Thienopyridone is a potent and selective phosphatase of regenerating liver (PRL) phosphatase inhibitor with IC50s of 173 nM, 277 nM and 128 nM for PRL-1, PRL-2, and PRL-3, respectively. Thienopyridone shows minimal effects on other phosphatases. Thienopyridone induces p130Cas cleavage and apoptosis and has anticancer effects[1].
Molekulargewicht:
242.30
Reinheit:
98.05
CAS Nummer:
[1018454-97-1]
Formel:
C13H10N2OS
Target-Kategorie:
Apoptosis,Phosphatase
Anwendungsbeschreibung:
MCE Product type: Reference compound
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