货号:A517196
同义名:
DZL-221; DM9384
Nefiracetam is a neuronal systems enhancer for Ro 5-4864-induced convulsions. Nefiracetam has GABAergic, cholinergic, and monoaminergic properties.
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产品名称 | GABA receptor ↓ ↑ | GABAA receptor ↓ ↑ | 其他靶点 | 纯度 | |||||||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Niflumic Acid | ✔ | 98% | |||||||||||||||||
Ginkgolide A |
++
GABA receptor, Ki: 14.5 μM |
98% | |||||||||||||||||
Valproic acid sodium | ✔ | Autophagy,HDAC | 97% | ||||||||||||||||
Flumazenil | ✔ | 95% | |||||||||||||||||
Bemegride | ✔ | 98% | |||||||||||||||||
Bicuculline |
+++
GABAA receptor, IC50: 2 μM |
99% | |||||||||||||||||
1. 鼠标悬停在“+”上可以显示相关IC50的具体数值。"+"越多,抑制作用越强。2. "✔"表示该化合物对相应的亚型有抑制作用,但抑制强度暂时没有相关数据。 |
描述 | Nefiracetam enhances neuronal systems related to GABAergic, cholinergic, and monoaminergic pathways and is used to manage Ro 5-4864-induced convulsions. It targets the GABA Receptor. At submicromolar concentrations (0.01-0.1 μM), Nefiracetam leads to a short-term reduction of ACh-evoked currents, decreasing them to 30% and 38% of the baseline after a 10-minute exposure, respectively. At higher micromolar concentrations (1-10 μM), it causes a long-term enhancement of these currents. This interaction with PKA and PKC pathways might explain the cellular mechanisms underlying the cognitive enhancement provided by Nefiracetam[1]. Orally administered, Nefiracetam prevents Ro 5-4864-induced convulsions in EL and DDY mice, particularly at doses exceeding 10 mg/kg[2]. Administering Nefiracetam 1 hour prior to each training session on a daily basis enhances the learning of the avoidance behavior [3]. |
计算器 | ||||
存储液制备 | ![]() |
1mg | 5mg | 10mg |
1 mM 5 mM 10 mM |
4.06mL 0.81mL 0.41mL |
20.30mL 4.06mL 2.03mL |
40.60mL 8.12mL 4.06mL |
CAS号 | 77191-36-7 |
分子式 | C14H18N2O2 |
分子量 | 246.3 |
SMILES Code | O=C(NC1=C(C)C=CC=C1C)CN2C(CCC2)=O |
MDL No. | MFCD00209882 |
别名 | DZL-221; DM9384 |
运输 | 蓝冰 |
InChI Key | NGHTXZCKLWZPGK-UHFFFAOYSA-N |
Pubchem ID | 71157 |
存储条件 |
In solvent -20°C:3-6个月-80°C:12个月 Pure form Sealed in dry,2-8°C |
溶解方案 |
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