FCPR16 is a selective inhibitor of Phosphodiesterase 4 (PDE4), a crucial enzyme involved in the hydrolysis of cyclic adenosine monophosphate (cAMP). By inhibiting PDE4, FCPR16 effectively increases cAMP levels in SH-SY5Y neuroblastoma cells, facilitating enhanced signaling pathways associated with neuronal functions. This compound is valuable for research investigating the molecular mechanisms underlying Parkinson's disease and other neurodegenerative disorders.
FCPR16 is a selective inhibitor of Phosphodiesterase 4 (PDE4), a crucial enzyme involved in the hydrolysis of cyclic adenosine monophosphate (cAMP). By inhibiting PDE4, FCPR16 effectively increases cAMP levels in SH-SY5Y neuroblastoma cells, facilitating enhanced signaling pathways associated with neuronal functions. This compound is valuable for research investigating the molecular mechanisms underlying Parkinson's disease and other neurodegenerative disorders.
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