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Merck
CN

U120

Sigma-Aldrich

U0126 钛酸乙酯 单乙醇盐

≥98% (HPLC), powder

别名:

1,4-二氨基-2,3-二氰基-1,4-双(邻-氨基苯硫醇)丁二烯钛酸乙酯 单乙醇盐

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About This Item

经验公式(希尔记法):
C18H16N6S2 · C2H5OH
分子量:
426.56
MDL编号:
UNSPSC代码:
12352200
PubChem化学物质编号:
NACRES:
NA.77

质量水平

方案

≥98% (HPLC)

表单

powder

储存条件

protect from light

颜色

white to off-white

溶解性

DMSO: >10 mg/mL (Stock solutions in DMSO should be used within a month. Acidic solutions exhibit weaker inhibition)

储存温度

2-8°C

SMILES字符串

N#CC(C(C#N)=C(N)SC1=C(N)C=CC=C1)=C(N)SC2=C(N)C=CC=C2.CCO

InChI

1S/C18H16N6S2.C2H6O/c19-9-11(17(23)25-15-7-3-1-5-13(15)21)12(10-20)18(24)26-16-8-4-2-6-14(16)22;1-2-3/h1-8H,21-24H2;3H,2H2,1H3

InChI key

CFQULUVMLGZVAF-UHFFFAOYSA-N

基因信息

相关类别

应用

U0126乙醇盐已用作一种MEK抑制剂,用在鸡胚乳房肌衍生的单核肌原细胞中。U0126 也已用于研究淀粉样蛋白前体蛋白(APP)敲除(KO)小鼠神经元中的 ERK2 功能

生化/生理作用

U0126 是 MEK1 和 MEK2(MAP 激酶激酶;MAPKK)的特异性抑制剂;还抑制 MEK 的组成型活性突变形式。
U0126,1,4-二氨基-2,3-二氰基-1,4-双[2-氨基苯硫基]丁二烯是 MEK1 和 MEK2 的高选择性抑制剂。 U0126 通过非竞争性抑制双特异性激酶 MEK,在功能上拮抗 AP-1 转录活性,MEK1的 IC50 为 72nM,MEK2 的 IC50 为 58nM。 U0126 通过同时阻断细胞外信号调节激酶(ERK)和哺乳动物雷帕霉素靶蛋白(mTOR)-p70(S6K)途径,抑制 Ki-ras 转化的大鼠成纤维细胞的贴壁依赖性生长。U0126 对 8 种人乳腺癌细胞系生长的影响表明,U0126 选择性地抑制 MDA-MB231 和HBC4 细胞的锚定非依赖性生长,这两种细胞具有组成型激活的 ERK。在许多正常细胞类型中,与基质失去接触会引发细胞凋亡,这种现象称为失巢凋亡。U0126 使得 MDA-MB231 和 HBC4 对失巢凋亡敏感,即在用 U0126 处理后,失去锚定的细胞将进入凋亡。

特点和优势

《受体分类和信号转导》手册的 MAPK 页面有该化合物的介绍。如需浏览其他手册页面,请点击此处
该化合物是激酶磷酸酶生物学研究的特色产品。点击此处 ,查看更多激酶磷酸酶生物学精选产品。了解更多有关用于其他研究领域的生物活性小分子的信息,请访问 sigma.com/discover-bsm

注意

光敏感的

制备说明

U0126乙醇盐可以>10 mg/ml的浓度溶于DMSO。本产品在 DMSO 中的储备溶液应在一个月内使用。本产品的酸性溶液表现出较弱的 MEK 抑制功能。

储存分类代码

11 - Combustible Solids

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

个人防护装备

Eyeshields, Gloves, type N95 (US)


历史批次信息供参考:

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Journal of immunology (Baltimore, Md. : 1950), 160(9), 4175-4181 (1998-05-09)
Three mitogen-activated protein kinase pathways are up-regulated during the activation of T lymphocytes, the extracellular signal-regulated kinase (ERK), Jun NH2-terminal kinase, and p38 mitogen-activated protein kinase pathways. To examine the effects of blocking the ERK pathway on T cell activation
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