SB 220025 is a reversible, orally active, cell-permeable, ATP-competitive and selective human p38 MAPK inhibitor (IC50 = 60 nM). SB 220025 also inhibits p56Lck and PKC with IC50 values of 3.5 and 2.89 µM, respectively. SB 220025 inhibits the expression of IL-8 gene in response to globular adiponectin (gAd), reduces inflammatory cytokine production and inhibits angiogenesis. SB 220025 effectively prevents the progression of arthritis in a chronic inflammatory disease model and can be used in the study of inflammation[1][2].
Molekulargewicht:
338.38
Reinheit:
99.90
CAS Nummer:
[165806-53-1]
Formel:
C18H19FN6
Target-Kategorie:
p38 MAPK,PKC,Src
Anwendungsbeschreibung:
MCE Product type: Reference compound
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