JP2013544846A5 - - Google Patents
Download PDFInfo
- Publication number
- JP2013544846A5 JP2013544846A5 JP2013542201A JP2013542201A JP2013544846A5 JP 2013544846 A5 JP2013544846 A5 JP 2013544846A5 JP 2013542201 A JP2013542201 A JP 2013542201A JP 2013542201 A JP2013542201 A JP 2013542201A JP 2013544846 A5 JP2013544846 A5 JP 2013544846A5
- Authority
- JP
- Japan
- Prior art keywords
- alkyl
- halo
- cycloalkyl
- alkoxyl
- alkylamino
- 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
- 125000005843 halogen group Chemical group 0.000 claims 18
- 150000001875 compounds Chemical class 0.000 claims 17
- 125000006552 (C3-C8) cycloalkyl group Chemical group 0.000 claims 16
- 125000003118 aryl group Chemical group 0.000 claims 13
- 125000000592 heterocycloalkyl group Chemical group 0.000 claims 12
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 11
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 claims 10
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims 10
- GBXQPDCOMJJCMJ-UHFFFAOYSA-M trimethyl-[6-(trimethylazaniumyl)hexyl]azanium;bromide Chemical compound [Br-].C[N+](C)(C)CCCCCC[N+](C)(C)C GBXQPDCOMJJCMJ-UHFFFAOYSA-M 0.000 claims 10
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims 9
- 125000004093 cyano group Chemical group *C#N 0.000 claims 9
- -1 cyano, hydroxyl Chemical group 0.000 claims 9
- 125000006570 (C5-C6) heteroaryl group Chemical group 0.000 claims 8
- 125000003601 C2-C6 alkynyl group Chemical group 0.000 claims 8
- 125000001424 substituent group Chemical group 0.000 claims 8
- 239000000203 mixture Substances 0.000 claims 5
- 238000000034 method Methods 0.000 claims 4
- 125000001313 C5-C10 heteroaryl group Chemical group 0.000 claims 3
- 208000032839 leukemia Diseases 0.000 claims 3
- 230000001404 mediated effect Effects 0.000 claims 3
- 125000006568 (C4-C7) heterocycloalkyl group Chemical group 0.000 claims 2
- 125000000753 cycloalkyl group Chemical group 0.000 claims 2
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims 2
- 239000003937 drug carrier Substances 0.000 claims 2
- 229910052757 nitrogen Inorganic materials 0.000 claims 2
- 125000004433 nitrogen atom Chemical group N* 0.000 claims 2
- 239000008194 pharmaceutical composition Substances 0.000 claims 2
- 150000003839 salts Chemical class 0.000 claims 2
- 238000002560 therapeutic procedure Methods 0.000 claims 2
- 125000004739 (C1-C6) alkylsulfonyl group Chemical group 0.000 claims 1
- 208000024893 Acute lymphoblastic leukemia Diseases 0.000 claims 1
- 208000014697 Acute lymphocytic leukaemia Diseases 0.000 claims 1
- 208000031261 Acute myeloid leukaemia Diseases 0.000 claims 1
- 102100039489 Histone-lysine N-methyltransferase, H3 lysine-79 specific Human genes 0.000 claims 1
- 101000963360 Homo sapiens Histone-lysine N-methyltransferase, H3 lysine-79 specific Proteins 0.000 claims 1
- 208000033776 Myeloid Acute Leukemia Diseases 0.000 claims 1
- 150000001204 N-oxides Chemical class 0.000 claims 1
- 206010028980 Neoplasm Diseases 0.000 claims 1
- 208000006664 Precursor Cell Lymphoblastic Leukemia-Lymphoma Diseases 0.000 claims 1
- 201000011510 cancer Diseases 0.000 claims 1
- 229910052799 carbon Inorganic materials 0.000 claims 1
- 210000000349 chromosome Anatomy 0.000 claims 1
- 201000005787 hematologic cancer Diseases 0.000 claims 1
- 208000024200 hematopoietic and lymphoid system neoplasm Diseases 0.000 claims 1
- 125000001072 heteroaryl group Chemical group 0.000 claims 1
- 125000005842 heteroatom Chemical group 0.000 claims 1
- 229910052739 hydrogen Inorganic materials 0.000 claims 1
- 125000003566 oxetanyl group Chemical group 0.000 claims 1
- 229910052760 oxygen Inorganic materials 0.000 claims 1
- 230000019639 protein methylation Effects 0.000 claims 1
- 108090000623 proteins and genes Proteins 0.000 claims 1
- 229910052717 sulfur Inorganic materials 0.000 claims 1
- 230000005945 translocation Effects 0.000 claims 1
- LXFOLMYKSYSZQS-LURJZOHASA-N CC(C)N(C[C@H]([C@H]([C@H]1O)O)O[C@H]1[n]1c(ncnc2N)c2nc1)[C@H]1C[C@@H](CCc2nc3cc(C(C)(C)C)ccc3[nH]2)C1 Chemical compound CC(C)N(C[C@H]([C@H]([C@H]1O)O)O[C@H]1[n]1c(ncnc2N)c2nc1)[C@H]1C[C@@H](CCc2nc3cc(C(C)(C)C)ccc3[nH]2)C1 LXFOLMYKSYSZQS-LURJZOHASA-N 0.000 description 1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US41966110P | 2010-12-03 | 2010-12-03 | |
| US61/419,661 | 2010-12-03 | ||
| PCT/US2011/063044 WO2012075381A1 (en) | 2010-12-03 | 2011-12-02 | Substituted purine and 7 - deazapurine compounds as modulators of epigenetic enzymes |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2013544846A JP2013544846A (ja) | 2013-12-19 |
| JP2013544846A5 true JP2013544846A5 (https=) | 2015-01-15 |
| JP5931905B2 JP5931905B2 (ja) | 2016-06-08 |
Family
ID=45444712
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2013542201A Expired - Fee Related JP5931905B2 (ja) | 2010-12-03 | 2011-12-02 | 置換プリン及び７‐デアザプリン化合物 |
Country Status (18)
| Country | Link |
|---|---|
| US (5) | US8580762B2 (https=) |
| EP (1) | EP2646444B1 (https=) |
| JP (1) | JP5931905B2 (https=) |
| KR (1) | KR101923746B1 (https=) |
| CN (1) | CN103391939B (https=) |
| AR (1) | AR084408A1 (https=) |
| AU (1) | AU2011336415B2 (https=) |
| BR (1) | BR112013013659B8 (https=) |
| CA (1) | CA2819648C (https=) |
| DK (1) | DK2646444T3 (https=) |
| ES (1) | ES2577027T3 (https=) |
| HR (1) | HRP20160655T1 (https=) |
| IL (1) | IL226651A (https=) |
| MX (1) | MX2013006251A (https=) |
| RU (1) | RU2606514C2 (https=) |
| SI (1) | SI2646444T1 (https=) |
| TW (1) | TWI537271B (https=) |
| WO (1) | WO2012075381A1 (https=) |
Families Citing this family (57)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CA2819734A1 (en) | 2010-12-03 | 2012-06-07 | Epizyme, Inc. | Carbocycle-substituted purine and 7-deazapurine compounds |
| EP2646455A4 (en) | 2010-12-03 | 2014-04-02 | Epizyme Inc | Modulators of histone methyltransferase, and methods of use thereof |
| WO2012075381A1 (en) * | 2010-12-03 | 2012-06-07 | Epizyme, Inc. | Substituted purine and 7 - deazapurine compounds as modulators of epigenetic enzymes |
| US9145438B2 (en) | 2010-12-03 | 2015-09-29 | Epizyme, Inc. | 7-deazapurine modulators of histone methyltransferase, and methods of use thereof |
| WO2013055397A1 (en) | 2011-10-14 | 2013-04-18 | Children's Medical Center Corporation | Inhibition and enhancement of reprogramming by chromatin modifying enzymes |
| SG10201913554YA (en) | 2011-12-22 | 2020-03-30 | Alios Biopharma Inc | Substituted nucleosides, nucleotides and analogs thereof |
| USRE48171E1 (en) | 2012-03-21 | 2020-08-25 | Janssen Biopharma, Inc. | Substituted nucleosides, nucleotides and analogs thereof |
| US9441007B2 (en) | 2012-03-21 | 2016-09-13 | Alios Biopharma, Inc. | Substituted nucleosides, nucleotides and analogs thereof |
| WO2014026198A1 (en) | 2012-08-10 | 2014-02-13 | Epizyme, Inc. | Inhibitors of protein methyltransferase dot1l and methods of use thereof |
| US9597348B2 (en) * | 2012-09-06 | 2017-03-21 | Epizyme, Inc. | Method of treating leukemia |
| CA2894220A1 (en) * | 2012-12-21 | 2014-06-26 | Epizyme, Inc. | Dot1l inhibitors for use in the treatment of leukemia |
| GEP201606600B (en) | 2013-02-22 | 2017-01-10 | Pfizer | Pyrrolo [2, 3 -d]pyrimidine derivatives as inhibitors of janus- related kinases (jak) |
| WO2014153172A1 (en) | 2013-03-14 | 2014-09-25 | Epizyme, Inc. | Pyrazole derivatives as prmt1 inhibitors and uses thereof |
| US9446064B2 (en) * | 2013-03-14 | 2016-09-20 | Epizyme, Inc. | Combination therapy for treating cancer |
| EP2970137A1 (en) | 2013-03-14 | 2016-01-20 | Epizyme, Inc. | Pyrazole derivatives as arginine methyltransferase inhibitors and uses thereof |
| JP2016517434A (ja) * | 2013-03-14 | 2016-06-16 | エピザイム，インコーポレイティド | 癌を処置するための併用療法 |
| WO2014153100A2 (en) | 2013-03-14 | 2014-09-25 | Epizyme, Inc. | Arginine methyltransferase inhibitors and uses thereof |
| WO2014152261A1 (en) * | 2013-03-14 | 2014-09-25 | Epizyme, Inc. | Substituted 7-deazapurine compounds |
| JP2016518336A (ja) | 2013-03-14 | 2016-06-23 | エピザイム，インコーポレイティド | Ｐｒｍｔ１阻害剤としてのピラゾール誘導体およびその使用 |
| US9120757B2 (en) | 2013-03-14 | 2015-09-01 | Epizyme, Inc. | Arginine methyltransferase inhibitors and uses thereof |
| KR102028793B1 (ko) | 2013-03-14 | 2019-10-07 | 에피자임, 인코포레이티드 | 아르기닌 메틸기 전이효소 억제제 및 이의 용도 |
| WO2014153208A1 (en) | 2013-03-14 | 2014-09-25 | Epizyme, Inc. | Arginine methyltransferase inhibitors and uses thereof |
| WO2014153214A1 (en) | 2013-03-14 | 2014-09-25 | Epizyme, Inc. | Arginine methyl transferase inhibtors and uses thereof |
| US9765035B2 (en) | 2013-03-14 | 2017-09-19 | Epizyme, Inc. | Arginine methyltransferase inhibitors and uses thereof |
| EP2970135B1 (en) | 2013-03-14 | 2018-07-18 | Epizyme, Inc. | Pyrazole derivatives as prmt1 inhibitors and uses thereof |
| JP2016517426A (ja) * | 2013-03-15 | 2016-06-16 | エピザイム，インコーポレイティド | 置換プリン化合物の合成方法 |
| WO2014152562A1 (en) * | 2013-03-15 | 2014-09-25 | Epizyme, Inc. | Injectable formulations for treating cancer |
| US9688714B2 (en) | 2013-07-03 | 2017-06-27 | Epizyme, Inc. | Substituted purine compounds |
| EP3027195B1 (en) * | 2013-07-29 | 2019-02-06 | Dana-Farber Cancer Institute, Inc. | Dot1l probes |
| AU2014295980B2 (en) | 2013-08-02 | 2020-08-27 | Memorial Sloan-Kettering Cancer Center | Methods for the detection and treatment of leukemias that are responsive to DOT1L inhibition |
| US10143704B2 (en) * | 2013-11-13 | 2018-12-04 | Epizyme, Inc. | Methods for treating cancer |
| US20170198006A1 (en) * | 2014-06-25 | 2017-07-13 | Epizyme, Inc. | Prmt5 inhibitors and uses thereof |
| WO2016024185A1 (en) | 2014-08-12 | 2016-02-18 | Pfizer Inc. | Pyrrolo[2,3-d]pyrimidine derivatives useful for inhibiting janus kinase |
| AU2015301746A1 (en) * | 2014-08-13 | 2017-02-16 | Celgene Corporation | Combination therapy for treating cancer |
| US9458165B2 (en) | 2014-08-27 | 2016-10-04 | Dana-Farber Cancer Institute, Inc. | DOT1L inhibitors |
| WO2016044649A1 (en) * | 2014-09-17 | 2016-03-24 | Epizyme, Inc. | Injectable formulations for treating cancer |
| EP3193884A4 (en) * | 2014-09-17 | 2018-06-20 | Epizyme, Inc. | Combination therapy for treating cancer |
| EP3200826B1 (en) * | 2014-09-30 | 2021-04-21 | Vecht-lifshitz, Susan Eve | Pharmaceutical compositions for treating ebola virus disease |
| WO2016123626A1 (en) * | 2015-01-30 | 2016-08-04 | Epizyme, Inc. | Combination therapy for treating cancer |
| US11453697B1 (en) | 2015-08-13 | 2022-09-27 | Merck Sharp & Dohme Llc | Cyclic di-nucleotide compounds as sting agonists |
| US10869868B2 (en) | 2016-01-26 | 2020-12-22 | Memorial Sloan Kettering Cancer Center | Targeting chromatin regulators inhibits leukemogenic gene expression in NPM1 mutant leukemia |
| ES3057783T3 (en) | 2016-03-15 | 2026-03-04 | Oryzon Genomics Sa | Combinations of lsd1 inhibitors for use in the treatment of neoplastic diseases |
| CA3017408C (en) | 2016-03-15 | 2025-08-19 | Oryzon Genomics, S.A. | LSD1 INHIBITOR COMBINATIONS FOR THE TREATMENT OF HEMATOLOGICAL MALIGNITIS |
| CN106432095B (zh) * | 2016-09-09 | 2019-04-16 | 东南大学 | 匹莫苯丹关键中间体6-(3,4-二氨基苯基)-5-甲基-4,5-二氢哒嗪-3(2h)-酮的制备 |
| WO2018175746A1 (en) | 2017-03-24 | 2018-09-27 | Kura Oncology, Inc. | Methods for treating hematological malignancies and ewing's sarcoma |
| CN109748944B (zh) * | 2017-11-03 | 2021-12-10 | 中国科学院上海药物研究所 | 5’-脱氧-5’-异丙基取代氨基核苷类化合物、其制备方法和用途 |
| CN109748943A (zh) * | 2017-11-03 | 2019-05-14 | 中国科学院上海药物研究所 | 2’-c-甲基取代核苷类化合物及其制备与用途 |
| JP2021505583A (ja) * | 2017-12-05 | 2021-02-18 | エンジェクス ファーマシューティカル インコーポレイテッド | Ｐｍｒｔ５阻害剤としての複素環式化合物 |
| KR102118891B1 (ko) | 2018-10-04 | 2020-06-04 | 성균관대학교산학협력단 | 매소니아노사이드 b를 유효성분으로 포함하는 혼합 직계성 백혈병 유전자 재배열 동반 백혈병 예방 및 치료용 약학적 조성물 |
| CA3126141A1 (en) | 2019-01-09 | 2020-07-16 | Dana-Farber Cancer Institute, Inc. | Dot1l degraders and uses thereof |
| BR112021017831A2 (pt) * | 2019-03-11 | 2021-11-30 | Collaborative Medicinal Dev Llc | Derivados heteroaromáticos e aromáticos heterobicíclicos para o tratamento de distúrbios relacionados com ferroptose |
| CN110092804A (zh) * | 2019-03-29 | 2019-08-06 | 广州盈升生物科技有限公司 | 一种含双环基团的嘌呤化合物及其制备方法 |
| MA55556A (fr) | 2019-04-02 | 2022-02-09 | Aligos Therapeutics Inc | Composés ciblant prmt5 |
| CN113024620B (zh) * | 2021-03-11 | 2023-02-28 | 沈阳药科大学 | 一种嘌呤衍生物及其制备方法和用途 |
| WO2022271540A1 (en) * | 2021-06-21 | 2022-12-29 | Mayo Foundation For Medical Education And Research | Inhibitors of dot1l |
| CA3226162A1 (en) | 2021-07-09 | 2023-01-12 | Plexium, Inc. | Aryl compounds and pharmaceutical compositions that modulate ikzf2 |
| US20240335438A1 (en) * | 2021-07-19 | 2024-10-10 | Dana-Farber Cancer Institute, Inc. | Targeting dot1l and smarca4/2 for the treatment of mllr leukemia |
Family Cites Families (41)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4522811A (en) | 1982-07-08 | 1985-06-11 | Syntex (U.S.A.) Inc. | Serial injection of muramyldipeptides and liposomes enhances the anti-infective activity of muramyldipeptides |
| US5763263A (en) | 1995-11-27 | 1998-06-09 | Dehlinger; Peter J. | Method and apparatus for producing position addressable combinatorial libraries |
| US20020127598A1 (en) | 2000-03-27 | 2002-09-12 | Wenqiang Zhou | Solution-phase combinatorial library synthesis and pharmaceutically active compounds produced thereby |
| EP1138689A1 (en) | 2000-03-28 | 2001-10-04 | Roche Diagnostics GmbH | N8- and C8-linked purine bases as universal nucleosides used for oligonucleotide hybridization |
| EP1138688A1 (en) | 2000-03-28 | 2001-10-04 | Roche Diagnostics GmbH | N8- and C8- linked purine bases as universal nucleosides used for oligonucleotide hybridization |
| US6534651B2 (en) | 2000-04-06 | 2003-03-18 | Inotek Pharmaceuticals Corp. | 7-Substituted isoindolinone inhibitors of inflammation and reperfusion injury and methods of use thereof |
| US20040043959A1 (en) | 2002-03-04 | 2004-03-04 | Bloom Laura A. | Combination therapies for treating methylthioadenosine phosphorylase deficient cells |
| EP1556399A4 (en) * | 2002-07-16 | 2007-09-26 | Merck & Co Inc | Nucleoside derivatives as inhibitors of RNA-dependent viral RNA polymerase |
| AU2002951247A0 (en) | 2002-09-06 | 2002-09-19 | Alchemia Limited | Compounds that interact with kinases |
| EP1572097A4 (en) | 2002-09-30 | 2010-02-17 | Smithkline Beecham Corp | NUCLEOSIDE DERIVATIVES FOR THE TREATMENT OF INFECTIONS WITH THE HEPATITIS C-VIRUS |
| GB0301450D0 (en) * | 2003-01-22 | 2003-02-19 | Medical Res Council | Protein crystal structure |
| PL1697394T3 (pl) * | 2003-12-19 | 2007-08-31 | Hoffmann La Roche | Inhibitory COMT |
| AU2005267706B2 (en) | 2004-08-02 | 2011-12-08 | University Of Virginia Patent Foundation | 2-propynyl adenosine analogs with modified 5'-ribose groups having A2A agonist activity |
| US7576069B2 (en) | 2004-08-02 | 2009-08-18 | University Of Virginia Patent Foundation | 2-polycyclic propynyl adenosine analogs having A2A agonist activity |
| US8058762B2 (en) * | 2005-01-19 | 2011-11-15 | Daikin Industries, Ltd. | Rotor, axial gap type motor, method of driving motor, and compressor |
| WO2006078752A2 (en) | 2005-01-21 | 2006-07-27 | Methylgene, Inc. | Inhibitors of dna methyltransferase |
| PT1848718E (pt) | 2005-02-04 | 2012-10-11 | Millennium Pharm Inc | Inibidores de enzimas de activação e1 |
| US20060235037A1 (en) | 2005-04-15 | 2006-10-19 | Purandare Ashok V | Heterocyclic inhibitors of protein arginine methyl transferases |
| WO2006113615A2 (en) | 2005-04-15 | 2006-10-26 | Sloan-Kettering Institute For Cancer Research | Anti-microbial agents and uses thereof |
| KR101450535B1 (ko) | 2006-02-02 | 2014-10-14 | 밀레니엄 파머슈티컬스 인코퍼레이티드 | Ｅ１ 활성화 효소의 억제제 |
| AU2006339445A1 (en) | 2006-03-02 | 2007-09-07 | Agency For Science, Technology And Research | Methods for cancer therapy and stem cell modulation |
| GB0607953D0 (en) | 2006-04-21 | 2006-05-31 | Novartis Ag | Organic compounds |
| US8188063B2 (en) | 2006-06-19 | 2012-05-29 | University Of Virginia Patent Foundation | Use of adenosine A2A modulators to treat spinal cord injury |
| US20080132525A1 (en) | 2006-12-04 | 2008-06-05 | Methylgene Inc. | Inhibitors of DNA Methyltransferase |
| US20080312160A1 (en) | 2007-04-09 | 2008-12-18 | Guerrant Richard L | Method of treating enteritis, intestinal damage, and diarrhea from c. difficile with an a2a adenosine receptor agonist |
| CN101417967A (zh) | 2007-10-26 | 2009-04-29 | 浙江海正药业股份有限公司 | 组蛋白去乙酰酶抑制剂、其组合物及其应用 |
| CN101910150B (zh) | 2007-11-05 | 2013-09-18 | 诺瓦提斯公司 | 作为cetp抑制剂、可用于治疗疾病如高脂血症或动脉硬化的4-苄基氨基-1-羧基酰基哌啶衍生物 |
| CN101938904A (zh) | 2008-01-09 | 2011-01-05 | PGx健康有限责任公司 | 用a2ar激动剂鞘内治疗神经性疼痛 |
| AR072906A1 (es) | 2008-08-06 | 2010-09-29 | Novartis Ag | Nucleosidos modificados utiles como antivirales |
| JPWO2010027005A1 (ja) | 2008-09-05 | 2012-02-02 | 壽製薬株式会社 | 置換アミン誘導体及びこれを有効成分とする医薬組成物 |
| WO2010048149A2 (en) | 2008-10-20 | 2010-04-29 | Kalypsys, Inc. | Heterocyclic modulators of gpr119 for treatment of disease |
| IN2012DN01983A (https=) * | 2009-08-24 | 2015-07-24 | Ascepion Pharmaceuticals Inc | |
| WO2012075381A1 (en) * | 2010-12-03 | 2012-06-07 | Epizyme, Inc. | Substituted purine and 7 - deazapurine compounds as modulators of epigenetic enzymes |
| EP2646455A4 (en) | 2010-12-03 | 2014-04-02 | Epizyme Inc | Modulators of histone methyltransferase, and methods of use thereof |
| US9145438B2 (en) | 2010-12-03 | 2015-09-29 | Epizyme, Inc. | 7-deazapurine modulators of histone methyltransferase, and methods of use thereof |
| CA2819734A1 (en) | 2010-12-03 | 2012-06-07 | Epizyme, Inc. | Carbocycle-substituted purine and 7-deazapurine compounds |
| US9597348B2 (en) * | 2012-09-06 | 2017-03-21 | Epizyme, Inc. | Method of treating leukemia |
| US9446064B2 (en) * | 2013-03-14 | 2016-09-20 | Epizyme, Inc. | Combination therapy for treating cancer |
| JP2016517426A (ja) | 2013-03-15 | 2016-06-16 | エピザイム，インコーポレイティド | 置換プリン化合物の合成方法 |
| AU2014295980B2 (en) * | 2013-08-02 | 2020-08-27 | Memorial Sloan-Kettering Cancer Center | Methods for the detection and treatment of leukemias that are responsive to DOT1L inhibition |
| US10143704B2 (en) * | 2013-11-13 | 2018-12-04 | Epizyme, Inc. | Methods for treating cancer |
-
2011
- 2011-12-02 WO PCT/US2011/063044 patent/WO2012075381A1/en not_active Ceased
- 2011-12-02 RU RU2013130250A patent/RU2606514C2/ru active
- 2011-12-02 MX MX2013006251A patent/MX2013006251A/es active IP Right Grant
- 2011-12-02 EP EP11804836.2A patent/EP2646444B1/en active Active
- 2011-12-02 ES ES11804836.2T patent/ES2577027T3/es active Active
- 2011-12-02 BR BR112013013659A patent/BR112013013659B8/pt not_active IP Right Cessation
- 2011-12-02 SI SI201130856A patent/SI2646444T1/sl unknown
- 2011-12-02 US US13/310,157 patent/US8580762B2/en not_active Expired - Fee Related
- 2011-12-02 KR KR1020137017337A patent/KR101923746B1/ko not_active Expired - Fee Related
- 2011-12-02 DK DK11804836.2T patent/DK2646444T3/da active
- 2011-12-02 HR HRP20160655TT patent/HRP20160655T1/hr unknown
- 2011-12-02 CN CN201180066760.7A patent/CN103391939B/zh not_active Expired - Fee Related
- 2011-12-02 JP JP2013542201A patent/JP5931905B2/ja not_active Expired - Fee Related
- 2011-12-02 CA CA2819648A patent/CA2819648C/en active Active
- 2011-12-02 AU AU2011336415A patent/AU2011336415B2/en not_active Ceased
- 2011-12-05 TW TW100144669A patent/TWI537271B/zh not_active IP Right Cessation
- 2011-12-05 AR ARP110104537A patent/AR084408A1/es active IP Right Grant
-
2013
- 2013-05-30 IL IL226651A patent/IL226651A/en active IP Right Grant
- 2013-10-16 US US14/055,510 patent/US9096634B2/en active Active
-
2015
- 2015-06-26 US US14/752,023 patent/US20150366893A1/en not_active Abandoned
-
2017
- 2017-11-03 US US15/802,979 patent/US20180280422A1/en not_active Abandoned
-
2020
- 2020-06-10 US US16/897,690 patent/US20210252035A1/en not_active Abandoned
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| JP2013544846A5 (https=) | ||
| RU2013130250A (ru) | Замещенные пуриновые и 7-деазапуриновые соединения | |
| JP2017526677A5 (https=) | ||
| JP2013522292A5 (https=) | ||
| JP2018504378A5 (https=) | ||
| JP2018504379A5 (https=) | ||
| JP2015509098A5 (https=) | ||
| JP2016523974A5 (https=) | ||
| JP2021523159A5 (https=) | ||
| JP2018517746A5 (https=) | ||
| JP2019537570A5 (https=) | ||
| JP2016506962A5 (https=) | ||
| JP2017536344A5 (https=) | ||
| JP2013537203A5 (https=) | ||
| JP2016506960A5 (https=) | ||
| JP2016503414A5 (https=) | ||
| RU2013109132A (ru) | Химические соединения | |
| JP2018511590A5 (https=) | ||
| RU2012151012A (ru) | Циклопропиловые дикарбоксамиды и аналоги, обладающие противораковым и антипролиферативным действием | |
| JP2017525730A5 (https=) | ||
| JP2018507197A5 (https=) | ||
| JP2012153722A5 (https=) | ||
| JP2013525458A5 (https=) | ||
| RU2015118647A (ru) | Аминопиримидиновые соединения в качестве ингибиторов содержащих т790м мутантных egfr | |
| JP2017511321A5 (https=) |