Potent, cell permeable and specific inhibitor of protein arginine N-methyltransferases (PRMTs) (IC50=8.8µM for human PRMT1 and 3.0µM for yeast Hmt1p). Does not compete for the AdoMet (S-adenosyl-L-methionine, SAM) binding site. Exhibits only minimal effe
Molecular Weight:
592.4
Purity:
98% (HPLC)
CAS Number:
[20324-87-2]
Formula:
C21H12N2O9S2Na4
Target:
PRMT
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