Cat. No.: B 001-05 Unit: 5 μmol / ~2.2 mg
DESCRIPTION: 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)
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