Sp-8-pCPT-cAMPS structure
|
Common Name | Sp-8-pCPT-cAMPS | ||
|---|---|---|---|---|
| CAS Number | 129693-13-6 | Molecular Weight | 509.85900 | |
| Density | N/A | Boiling Point | N/A | |
| Molecular Formula | C16H14ClN5NaO5PS2 | Melting Point | N/A | |
| MSDS | N/A | Flash Point | N/A | |
Use of Sp-8-pCPT-cAMPSSp-8-CPT-cAMPS, a cAMP analog, is a potent and selective activator of the cAMP-dependent protein kinas A (PKA I and PKA II). Sp-8-CPT-cAMPS selects site A of RI compares to site A of RII by 153-fold and site B of RII compares to site B of RI by 59-fold[1][2]. |
| Name | 8-(4-chlorophenylthio) adenosine-3',5'-cyclic monophosphorothioate, sp-isomer sodium salt |
|---|
| Description | Sp-8-CPT-cAMPS, a cAMP analog, is a potent and selective activator of the cAMP-dependent protein kinas A (PKA I and PKA II). Sp-8-CPT-cAMPS selects site A of RI compares to site A of RII by 153-fold and site B of RII compares to site B of RI by 59-fold[1][2]. |
|---|---|
| Related Catalog | |
| Target |
PKA[1] |
| In Vitro | Sp-8-CPT-cAMPS (100 μM; 24 h) enhances the IL-1β-stimulated nitrite release, and increases the release ofnitrite by vascular smooth muscle cells by 3 fold in the absence of IL-1β in vascular smooth muscle cells[2]. Sp-8-CPT-cAMPS (100 μM; 24 h) increases IL-1β-induced expression of iNOS protein in rat aortic smooth muscle cells[2]. Sp-8-CPT-cAMPS (10 μM; 30 min) exhibits anti-spasmogenic activity on ACh-induced tension development in guinea-pig trachealis[3]. |
| References |
| Molecular Formula | C16H14ClN5NaO5PS2 |
|---|---|
| Molecular Weight | 509.85900 |
| Exact Mass | 508.97600 |
| PSA | 207.80000 |
| LogP | 3.77360 |
| InChIKey | IVNQJYQKSYRLTE-IYKFWPKASA-N |
| SMILES | Nc1ncnc2c1nc(Sc1ccc(Cl)cc1)n2C1OC2COP(O)(=S)OC2C1O |