For other salt forms please inquire. Lipophilic analogue of the cyclic AMP antagonist Rp-cAMPS. Prefers type I of protein kinase A. Resistant against mammalian cyclic nucleotide-dependent phosphodiesterases. Significantly more lipophilic and membrane-permeant compared to Rp-cAMPS (
Cat. No. A 002) or 8-Br-cAMP (
Cat. No. B 007). Detailed technical information and updated reference list available on request. References: Gjertsen et al.,
J. Biol. Chem.,
270, 20599 - 20607 (1995), Aandahl et al.,
FASEB J.,
12, 855 - 863 (1998).