JP6182549B2 - 選択的サイクリン依存性キナーゼ阻害剤としてのピラゾロ−トリアジン誘導体 - Google Patents
選択的サイクリン依存性キナーゼ阻害剤としてのピラゾロ−トリアジン誘導体 Download PDFInfo
- Publication number
- JP6182549B2 JP6182549B2 JP2014559259A JP2014559259A JP6182549B2 JP 6182549 B2 JP6182549 B2 JP 6182549B2 JP 2014559259 A JP2014559259 A JP 2014559259A JP 2014559259 A JP2014559259 A JP 2014559259A JP 6182549 B2 JP6182549 B2 JP 6182549B2
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- JP
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- Prior art keywords
- triazine
- pyrazolo
- isopropyl
- amine
- benzyl
- 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.)
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- 0 C**(C1(C)CCN)C1(N)N1CC1 Chemical compound C**(C1(C)CCN)C1(N)N1CC1 0.000 description 12
- RYZNTSNBHJFXIK-UHFFFAOYSA-N CC(C)c(cn[nH]1)c1/N=C(\N=C(/C)\O)/OC1CCN(C)CC1 Chemical compound CC(C)c(cn[nH]1)c1/N=C(\N=C(/C)\O)/OC1CCN(C)CC1 RYZNTSNBHJFXIK-UHFFFAOYSA-N 0.000 description 1
- RRBPEHJNXHJYQN-UHFFFAOYSA-N CC(C)c(cn[n]1c(Cl)n2)c1nc2SC Chemical compound CC(C)c(cn[n]1c(Cl)n2)c1nc2SC RRBPEHJNXHJYQN-UHFFFAOYSA-N 0.000 description 1
- RKZVXCFEGXDBPD-UHFFFAOYSA-N CC(C)c(cn[n]1c(NCc2ccccc2)n2)c1nc2/[O]=C1/CNCCC1 Chemical compound CC(C)c(cn[n]1c(NCc2ccccc2)n2)c1nc2/[O]=C1/CNCCC1 RKZVXCFEGXDBPD-UHFFFAOYSA-N 0.000 description 1
- BWJDMRPMFRWAOP-UHFFFAOYSA-N CC(C)c(cn[n]1c(NCc2ccccc2)n2)c1nc2OC1CCN(C)CC1 Chemical compound CC(C)c(cn[n]1c(NCc2ccccc2)n2)c1nc2OC1CCN(C)CC1 BWJDMRPMFRWAOP-UHFFFAOYSA-N 0.000 description 1
- XGMRHIVZRRHUJF-QGZVFWFLSA-N CC(C)c(cn[n]1c(NCc2ccccc2OC(C)=O)n2)c1nc2O[C@H]1CNCCC1 Chemical compound CC(C)c(cn[n]1c(NCc2ccccc2OC(C)=O)n2)c1nc2O[C@H]1CNCCC1 XGMRHIVZRRHUJF-QGZVFWFLSA-N 0.000 description 1
- ODSNLAHWJMQSAD-UHFFFAOYSA-N CC(C)c(cn[n]1c(O)n2)c1nc2S(C)(=O)=O Chemical compound CC(C)c(cn[n]1c(O)n2)c1nc2S(C)(=O)=O ODSNLAHWJMQSAD-UHFFFAOYSA-N 0.000 description 1
- FIDVAOGPIORFCW-UHFFFAOYSA-N CC(C)c(cn[n]1c(OCc2ccccc2)n2)c1nc2SC Chemical compound CC(C)c(cn[n]1c(OCc2ccccc2)n2)c1nc2SC FIDVAOGPIORFCW-UHFFFAOYSA-N 0.000 description 1
- WILPWKRSABABGR-UHFFFAOYSA-N CC1(N)OC(N)=C1N Chemical compound CC1(N)OC(N)=C1N WILPWKRSABABGR-UHFFFAOYSA-N 0.000 description 1
- BAUWRHPMUVYFOD-UHFFFAOYSA-N CN(CC1)CCC1O Chemical compound CN(CC1)CCC1O BAUWRHPMUVYFOD-UHFFFAOYSA-N 0.000 description 1
- AIKUBOPKWKZULG-UHFFFAOYSA-N Cc1ccnnc1 Chemical compound Cc1ccnnc1 AIKUBOPKWKZULG-UHFFFAOYSA-N 0.000 description 1
- CAWHJQAVHZEVTJ-UHFFFAOYSA-N Cc1cnccn1 Chemical compound Cc1cnccn1 CAWHJQAVHZEVTJ-UHFFFAOYSA-N 0.000 description 1
- TWGNOYAGHYUFFR-UHFFFAOYSA-N Cc1cncnc1 Chemical compound Cc1cncnc1 TWGNOYAGHYUFFR-UHFFFAOYSA-N 0.000 description 1
- LNJMHEJAYSYZKK-UHFFFAOYSA-N Cc1ncccn1 Chemical compound Cc1ncccn1 LNJMHEJAYSYZKK-UHFFFAOYSA-N 0.000 description 1
- LVILGAOSPDLNRM-UHFFFAOYSA-N Cc1ncncc1 Chemical compound Cc1ncncc1 LVILGAOSPDLNRM-UHFFFAOYSA-N 0.000 description 1
- YIUOAAUFVBZQPM-UHFFFAOYSA-N Cc1ncncn1 Chemical compound Cc1ncncn1 YIUOAAUFVBZQPM-UHFFFAOYSA-N 0.000 description 1
- MXDRPNGTQDRKQM-UHFFFAOYSA-N Cc1nnccc1 Chemical compound Cc1nnccc1 MXDRPNGTQDRKQM-UHFFFAOYSA-N 0.000 description 1
- RFOWTCHRQOMTNI-UHFFFAOYSA-N [O-][NH+]=CC1CCC1 Chemical compound [O-][NH+]=CC1CCC1 RFOWTCHRQOMTNI-UHFFFAOYSA-N 0.000 description 1
Classifications
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- C07D491/02—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains two hetero rings
- C07D491/10—Spiro-condensed systems
- C07D491/107—Spiro-condensed systems with only one oxygen atom as ring hetero atom in the oxygen-containing ring
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- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/53—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with three nitrogens as the only ring hetero atoms, e.g. chlorazanil, melamine
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/10—Spiro-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D519/00—Heterocyclic compounds containing more than one system of two or more relevant hetero rings condensed among themselves or condensed with a common carbocyclic ring system not provided for in groups C07D453/00 or C07D455/00
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- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Veterinary Medicine (AREA)
- Medicinal Chemistry (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- Public Health (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Oncology (AREA)
- Communicable Diseases (AREA)
- Immunology (AREA)
- Diabetes (AREA)
- Physical Education & Sports Medicine (AREA)
- Pulmonology (AREA)
- Rheumatology (AREA)
- Hematology (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Cardiology (AREA)
- Virology (AREA)
- Heart & Thoracic Surgery (AREA)
- Dermatology (AREA)
- Neurology (AREA)
- Tropical Medicine & Parasitology (AREA)
- AIDS & HIV (AREA)
- Gastroenterology & Hepatology (AREA)
- Urology & Nephrology (AREA)
- Molecular Biology (AREA)
- Vascular Medicine (AREA)
- Ophthalmology & Optometry (AREA)
- Transplantation (AREA)
- Obesity (AREA)
- Endocrinology (AREA)
- Pain & Pain Management (AREA)
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP12157751.4 | 2012-03-01 | ||
EP12157751.4A EP2634190A1 (en) | 2012-03-01 | 2012-03-01 | Pyrazolo-triazine derivatives as selective cyclin-dependent kinase inhinitors |
PCT/EP2013/054224 WO2013128028A1 (en) | 2012-03-01 | 2013-03-01 | Pyrazolo - triazine derivatives as selective cyclin- dependent kinase inhinitors |
Publications (3)
Publication Number | Publication Date |
---|---|
JP2015511952A JP2015511952A (ja) | 2015-04-23 |
JP2015511952A5 JP2015511952A5 (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | 2017-08-03 |
JP6182549B2 true JP6182549B2 (ja) | 2017-08-16 |
Family
ID=47757629
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2014559259A Active JP6182549B2 (ja) | 2012-03-01 | 2013-03-01 | 選択的サイクリン依存性キナーゼ阻害剤としてのピラゾロ−トリアジン誘導体 |
Country Status (17)
Families Citing this family (33)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
UA119247C2 (uk) | 2013-09-06 | 2019-05-27 | РОЙВЕНТ САЙЕНСИЗ ҐмбГ | Спіроциклічні сполуки як інгібітори триптофангідроксилази |
GB201403093D0 (en) | 2014-02-21 | 2014-04-09 | Cancer Rec Tech Ltd | Therapeutic compounds and their use |
ES2702951T3 (es) | 2014-04-04 | 2019-03-06 | Syros Pharmaceuticals Inc | Inhibidores de quinasas dependientes de ciclina 7 (cdk7) |
EP3129371B1 (en) * | 2014-04-05 | 2020-07-29 | Syros Pharmaceuticals, Inc. | Inhibitors of cyclin-dependent kinase 7 (cdk7) |
AU2015337607B2 (en) | 2014-10-31 | 2020-04-09 | Ube Corporation | Substituted dihydropyrrolopyrazole compound |
CA2978170C (en) * | 2015-03-09 | 2024-02-27 | Aurigene Discovery Technologies Limited | Pyrazolo[1,5-a][1,3,5]triazine and pyrazolo[1,5-a]pyrimidine derivatives as cdk inhibitors |
US10273252B2 (en) | 2015-06-15 | 2019-04-30 | Ube Industries, Ltd. | Substituted dihydropyrrolopyrazole derivative |
WO2016206999A1 (en) * | 2015-06-24 | 2016-12-29 | Apodemus Ab | Pyrazolo[1,5-a]triazin-4-amine derivatives useful in therapy |
SI3432916T1 (sl) | 2016-09-13 | 2020-01-31 | Allergan, Inc. | Stabilizirani ne-protein klostridijski toksin sestavki |
CN106432249B (zh) * | 2016-09-30 | 2018-12-04 | 陕西科技大学 | 一类吡咯并[2,1-f][1,2,4]三嗪母核化合物的合成及其医药用途 |
WO2019032720A1 (en) | 2017-08-09 | 2019-02-14 | Sanford Burnham Prebys Medical Discovery Institute | APELIN RECEPTOR AGONISTS AND METHODS OF USE |
GB201715194D0 (en) | 2017-09-20 | 2017-11-01 | Carrick Therapeutics Ltd | Compounds and their therapeutic use |
US11649238B2 (en) | 2018-01-17 | 2023-05-16 | Glaxosmithkline Intellectual Property Development Limited | Substituted pyrazolo[1,5-a]pyrimidines as PI4K inhibitors |
IL277770B2 (en) * | 2018-04-11 | 2024-01-01 | Qurient Co Ltd | Pyrazolo-triazine and/or pyrazolo-pyrimidine derivatives as selective inhibitor of cyclin dependent kinase |
WO2019197546A1 (en) * | 2018-04-11 | 2019-10-17 | Qurient Co., Ltd. | Pharmaceutically active pyrazolo-triazine and/or pyrazolo-pyrimidine derivatives |
WO2020051689A1 (en) * | 2018-09-12 | 2020-03-19 | The Governing Council Of The University Of Toronto | Compounds and methods for treating nematode infections |
US11517568B2 (en) | 2018-09-12 | 2022-12-06 | The Governing Council Of The University Of Toronto | Compounds and methods for treating nematode infections |
IL282737B2 (en) | 2018-11-01 | 2025-05-01 | Syros Pharmaceuticals Inc | Cyclin-dependent kinase 7 (CDK7) inhibitors |
US12304913B2 (en) | 2018-11-14 | 2025-05-20 | Ube Industries, Ltd. | Dihydropyrrolopyrazole derivative |
CN110101703B (zh) * | 2019-05-06 | 2021-06-11 | 暨南大学 | Cdk7抑制剂在制备溃疡性结肠炎或结肠癌药物的应用 |
RU2713152C1 (ru) * | 2019-08-30 | 2020-02-04 | Федеральное государственное бюджетное образовательное учреждение высшего образования "Алтайский государственный медицинский университет" Министерства здравоохранения Российской Федерации | Способ лечения хронической аллергической крапивницы на фоне описторхоза |
TW202146416A (zh) * | 2019-12-11 | 2021-12-16 | 德商拜耳廠股份有限公司 | 吡唑并三𠯤 |
GB201918541D0 (en) * | 2019-12-16 | 2020-01-29 | Carrick Therapeutics Ltd | Therapeutic compounds and their use |
CN110950871B (zh) * | 2019-12-25 | 2022-05-17 | 陕西师范大学 | 2-取代-4-芳氨基吡唑并三嗪衍生物及制备抗肿瘤药物的应用 |
CN116964061A (zh) * | 2020-12-21 | 2023-10-27 | 詹森药业有限公司 | 作为细胞周期蛋白依赖性激酶7(cdk7)抑制剂的三环嘧啶 |
EP4305040A1 (en) * | 2021-03-09 | 2024-01-17 | JANSSEN Pharmaceutica NV | Tricyclic pyridines as cyclin-dependent kinase 7 (cdk7) inhibitors |
US20250042903A1 (en) * | 2021-06-17 | 2025-02-06 | H. Lee Moffitt Cancer Center And Research Institute, Inc. | Triazine inhibitors of cyclin-dependent kinases |
WO2023001061A1 (en) * | 2021-07-17 | 2023-01-26 | Jingrui Biopharma Co., Ltd. | Cdk7 selective inhibitors as anticancer agents |
US20240327397A1 (en) | 2021-07-29 | 2024-10-03 | Syngenta Crop Protection Ag | Pesticidally Active Fused Bicyclic Heteroaromatic Compounds |
JP2024541474A (ja) * | 2021-11-23 | 2024-11-08 | オリゲニス ゲーエムベーハー | Cdk9阻害剤として有用なピラゾロトリアジン誘導体 |
CN114181217B (zh) * | 2022-01-10 | 2022-12-27 | 陕西师范大学 | 吡唑并[1,5-a][1,3,5]三嗪衍生物及其盐和在制备抗癌药物中的应用 |
WO2023175173A1 (en) * | 2022-03-18 | 2023-09-21 | Qurient Co., Ltd. | Cdk7 inhibitors for antiviral treatment |
WO2024175024A1 (zh) * | 2023-02-21 | 2024-08-29 | 杭州德睿智药科技有限公司 | 作为CDKs抑制剂的新型并杂环类新化合物及其应用 |
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US615968A (en) | 1898-12-13 | Apparatus for treating ores | ||
BR0007919A (pt) * | 1999-02-01 | 2002-04-09 | Cv Therapeutics Inc | Composição purina 2,6,9-trisubstituìda |
US7119200B2 (en) * | 2002-09-04 | 2006-10-10 | Schering Corporation | Pyrazolopyrimidines as cyclin dependent kinase inhibitors |
PE20051128A1 (es) | 2004-02-25 | 2006-01-16 | Schering Corp | Pirazolotriazinas como inhibidores de quinasa |
CZ302122B6 (cs) * | 2009-01-28 | 2010-10-20 | Univerzita Palackého v Olomouci | Substituované deriváty 6-(2-aminobenzylamino)purinu, jejich použití jako léciva a prípravky tyto slouceniny obsahující |
FR2943058B1 (fr) * | 2009-03-11 | 2011-06-03 | Centre Nat Rech Scient | Derives de pyrazolo°1,5-a!-1,3,5-triazines, leur preparation et leur application en therapeutique. |
CZ302711B6 (cs) * | 2009-06-03 | 2011-09-14 | Univerzita Palackého v Olomouci | Substituované deriváty 6-(2-hydroxybenzylamino)purinu, jejich použití jako léciva a farmaceutické prípravky tyto slouceniny obsahující |
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JP2015511952A (ja) | 2015-04-23 |
KR101821452B1 (ko) | 2018-01-23 |
ZA201406078B (en) | 2016-08-31 |
HUE029264T2 (en) | 2017-02-28 |
EP2820020B1 (en) | 2016-04-06 |
DK2820020T3 (en) | 2016-07-04 |
AU2013224848A1 (en) | 2014-08-28 |
RU2645347C2 (ru) | 2018-02-21 |
MX347359B (es) | 2017-04-06 |
EP2634190A1 (en) | 2013-09-04 |
US20150018329A1 (en) | 2015-01-15 |
SG11201405129RA (en) | 2014-09-26 |
RU2014139705A (ru) | 2016-04-20 |
BR112014021189A2 (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | 2017-06-20 |
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IL234183A (en) | 2016-11-30 |
MX2014010494A (es) | 2015-04-08 |
CN104350054A (zh) | 2015-02-11 |
KR20140131994A (ko) | 2014-11-14 |
WO2013128028A8 (en) | 2014-10-02 |
WO2013128028A1 (en) | 2013-09-06 |
BR112014021189B1 (pt) | 2022-08-16 |
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