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Alternative structural projections:


8- Piperidinoadenosine- 3', 5'- cyclic monophosphorothioate, Sp- isomer ( Sp-8-PIP-cAMPS ), sodium salt
Site selective analogue of the PDE-resistant PKA agonist Sp-cAMPS
Cat. No.: P 005
CAS No.: [156816-35-2]
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Product Name Price (net) Qty
Cat. No.: P 005-05
Unit: 5 µmol / ~2.3 mg
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).
Cat. No. P 005
CAS number [156816-35-2]
Purity > 98% HPLC
Salt form Sodium
Storage temperature -20°C / -4°F
Molecular formula C₁₅H₂₀N₆O₅PS · Na
Molecular weight [g/mol] 450,4
Modifications 8-cAMP
Target PKA (cAK) Activator
Lipophilicity 2.39
Absorption max [nm] 273
Molar extinction coefficient ε [L·mol⁻¹·cm⁻¹] 15000