ATE524459T1 - Pyrazolederivate und ihr einsatz als hemmer von cyclinabhängigen kinasen - Google Patents

Pyrazolederivate und ihr einsatz als hemmer von cyclinabhängigen kinasen

Info

Publication number
ATE524459T1
ATE524459T1 AT08857078T AT08857078T ATE524459T1 AT E524459 T1 ATE524459 T1 AT E524459T1 AT 08857078 T AT08857078 T AT 08857078T AT 08857078 T AT08857078 T AT 08857078T AT E524459 T1 ATE524459 T1 AT E524459T1
Authority
AT
Austria
Prior art keywords
cyclin
inhibitors
pyrazole derivatives
dependent kinases
useful
Prior art date
Application number
AT08857078T
Other languages
English (en)
Inventor
Christopher Thomas Brain
Young Shin Cho
Ying Hou
Moo Sung
Original Assignee
Novartis Ag
Astex Therapeutics Ltd
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 Novartis Ag, Astex Therapeutics Ltd filed Critical Novartis Ag
Application granted granted Critical
Publication of ATE524459T1 publication Critical patent/ATE524459T1/de

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D401/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
    • C07D401/02Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
    • C07D401/04Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D401/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
    • C07D401/14Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing three or more hetero rings
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D403/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
    • C07D403/02Heterocyclic 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
    • C07D403/04Heterocyclic 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 directly linked by a ring-member-to-ring-member bond
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D403/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
    • C07D403/14Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing three or more hetero rings
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D405/00Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
    • C07D405/14Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing three or more hetero rings
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D453/00Heterocyclic compounds containing quinuclidine or iso-quinuclidine ring systems, e.g. quinine alkaloids
    • C07D453/02Heterocyclic compounds containing quinuclidine or iso-quinuclidine ring systems, e.g. quinine alkaloids containing not further condensed quinuclidine ring systems

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Veterinary Medicine (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Public Health (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
AT08857078T 2007-12-07 2008-12-08 Pyrazolederivate und ihr einsatz als hemmer von cyclinabhängigen kinasen ATE524459T1 (de)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US1227607P 2007-12-07 2007-12-07
PCT/EP2008/067037 WO2009071701A1 (en) 2007-12-07 2008-12-08 Pyrazole derivatives and use thereof as inhibitors of cyclin dependent kinases

Publications (1)

Publication Number Publication Date
ATE524459T1 true ATE524459T1 (de) 2011-09-15

Family

ID=40343520

Family Applications (1)

Application Number Title Priority Date Filing Date
AT08857078T ATE524459T1 (de) 2007-12-07 2008-12-08 Pyrazolederivate und ihr einsatz als hemmer von cyclinabhängigen kinasen

Country Status (15)

Country Link
US (1) US8367687B2 (de)
EP (1) EP2231636B1 (de)
JP (1) JP2011506303A (de)
KR (1) KR20100098521A (de)
CN (1) CN101883764B (de)
AT (1) ATE524459T1 (de)
AU (1) AU2008333136B2 (de)
BR (1) BRPI0821151A2 (de)
CA (1) CA2707989A1 (de)
EA (1) EA018459B1 (de)
ES (1) ES2374480T3 (de)
MX (1) MX2010006203A (de)
PL (1) PL2231636T3 (de)
PT (1) PT2231636E (de)
WO (1) WO2009071701A1 (de)

Families Citing this family (30)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101910150B (zh) 2007-11-05 2013-09-18 诺瓦提斯公司 作为cetp抑制剂、可用于治疗疾病如高脂血症或动脉硬化的4-苄基氨基-1-羧基酰基哌啶衍生物
MX2010006063A (es) 2007-12-03 2010-07-01 Novartis Ag Derivados de 4-bencil-amino-pirrolidina 1,2-disustituida como inhibidores de la proteina de transferencia de colesteril-ester (cetp) utiles para el tratamiento de las enfermedades tales como hiperlipidemia o arterioesclerosis.
MX2011012343A (es) * 2009-05-19 2011-12-14 Dow Agrosciences Llc Compuestos y metodos para controlar hongos.
EP2558092B1 (de) * 2010-04-13 2018-06-27 Novartis AG Kombination mit einem hemmer der cyclin-abhängigen kinase-4 oder cyclinabhängigen kinase-6 (cdk4/6) und everolimus zur behandlung von krebs
ES2577829T3 (es) 2010-06-04 2016-07-19 F. Hoffmann-La Roche Ag Derivados de aminopirimidina como moduladores de la LRRK2
GB201017345D0 (en) 2010-10-14 2010-11-24 Proximagen Ltd Receptor antagonists
NO2638031T3 (de) 2010-11-10 2018-03-10
CN103547580B (zh) 2011-03-22 2016-12-07 阿迪维纳斯疗法有限公司 取代的稠合三环化合物、其组合物及医药用途
CA2851788C (en) 2011-10-11 2022-11-29 Dana-Farber Cancer Institute, Inc. Pyrazol-3-ones that activate pro-apoptotic bax
US9593115B2 (en) 2012-09-21 2017-03-14 Advinus Therapeutics Ltd. Substituted fused tricyclic compounds, compositions, and medicinal applications thereof
NZ746607A (en) 2012-11-21 2019-11-29 Ptc Therapeutics Inc Substituted reverse pyrimidine bmi-1 inhibitors
EA034866B1 (ru) 2013-08-30 2020-03-31 ПиТиСи ТЕРАПЬЮТИКС, ИНК. Замещенные пиримидиновые ингибиторы bmi-1
WO2015076800A1 (en) 2013-11-21 2015-05-28 Ptc Therapeutics, Inc. Substituted pyridine and pyrazine bmi-1 inhibitors
AU2016242118B2 (en) 2015-04-02 2021-07-08 Proximagen, Llc Novel therapies for cancer
US10376511B2 (en) 2015-08-04 2019-08-13 Yissum Research Development Company Of The Hebrew University Of Jerusalem Ltd. Pyrazole pyrimidine derivative and uses thereof
BR112020018094A2 (pt) 2018-03-08 2020-12-22 Incyte Corporation Compostos de aminopirazina diol como inibidores de pi3k-¿
US11046658B2 (en) 2018-07-02 2021-06-29 Incyte Corporation Aminopyrazine derivatives as PI3K-γ inhibitors
EP3836932A2 (de) 2018-08-17 2021-06-23 PTC Therapeutics, Inc. Verfahren zur behandlung von bauchspeicheldrüsenkrebs
US11066404B2 (en) 2018-10-11 2021-07-20 Incyte Corporation Dihydropyrido[2,3-d]pyrimidinone compounds as CDK2 inhibitors
US11384083B2 (en) 2019-02-15 2022-07-12 Incyte Corporation Substituted spiro[cyclopropane-1,5′-pyrrolo[2,3-d]pyrimidin]-6′(7′h)-ones as CDK2 inhibitors
TW202100520A (zh) 2019-03-05 2021-01-01 美商英塞特公司 作為cdk2 抑制劑之吡唑基嘧啶基胺化合物
WO2020205560A1 (en) 2019-03-29 2020-10-08 Incyte Corporation Sulfonylamide compounds as cdk2 inhibitors
WO2020223469A1 (en) 2019-05-01 2020-11-05 Incyte Corporation N-(1-(methylsulfonyl)piperidin-4-yl)-4,5-di hydro-1h-imidazo[4,5-h]quinazolin-8-amine derivatives and related compounds as cyclin-dependent kinase 2 (cdk2) inhibitors for treating cancer
US11447494B2 (en) 2019-05-01 2022-09-20 Incyte Corporation Tricyclic amine compounds as CDK2 inhibitors
CA3150681A1 (en) 2019-08-14 2021-02-18 Incyte Corporation Imidazolyl pyrimidinylamine compounds as cdk2 inhibitors
US11851426B2 (en) 2019-10-11 2023-12-26 Incyte Corporation Bicyclic amines as CDK2 inhibitors
US11981671B2 (en) 2021-06-21 2024-05-14 Incyte Corporation Bicyclic pyrazolyl amines as CDK2 inhibitors
US11976073B2 (en) 2021-12-10 2024-05-07 Incyte Corporation Bicyclic amines as CDK2 inhibitors
US12084453B2 (en) 2021-12-10 2024-09-10 Incyte Corporation Bicyclic amines as CDK12 inhibitors
EP4725942A1 (de) 2024-10-09 2026-04-15 Sibylla Biotech S.p.A. Verbindungen mit wirkung auf den cyclin-d1-pfad und ihre verwendung

Family Cites Families (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6979686B1 (en) * 2001-12-07 2005-12-27 Pharmacia Corporation Substituted pyrazoles as p38 kinase inhibitors
GB9919778D0 (en) * 1999-08-21 1999-10-27 Zeneca Ltd Chemical compounds
ATE407132T1 (de) 2000-12-05 2008-09-15 Vertex Pharma Inhibitoren von c-jun n-terminalen kinasen (jnk) und anderen proteinkinasen
GB0107901D0 (en) * 2001-03-29 2001-05-23 Cyclacel Ltd Anti-cancer compounds
WO2002092573A2 (en) * 2001-05-16 2002-11-21 Vertex Pharmaceuticals Incorporated Heterocyclic substituted pyrazoles as inhibitors of src and other protein kinases
WO2003051886A1 (en) * 2001-12-17 2003-06-26 Smithkline Beecham Corporation Pyrazolopyridazine derivatives
GB0215844D0 (en) 2002-07-09 2002-08-14 Novartis Ag Organic compounds
EP1551842A1 (de) 2002-10-15 2005-07-13 Smithkline Beecham Corporation Pyridazinverbindungen als gsk-3-inhibitoren
GB0409080D0 (en) * 2004-04-23 2004-05-26 Biofocus Discovery Ltd Compounds which interact with protein kinases
US20080242667A1 (en) 2005-08-26 2008-10-02 Smithkline Beecham Corporation Pyrimidinyl-Pyrazole Inhibitors of Aurora Kinases
EA200802050A1 (ru) * 2006-04-19 2009-04-28 Лаборатуар Сероно Са Новые гетероарилзамещенные ариламинопиридиновые производные в качестве мек ингибиторов
WO2007132220A1 (en) 2006-05-12 2007-11-22 Cyclacel Limited Combination of a 2-substituted-4-heter0aryl-pyrimidine amine with a cytotoxic drug and use thereof in the treatment of a proliferative disorder
JP2010533147A (ja) * 2007-07-13 2010-10-21 アデックス ファルマ エス.エイ. 代謝調節型グルタミン酸レセプターのモジュレーターとしてのピラゾール誘導体

Also Published As

Publication number Publication date
EA201000879A1 (ru) 2010-12-30
US20100280033A1 (en) 2010-11-04
JP2011506303A (ja) 2011-03-03
ES2374480T3 (es) 2012-02-17
WO2009071701A1 (en) 2009-06-11
EP2231636B1 (de) 2011-09-14
BRPI0821151A2 (pt) 2015-06-16
MX2010006203A (es) 2010-06-25
KR20100098521A (ko) 2010-09-07
EA018459B1 (ru) 2013-08-30
AU2008333136A1 (en) 2009-06-11
CA2707989A1 (en) 2009-06-11
CN101883764A (zh) 2010-11-10
PL2231636T3 (pl) 2012-04-30
AU2008333136B2 (en) 2012-05-10
CN101883764B (zh) 2013-11-13
EP2231636A1 (de) 2010-09-29
PT2231636E (pt) 2012-01-02
US8367687B2 (en) 2013-02-05

Similar Documents

Publication Publication Date Title
ATE524459T1 (de) Pyrazolederivate und ihr einsatz als hemmer von cyclinabhängigen kinasen
JO3235B1 (ar) مركبات بيررولوبيريميدين و استعمالاتها
EA200900798A1 (ru) Производные индол-4-илпиримидинил-2-иламина и их применение в качестве ингибиторов циклинзависимой киназы
MX2009006536A (es) Compuestos de heteroaril-heteroarilo como inhibidores de cdk para el tratamiento de cancer, inflamacion e infecciones virales.
EA200970738A1 (ru) Ингибиторы активности akt
EA200900819A1 (ru) Хиназолины для ингибирования pdk1
EA201101477A1 (ru) Органические соединения и их применение
EA200900571A1 (ru) Композиции chk1 ингибиторов
ECSP099414A (es) Derivados de dihidropiridina de utilidad como inhibidores de la proteína quinasa
NO20092658L (no) New compounds
EA200901144A1 (ru) Ингибиторы киназы pim и способы их применения
ATE516286T1 (de) 5-(ä1,3,4üoxadiazol-2-yl)-1h-indazol und 5-(ä1,3, 4üthiadiazol-2-yl)-1h-indazol derivate als sgk- inhibitoren zur behandlung von diabetes
TW200801008A (en) Protein kinase inhibitors
EA200800441A1 (ru) Замещенные бензимидазолы в качестве ингибиторов киназ
EA201101521A1 (ru) Способы лечения онкологических заболеваний, использующие эпиметаболические переключатели, многоаспектные внутриклеточные молекулы или факторы влияния
UA101478C2 (ru) Соединения, полезные как ингибиторы raf-киназы
EA201170252A1 (ru) Амидофеноксиндазолы в качестве ингибиторов c-мет
EA201200323A1 (ru) Соединения и композиции, как ингибиторы протеинкиназы
BRPI0915105A2 (pt) composto de 2,4'-biripidinila como inibidores da proteína cinase d úteis para o tratamento de ia insuficiência cardíaca e cancer
NO20084749L (no) Organiske forbindelser og deres anvendelser
ATE502944T1 (de) 2-amino-5,7-dihydro-6h-pyrroloä3,4- düpyrimidinderivate als hsp-90-inhibitoren zur behandlung von krebs
UA95627C2 (ru) Аминотиазолы и их применение
WO2007016338A3 (en) Use of chk2 kinase inhibitors for cancer treatment
TN2009000495A1 (en) Macrocycles and their uses
EA200971067A1 (ru) Триазолиламинопиримидиновые соединения

Legal Events

Date Code Title Description
UEP Publication of translation of european patent specification

Ref document number: 2231636

Country of ref document: EP