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Product details
名称
PF-04856264
分子类型
小分子
英文名称
PF-04856264
货号
P654480-1ml
包装规格
1ml
浓度
10mM in DMSO
储存温度
-80℃储存
运输条件
超低温冰袋运输
产品介绍
PF-04856264 is a potent and selective Nav1.7 inhibitor, with IC 50 s of 28, 131, 19, and 42 nM for human, mouse, cynomolgus monkey and dog Nav1.7, respectively. PF-04856264 has low potency against the rat Nav1.7 channel. PF-04856264 shows analgesic effect In Vivo PF-04856264 (3-30 mg/kg; i.p.) reverses OD1-induced pain behaviors. MCE has not independently confirmed the accuracy of these methods. They are for reference only. Animal Model: 6-8 weeks adult male C57BL/6J mice (OD1-induced spontaneous pain model)Dosage: 3, 30 mg/kg Administration: I.p. Result: Significantly reduced spontaneous pain behaviors in mice. IC50& Target:IC50: 28 (human Nav1.7), 131 nM (mouse Nav1.7), 19 nM (cynomolgus monkey Nav1.7), 42 nM (dog Nav1.7)
生化机理
PF-04856264 是一种强效的选择性 Nav1.7 抑制剂,对人、小鼠、猴和狗 Nav1.7 的 IC 50 s 分别为 28、131、19 和 42 nM。PF-04856264 对大鼠 Nav1.7 通道的效力较低。PF-04856264 具有镇痛作用
CAS号
1235397-05-3(DMSO)
分子式
C20H15N5O3S2
分子量
437.49 g/mol
Smiles
CN1C(=CC=N1)C2=CC=CC=C2OC3=C(C=C(C=C3)S(=O)(=O)NC4=NC=CS4)C#N
Safety
「No Dangerous Attributes」
Related
「No upstream and downstream information yet」
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PF-04856264 1ml

PF-04856264 1ml; supplied for laboratory research, analysis, inspection, and scientific procurement use; specifications: 1ml.

item number:P654480-1ml
Product model:1ml
level: 1ml
Lead Time:30days
sold 671 Items
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1ml

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