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- 详细信息
- 技术资料
- 保存条件:
Powder: -20°C, 3 years; 4°C, 2 years. In solvent: -80°C, 6 months; -20°C, 1 month.
- 库存:
货期:1-2天
- 供应商:
MedChemExpress LLC
- CAS号:
1266212-81-0
- 规格:
10 mM * 1 mL/1 mg/5 mg/10 mg/25 mg/50 mg
| 规格: | 10 mM * 1 mL | 产品价格: | ¥1595.0 |
|---|---|---|---|
| 规格: | 1 mg | 产品价格: | ¥659.0 |
| 规格: | 5 mg | 产品价格: | ¥1450.0 |
| 规格: | 10 mg | 产品价格: | ¥2550.0 |
| 规格: | 25 mg | 产品价格: | ¥5500.0 |
| 规格: | 50 mg | 产品价格: | ¥9500.0 |
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A-887826
CAS No. : 1266212-81-0
MCE 国际站:A-887826
产品活性:A-887826 是一种高效、选择性的,口服有效的,电压依赖性的 Na(v)1.8 钠通道阻滞剂,其 IC50 值为 11 nM。在体内,A-88782 6可减轻神经性触觉痛。
研究领域:Membrane Transporter/Ion Channel
作用靶点:Sodium Channel
In Vitro: A-887826 is approximately 3 fold less potent to block Na(v)1.2, approximately 10 fold less potent to block tetrodotoxin-sensitive sodium (TTX-S Na(+)) currents and is >30 fold less potent to block Na(v)1.5 channels.
A-887826 potently blocks tetrodotoxin-resistant sodium (TTX-R Na(+)) currents (IC50=8 nM) from small diameter rat dorsal root ganglion (DRG) neurons in a voltage-dependent fashion.
A-887826 effectively suppresses evoked action potential firing when DRG neurons are held at depolarized potentials and reversibly suppresses spontaneous firing in small diameter DRG neurons from complete Freund's adjuvant inflamed rats.
A-887826 (100 nM) shifts the mid-point of voltage-dependent inactivation of TTX-R currents by approximately 4mV without affecting voltage-dependent activation and do not exhibit frequency-dependent inhibition.
In Vivo: A-887826 (3-30 mg/kg; p.o.; 1 hour pre-treatment) significantly attenuates tactile allodynia in a rat neuropathic pain model.
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