EA200802407A1 - Замещенные аминопиразолопиридины и их соли, их получения и фармацевтические композиции, которые их содержат - Google Patents

Замещенные аминопиразолопиридины и их соли, их получения и фармацевтические композиции, которые их содержат

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Publication number
EA200802407A1
EA200802407A1 EA200802407A EA200802407A EA200802407A1 EA 200802407 A1 EA200802407 A1 EA 200802407A1 EA 200802407 A EA200802407 A EA 200802407A EA 200802407 A EA200802407 A EA 200802407A EA 200802407 A1 EA200802407 A1 EA 200802407A1
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EA
Eurasian Patent Office
Prior art keywords
substituted
salts
pharmaceutical compositions
aminopyrazolopiridines
contain
Prior art date
Application number
EA200802407A
Other languages
English (en)
Inventor
Инго Хартунг
Стьюарт Инс
Георг Кеттшау
Карл-Хайнц Тираух
Ханс Брим
Ульф Бёмер
Original Assignee
Байер Шеринг Фарма Акциенгезельшафт
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
Priority claimed from EP06090109A external-priority patent/EP1867648A1/en
Application filed by Байер Шеринг Фарма Акциенгезельшафт filed Critical Байер Шеринг Фарма Акциенгезельшафт
Publication of EA200802407A1 publication Critical patent/EA200802407A1/ru

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    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D213/00Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
    • C07D213/02Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
    • C07D213/04Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D213/60Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D213/78Carbon atoms having three bonds to hetero atoms, with at the most one bond to halogen, e.g. ester or nitrile radicals
    • C07D213/84Nitriles
    • C07D213/85Nitriles in position 3
    • AHUMAN NECESSITIES
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    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
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    • AHUMAN NECESSITIES
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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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    • A61P35/00Antineoplastic agents
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    • 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
    • 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

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  • Health & Medical Sciences (AREA)
  • Organic Chemistry (AREA)
  • Chemical & Material Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • General Chemical & Material Sciences (AREA)
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  • Heart & Thoracic Surgery (AREA)
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  • Rheumatology (AREA)
  • Urology & Nephrology (AREA)
  • Dermatology (AREA)
  • Physical Education & Sports Medicine (AREA)
  • Biomedical Technology (AREA)
  • Transplantation (AREA)
  • Ophthalmology & Optometry (AREA)
  • Pain & Pain Management (AREA)
  • Neurology (AREA)
  • Orthopedic Medicine & Surgery (AREA)
  • Vascular Medicine (AREA)
  • Neurosurgery (AREA)
  • Endocrinology (AREA)
  • Reproductive Health (AREA)
  • Oncology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Plural Heterocyclic Compounds (AREA)

Abstract

Изобретение относится к замещенным пиразолопиридинам согласно общей формуле (I)в которой А, В, D, Е, R, R, R, R, R, Rи q имеют значения, указанные в пунктах формулы изобретения, и их солям, к фармацевтическим композициям, содержащим указанные замещенные пиразолопиридиновые соединения, к способам получения указанных замещенных пиразолопиридинов, а также к их применению для приготовления фармацевтической композиции для лечения заболеваний нарушенной регуляции роста сосудов или заболеваний, которые сопровождаются нарушенной регуляции роста сосудов, где соединения эффективно препятствуют передаче сигналов посредством Tie2.
EA200802407A 2006-06-13 2007-06-12 Замещенные аминопиразолопиридины и их соли, их получения и фармацевтические композиции, которые их содержат EA200802407A1 (ru)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
EP06090109A EP1867648A1 (en) 2006-06-13 2006-06-13 Substituted aminopyrazolopyridines and salts thereof, their preparations and pharmaceutical compositions comprising them.
EP07090020 2007-02-15
PCT/EP2007/005432 WO2007144204A1 (en) 2006-06-13 2007-06-12 Substituted aminopyrazolopyridines and salts thereof, their preparations and pharmaceutical compositions comprising them

Publications (1)

Publication Number Publication Date
EA200802407A1 true EA200802407A1 (ru) 2009-06-30

Family

ID=38445661

Family Applications (1)

Application Number Title Priority Date Filing Date
EA200802407A EA200802407A1 (ru) 2006-06-13 2007-06-12 Замещенные аминопиразолопиридины и их соли, их получения и фармацевтические композиции, которые их содержат

Country Status (21)

Country Link
US (1) US7846928B2 (ru)
EP (1) EP2061790B1 (ru)
JP (1) JP5475442B2 (ru)
KR (1) KR20090018212A (ru)
AR (1) AR061346A1 (ru)
AU (1) AU2007260216A1 (ru)
BR (1) BRPI0711961A2 (ru)
CA (1) CA2654789C (ru)
CL (1) CL2007001711A1 (ru)
CR (1) CR10505A (ru)
EA (1) EA200802407A1 (ru)
EC (1) ECSP088963A (ru)
ES (1) ES2515117T3 (ru)
GT (1) GT200800285A (ru)
IL (1) IL195813A0 (ru)
MX (1) MX2008015955A (ru)
NO (1) NO20090171L (ru)
PE (1) PE20080205A1 (ru)
TW (1) TW200815438A (ru)
UY (1) UY30409A1 (ru)
WO (1) WO2007144204A1 (ru)

Families Citing this family (14)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
PE20061119A1 (es) * 2005-01-19 2006-11-27 Aventis Pharma Sa PIRAZOLO PIRIDINAS SUSTITUIDAS COMO INHIBIDORES DE CINASAS FAK, KDR Y Tie
CN101903384A (zh) * 2007-11-02 2010-12-01 沃泰克斯药物股份有限公司 作为蛋白激酶Cθ抑制剂的[1H-吡唑并[3,4-B]吡啶-4-基]-苯基或-吡啶-2-基衍生物
EP2300427A1 (en) * 2008-05-05 2011-03-30 Amgen Inc. Urea compounds as gamma secretase modulators
AU2009262199B2 (en) 2008-06-27 2012-08-09 Amgen Inc. Ang-2 inhibition to treat multiple sclerosis
SG171765A1 (en) 2008-11-20 2011-07-28 Genentech Inc Pyrazolopyridine pi3k inhibitor compounds and methods of use
EP2789615B1 (en) 2009-08-11 2017-05-03 Bristol-Myers Squibb Company Azaindazoles as Btk kinase modulators and use thereof
EP2516437B1 (en) 2009-12-21 2014-01-29 Novartis AG Disubstituted heteroaryl-fused pyridines
WO2013148460A1 (en) * 2012-03-26 2013-10-03 Swenson Rolf E Novel sphingosine 1-phosphate receptor antagonists
WO2013188848A2 (en) * 2012-06-15 2013-12-19 The Regents Of The University Of California Antiviral compounds and methods of use
WO2017053604A1 (en) 2015-09-23 2017-03-30 The Regents Of The University Of California Potent antiviral pyrazolopyridine compounds
JOP20190024A1 (ar) 2016-08-26 2019-02-19 Gilead Sciences Inc مركبات بيروليزين بها استبدال واستخداماتها
MX2020003671A (es) 2017-10-06 2020-08-03 Forma Therapeutics Inc Inhibicion de peptidasa especifica de ubiquitina 30.
ES2962605T3 (es) 2018-02-26 2024-03-20 Gilead Sciences Inc Compuestos de pirrolizina sustituidos como inhibidores de la replicación del VHB
EP4218934A1 (en) 2018-10-05 2023-08-02 Forma Therapeutics, Inc. Inhibiting ubiquitin-specific protease 30 (usp30)

Family Cites Families (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6670364B2 (en) * 2001-01-31 2003-12-30 Telik, Inc. Antagonists of MCP-1 function and methods of use thereof
EP1638941B1 (en) 2003-05-22 2010-06-02 Abbott Laboratories Indazole, benzisoxazole, and benzisothiazole kinase inhibitors
US20070293511A1 (en) * 2003-12-22 2007-12-20 Sb Pharmco Puerto Rico Inc. And Neurocrine Biosciences, Inc., A Corporation Crf Receptor Antagonists and Methods
FR2876691B1 (fr) * 2004-10-18 2006-12-29 Sanofi Aventis Sa Derives de pyridine, leur preparation, leur application en therapeutique
WO2006050109A2 (en) * 2004-10-29 2006-05-11 Abbott Laboratories Novel kinase inhibitors
PE20061119A1 (es) * 2005-01-19 2006-11-27 Aventis Pharma Sa PIRAZOLO PIRIDINAS SUSTITUIDAS COMO INHIBIDORES DE CINASAS FAK, KDR Y Tie
EP1683796A1 (en) * 2005-01-24 2006-07-26 Schering Aktiengesellschaft Pyrazolopyridines, their preparation and their medical use
ATE423118T1 (de) * 2005-06-27 2009-03-15 Sanofi Aventis Pyrazolopyridinderivate als inhibitoren der kinase 1 des beta-adrenergen rezeptors

Also Published As

Publication number Publication date
US20080058326A1 (en) 2008-03-06
JP2009539914A (ja) 2009-11-19
CA2654789C (en) 2014-08-05
CL2007001711A1 (es) 2008-01-04
CA2654789A1 (en) 2007-12-21
ECSP088963A (es) 2009-01-30
MX2008015955A (es) 2009-01-09
WO2007144204A1 (en) 2007-12-21
PE20080205A1 (es) 2008-06-01
IL195813A0 (en) 2009-09-22
ES2515117T3 (es) 2014-10-29
AR061346A1 (es) 2008-08-20
BRPI0711961A2 (pt) 2012-01-17
NO20090171L (no) 2009-03-12
US7846928B2 (en) 2010-12-07
KR20090018212A (ko) 2009-02-19
CR10505A (es) 2009-03-20
JP5475442B2 (ja) 2014-04-16
TW200815438A (en) 2008-04-01
EP2061790B1 (en) 2014-08-13
UY30409A1 (es) 2008-01-31
GT200800285A (es) 2009-03-09
EP2061790A1 (en) 2009-05-27
AU2007260216A1 (en) 2007-12-21

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