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Merck
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文件

527450

Sigma-Aldrich

Imidazolo-oxindole PKR inhibitor C16

≥90% (HPLC), solid, PKR inhibitor, Calbiochem®

别名:

PKR 抑制剂

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About This Item

经验公式(希尔记法):
C13H8N4OS
分子量:
268.29
MDL號碼:
分類程式碼代碼:
12352200
NACRES:
NA.77

product name

PKR 抑制剂, The PKR Inhibitor, also referenced under CAS 608512-97-6, controls the biological activity of PKR. This small molecule/inhibitor is primarily used for Phosphorylation & Dephosphorylation applications.

品質等級

化驗

≥90% (HPLC)

形狀

solid

製造商/商標名

Calbiochem®

儲存條件

OK to freeze
protect from light

顏色

orange to orange-brown

溶解度

DMSO: 5 mg/mL

運輸包裝

ambient

儲存溫度

2-8°C

InChI

1S/C13H8N4OS/c18-13-8(3-7-4-14-5-15-7)11-9(17-13)1-2-10-12(11)19-6-16-10/h1-6H,(H,14,15)(H,17,18)/b8-3-

InChI 密鑰

VFBGXTUGODTSPK-BAQGIRSFSA-N

一般說明

一种咪唑-羟吲哚化合物,作为PKR的一种有效的ATP结合位点定向抑制剂。显示可有效抑制RNA诱导的PKR自磷酸化(IC50 =210 nM)并挽救PKR依赖性翻译阻断(IC50=100 nM)。也可以使用非活性对照(目录号 527455。显示可增加持久突触增强的晚期阶段,并增强小鼠的长期记忆。也可以50 mM的DMSO溶液(货号527451)提供。
一种咪唑-羟吲哚化合物,作为PKR的一种有效的ATP结合位点定向抑制剂。显示可有效抑制RNA诱导的PKR自磷酸化(IC50 =210 nM)并挽救PKR依赖性翻译阻断(IC50=100 nM)。显示可增加持久突触增强的晚期阶段,并增强小鼠的长期记忆。也可以使用非活性对照(目录号527455)。

生化/生理作用

主要靶标
PKR
产物不与ATP竞争。
可逆:否
细胞渗透性:否
靶标IC50:210 nM抑制RNA诱导的PKR自磷酸化,100 nM挽救PKR依赖性翻译阻断

包裝

用惰性气体包装

警告

毒性:致癌/致畸(D)

重構

复溶后,等分并冷冻保存(-20°C)。贮备液在-20°C下可稳定保存至多3个月。

其他說明

Zhu, P.J., et al. 2011.Cell147, 1384.
Jammi, N.V., et al. 2003.Biochem.Biophys.Res. Commun.308, 50.

法律資訊

CALBIOCHEM is a registered trademark of Merck KGaA, Darmstadt, Germany

儲存類別代碼

11 - Combustible Solids

水污染物質分類(WGK)

WGK 3

閃點(°F)

Not applicable

閃點(°C)

Not applicable


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