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PE20081534A1 - Piperidinas sustituidas que tienen actividad inhibidoras de la proteina cinasa - Google Patents

Piperidinas sustituidas que tienen actividad inhibidoras de la proteina cinasa

Info

Publication number
PE20081534A1
PE20081534A1 PE2008000027A PE2008000027A PE20081534A1 PE 20081534 A1 PE20081534 A1 PE 20081534A1 PE 2008000027 A PE2008000027 A PE 2008000027A PE 2008000027 A PE2008000027 A PE 2008000027A PE 20081534 A1 PE20081534 A1 PE 20081534A1
Authority
PE
Peru
Prior art keywords
protein kinase
substituted
piperidins
inhibiting activity
kinase inhibiting
Prior art date
Application number
PE2008000027A
Other languages
English (en)
Inventor
Steven John Woodhead
Martyn Frederickson
Christopher Hamlett
Hannah Fiona Sore
David Winter Walker
Peter Blurton
Ian Collins
Kwai Ming Cheung
John Caldwell
Fonseca Mchary Tatiana Faria Da
Richard William Arthur Luke
Zbigniew Stanley Matusiak
Andrew Leach
Jeffrey James Morris
Original Assignee
Astex Therapeutics Ltd
Cancer Research Technology Ltd Inst Cancer Res Royal Cancer Hospital
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=PE20081534(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 Research Technology Ltd Inst Cancer Res Royal Cancer Hospital, Astrazeneca Ab filed Critical Astex Therapeutics Ltd
Publication of PE20081534A1 publication Critical patent/PE20081534A1/es

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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
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P1/00Drugs for disorders of the alimentary tract or the digestive system
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    • AHUMAN NECESSITIES
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    • A61P17/00Drugs for dermatological disorders
    • A61P17/04Antipruritics
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    • A61P17/00Drugs for dermatological disorders
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    • A61P19/00Drugs for skeletal disorders
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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
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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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    • A61P25/28Drugs 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
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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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    • A61P31/20Antivirals for DNA viruses
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    • A61P9/00Drugs for disorders of the cardiovascular system
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    • A61P9/00Drugs for disorders of the cardiovascular system
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    • 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)
  • Organic Chemistry (AREA)
  • Chemical & Material Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Public Health (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
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  • Diabetes (AREA)
  • Communicable Diseases (AREA)
  • Orthopedic Medicine & Surgery (AREA)
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  • Dermatology (AREA)
  • Pulmonology (AREA)
  • Hematology (AREA)
  • Immunology (AREA)
  • Obesity (AREA)
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  • Urology & Nephrology (AREA)
  • Heart & Thoracic Surgery (AREA)
  • AIDS & HIV (AREA)
  • Psychology (AREA)
  • Vascular Medicine (AREA)
  • Child & Adolescent Psychology (AREA)
  • Ophthalmology & Optometry (AREA)
  • Pain & Pain Management (AREA)

Abstract

SE REFIERE A UN COMPUESTO DE FORMULA I, DONDE E ES HETEROARILO DE 5 MIEMBROSCON 1-4 HETEROATOMOS SELECCIONADOS DE O, N Y S; q Y r SON CADA UNO 0-1, CON TAL QUE LA SUMA DE q + r SEA 1-2; T ES N, CR5; J1-J2 ES UN GRUPO N=C(R6), (R7)C=N, N=N, ENTRE OTROS; Q3 ES UN ENLACE, ENLAZADOR DE HIDROCARBURO SATURADO QUE CONTIENE1-3 ATOMOS DE CARBONO SUSTITUIDO O NO; G ES NR2R3, CN, OH; R1a Y R1b SON CADA UNO H, R10 O JUNTOS FORMAN ARILO, HETEROARILO, DE 5-6 MIEMBROS SUSTITUIDOS O NO; R3 Y R3 SON CADA UNO H, HIDROCARBILO C1-C4, ACILO C1-C4 SUSTITUIDOS O NO, ENTRE OTROS; R4 Y R6 SON CADA UNO H, HALOGENO, HIDROCARBILO C1-C5 SATURADO, CIANO, CONH2, CF3 Y NH2; R5 Y R7 SON CADA UNO H, HALOGENO, CIANO, ENTRE OTROS. UN COMPUESTO ES 4-(7-(BENCILOXI)-1H-BENZO[d]IMIDAZO-2-LIL)-1-(7H-PIRROLO[2,3-d]PIRIMIDI-4-NIL)PIPERIDI-1-NAMINA. DICHOS COMPUESTOS SON INHIBIDORES DE LA PROTEINA QUINASA B Y/O LA PROTEINA CINASA A
PE2008000027A 2006-12-21 2008-01-02 Piperidinas sustituidas que tienen actividad inhibidoras de la proteina cinasa PE20081534A1 (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
PE20081534A1 true PE20081534A1 (es) 2008-12-19

Family

ID=39283821

Family Applications (1)

Application Number Title Priority Date Filing Date
PE2008000027A PE20081534A1 (es) 2006-12-21 2008-01-02 Piperidinas sustituidas que tienen actividad inhibidoras de la proteina cinasa

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
EP3421471B1 (en) 2006-04-25 2021-05-26 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
ES2522365T3 (es) 2007-10-11 2014-11-14 Astrazeneca Ab Derivados de pirrolo [2,3-D] pirimidina como inhibidores de proteína quinasas B
EP2297153B1 (en) * 2008-04-21 2015-05-27 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
AU2009314336B2 (en) 2008-11-11 2013-09-12 Eli Lilly And Company P70 S6 kinase inhibitor and EGFR inhibitor combination therapy
CA2743242A1 (en) * 2008-11-11 2010-05-20 Eli Lilly And Company P70 s6 kinase inhibitor and mtor inhibitor combination therapy
JOP20190230A1 (ar) 2009-01-15 2017-06-16 Incyte Corp طرق لاصلاح مثبطات انزيم jak و المركبات الوسيطة المتعلقة به
ES2465094T3 (es) 2009-10-23 2014-06-05 Eli Lilly And Company Inhibidores de AKT
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
WO2012044537A1 (en) 2010-10-01 2012-04-05 Bristol-Myers 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
ES2617339T3 (es) 2010-12-16 2017-06-16 Calchan Limited Derivados de pirrolopirimidina inhibidores de ASK1
EA201300846A1 (ru) * 2011-01-21 2013-12-30 Бёрингер Ингельхайм Интернациональ Гмбх Конденсированные дигидрофураны в качестве модуляторов gpr119, предназначенные для лечения диабета, ожирения и родственных нарушений
US9402847B2 (en) 2011-04-01 2016-08-02 Astrazeneca Ab Combinations comprising (S)-4-amino-N-(1-(4-chlorophenyl)-3-hydroxypropyl)-1-(7H-pyrrolo[2,3-d]pyrimidin-4-yl)piperidine-4-carboxamide
EP2707373A1 (de) 2011-05-10 2014-03-19 Bayer Intellectual Property GmbH Bicyclische (thio)carbonylamidine
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CA2890345A1 (en) 2012-11-16 2014-05-22 Merck Patent Gmbh Imidazol-piperidinyl derivatives as modulators of kinase activity
ES2620119T3 (es) * 2012-11-16 2017-06-27 Merck Patent Gmbh Derivados heterocíclicos novedosos como moduladores de la actividad de quinasa
HK1218756A1 (zh) * 2013-03-11 2017-03-10 默克专利有限公司 用作激酶活性调节剂的6-[4-(1h-咪唑-2-基)哌啶-1-基]嘧啶-4-胺衍生物
US9771369B2 (en) 2014-03-04 2017-09-26 Plexxikon Inc. Compounds and methods for kinase modulation, and indications therefor
DK3134383T3 (da) * 2014-04-25 2020-06-29 Bayer Cropscience Ag Fremgangsmåde til fremstilling af biphenylaminer af anilider ved hjælp af rutheniumkatalyse
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
CN109476669A (zh) * 2016-05-18 2019-03-15 富荣吉有限责任公司 Lim激酶抑制剂
CA3024831C (en) * 2016-05-20 2021-06-08 Taiho Pharmaceutical Co., Ltd. Novel 5h-pyrrolo[2,3-d]pyrimidin-6(7h)-one derivative
US12344592B2 (en) * 2020-01-17 2025-07-01 Lupin Limited Methods, processes and intermediates for preparing chroman compounds
JP2023520140A (ja) 2020-03-17 2023-05-16 江蘇恒瑞医薬股▲ふん▼有限公司 縮合二環系誘導体、その調製方法及びその医薬的応用
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
JP2024535857A (ja) 2021-09-17 2024-10-02 江▲蘇▼恒瑞医▲薬▼股▲フン▼有限公司 縮合二環系誘導体の薬学的に許容される塩、結晶及びそれらの調製方法
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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
TW200738709A (en) * 2006-01-19 2007-10-16 Osi Pharm Inc Fused heterobicyclic kinase inhibitors

Also Published As

Publication number Publication date
CL2007003791A1 (es) 2008-08-22
EP2125805A1 (en) 2009-12-02
US20100093748A1 (en) 2010-04-15
JP2010514675A (ja) 2010-05-06
WO2008075109A1 (en) 2008-06-26
TW200833676A (en) 2008-08-16
UY30830A1 (es) 2008-07-31
AR064416A1 (es) 2009-04-01

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