2 - 吡啶甲酰胺,6 - 氨基-N-甲基-5 - (2,3,5 - 三氯苯基) -
- CAS号:875051-72-2
- 英文名:PF-01247324
- 中文名:2 - 吡啶甲酰胺,6 - 氨基-N-甲基-5 - (2,3,5 - 三氯苯基) -
- CBNumber:CB42682530
- 分子式:C13H10Cl3N3O
- 分子量:330.6
- MOL File:875051-72-2.mol
- 沸点 :477.7±45.0 °C(Predicted)
- 密度 :1.460±0.06 g/cm3(Predicted)
- 储存条件 :room temp
- 溶解度 :DMF: 30 mg/ml; DMSO: 30 mg/ml; Ethanol: 30 mg/ml; Ethanol:PBS (pH 7.2) (1:4): 0.2 mg/ml
- 酸度系数(pKa) :6.56±0.46(Predicted)
- 形态 :powder
- 颜色 :white to beige
- 危险品运输编号 :UN 2811 6.1 / PGIII
2 - 吡啶甲酰胺,6 - 氨基-N-甲基-5 - (2,3,5 - 三氯苯基) -性质、用途与生产工艺
- 生物活性 PF-01247324是选择性且有口服活性的Nav1.8通道阻断物,对人类重组Nav1.8 的IC50值为196 nM。
-
靶点
IC50: 196 nM (hNa v 1.8)
-
体外研究
PF-01247324 inhibits native tetrodotoxin-resistant (TTX-R) currents in human dorsal root ganglion (DRG) neurons (IC 50 =331 nM) and in recombinantly expressed h Na v 1.8 channels (IC 50 =196 nM), with 50-fold selectivity over recombinantly expressed TTX-R hNav1.5 channels (IC 50 =10 μM) and 65-100-fold selectivity over TTX-sensitive (TTX-S) channels (IC 50 =10-18 μM). In vitro current clamp shows that PF-01247324 reduces excitability in both rat and human DRG neurons and also alters the waveform of the action potential.
-
体内研究
Experiments n rodents demonstrates efficacy in both inflammatory and neuropathic pain models. PF-01247324 reduces phase 2 flinching by 37% at 100 mg/kg. There is a significant effect of 30 mg/kg of PF-01247324 in the rat model carrageenan-induced thermal hyperalgesia and in CFA-induced mechanical hyperalgesia at exposures of 0.218 and 0.126 μM respectively. Mice that received PF-01247324 shows significant improvements in motor coordination and cerebellar-like symptoms compared to control.
- 更新日期:2024/11/08
- 产品编号:HY-101383
- 产品名称:2 - 吡啶甲酰胺,6 - 氨基-N-甲基-5 - (2,3,5 - 三氯苯基) - PF-01247324
- CAS编号:875051-72-2
- 包装:5mg
- 价格:700元
- 更新日期:2024/11/08
- 产品编号:HY-101383
- 产品名称:2 - 吡啶甲酰胺,6 - 氨基-N-甲基-5 - (2,3,5 - 三氯苯基) - PF-01247324
- CAS编号:875051-72-2
- 包装:10mM * 1mLin DMSO
- 价格:770元
- 公司名称:TargetMol Chemicals Inc.
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