产品
编 号:F691207
分子式:C19H18F4N4O5
分子量:458.36
产品类型
结构图
CAS No: 1476727-50-0
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产品详情
生物活性:
TAK-915 is a potent, selective, brain-penetrant and orally active phosphodiesterase 2A (PDE2A) inhibitor with an IC50 of 0.61 nM. TAK-915 is >4100-fold more selectivity for PDE2A than PDE1A. TAK-915 has the potential for neuropsychiatric and neurodegenerative disorders treatment.
体内研究:
TAK-915 (3 mg/kg; oral administration; daily; for 4 days; male F344 rats) treatment significantly reduces escape latency in aged rats in the Morris water maze task.TAK-915 (1, 3, and 10?mg/kg, p.o.) dose-dependently attenuates the non-selective muscarinic antagonist scopolamine-induced memory deficits in rats. Oral dosing of TAK-915 (compound 36) (3 or 10 mg/kg) in mice produces a dose-dependent increase in 3',5'-cyclic guanosine monophosphate (cGMP) levels, with significant cGMP increases observed at a dose of 10 mg/kg.Animal Model:Male F344 rats (10-week-old and 26-month-old) bearing morris water maze task
Dosage:3 mg/kg
Administration:Oral administration; daily; for 4 days
Result:Significantly reduced escape latency in aged rats in the Morris water maze task.