Lipophilic precursor of Rp-cAMPS, a competitive inhibitor of protein kinase A type I and II ( cyclic AMP antagonist). During metabolic activation by esterases the inhibitor and butyrate are released. Significantly more lipophilic and membrane permeant compared to Rp-cAMPS. Resistant against mammalian cyclic nucleotide-dependent phosphodiesterases.
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