| Bioactivity | 8-Benzylthio-cAMP is a derivative of cyclic adenosine monophosphate (cAMP). 8-Bn-cAMP is a site-selective activator of cAMP-dependent protein kinases. Compared with cyclic adenosine monophosphate, it is more stable to phosphodiesterase (PDE) hydrolysis and has higher membrane permeability. 8-Bn-cAMP can be used to study the role of cAMP in regulating cell proliferation, differentiation and apoptosis[1]. |
| CAS | 50655-17-9 |
| Formula | C17H17N5NaO6PS |
| Molar Mass | 473.38 |
| Transport | Room temperature in continental US; may vary elsewhere. |
| Storage | Please store the product under the recommended conditions in the Certificate of Analysis. |
| Reference | [1]. KATAOKA S, et al. Studies on the Synthesis of Compounds Related to Adenosine 3', 5'-Cyclic Phosphate. V.: Synthesis and Cardiac Effect of N6-Alkyladenosine 3', 5'-Cyclic Phosphates and Their 8-Benzylthio Derivatives[J]. Chemical and pharmaceutical bulletin, 1988, 36(6): 2212-2219. |
8-Benzylthio-cAMP
CAS: 50655-17-9 F: C17H17N5NaO6PS W: 473.38
8-Benzylthio-cAMP is a derivative of cyclic adenosine monophosphate (cAMP). 8-Bn-cAMP is a site-selective activator of c
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