SG11202104229WA - Compounds, compositions, and methods for modulating cdk9 activity - Google Patents

Compounds, compositions, and methods for modulating cdk9 activity

Info

Publication number
SG11202104229WA
SG11202104229WA SG11202104229WA SG11202104229WA SG11202104229WA SG 11202104229W A SG11202104229W A SG 11202104229WA SG 11202104229W A SG11202104229W A SG 11202104229WA SG 11202104229W A SG11202104229W A SG 11202104229WA SG 11202104229W A SG11202104229W A SG 11202104229WA
Authority
SG
Singapore
Prior art keywords
modulating
compositions
compounds
methods
cdk9 activity
Prior art date
Application number
SG11202104229WA
Other languages
English (en)
Inventor
Peter Mikochik
Joseph VACCA
David Freeman
Andrew Tasker
Original Assignee
Kronos Bio Inc
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Kronos Bio Inc filed Critical Kronos Bio Inc
Publication of SG11202104229WA publication Critical patent/SG11202104229WA/en

Links

Classifications

    • 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

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Medicinal Chemistry (AREA)
  • Public Health (AREA)
  • Epidemiology (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
SG11202104229WA 2018-10-30 2019-10-29 Compounds, compositions, and methods for modulating cdk9 activity SG11202104229WA (en)

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
US201862752635P 2018-10-30 2018-10-30
US201962884993P 2019-08-09 2019-08-09
US201962910058P 2019-10-03 2019-10-03
PCT/US2019/058482 WO2020092314A1 (en) 2018-10-30 2019-10-29 Compounds, compositions, and methods for modulating cdk9 activity

Publications (1)

Publication Number Publication Date
SG11202104229WA true SG11202104229WA (en) 2021-05-28

Family

ID=70328627

Family Applications (1)

Application Number Title Priority Date Filing Date
SG11202104229WA SG11202104229WA (en) 2018-10-30 2019-10-29 Compounds, compositions, and methods for modulating cdk9 activity

Country Status (20)

Country Link
US (3) US11155560B2 (ja)
EP (1) EP3873911A4 (ja)
JP (1) JP7385658B2 (ja)
KR (1) KR20210068597A (ja)
CN (1) CN112996790B (ja)
AU (1) AU2019370200A1 (ja)
BR (1) BR112021008176A2 (ja)
CA (1) CA3118472A1 (ja)
CO (1) CO2021005502A2 (ja)
CR (1) CR20210202A (ja)
DO (1) DOP2021000066A (ja)
IL (1) IL282254A (ja)
MA (1) MA54092A (ja)
MD (1) MD20210033A2 (ja)
MX (1) MX2021004769A (ja)
PE (1) PE20212196A1 (ja)
PH (1) PH12021550857A1 (ja)
SG (1) SG11202104229WA (ja)
WO (1) WO2020092314A1 (ja)
ZA (1) ZA202102609B (ja)

Families Citing this family (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
PE20212196A1 (es) * 2018-10-30 2021-11-16 Kronos Bio Inc Compuestos, composiciones, y metodos para modular la actividad cdk9
US20230158159A1 (en) * 2020-04-24 2023-05-25 Massachusetts Institute Of Technology Chimeric degraders of cyclin-dependent kinase 9 and uses thereof
EP4240422A1 (en) * 2020-11-05 2023-09-13 Kronos Bio, Inc. Compounds and methods for modulating cdk9 activity
WO2023096922A1 (en) * 2021-11-24 2023-06-01 Kronos Bio, Inc. Polymorphic and salt forms of (ls,3s)-n1-(5-(pentan-3- yl)pyrazolo[l,5-a]pyrimidin-7-yl)cyclopentane-l,3-diamine
WO2024017365A1 (zh) * 2022-07-22 2024-01-25 上海海雁医药科技有限公司 取代的吡唑并[1,5-a]嘧啶-7-胺衍生物的药学上可接受的盐和多晶型物及其应用

Family Cites Families (67)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5389632A (en) 1992-02-24 1995-02-14 Laboratoires Upsa Pyrazolopyrimidine derivatives which are angiotensin II receptor antagonists
KR100315837B1 (ko) 1994-06-21 2002-02-28 고리 히데아끼 피라졸로[1,5-a]피리미딘유도체
EP0915880B1 (en) 1996-07-24 2007-10-10 Bristol-Myers Squibb Pharma Company Azolo triazines and pyrimidines
US20010007867A1 (en) 1999-12-13 2001-07-12 Yuhpyng L. Chen Substituted 6,5-hetero-bicyclic derivatives
YU23602A (sh) 1999-09-30 2004-09-03 Neurogen Corporation Amino supstituisani pirazolo /1,5/a/-1,5-pirimidini i pirazolo /1,5-a/-1,3,5-triazini
CZ20021067A3 (cs) 1999-09-30 2002-11-13 Neurogen Corporation Určité alkylendiaminové substituované pyrazolo[1,5-a]- 1,5-pyrimidiny a pyrazolo[1,5-a]-1,3,5-triaziny
JP2002308879A (ja) 2001-04-13 2002-10-23 Nippon Soda Co Ltd 5−ハロアルキル−アゾロピリミジン化合物、製造方法及び有害生物防除剤
KR20040097375A (ko) 2002-04-23 2004-11-17 시오노기 앤드 컴파니, 리미티드 피라졸로[1, 5-에이]피리미딘 유도체 및 이를 함유한엔에이디(피)에이취 산화효소 저해제
WO2003095455A2 (en) 2002-05-10 2003-11-20 Smithkline Beecham Corporation Substituted pyrazolopyrimidines
ES2304511T3 (es) 2002-06-04 2008-10-16 Schering Corporation Compuestos de pirazolo(1,5-a)pirimidina como agentes antivirales.
AU2003263071B2 (en) 2002-09-04 2007-03-15 Merck Sharp & Dohme Llc Pyrazolopyrimidines as cyclin-dependent kinase inhibitors
US7196078B2 (en) 2002-09-04 2007-03-27 Schering Corpoartion Trisubstituted and tetrasubstituted pyrazolopyrimidines as cyclin dependent kinase inhibitors
US7119200B2 (en) 2002-09-04 2006-10-10 Schering Corporation Pyrazolopyrimidines as cyclin dependent kinase inhibitors
US7605155B2 (en) 2002-09-04 2009-10-20 Schering Corporation Substituted pyrazolo[1,5-a]pyrimidines as protein kinase inhibitors
US7205308B2 (en) 2002-09-04 2007-04-17 Schering Corporation Trisubstituted 7-aminopyrazolopyrimidines as cyclin dependent kinase inhibitors
US8580782B2 (en) 2002-09-04 2013-11-12 Merck Sharp & Dohme Corp. Substituted pyrazolo[1,5-a]pyrimidines as cyclin dependent kinase inhibitors
US7563798B2 (en) 2002-09-04 2009-07-21 Schering Corporation Substituted pyrazolo[1,5-a]pyrimidines as protein kinase inhibitors
DE60313872T2 (de) 2002-09-04 2008-01-17 Schering Corp. Pyrazoloä1,5-aüpyrimidine als hemmstoffe cyclin-abhängiger kinasen
US7161003B1 (en) 2002-09-04 2007-01-09 Schering Corporation Pyrazolopyrimidines as cyclin dependent kinase inhibitors
GB0305559D0 (en) 2003-03-11 2003-04-16 Teijin Ltd Compounds
US20070179161A1 (en) 2003-03-31 2007-08-02 Vernalis (Cambridge) Limited. Pyrazolopyrimidine compounds and their use in medicine
US7501405B2 (en) 2003-04-11 2009-03-10 High Point Pharmaceuticals, Llc Combination therapy using an 11β-hydroxysteroid dehydrogenase type 1 inhibitor and an antihypertensive agent for the treatment of metabolic syndrome and related diseases and disorders
EP1615697A2 (en) 2003-04-11 2006-01-18 Novo Nordisk A/S New pyrazolo[1,5-a] pyrimidine derivatives and pharmaceutical use thereof
JP2005008581A (ja) 2003-06-20 2005-01-13 Kissei Pharmaceut Co Ltd 新規なピラゾロ[1,5−a]ピリミジン誘導体、それを含有する医薬組成物およびそれらの用途
EP1671962A1 (en) 2003-10-10 2006-06-21 Ono Pharmaceutical Co., Ltd. Novel fused heterocyclic compound and use thereof
EP1697369A1 (en) 2003-12-22 2006-09-06 SB Pharmco Puerto Rico Inc Crf receptor antagonists and methods relating thereto
US8018479B2 (en) 2008-08-27 2011-09-13 Lexmark International, Inc. Method and system for correcting the linearity error in electrophotographic devices
BRPI0514187A (pt) * 2004-08-13 2008-06-03 Teijin Pharma Ltd composto, e, droga preventiva ou uma droga terapêutica
EP1836205B1 (en) 2004-12-21 2009-06-10 Schering Corporation PYRAZOLO[1,5-A]PYRIMIDINE ADENOSINE A2a RECEPTOR ANTAGONISTS
DE102005007534A1 (de) 2005-02-17 2006-08-31 Bayer Cropscience Ag Pyrazolopyrimidine
NZ567151A (en) 2005-10-06 2012-03-30 Schering Corp Pyrazolo [1,5 -A] pyrimidine derivatives and their use for inhibiting Checkpoint kinases
WO2007044407A2 (en) 2005-10-06 2007-04-19 Schering Corporation Pyrazolo (1 , 5a) pyrimidines as protein kinase inhibitors
AR056876A1 (es) 2005-10-21 2007-10-31 Tanabe Seiyaku Co Compuestos de pirazolo[1-5-a]pirimidina, antagonistas de receptores canabinoides cb1, composiciones farmaceuticas que los contienen y usos en el tratamiento de enfermedades del sistema nervioso central, tales como trastornos psicoticos, neurologicos y similares
WO2007109571A2 (en) 2006-03-17 2007-09-27 Prometheus Laboratories, Inc. Methods of predicting and monitoring tyrosine kinase inhibitor therapy
CA2653076A1 (en) 2006-05-22 2007-12-06 Schering Corporation Pyrazolo [1, 5-a] pyrimidines as cdk inhibitors
EP2170073A4 (en) 2007-06-05 2011-07-27 Univ Emory SELECTIVE INHIBITORS FOR CYCLINE-RELATED KINASES
EP2173346A2 (en) 2007-06-27 2010-04-14 Summit Corporation Plc Use of compounds for preparing anti-tuberculosis agents
CN102143746A (zh) 2008-07-03 2011-08-03 埃克塞利希斯股份有限公司 Cdk 调节剂
WO2010074284A1 (ja) 2008-12-26 2010-07-01 味の素株式会社 ピラゾロピリミジン化合物
US8993612B2 (en) 2009-10-08 2015-03-31 Rhizen Pharmaceuticals Sa Modulators of calcium release-activated calcium channel and methods for treatment of non-small cell lung cancer
AU2010326268B2 (en) 2009-12-04 2016-11-03 Senhwa Biosciences, Inc. Pyrazolopyrimidines and related heterocycles as CK2 inhibitors
ES2540867T3 (es) 2010-02-26 2015-07-14 Mitsubishi Tanabe Pharma Corporation Compuestos de pirazolopirimidina y su uso como inhibidores de PDE10
CA2792102C (en) 2010-03-05 2015-06-09 Kyowa Hakko Kirin Co., Ltd. Pyrazolopyrimidine derivative
ES2700542T3 (es) 2010-06-24 2019-02-18 Gilead Sciences Inc Composición farmacéutica que comprende un derivado de pirazolo[1,5-A]pirimidina como un agente antiviral
RU2604062C2 (ru) 2010-07-13 2016-12-10 Ф.Хоффманн-Ля Рош Аг ПРОИЗВОДНЫЕ ПИРАЗОЛО[1,5-a]ПИРИМИДИНА И ТИЕНО[3,2-b]ПИРИМИДИНА В КАЧЕСТВЕ МОДУЛЯТОРОВ IRAK-4
EP2608669B1 (en) 2010-08-23 2016-06-22 Merck Sharp & Dohme Corp. NOVEL PYRAZOLO[1,5-a]PYRIMIDINE DERIVATIVES AS mTOR INHIBITORS
EP2621926B1 (en) 2010-09-30 2017-08-30 Merck Sharp & Dohme Corp. Pyrazolopyrimidine pde10 inhibitors
WO2012170827A2 (en) 2011-06-08 2012-12-13 Cylene Pharmaceuticals, Inc. Pyrazolopyrimidines and related heterocycles as ck2 inhibitors
JP6106694B2 (ja) 2012-01-10 2017-04-05 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 Aktキナーゼ阻害剤としての置換ピラゾロピリミジン類
SG11201404757WA (en) 2012-02-17 2014-09-26 Millennium Pharm Inc Pyrazolopyrimidinyl inhibitors of ubiquitin-activating enzyme
WO2013130943A1 (en) 2012-03-02 2013-09-06 Genentech, Inc. Alkyl-and di-substituted amido-benzyl sulfonamide derivatives
NZ707432A (en) 2012-11-16 2020-01-31 Univ Health Network Pyrazolopyrimidine compounds
RU2678196C2 (ru) 2013-03-14 2019-01-24 Селтакссис, Инк. Производные 2-фениламино-3-цианопиразоло[1,5-а]пиримидина, полезные в качестве ингибитора лейкотриен-a4-гидролазы
GB201403093D0 (en) * 2014-02-21 2014-04-09 Cancer Rec Tech Ltd Therapeutic compounds and their use
WO2015153732A2 (en) 2014-04-01 2015-10-08 Cornell University Use of double-stranded dna in exosomes: a novel biomarker in cancer detection
EP3805218A1 (en) 2014-04-05 2021-04-14 Syros Pharmaceuticals, Inc. Inhibitors of cyclin-dependent kinase 7 (cdk7)
EP3268000B1 (en) 2015-03-09 2021-08-04 Aurigene Discovery Technologies Limited Pyrazolo[1,5-a][1,3,5]triazine and pyrazolo[1,5-a]pyrimidine derivatives as cdk inhibitors
US10550121B2 (en) 2015-03-27 2020-02-04 Dana-Farber Cancer Institute, Inc. Inhibitors of cyclin-dependent kinases
US9828381B2 (en) 2015-04-20 2017-11-28 AbbVie Deutschland GmbH & Co. KG Substituted pyrazolopyrimidines and method of use
AU2016276963C1 (en) * 2015-06-12 2021-08-05 Dana-Farber Cancer Institute, Inc. Combination therapy of transcription inhibitors and kinase inhibitors
WO2017059080A1 (en) 2015-10-01 2017-04-06 Bristol-Myers Squibb Company Biaryl kinase inhibitors
JP2018199623A (ja) 2015-10-22 2018-12-20 大正製薬株式会社 含窒素縮合複素環化合物
SG10201912607SA (en) 2015-11-19 2020-02-27 Blueprint Medicines Corp Compounds and compositions useful for treating disorders related to ntrk
WO2017180499A2 (en) 2016-04-13 2017-10-19 President And Fellows Of Harvard College Methods for capturing, isolation, and targeting of circulating tumor cells and diagnostic and therapeutic applications thereof
CN117946115A (zh) 2017-07-28 2024-04-30 武田药品工业株式会社 Tyk2抑制剂与其用途
WO2019023654A2 (en) * 2017-07-28 2019-01-31 Massachusetts Institute Of Technology DISCOVERING SMALL MOLECULES TARGETING THE ANDROGEN RECEPTOR AND USES THEREOF
PE20212196A1 (es) * 2018-10-30 2021-11-16 Kronos Bio Inc Compuestos, composiciones, y metodos para modular la actividad cdk9

Also Published As

Publication number Publication date
PE20212196A1 (es) 2021-11-16
MD20210033A2 (ro) 2021-10-31
MX2021004769A (es) 2021-08-24
JP2022505268A (ja) 2022-01-14
US11155560B2 (en) 2021-10-26
IL282254A (en) 2021-05-31
US20200131189A1 (en) 2020-04-30
US20220002305A1 (en) 2022-01-06
CR20210202A (es) 2022-02-08
US11845754B2 (en) 2023-12-19
CN112996790B (zh) 2023-11-03
EP3873911A1 (en) 2021-09-08
US20240132506A1 (en) 2024-04-25
CA3118472A1 (en) 2020-05-07
MA54092A (fr) 2021-09-08
WO2020092314A1 (en) 2020-05-07
AU2019370200A1 (en) 2021-06-10
JP7385658B2 (ja) 2023-11-22
BR112021008176A2 (pt) 2021-08-03
CO2021005502A2 (es) 2021-09-20
KR20210068597A (ko) 2021-06-09
DOP2021000066A (es) 2021-10-31
PH12021550857A1 (en) 2021-12-06
CN112996790A (zh) 2021-06-18
EP3873911A4 (en) 2022-06-22
ZA202102609B (en) 2023-02-22

Similar Documents

Publication Publication Date Title
HK1258811A1 (zh) 用於調節cftr 的化合物、組合物和方法
IL272089A (en) Compounds, preparations and methods
HRP20200201T1 (hr) Spojevi i sastavi za moduliranje aktivnosti mutantne egfr kinaze
IL273752A (en) Ingredients, compounds and methods for increasing cftr activity
EP3642182A4 (en) COMPOUNDS, COMPOSITIONS AND SYNTHESIS METHODS
IL271149A (en) Compounds for modulating s1p1 activity and methods of using them
PL3676297T3 (pl) Związki, kompozycje i sposoby
ZA202102609B (en) Compounds, compositions, and methods for modulating cdk9 activity
IL285302A (en) Compounds, preparations and methods
IL280809B (en) New preparations, their use and methods of their creation
EP3265098A4 (en) COMPOSITIONS FOR MODULATING MECP2 EXPRESSION
EP3634429A4 (en) SYNTHETIC COMPOSITION FOR MICROBIOTE MODULATION
EP3589139A4 (en) SYNTHETIC COMPOSITION FOR MICROBIOTE MODULATION
IL287079A (en) Compositions and methods for regulating complement activity
IL287120A (en) Compounds, preparations and methods
EP3551613A4 (en) COMPOUNDS AND PHARMACEUTICAL COMPOSITIONS FOR MODULATING SGK ACTIVITY AND METHOD THEREFOR
IL286681A (en) Compounds and methods for modulating ube3a-ats
EP3220940A4 (en) Compositions and methods for modulating at2r activity
IL270505B1 (en) Compounds, preparations and methods
EP3331536A4 (en) COMPOSITIONS AND METHODS FOR MODULATING ABHD2 ACTIVITY
EP3352778A4 (en) METHODS, COMPOUNDS AND COMPOSITIONS FOR MODULATING THE INTEGRITY OF THE HEMATO-ENCEPHALIC BARRIER AND REMYLELINING