For other salt forms or higher purity please inquire. Hydrolysis-resistant putative agonist of the second messenger cyclic ADP ribose (Cat. No. C 005) with significantly increased lipophilicity and membrane permeability. The parent compound N1-cIDPR (Cat. No. C 098) is offered as well. Detailed technical information available. Reference for structurally related agonistic N1-cIDPR analogues: Moreau et al., J. Med. Chem., 49, 5162 - 5176 (2006).
| Cat. No. | C 100 |
| CAS number | [pending] |
| Purity | > 97 % HPLC |
| Salt form | Sodium |
| Storage temperature | -70°C / -94°F |
| Molecular formula | C₂₁H₂₃ClN₄O₁₄P₂S (free acid) |
| Molecular weight [g/mol] | 684.9 (free acid) |
| Absorption max [nm] | 274 |
| Molar extinction coefficient ε [L·mol⁻¹·cm⁻¹] | 11000 (est.) |
| UV pH value | 5.5 |
- 1. Moreau C., Wagner G. K., Weber K., Guse A. H.Potter B. V., J. Med. Chem., 49, 5162 - 5172 (2006), "Structural Determinants for N1/N7 Cyclization of Nicotinamide Hypoxanthine 5'-Dinucleotide (NHD+) Derivatives by ADP-Ribosyl Cyclase from Aplysia Californica: Ca2+-Mobilizing Activity of 8-Substituted Cyclic Inosine 5'-Diphosphoribose Analogues in T-Lymphocytes"
