For other salt forms please inquire. Fluorescent activator of cyclic GMP-dependent protein kinase (λexc 494 nm, λem 517 nm), but most probably inhibitor of the retinal type cGMP-gated ion channel, thus suitable for distinction between kinase and ion channel mediated effects. Resistant against mammalian cyclic nucleotide-dependent phosphodiesterases.
The category "Future Products" lists structures that are already "in the pipeline" and nearly ready to be offered as regular products. Please just inquire, your interest will certainly accelerate the process.
Cat. No. | F 013 |
CAS number | [pending] |
Purity | > 95% |
Salt form | Sodium |
Appearance | Solid |
Storage temperature | -20°C / -4°F |
Light-sensitive | Yes |
Molecular formula | C₄₅H₃₈N₆O₁₃PS · Na |
Molecular weight [g/mol] | 956.9 |
Modifications | 1-cGMP, 2-cGMP, 8-cGMP |
Target | PKG (cGK) Activator |
Excitation max [nm] | 494 |
Emission max [nm] | 517 |
Absorption max [nm] | 499 |
Molar extinction coefficient ε [L·mol⁻¹·cm⁻¹] | 79000 |
UV pH value | 9 |
Solvent for UV data | Water |