WO2004054505A3 - Procede d'utilisation de composes d'aminocyanopyridine en tant qu'inhibiteurs de la proteine mapkap kinase-2 - Google Patents

Procede d'utilisation de composes d'aminocyanopyridine en tant qu'inhibiteurs de la proteine mapkap kinase-2 Download PDF

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Publication number
WO2004054505A3
WO2004054505A3 PCT/US2003/039166 US0339166W WO2004054505A3 WO 2004054505 A3 WO2004054505 A3 WO 2004054505A3 US 0339166 W US0339166 W US 0339166W WO 2004054505 A3 WO2004054505 A3 WO 2004054505A3
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WO
WIPO (PCT)
Prior art keywords
protein kinase
activated protein
inhibitors
mitogen
aminocyanopyridine compounds
Prior art date
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PCT/US2003/039166
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English (en)
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WO2004054505A2 (fr
Inventor
Emily J Reinhard
Stephen A Kolodziej
David R Anderson
Nathan W Stehle
William F Vernier
Len F Lee
Shridhar G Hegde
Original Assignee
Pharmacia Corp
Emily J Reinhard
Stephen A Kolodziej
David R Anderson
Nathan W Stehle
William F Vernier
Len F Lee
Shridhar G Hegde
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Publication date
Application filed by Pharmacia Corp, Emily J Reinhard, Stephen A Kolodziej, David R Anderson, Nathan W Stehle, William F Vernier, Len F Lee, Shridhar G Hegde filed Critical Pharmacia Corp
Priority to MXPA05006367A priority Critical patent/MXPA05006367A/es
Priority to AU2003296414A priority patent/AU2003296414A1/en
Priority to CA002508780A priority patent/CA2508780A1/fr
Priority to BR0317183-3A priority patent/BR0317183A/pt
Priority to JP2004560746A priority patent/JP2006512338A/ja
Priority to EP03813364A priority patent/EP1569645A2/fr
Publication of WO2004054505A2 publication Critical patent/WO2004054505A2/fr
Publication of WO2004054505A3 publication Critical patent/WO2004054505A3/fr

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    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/47Quinolines; Isoquinolines
    • A61K31/4738Quinolines; Isoquinolines ortho- or peri-condensed with heterocyclic ring systems
    • A61K31/4745Quinolines; Isoquinolines ortho- or peri-condensed with heterocyclic ring systems condensed with ring systems having nitrogen as a ring hetero atom, e.g. phenantrolines
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    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/41Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
    • A61K31/4151,2-Diazoles
    • A61K31/41621,2-Diazoles condensed with heterocyclic ring systems
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    • 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
    • A61K31/41Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
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    • A61K31/41Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
    • A61K31/41641,3-Diazoles
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    • A61K31/435Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
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    • A61K31/435Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
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Abstract

La présente invention a trait à un procédé permettant l'inhibition de la protéine MAPKKK chez un sujet qui en a besoin, qui comprend l'administration au sujet d'un composé d'aminocyanopyridine MK-2, ou un de ses sels pharmaceutiquement acceptables.
PCT/US2003/039166 2002-12-12 2003-12-09 Procede d'utilisation de composes d'aminocyanopyridine en tant qu'inhibiteurs de la proteine mapkap kinase-2 WO2004054505A2 (fr)

Priority Applications (6)

Application Number Priority Date Filing Date Title
MXPA05006367A MXPA05006367A (es) 2002-12-12 2003-12-09 Metodo de uso de compuestos de aminocianopiridina como inhibidores de cinasa-2 de proteina activada de cinasa de proteina activada por mitogeno.
AU2003296414A AU2003296414A1 (en) 2002-12-12 2003-12-09 Method of using aminocyanopyridine compounds as mitogen activated protein kinase-activated protein kinase-2 inhibitors
CA002508780A CA2508780A1 (fr) 2002-12-12 2003-12-09 Procede d'utilisation de composes d'aminocyanopyridine en tant qu'inhibiteurs de la proteine mapkap kinase-2
BR0317183-3A BR0317183A (pt) 2002-12-12 2003-12-09 Método de usar compostos de aminocianopiridina como inibidores de proteìna quinase-2 ativada por proteìna quinase ativada por mitógeno
JP2004560746A JP2006512338A (ja) 2002-12-12 2003-12-09 マイトジェン活性化プロテインキナーゼ−活性化プロテインキナーゼ−2阻害剤としてのアミノシアノピリジンの使用法
EP03813364A EP1569645A2 (fr) 2002-12-12 2003-12-09 Procede d'utilisation de composes d'aminocyanopyridine en tant qu'inhibiteurs de la proteine mapkap kinase-2

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US43280702P 2002-12-12 2002-12-12
US60/432,807 2002-12-12

Publications (2)

Publication Number Publication Date
WO2004054505A2 WO2004054505A2 (fr) 2004-07-01
WO2004054505A3 true WO2004054505A3 (fr) 2004-09-02

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PCT/US2003/039166 WO2004054505A2 (fr) 2002-12-12 2003-12-09 Procede d'utilisation de composes d'aminocyanopyridine en tant qu'inhibiteurs de la proteine mapkap kinase-2

Country Status (7)

Country Link
EP (1) EP1569645A2 (fr)
JP (1) JP2006512338A (fr)
AU (1) AU2003296414A1 (fr)
BR (1) BR0317183A (fr)
CA (1) CA2508780A1 (fr)
MX (1) MXPA05006367A (fr)
WO (1) WO2004054505A2 (fr)

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AU2003296414A8 (en) 2004-07-09
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BR0317183A (pt) 2005-11-01
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