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Merck
CN

90221

Supelco

瑞替加滨

analytical standard

别名:

D-23129, N-(2-氨基-4-(4-氟苄基氨基)苯基)氨基甲酸乙酯, 依佐加滨

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About This Item

经验公式(希尔记法):
C16H18FN3O2
分子量:
303.33
Beilstein:
8072099
MDL编号:
UNSPSC代码:
41116107
PubChem化学物质编号:
NACRES:
NA.24

等级

analytical standard

质量水平

方案

≥98.0% (HPLC)

保质期

limited shelf life, expiry date on the label

药品控制

USDEA Schedule IV

技术

HPLC: suitable
gas chromatography (GC): suitable

杂质

≤1.0% water (calc. from elemental analysis)

应用

forensics and toxicology
veterinary

包装形式

neat

储存温度

2-8°C

SMILES字符串

FC1=CC=C(CNC2=CC(N)=C(NC(OCC)=O)C=C2)C=C1

InChI

1S/C16H18FN3O2/c1-2-22-16(21)20-15-8-7-13(9-14(15)18)19-10-11-3-5-12(17)6-4-11/h3-9,19H,2,10,18H2,1H3,(H,20,21)

InChI key

PCOBBVZJEWWZFR-UHFFFAOYSA-N

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相关类别

一般描述

瑞替加滨是一种抗癫痫药物,它通过诱导稳态激活的大型超极化转变(hyperpolarizing shift)来激活神经元 KCNQ 型 K+ 通道。

应用

瑞替加滨可用作参考标准品,用于通过高效液相色谱结合串联质谱和正离子大气压化学电离(HPLC-APCI-MS/MS)测定生物基质中的瑞替加滨。

生化/生理作用

瑞替加滨是一种 Kv7.2-7.5 钾通道激活剂; 抗惊厥药。
瑞替加滨(依佐加滨)是一种具有抗惊厥活性的 Kv7.2-7.5 (KCNQ2-5)神经元钾通道开放剂。

象形图

Skull and crossbonesEnvironment

警示用语:

Danger

危险声明

危险分类

Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Aquatic Acute 1 - Aquatic Chronic 1

储存分类代码

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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访问文档库

The new anticonvulsant retigabine favors voltage-dependent opening of the Kv7. 2 (KCNQ2) channel by binding to its activation gate.
Wuttke VT, et al.
Molecular Pharmacology, 94, 71-76 (2005)
Identification, characterization, synthesis and HPLC quantification of new process-related impurities and degradation products in retigabine.
Dousa M, et al.
Journal of Pharmaceutical and Biomedical Analysis, 94, 71-76 (2014)
Determination of retigabine and its acetyl metabolite in biological matrices by on-line solid-phase extraction (column switching) liquid chromatography with tandem mass spectrometry.
Knebel GN, et al.
Journal of Chromatography. B, Biomedical Sciences and Applications, 748(1), 97-111 (2000)
Lyubov I Brueggemann et al.
Molecular pharmacology, 86(3), 330-341 (2014-06-20)
Recent research suggests that smooth muscle cells express Kv7.4 and Kv7.5 voltage-activated potassium channels, which contribute to maintenance of their resting membrane voltage. New pharmacologic activators of Kv7 channels, ML213 (N-mesitybicyclo[2.2.1]heptane-2-carboxamide) and ICA-069673 N-(6-chloropyridin-3-yl)-3,4-difluorobenzamide), have been reported to discriminate among

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