PU3 is an Hsp90 inhibitor that competes with geldanamycin (GM) and others for the conserved ATP/ADP pocket of Hsp90. PU3 also induces degradation of proteins such as Her2 and inhibits breast cancer cell growth by causing retinoblastoma protein hypophosphorylation, G1 arrest, and cell differentiation. PU3 has the potential to be a cancer inhibitor.[1].
Molekulargewicht:
371.43
CAS Nummer:
[352519-21-2]
Formel:
C19H25N5O3
Target-Kategorie:
HSP
Anwendungsbeschreibung:
MCE Product type: Reference compound1
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