JP2016528209A5 - - Google Patents
Download PDFInfo
- Publication number
- JP2016528209A5 JP2016528209A5 JP2016525833A JP2016525833A JP2016528209A5 JP 2016528209 A5 JP2016528209 A5 JP 2016528209A5 JP 2016525833 A JP2016525833 A JP 2016525833A JP 2016525833 A JP2016525833 A JP 2016525833A JP 2016528209 A5 JP2016528209 A5 JP 2016528209A5
- Authority
- JP
- Japan
- Prior art keywords
- alkyl
- optionally substituted
- halo
- cancer
- independently
- 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.)
- Granted
Links
- 125000000217 alkyl group Chemical group 0.000 claims 87
- 150000001875 compounds Chemical class 0.000 claims 49
- 125000001475 halogen functional group Chemical group 0.000 claims 30
- 125000004122 cyclic group Chemical group 0.000 claims 29
- 125000003545 alkoxy group Chemical group 0.000 claims 19
- -1 where Z Chemical compound 0.000 claims 19
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims 18
- 206010028980 Neoplasm Diseases 0.000 claims 16
- 150000003973 alkyl amines Chemical class 0.000 claims 13
- 208000035475 disorder Diseases 0.000 claims 10
- 230000002062 proliferating effect Effects 0.000 claims 9
- 208000023275 Autoimmune disease Diseases 0.000 claims 8
- 208000003556 Dry Eye Syndromes Diseases 0.000 claims 8
- 206010013774 Dry eye Diseases 0.000 claims 8
- 201000004681 Psoriasis Diseases 0.000 claims 8
- 201000011510 cancer Diseases 0.000 claims 8
- 201000010099 disease Diseases 0.000 claims 8
- 239000003814 drug Substances 0.000 claims 8
- 208000027866 inflammatory disease Diseases 0.000 claims 8
- 206010025135 lupus erythematosus Diseases 0.000 claims 8
- 238000000034 method Methods 0.000 claims 8
- 125000003342 alkenyl group Chemical group 0.000 claims 7
- 108010024121 Janus Kinases Proteins 0.000 claims 6
- 102000015617 Janus Kinases Human genes 0.000 claims 6
- 238000004519 manufacturing process Methods 0.000 claims 6
- 150000003839 salts Chemical class 0.000 claims 6
- 125000004433 nitrogen atom Chemical group N* 0.000 claims 4
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 3
- 239000008194 pharmaceutical composition Substances 0.000 claims 3
- 206010006187 Breast cancer Diseases 0.000 claims 2
- 208000026310 Breast neoplasm Diseases 0.000 claims 2
- 206010008342 Cervix carcinoma Diseases 0.000 claims 2
- 206010009944 Colon cancer Diseases 0.000 claims 2
- 201000008808 Fibrosarcoma Diseases 0.000 claims 2
- 101000692455 Homo sapiens Platelet-derived growth factor receptor beta Proteins 0.000 claims 2
- 101000932478 Homo sapiens Receptor-type tyrosine-protein kinase FLT3 Proteins 0.000 claims 2
- 101000997835 Homo sapiens Tyrosine-protein kinase JAK1 Proteins 0.000 claims 2
- 101000997832 Homo sapiens Tyrosine-protein kinase JAK2 Proteins 0.000 claims 2
- 101000934996 Homo sapiens Tyrosine-protein kinase JAK3 Proteins 0.000 claims 2
- 208000008839 Kidney Neoplasms Diseases 0.000 claims 2
- 206010058467 Lung neoplasm malignant Diseases 0.000 claims 2
- 206010025323 Lymphomas Diseases 0.000 claims 2
- 206010033128 Ovarian cancer Diseases 0.000 claims 2
- 206010061535 Ovarian neoplasm Diseases 0.000 claims 2
- 206010061902 Pancreatic neoplasm Diseases 0.000 claims 2
- 102100026547 Platelet-derived growth factor receptor beta Human genes 0.000 claims 2
- 206010060862 Prostate cancer Diseases 0.000 claims 2
- 208000000236 Prostatic Neoplasms Diseases 0.000 claims 2
- 108090000412 Protein-Tyrosine Kinases Proteins 0.000 claims 2
- 102000004022 Protein-Tyrosine Kinases Human genes 0.000 claims 2
- 102100020718 Receptor-type tyrosine-protein kinase FLT3 Human genes 0.000 claims 2
- 206010038389 Renal cancer Diseases 0.000 claims 2
- 206010039491 Sarcoma Diseases 0.000 claims 2
- 208000000453 Skin Neoplasms Diseases 0.000 claims 2
- 102100033438 Tyrosine-protein kinase JAK1 Human genes 0.000 claims 2
- 102100033444 Tyrosine-protein kinase JAK2 Human genes 0.000 claims 2
- 102100025387 Tyrosine-protein kinase JAK3 Human genes 0.000 claims 2
- 208000006105 Uterine Cervical Neoplasms Diseases 0.000 claims 2
- 201000007455 central nervous system cancer Diseases 0.000 claims 2
- 201000010881 cervical cancer Diseases 0.000 claims 2
- 208000029742 colonic neoplasm Diseases 0.000 claims 2
- 230000000694 effects Effects 0.000 claims 2
- 102000052116 epidermal growth factor receptor activity proteins Human genes 0.000 claims 2
- 108700015053 epidermal growth factor receptor activity proteins Proteins 0.000 claims 2
- 206010017758 gastric cancer Diseases 0.000 claims 2
- 208000010749 gastric carcinoma Diseases 0.000 claims 2
- 201000010536 head and neck cancer Diseases 0.000 claims 2
- 208000014829 head and neck neoplasm Diseases 0.000 claims 2
- 125000000623 heterocyclic group Chemical group 0.000 claims 2
- 230000002401 inhibitory effect Effects 0.000 claims 2
- 201000010982 kidney cancer Diseases 0.000 claims 2
- 208000032839 leukemia Diseases 0.000 claims 2
- 201000007270 liver cancer Diseases 0.000 claims 2
- 208000014018 liver neoplasm Diseases 0.000 claims 2
- 201000005202 lung cancer Diseases 0.000 claims 2
- 208000020816 lung neoplasm Diseases 0.000 claims 2
- 208000015486 malignant pancreatic neoplasm Diseases 0.000 claims 2
- 201000001441 melanoma Diseases 0.000 claims 2
- YOHYSYJDKVYCJI-UHFFFAOYSA-N n-[3-[[6-[3-(trifluoromethyl)anilino]pyrimidin-4-yl]amino]phenyl]cyclopropanecarboxamide Chemical compound FC(F)(F)C1=CC=CC(NC=2N=CN=C(NC=3C=C(NC(=O)C4CC4)C=CC=3)C=2)=C1 YOHYSYJDKVYCJI-UHFFFAOYSA-N 0.000 claims 2
- 208000002154 non-small cell lung carcinoma Diseases 0.000 claims 2
- 201000002528 pancreatic cancer Diseases 0.000 claims 2
- 208000008443 pancreatic carcinoma Diseases 0.000 claims 2
- 230000037361 pathway Effects 0.000 claims 2
- 230000002265 prevention Effects 0.000 claims 2
- 230000000069 prophylactic effect Effects 0.000 claims 2
- 201000000849 skin cancer Diseases 0.000 claims 2
- 206010041823 squamous cell carcinoma Diseases 0.000 claims 2
- 201000000498 stomach carcinoma Diseases 0.000 claims 2
- 229940124597 therapeutic agent Drugs 0.000 claims 2
- 208000029729 tumor suppressor gene on chromosome 11 Diseases 0.000 claims 2
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 claims 1
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 claims 1
- 239000003937 drug carrier Substances 0.000 claims 1
- 239000000546 pharmaceutical excipient Substances 0.000 claims 1
- 125000000472 sulfonyl group Chemical group *S(*)(=O)=O 0.000 claims 1
Applications Claiming Priority (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201361845342P | 2013-07-11 | 2013-07-11 | |
| US61/845,342 | 2013-07-11 | ||
| US201461923179P | 2014-01-02 | 2014-01-02 | |
| US61/923,179 | 2014-01-02 | ||
| PCT/US2014/046442 WO2015006754A2 (en) | 2013-07-11 | 2014-07-11 | Heterocyclic compounds and uses thereof |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2016528209A JP2016528209A (ja) | 2016-09-15 |
| JP2016528209A5 true JP2016528209A5 (enExample) | 2017-08-17 |
| JP6564771B2 JP6564771B2 (ja) | 2019-08-21 |
Family
ID=51298956
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2016525833A Active JP6564771B2 (ja) | 2013-07-11 | 2014-07-11 | キナーゼ阻害剤としてのピリミジン誘導体 |
Country Status (16)
| Country | Link |
|---|---|
| US (1) | US10562918B2 (enExample) |
| EP (1) | EP3019496B1 (enExample) |
| JP (1) | JP6564771B2 (enExample) |
| KR (1) | KR102173433B1 (enExample) |
| CN (3) | CN117486865A (enExample) |
| AU (1) | AU2014287016B2 (enExample) |
| BR (1) | BR112016000195A8 (enExample) |
| CA (1) | CA2917364C (enExample) |
| DK (1) | DK3019496T3 (enExample) |
| ES (1) | ES2761572T3 (enExample) |
| IL (1) | IL243420A0 (enExample) |
| MX (1) | MX368491B (enExample) |
| NZ (1) | NZ715687A (enExample) |
| RU (1) | RU2677653C2 (enExample) |
| SG (1) | SG11201600062RA (enExample) |
| WO (1) | WO2015006754A2 (enExample) |
Families Citing this family (60)
| 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 |
| CN104203924B (zh) | 2012-01-13 | 2019-06-11 | 艾森生物科学公司 | 杂环化合物及其作为抗癌药的用途 |
| US9464089B2 (en) | 2012-01-13 | 2016-10-11 | Acea Biosciences Inc. | Heterocyclic compounds and uses thereof |
| US9034885B2 (en) | 2012-01-13 | 2015-05-19 | Acea Biosciences Inc. | EGFR modulators and uses thereof |
| PH12019502809B1 (en) | 2012-06-13 | 2024-04-24 | Incyte Holdings Corp | Substituted tricyclic compounds as fgfr inhibitors |
| WO2014026125A1 (en) | 2012-08-10 | 2014-02-13 | Incyte Corporation | Pyrazine derivatives as fgfr inhibitors |
| US9266892B2 (en) | 2012-12-19 | 2016-02-23 | Incyte Holdings Corporation | Fused pyrazoles as FGFR inhibitors |
| MY181497A (en) | 2013-04-19 | 2020-12-23 | Incyte Holdings Corp | Bicyclic heterocycles as fgfr inhibitors |
| BR112016000195A8 (pt) | 2013-07-11 | 2019-12-31 | Acea Biosciences Inc | compostos heterocíclicos, composição farmacêutica, combinação, seu uso, e método para inibir uma atividade da tirosina quinase btk ou jak, egfr, alk, pdgfr, blk, bmx/etk, flt3(d835y), itk, tec, txk, e suas respectivas vias |
| US9550770B2 (en) | 2013-08-23 | 2017-01-24 | Neupharma, Inc. | Substituted quinazolines for inhibiting kinase activity |
| CN111170999B (zh) * | 2014-10-11 | 2023-06-30 | 上海翰森生物医药科技有限公司 | Egfr抑制剂及其制备和应用 |
| US10851105B2 (en) | 2014-10-22 | 2020-12-01 | Incyte Corporation | Bicyclic heterocycles as FGFR4 inhibitors |
| EP3236959B1 (en) | 2014-12-23 | 2025-09-24 | Dana-Farber Cancer Institute, Inc. | Inhibitors of cyclin-dependent kinase 7 (cdk7) |
| CN105884695B (zh) * | 2015-02-13 | 2019-02-26 | 山东轩竹医药科技有限公司 | 杂环衍生物类酪氨酸激酶抑制剂 |
| MA41551A (fr) | 2015-02-20 | 2017-12-26 | Incyte Corp | Hétérocycles bicycliques utilisés en tant qu'inhibiteurs de fgfr4 |
| WO2016134294A1 (en) | 2015-02-20 | 2016-08-25 | Incyte Corporation | Bicyclic heterocycles as fgfr4 inhibitors |
| PE20171514A1 (es) | 2015-02-20 | 2017-10-20 | Incyte Corp | Heterociclos biciclicos como inhibidores de fgfr |
| JP6861166B2 (ja) | 2015-03-27 | 2021-04-21 | ダナ−ファーバー キャンサー インスティテュート, インコーポレイテッド | サイクリン依存性キナーゼの阻害剤 |
| CN106146515B (zh) | 2015-04-17 | 2020-09-04 | 常州隆赛医药科技有限公司 | 新型激酶抑制剂的制备及应用 |
| KR101778004B1 (ko) * | 2015-06-22 | 2017-09-15 | (주) 에빅스젠 | 이마티닙을 유효성분으로 포함하는 안구 건조 질환 예방 및 치료용 약학 조성물 |
| EP3319960B1 (en) * | 2015-07-09 | 2020-11-18 | Merck Patent GmbH | Pyrimidine derivatives as btk inhibitors and uses thereof |
| WO2017059702A1 (en) * | 2015-10-09 | 2017-04-13 | Acea Biosciences, Inc | Pharmaceutical salts, physical forms, and compositions of pyrrolopyrimidine kinase inhibitors, and methods of making same |
| CN106608868A (zh) * | 2015-10-21 | 2017-05-03 | 复旦大学 | 5-(硫醚基)嘧啶类化合物及其药用组合物和应用 |
| KR20170050453A (ko) * | 2015-10-30 | 2017-05-11 | 한미약품 주식회사 | 싸이에노피리미딘 화합물의 신규 제조방법 및 이에 사용되는 중간체 |
| WO2017097113A1 (zh) * | 2015-12-10 | 2017-06-15 | 深圳市塔吉瑞生物医药有限公司 | 用于抑制蛋白酪氨酸激酶活性的氨基嘧啶类化合物 |
| WO2018004306A1 (en) * | 2016-06-30 | 2018-01-04 | Daewoong Pharmaceutical Co., Ltd. | Pyrazolopyrimidine derivatives as kinase inhibitor |
| EP4006035B1 (en) | 2016-08-15 | 2023-11-22 | Neupharma, Inc. | Quinazoline derivatives as tyrosine kinase inhibitors for the treatment of cancer |
| CN106749042B (zh) * | 2016-11-16 | 2019-01-22 | 大连医科大学 | 磺酰胺基嘧啶类化合物,组合物及用途 |
| KR20180075228A (ko) * | 2016-12-26 | 2018-07-04 | 한미약품 주식회사 | 싸이에노피리미딘 화합물의 신규 제조방법 및 중간체 |
| JP7076741B2 (ja) | 2016-12-27 | 2022-05-30 | 国立研究開発法人理化学研究所 | Bmpシグナル阻害化合物 |
| WO2018139883A1 (ko) * | 2017-01-26 | 2018-08-02 | 부광약품 주식회사 | 다중 표적 키나아제 저해제로서 융합피리미딘 유도체 |
| US11608334B2 (en) * | 2017-02-08 | 2023-03-21 | The National Institutes of Pharmaceutical R&D Co., Ltd. | Pyrrolo-aromatic heterocyclic compound, preparation method therefor, and medical use thereof |
| CA3059072A1 (en) | 2017-04-07 | 2018-10-11 | ACEA Therapeutics, Inc. | Pharmaceutical salts, physical forms, and compositions of pyrrolopyrimidine kinase inhibitors, and methods of making same |
| AR111960A1 (es) | 2017-05-26 | 2019-09-04 | Incyte Corp | Formas cristalinas de un inhibidor de fgfr y procesos para su preparación |
| JOP20180094A1 (ar) | 2017-10-18 | 2019-04-18 | Hk Inno N Corp | مركب حلقي غير متجانس كمثبط بروتين كيناز |
| CN112867716B (zh) | 2018-05-04 | 2024-09-13 | 因赛特公司 | Fgfr抑制剂的固体形式和其制备方法 |
| JP7568512B2 (ja) | 2018-05-04 | 2024-10-16 | インサイト・コーポレイション | Fgfr阻害剤の塩 |
| CA3099763A1 (en) | 2018-06-25 | 2020-01-02 | Dana-Farber Cancer Institute, Inc. | Taire family kinase inhibitors and uses thereof |
| JP7675647B2 (ja) * | 2018-08-09 | 2025-05-13 | エイシア セラピューティクス, インコーポレイテッド | (s)-n-(3-((2-((4-((1-アセチルピロリジン-3-イル)(メチル)アミノ)フェニル)アミノ)-5-メトキシピリミジン-4-イル)オキシ)フェニル)アクリルアミドの製造のためのプロセスおよびその製剤 |
| KR102195348B1 (ko) | 2018-11-15 | 2020-12-24 | 에이치케이이노엔 주식회사 | 단백질 키나제 억제제로서의 신규 화합물 및 이를 포함하는 약제학적 조성물 |
| US12281126B2 (en) | 2018-12-28 | 2025-04-22 | Dana-Farber Cancer Institute, Inc. | Inhibitors of cyclin-dependent kinase 7 and uses thereof |
| WO2020185532A1 (en) | 2019-03-08 | 2020-09-17 | Incyte Corporation | Methods of treating cancer with an fgfr inhibitor |
| WO2021007269A1 (en) | 2019-07-09 | 2021-01-14 | Incyte Corporation | Bicyclic heterocycles as fgfr inhibitors |
| 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 |
| IL293211A (en) * | 2019-11-22 | 2022-07-01 | Medshine Discovery Inc | Pyrimidopyrrole spiro compounds and derivatives thereof as dna-pk inhibitors |
| CN111018842B (zh) * | 2019-12-04 | 2021-02-12 | 宜春市人民医院 | 一种唑代嘧啶衍生物、其药物组合物和在抗肿瘤中的应用 |
| WO2021113462A1 (en) | 2019-12-04 | 2021-06-10 | Incyte Corporation | Derivatives of an fgfr inhibitor |
| US11897891B2 (en) | 2019-12-04 | 2024-02-13 | Incyte Corporation | Tricyclic heterocycles as FGFR inhibitors |
| WO2021146424A1 (en) | 2020-01-15 | 2021-07-22 | Incyte Corporation | Bicyclic heterocycles as fgfr inhibitors |
| CN111848631B (zh) * | 2020-08-28 | 2022-04-19 | 四川大学华西医院 | 一种靶向EGFR突变的吡咯并[2,3-d]嘧啶衍生物及其制备方法和用途 |
| US20240100172A1 (en) | 2020-12-21 | 2024-03-28 | Hangzhou Jijing Pharmaceutical Technology Limited | Methods and compounds for targeted autophagy |
| CA3215903A1 (en) | 2021-04-12 | 2022-10-20 | Incyte Corporation | Combination therapy comprising an fgfr inhibitor and a nectin-4 targeting agent |
| US11939331B2 (en) | 2021-06-09 | 2024-03-26 | Incyte Corporation | Tricyclic heterocycles as FGFR inhibitors |
| JP2024522188A (ja) | 2021-06-09 | 2024-06-11 | インサイト・コーポレイション | Fgfr阻害剤としての三環式ヘテロ環 |
| CN114184671B (zh) * | 2021-12-09 | 2024-02-06 | 中国石油大学(北京) | 用于确定表面活性剂在岩石表面的吸附层数的方法 |
| CA3238851A1 (en) * | 2021-12-21 | 2023-06-29 | Yuli Xie | Compound as fak inhibitor and use thereof |
| WO2024092047A1 (en) * | 2022-10-26 | 2024-05-02 | Sorrento Therapeutics, Inc. | Administration of pyrrolopyrimidine-based kinase inhibitors for treatment of psoriasis |
| CN117586235B (zh) * | 2023-11-27 | 2025-08-22 | 广东省人民医院 | 增强线粒体自噬的嵌合分子及其应用 |
Family Cites Families (64)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3974277A (en) | 1974-09-06 | 1976-08-10 | Diamond Shamrock Corporation | 2-[2-(5-Nitro-2-furyl)vinyl]-4-(anilino)quinazolines as growth promotants and feed efficiency enhancing agents |
| SV2002000205A (es) | 1999-11-01 | 2002-06-07 | Lilly Co Eli | Compuestos farmaceuticos ref. x-01095 |
| CN1264824C (zh) | 2001-02-21 | 2006-07-19 | 三菱制药株式会社 | 喹唑啉衍生物 |
| US6881737B2 (en) | 2001-04-11 | 2005-04-19 | Amgen Inc. | Substituted triazinyl acrylamide derivatives and methods of use |
| WO2003026665A1 (en) | 2001-09-26 | 2003-04-03 | Bayer Pharmaceuticals Corporation | 2-phenylamino-4-(5-pyrazolylamino)-pyrimidine derivatives as kinase inhibitors, in particular, src kinase inhibitors |
| US7732127B2 (en) | 2002-12-20 | 2010-06-08 | Acea Biosciences, Inc. | Dynamic monitoring of cell adhesion and spreading using the RT-CES system |
| US7470533B2 (en) | 2002-12-20 | 2008-12-30 | Acea Biosciences | Impedance based devices and methods for use in assays |
| US7560269B2 (en) | 2002-12-20 | 2009-07-14 | Acea Biosciences, Inc. | Real time electronic cell sensing system and applications for cytotoxicity profiling and compound assays |
| US7468255B2 (en) | 2002-12-20 | 2008-12-23 | Acea Biosciences | Method for assaying for natural killer, cytotoxic T-lymphocyte and neutrophil-mediated killing of target cells using real-time microelectronic cell sensing technology |
| JP2005537498A (ja) | 2002-07-20 | 2005-12-08 | アセア バイオサイエンシーズ,インク. | インピーダンスによる測定装置および方法 |
| WO2004021979A2 (en) | 2002-09-06 | 2004-03-18 | Smithkline Beecham Corporation | PYRROLO[2, 3-d]PYRIMIDINE-4-YL AND PURIN-6-YL UREA COMPOUNDS |
| TW200416034A (en) | 2002-11-15 | 2004-09-01 | Mitsubishi Pharma Corp | Medicinal composition |
| CA2550274A1 (en) | 2003-11-12 | 2005-05-26 | Acea Biosciences, Inc. | Real time electronic cell sensing systems and applications for cell-based assays |
| PT1696920E (pt) | 2003-12-19 | 2015-01-14 | Plexxikon Inc | Compostos e métodos para o desenvolvimento de moduladores de ret |
| JP5283336B2 (ja) | 2004-01-12 | 2013-09-04 | ワイエム・バイオサイエンシズ・オーストラリア・ピーティーワイ・リミテッド | 選択的キナーゼ阻害剤 |
| AU2005218655A1 (en) | 2004-03-02 | 2005-09-15 | Neurogen Corporation | Aryl substituted purine analogues |
| AU2005265017A1 (en) | 2004-06-17 | 2006-01-26 | Plexxikon, Inc. | Azaindoles modulating c-kit activity and uses therefor |
| WO2006014325A2 (en) | 2004-07-02 | 2006-02-09 | Exelixis, Inc. | C-met modulators and method of use |
| AU2006298882B2 (en) | 2005-09-21 | 2011-10-27 | 4Sc Ag | Novel sulphonylpyrroles as inhibitors of HDAC S novel sulphonylpyrroles |
| EA200800664A1 (ru) | 2005-10-13 | 2009-02-27 | Глаксо Груп Лимитед | Производные пирролопиримидина в качестве ингибиторов syk |
| KR100832594B1 (ko) | 2005-11-08 | 2008-05-27 | 한미약품 주식회사 | 다중저해제로서의 퀴나졸린 유도체 및 이의 제조방법 |
| GB0526246D0 (en) | 2005-12-22 | 2006-02-01 | Novartis Ag | Organic compounds |
| AU2007224162A1 (en) | 2006-03-03 | 2007-09-13 | Aveo Pharmaceuticals, Inc. | Processes for synthesizing 7-alkynyl-4-aminoquinazolines and a related intermediate |
| EA200870385A1 (ru) | 2006-03-29 | 2009-04-28 | Фолдркс Фармасьютикалз, Инк. | Ингибирование токсичности альфа-синуклеина |
| US8314234B2 (en) | 2006-09-25 | 2012-11-20 | Janssen Pharmaceutica N.V. | Bicyclic pyrimidine kinase inhibitors |
| MX2009006081A (es) | 2006-12-08 | 2009-06-17 | Irmc Llc | Compuestos y composiciones como inhibidores de cinasa de proteina. |
| CN101622001A (zh) | 2007-01-26 | 2010-01-06 | Irm责任有限公司 | 作为激酶抑制剂用于治疗疟原虫相关疾病的嘌呤化合物和组合物 |
| CA2702647C (en) | 2007-01-31 | 2016-03-22 | Ym Biosciences Australia Pty Ltd | Thiopyrimidine-based compounds and uses thereof |
| TWI377944B (en) | 2007-06-05 | 2012-12-01 | Hanmi Holdings Co Ltd | Novel amide derivative for inhibiting the growth of cancer cells |
| WO2009017838A2 (en) | 2007-08-01 | 2009-02-05 | Exelixis, Inc. | Combinations of jak-2 inhibitors and other agents |
| JP5298128B2 (ja) | 2007-08-08 | 2013-09-25 | グラクソスミスクライン エルエルシー | 癌の治療用のIGF−1R阻害剤としての2−[(2−{フェニルアミノ}−1H−ピロロ[2,3−d]ピリミジン−4−イル)アミノ]ベンズアミド誘導体 |
| WO2009032703A1 (en) | 2007-08-28 | 2009-03-12 | Irm Llc | 2- (het) arylamino-6-aminopyridine derivatives and fused forms thereof as anaplastic lymphoma kinase inhibitors |
| AU2008314632B2 (en) | 2007-10-19 | 2015-05-28 | Celgene Avilomics Research, Inc. | Heteroaryl compounds and uses thereof |
| US7989465B2 (en) | 2007-10-19 | 2011-08-02 | Avila Therapeutics, Inc. | 4,6-disubstituted pyrimidines useful as kinase inhibitors |
| AU2009238590A1 (en) | 2008-04-22 | 2009-10-29 | Portola Pharmaceuticals, Inc. | Inhibitors of protein kinases |
| ES2645689T5 (en) | 2008-05-21 | 2025-06-24 | Takeda Pharmaceuticals Co | Phosphorous derivatives as kinase inhibitors |
| TWI546290B (zh) | 2008-06-27 | 2016-08-21 | 賽基艾維洛米斯研究股份有限公司 | 雜芳基化合物及其用途 |
| US8338439B2 (en) * | 2008-06-27 | 2012-12-25 | Celgene Avilomics Research, Inc. | 2,4-disubstituted pyrimidines useful as kinase inhibitors |
| WO2010045451A1 (en) | 2008-10-16 | 2010-04-22 | Glaxosmithkline Llc | Pyrrolopyrimidine compounds |
| WO2010090764A1 (en) | 2009-02-09 | 2010-08-12 | Supergen, Inc. | Pyrrolopyrimidinyl axl kinase inhibitors |
| CN102482277B (zh) * | 2009-05-05 | 2017-09-19 | 达纳-法伯癌症研究所有限公司 | 表皮生长因子受体抑制剂及治疗障碍的方法 |
| CA2777773C (en) * | 2009-10-22 | 2017-10-17 | Marcel Peter Gerard Maes | Signaling system having improved contrast ratio |
| WO2011079231A1 (en) * | 2009-12-23 | 2011-06-30 | Gatekeeper Pharmaceutical, Inc. | Compounds that modulate egfr activity and methods for treating or preventing conditions therewith |
| JP6147503B2 (ja) | 2009-12-28 | 2017-06-14 | ペトロレオ ブラジレイロ ソシエダ アノニマ − ペトロブラス | 軽質オレフィンを製造する高性能燃焼装置及び流動接触分解方法 |
| WO2011140338A1 (en) | 2010-05-05 | 2011-11-10 | Gatekeeper Pharmaceuticals, Inc. | Compounds that modulate egfr activity and methods for treating or preventing conditions therewith |
| USRE46511E1 (en) * | 2010-06-23 | 2017-08-15 | Hanmi Science Co., Ltd. | Fused pyrimidine derivatives for inhibition of tyrosine kinase activity |
| BR112013010564B1 (pt) | 2010-11-01 | 2021-09-21 | Celgene Car Llc | Compostos heterocíclicos e composições compreendendo os mesmos |
| JP5956999B2 (ja) * | 2010-11-01 | 2016-07-27 | セルジーン アヴィロミクス リサーチ, インコーポレイテッド | ヘテロアリール化合物およびその使用 |
| EP2637502B1 (en) * | 2010-11-10 | 2018-01-10 | Celgene CAR LLC | Mutant-selective egfr inhibitors and uses thereof |
| CN102583089B (zh) | 2011-01-11 | 2015-11-25 | 山东新北洋信息技术股份有限公司 | 薄片类介质处理装置 |
| CA2826864A1 (en) | 2011-03-07 | 2012-09-13 | Fondazione Telethon | Tfeb variants and uses thereof |
| US8703767B2 (en) | 2011-04-01 | 2014-04-22 | University Of Utah Research Foundation | Substituted N-(3-(pyrimidin-4-yl)phenyl)acrylamide analogs as tyrosine receptor kinase BTK inhibitors |
| KR101884010B1 (ko) * | 2011-05-04 | 2018-07-31 | 어리어드 파마슈티칼스, 인코포레이티드 | Egfr-유도된 암의 세포 증식을 억제하는 화합물 |
| US8828391B2 (en) | 2011-05-17 | 2014-09-09 | Boehringer Ingelheim International Gmbh | Method for EGFR directed combination treatment of non-small cell lung cancer |
| HUE048834T2 (hu) * | 2011-05-17 | 2020-08-28 | Univ California | Kináz inhibitorok |
| US9034885B2 (en) | 2012-01-13 | 2015-05-19 | Acea Biosciences Inc. | EGFR modulators and uses thereof |
| CN104203924B (zh) | 2012-01-13 | 2019-06-11 | 艾森生物科学公司 | 杂环化合物及其作为抗癌药的用途 |
| US9464089B2 (en) | 2012-01-13 | 2016-10-11 | Acea Biosciences Inc. | Heterocyclic compounds and uses thereof |
| US9586965B2 (en) | 2012-01-13 | 2017-03-07 | Acea Biosciences Inc. | Pyrrolo[2,3-d]pyrimidine compounds as inhibitors of protein kinases |
| RU2645672C2 (ru) | 2012-08-06 | 2018-02-27 | Ацея Байосайенсиз Инк. | Новые соединения пирролопиримидина в качестве ингибиторов протеинкиназ |
| BR112016000195A8 (pt) | 2013-07-11 | 2019-12-31 | Acea Biosciences Inc | compostos heterocíclicos, composição farmacêutica, combinação, seu uso, e método para inibir uma atividade da tirosina quinase btk ou jak, egfr, alk, pdgfr, blk, bmx/etk, flt3(d835y), itk, tec, txk, e suas respectivas vias |
| CN104306348B (zh) | 2014-09-30 | 2017-05-31 | 地奥集团成都药业股份有限公司 | 一种辛伐他汀片及其制备方法 |
| WO2017059702A1 (en) | 2015-10-09 | 2017-04-13 | Acea Biosciences, Inc | Pharmaceutical salts, physical forms, and compositions of pyrrolopyrimidine kinase inhibitors, and methods of making same |
| CA3059072A1 (en) | 2017-04-07 | 2018-10-11 | ACEA Therapeutics, Inc. | Pharmaceutical salts, physical forms, and compositions of pyrrolopyrimidine kinase inhibitors, and methods of making same |
-
2014
- 2014-07-11 BR BR112016000195A patent/BR112016000195A8/pt not_active Application Discontinuation
- 2014-07-11 EP EP14748351.5A patent/EP3019496B1/en active Active
- 2014-07-11 KR KR1020167002970A patent/KR102173433B1/ko active Active
- 2014-07-11 NZ NZ715687A patent/NZ715687A/en not_active IP Right Cessation
- 2014-07-11 SG SG11201600062RA patent/SG11201600062RA/en unknown
- 2014-07-11 ES ES14748351T patent/ES2761572T3/es active Active
- 2014-07-11 CA CA2917364A patent/CA2917364C/en active Active
- 2014-07-11 CN CN202310865044.XA patent/CN117486865A/zh active Pending
- 2014-07-11 RU RU2016104388A patent/RU2677653C2/ru active
- 2014-07-11 CN CN202011022304.XA patent/CN112592334B/zh active Active
- 2014-07-11 WO PCT/US2014/046442 patent/WO2015006754A2/en not_active Ceased
- 2014-07-11 MX MX2016000261A patent/MX368491B/es active IP Right Grant
- 2014-07-11 DK DK14748351T patent/DK3019496T3/da active
- 2014-07-11 JP JP2016525833A patent/JP6564771B2/ja active Active
- 2014-07-11 CN CN201480049793.4A patent/CN105916851A/zh active Pending
- 2014-07-11 AU AU2014287016A patent/AU2014287016B2/en active Active
-
2015
- 2015-12-30 IL IL243420A patent/IL243420A0/en unknown
-
2018
- 2018-01-29 US US15/882,924 patent/US10562918B2/en active Active
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| JP2016528209A5 (enExample) | ||
| RU2016104388A (ru) | Производные пиримидина в качестве ингибиторов киназы | |
| WO2023015559A1 (en) | Macrocycle compounds as inhibitors of ras | |
| ES2558780T3 (es) | Imidazopiridazinas como inhibidores de la cinasa Akt | |
| JP2016528197A5 (enExample) | ||
| JP2016530283A5 (enExample) | ||
| RU2015133528A (ru) | Замещенные полициклические пиразольные ингибиторы киназной активности и их применение | |
| CN114835680A (zh) | 卤素取代异吲哚啉化合物及其应用 | |
| CN103429591A (zh) | 在治疗过度增殖性病症中用作mps-1和tkk抑制剂的6-取代的咪唑并吡嗪 | |
| ES2822654T3 (es) | Benzimidazol-2-aminas como inhibidores de mIDH1 | |
| JP2018516238A5 (enExample) | ||
| CN116514846A (zh) | 杂环类衍生物、其制备方法及其医药上的用途 | |
| KR20140003436A (ko) | 과증식성 장애 및 혈관형성과 관련된 질환 치료에 유용한 아미노알코올 치환된 2,3-디하이드로이미다조[1,2-c]퀴나졸린 유도체 | |
| RU2642779C2 (ru) | Ингибиторы сомт | |
| TWI848400B (zh) | 雜環化合物及醫藥 | |
| JP2014518544A5 (enExample) | ||
| CN117794929A (zh) | 选择性bcl-xl protac化合物及使用方法 | |
| RU2014135436A (ru) | Комбинация ингибитора rtk с антиэстрогеном и ее применение для лечения рака | |
| JP2017514806A5 (enExample) | ||
| JP7732668B2 (ja) | 窒素含有多環式縮合環系化合物、その薬学的組成物、製造方法及び用途 | |
| CN106211770A (zh) | 作为γ‑分泌酶调节剂的色烯和1,1A,2,7B‑四氢环丙烷并[c]色烯吡啶并吡嗪二酮 | |
| CN114437074A (zh) | 一种化合物、含该化合物的药物组合物及其用途 | |
| JP2016525142A5 (enExample) | ||
| JP2018534314A5 (enExample) | ||
| AU2016298962A1 (en) | Compounds and pharmaceutical composition associated with ubiquitination-proteasome system |