition containing it, and the method for using it. |
| HK1258570A1 (en) | 2015-09-30 | 2019-11-15 | Vertex Pharmaceuticals Inc. | Method for treating cancer using a combination of dna damaging agents and atr inhibitors |
| AU2016348639B2 (en) | 2015-11-06 | 2022-09-08 | Samumed, Llc | Treatment of osteoarthritis |
| TW201720828A (en) * | 2015-11-23 | 2017-06-16 | 赫孚孟拉羅股份公司 | Therapeutic compounds and compositions, and methods of use thereof |
| JP6936236B2 (en) * | 2016-02-18 | 2021-09-15 | エフ.ホフマン−ラ ロシュ アーゲーF. Hoffmann−La Roche Aktiengesellschaft | Use of therapeutic compounds, compositions and methods thereof |
| WO2017161116A1 (en) | 2016-03-17 | 2017-09-21 | Infinity Pharmaceuticals, Inc. | Isotopologues of isoquinolinone and quinazolinone compounds and uses thereof as pi3k kinase inhibitors |
| SG10201912248RA (en) | 2016-06-01 | 2020-02-27 | Samumed Llc | Process for preparing n-(5-(3-(7-(3-fluorophenyl)-3h-imidazo[4,5-c]pyridin-2-yl)-1h-indazol-5-yl)pyridin-3-yl)-3-methylbutanamide |
| WO2017214269A1 (en) | 2016-06-08 | 2017-12-14 | Infinity Pharmaceuticals, Inc. | Heterocyclic compounds and uses thereof |
| CN106008525B (en) * | 2016-06-16 | 2018-08-07 | 南京工业大学 | Micromolecule organic nano tumor photothermal treatment reagent and preparation method thereof |
| CR20190310A (en) * | 2016-12-29 | 2019-08-21 | Hoffmann La Roche | PYRAZOLOPYRIMIDINE COMPOUNDS AND METHODS OF USE OF THEM |
| CN110139853B (en) | 2016-12-29 | 2023-06-16 | 美国陶氏益农公司 | Process for the preparation of pesticidal compounds |
| US10233155B2 (en) | 2016-12-29 | 2019-03-19 | Dow Agrosciences Llc | Processes for the preparation of pesticide compounds |
| JP6986086B2 (en) * | 2017-01-17 | 2021-12-22 | アストラゼネカ・アクチエボラーグAstrazeneca Aktiebolag | JAK1 Selective Inhibitor |
| JP2020510061A (en) * | 2017-03-14 | 2020-04-02 | エフ.ホフマン−ラ ロシュ アーゲーF. Hoffmann−La Roche Aktiengesellschaft | Pyrazolochlorophenyl compounds, compositions and methods of using same |
| WO2018167283A1 (en) | 2017-03-17 | 2018-09-20 | INSERM (Institut National de la Santé et de la Recherche Médicale) | Methods for the diagnosis and treatment of pancreatic ductal adenocarcinoma associated neural remodeling |
| US20200088732A1 (en) | 2017-04-13 | 2020-03-19 | INSERM (Institut National de la Santé et de la Recherche Mèdicale) | Methods for the diagnosis and treatment of pancreatic ductal adenocarcinoma |
| PL233595B1 (en) * | 2017-05-12 | 2019-11-29 | Celon Pharma Spolka Akcyjna | Derivatives of pyrazolo[1,5-a]pyrimidine as inhibitors of kinase JAK |
| US20180334465A1 (en) * | 2017-05-22 | 2018-11-22 | Genentech, Inc. | Therapeutic compounds and compositions, and methods of use thereof |
| CR20190520A (en) * | 2017-05-22 | 2020-01-21 | Hoffmann La Roche | Therapeutic compounds and compositions, and methods of use thereof |
| JP2020527562A (en) | 2017-07-18 | 2020-09-10 | バイエル・クロップサイエンス・アクチェンゲゼルシャフト | Substitution 3-heteroaryloxy-1H-pyrazoles and their salts, and their use as herbicidal active substances |
| CN107686456B (en) * | 2017-07-25 | 2018-10-23 | 杭州师范大学 | A kind of quinolione key intermediate ethyl ester aminate and its preparation method and application |
| CN109422751B (en) * | 2017-09-03 | 2022-04-22 | 上海美志医药科技有限公司 | Compound with activity of degrading tyrosine protein kinase JAK3 |
| WO2019113487A1 (en) | 2017-12-08 | 2019-06-13 | Incyte Corporation | Low dose combination therapy for treatment of myeloproliferative neoplasms |
| CN111587250A (en) * | 2018-01-15 | 2020-08-25 | 豪夫迈·罗氏有限公司 | Pyrazolopyrimidine Compounds as JAK Inhibitors |
| TWI795510B (en) * | 2018-01-17 | 2023-03-11 | 英商葛蘭素史密斯克藍智慧財產發展有限公司 | PI4KIIIβ INHIBITORS |
| AU2019213665B2 (en) | 2018-01-30 | 2024-06-13 | Incyte Corporation | Processes for preparing (1 -(3-fluoro-2-(trifluoromethyl)isonicotinyl)piperidine-4-one) |
| JPWO2019172243A1 (en) | 2018-03-07 | 2020-04-16 | 三菱ケミカル株式会社 | Transparent resin composition, resin molding, lamp cover, vehicle lamp cover, combination lamp cover and vehicle |
| SG11202009441PA (en) | 2018-03-30 | 2020-10-29 | Incyte Corp | Treatment of hidradenitis suppurativa using jak inhibitors |
| MX2020010815A (en) | 2018-04-13 | 2020-12-11 | Incyte Corp | Biomarkers for graft-versus-host disease. |
| WO2020092015A1 (en) | 2018-11-02 | 2020-05-07 | University Of Rochester | Therapeutic mitigation of epithelial infection |
| WO2020150552A2 (en) * | 2019-01-17 | 2020-07-23 | Samumed, Llc | Methods of treating cartilage disorders through inhibition of clk and dyrk |
| MX2021009863A (en) | 2019-03-21 | 2021-11-12 | Onxeo | A dbait molecule in combination with kinase inhibitor for the treatment of cancer. |
| EP3986899A1 (en) | 2019-06-18 | 2022-04-27 | F. Hoffmann-La Roche AG | Pyrazolopyrimidine aryl ether inhibitors of jak kinases and uses thereof |
| AU2020297415A1 (en) * | 2019-06-18 | 2022-01-06 | F. Hoffmann-La Roche Ag | Pyrazolopyrimidine sulfone inhibitors of JAK kinases and uses thereof |
| WO2020257142A1 (en) | 2019-06-18 | 2020-12-24 | Genentech, Inc. | Tetrazole-substituted pyrazolopyrimidine inhibitors of jak kinases and uses thereof |
| US12360120B2 (en) | 2019-10-10 | 2025-07-15 | Incyte Corporation | Biomarkers for graft-versus-host disease |
| EP4041204A1 (en) | 2019-10-10 | 2022-08-17 | Incyte Corporation | Biomarkers for graft-versus-host disease |
| KR20220098759A (en) | 2019-11-08 | 2022-07-12 | 인쎄름 (엥스띠뛰 나씨오날 드 라 쌍떼 에 드 라 흐쉐르슈 메디깔) | A method of treating cancer that has acquired resistance to a kinase inhibitor |
| WO2021148581A1 (en) | 2020-01-22 | 2021-07-29 | Onxeo | Novel dbait molecule and its use |
| CN115003667B (en) * | 2020-02-26 | 2025-04-15 | 百济神州有限公司 | TYK-2 inhibitors |
| BR112022022986A2 (en) | 2020-05-13 | 2023-01-17 | Disc Medicine Inc | ANTI-HEMOJUVELIN (HJV) ANTIBODIES TO TREAT MYELOFIBROSIS |
| US11833155B2 (en) | 2020-06-03 | 2023-12-05 | Incyte Corporation | Combination therapy for treatment of myeloproliferative neoplasms |
| WO2022256358A1 (en) | 2021-06-03 | 2022-12-08 | Genentech, Inc. | Process for preparing medicaments |
| CN115466227B (en) * | 2022-06-30 | 2024-07-19 | 杭州国瑞生物科技有限公司 | Preparation method of 3- (chloromethyl) -1-methyl-1H-1, 2, 4-triazole hydrochloride |
| WO2024262911A1 (en) * | 2023-06-19 | 2024-12-26 | 주식회사 에이조스바이오 | Novel pyrazolo pyrimidine-based compound and use thereof |
Family Cites Families (60)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| ES8401486A1 (en) | 1981-11-10 | 1983-12-01 | Wellcome Found | New imidazo[4,5-c]pyridine derivatives, processes for their preparation and pharmaceutical formulations containing such compounds. |
| US4602035A (en) | 1983-12-07 | 1986-07-22 | Hoechst-Roussel Pharmaceuticals Inc. | Antidepressant (3-aryl-2,3-dihydrobenzofuran-3-yl)alkylamines |
| US4847256A (en) | 1986-10-16 | 1989-07-11 | American Cyanamid Company | 4,5-dihydro and 4,5,6,7-tetrahydropyrazolo(1,5-A)-pyrimidines |
| US5728536A (en) | 1993-07-29 | 1998-03-17 | St. Jude Children's Research Hospital | Jak kinases and regulation of Cytokine signal transduction |
| US6136595A (en) | 1993-07-29 | 2000-10-24 | St. Jude Children's Research Hospital | Jak kinases and regulations of cytokine signal transduction |
| US5543523A (en) | 1994-11-15 | 1996-08-06 | Regents Of The University Of Minnesota | Method and intermediates for the synthesis of korupensamines |
| US5705625A (en) | 1994-12-15 | 1998-01-06 | The Johns Hopkins University School Of Medicine | Nucleic Acid Encoding novel protein tyrosine kinase |
| US7070972B1 (en) | 1995-01-13 | 2006-07-04 | The United States Of America As Represented By The Department Of Health And Human Services | Janus family kinases and identification of immune modulators |
| US7091020B1 (en) | 1995-12-05 | 2006-08-15 | Incyte Corporation | Human Jak2 kinase |
| ID18494A (en) | 1996-10-02 | 1998-04-16 | Novartis Ag | PIRAZOLA DISTRIBUTION IN THE SEQUENCE AND THE PROCESS OF MAKING IT |
| US6235741B1 (en) | 1997-05-30 | 2001-05-22 | Merck & Co., Inc. | Angiogenesis inhibitors |
| FR2791562B1 (en) | 1999-03-29 | 2004-03-05 | Oreal | TINCTORIAL COMPOSITION CONTAINING PYRAZOLO- [1,5-A] - PYRIMIDINE AND A MONOCYCLIC POLYAMINOPYRIMIDINE AS OXIDATION BASES AND A COUPLER, AND DYEING METHODS |
| PT1221444E (en) | 1999-07-02 | 2005-11-30 | Eisai Co Ltd | CONDENSED IMIDAZOLE DERIVATIVES AND MEDICINES FOR DIABETES MELLITUS |
| HU229671B1 (en) | 1999-12-10 | 2014-04-28 | Pfizer Prod Inc | Pyrrolo[2,3-d]pirimidine compounds |
| BR0309475A (en) | 2002-04-23 | 2005-03-01 | Shionogi & Co | Pyrazolo [1,5-a] pyrimidine derivatives and nad (p) h oxidase inhibitors containing them |
| US8580782B2 (en) | 2002-09-04 | 2013-11-12 | Merck Sharp & Dohme Corp. | Substituted pyrazolo[1,5-a]pyrimidines as cyclin dependent kinase inhibitors |
| US7161003B1 (en) | 2002-09-04 | 2007-01-09 | Schering Corporation | Pyrazolopyrimidines as cyclin dependent kinase inhibitors |
| US7129239B2 (en) | 2002-10-28 | 2006-10-31 | Pfizer Inc. | Purine compounds and uses thereof |
| US7199119B2 (en) | 2002-10-31 | 2007-04-03 | Amgen Inc. | Antiinflammation agents |
| US7550470B2 (en) | 2002-12-11 | 2009-06-23 | Merck & Co. Inc. | Substituted pyrazolo[1,5-A]pyrimidines as tyrosine kinase inhibitors |
| WO2004089471A2 (en) | 2003-04-11 | 2004-10-21 | Novo Nordisk A/S | NEW PYRAZOLO[1,5-a] PYRIMIDINES DERIVATIVES AND PHARMACEUTICAL USE THEREOF |
| US20070270408A1 (en) | 2003-04-11 | 2007-11-22 | Novo Nordisk A/S | Pharmaceutical use of substituted pyrazolo[1,5-a]pyrimidines |
| SE0301372D0 (en) * | 2003-05-09 | 2003-05-09 | Astrazeneca Ab | Novel compounds |
| WO2005004810A2 (en) * | 2003-07-02 | 2005-01-20 | Merck & Co., Inc. | Arylsulfonamide derivatives |
| TWI372050B (en) * | 2003-07-03 | 2012-09-11 | Astex Therapeutics Ltd | (morpholin-4-ylmethyl-1h-benzimidazol-2-yl)-1h-pyrazoles |
| GB0329214D0 (en) | 2003-12-17 | 2004-01-21 | Glaxo Group Ltd | Novel compounds |
| AR048454A1 (en) * | 2004-03-30 | 2006-04-26 | Vertex Pharma | USEFUL AZAINDOLS AS INHIBITORS OF JAK PROTEIN KINES OR OTHER KINASE PROTEINS |
| US7306631B2 (en) | 2004-03-30 | 2007-12-11 | The Procter & Gamble Company | Keratin dyeing compounds, keratin dyeing compositions containing them, and use thereof |
| CA2563305A1 (en) | 2004-04-09 | 2005-11-24 | University Of South Florida | Combination therapies for cancer and proliferative angiopathies |
| JP2007535560A (en) | 2004-04-28 | 2007-12-06 | シーブイ・セラピューティクス・インコーポレイテッド | A1 adenosine receptor antagonist |
| AU2005260031B2 (en) | 2004-06-25 | 2008-10-09 | Amgen Inc. | Condensed triazoles and indazoles useful in treating citokines mediated diseases and other diseases |
| CN101094853B (en) | 2004-11-04 | 2011-07-13 | 沃泰克斯药物股份有限公司 | Pyrazolo[1,5-a]pyrimidines useful as protein kinase inhibitors |
| JP2009502734A (en) | 2005-07-29 | 2009-01-29 | アステラス製薬株式会社 | Fused heterocycles as Lck inhibitors |
| WO2007039797A1 (en) | 2005-10-03 | 2007-04-12 | Pfizer Products Inc. | Use of cannabinoid receptor-1 antagonist for treating inflammation and arthritis |
| CA2624500A1 (en) | 2005-10-06 | 2007-04-19 | Schering Corporation | Pyrazolopyrimidines as protein kinase inhibitors |
| TW200745123A (en) * | 2005-10-06 | 2007-12-16 | Schering Corp | Pyrazolopyrimidines as protein kinase inhibitors |
| WO2007048065A2 (en) | 2005-10-21 | 2007-04-26 | Exelixis, Inc. | Pyrimidinones as casein kinase ii (ck2) modulators |
| KR20080074161A (en) | 2005-12-08 | 2008-08-12 | 노파르티스 아게 | Pyrazolo [1,5-a] pyridine-3-carboxylic acid as EPHH and EVFR2 kinase inhibitor |
| US8541406B2 (en) | 2006-02-07 | 2013-09-24 | Nv Remynd | Thiadiazole derivatives for the treatment of neurodegenerative diseases |
| TW200800997A (en) | 2006-03-22 | 2008-01-01 | Astrazeneca Ab | Chemical compounds |
| AU2007235487A1 (en) * | 2006-04-05 | 2007-10-18 | Vertex Pharmaceuticals Incorporated | Deazapurines useful as inhibitors of janus kinases |
| US8796246B2 (en) | 2006-06-02 | 2014-08-05 | Nippon Shinyaku Co., Ltd. | 9, 10-secopregnane derivative and pharmaceutical |
| AR061793A1 (en) | 2006-07-05 | 2008-09-24 | Mitsubishi Tanabe Pharma Corp | PIRAZOLO COMPOUND [1,5-A] PYRIMIDINE AND PHARMACEUTICAL COMPOSITION |
| PE20080403A1 (en) | 2006-07-14 | 2008-04-25 | Amgen Inc | FUSED HETEROCYCLIC DERIVATIVES AND METHODS OF USE |
| JP2010508315A (en) | 2006-10-30 | 2010-03-18 | ノバルティス アーゲー | Heterocyclic compounds as anti-inflammatory agents |
| EP2102211A2 (en) | 2006-11-20 | 2009-09-23 | Alantos Pharmaceuticals Holding, Inc. | Heterobicyclic metalloprotease inhibitors |
| WO2009017954A1 (en) | 2007-08-01 | 2009-02-05 | Phenomix Corporation | Inhibitors of jak2 kinase |
| KR20100090772A (en) * | 2007-10-12 | 2010-08-17 | 인게니움 파르마코이티칼스 게엠베하 | Inhibitors of protein kinases |
| CN104327084B (en) | 2007-11-28 | 2017-06-06 | 达那-法伯癌症研究所 | The small molecule myristate inhibitors and its application method of BCR ABL |
| US8642660B2 (en) * | 2007-12-21 | 2014-02-04 | The University Of Rochester | Method for altering the lifespan of eukaryotic organisms |
| WO2010019762A1 (en) | 2008-08-13 | 2010-02-18 | Jenrin Discovery | Purine compounds as cannabinoid receptor blockers |
| EP2962566A1 (en) * | 2008-10-31 | 2016-01-06 | Genentech, Inc. | Pyrazolopyrimidine jak inhibitor compounds and methods |
| WO2010063487A1 (en) | 2008-12-05 | 2010-06-10 | Merz Pharma Gmbh & Co. Kgaa | Pyrazolopyrimidines, a process for their preparation and their use as medicine |
| UA106360C2 (en) | 2009-02-06 | 2014-08-26 | Янссен Фармасьютікелз, Інк | Substituted bicyclic heterocyclic compounds as gamma secretase modulators |
| TWI461425B (en) | 2009-02-19 | 2014-11-21 | Janssen Pharmaceuticals Inc | Novel substituted benzoxazole, benzimidazole, oxazolopyridine and imidazopyridine derivatives as gamma secretase modulators |
| UA110324C2 (en) | 2009-07-02 | 2015-12-25 | Genentech Inc | Jak inhibitory compounds based on pyrazolo pyrimidine |
| AR077468A1 (en) | 2009-07-09 | 2011-08-31 | Array Biopharma Inc | PIRAZOLO COMPOUNDS (1,5-A) PYRIMIDINE SUBSTITUTED AS TRK-QUINASA INHIBITORS |
| CN102666545B (en) | 2009-10-20 | 2016-04-06 | 塞尔卓姆有限公司 | As the heterocycle Pyrazolopyrimidine analogs of JAK inhibitor |
| EP2547338A2 (en) | 2010-03-17 | 2013-01-23 | F. Hoffmann-La Roche AG | Imidazopyridine compounds, compositions and methods of use |
| MX2012012328A (en) | 2010-04-30 | 2013-05-06 | Cellzome Ltd | Pyrazole compounds as jak inhibitors. |
-
2010
- 2010-02-07 UA UAA201201035A patent/UA110324C2/en unknown
- 2010-07-02 SG SG10201509607XA patent/SG10201509607XA/en unknown
- 2010-07-02 PE PE2012000003A patent/PE20120575A1/en active IP Right Grant
- 2010-07-02 PL PL10794815T patent/PL2448941T3/en unknown
- 2010-07-02 WO PCT/US2010/040906 patent/WO2011003065A2/en active Application Filing
- 2010-07-02 CR CR20170115A patent/CR20170115A/en unknown
- 2010-07-02 US US13/382,145 patent/US8999998B2/en active Active
- 2010-07-02 SI SI201031625T patent/SI2448941T1/en unknown
- 2010-07-02 HR HRP20180157TT patent/HRP20180157T1/en unknown
- 2010-07-02 NZ NZ738778A patent/NZ738778A/en not_active IP Right Cessation
- 2010-07-02 DK DK10794815.0T patent/DK2448941T3/en active
- 2010-07-02 IN IN755DEN2012 patent/IN2012DN00755A/en unknown
- 2010-07-02 NZ NZ706218A patent/NZ706218A/en not_active IP Right Cessation
- 2010-07-02 RS RS20171278A patent/RS56671B1/en unknown
- 2010-07-02 JP JP2012517917A patent/JP5769261B2/en active Active
- 2010-07-02 NZ NZ719972A patent/NZ719972A/en not_active IP Right Cessation
- 2010-07-02 KR KR1020177012984A patent/KR101903305B1/en not_active Expired - Fee Related
- 2010-07-02 KR KR1020127002790A patent/KR101825754B1/en not_active Expired - Fee Related
- 2010-07-02 CN CN201080039041.1A patent/CN102482284B/en active Active
- 2010-07-02 ES ES10794815.0T patent/ES2657839T3/en active Active
- 2010-07-02 SG SG2011097623A patent/SG177454A1/en unknown
- 2010-07-02 AU AU2010266188A patent/AU2010266188B2/en not_active Ceased
- 2010-07-02 NO NO10794815A patent/NO2448941T3/no unknown
- 2010-07-02 RU RU2015133989A patent/RU2675857C2/en not_active IP Right Cessation
- 2010-07-02 PT PT107948150T patent/PT2448941T/en unknown
- 2010-07-02 LT LTEP10794815.0T patent/LT2448941T/en unknown
- 2010-07-02 NZ NZ622283A patent/NZ622283A/en not_active IP Right Cessation
- 2010-07-02 CN CN201510276276.7A patent/CN104910161B/en active Active
- 2010-07-02 EP EP17192475.6A patent/EP3333169B1/en active Active
- 2010-07-02 MX MX2012000169A patent/MX2012000169A/en active IP Right Grant
- 2010-07-02 EP EP19211640.8A patent/EP3670514A1/en not_active Withdrawn
- 2010-07-02 EP EP10794815.0A patent/EP2448941B1/en active Active
- 2010-07-02 CA CA2767097A patent/CA2767097A1/en not_active Abandoned
- 2010-07-02 PE PE2015000692A patent/PE20151249A1/en not_active Application Discontinuation
- 2010-07-02 MY MYPI2011006384A patent/MY160156A/en unknown
- 2010-07-02 MA MA34594A patent/MA33502B1/en unknown
- 2010-07-02 HU HUE10794815A patent/HUE035537T2/en unknown
- 2010-07-02 RU RU2012103487/04A patent/RU2567238C2/en not_active IP Right Cessation
- 2010-07-02 KR KR1020187027109A patent/KR20180108858A/en not_active Ceased
- 2010-07-02 BR BRPI1010197A patent/BRPI1010197A2/en not_active Application Discontinuation
-
2011
- 2011-12-27 IL IL217224A patent/IL217224B/en not_active IP Right Cessation
-
2012
- 2012-01-02 CL CL2012000001A patent/CL2012000001A1/en unknown
- 2012-01-20 ZA ZA2012/00490A patent/ZA201200490B/en unknown
- 2012-01-25 CO CO12011326A patent/CO6491081A2/en active IP Right Grant
- 2012-01-30 CR CR20120053A patent/CR20120053A/en unknown
- 2012-02-02 EC ECSP12011645 patent/ECSP12011645A/en unknown
-
2013
- 2013-10-02 ZA ZA2013/07356A patent/ZA201307356B/en unknown
-
2015
- 2015-02-06 US US14/615,873 patent/US20150152117A1/en not_active Abandoned
- 2015-03-25 PH PH12015500666A patent/PH12015500666A1/en unknown
- 2015-06-17 JP JP2015122441A patent/JP6312634B2/en active Active
- 2015-12-09 IL IL242999A patent/IL242999B/en not_active IP Right Cessation
-
2017
- 2017-06-20 US US15/627,847 patent/US20170283424A1/en not_active Abandoned
-
2018
- 2018-01-04 JP JP2018000305A patent/JP2018083828A/en not_active Withdrawn
- 2018-01-15 IL IL256921A patent/IL256921A/en unknown
-
2019
- 2019-06-07 JP JP2019106948A patent/JP2019194199A/en active Pending
- 2019-09-05 US US16/561,432 patent/US20200002345A1/en not_active Abandoned
-
2022
- 2022-01-14 US US17/648,045 patent/US20220389020A1/en not_active Abandoned
-
2023
- 2023-11-13 US US18/507,678 patent/US20240150364A1/en active Pending
Also Published As
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| IN2012DN00755A (en) | ||
| EP2288260A4 (en) | Triazolopyridine jak inhibitor compounds and methods | |
| MX336271B (en) | Triazolopyridine jak inhibitor compounds and methods. | |
| WO2017089390A8 (en) | Janus kinases inhibitors, compositions thereof and use thereof | |
| CR20200286A (en) | Dihydro-benzo-oxazine and dihydro-pyrido-oxazine derivatives | |
| ATE456565T1 (en) | PYRIDINE AND PYRAZINE DERIVATIVES AS MNK KINASE INHIBITORS | |
| MX2010009207A (en) | Heterocyclic compounds and compositions as c-kit and pdgfr kinase inhibitors. | |
| MX350761B (en) | Isoindolinone inhibitors of phosphatidylinositol 3-kinase. | |
| PH12012500903A1 (en) | N1 - pyrazolospiroketone acetyl-coa carboxylase inhibitors | |
| MA32272B1 (en) | Inhibitors of pyrazole [3,4-b] pyridine raf | |
| AU2012258977A8 (en) | Inhibitors of LRRK2 kinase activity | |
| IN2012DN01641A (en) | ||
| MX2009011950A (en) | Pyrimidine derivatives and compositions as c-kit and pdgfr kinase inhibitors. | |
| WO2011052923A3 (en) | Novel 1,6-disubstituted indole compounds as protein kinase inhibitors | |
| PH12012501693A1 (en) | 4 - [cycloalkyloxy (hetero) arylamino] thieno [2,3 - d] pyrimidines having mnkl/mnk2 inhibiting activity for pharmaceutical compositions | |
| NO20091590L (en) | Heterocyclic amide compounds useful as kinase inhibitors | |
| MY147188A (en) | Substituted imidazole compounds as ksp inhibitors | |
| PH12019502601A1 (en) | Therapeutic compounds and compositions, and methods of use thereof | |
| MY151835A (en) | Kinase inhibitors and methods of use thereof | |
| WO2009094560A3 (en) | Thienopyranones as kinase inhibitors | |
| IN2012DN01642A (en) | ||
| MX2009011059A (en) | Aminopyrimidines useful as kinase inhibitors. | |
| MX2013008161A (en) | Solid forms of gyrase inhibitor (r)-1-ethyl-3-[6-fluoro-5-[2-(1-h ydroxy-1-methyl-ethyl) pyrimidin-5-yl]-7-(tetrahydrofuran-2-yl)-1 h-benzimidazol-2-yl]urea. | |
| PL1753723T3 (en) | Substituted quinoline derivatives as mitotic kinesin inhibitors | |
| MX2013008163A (en) | Solid forms of gyrase inhibitor (r)-1-ethyl-3-[5-[2-{1-hydroxy-1- methyl-ethyl}pyrimidin-5-yl]-7-(tetrahydrofuran-2-yl}-1h-benzimi dazol-2-yl]urea. |