CA2939786C - Pyrazolo[1,5-a]pyrimidine-5,7-diamine compounds as cdk inhibitors and their therapeutic use - Google Patents

Pyrazolo[1,5-a]pyrimidine-5,7-diamine compounds as cdk inhibitors and their therapeutic use Download PDF

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Publication number
CA2939786C
CA2939786C CA2939786A CA2939786A CA2939786C CA 2939786 C CA2939786 C CA 2939786C CA 2939786 A CA2939786 A CA 2939786A CA 2939786 A CA2939786 A CA 2939786A CA 2939786 C CA2939786 C CA 2939786C
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compound according
independently
ppda
piperazino
compound
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CA2939786A
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English (en)
French (fr)
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CA2939786A1 (en
Inventor
Alexander BONDKE
Sebastian KROLL
Anthony Barrett
Matthew FUCHTER
Brian SLAFER
Simak Ali
Charles COOMBES
James Patrick Snyder
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Cancer Research Technology Ltd
Ip2ipo Innovations Ltd
Emory University
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Cancer Research Technology Ltd
Ip2ipo Innovations Ltd
Emory University
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Publication of CA2939786A1 publication Critical patent/CA2939786A1/en
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    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D487/00Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
    • C07D487/02Heterocyclic 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
    • C07D487/04Ortho-condensed systems
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/495Heterocyclic 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
    • A61K31/505Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
    • A61K31/519Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • A61P35/04Antineoplastic agents specific for metastasis

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  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • General Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Animal Behavior & Ethology (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Oncology (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Epidemiology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Medicines Containing Antibodies Or Antigens For Use As Internal Diagnostic Agents (AREA)
CA2939786A 2014-02-21 2015-02-20 Pyrazolo[1,5-a]pyrimidine-5,7-diamine compounds as cdk inhibitors and their therapeutic use Active CA2939786C (en)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
GB1403093.6 2014-02-21
GB201403093A GB201403093D0 (en) 2014-02-21 2014-02-21 Therapeutic compounds and their use
PCT/GB2015/050494 WO2015124941A1 (en) 2014-02-21 2015-02-20 Pyrazolo[1,5-a]pyrimidine-5,7-diamine compounds as cdk inhibitors and their therapeutic use

Publications (2)

Publication Number Publication Date
CA2939786A1 CA2939786A1 (en) 2015-08-27
CA2939786C true CA2939786C (en) 2022-03-08

Family

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Family Applications (1)

Application Number Title Priority Date Filing Date
CA2939786A Active CA2939786C (en) 2014-02-21 2015-02-20 Pyrazolo[1,5-a]pyrimidine-5,7-diamine compounds as cdk inhibitors and their therapeutic use

Country Status (23)

Country Link
US (4) US9932344B2 (en, 2012)
EP (1) EP3107914B8 (en, 2012)
JP (1) JP6498212B2 (en, 2012)
CN (1) CN106103445B (en, 2012)
AU (1) AU2015220560B2 (en, 2012)
BR (1) BR112016018633B1 (en, 2012)
CA (1) CA2939786C (en, 2012)
CY (1) CY1121588T1 (en, 2012)
DK (1) DK3107914T3 (en, 2012)
ES (1) ES2721268T3 (en, 2012)
GB (1) GB201403093D0 (en, 2012)
HR (1) HRP20190685T1 (en, 2012)
HU (1) HUE043122T2 (en, 2012)
LT (1) LT3107914T (en, 2012)
ME (1) ME03427B (en, 2012)
NZ (1) NZ724323A (en, 2012)
PL (1) PL3107914T3 (en, 2012)
PT (1) PT3107914T (en, 2012)
RS (1) RS58704B1 (en, 2012)
SI (1) SI3107914T1 (en, 2012)
SM (1) SMT201900266T1 (en, 2012)
TR (1) TR201905647T4 (en, 2012)
WO (1) WO2015124941A1 (en, 2012)

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CA2970574C (en) 2014-12-17 2023-09-19 King's College London Bicycloheteroaryl-heteroaryl-benzoic acid compounds as retinoic acid receptor beta (rar.beta.) agonists
CA2976109A1 (en) * 2015-02-13 2016-08-18 Dana-Farber Cancer Institute, Inc. Substituted pyrrolopyrimidine, pyrazolopyrimidine and purine derivatives and use thereof as lrrk2 inhibitors
EP3309163A4 (en) 2015-06-15 2019-01-09 UBE Industries, Ltd. SUBSTITUTED DIHYDROPYRROLO PYRAZOL DERIVATIVE
US20200123499A1 (en) 2015-12-02 2020-04-23 Massachusetts Institute Of Technology Method for efficient generation of neurons from non-neuronal cells
EP3507290A1 (en) 2016-08-31 2019-07-10 Agios Pharmaceuticals, Inc. Inhibitors of cellular metabolic processes
EP4438117A3 (en) 2017-07-28 2024-12-18 Takeda Pharmaceutical Company Limited Tyk2 inhibitors and uses thereof
MX2020001531A (es) * 2017-08-07 2020-03-20 Biocad Joint Stock Co Nuevos compuestos hetorociclicos como inhibidores de cdk8/19.
US20200197392A1 (en) * 2017-08-15 2020-06-25 The Brigham & Women's Hospital, Inc. Compositions and methods for treating tuberous sclerosis complex
GB201715194D0 (en) * 2017-09-20 2017-11-01 Carrick Therapeutics Ltd Compounds and their therapeutic use
TWI703149B (zh) * 2017-11-16 2020-09-01 美商美國禮來大藥廠 用於抑制cdk7之化合物
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
EP3787629A4 (en) 2018-05-02 2022-01-05 Kinnate Biopharma Inc. CYCLINE-DEPENDENT KINASE INHIBITORS
MX2020014245A (es) 2018-06-29 2021-05-12 Kinnate Biopharma Inc Inhibidores de quinasas dependientes de ciclinas.
IL282254B1 (en) * 2018-10-30 2025-04-01 Kronos Bio Inc Compounds, compositions, and methods for modulating CDK9 activity
WO2020100944A1 (ja) 2018-11-14 2020-05-22 宇部興産株式会社 ジヒドロピロロピラゾール誘導体
CN109860354B (zh) 2018-12-28 2020-05-19 南京邮电大学 同质集成红外光子芯片及其制备方法
WO2020186196A1 (en) * 2019-03-13 2020-09-17 The Translational Genomics Research Institute Trisubstituted pyrazolo [1,5-a] pyrimidine compounds as cdk7 inhibitors
WO2021003517A1 (en) * 2019-07-10 2021-01-14 Aucentra Therapeutics Pty Ltd Derivatives of 4-(imidazo[l,2-a]pyridin-3-yl)-n-(pyridinyl)pyrimidin- 2-amine as therapeutic agents
WO2021087138A1 (en) * 2019-10-29 2021-05-06 Syros Pharmaceuticals, Inc. Methods of treating cancer in biomarker-identified patients with inhibitors of cyclin-dependent kinase 7 (cdk7)
GB201918541D0 (en) * 2019-12-16 2020-01-29 Carrick Therapeutics Ltd Therapeutic compounds and their use
JP2023517034A (ja) * 2020-03-06 2023-04-21 バイエル アクチェンゲゼルシャフト Cdk12の阻害を介してがんに作用するイミダゾトリアジン
US20230158159A1 (en) * 2020-04-24 2023-05-25 Massachusetts Institute Of Technology Chimeric degraders of cyclin-dependent kinase 9 and uses thereof
WO2022156779A1 (zh) * 2021-01-22 2022-07-28 上海海雁医药科技有限公司 取代的吡唑并[1,5-a]嘧啶-7-胺衍生物、其组合物及医药上的用途
US12097261B2 (en) 2021-05-07 2024-09-24 Kymera Therapeutics, Inc. CDK2 degraders and uses thereof
GB202108572D0 (en) * 2021-06-16 2021-07-28 Carrick Therapeutics Ltd Therapeutic compounds and their use
WO2023001061A1 (en) * 2021-07-17 2023-01-26 Jingrui Biopharma Co., Ltd. Cdk7 selective inhibitors as anticancer agents
KR20240110634A (ko) * 2021-11-24 2024-07-15 크로노스 바이오, 인코포레이티드 (1s,3s)-n1-(5-(펜탄-3-일)피라졸로[1,5-a]피리미딘-7-일)시클로펜탄-1,3-디아민의다형체 및 염 형태
WO2024102447A1 (en) * 2022-11-10 2024-05-16 Emory University Uses of hydroimidazopyridopyrimidinone derivatives for managing aneurysms or other vascular conditions or diseases
WO2024174949A1 (zh) * 2023-02-20 2024-08-29 江苏正大丰海制药有限公司 作为cdk7激酶抑制剂的杂芳环化合物及其制备和应用
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
TW202500147A (zh) 2023-06-27 2025-01-01 美商亞文納營運公司 雌激素受體降解劑與cdk7抑制劑之組合
WO2025057087A1 (en) 2023-09-11 2025-03-20 Assia Chemical Industries Ltd. Solid state forms of samuraciclib

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JP4881558B2 (ja) 2002-09-04 2012-02-22 シェーリング コーポレイション サイクリン依存性キナーゼインヒビターとしてのピラゾロピリミジン
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WO2004087707A1 (en) * 2003-03-31 2004-10-14 Vernalis (Cambridge) Limited Pyrazolopyrimidine compounds and their use in medicine
JO2478B1 (en) 2003-06-19 2009-01-20 جانسين فارماسوتيكا ان. في. (Aminomethyl) -biperidine benzamides as 5 HT4 antagonists
CA2627623C (en) * 2005-10-06 2014-04-22 Schering Corporation Methods for inhibiting protein kinases
EP2170073A4 (en) 2007-06-05 2011-07-27 Univ Emory SELECTIVE INHIBITORS FOR CYCLINE-RELATED KINASES
SG181507A1 (en) 2009-12-04 2012-07-30 Cylene Pharmaceuticals Inc Pyrazolopyrimidines and related heterocycles as ck2 inhibitors
WO2012059932A1 (en) 2010-11-01 2012-05-10 Aurigene Discovery Technologies Limited 2, 4 -diaminopyrimidine derivatives as protein kinase inhibitors
EP3812387A1 (en) * 2011-07-21 2021-04-28 Sumitomo Dainippon Pharma Oncology, Inc. Heterocyclic protein kinase inhibitors
EP2634189A1 (en) 2012-03-01 2013-09-04 Lead Discovery Center GmbH Pyrazolo-triazine derivatives as selective cyclin-dependent kinase inhibitors
EP2634190A1 (en) 2012-03-01 2013-09-04 Lead Discovery Center GmbH Pyrazolo-triazine derivatives as selective cyclin-dependent kinase inhinitors
GB201403093D0 (en) 2014-02-21 2014-04-09 Cancer Rec Tech Ltd Therapeutic compounds and their use

Also Published As

Publication number Publication date
DK3107914T3 (en) 2019-04-29
LT3107914T (lt) 2019-05-27
AU2015220560A1 (en) 2016-10-06
EP3107914B1 (en) 2019-01-30
CN106103445B (zh) 2019-08-09
NZ724323A (en) 2022-02-25
US20180273540A1 (en) 2018-09-27
CN106103445A (zh) 2016-11-09
ES2721268T3 (es) 2019-07-30
JP6498212B2 (ja) 2019-04-10
TR201905647T4 (tr) 2019-05-21
EP3107914A1 (en) 2016-12-28
US10927119B2 (en) 2021-02-23
RS58704B1 (sr) 2019-06-28
BR112016018633B1 (pt) 2022-08-30
US11566029B2 (en) 2023-01-31
HUE043122T2 (hu) 2019-08-28
US20210253583A1 (en) 2021-08-19
WO2015124941A1 (en) 2015-08-27
EP3107914B8 (en) 2019-07-17
CA2939786A1 (en) 2015-08-27
ME03427B (me) 2020-01-20
US20160362410A1 (en) 2016-12-15
US9932344B2 (en) 2018-04-03
BR112016018633A2 (en, 2012) 2017-08-08
HRP20190685T1 (hr) 2019-06-14
GB201403093D0 (en) 2014-04-09
US10414772B2 (en) 2019-09-17
US20200055862A1 (en) 2020-02-20
JP2017506250A (ja) 2017-03-02
PT3107914T (pt) 2019-05-20
SI3107914T1 (sl) 2019-05-31
AU2015220560B2 (en) 2019-05-16
CY1121588T1 (el) 2020-05-29
PL3107914T3 (pl) 2019-09-30
SMT201900266T1 (it) 2019-07-11

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