EA201300997A1 - ПИРИДО[2,3-b]ПИРАЗИНОВЫЕ ПРОИЗВОДНЫЕ И ИХ ТЕРАПЕВТИЧЕСКИЕ ПРИМЕНЕНИЯ - Google Patents

ПИРИДО[2,3-b]ПИРАЗИНОВЫЕ ПРОИЗВОДНЫЕ И ИХ ТЕРАПЕВТИЧЕСКИЕ ПРИМЕНЕНИЯ

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Publication number
EA201300997A1
EA201300997A1 EA201300997A EA201300997A EA201300997A1 EA 201300997 A1 EA201300997 A1 EA 201300997A1 EA 201300997 A EA201300997 A EA 201300997A EA 201300997 A EA201300997 A EA 201300997A EA 201300997 A1 EA201300997 A1 EA 201300997A1
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EA
Eurasian Patent Office
Prior art keywords
pyrido
therapeutic applications
kinases
derivatives
pirazine
Prior art date
Application number
EA201300997A
Other languages
English (en)
Inventor
Дитер Дорш
Альфред Йончик
Гюнтер Хёльцеманн
Кристиане Амендт
Франк Ценке
Original Assignee
Мерк Патент Гмбх
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.)
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Application filed by Мерк Патент Гмбх filed Critical Мерк Патент Гмбх
Publication of EA201300997A1 publication Critical patent/EA201300997A1/ru

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    • 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
    • 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
    • A61K31/4985Pyrazines or piperazines ortho- or peri-condensed with heterocyclic ring systems
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
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    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P29/00Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
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    • C07D491/00Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00
    • C07D491/02Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains two hetero rings
    • C07D491/04Ortho-condensed systems
    • C07D491/044Ortho-condensed systems with only one oxygen atom as ring hetero atom in the oxygen-containing ring
    • C07D491/048Ortho-condensed systems with only one oxygen atom as ring hetero atom in the oxygen-containing ring the oxygen-containing ring being five-membered

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Abstract

Настоящее изобретение относится к новым пиридо[2,3-b]пиразиновым производным формулы (I) и к применению таких соединений, при котором играет роль ингибирование, регуляция и/или модуляция передачи сигналов с помощью АТФ-связывающих белков, подобных киназам, в частности к ингибиторам TGF-бета рецепторных киназ, и к применению таких соединений для лечения заболеваний, индуцированных киназами, в частности для лечения опухолей.
EA201300997A 2011-03-09 2012-02-13 ПИРИДО[2,3-b]ПИРАЗИНОВЫЕ ПРОИЗВОДНЫЕ И ИХ ТЕРАПЕВТИЧЕСКИЕ ПРИМЕНЕНИЯ EA201300997A1 (ru)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
EP11001944 2011-03-09
PCT/EP2012/000630 WO2012119690A1 (en) 2011-03-09 2012-02-13 Pyrido [2, 3 - b] pyrazine derivatives and their therapeutical uses

Publications (1)

Publication Number Publication Date
EA201300997A1 true EA201300997A1 (ru) 2014-02-28

Family

ID=45607719

Family Applications (1)

Application Number Title Priority Date Filing Date
EA201300997A EA201300997A1 (ru) 2011-03-09 2012-02-13 ПИРИДО[2,3-b]ПИРАЗИНОВЫЕ ПРОИЗВОДНЫЕ И ИХ ТЕРАПЕВТИЧЕСКИЕ ПРИМЕНЕНИЯ

Country Status (16)

Country Link
US (1) US9051318B2 (ru)
EP (1) EP2683715B1 (ru)
JP (1) JP6104824B2 (ru)
KR (1) KR20140022829A (ru)
CN (1) CN103391938B (ru)
AR (1) AR085637A1 (ru)
AU (1) AU2012224979B2 (ru)
BR (1) BR112013022948A2 (ru)
CA (1) CA2829287C (ru)
EA (1) EA201300997A1 (ru)
ES (1) ES2542647T3 (ru)
IL (1) IL228265A (ru)
MX (1) MX2013010163A (ru)
SG (1) SG193301A1 (ru)
WO (1) WO2012119690A1 (ru)
ZA (1) ZA201307511B (ru)

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CA2829287C (en) * 2011-03-09 2019-12-17 Merck Patent Gmbh Pyrido [2,3-b] pyrazine derivatives and their therapeutical uses
AU2014373773C1 (en) 2014-01-01 2019-06-27 Medivation Technologies Llc Compounds and methods of use
JP6767875B2 (ja) * 2014-04-08 2020-10-14 ライジェル ファーマシューティカルズ, インコーポレイテッド Tgf−ベータ阻害剤としての2,3−二置換ピリジン化合物および使用方法
US10342786B2 (en) 2017-10-05 2019-07-09 Fulcrum Therapeutics, Inc. P38 kinase inhibitors reduce DUX4 and downstream gene expression for the treatment of FSHD
CA3128468A1 (en) 2017-10-05 2019-04-11 Fulcrum Therapeutics, Inc. P38 kinase inhibitors reduce dux4 and downstream gene expression for the treatment of fshd
CN109053598B (zh) * 2018-06-14 2021-04-13 温州大学 一种芳基取代喹唑啉化合物及其合成方法
US20230090552A1 (en) 2020-01-08 2023-03-23 Synthis Therapeutics, Inc. Alk5 inhibitor conjugates and uses thereof

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AU1918299A (en) 1998-02-23 1999-09-06 Warner-Lambert Company Substituted quinoxaline derivatives as interleukin-8 receptor antagonists
US6184226B1 (en) 1998-08-28 2001-02-06 Scios Inc. Quinazoline derivatives as inhibitors of P-38 α
GB9904387D0 (en) 1999-02-25 1999-04-21 Pharmacia & Upjohn Spa Antitumour synergistic composition
WO2000061186A1 (en) 1999-04-08 2000-10-19 Arch Development Corporation Use of anti-vegf antibody to enhance radiation in cancer therapy
AU2003229305A1 (en) 2002-05-17 2003-12-02 Scios, Inc. TREATMENT OF FIBROPROLIFERATIVE DISORDERS USING TGF-Beta INHIBITORS
EP1575506A4 (en) 2002-07-25 2008-04-23 Scios Inc METHOD FOR IMPROVING LUNG FUNCTION WITH TGF-BETA INHIBITORS
EP1603908B1 (en) * 2003-03-12 2008-06-11 Millennium Pharmaceuticals, Inc. Quinazoline derivatives as tgf-beta inhibitors
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WO2005023807A2 (en) 2003-09-09 2005-03-17 Neurogen Corporation 4 - heterobicyclyamino - substituted quinazolines and analogues therof as capsaicin - antagonists
WO2005042498A2 (en) 2003-10-31 2005-05-12 Neurogen Corporation 4-amino (aza) quinoline derivatives as capsaicin receptor agonists
US20050245508A1 (en) 2003-12-24 2005-11-03 Scios, Inc. Treatment of malignant gliomas with TGF-beta inhibitors
TW200621251A (en) 2004-10-12 2006-07-01 Neurogen Corp Substituted biaryl quinolin-4-ylamine analogues
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Also Published As

Publication number Publication date
SG193301A1 (en) 2013-10-30
AU2012224979A1 (en) 2013-10-24
CA2829287C (en) 2019-12-17
JP6104824B2 (ja) 2017-03-29
IL228265A (en) 2016-12-29
AU2012224979B2 (en) 2017-01-19
US9051318B2 (en) 2015-06-09
MX2013010163A (es) 2013-10-30
EP2683715A1 (en) 2014-01-15
ZA201307511B (en) 2016-08-31
CN103391938A (zh) 2013-11-13
WO2012119690A1 (en) 2012-09-13
KR20140022829A (ko) 2014-02-25
EP2683715B1 (en) 2015-04-15
CN103391938B (zh) 2016-02-24
BR112013022948A2 (pt) 2016-12-06
IL228265A0 (en) 2013-11-25
AR085637A1 (es) 2013-10-16
ES2542647T3 (es) 2015-08-07
US20130345227A1 (en) 2013-12-26
JP2014511390A (ja) 2014-05-15
CA2829287A1 (en) 2012-09-13

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