JP2013534804A5 - - Google Patents
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- JP2013534804A5 JP2013534804A5 JP2013505074A JP2013505074A JP2013534804A5 JP 2013534804 A5 JP2013534804 A5 JP 2013534804A5 JP 2013505074 A JP2013505074 A JP 2013505074A JP 2013505074 A JP2013505074 A JP 2013505074A JP 2013534804 A5 JP2013534804 A5 JP 2013534804A5
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- Prior art keywords
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- FWMNVWWHGCHHJJ-SKKKGAJSSA-N 4-amino-1-[(2r)-6-amino-2-[[(2r)-2-[[(2r)-2-[[(2r)-2-amino-3-phenylpropanoyl]amino]-3-phenylpropanoyl]amino]-4-methylpentanoyl]amino]hexanoyl]piperidine-4-carboxylic acid Chemical compound C([C@H](C(=O)N[C@H](CC(C)C)C(=O)N[C@H](CCCCN)C(=O)N1CCC(N)(CC1)C(O)=O)NC(=O)[C@H](N)CC=1C=CC=CC=1)C1=CC=CC=C1 FWMNVWWHGCHHJJ-SKKKGAJSSA-N 0.000 claims 116
- 125000000539 amino acid group Chemical group 0.000 claims 116
- 102100033793 ALK tyrosine kinase receptor Human genes 0.000 claims 108
- 101710168331 ALK tyrosine kinase receptor Proteins 0.000 claims 108
- 229920001184 polypeptide Polymers 0.000 claims 91
- 102000004196 processed proteins & peptides Human genes 0.000 claims 91
- 108090000765 processed proteins & peptides Proteins 0.000 claims 91
- 239000002157 polynucleotide Substances 0.000 claims 65
- 102000040430 polynucleotide Human genes 0.000 claims 65
- 108091033319 polynucleotide Proteins 0.000 claims 65
- 125000003275 alpha amino acid group Chemical group 0.000 claims 59
- 150000003384 small molecules Chemical class 0.000 claims 48
- 229940043355 kinase inhibitor Drugs 0.000 claims 47
- 239000003757 phosphotransferase inhibitor Substances 0.000 claims 47
- 239000002773 nucleotide Substances 0.000 claims 45
- 125000003729 nucleotide group Chemical group 0.000 claims 45
- 230000000694 effects Effects 0.000 claims 42
- 108091000080 Phosphotransferase Proteins 0.000 claims 37
- 102000020233 phosphotransferase Human genes 0.000 claims 37
- 230000035772 mutation Effects 0.000 claims 34
- 238000000034 method Methods 0.000 claims 29
- 229940122531 Anaplastic lymphoma kinase inhibitor Drugs 0.000 claims 28
- 125000003588 lysine group Chemical group [H]N([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])(N([H])[H])C(*)=O 0.000 claims 28
- 239000012472 biological sample Substances 0.000 claims 26
- 206010028980 Neoplasm Diseases 0.000 claims 22
- 201000011510 cancer Diseases 0.000 claims 22
- 125000003295 alanine group Chemical group N[C@@H](C)C(=O)* 0.000 claims 14
- 108020001507 fusion proteins Proteins 0.000 claims 14
- 102000037865 fusion proteins Human genes 0.000 claims 14
- 125000002987 valine group Chemical group [H]N([H])C([H])(C(*)=O)C([H])(C([H])([H])[H])C([H])([H])[H] 0.000 claims 14
- 231100000590 oncogenic Toxicity 0.000 claims 13
- 230000002246 oncogenic effect Effects 0.000 claims 13
- 125000001360 methionine group Chemical group N[C@@H](CCSC)C(=O)* 0.000 claims 11
- 125000000637 arginyl group Chemical group N[C@@H](CCCNC(N)=N)C(=O)* 0.000 claims 7
- 125000000613 asparagine group Chemical group N[C@@H](CC(N)=O)C(=O)* 0.000 claims 7
- 125000000151 cysteine group Chemical group N[C@@H](CS)C(=O)* 0.000 claims 7
- 125000000741 isoleucyl group Chemical group [H]N([H])C(C(C([H])([H])[H])C([H])([H])C([H])([H])[H])C(=O)O* 0.000 claims 7
- 125000001909 leucine group Chemical group [H]N(*)C(C(*)=O)C([H])([H])C(C([H])([H])[H])C([H])([H])[H] 0.000 claims 7
- 125000003607 serino group Chemical group [H]N([H])[C@]([H])(C(=O)[*])C(O[H])([H])[H] 0.000 claims 7
- 125000001493 tyrosinyl group Chemical group [H]OC1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])C([H])(N([H])[H])C(*)=O 0.000 claims 7
- 239000003153 chemical reaction reagent Substances 0.000 claims 6
- 239000008194 pharmaceutical composition Substances 0.000 claims 6
- 229940126069 ALK kinase inhibitor Drugs 0.000 claims 5
- 230000001594 aberrant effect Effects 0.000 claims 5
- 230000030279 gene silencing Effects 0.000 claims 4
- 108090000623 proteins and genes Proteins 0.000 claims 4
- 239000003795 chemical substances by application Substances 0.000 claims 3
- 241001465754 Metazoa Species 0.000 claims 2
- 230000009261 transgenic effect Effects 0.000 claims 2
- 230000002159 abnormal effect Effects 0.000 claims 1
- 230000000711 cancerogenic effect Effects 0.000 claims 1
- 231100000315 carcinogenic Toxicity 0.000 claims 1
- 230000004927 fusion Effects 0.000 claims 1
- 239000003112 inhibitor Substances 0.000 claims 1
- 230000002401 inhibitory effect Effects 0.000 claims 1
- 235000018102 proteins Nutrition 0.000 claims 1
- 102000004169 proteins and genes Human genes 0.000 claims 1
- 230000008685 targeting Effects 0.000 claims 1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US12/761,050 | 2010-04-15 | ||
| US12/761,050 US8383793B2 (en) | 2010-04-15 | 2010-04-15 | Methods and compositions for the diagnosis and treatment of cancer resistant to anaplastic lymphoma kinase (ALK) kinase inhibitors |
| PCT/US2011/032204 WO2011130340A1 (en) | 2010-04-15 | 2011-04-13 | Methods and compositions for the diagnosis and treatment of cancer resistant to anaplastic lymphoma kinase (alk) kinase inhibitors |
Related Child Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2016195911A Division JP2017018141A (ja) | 2010-04-15 | 2016-10-03 | 未分化リンパ腫キナーゼ(alk)キナーゼ阻害剤に耐性である癌の診断および治療のための方法および組成物 |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2013534804A JP2013534804A (ja) | 2013-09-09 |
| JP2013534804A5 true JP2013534804A5 (enExample) | 2014-05-29 |
| JP6223822B2 JP6223822B2 (ja) | 2017-11-01 |
Family
ID=44314994
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2013505074A Expired - Fee Related JP6223822B2 (ja) | 2010-04-15 | 2011-04-13 | 未分化リンパ腫キナーゼ(alk)キナーゼ阻害剤に耐性である癌の診断および治療のための方法および組成物 |
| JP2016195911A Pending JP2017018141A (ja) | 2010-04-15 | 2016-10-03 | 未分化リンパ腫キナーゼ(alk)キナーゼ阻害剤に耐性である癌の診断および治療のための方法および組成物 |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2016195911A Pending JP2017018141A (ja) | 2010-04-15 | 2016-10-03 | 未分化リンパ腫キナーゼ(alk)キナーゼ阻害剤に耐性である癌の診断および治療のための方法および組成物 |
Country Status (10)
| Country | Link |
|---|---|
| US (2) | US8383793B2 (enExample) |
| EP (1) | EP2558490B1 (enExample) |
| JP (2) | JP6223822B2 (enExample) |
| KR (1) | KR20130064067A (enExample) |
| CN (1) | CN103201286B (enExample) |
| AU (1) | AU2011240636B2 (enExample) |
| BR (1) | BR112012026239A2 (enExample) |
| CA (1) | CA2796306A1 (enExample) |
| RU (1) | RU2012148450A (enExample) |
| WO (1) | WO2011130340A1 (enExample) |
Families Citing this family (33)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20110206691A1 (en) * | 2008-02-15 | 2011-08-25 | Mosse Yael P | Methods and Compositions for Treating Neuroblastoma |
| WO2009103061A2 (en) * | 2008-02-15 | 2009-08-20 | The Children's Hospital Of Philadelphia | Methods and compositions for identifying, diagnosing, and treating neuroblastoma |
| US9273077B2 (en) | 2008-05-21 | 2016-03-01 | Ariad Pharmaceuticals, Inc. | Phosphorus derivatives as kinase inhibitors |
| PT2300013T (pt) | 2008-05-21 | 2017-10-31 | Ariad Pharma Inc | Derivados de fósforo como inibidores de cinases |
| SI2350075T1 (sl) | 2008-09-22 | 2014-06-30 | Array Biopharma, Inc. | Substituirane imidazo (1,2b)piridazinske spojine kot Trk kinazni inhibitorji |
| SG10201914059WA (en) | 2008-10-22 | 2020-03-30 | Array Biopharma Inc | Substituted pyrazolo[1,5-a]pyrimidine compounds as trk kinase inhibitors |
| AR077468A1 (es) | 2009-07-09 | 2011-08-31 | Array Biopharma Inc | Compuestos de pirazolo (1,5 -a) pirimidina sustituidos como inhibidores de trk- quinasa |
| EP2464954B1 (en) | 2009-08-13 | 2019-06-05 | Teleflex Life Sciences Unlimited Company | Pressure indicator |
| EP2918588B1 (en) | 2010-05-20 | 2017-05-03 | Array Biopharma, Inc. | Macrocyclic compounds as TRK kinase inhibitors |
| US20130288240A1 (en) * | 2010-05-21 | 2013-10-31 | Cell Signaling Technology, Inc. | Alk and ros kinase in cancer |
| US10549054B2 (en) | 2011-02-02 | 2020-02-04 | Teleflex Life Sciences Unlimited Company | Artificial airway |
| EP2704572B1 (en) | 2011-05-04 | 2015-12-30 | Ariad Pharmaceuticals, Inc. | Compounds for inhibiting cell proliferation in egfr-driven cancers |
| EP2822953B9 (en) | 2012-03-06 | 2017-06-21 | Pfizer Inc | Macrocyclic derivatives for the treatment of proliferative diseases |
| AU2013204563B2 (en) | 2012-05-05 | 2016-05-19 | Takeda Pharmaceutical Company Limited | Compounds for inhibiting cell proliferation in EGFR-driven cancers |
| JP6205216B2 (ja) * | 2012-09-24 | 2017-09-27 | アークレイ株式会社 | 変異検出用プローブ、変異検出方法、薬効判定方法及び変異検出用キット |
| US9611283B1 (en) | 2013-04-10 | 2017-04-04 | Ariad Pharmaceuticals, Inc. | Methods for inhibiting cell proliferation in ALK-driven cancers |
| CN104513253A (zh) | 2013-10-01 | 2015-04-15 | 南京波尔泰药业科技有限公司 | 用于治疗增殖性疾病的大环化合物 |
| ES2811927T3 (es) * | 2014-04-10 | 2021-03-15 | Memorial Sloan Kettering Cancer Center | Isoforma novedosa de cinasa de linfoma anaplásico y sus usos |
| US9428812B2 (en) * | 2014-04-28 | 2016-08-30 | Insight Genetics, Inc. | Kit comprising primers for amplifying ALK kinase domain nucleic acids |
| US10799505B2 (en) | 2014-11-16 | 2020-10-13 | Array Biopharma, Inc. | Crystalline form of (S)-N-(5-((R)-2-(2,5-difluorophenyl)-pyrrolidin-1-yl)-pyrazolo[1,5-A]pyrimidin-3-yl)-3-hydroxypyrrolidine-1-carboxamide hydrogen sulfate |
| EP3244927A1 (en) * | 2015-01-16 | 2017-11-22 | Vedantra Pharmaceuticals Inc. | Multilamellar lipid vesicle compositions including a conjugated anaplastic lymphoma kinase (alk) variant and uses thereof |
| EP3303382A4 (en) * | 2015-05-29 | 2018-12-19 | Ignyta, Inc. | Compositions and methods for treating patients with rtk mutant cells |
| JP2018534296A (ja) | 2015-10-26 | 2018-11-22 | ロクソ オンコロジー, インコーポレイテッドLoxo Oncology, Inc. | Trk阻害薬耐性がんにおける点変異およびそれに関連する方法 |
| US10045991B2 (en) | 2016-04-04 | 2018-08-14 | Loxo Oncology, Inc. | Methods of treating pediatric cancers |
| MX386416B (es) | 2016-04-04 | 2025-03-18 | Loxo Oncology Inc | Formulaciones liquidas de (s)-n-(5-((r)-2-(2,5-difluorofenil)-pirrolidin-1-il)-pirazolo[1,5-a]pirimidin-3-il)-3-hidroxipirrolidina-1-carboxamida. |
| HUE063877T2 (hu) | 2016-05-18 | 2024-02-28 | Loxo Oncology Inc | (S)-N-(5-((R)-2-(2,5-dlfluorofenil)pirolidin-1-il)plrazolo[1,5-A]pirimidin-3-il) -3-hidroxipirolidin-1-karboxamid elõállítása |
| CN107885972B (zh) * | 2016-09-30 | 2021-07-27 | 广州华大基因医学检验所有限公司 | 一种基于单端测序的融合基因检测方法及其应用 |
| JOP20190092A1 (ar) | 2016-10-26 | 2019-04-25 | Array Biopharma Inc | عملية لتحضير مركبات بيرازولو[1، 5-a]بيريميدين وأملاح منها |
| JOP20190213A1 (ar) | 2017-03-16 | 2019-09-16 | Array Biopharma Inc | مركبات حلقية ضخمة كمثبطات لكيناز ros1 |
| CN110716042A (zh) * | 2019-10-23 | 2020-01-21 | 郑州大学 | 一种用于卵巢癌早期筛查和诊断的血清蛋白标志物、试剂盒及检测方法 |
| CN111235272B (zh) * | 2020-01-10 | 2023-07-07 | 厦门艾德生物医药科技股份有限公司 | 一次性检测肺癌多重基因突变的组合物及其应用 |
| IL297442A (en) | 2020-04-22 | 2022-12-01 | Iovance Biotherapeutics Inc | Systems and methods for coordinating production of cells for patient-specific immunotherapy |
| CN112391390A (zh) * | 2020-11-19 | 2021-02-23 | 山西大学 | 飞蝗网格蛋白重链基因及其靶向dsRNA的合成与应用 |
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-
2010
- 2010-04-15 US US12/761,050 patent/US8383793B2/en not_active Expired - Fee Related
-
2011
- 2011-04-13 KR KR1020127029988A patent/KR20130064067A/ko not_active Withdrawn
- 2011-04-13 BR BR112012026239A patent/BR112012026239A2/pt not_active IP Right Cessation
- 2011-04-13 EP EP11721840.4A patent/EP2558490B1/en not_active Not-in-force
- 2011-04-13 AU AU2011240636A patent/AU2011240636B2/en not_active Ceased
- 2011-04-13 CN CN201180023776.XA patent/CN103201286B/zh not_active Expired - Fee Related
- 2011-04-13 CA CA2796306A patent/CA2796306A1/en not_active Abandoned
- 2011-04-13 RU RU2012148450/10A patent/RU2012148450A/ru not_active Application Discontinuation
- 2011-04-13 JP JP2013505074A patent/JP6223822B2/ja not_active Expired - Fee Related
- 2011-04-13 WO PCT/US2011/032204 patent/WO2011130340A1/en not_active Ceased
-
2013
- 2013-02-20 US US13/771,948 patent/US9458508B2/en not_active Expired - Fee Related
-
2016
- 2016-10-03 JP JP2016195911A patent/JP2017018141A/ja active Pending
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