UY30830A1 - Piperidinas sustituidas que presentan actividad inhibitoria de proteinquinasa - Google Patents

Piperidinas sustituidas que presentan actividad inhibitoria de proteinquinasa

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Publication number
UY30830A1
UY30830A1 UY30830A UY30830A UY30830A1 UY 30830 A1 UY30830 A1 UY 30830A1 UY 30830 A UY30830 A UY 30830A UY 30830 A UY30830 A UY 30830A UY 30830 A1 UY30830 A1 UY 30830A1
Authority
UY
Uruguay
Prior art keywords
substituted
proteinquinasa
piperidins
presenting
inhibitory activity
Prior art date
Application number
UY30830A
Other languages
English (en)
Inventor
Peter Blurton
Andrew James Woodhead
Martin Frederickson
Jeffrey James Morris
Zbigniew Stanley Matsuiakz
Kwai Ming Cheung
Andrew Leach
Christopher Hamlett
Tatiana Faria Da Fonseca
John Caldwell
Marinus Leendert Verdonk
Collins Ian
Walker David Winter
Sore Hannah Fiona
Woodhead Steven John
Luke Richard William Arthur
Original Assignee
Astex Therapeutics Ltd
Cancer Res Inst Royal
Cancer Resarch Technology Ltd
Astrazeneca Ab
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
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=39283821&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=UY30830(A1) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Priority claimed from GB0625668A external-priority patent/GB0625668D0/en
Application filed by Astex Therapeutics Ltd, Cancer Res Inst Royal, Cancer Resarch Technology Ltd, Astrazeneca Ab filed Critical Astex Therapeutics Ltd
Publication of UY30830A1 publication Critical patent/UY30830A1/es

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    • 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
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    • A61P1/00Drugs for disorders of the alimentary tract or the digestive system
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    • A61P17/00Drugs for dermatological disorders
    • A61P17/04Antipruritics
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    • A61P17/00Drugs for dermatological disorders
    • A61P17/06Antipsoriatics
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    • A61P19/00Drugs for skeletal disorders
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
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    • A61P19/00Drugs for skeletal disorders
    • A61P19/02Drugs for skeletal disorders for joint disorders, e.g. arthritis, arthrosis
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    • A61P19/00Drugs for skeletal disorders
    • A61P19/08Drugs for skeletal disorders for bone diseases, e.g. rachitism, Paget's disease
    • A61P19/10Drugs for skeletal disorders for bone diseases, e.g. rachitism, Paget's disease for osteoporosis
    • AHUMAN NECESSITIES
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    • A61P21/00Drugs for disorders of the muscular or neuromuscular system
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    • A61P25/00Drugs for disorders of the nervous system
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    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/14Drugs for disorders of the nervous system for treating abnormal movements, e.g. chorea, dyskinesia
    • A61P25/16Anti-Parkinson drugs
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    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/28Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
    • AHUMAN NECESSITIES
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    • A61P27/00Drugs for disorders of the senses
    • A61P27/02Ophthalmic agents
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    • A61P29/00Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
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    • A61P9/00Drugs for disorders of the cardiovascular system
    • A61P9/10Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D471/00Heterocyclic 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
    • C07D471/02Heterocyclic 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
    • C07D471/04Ortho-condensed systems
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D473/00Heterocyclic compounds containing purine ring systems
    • C07D473/26Heterocyclic compounds containing purine ring systems with an oxygen, sulphur, or nitrogen atom directly attached in position 2 or 6, but not in both
    • C07D473/32Nitrogen atom
    • C07D473/34Nitrogen atom attached in position 6, e.g. adenine
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D519/00Heterocyclic 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)
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  • Chemical & Material Sciences (AREA)
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  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
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Abstract

La invencion proporciona compuestos inhibidores de quinasas PKA y PKB de formula I o sales, solvatos, tautomeros o N-oxidos del mísmo, donde E es un anillo heteroarilo de cinco miembros conteniendo 1, 2, 4 o 4 heteroatomos seleccionados de O, N y S siempre que no más de un heteroátomo sea distinto de N; cada q y r son 0 o 1 ; siempre que q+r sea 1 o 2; T es N o un grupo CR5; J1- J2 es N=C(R6), (R7)C=N, (R8)N-C(O), (R8)2C-C(O), N=N o (R7)C=C(R6), Q3 es un enlace o un grupo hidrocarburo C1-C3 enlazador saturado opcionalmente sustituido por fluoro e hidroxi ; G es NR2R3, CN o OH; cáda m y n es 0 o 1, siempre que m+n sea 1 o 2, y siempre que también cada m o n sea 0 cuando los miembros adyacentes en el anillo del anillo E sean S u O; R1a y R1b son iguales o diferentes y cada uno es hidrogeno o un sustituyente R10; o R1a y R1b junto con los átomos de carbono o heteroatomos a los que están unidos forman un anillo arilo o heteroarilo de 5 o 6 miembros, donde el anillo arilo o heteroarilo se sustituye opcionalmente con uno más sustituyentes R10; y R2, R3, R4, R5, R7, R8, y R10 son como se los define en las reivindicaciones.
UY30830A 2006-12-21 2007-12-21 Piperidinas sustituidas que presentan actividad inhibitoria de proteinquinasa UY30830A1 (es)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US87138606P 2006-12-21 2006-12-21
GB0625668A GB0625668D0 (en) 2006-12-21 2006-12-21 Pharmaceutical compounds
US98263307P 2007-10-25 2007-10-25

Publications (1)

Publication Number Publication Date
UY30830A1 true UY30830A1 (es) 2008-07-31

Family

ID=39283821

Family Applications (1)

Application Number Title Priority Date Filing Date
UY30830A UY30830A1 (es) 2006-12-21 2007-12-21 Piperidinas sustituidas que presentan actividad inhibitoria de proteinquinasa

Country Status (9)

Country Link
US (1) US20100093748A1 (es)
EP (1) EP2125805A1 (es)
JP (1) JP2010514675A (es)
AR (1) AR064416A1 (es)
CL (1) CL2007003791A1 (es)
PE (1) PE20081534A1 (es)
TW (1) TW200833676A (es)
UY (1) UY30830A1 (es)
WO (1) WO2008075109A1 (es)

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MY179032A (en) 2004-10-25 2020-10-26 Cancer Research Tech Ltd Ortho-condensed pyridine and pyrimidine derivatives (e.g.purines) as protein kinase inhibitors
EP2043655A2 (en) 2006-04-25 2009-04-08 Astex Therapeutics Limited Purine and deazapurine derivatives as pharmaceutical compounds
UA99284C2 (ru) * 2007-05-11 2012-08-10 Елі Ліллі Енд Компані ИНГИБИТОРЫ р70 S6-КИНАЗЫ
PL2201012T3 (pl) 2007-10-11 2014-11-28 Astrazeneca Ab Pochodne pirolo[2,3-d]pirymidyny jako inhibitory kinazy białkowej b
AU2009239500B2 (en) * 2008-04-21 2014-01-30 Lexicon Pharmaceuticals, Inc. LIMK2 inhibitors, compositions comprising them, and methods of their use
AR074072A1 (es) 2008-11-11 2010-12-22 Lilly Co Eli Compuesto de imidazol -piperidin -pirrol-pirimidin-6-ona, composicion farmaceutica que lo comprende y su uso para preparar un medicamento util para tratar el glioblastoma multiforme
JP2012508240A (ja) * 2008-11-11 2012-04-05 イーライ リリー アンド カンパニー P70s6キナーゼ阻害剤およびegfr阻害剤の併用療法
JP2012508239A (ja) * 2008-11-11 2012-04-05 イーライ リリー アンド カンパニー P70s6キナーゼ阻害剤およびmtor阻害剤の併用療法
JOP20190230A1 (ar) 2009-01-15 2017-06-16 Incyte Corp طرق لاصلاح مثبطات انزيم jak و المركبات الوسيطة المتعلقة به
EP2491032B1 (en) * 2009-10-23 2014-04-16 Eli Lilly and Company Akt inhibitors
WO2012020725A1 (ja) * 2010-08-10 2012-02-16 塩野義製薬株式会社 Npy y5受容体拮抗作用を有するヘテロ環誘導体
US9133160B2 (en) 2010-10-01 2015-09-15 Bristol-Meyers Squibb Company Substituted benzimidazole and imidazopyridine compounds useful as CYP17 modulators
US9266880B2 (en) 2010-11-12 2016-02-23 Bristol-Myers Squibb Company Substituted azaindazole compounds
US9045485B2 (en) 2010-12-16 2015-06-02 Convergence Pharmaceuticals Limited ASK 1 inhibiting pyrrolopyrimidine derivatives
MX2013008083A (es) * 2011-01-21 2013-09-13 Boehringer Ingelheim Int Dihidrofuranos fusionados como moduladores de gpr119 para el tratamiento de diabetes, obesidad y trastornos relacionados.
ES2761311T3 (es) 2011-04-01 2020-05-19 Astrazeneca Ab Tratamiento terapéutico
EP2707373A1 (de) 2011-05-10 2014-03-19 Bayer Intellectual Property GmbH Bicyclische (thio)carbonylamidine
MX346095B (es) * 2011-09-12 2017-03-07 Merck Patent Gmbh Nuevas imidazol-aminas como moduladores de la actividad de cinasas.
US8969586B2 (en) 2011-09-27 2015-03-03 Bristol-Myers Squibb Company Substituted bicyclic heteroaryl compounds
MY175800A (en) 2011-11-30 2020-07-09 Astrazeneca Ab Combination treatment of cancer
AU2013204533B2 (en) 2012-04-17 2017-02-02 Astrazeneca Ab Crystalline forms
CN105102435A (zh) 2012-11-16 2015-11-25 默克专利有限公司 用作激酶活性调节剂的新颖的咪唑-哌啶基衍生物
AU2013344552B2 (en) * 2012-11-16 2018-03-15 Xiaoling Chen Novel heterocyclic derivatives as modulators of kinase activity
KR20150124957A (ko) * 2013-03-11 2015-11-06 메르크 파텐트 게엠베하 키나아제 활성의 조절인자로서 (6-[4-1h-이미다졸-2-일)피페리딘-1-일]피리미딘-4-아민 유도체
WO2015134536A1 (en) * 2014-03-04 2015-09-11 Plexxikon Inc. Compounds and methods for kinase modulation, and indications therefor
JP6588924B2 (ja) * 2014-04-25 2019-10-09 バイエル・クロップサイエンス・アクチェンゲゼルシャフト ルテニウムの触媒作用によってアニリド類からビフェニルアミン類を製造する方法
CZ306987B6 (cs) * 2015-10-26 2017-11-01 Ústav experimentální botaniky AV ČR, v. v. i. 2,6-disubstituované puriny pro použití jako léčiva a farmaceutické přípravky je obsahující
WO2017201187A1 (en) * 2016-05-18 2017-11-23 Virongy, Llc Lim kinase inhibitors
TWI732187B (zh) * 2016-05-20 2021-07-01 日商大鵬藥品工業股份有限公司 新穎5H-吡咯并[2, 3-d]嘧啶-6(7H)-酮衍生物
BR112022017856A2 (pt) * 2020-03-17 2022-11-01 Jiangsu Hengrui Pharmaceuticals Co Ltd Derivado bicíclico fundido, método de preparação do mesmo e uso farmacêutico do mesmo
CN113444110B (zh) * 2020-03-25 2023-05-12 江苏恒瑞医药股份有限公司 四氢吡咯并吡唑类衍生物、其制备方法及其在医药上的应用
CA3231865A1 (en) 2021-09-17 2023-03-23 Tingting SHANG Fused bicyclic derivative, pharmaceutically acceptable salt, crystal form thereof and preparation method therefor
AR128669A1 (es) 2022-03-01 2024-06-05 Insilico Medicine Ip Ltd INHIBIDORES DE DIACILGLICEROL CINASA (DGK) a Y USOS DE LOS MISMOS

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MY179032A (en) * 2004-10-25 2020-10-26 Cancer Research Tech Ltd Ortho-condensed pyridine and pyrimidine derivatives (e.g.purines) as protein kinase inhibitors
WO2007084667A2 (en) * 2006-01-19 2007-07-26 Osi Pharmaceutical, Inc. Fused heterobicyclic kinase inhibitors

Also Published As

Publication number Publication date
WO2008075109A1 (en) 2008-06-26
AR064416A1 (es) 2009-04-01
US20100093748A1 (en) 2010-04-15
CL2007003791A1 (es) 2008-08-22
JP2010514675A (ja) 2010-05-06
PE20081534A1 (es) 2008-12-19
TW200833676A (en) 2008-08-16
EP2125805A1 (en) 2009-12-02

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