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贝美格 /Bemegride {[allProObj[0].p_purity_real_show]}

货号:A149990 同义名: Bemegrid;3-Ethyl-3-methylglutarimide

Bemegride can stimulate central nervous system and release barbiturate poisoning.

Bemegride 化学结构 CAS号:64-65-3
Bemegride 化学结构
CAS号:64-65-3
Bemegride 3D分子结构
CAS号:64-65-3
Bemegride 化学结构 CAS号:64-65-3
Bemegride 3D分子结构 CAS号:64-65-3
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Bemegride 纯度/质量文件 产品仅供科研

货号:A149990 标准纯度: {[allProObj[0].p_purity_real_show]}
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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 HDAC,Autophagy 97%
Flumazenil 95%
Bemegride 98%
Bicuculline +++

GABAA receptor, IC50: 2 μM

98+%
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。

Bemegride 生物活性

靶点
  • GABAA receptor

描述 Bemegride had an antagonistic action on the GABAA receptor, suppressing both GABA- and pentobarbitone-evoked whole-cell currents to similar extents[3]. The intensity of withdrawal syndrome in rats treated with barbital alone or in combination with the stimulant bemegride or pentylenettrazol was approximately parallel to the degree of related central nervous system depression[4]. The bemegride discriminative stimulus generalized to PTZ (20mg/kg) and was antagonized by chlordiazepoxide (10 mg/kg). Bemegride and cocaine generalized to the PTZ (pentylenetetrazol) discriminative stimulus in a dose-dependent manner, but d-amphetamine, methylphenidate, and nicotine did not[5]. Administration of subconvulsant doses of bemegride results in extensive enhancement of sensory responsiveness to auditory, visual, somatosensory and vibrissa stimulation of neurons in the medullary and mesencephalic reticular formation (RF)[6].

Bemegride 参考文献

[1]Mistry DK, Cottrell GA. Actions of steroids and bemegride on the GABAA receptor of mouse spinal neurones in culture. Exp Physiol. 1990 Mar;75(2):199-209.

[2]Arblaster CI, Cameron DW, et al. Studies on the development of physical dependence on barbitone in the rat and rat atrium. Farmaco Sci. 1986 Jan;41(1):3-22.

[3]Mistry DK, Cottrell GA. Actions of steroids and bemegride on the GABAA receptor of mouse spinal neurones in culture. Exp Physiol. 1990 Mar;75(2):199-209

[4]Arblaster CI, Cameron DW, Laycock GM, Shulman A. Studies on the development of physical dependence on barbitone in the rat and rat atrium. Farmaco Sci. 1986 Jan;41(1):3-22

[5]Shearman G, Lal H. Discriminative stimulus properties of pentylenetetrazol and bemegride: some generalization and antagonism tests. Psychopharmacology (Berl). 1979 Sep;64(3):315-9

[6]Faingold CL, Hoffmann WE. Effects of bemegride on the sensory responses of neurons in the hippocampus and brain stem reticular formation. Electroencephalogr Clin Neurophysiol. 1981 Oct;52(4):316-27

Bemegride 实验方案

计算器
存储液制备 1mg 5mg 10mg

1 mM

5 mM

10 mM

6.44mL

1.29mL

0.64mL

32.22mL

6.44mL

3.22mL

64.44mL

12.89mL

6.44mL

Bemegride 技术信息

CAS号64-65-3
分子式C8H13NO2
分子量 155.194
别名 Bemegrid;3-Ethyl-3-methylglutarimide;Zentraleptin;Mikedimide;Malysol;Eukraton;Ahypnon;Agipnon;Antibarbi
运输蓝冰
存储条件

液体 -20°C:3-6个月-80°C:12个月

粉末 Sealed in dry,2-8°C

溶解度

DMSO: 30 mg/mL(193.31 mM),注意:DMSO长时间开封后,会吸水并导致溶解能力下降,请避免使用长期开封的DMSO

动物实验配方
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