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Merck
CN

I1661

Sigma-Aldrich

ICA-105574

≥98% (HPLC)

别名:

3-nitro-N-(4-phenoxyphenyl)-benzamide

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关于此项目

经验公式(希尔记法):
C19H14N2O4
化学文摘社编号:
分子量:
334.33
MDL编号:
UNSPSC代码:
12352200
PubChem化学物质编号:
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方案

≥98% (HPLC)

表单

powder

颜色

off-white to light tan

溶解性

DMSO: >20 mg/mL

储存温度

room temp

SMILES字符串

[O-][N+](=O)c1cccc(c1)C(=O)Nc2ccc(Oc3ccccc3)cc2

InChI

1S/C19H14N2O4/c22-19(14-5-4-6-16(13-14)21(23)24)20-15-9-11-18(12-10-15)25-17-7-2-1-3-8-17/h1-13H,(H,20,22)

InChI key

GDWKBKTVROCPNZ-UHFFFAOYSA-N

生化/生理作用

ICA-105574 is a potent and efficacious hERG potassium channel activator, that removes hERG inactivation.
hERG (Kv11.1) is a voltage-gated potassium channel with important cardiovascular function. Many potential and marketed drugs bind to and inhibit hERG function, causing prolongation of the electrocardiogram QT interval, which leads to life-threatening ventricular arrhythmias. Understanding of hERG function is critical for drug discovery and development. hERG exhibits a unique bell-shaped current-voltage relationship which is a result of very rapid inactivation of the channel upon voltage activation. ICA-105574 is a small molecule activator of hERG that binds to the channel to remove inactivation, thereby increasing peak current amplitude and shortening the action potential. It also modulates activation kinetics of the channel. ICA-105574 differs in efficacy, mechanism of action, and/or binding site from other known hERG activators and enhancers. This compound is a valuable tool for furthering understanding of hERG biophysics and physiology, expecially the structural transitions that occur during inactivation.

特点和优势

This compound is featured on the Potassium Channels page of the Handbook of Receptor Classification and Signal Transduction. To browse other handbook pages, click here.

象形图

Exclamation markEnvironment

警示用语:

Warning

危险声明

危险分类

Aquatic Acute 1 - Eye Irrit. 2 - Skin Sens. 1

储存分类代码

13 - Non Combustible Solids

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

法规信息

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历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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Jared N Tschirhart et al.
Molecular pharmacology, 95(4), 386-397 (2019-01-23)
The human ether-a-go-go-related gene (hERG) encodes the pore-forming subunit of the rapidly activating delayed rectifier potassium channel (IKr). Drug-mediated or medical condition-mediated disruption of hERG function is the primary cause of acquired long-QT syndrome, which predisposes affected individuals to ventricular

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