For other salt forms or metabolites please inquire. Potent site-selective and highly membrane-permeant activator of protein kinase A showing strong preference for site A of both isozymes. Together with e.g. SP-5,6-DCl-cBIMPS (Cat. No. D 014) selective stimulation of type II can be achieved. Highly membrane-permeant analogue. Available with phosphorothioate modification (Cat. No. P 018) as well. Detailed technical information and updated reference list available. Reference: Kloss et al., Mol. Pharmacol., 65, 1440 - 1451 (2004).