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Alternative structural projections:


N6- Phenyladenosine- 3', 5'- cyclic monophosphate ( 6-Phe-cAMP ), sodium salt

Site-selective PKA agonist, Epac-negative control
Cat. No.: P 006
CAS No.: [34051-30-4]
Shipping: ambient
Product Name Price (net) Qty
Cat. No.: P 006-05
Unit: 5 µmol / ~2.1 mg
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).
Cat. No. P 006
CAS number [34051-30-4]
Purity > 98% HPLC
Salt form Sodium
Storage temperature -20°C / -4°F
Molecular formula C₁₆H₁₅N₅O₆P · Na
Molecular weight [g/mol] 427.3
Target PKA (cAK) Activator
Lipophilicity 2.46
Absorption max [nm] 288
Molar extinction coefficient ε [L·mol⁻¹·cm⁻¹] 20800
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