JP2017160233A5 - - Google Patents
Download PDFInfo
- Publication number
- JP2017160233A5 JP2017160233A5 JP2017088732A JP2017088732A JP2017160233A5 JP 2017160233 A5 JP2017160233 A5 JP 2017160233A5 JP 2017088732 A JP2017088732 A JP 2017088732A JP 2017088732 A JP2017088732 A JP 2017088732A JP 2017160233 A5 JP2017160233 A5 JP 2017160233A5
- Authority
- JP
- Japan
- Prior art keywords
- alkyl
- alkoxy
- group
- pharmaceutical composition
- change
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Pending
Links
- 238000000034 method Methods 0.000 claims description 5
- 125000000217 alkyl group Chemical group 0.000 claims 32
- 125000003545 alkoxy group Chemical group 0.000 claims 16
- 208000006990 cholangiocarcinoma Diseases 0.000 claims 14
- 239000008194 pharmaceutical composition Substances 0.000 claims 13
- 102100031734 Fibroblast growth factor 19 Human genes 0.000 claims 10
- 102100027844 Fibroblast growth factor receptor 4 Human genes 0.000 claims 10
- 101000846394 Homo sapiens Fibroblast growth factor 19 Proteins 0.000 claims 10
- 101000917134 Homo sapiens Fibroblast growth factor receptor 4 Proteins 0.000 claims 10
- 229910052739 hydrogen Inorganic materials 0.000 claims 10
- 239000001257 hydrogen Substances 0.000 claims 10
- 150000003839 salts Chemical class 0.000 claims 10
- 206010004593 Bile duct cancer Diseases 0.000 claims 9
- 208000026900 bile duct neoplasm Diseases 0.000 claims 9
- 150000002431 hydrogen Chemical class 0.000 claims 6
- 125000004356 hydroxy functional group Chemical group O* 0.000 claims 6
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 4
- 150000001875 compounds Chemical class 0.000 claims 4
- 125000005843 halogen group Chemical group 0.000 claims 4
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 4
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 4
- 125000004390 alkyl sulfonyl group Chemical group 0.000 claims 2
- 239000012472 biological sample Substances 0.000 claims 2
- 125000001309 chloro group Chemical group Cl* 0.000 claims 2
- 125000001153 fluoro group Chemical group F* 0.000 claims 2
- 125000000623 heterocyclic group Chemical group 0.000 claims 2
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims 2
- 239000003814 drug Substances 0.000 claims 1
- 238000004519 manufacturing process Methods 0.000 claims 1
- MBWRLLRCTIYXDW-UHFFFAOYSA-N N-[2-[[6-[(2,6-dichloro-3,5-dimethoxyphenyl)carbamoyl-methylamino]pyrimidin-4-yl]amino]-5-(4-ethylpiperazin-1-yl)phenyl]prop-2-enamide Chemical compound ClC1=C(C(=C(C=C1OC)OC)Cl)NC(N(C)C1=CC(=NC=N1)NC1=C(C=C(C=C1)N1CCN(CC1)CC)NC(C=C)=O)=O MBWRLLRCTIYXDW-UHFFFAOYSA-N 0.000 description 1
- XGVXKJKTISMIOW-ZDUSSCGKSA-N simurosertib Chemical compound N1N=CC(C=2SC=3C(=O)NC(=NC=3C=2)[C@H]2N3CCC(CC3)C2)=C1C XGVXKJKTISMIOW-ZDUSSCGKSA-N 0.000 description 1
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201361892881P | 2013-10-18 | 2013-10-18 | |
| US61/892,881 | 2013-10-18 |
Related Parent Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2016523266A Division JP6139788B2 (ja) | 2013-10-18 | 2014-10-16 | ピリミジンｆｇｆｒ４阻害剤 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2017160233A JP2017160233A (ja) | 2017-09-14 |
| JP2017160233A5 true JP2017160233A5 (OSRAM) | 2017-11-16 |
Family
ID=51842899
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2016523266A Active JP6139788B2 (ja) | 2013-10-18 | 2014-10-16 | ピリミジンｆｇｆｒ４阻害剤 |
| JP2017088732A Pending JP2017160233A (ja) | 2013-10-18 | 2017-04-27 | ピリミジンｆｇｆｒ４阻害剤 |
Family Applications Before (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2016523266A Active JP6139788B2 (ja) | 2013-10-18 | 2014-10-16 | ピリミジンｆｇｆｒ４阻害剤 |
Country Status (33)
| Country | Link |
|---|---|
| US (4) | US9434697B2 (OSRAM) |
| EP (2) | EP3057943B1 (OSRAM) |
| JP (2) | JP6139788B2 (OSRAM) |
| KR (1) | KR101826015B1 (OSRAM) |
| CN (2) | CN110354128A (OSRAM) |
| AR (1) | AR098048A1 (OSRAM) |
| AU (2) | AU2014337291B9 (OSRAM) |
| BR (1) | BR112016008110B1 (OSRAM) |
| CA (1) | CA2924206C (OSRAM) |
| CL (1) | CL2016000918A1 (OSRAM) |
| CY (1) | CY1121129T1 (OSRAM) |
| DK (1) | DK3057943T3 (OSRAM) |
| ES (1) | ES2679521T3 (OSRAM) |
| HR (1) | HRP20181129T1 (OSRAM) |
| HU (1) | HUE039268T2 (OSRAM) |
| IL (1) | IL244373B (OSRAM) |
| JO (1) | JO3515B1 (OSRAM) |
| LT (1) | LT3057943T (OSRAM) |
| MX (1) | MX378288B (OSRAM) |
| MY (1) | MY184733A (OSRAM) |
| NZ (1) | NZ717559A (OSRAM) |
| PE (1) | PE20160679A1 (OSRAM) |
| PH (1) | PH12016500676B1 (OSRAM) |
| PL (1) | PL3057943T3 (OSRAM) |
| PT (1) | PT3057943T (OSRAM) |
| RS (1) | RS57444B1 (OSRAM) |
| RU (1) | RU2715708C2 (OSRAM) |
| SG (1) | SG11201602069WA (OSRAM) |
| SI (1) | SI3057943T1 (OSRAM) |
| SM (1) | SMT201800379T1 (OSRAM) |
| TW (1) | TWI597268B (OSRAM) |
| UA (1) | UA116920C2 (OSRAM) |
| WO (2) | WO2015057963A1 (OSRAM) |
Families Citing this family (73)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US8754114B2 (en) | 2010-12-22 | 2014-06-17 | Incyte Corporation | Substituted imidazopyridazines and benzimidazoles as inhibitors of FGFR3 |
| PE20190736A1 (es) | 2012-06-13 | 2019-05-23 | Incyte Holdings Corp | Compuestos triciclicos sustituidos como inhibidores del receptor del factor de crecimiento de fibroblastos (fgfr) |
| US8802697B2 (en) | 2012-07-11 | 2014-08-12 | Blueprint Medicines Corporation | Inhibitors of the fibroblast growth factor receptor |
| WO2014026125A1 (en) | 2012-08-10 | 2014-02-13 | Incyte Corporation | Pyrazine derivatives as fgfr inhibitors |
| TWI647220B (zh) | 2013-03-15 | 2019-01-11 | 美商西建卡爾有限責任公司 | 雜芳基化合物及其用途 |
| ES2892423T3 (es) | 2013-03-15 | 2022-02-04 | Celgene Car Llc | Compuestos de heteroarilo y usos de los mismos |
| AU2014228746B2 (en) | 2013-03-15 | 2018-08-30 | Celgene Car Llc | Heteroaryl compounds and uses thereof |
| KR102269032B1 (ko) | 2013-04-19 | 2021-06-24 | 인사이트 홀딩스 코포레이션 | Fgfr 저해제로서 이환식 헤테로사이클 |
| CN110354128A (zh) | 2013-10-18 | 2019-10-22 | 卫材R&D管理有限公司 | 嘧啶fgfr4抑制剂 |
| AU2014339972B9 (en) | 2013-10-25 | 2019-05-30 | Blueprint Medicines Corporation | Inhibitors of the fibroblast growth factor receptor |
| MX367723B (es) | 2013-10-25 | 2019-09-03 | Novartis Ag | Compuestos de anillos fusionados bicíclicos derivados de piridilo como inhibidores de fgfr4. |
| WO2015108992A1 (en) | 2014-01-15 | 2015-07-23 | Blueprint Medicines Corporation | Heterobicyclic compounds and their use as fgfr4 receptor inhibitors |
| EP3200786B1 (en) | 2014-10-03 | 2019-08-28 | Novartis AG | Use of ring-fused bicyclic pyridyl derivatives as fgfr4 inhibitors |
| US10851105B2 (en) | 2014-10-22 | 2020-12-01 | Incyte Corporation | Bicyclic heterocycles as FGFR4 inhibitors |
| ES2895769T3 (es) | 2015-02-20 | 2022-02-22 | Incyte Corp | Heterociclos bicíclicos como inhibidores de FGFR |
| MA41551A (fr) | 2015-02-20 | 2017-12-26 | Incyte Corp | Hétérocycles bicycliques utilisés en tant qu'inhibiteurs de fgfr4 |
| US9580423B2 (en) | 2015-02-20 | 2017-02-28 | Incyte Corporation | Bicyclic heterocycles as FGFR4 inhibitors |
| US9802917B2 (en) | 2015-03-25 | 2017-10-31 | Novartis Ag | Particles of N-(5-cyano-4-((2-methoxyethyl)amino)pyridin-2-yl)-7-formyl-6-((4-methyl-2-oxopiperazin-1-yl)methyl)-3,4-dihydro-1,8-naphthyridine-1(2H)-carboxamide |
| WO2016164703A1 (en) * | 2015-04-09 | 2016-10-13 | Eisai R & D Management Co., Ltd. | Fgfr4 inhibitors |
| CA2982562C (en) * | 2015-04-14 | 2023-06-13 | Eisai R&D Management Co., Ltd. | Crystalline fgfr4 inhibitor compound and uses thereof |
| US10624897B2 (en) | 2015-07-20 | 2020-04-21 | Taipei Medical University | Chlorobenzene substituted azaaryl compounds |
| US10550112B2 (en) | 2015-07-20 | 2020-02-04 | Dana-Farber Cancer Institute, Inc. | Pyrimidines as EGFR inhibitors and methods of treating disorders |
| CN105418441A (zh) * | 2015-12-22 | 2016-03-23 | 中国工程物理研究院化工材料研究所 | 2,3-二氯-4-羟基苯胺的制备方法 |
| US10934311B2 (en) | 2016-01-08 | 2021-03-02 | Hangzhou Innogate Pharma Co., Ltd. | Heterocyclic compound used as FGFR inhibitor |
| JP7372740B2 (ja) * | 2016-05-10 | 2023-11-01 | エーザイ・アール・アンド・ディー・マネジメント株式会社 | 細胞生存性及び／又は細胞増殖を低減するための薬物の組み合わせ |
| CN107400092B (zh) * | 2016-05-20 | 2021-08-24 | 浙江海正药业股份有限公司 | 嘧啶类衍生物及其制备方法和其在医药上的用途 |
| TWI669300B (zh) * | 2016-05-20 | 2019-08-21 | 浙江海正藥業股份有限公司 | 嘧啶類衍生物、其製備方法、其藥物組合物以及其在醫藥上的用途 |
| CN105884760B (zh) * | 2016-06-13 | 2019-01-04 | 厦门市蔚嘉化学科技有限公司 | 一种可比司他中间体的制备方法 |
| IL264950B2 (en) * | 2016-08-23 | 2024-01-01 | Eisai R&D Man Co Ltd | Combined treatments for the treatment of malignant liver cell carcinoma |
| CN110022900A (zh) | 2016-09-08 | 2019-07-16 | 蓝图药品公司 | 成纤维细胞生长因子受体4抑制剂与细胞周期蛋白依赖性激酶抑制剂的组合 |
| WO2018055503A1 (en) | 2016-09-20 | 2018-03-29 | Novartis Ag | Combination comprising a pd-1 antagonist and an fgfr4 inhibitor |
| ES2934341T3 (es) | 2016-11-02 | 2023-02-21 | Novartis Ag | Combinaciones de inhibidores de FGFR4 y secuestrantes de ácidos biliares |
| EP3543227B1 (en) * | 2016-11-17 | 2020-12-30 | Guangdong Zhongsheng Pharmaceutical Co., Ltd | Fgfr4 inhibitor and preparation method and use thereof |
| KR101812266B1 (ko) | 2016-11-25 | 2017-12-27 | 한국과학기술연구원 | 4-((2-아크릴아미도페닐)아미노)티에노[3,2-d]피리미딘-7-카복스아미드 유도체 및 그의 약학적 활용 |
| CN108239069B (zh) * | 2016-12-26 | 2021-01-05 | 南京药捷安康生物科技有限公司 | 一种用于成纤维细胞生长因子受体的抑制剂及其用途 |
| CN108503593B (zh) * | 2017-02-28 | 2021-04-27 | 暨南大学 | 2-氨基嘧啶类化合物及其应用 |
| AR111960A1 (es) | 2017-05-26 | 2019-09-04 | Incyte Corp | Formas cristalinas de un inhibidor de fgfr y procesos para su preparación |
| WO2019024876A1 (zh) * | 2017-08-04 | 2019-02-07 | 上海和誉生物医药科技有限公司 | 一种具有fgfr4抑制活性的醛基吡啶衍生物、其制备方法和应用 |
| CN109422760B (zh) * | 2017-09-01 | 2022-05-27 | 南京圣和药物研发有限公司 | Fgfr4抑制剂及其应用 |
| SG11202001979PA (en) | 2017-09-05 | 2020-04-29 | Bioardis Llc | Aromatic derivative, preparation method for same, and medical applications thereof |
| MA51570A (fr) | 2018-01-10 | 2020-11-18 | Eisai R&D Man Co Ltd | Polythérapies pour le traitement du carcinome hépatocellulaire |
| SI3788047T1 (sl) | 2018-05-04 | 2024-11-29 | Incyte Corporation | Trdne oblike inhibitorja fgfr in postopki priprave le-teh |
| SG11202010882XA (en) | 2018-05-04 | 2020-11-27 | Incyte Corp | Salts of an fgfr inhibitor |
| WO2019242689A1 (zh) * | 2018-06-22 | 2019-12-26 | 北京赛特明强医药科技有限公司 | 一种氰基取代吡啶及氰基取代嘧啶类化合物、制备方法及其应用 |
| WO2020177067A1 (en) | 2019-03-05 | 2020-09-10 | Bioardis Llc | Aromatic derivatives, preparation methods, and medical uses thereof |
| WO2020185532A1 (en) | 2019-03-08 | 2020-09-17 | Incyte Corporation | Methods of treating cancer with an fgfr inhibitor |
| HUE065486T2 (hu) | 2019-05-10 | 2024-05-28 | Deciphera Pharmaceuticals Llc | Fenilaminopirimidinamid autophágia inhibitorok és azok felhasználási eljárásai |
| PL3966206T3 (pl) | 2019-05-10 | 2024-01-29 | Deciphera Pharmaceuticals, Llc | Heteroaryloaminopirymidynoamidowe inhibitory autofagii i sposoby ich zastosowania |
| AU2020297422B2 (en) | 2019-06-17 | 2024-03-21 | Deciphera Pharmaceuticals, Llc | Aminopyrimidine amide autophagy inhibitors and methods of use thereof |
| US11591329B2 (en) | 2019-07-09 | 2023-02-28 | Incyte Corporation | Bicyclic heterocycles as FGFR inhibitors |
| CN112341344B (zh) * | 2019-08-09 | 2021-10-26 | 上海喀露蓝科技有限公司 | 一种激酶抑制剂中间体的制备方法 |
| WO2021067374A1 (en) | 2019-10-01 | 2021-04-08 | Incyte Corporation | Bicyclic heterocycles as fgfr inhibitors |
| US11607416B2 (en) | 2019-10-14 | 2023-03-21 | Incyte Corporation | Bicyclic heterocycles as FGFR inhibitors |
| US11566028B2 (en) | 2019-10-16 | 2023-01-31 | Incyte Corporation | Bicyclic heterocycles as FGFR inhibitors |
| WO2021113462A1 (en) | 2019-12-04 | 2021-06-10 | Incyte Corporation | Derivatives of an fgfr inhibitor |
| EP4069696A1 (en) | 2019-12-04 | 2022-10-12 | Incyte Corporation | Tricyclic heterocycles as fgfr inhibitors |
| KR102797616B1 (ko) * | 2019-12-23 | 2025-04-21 | 베이징 사이텍-엠큐 파마슈티컬즈 리미티드 | 시아노-치환된 피리딘 및 시아노-치환된 피리미딘 화합물 및 이의 제조방법 및 이의 적용 |
| WO2021146424A1 (en) | 2020-01-15 | 2021-07-22 | Incyte Corporation | Bicyclic heterocycles as fgfr inhibitors |
| WO2021230886A1 (en) | 2020-05-15 | 2021-11-18 | Eisai R&D Management Co., Ltd. | A method for treating cancer with an oral dosage form of an fgfr4 inhibitor |
| US20230172867A1 (en) | 2020-05-15 | 2023-06-08 | Eisai R&D Management Co., Ltd. | A method for treating cancer with an oral dosage form of an fgfr4 inhibitor |
| CN113943251A (zh) * | 2020-07-16 | 2022-01-18 | 正大天晴药业集团股份有限公司 | 双环庚烯基氨基取代的氮杂芳环类化合物及其医药用途 |
| WO2022075482A1 (ja) | 2020-10-05 | 2022-04-14 | 株式会社カイオム・バイオサイエンス | がん治療用医薬 |
| CN114621106A (zh) * | 2020-12-11 | 2022-06-14 | 重庆医药工业研究院有限责任公司 | 一种酪氨酸激酶药物中间体的制备方法 |
| WO2022221170A1 (en) | 2021-04-12 | 2022-10-20 | Incyte Corporation | Combination therapy comprising an fgfr inhibitor and a nectin-4 targeting agent |
| WO2022261160A1 (en) | 2021-06-09 | 2022-12-15 | Incyte Corporation | Tricyclic heterocycles as fgfr inhibitors |
| WO2022261159A1 (en) | 2021-06-09 | 2022-12-15 | Incyte Corporation | Tricyclic heterocycles as fgfr inhibitors |
| CN115490670A (zh) * | 2021-06-17 | 2022-12-20 | 浙江海正药业股份有限公司 | Fgfr4选择性抑制剂的盐及其制备方法和用途 |
| CN115504965A (zh) | 2021-06-23 | 2022-12-23 | 浙江海正药业股份有限公司 | 嘧啶类衍生物的晶型及其制备方法 |
| CN114276266B (zh) * | 2021-12-30 | 2024-10-11 | 兰州康鹏威耳化工有限公司 | 一种4-氨基-2-氟苯甲酰胺的制备方法 |
| CN114560815A (zh) * | 2022-03-04 | 2022-05-31 | 北京工业大学 | (2-((5-氯-取代苯基氨基嘧啶-2-基)氨基)苯基)氨基甲酸叔丁酯类衍生物 |
| CN116947825B (zh) * | 2022-04-14 | 2025-11-28 | 浙江海正药业股份有限公司 | Fgfr4选择性抑制剂化合物的晶型及其制备方法和用途 |
| CN114835640B (zh) * | 2022-05-24 | 2024-02-13 | 中国药科大学 | 成纤维细胞生长因子受体抑制剂、制备方法及应用 |
| EP4509142A1 (en) | 2023-08-16 | 2025-02-19 | Ona Therapeutics S.L. | Fgfr4 as target in cancer treatment |
Family Cites Families (30)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0310550B1 (de) * | 1987-09-28 | 1993-05-26 | Ciba-Geigy Ag | Schädlingsbekämpfungsmittel |
| ES2310039T3 (es) | 1998-05-26 | 2008-12-16 | Warner-Lambert Company Llc | Pirimidinas biciclicas y 3,4-dihidropirimidinas biciclicas como inhibidores de la proliferacion celular. |
| GB0103926D0 (en) | 2001-02-17 | 2001-04-04 | Astrazeneca Ab | Chemical compounds |
| WO2004037212A2 (en) | 2002-10-24 | 2004-05-06 | Sepracor, Inc. | Compositions comprising zopiclone derivatives and methods of making and using the same |
| CN1860118A (zh) | 2003-07-29 | 2006-11-08 | Irm责任有限公司 | 作为蛋白激酶抑制剂的化合物和组合物 |
| GB0512324D0 (en) * | 2005-06-16 | 2005-07-27 | Novartis Ag | Organic compounds |
| WO2006038112A1 (en) | 2004-10-01 | 2006-04-13 | Warner-Lambert Company Llc | Use of kinase inhibitors to promote neochondrogenesis |
| CN101336237B (zh) | 2005-12-21 | 2015-09-30 | 诺华股份有限公司 | 作为fgf抑制剂的嘧啶基芳基脲衍生物 |
| EP1918376A1 (en) | 2006-11-03 | 2008-05-07 | Max-Planck-Gesellschaft zur Förderung der Wissenschaften e.V. | FGFR4 promotes cancer cell resistance in response to chemotherapeutic drugs |
| AU2008210266B2 (en) * | 2007-01-31 | 2013-09-05 | Ym Biosciences Australia Pty Ltd | Thiopyrimidine-based compounds and uses thereof |
| US20090062320A1 (en) | 2007-08-28 | 2009-03-05 | Vito Guagnano | Method of Treating Disorders Mediated by the Fibroblast Growth Factor Receptor |
| EP2361248B1 (en) | 2008-06-27 | 2018-09-19 | Celgene CAR LLC | Heteroaryl compounds and uses thereof |
| AR079257A1 (es) * | 2009-12-07 | 2012-01-04 | Novartis Ag | Formas cristalinas de 3-(2,6-dicloro-3-5-dimetoxi-fenil)-1-{6-[4-(4-etil-piperazin-1-il)-fenil-amino]-pirimidin-4-il}-1-metil-urea y sales de las mismas |
| CA2784807C (en) | 2009-12-29 | 2021-12-14 | Dana-Farber Cancer Institute, Inc. | Type ii raf kinase inhibitors |
| WO2011088196A2 (en) | 2010-01-14 | 2011-07-21 | Yale University | Inhibitors of receptor tyrosine kinases (rtk) and methods of use thereof |
| WO2011153553A2 (en) | 2010-06-04 | 2011-12-08 | The Regents Of The University Of California | Methods and compositions for kinase inhibition |
| AR085934A1 (es) | 2011-04-08 | 2013-11-06 | Ab Science | Tratamiento de mieloma multiple con masitinib |
| CN102816162B (zh) | 2011-06-10 | 2016-04-27 | 中国科学院广州生物医药与健康研究院 | 嘧啶并嘧啶酮类化合物及其药用组合物和应用 |
| BR112014017626A2 (pt) | 2012-01-18 | 2018-05-22 | Genentech Inc | métodos para tratar uma doença ou disfunção, métodos de identificação de um indivíduo, método para prever se um indivíduo com uma doença ou disfunção tem mais ou menos probabilidade para desenvolver toxicidade ao tratamento, método para determinar se um indivíduo com uma doença ou disfunção deve continuar ou suspender o tratamento que compreende um modulador de fgf19, método de otimização de eficácia terapêutica e método de ensaio |
| ES2746288T3 (es) | 2012-02-28 | 2020-03-05 | Astellas Pharma Inc | Compuesto heterocíclico aromático que contiene nitrógeno |
| US8802697B2 (en) * | 2012-07-11 | 2014-08-12 | Blueprint Medicines Corporation | Inhibitors of the fibroblast growth factor receptor |
| KR20150133172A (ko) * | 2013-03-15 | 2015-11-27 | 셀진 아빌로믹스 리서치, 인코포레이티드 | Mk2 억제제 및 이의 용도 |
| AU2014228746B2 (en) * | 2013-03-15 | 2018-08-30 | Celgene Car Llc | Heteroaryl compounds and uses thereof |
| AU2014287209B2 (en) | 2013-07-09 | 2019-01-24 | Dana-Farber Cancer Institute, Inc. | Kinase inhibitors for the treatment of disease |
| TW201605452A (zh) | 2013-08-28 | 2016-02-16 | 安斯泰來製藥股份有限公司 | 以嘧啶化合物作爲有效成分之醫藥組成物 |
| CN110354128A (zh) * | 2013-10-18 | 2019-10-22 | 卫材R&D管理有限公司 | 嘧啶fgfr4抑制剂 |
| AU2014339972B9 (en) | 2013-10-25 | 2019-05-30 | Blueprint Medicines Corporation | Inhibitors of the fibroblast growth factor receptor |
| WO2015108992A1 (en) | 2014-01-15 | 2015-07-23 | Blueprint Medicines Corporation | Heterobicyclic compounds and their use as fgfr4 receptor inhibitors |
| TWI669300B (zh) | 2016-05-20 | 2019-08-21 | 浙江海正藥業股份有限公司 | 嘧啶類衍生物、其製備方法、其藥物組合物以及其在醫藥上的用途 |
| US11667631B2 (en) | 2016-05-20 | 2023-06-06 | Jiangsu Hansoh Pharmaceutical Group Co., Ltd. | FGFR4 inhibitor, preparation method therefor, and applications thereof |
-
2014
- 2014-10-16 CN CN201910565163.7A patent/CN110354128A/zh active Pending
- 2014-10-16 KR KR1020167009625A patent/KR101826015B1/ko active Active
- 2014-10-16 TW TW103135880A patent/TWI597268B/zh active
- 2014-10-16 JP JP2016523266A patent/JP6139788B2/ja active Active
- 2014-10-16 PH PH1/2016/500676A patent/PH12016500676B1/en unknown
- 2014-10-16 SG SG11201602069WA patent/SG11201602069WA/en unknown
- 2014-10-16 PE PE2016000460A patent/PE20160679A1/es unknown
- 2014-10-16 SI SI201430792T patent/SI3057943T1/en unknown
- 2014-10-16 EP EP14790956.8A patent/EP3057943B1/en active Active
- 2014-10-16 AR ARP140103845A patent/AR098048A1/es active IP Right Grant
- 2014-10-16 NZ NZ717559A patent/NZ717559A/en unknown
- 2014-10-16 PT PT147909568T patent/PT3057943T/pt unknown
- 2014-10-16 HR HRP20181129TT patent/HRP20181129T1/hr unknown
- 2014-10-16 RU RU2016118981A patent/RU2715708C2/ru active
- 2014-10-16 EP EP18167989.5A patent/EP3421457B1/en active Active
- 2014-10-16 ES ES14790956.8T patent/ES2679521T3/es active Active
- 2014-10-16 JO JOP/2014/0297A patent/JO3515B1/ar active
- 2014-10-16 MY MYPI2016000489A patent/MY184733A/en unknown
- 2014-10-16 AU AU2014337291A patent/AU2014337291B9/en active Active
- 2014-10-16 PL PL14790956T patent/PL3057943T3/pl unknown
- 2014-10-16 BR BR112016008110-2A patent/BR112016008110B1/pt active IP Right Grant
- 2014-10-16 HU HUE14790956A patent/HUE039268T2/hu unknown
- 2014-10-16 RS RS20180834A patent/RS57444B1/sr unknown
- 2014-10-16 DK DK14790956.8T patent/DK3057943T3/en active
- 2014-10-16 SM SM20180379T patent/SMT201800379T1/it unknown
- 2014-10-16 CA CA2924206A patent/CA2924206C/en active Active
- 2014-10-16 WO PCT/US2014/060902 patent/WO2015057963A1/en not_active Ceased
- 2014-10-16 LT LTEP14790956.8T patent/LT3057943T/lt unknown
- 2014-10-16 CN CN201480056358.4A patent/CN105899490B/zh active Active
- 2014-10-16 WO PCT/US2014/060857 patent/WO2015057938A1/en not_active Ceased
- 2014-10-16 MX MX2016004933A patent/MX378288B/es unknown
- 2014-10-16 UA UAA201605322A patent/UA116920C2/uk unknown
-
2016
- 2016-01-19 US US15/000,659 patent/US9434697B2/en active Active
- 2016-03-01 IL IL244373A patent/IL244373B/en active IP Right Grant
- 2016-04-18 CL CL2016000918A patent/CL2016000918A1/es unknown
- 2016-07-27 US US15/221,018 patent/US9730931B2/en active Active
-
2017
- 2017-04-27 JP JP2017088732A patent/JP2017160233A/ja active Pending
- 2017-06-20 US US15/627,851 patent/US10537571B2/en active Active
-
2018
- 2018-07-18 CY CY181100754T patent/CY1121129T1/el unknown
- 2018-11-27 AU AU2018271284A patent/AU2018271284B2/en active Active
-
2019
- 2019-12-17 US US16/717,080 patent/US10912774B2/en active Active
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| JP2017160233A5 (OSRAM) | ||
| EA200500304A1 (ru) | Производные 3-(сульфонамидоэтил)индола, предназначенные для использования в качестве миметиков глюкокортикоидов при лечении воспалительных, аллергических и пролиферативных заболеваний | |
| RU2017127135A (ru) | Терапевтическое средство против рака желчных протоков | |
| JP2014500265A5 (OSRAM) | ||
| JP2006517939A5 (OSRAM) | ||
| JP2017537940A5 (OSRAM) | ||
| JP2005534623A5 (OSRAM) | ||
| ME02382B (me) | 2-(2,4,5-supstituisani-anilino) piramidisnki derivati kao egfr modulatori korisni za tretman raka | |
| PE20090617A1 (es) | Compuestos amino-5-[-4-(difluorometoxi)fenil]-5-fenilimidazolona para la inhibicion de -secretasa | |
| JP2010529118A5 (OSRAM) | ||
| TW200716648A (en) | Heterocycles as nicotinic acid receptor agonists for the treatment of dyslipidemia | |
| NO20091596L (no) | Benzoylamino-heterocykliske forbindelser som Glucokinase-(GLK)-activatorer | |
| JP2009534386A5 (OSRAM) | ||
| JP2011529049A5 (OSRAM) | ||
| JP2012522847A5 (OSRAM) | ||
| JP2012516894A5 (OSRAM) | ||
| US20050032786A1 (en) | 1, 3-benzothiazinone derivatives and use thereof | |
| JP2020510661A5 (OSRAM) | ||
| NO20085271L (no) | Muscarin reseptoragonister som er effektive i behandling av smerte, Alzheimers sykdom og schizofreni | |
| PL1891029T3 (pl) | Związki organiczne do leczenia stanów zapalnych lub alergicznych | |
| SI3038622T1 (en) | Heterocyclic compounds and methods of use | |
| JP2010521516A5 (OSRAM) | ||
| JP2019520344A5 (OSRAM) | ||
| JP2007500222A5 (OSRAM) | ||
| DE502007001402D1 (de) | Aminoacyl-prodrug derivate und arzneimittel zur behandlung von thromboembolischen erkrankungen |