8- Piperidinoadenosine- 3', 5'- cyclic monophosphorothioate, Sp- isomer ( Sp-8-PIP-cAMPS )

Site selective analogue of the PDE-resistant PKA agonist Sp-cAMPS
Cat. No.: P 005   CAS No.: [156816-35-2]   
Product Image



C15H20N6O5PS•Na; MW 450.4; λmax 273 nm; ε 15000; sodium salt; purity > 98%. For other salt forms please inquire. Lipophilic site-selective cyclic AMP analogue with extremely high selectivity for site B of protein kinase A type II. Acts synergistically with site A activating analogues for selective activation of type II. Metabolically stable and good membrane permeability. Detailed technical information and updated reference list available. Reference: Øgreid et al., Eur. J. Biochem., 221, 1089 - 1094 (1994).

Protected under patent DE 3802865.4 exclusively licensed to BIOLOG LSI

 



Forgot your password?
Register
Username:
Password:
What is new!

January 13, 2012

6-Fu-ATP-γ-S reference

Lo & Hollingsworth have successfully used 6-Fu-ATP-γ-S (Cat. No. F 008) from BIOLOG in... [more...]

August 18, 2011

New fluorescent cAMP analogue !

Using the fluorescent cAMP analogue 8-[DY-547]-AET-cAMP (or fcAMP) synthesized by BIOLOG, Ku... [more...]