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
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- 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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- A61K31/505—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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- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/14—Vasoprotectives; Antihaemorrhoidals; Drugs for varicose therapy; Capillary stabilisers
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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)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Organic Chemistry (AREA)
- Epidemiology (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Biomedical Technology (AREA)
- Neurology (AREA)
- Neurosurgery (AREA)
- Oncology (AREA)
- Heart & Thoracic Surgery (AREA)
- Cardiology (AREA)
- Immunology (AREA)
- Hospice & Palliative Care (AREA)
- Communicable Diseases (AREA)
- Psychiatry (AREA)
- Hematology (AREA)
- Pain & Pain Management (AREA)
- Rheumatology (AREA)
- Vascular Medicine (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 (OSRAM) | 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 (OSRAM) |
| EP (1) | EP2509602B9 (OSRAM) |
| JP (1) | JP5802676B2 (OSRAM) |
| KR (1) | KR101851130B1 (OSRAM) |
| CN (1) | CN102762208A (OSRAM) |
| AU (1) | AU2010326268B2 (OSRAM) |
| BR (1) | BR112012013508A2 (OSRAM) |
| CA (1) | CA2782684C (OSRAM) |
| ES (1) | ES2629170T3 (OSRAM) |
| IL (1) | IL220086B (OSRAM) |
| PL (1) | PL2509602T3 (OSRAM) |
| RU (1) | RU2607453C2 (OSRAM) |
| SG (1) | SG181507A1 (OSRAM) |
| WO (1) | WO2011068667A1 (OSRAM) |
Families Citing this family (54)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP5824040B2 (ja) * | 2010-06-01 | 2015-11-25 | バイエル・インテレクチュアル・プロパティ・ゲゼルシャフト・ミット・ベシュレンクテル・ハフツングBayer Intellectual Property GmbH | 置換イミダゾピラジン |
| NZ604040A (en) | 2010-06-03 | 2015-02-27 | Pharmacyclics Inc | 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 |
| JP2014517079A (ja) | 2011-06-22 | 2014-07-17 | 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 | Atrキナーゼ阻害剤として有用な化合物 |
| JP5408389B1 (ja) * | 2012-04-27 | 2014-02-05 | 新日鐵住金株式会社 | 継目無鋼管及びその製造方法 |
| AU2013280644B2 (en) | 2012-06-26 | 2018-08-02 | Jeffrey A. BACHA | Methods for treating tyrosine-kinase-inhibitor-resistant malignancies in patients with genetic polymorphisms or AHI1 dysregulations or mutations employing dianhydrogalactitol, diacetyldianhydrogalactitol, dibromodulcitol, or analogs or derivatives thereof |
| 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 |
| KR20150032340A (ko) | 2012-07-24 | 2015-03-25 | 파마시클릭스, 인코포레이티드 | 브루톤 티로신 키나제(btk)의 억제제에 대한 내성과 관련된 돌연변이 |
| PT4190786T (pt) | 2012-12-07 | 2025-05-29 | Vertex Pharma | Compostos úteis como inibidores da quinase atr |
| JP6437452B2 (ja) | 2013-01-14 | 2018-12-12 | インサイト・ホールディングス・コーポレイションIncyte Holdings Corporation | Pimキナーゼ阻害剤として有用な二環式芳香族カルボキサミド化合物 |
| LT2945939T (lt) | 2013-01-15 | 2020-07-27 | Incyte Holdings Corporation | Triazolkarboksamidai ir piridinkarboksamido junginiai, naudotini kaip pim kinazės inhibitoriai |
| EP2970286A1 (en) | 2013-03-15 | 2016-01-20 | Vertex Pharmaceuticals Inc. | Fused pyrazolopyrimidine derivatives useful as inhibitors of atr kinase |
| JP2016512816A (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化合物 |
| JP2016512239A (ja) | 2013-03-15 | 2016-04-25 | 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化合物 |
| JP2016519684A (ja) | 2013-04-08 | 2016-07-07 | デニス エム ブラウン | 準最適に投与された薬物療法の有効性を改善するための及び/又は副作用を低減するための方法および組成物 |
| 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 |
| EP3036238A1 (en) | 2013-08-23 | 2016-06-29 | 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 |
| PE20170189A1 (es) * | 2014-05-28 | 2017-03-15 | Novartis Ag | Nuevos derivados de pirazolo pirimidina y su uso como inhibidores de malt1 |
| KR102575125B1 (ko) | 2014-06-05 | 2023-09-07 | 버텍스 파마슈티칼스 인코포레이티드 | Atr 키나제의 저해제로서 유용한 2-아미노-6-플루오로-n-[5-플루오로-피리딘-3-일]-피라졸로[1,5-a]피리미딘-3-카복스아미드 화합물의 방사성표지된 유도체, 상기 화합물의 제조 및 이의 다양한 고체 형태 |
| RU2736219C2 (ru) | 2014-06-17 | 2020-11-12 | Вертекс Фармасьютикалз Инкорпорейтед | Способ лечения рака с использованием комбинации ингибиторов снк1 и atr |
| US9580418B2 (en) | 2014-07-14 | 2017-02-28 | Incyte Corporation | Bicyclic aromatic carboxamide compounds useful as Pim kinase inhibitors |
| US9822124B2 (en) | 2014-07-14 | 2017-11-21 | 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 |
| AU2016208528B2 (en) * | 2015-01-23 | 2019-02-21 | Glaxosmithkline Intellectual Property Development Limited | Pyrazolo[3,4-d]pyrimidin derivative and its use for the treatment of leishmaniasis |
| US9540347B2 (en) | 2015-05-29 | 2017-01-10 | 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 |
| AU2016331955B2 (en) | 2015-09-30 | 2022-07-21 | 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 |
| EP3416950A1 (en) | 2016-02-16 | 2018-12-26 | Massachusetts Institute of Technology | Max binders as myc modulators and uses thereof |
| EP3474855B1 (en) | 2016-06-24 | 2022-01-26 | Polaris Pharmaceuticals, Inc. | Ck2 inhibitors, compositions and methods thereof |
| KR102668371B1 (ko) | 2017-04-21 | 2024-05-28 | 이케나 온콜로지, 인코포레이티드 | 인돌 ahr 억제제 및 이의 용도 |
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| RU2607453C2 (ru) | 2017-01-10 |
| KR20130067486A (ko) | 2013-06-25 |
| AU2010326268A1 (en) | 2012-07-26 |
| CN102762208A (zh) | 2012-10-31 |
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