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PF-04449613 Sale

目录号 : GC47939

A PDE9A inhibitor

PF-04449613 Chemical Structure

Cas No.:1236858-52-8

规格 价格 库存 购买数量
1 mg
¥274.00
现货
5 mg
¥1,298.00
现货
10 mg
¥2,225.00
现货
25 mg
¥4,895.00
现货

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Sample solution is provided at 25 µL, 10mM.

Description

PF-04449613 is a phosphodiesterase 9A (PDE9A) inhibitor (IC50 = 22 nM).1 It is selective for PDE9A over PDE1C (IC50 = >1,000 nM), as well as over a variety of other PDEs, inhibiting PDE2-8, -10, and -11 activity by less than 30% in a panel of enzymes, ion channels, and transporters at 1 µM but does inhibit the human dopamine transporter (DAT; Ki = 293 nM). PF-04449613 (0.1-100 mg/kg, s.c.) increases cerebrospinal fluid (CSF) levels of cyclic GMP (cGMP) in rats. Subcutaneous administration of PF-04449613 (10 mg/kg) increases the rate of dendritic spine formation and elimination in mouse primary motor cortex pyramidal neurons in vivo.2 It increases the average running speed of mice in an accelerating rotarod task, indicating improved motor learning, at the same dose.

1.Claffey, M.M., Helal, C.J., Verhoest, P.R., et al.Application of structure-based drug design and parallel chemistry to identify selective, brain penetrant, in vivo active phosphodiesterase 9A inhibitorsJ. Med. Chem.55(21)9055-9068(2012) 2.Lai, B., Li, M., Hu, A., et al.The phosphodiesterase 9 inhibitor PF-04449613 promotes dendritic spine formation and performance improvement after motor learningDev. Neurobiol.78(9)859-872(2018)

化学性质

Cas No. 1236858-52-8 SDF
Canonical SMILES O=C1N=C([C@@H](C)N2CC(OC3=CC=CC=C3)C2)NC4=C1C=NN4C5CCOCC5
分子式 C21H25N5O3 分子量 395.5
溶解度 DMSO: 10 mg/ml 储存条件 Store at -20°C
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储备液的保存方式和期限:-80°C 储存时,请在 6 个月内使用,-20°C 储存时,请在 1 个月内使用。
为了提高溶解度,请将管子加热至37℃,然后在超声波浴中震荡一段时间。
Shipping Condition 评估样品解决方案:配备蓝冰进行发货。所有其他可用尺寸:配备RT,或根据请求配备蓝冰。

溶解性数据

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1 mg 5 mg 10 mg
1 mM 2.5284 mL 12.6422 mL 25.2845 mL
5 mM 0.5057 mL 2.5284 mL 5.0569 mL
10 mM 0.2528 mL 1.2642 mL 2.5284 mL
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