CBT-295 is an orally active autotaxin (ATX) inhibitor. CBT-295 exhibits a significant reduction in inflammatory cytokines like TGF-beta, TNF-alpha and IL-6 levels, also reduced bile duct proliferation marker CK-19 and lowered liver fibrosis. The reversal of liver fibrosis with CBT-295 led to a reduction in blood and brain ammonia levels. CBT-295 also reduced neuroinflammation induced by ammonia. CBT-295 is promising for research of liver cirrhosis and associated encephalopathy[1].
Molekulargewicht:
329.82
Reinheit:
99.34
Formel:
C18H20ClN3O
Target-Kategorie:
Interleukin Related,TGF-beta/Smad
Anwendungsbeschreibung:
MCE Product type: Reference compound
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