JP5802676B2 - Ck2阻害剤としてのピラゾロピリミジンおよび関連複素環化合物 - Google Patents
Ck2阻害剤としてのピラゾロピリミジンおよび関連複素環化合物 Download PDFInfo
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- JP5802676B2 JP5802676B2 JP2012542060A JP2012542060A JP5802676B2 JP 5802676 B2 JP5802676 B2 JP 5802676B2 JP 2012542060 A JP2012542060 A JP 2012542060A JP 2012542060 A JP2012542060 A JP 2012542060A JP 5802676 B2 JP5802676 B2 JP 5802676B2
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- 0 CCCCCCICC(C)C(*)**(*C(C)N)C(C(C)C)C(*)NI Chemical compound CCCCCCICC(C)C(*)**(*C(C)N)C(C(C)C)C(*)NI 0.000 description 25
- KPIGTOBEYDEFHW-NHDPSOOVSA-N C=C1NC2OC2N/C1=C\c(cn[n]1c(NCC2(CN3CCCC3)CC2)c2)c1nc2Nc1cccc(Cl)c1 Chemical compound C=C1NC2OC2N/C1=C\c(cn[n]1c(NCC2(CN3CCCC3)CC2)c2)c1nc2Nc1cccc(Cl)c1 KPIGTOBEYDEFHW-NHDPSOOVSA-N 0.000 description 1
- WEZJDTIOVDYLCA-UHFFFAOYSA-N CC(C)C(C)CCN Chemical compound CC(C)C(C)CCN WEZJDTIOVDYLCA-UHFFFAOYSA-N 0.000 description 1
- BTGXNWANKBSFRW-UHFFFAOYSA-N CC(C1)(C2C3C4)C2C4C3C1C=C Chemical compound CC(C1)(C2C3C4)C2C4C3C1C=C BTGXNWANKBSFRW-UHFFFAOYSA-N 0.000 description 1
- CRMGTMDZHPSVIF-IUXPMGMMSA-N CC(C=C)Nc1cc(-c2cccc(CO)c2)nc2c(/C=C(/C(N3)=O)\NC3=O)cn[n]12 Chemical compound CC(C=C)Nc1cc(-c2cccc(CO)c2)nc2c(/C=C(/C(N3)=O)\NC3=O)cn[n]12 CRMGTMDZHPSVIF-IUXPMGMMSA-N 0.000 description 1
- SNGBPSQAUOVPHC-UHFFFAOYSA-N CCC(CC)CC(C)CCCN Chemical compound CCC(CC)CC(C)CCCN SNGBPSQAUOVPHC-UHFFFAOYSA-N 0.000 description 1
- YULCLPOCSKDUBP-JAIQZWGSSA-N CN1CCN(CC2(CNc3cc(NC(C4)=CC=CC4Cl)nc4c(/C=C(/C(N5)=O)\NC5=O)cn[n]34)CC2)CC1 Chemical compound CN1CCN(CC2(CNc3cc(NC(C4)=CC=CC4Cl)nc4c(/C=C(/C(N5)=O)\NC5=O)cn[n]34)CC2)CC1 YULCLPOCSKDUBP-JAIQZWGSSA-N 0.000 description 1
- RIRARCHMRDHZAR-PKPIPKONSA-N C[C@@H]1C(C)CCC1 Chemical compound C[C@@H]1C(C)CCC1 RIRARCHMRDHZAR-PKPIPKONSA-N 0.000 description 1
- BTRQSBOYOIKTSH-ACAGNQJTSA-N O=C(/C(/S1)=C/c(cn[n]2c(NC3CC3)c3)c2nc3-c2cc(F)ncc2)NC1=S Chemical compound O=C(/C(/S1)=C/c(cn[n]2c(NC3CC3)c3)c2nc3-c2cc(F)ncc2)NC1=S BTRQSBOYOIKTSH-ACAGNQJTSA-N 0.000 description 1
- REDYAYDTOMHCMU-IUXPMGMMSA-N OC(C1CCNCC1)Nc1cc(Nc2cccc(Cl)c2)nc2c(/C=C(/CN3)\NC3O)cn[n]12 Chemical compound OC(C1CCNCC1)Nc1cc(Nc2cccc(Cl)c2)nc2c(/C=C(/CN3)\NC3O)cn[n]12 REDYAYDTOMHCMU-IUXPMGMMSA-N 0.000 description 1
- DVGNWBWHPCGJRN-UHFFFAOYSA-N OCc1cccc(-c2nc3c(C=O)cn[n]3c(NC3CC3)c2)c1 Chemical compound OCc1cccc(-c2nc3c(C=O)cn[n]3c(NC3CC3)c2)c1 DVGNWBWHPCGJRN-UHFFFAOYSA-N 0.000 description 1
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- 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
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- 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
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- A61K31/535—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one oxygen as the ring hetero atoms, e.g. 1,2-oxazines
- A61K31/5375—1,4-Oxazines, e.g. morpholine
- A61K31/5377—1,4-Oxazines, e.g. morpholine not condensed and containing further heterocyclic rings, e.g. timolol
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- A61K31/553—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole having at least one nitrogen and one oxygen as ring hetero atoms, e.g. loxapine, staurosporine
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- 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
- C07D403/02—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 two hetero rings
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- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Veterinary Medicine (AREA)
- Life Sciences & Earth Sciences (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- Organic Chemistry (AREA)
- Epidemiology (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Biomedical Technology (AREA)
- Neurology (AREA)
- Neurosurgery (AREA)
- Oncology (AREA)
- Immunology (AREA)
- Cardiology (AREA)
- Heart & Thoracic Surgery (AREA)
- Vascular Medicine (AREA)
- Communicable Diseases (AREA)
- Rheumatology (AREA)
- Hospice & Palliative Care (AREA)
- Psychiatry (AREA)
- Hematology (AREA)
- Pain & Pain Management (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Peptides Or Proteins (AREA)
Applications Claiming Priority (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US26680109P | 2009-12-04 | 2009-12-04 | |
| US61/266,801 | 2009-12-04 | ||
| US35416510P | 2010-06-11 | 2010-06-11 | |
| US61/354,165 | 2010-06-11 | ||
| PCT/US2010/056712 WO2011068667A1 (en) | 2009-12-04 | 2010-11-15 | Pyrazolopyrimidines and related heterocycles as ck2 inhibitors |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2013512903A JP2013512903A (ja) | 2013-04-18 |
| JP2013512903A5 JP2013512903A5 (enExample) | 2013-12-19 |
| JP5802676B2 true JP5802676B2 (ja) | 2015-10-28 |
Family
ID=44115232
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2012542060A Active JP5802676B2 (ja) | 2009-12-04 | 2010-11-15 | Ck2阻害剤としてのピラゾロピリミジンおよび関連複素環化合物 |
Country Status (14)
| Country | Link |
|---|---|
| US (2) | US8575177B2 (enExample) |
| EP (1) | EP2509602B9 (enExample) |
| JP (1) | JP5802676B2 (enExample) |
| KR (1) | KR101851130B1 (enExample) |
| CN (1) | CN102762208A (enExample) |
| AU (1) | AU2010326268B2 (enExample) |
| BR (1) | BR112012013508A2 (enExample) |
| CA (1) | CA2782684C (enExample) |
| ES (1) | ES2629170T3 (enExample) |
| IL (1) | IL220086B (enExample) |
| PL (1) | PL2509602T3 (enExample) |
| RU (1) | RU2607453C2 (enExample) |
| SG (1) | SG181507A1 (enExample) |
| WO (1) | WO2011068667A1 (enExample) |
Families Citing this family (54)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CA2801031A1 (en) * | 2010-06-01 | 2011-12-08 | Bayer Intellectual Property Gmbh | Substituted imidazopyrazines |
| NZ736048A (en) | 2010-06-03 | 2019-09-27 | Pharmacyclics Llc | The use of inhibitors of bruton’s tyrosine kinase (btk) |
| WO2012170827A2 (en) * | 2011-06-08 | 2012-12-13 | Cylene Pharmaceuticals, Inc. | Pyrazolopyrimidines and related heterocycles as ck2 inhibitors |
| EP2723746A1 (en) | 2011-06-22 | 2014-04-30 | Vertex Pharmaceuticals Inc. | Compounds useful as inhibitors of atr kinase |
| CN104271786B (zh) * | 2012-04-27 | 2016-07-06 | 新日铁住金株式会社 | 无缝钢管及其制造方法 |
| MX367055B (es) | 2012-06-26 | 2019-08-02 | Del Mar Pharmaceuticals | El uso de una composición que comprende dianhidrogalactitol, diacetildianhidrogalactitol, y dibromodulcitol, y análogos o derivados de cada uno para el tratamiento de malignidades resistentes a inhibidores de tirosina cinasa. |
| TW201414737A (zh) * | 2012-07-13 | 2014-04-16 | 必治妥美雅史谷比公司 | 作爲激酶抑制劑之咪唑并三□甲腈 |
| KR20180088926A (ko) | 2012-07-24 | 2018-08-07 | 파마싸이클릭스 엘엘씨 | 브루톤 티로신 키나제(btk)의 억제제에 대한 내성과 관련된 돌연변이 |
| LT3486245T (lt) | 2012-12-07 | 2021-08-25 | Vertex Pharmaceuticals Incorporated | 2-amino-n-(piperidin-1-il-piridin-3-il)pirazolo[1,5alfa]pirimidin-3-karboksamidas, kaip atr kinazės inhibitorius |
| US9278950B2 (en) | 2013-01-14 | 2016-03-08 | Incyte Corporation | Bicyclic aromatic carboxamide compounds useful as Pim kinase inhibitors |
| AU2014207691B2 (en) | 2013-01-15 | 2018-08-30 | Incyte Holdings Corporation | Thiazolecarboxamides and pyridinecarboxamide compounds useful as Pim kinase inhibitors |
| EP2970288A1 (en) | 2013-03-15 | 2016-01-20 | Vertex Pharmaceuticals Incorporated | Compounds useful as inhibitors of atr kinase |
| JP2016512815A (ja) | 2013-03-15 | 2016-05-09 | バーテックス ファーマシューティカルズ インコーポレイテッドVertex Pharmaceuticals Incorporated | Atrキナーゼの阻害剤として有用な縮合ピラゾロピリミジン誘導体 |
| WO2014143241A1 (en) | 2013-03-15 | 2014-09-18 | Vertex Pharmaceuticals Incorporated | Compounds useful as inhibitors of atr kinase |
| CN105492011A (zh) | 2013-04-08 | 2016-04-13 | 丹尼斯·M·布朗 | 不理想给药化学化合物的治疗增效 |
| CN103360399B (zh) * | 2013-08-02 | 2016-03-02 | 北京大学 | 6-芳基取代-咪唑-[1,2-b]哒嗪类衍生物,其制备方法及用途 |
| WO2015027124A1 (en) | 2013-08-23 | 2015-02-26 | Incyte Corporation | Furo- and thieno-pyridine carboxamide compounds useful as pim kinase inhibitors |
| CN103570728B (zh) * | 2013-11-12 | 2015-12-30 | 山东大学 | 一种取代吡唑并[1,5-a]嘧啶类衍生物及其制备方法与应用 |
| CA2932757C (en) | 2013-12-06 | 2023-10-31 | Vertex Pharmaceuticals Incorporated | 2-amino-6-fluoro-n-[5-fluoro-pyridin-3-yl]pyrazolo[1,5-a]pyrimidin-3-carboxamide compound useful as atr kinase inhibitor, its preparation, different solid forms and radiolabelled derivatives thereof |
| EP3080131B1 (en) * | 2013-12-10 | 2018-10-10 | Bristol-Myers Squibb Company | Imidazopyridazine compounds useful as modulators of il-12, il-23 and/or ifn alpha responses |
| TWI534148B (zh) * | 2014-02-13 | 2016-05-21 | 生華生物科技股份有限公司 | 吡唑並嘧啶前藥及其使用方法 |
| GB201403093D0 (en) | 2014-02-21 | 2014-04-09 | Cancer Rec Tech Ltd | Therapeutic compounds and their use |
| ES2738695T3 (es) * | 2014-05-28 | 2020-01-24 | Novartis Ag | Nuevos Derivados de Pirazolo Pirimidina y su uso como inhibidores de MALT1 |
| AU2015271030B2 (en) | 2014-06-05 | 2019-05-16 | Vertex Pharmaceuticals Incorporated | Radiolabelled derivatives of a 2-amino-6-fluoro-n-[5-fluoro-pyridin-3-yl]- pyrazolo [1,5-a] pyrimidin-3-carboxamide compound useful as ATR kinase inhibitor, the preparation of said compound and different solid forms thereof |
| LT3157566T (lt) | 2014-06-17 | 2019-08-12 | Vertex Pharmaceuticals Incorporated | Vėžio gydymo būdas, panaudojant chk1 ir atr inhibitorių derinį |
| US9580418B2 (en) | 2014-07-14 | 2017-02-28 | Incyte Corporation | Bicyclic aromatic carboxamide compounds useful as Pim kinase inhibitors |
| WO2016010897A1 (en) | 2014-07-14 | 2016-01-21 | Incyte Corporation | Bicyclic heteroaromatic carboxamide compounds useful as pim kinase inhibitors |
| CN105457029A (zh) * | 2014-09-29 | 2016-04-06 | 中国科学院上海巴斯德研究所 | 抑制酪蛋白激酶2活性在促进i型干扰素表达的应用 |
| WO2016094688A1 (en) * | 2014-12-10 | 2016-06-16 | Massachusetts Institute Of Technology | Fused 1,3-azole derivatives useful for the treatment of proliferative diseases |
| CR20170339A (es) * | 2015-01-23 | 2018-01-22 | Glaxosmithkline Ip Dev Ltd | Derivados de pirazol[3,4-d] pirimidina y su uso para el tratamiento de leshmaniasis |
| WO2016196244A1 (en) | 2015-05-29 | 2016-12-08 | Incyte Corporation | Pyridineamine compounds useful as pim kinase inhibitors |
| AR105967A1 (es) | 2015-09-09 | 2017-11-29 | Incyte Corp | Sales de un inhibidor de pim quinasa |
| WO2017059357A1 (en) | 2015-09-30 | 2017-04-06 | Vertex Pharmaceuticals Incorporated | Method for treating cancer using a combination of dna damaging agents and atr inhibitors |
| WO2017059251A1 (en) | 2015-10-02 | 2017-04-06 | Incyte Corporation | Heterocyclic compounds useful as pim kinase inhibitors |
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| EP3474855B1 (en) * | 2016-06-24 | 2022-01-26 | Polaris Pharmaceuticals, Inc. | Ck2 inhibitors, compositions and methods thereof |
| CN110831600B (zh) | 2017-04-21 | 2023-10-17 | 医肯纳肿瘤学公司 | 吲哚ahr抑制剂和其用途 |
| CN107188901A (zh) * | 2017-05-27 | 2017-09-22 | 无锡捷化医药科技有限公司 | 一种(3‑(3‑(二甲氨基)丙氧基)苯基)硼酸的制备方法 |
| KR102688084B1 (ko) | 2017-07-28 | 2024-07-24 | 주식회사유한양행 | 아미노피리미딘 유도체의 개선된 제조방법 |
| DK3658557T3 (da) | 2017-07-28 | 2024-07-29 | Takeda Pharmaceuticals Co | Tyk2-inhibitorer og anvendelser deraf |
| GB201715194D0 (en) | 2017-09-20 | 2017-11-01 | Carrick Therapeutics Ltd | Compounds and their therapeutic use |
| US10596161B2 (en) | 2017-12-08 | 2020-03-24 | Incyte Corporation | Low dose combination therapy for treatment of myeloproliferative neoplasms |
| US11071727B2 (en) | 2018-01-26 | 2021-07-27 | Northwestern University | Therapeutic targeting of proteolytic cleavage of the mixed lineage leukemia gene product (MLL1) by taspase1 using kinase inhibitors |
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| RU2607453C2 (ru) | 2017-01-10 |
| SG181507A1 (en) | 2012-07-30 |
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| JP2013512903A (ja) | 2013-04-18 |
| RU2012127792A (ru) | 2014-08-10 |
| ES2629170T3 (es) | 2017-08-07 |
| EP2509602A1 (en) | 2012-10-17 |
| US9303033B2 (en) | 2016-04-05 |
| AU2010326268A1 (en) | 2012-07-26 |
| US20140094448A1 (en) | 2014-04-03 |
| WO2011068667A1 (en) | 2011-06-09 |
| IL220086B (en) | 2018-02-28 |
| BR112012013508A2 (pt) | 2019-09-24 |
| US8575177B2 (en) | 2013-11-05 |
| CA2782684C (en) | 2018-09-04 |
| AU2010326268B2 (en) | 2016-11-03 |
| PL2509602T3 (pl) | 2017-08-31 |
| CN102762208A (zh) | 2012-10-31 |
| EP2509602A4 (en) | 2013-10-09 |
| EP2509602B9 (en) | 2017-11-01 |
| IL220086A0 (en) | 2012-09-24 |
| CA2782684A1 (en) | 2011-06-09 |
| KR20130067486A (ko) | 2013-06-25 |
| US20110152240A1 (en) | 2011-06-23 |
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