CL2016002877A1 - Compuestos de 2-cloro-2-difluorometoxifenil pirazolopirimidina, composiciones y métodos de uso de los mismos. - Google Patents
Compuestos de 2-cloro-2-difluorometoxifenil pirazolopirimidina, composiciones y métodos de uso de los mismos.Info
- Publication number
- CL2016002877A1 CL2016002877A1 CL2016002877A CL2016002877A CL2016002877A1 CL 2016002877 A1 CL2016002877 A1 CL 2016002877A1 CL 2016002877 A CL2016002877 A CL 2016002877A CL 2016002877 A CL2016002877 A CL 2016002877A CL 2016002877 A1 CL2016002877 A1 CL 2016002877A1
- Authority
- CL
- Chile
- Prior art keywords
- compounds
- chloro
- compositions
- methods
- difluoromethoxyphenyl pyrazolopyrimidine
- Prior art date
Links
- 150000001875 compounds Chemical class 0.000 title abstract 2
- OOIDKCUQCLTMNJ-UHFFFAOYSA-N FC(OC1(C=CC=CC1C1=NNC2=C1N=CN=C2)Cl)F Chemical compound FC(OC1(C=CC=CC1C1=NNC2=C1N=CN=C2)Cl)F OOIDKCUQCLTMNJ-UHFFFAOYSA-N 0.000 title 1
- 239000000203 mixture Substances 0.000 title 1
- 208000006673 asthma Diseases 0.000 abstract 1
- 208000027866 inflammatory disease Diseases 0.000 abstract 1
- 239000008194 pharmaceutical composition Substances 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/04—Ortho-condensed systems
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- 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
- A61P11/00—Drugs for disorders of the respiratory system
- A61P11/06—Antiasthmatics
-
- 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
- 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
- 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
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Medicinal Chemistry (AREA)
- Pulmonology (AREA)
- Epidemiology (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
Abstract
<p>COMPUESTOS DERIVADOS DE 2-CLORO-2-DIFLUOROMETOXIFENIL PIRAZOLOPIRIMIDINA; COMPOSICION FARMACEUTICA QUE LOS COMPRENDE; Y SU USO PARA EL TRATAMIENTO DE UNA ENFERMEDAD INFLAMATORIA TAL COMO ASMA.</p>
Applications Claiming Priority (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201462002547P | 2014-05-23 | 2014-05-23 | |
| US201562101234P | 2015-01-08 | 2015-01-08 | |
| US201562130098P | 2015-03-09 | 2015-03-09 | |
| CNPCT/CN2015/077176 | 2015-04-22 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CL2016002877A1 true CL2016002877A1 (es) | 2017-06-09 |
Family
ID=53276096
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CL2016002877A CL2016002877A1 (es) | 2014-05-23 | 2016-11-11 | Compuestos de 2-cloro-2-difluorometoxifenil pirazolopirimidina, composiciones y métodos de uso de los mismos. |
Country Status (20)
| Country | Link |
|---|---|
| US (5) | US9346815B2 (es) |
| EP (1) | EP3145929B1 (es) |
| JP (2) | JP2017516850A (es) |
| KR (1) | KR20170005870A (es) |
| CN (2) | CN109970743B (es) |
| AU (3) | AU2015261812B2 (es) |
| CA (1) | CA2948589A1 (es) |
| CL (1) | CL2016002877A1 (es) |
| EA (1) | EA032488B1 (es) |
| HR (1) | HRP20210935T1 (es) |
| HU (1) | HUE054784T2 (es) |
| IL (2) | IL248661B (es) |
| MX (1) | MX2016015062A (es) |
| PE (2) | PE20170663A1 (es) |
| PH (1) | PH12016502099A1 (es) |
| SG (1) | SG11201609830RA (es) |
| SI (1) | SI3145929T1 (es) |
| TW (1) | TWI699364B (es) |
| UA (1) | UA121658C2 (es) |
| WO (1) | WO2015177326A1 (es) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US11155557B2 (en) | 2016-12-29 | 2021-10-26 | Genentech, Inc. | Pyrazolopyrimidine compounds and methods of use thereof |
Families Citing this family (23)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| MX2016015062A (es) * | 2014-05-23 | 2017-02-27 | Hoffmann La Roche | Compuestos de 5-cloro-2-difluorometoxifenil pirazolopirimidina los cuales son inhibidores de janus cinasas (jak). |
| EP3200589A4 (en) | 2014-09-10 | 2018-07-25 | Temple University Of The Commonwealth System Of Higher Education | Novel 5-hydroxytryptamine receptor 7 activity modulators and their method of use |
| GB201506872D0 (en) | 2015-04-22 | 2015-06-03 | Ge Oil & Gas Uk Ltd | Novel compounds |
| WO2016183150A1 (en) * | 2015-05-12 | 2016-11-17 | Temple University-Of The Commonwealth System Of Higher Education | Novel sigma-2 receptor binders and their method of use |
| TW201720828A (zh) * | 2015-11-23 | 2017-06-16 | 赫孚孟拉羅股份公司 | 治療性化合物及組合物以及其使用方法 |
| EP3390402B1 (en) * | 2015-12-18 | 2020-01-15 | H. Hoffnabb-La Roche Ag | Therapeutic compounds, compositions and methods of use thereof |
| CN108473501B (zh) * | 2016-02-18 | 2021-07-16 | 豪夫迈·罗氏有限公司 | 治疗化合物、其组合物及使用方法 |
| EP3596072B1 (en) | 2017-03-14 | 2022-06-22 | F. Hoffmann-La Roche AG | Pyrazolochlorophenyl compounds, compositions and methods of use thereof |
| TW201900648A (zh) | 2017-05-22 | 2019-01-01 | 瑞士商赫孚孟拉羅股份公司 | 治療性化合物及組成物以及其使用方法 |
| RU2769696C2 (ru) | 2017-05-22 | 2022-04-05 | Ф. Хоффманн-Ля Рош Аг | Терапевтические соединения и композиции и способы их применения |
| AU2018351651B2 (en) | 2017-10-20 | 2023-01-05 | Vanderbilt University | Antagonists of the muscarinic acetylcholine receptor M4 |
| CA3081324A1 (en) | 2017-10-31 | 2019-05-09 | Vanderbilt University | Antagonists of the muscarinic acetylcholine receptor m4 |
| JP7339263B2 (ja) * | 2018-01-15 | 2023-09-05 | エフ. ホフマン-ラ ロシュ アーゲー | Jak阻害剤としてのピラゾロピリミジン化合物 |
| AU2019216492A1 (en) * | 2018-02-02 | 2020-08-20 | Vanderbilt University | Antagonists of the muscarinic acetylcholine receptor M4 |
| KR20200141041A (ko) * | 2018-03-28 | 2020-12-17 | 포천 파마슈티컬즈, 엘티디. | Trk 키나제 억제제로서의 마크로사이클릭 화합물 |
| US11034669B2 (en) | 2018-11-30 | 2021-06-15 | Nuvation Bio Inc. | Pyrrole and pyrazole compounds and methods of use thereof |
| EP3939954B1 (en) | 2019-03-13 | 2025-07-23 | Otsuka Pharmaceutical Co., Ltd. | Method for introducing deuterated lower alkyl into amine moiety of compound containing secondary amine |
| CN114008050B (zh) * | 2019-06-18 | 2024-12-31 | 豪夫迈·罗氏有限公司 | Jak激酶的吡唑并嘧啶芳基醚抑制剂及其用途 |
| TW202115068A (zh) | 2019-06-18 | 2021-04-16 | 瑞士商赫孚孟拉羅股份公司 | Jak激酶之吡唑并嘧啶碸抑制劑及其用途 |
| EP3986900A1 (en) | 2019-06-18 | 2022-04-27 | F. Hoffmann-La Roche AG | Tetrazole-substituted pyrazolopyrimidine inhibitors of jak kinases and uses thereof |
| WO2022059779A1 (ja) | 2020-09-18 | 2022-03-24 | 大日本住友製薬株式会社 | アミン誘導体 |
| EP4347568A1 (en) * | 2021-05-27 | 2024-04-10 | Protego Biopharma, Inc. | Heteroaryl diamide ire1/xbp1s activators |
| WO2022256358A1 (en) | 2021-06-03 | 2022-12-08 | Genentech, Inc. | Process for preparing medicaments |
Family Cites Families (67)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| ES517193A0 (es) | 1981-11-10 | 1983-12-01 | Wellcome Found | Un procedimiento para la preparacion de nuevos derivados de imidazo (4,5-c)piridina. |
| 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 |
| 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 (id) | 1996-10-02 | 1998-04-16 | Novartis Ag | Turunan pirazola leburan dan proses pembuatannya |
| US6235741B1 (en) | 1997-05-30 | 2001-05-22 | Merck & Co., Inc. | Angiogenesis inhibitors |
| FR2791562B1 (fr) | 1999-03-29 | 2004-03-05 | Oreal | Composition tinctoriale contenant une pyrazolo-[1,5-a]- pyrimidine et une polyaminopyrimidine monocyclique a titre de bases d'oxydation et un coupleur, et procedes de teinture |
| JP4324338B2 (ja) | 1999-07-02 | 2009-09-02 | エーザイ・アール・アンド・ディー・マネジメント株式会社 | 縮合イミダゾール化合物及び糖尿病治療薬 |
| RS51574B (sr) | 1999-12-10 | 2011-08-31 | Pfizer Products Inc. | JEDINJENJA PIROLO (2,3-d) PIRIMIDINA |
| JP4500055B2 (ja) | 2002-04-23 | 2010-07-14 | 塩野義製薬株式会社 | ピラゾロ[1,5−a]ピリミジン誘導体およびそれを含有するNAD(P)Hオキシダーゼ阻害剤 |
| US7161003B1 (en) | 2002-09-04 | 2007-01-09 | Schering Corporation | Pyrazolopyrimidines as cyclin dependent kinase inhibitors |
| US8580782B2 (en) | 2002-09-04 | 2013-11-12 | Merck Sharp & Dohme Corp. | Substituted pyrazolo[1,5-a]pyrimidines as cyclin dependent kinase inhibitors |
| US7129239B2 (en) | 2002-10-28 | 2006-10-31 | Pfizer Inc. | Purine compounds and uses thereof |
| WO2004041285A1 (en) | 2002-10-31 | 2004-05-21 | Amgen Inc. | Antiinflammation agents |
| WO2004052315A2 (en) | 2002-12-11 | 2004-06-24 | Merck & Co., Inc. | Tyrosine kinase inhibitors |
| US20070270408A1 (en) | 2003-04-11 | 2007-11-22 | Novo Nordisk A/S | Pharmaceutical use of substituted pyrazolo[1,5-a]pyrimidines |
| JP2006522750A (ja) | 2003-04-11 | 2006-10-05 | ノボ ノルディスク アクティーゼルスカブ | 代謝性症候群ならびに関連の疾患および障害を治療するために、11β−ヒドロキシステロイドデヒドロゲナーゼ1型阻害剤および抗高血圧剤を使用する併用療法 |
| EP1615697A2 (en) | 2003-04-11 | 2006-01-18 | Novo Nordisk A/S | New pyrazolo[1,5-a] pyrimidine derivatives and pharmaceutical use thereof |
| JP2006522744A (ja) | 2003-04-11 | 2006-10-05 | ノボ ノルディスク アクティーゼルスカブ | グルココルチコイド受容体アゴニスト療法に伴う副作用を最小化するための、11β−ヒドロキシステロイドデヒドロゲナーゼ1型阻害剤およびグルココルチコイド受容体アゴニストを使用する併用療法 |
| EP1643960A2 (en) | 2003-07-02 | 2006-04-12 | 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 |
| US7306631B2 (en) | 2004-03-30 | 2007-12-11 | The Procter & Gamble Company | Keratin dyeing compounds, keratin dyeing compositions containing them, and use thereof |
| EP1748772A2 (en) | 2004-04-09 | 2007-02-07 | University Of South Florida | Combination therapies for cancer and proliferative angiopathies |
| EP1751159A2 (en) | 2004-04-28 | 2007-02-14 | Cv Therapeutics, Inc. | Purine derivatives as a1 adenosine receptor antagonists |
| US20050288502A1 (en) | 2004-06-25 | 2005-12-29 | Andersen Denise L | Substituted heterocyclic compounds and methods of use |
| US7528138B2 (en) | 2004-11-04 | 2009-05-05 | Vertex Pharmaceuticals Incorporated | Pyrazolo[1,5-a]pyrimidines useful as inhibitors of protein kinases |
| JP2009502734A (ja) | 2005-07-29 | 2009-01-29 | アステラス製薬株式会社 | Lck阻害剤としての縮合複素環 |
| WO2007039797A1 (en) | 2005-10-03 | 2007-04-12 | Pfizer Products Inc. | Use of cannabinoid receptor-1 antagonist for treating inflammation and arthritis |
| JP5102212B2 (ja) | 2005-10-06 | 2012-12-19 | メルク・シャープ・アンド・ドーム・コーポレーション | プロテインキナーゼインヒビターとしてのピラゾロピリミジン |
| AU2006304875B2 (en) | 2005-10-21 | 2013-01-17 | Exelixis, Inc. | Pyrazolo-pyrimidines as casein kinase II (CK2) modulators |
| JP2009518340A (ja) | 2005-12-08 | 2009-05-07 | ノバルティス アクチエンゲゼルシャフト | EphBおよびVEGFR2キナーゼ阻害剤としてのピラゾロ[1,5−a]ピリジン−3−カルボン酸 |
| 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 |
| AR061793A1 (es) | 2006-07-05 | 2008-09-24 | Mitsubishi Tanabe Pharma Corp | Compuesto de pirazolo[1,5-a] pirimidina y composicion farmaceutica |
| US8217177B2 (en) | 2006-07-14 | 2012-07-10 | Amgen Inc. | Fused heterocyclic derivatives and methods of use |
| PE20080403A1 (es) | 2006-07-14 | 2008-04-25 | Amgen Inc | Derivados heterociclicos fusionados y metodos de uso |
| CN101522682A (zh) | 2006-10-30 | 2009-09-02 | 诺瓦提斯公司 | 作为抗炎剂的杂环化合物 |
| AU2007321924A1 (en) | 2006-11-20 | 2008-05-29 | Alantos Pharmaceuticals Holding, Inc. | Heterobicyclic metalloprotease inhibitors |
| WO2009017954A1 (en) | 2007-08-01 | 2009-02-05 | Phenomix Corporation | Inhibitors of jak2 kinase |
| SI2212297T1 (sl) | 2007-10-12 | 2011-09-30 | Ingenium Pharmaceuticals Gmbh | Inhibitorji protein kinaz |
| KR20100130583A (ko) | 2007-11-28 | 2010-12-13 | 다나-파버 캔서 인스티튜트 인크. | Bcr-abl의 소 분자 미리스테이트 억제제 및 이의 사용 방법 |
| US8642660B2 (en) | 2007-12-21 | 2014-02-04 | The University Of Rochester | Method for altering the lifespan of eukaryotic organisms |
| WO2009106443A1 (en) * | 2008-02-25 | 2009-09-03 | F. Hoffmann-La Roche Ag | Pyrrolopyrazine kinase inhibitors |
| WO2010001184A1 (en) | 2008-07-02 | 2010-01-07 | Novatech D.O.O. | Formulation based on micronized natural calcite mineral and micronized zeolite as an enhanced plant booster and mineral fertilizer |
| US8252791B2 (en) | 2008-08-13 | 2012-08-28 | Jenrin Discovery, Inc. | Purine compounds as cannabinoid receptor blockers |
| AU2009308675A1 (en) * | 2008-10-31 | 2010-05-06 | 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 |
| AU2010211109B2 (en) | 2009-02-06 | 2014-11-27 | Cellzome Limited | Novel substituted bicyclic heterocyclic compounds as gamma secretase modulators |
| TWI461425B (zh) | 2009-02-19 | 2014-11-21 | Janssen Pharmaceuticals Inc | 作為伽瑪分泌酶調節劑之新穎經取代的苯并唑、苯并咪唑、唑并吡啶及咪唑并吡啶衍生物類 |
| UA110324C2 (en) * | 2009-07-02 | 2015-12-25 | Genentech Inc | Jak inhibitory compounds based on pyrazolo pyrimidine |
| AR077468A1 (es) | 2009-07-09 | 2011-08-31 | Array Biopharma Inc | Compuestos de pirazolo (1,5 -a) pirimidina sustituidos como inhibidores de trk- quinasa |
| WO2011048082A1 (en) | 2009-10-20 | 2011-04-28 | Cellzome Limited | Heterocyclyl pyrazolopyrimidine analogues as jak inhibitors |
| CA2793024A1 (en) | 2010-03-17 | 2011-09-22 | F. Hoffmann-La Roche Ag | Imidazopyridine compounds, compositions and methods of use |
| CN103180322A (zh) | 2010-04-30 | 2013-06-26 | 塞尔佐姆有限公司 | 作为jak抑制剂的吡唑化合物 |
| MX358682B (es) | 2010-07-13 | 2018-08-31 | Hoffmann La Roche | Derivados de pirazolo [1,5a]pirimidina y de tieno[3,2b] pirimidina como moduladores de la cinasa asociada al receptor de la interleucina 4 (irak4). |
| WO2012075393A2 (en) | 2010-12-02 | 2012-06-07 | President And Fellows Of Harvard College | Activators of proteasomal degradation and uses thereof |
| EP2688872A4 (en) * | 2011-03-22 | 2014-08-27 | Merck Sharp & Dohme | AMIDOPYRAZOLHEMMER OF INTERLEUKIN RECEPTOR-MEDIATED KINASES |
| WO2015073267A1 (en) | 2013-11-15 | 2015-05-21 | Calitor Sciences, Llc | Substituted heteroaryl compounds and methods of use |
| MX2016015062A (es) | 2014-05-23 | 2017-02-27 | Hoffmann La Roche | Compuestos de 5-cloro-2-difluorometoxifenil pirazolopirimidina los cuales son inhibidores de janus cinasas (jak). |
| WO2016144846A1 (en) | 2015-03-12 | 2016-09-15 | Merck Sharp & Dohme Corp. | Pyrazolopyrimidine inhibitors of irak4 activity |
| WO2016144844A1 (en) | 2015-03-12 | 2016-09-15 | Merck Sharp & Dohme Corp. | Carboxamide inhibitors of irak4 activity |
| WO2016144848A1 (en) | 2015-03-12 | 2016-09-15 | Merck Sharp & Dohme Corp. | Pyrrolotriazine inhibitors of irak4 activity |
| WO2016144847A1 (en) | 2015-03-12 | 2016-09-15 | Merck Sharp & Dohme Corp. | Pyrrolopyridazine inhibitors of irak4 activity |
-
2015
- 2015-05-22 MX MX2016015062A patent/MX2016015062A/es unknown
- 2015-05-22 PE PE2016002240A patent/PE20170663A1/es unknown
- 2015-05-22 WO PCT/EP2015/061350 patent/WO2015177326A1/en not_active Ceased
- 2015-05-22 TW TW104116569A patent/TWI699364B/zh active
- 2015-05-22 PE PE2021000895A patent/PE20211782A1/es unknown
- 2015-05-22 JP JP2017513346A patent/JP2017516850A/ja not_active Withdrawn
- 2015-05-22 UA UAA201613029A patent/UA121658C2/uk unknown
- 2015-05-22 KR KR1020167036075A patent/KR20170005870A/ko not_active Ceased
- 2015-05-22 EA EA201692338A patent/EA032488B1/ru not_active IP Right Cessation
- 2015-05-22 AU AU2015261812A patent/AU2015261812B2/en active Active
- 2015-05-22 HU HUE15726064A patent/HUE054784T2/hu unknown
- 2015-05-22 CN CN201910249668.2A patent/CN109970743B/zh active Active
- 2015-05-22 SG SG11201609830RA patent/SG11201609830RA/en unknown
- 2015-05-22 HR HRP20210935TT patent/HRP20210935T1/hr unknown
- 2015-05-22 SI SI201531621T patent/SI3145929T1/sl unknown
- 2015-05-22 CA CA2948589A patent/CA2948589A1/en active Granted
- 2015-05-22 US US14/720,323 patent/US9346815B2/en active Active
- 2015-05-22 EP EP15726064.7A patent/EP3145929B1/en active Active
- 2015-05-22 CN CN201580026680.7A patent/CN106459039A/zh active Pending
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2016
- 2016-04-26 US US15/139,164 patent/US9604984B2/en active Active
- 2016-10-20 PH PH12016502099A patent/PH12016502099A1/en unknown
- 2016-10-31 IL IL24866116A patent/IL248661B/en active IP Right Grant
- 2016-11-11 CL CL2016002877A patent/CL2016002877A1/es unknown
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2017
- 2017-02-03 US US15/424,536 patent/US20170145020A1/en not_active Abandoned
- 2017-11-22 US US15/820,515 patent/US20180305355A1/en not_active Abandoned
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2019
- 2019-06-11 US US16/438,135 patent/US20190322661A1/en not_active Abandoned
- 2019-08-01 IL IL268446A patent/IL268446A/en unknown
- 2019-10-30 AU AU2019257450A patent/AU2019257450A1/en not_active Abandoned
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2020
- 2020-06-24 JP JP2020108861A patent/JP7041198B2/ja active Active
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2021
- 2021-06-07 AU AU2021203734A patent/AU2021203734A1/en not_active Abandoned
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US11155557B2 (en) | 2016-12-29 | 2021-10-26 | Genentech, Inc. | Pyrazolopyrimidine compounds and methods of use thereof |
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