Site selective cyclic AMP analogue with high selectivity for site A of protein kinase A type I and for site B of type II. Acts synergistically together with analogues having opposite site-selectivity. Combination with e.g. 8-HA-cAMP (Prod. No. BLG-H006) preferentially activates type I, while e.g. with 6-MBC-cAMP (Prod. No. BLG-M012) selects type II. Increased metabolic stability and membrane permeability compared to cAMP.
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