TAK-915 is a selective inhibitor of phosphodiesterase 2A (PDE2A) with an IC50 of 0.61 nM, demonstrating over 4100-fold selectivity for PDE2A compared to PDE1A. This brain-penetrant and orally active compound is of particular interest for research focused on neuropsychiatric and neurodegenerative disorders. Its unique mechanism of action positions TAK-915 as a valuable tool in the study of underlying pathways in these conditions.
TAK-915 is a selective inhibitor of phosphodiesterase 2A (PDE2A) with an IC50 of 0.61 nM, demonstrating over 4100-fold selectivity for PDE2A compared to PDE1A. This brain-penetrant and orally active compound is of particular interest for research focused on neuropsychiatric and neurodegenerative disorders. Its unique mechanism of action positions TAK-915 as a valuable tool in the study of underlying pathways in these conditions.
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