Design and synthesis of potent, selective, and orally bioavailable tetrasubstituted imidazole inhibitors of p38 mitogen-activated protein kinase 4-(Bromoacetyl)pyridine hydrobromide was used to prepare 2-Phenyl-4-(4-pyridyl)imidazole.
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Aplicaciones
Diseño y síntesis de inhibidores de imidazol potentes, selectivos y biodisponibles por vía oral tetrasustituidos de la proteína quinasa activada por mitógeno p38. Se utilizó hidrobromuro de 4-(bromoacetil)piridina para preparar 2-fenil-4-(4-piridil)imidazol.
Solubilidad
Soluble en agua.
Notas
Almacenar en un lugar fresco. Mantener el recipiente bien cerrado en un lugar seco y bien ventilado. Almacenar alejado de agentes oxidantes fuertes y bases.
RUO – Research Use Only
Nigel J. Liverton,; John W. Butcher,; Christopher F. Claiborne,; David A. Claremon,; Brian E. Libby,; Kevin T. Nguyen,; Steven M. Pitzenberger,; Harold G. Selnick,; Garry R. Smith,; Andrew Tebben. Design and Synthesis of Potent, Selective, and Orally Bioavailable Tetrasubstituted Imidazole Inhibitors of p38 Mitogen-Activated Protein Kinase . J. Med. Chem. 1999, 42 (12),2180-2190.