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
Molecular Weight:
482.5
Source:
Isolated from Streptomyces sp. MST-AS5345.
Purity:
99% (HPLC)
CAS Number:
[112953-11-4]
Formula:
C28H26N4O4
Target:
PKC
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