FCPR03 structure
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Common Name | FCPR03 | ||
|---|---|---|---|---|
| CAS Number | 1917347-65-9 | Molecular Weight | 299.318 | |
| Density | N/A | Boiling Point | N/A | |
| Molecular Formula | C15H19F2NO3 | Melting Point | N/A | |
| MSDS | N/A | Flash Point | N/A | |
Use of FCPR03FCPR03 is a novel potent, selective PDE4 inhibitor with IC50 of 60, 31 and 47 nM for PDE4CAT (PDE4 catalytic domain), PDE4B1 and PDE4D7, respectively; displays >2,000-fold selectivity over other PDEs; effectively increases the production of cAMP, promotes CREB phosphorylation, and inhibits NF-κB activation both in vitro and in vivo; displays anti-neuroinflammation potential, promising antidepressant-like effects in vivo. |
| Name | FCPR03 |
|---|
| Description | FCPR03 is a novel potent, selective PDE4 inhibitor with IC50 of 60, 31 and 47 nM for PDE4CAT (PDE4 catalytic domain), PDE4B1 and PDE4D7, respectively; displays >2,000-fold selectivity over other PDEs; effectively increases the production of cAMP, promotes CREB phosphorylation, and inhibits NF-κB activation both in vitro and in vivo; displays anti-neuroinflammation potential, promising antidepressant-like effects in vivo. |
|---|---|
| References | References 1. Zou ZQ, et al. J Pharmacol Exp Ther. 2017 Jul;362(1):67-77. 2. Zhou ZZ, et al. ACS Chem Neurosci. 2017 Jan 18;8(1):135-146. View Related Products by Target Phosphodiesterase (PDE) |
| Molecular Formula | C15H19F2NO3 |
|---|---|
| Molecular Weight | 299.318 |
| InChIKey | DLTIJXDCEGNJEW-UHFFFAOYSA-N |
| SMILES | CC(C)NC(=O)c1ccc(OC(F)F)c(OCC2CC2)c1 |