Potent (IC50=40nM) and selective (290X selectivity over other PDE isoforms) inhibitor of phosphodiesterase Type II (PDE2). Displayed no significant level of binding to neither a collection of 54 receptors and ion channels, nor to a panel of 30 kinases. B
Molecular Weight:
314.3
Purity:
98% (TLC)
Formula:
C14H10N4O3S
Target:
PDE2
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