跳转至内容
Merck
CN
所有图片(2)

文件

324879

Sigma-Aldrich

CCT020312

≥98% (HPLC), solid, EIF2AK3 activator, Calbiochem®

别名:

EIF2AK3活化剂,CCT020312, 6-溴-3-[5-(4-溴-苯基)-1-(3-二乙氨基-丙酰基)-4,5-二氢-1H-吡唑-3-基]-4-苯基-1H-喹啉-2-酮,PERK活化剂,CCT020312

登录查看公司和协议定价


About This Item

经验公式(希尔记法):
C31H30Br2N4O2
分子量:
650.40
MDL编号:
UNSPSC代码:
12352200
NACRES:
NA.77

product name

EIF2AK3活化剂,CCT020312, The EIF2AK3 Activator, CCT020312 modulates the biological activity of EIF2AK3.

质量水平

检测方案

≥98% (HPLC)

形式

solid

制造商/商品名称

Calbiochem®

储存条件

OK to freeze
protect from light

颜色

yellow-white

溶解性

DMSO: 50 mg/mL

运输

ambient

储存温度

−20°C

SMILES字符串

O=C1C(C2=NN(C(CCN(CC)CC)=O)C(C3=CC=C(Br)C=C3)C2)=C(C4=CC=CC=C4)C5=CC(Br)=CC=C5N1

一般描述

一种二氢吡唑衍生物,作为真核翻译起始因子2-α激酶3(eIF2AK3/PERK)的选择性激活剂,并增加HT29和MCF7细胞中EIF2A在Ser51位点的磷酸化。不抑制细胞周期蛋白依赖性激酶的活性,但引起细胞周期蛋白D表达的快速丧失。还显示阻断HT29细胞中的Rb蛋白磷酸化(EC50 = 4.2 µM)。据报道,可使紫杉烷诱导的EIF2A磷酸化缺陷的癌症细胞对紫杉醇治疗敏感。即使去除细胞增殖(GI50 = 3.1 µM),也能诱导长期抑制细胞增殖。

包装

用惰性气体包装

警告

毒性:标准处理(A)

重悬

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

其他说明

Stockwell, S. R., et al. 2011.Plos One In press.

法律信息

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

WGK

WGK 2

闪点(°F)

Not applicable

闪点(°C)

Not applicable


分析证书(COA)

输入产品批号来搜索 分析证书(COA) 。批号可以在产品标签上"批“ (Lot或Batch)字后找到。

已有该产品?

在文件库中查找您最近购买产品的文档。

访问文档库

Shin-Ichi Ikeda et al.
Nature communications, 13(1), 5859-5859 (2022-10-11)
Axial length is the primary determinant of eye size, and it is elongated in myopia. However, the underlying mechanism of the onset and progression of axial elongation remain unclear. Here, we show that endoplasmic reticulum (ER) stress in sclera is
Kai Chen et al.
Aging cell, 21(4), e13592-e13592 (2022-03-18)
Delirium is the most common postoperative complication in older patients after prolonged anesthesia and surgery and is associated with accelerated cognitive decline and dementia. The neuronal pathogenesis of postoperative delirium is largely unknown. The unfolded protein response (UPR) is an
Himanshu Soni et al.
Oncogenesis, 9(2), 18-18 (2020-02-15)
PKR-like kinase (PERK) plays a significant role in inducing angiogenesis in various cancer types including glioblastoma. By proteomics analysis of the conditioned medium from a glioblastoma cell line treated with a PERK inhibitor, we showed that peptidylglycine α-amidating monooxygenase (PAM)
Simon R Stockwell et al.
PloS one, 7(1), e28568-e28568 (2012-01-19)
Human cancers often contain genetic alterations that disable G1/S checkpoint control and loss of this checkpoint is thought to critically contribute to cancer generation by permitting inappropriate proliferation and distorting fate-driven cell cycle exit. The identification of cell permeable small

我们的科学家团队拥有各种研究领域经验,包括生命科学、材料科学、化学合成、色谱、分析及许多其他领域.

联系技术服务部门