Inhibitor of protein kinase C (PKC) and cyclin-dependent kinases (CDKs) resulting in accumulation of cells in the G1 phase and induction of apoptosis. Enhances the cytotoxicity of other anticancer drugs, such as DNA-damaging agents and anti-metabolite dr
Molekulargewicht:
482.5
Quelle:
Isolated from Streptomyces sp. MST-AS5345.
Reinheit:
99% (HPLC)
CAS Nummer:
[112953-11-4]
Formel:
C28H26N4O4
Target-Kategorie:
PKC
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