N6- Phenyladenosine- 3', 5'- cyclic monophosphorothioate, Sp- isomer ( Sp-6-Phe-cAMPS )

C16H15N5O5PS•Na; MW 443.4; λmax 288 nm; ε 20800; sodium salt; purity > 98% HPLC. PDE-resistant form of 6-Phe-cAMP (Cat. No. P 006), a potent site-selective, membrane-permeant activator of protein kinase A. Sp-6-Phe-cAMPS does not activate Epac and thus can be used as an Epac-negative control. For more details on site selectivity please inquire. Detailed technical information available. Reference: Gjertsen et al., J. Biol. Chem., 270, 20599 - 20607 (1995).
Protected under patent DE 3802865.4 exclusively licensed to BIOLOG LSI
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