您好,欢迎来到试剂仪器网! [登录] [免费注册]
试剂仪器网
位置:首页 > 产品库 > Flumazenil-d5
立即咨询
咨询类型:
     
*姓名:
*电话:
*单位:
Email:
*留言内容:
请详细说明您的需求。
*验证码:
 
Flumazenil-d5
本产品不向个人销售,仅用作科学研究,不用于任何人体实验及非科研性质的动物实验。
Flumazenil-d5图片
包装:2.5mg
规格:98%
市场价:4074元
分子量:308.3

产品介绍
C15H9D5FN3O3
货号:ajcx19428
CAS:N/A
分子式:C15H9D5FN3O3
分子量:308.3
溶解度:Soluble in DMSO
纯度:98%
存储:Store at -20°C
库存:现货

Background:

Flumazenil-d5 is intended for use as an internal standard for the quantification of flumazenil by GC- or LC-MS. Flumazenil is an imidazobenzodiazepine derivative that competitively inhibits benzodiazepine binding to GABAA receptors with an IC50 value of 2 nM.1 Flumazenil is non-selective for α1, α2, α3, or α5 subunit-containing GABAA receptors and antagonizes the actions of benzodiazepines on the central nervous system without producing the behavioral or neurological effects typical of the benzodiazepines.1,2 Formulations containing flumazenil have been used to reverse sedation induced by benzodiazepines and in the treatment of benzodiazepine overdose or withdrawal.

参考文献
1. Hunkeler, W., M•hler, H., Pieri, L., et al. Selective antagonists of benzodiazepines. Nature 290(5806), 514-516 (1981).
2. Atack, J.R., Smith, A.J., Emms, F., et al. Regional differences in the inhibition of mouse in vivo [3H]Ro 15-1788 binding reflect selectivity for α1 versus α2 and α3 subunit-containing GABAA receptors. Neuropsychopharmacology 20(3), 255-262 (1999).