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Erastin/爱拉斯汀 {[allProObj[0].p_purity_real_show]}

货号:A145112

Erastin is a compound that interacts with VDAC, blocks and reverses mitochondrial depolarization after microtubule destabilizers in intact cells and antagonized tubulin-induced VDAC blockage in planar bilayers. It is also a ferroptosis inducer.

Erastin/爱拉斯汀 化学结构 CAS号:571203-78-6
Erastin/爱拉斯汀 化学结构
CAS号:571203-78-6
Erastin/爱拉斯汀 3D分子结构
CAS号:571203-78-6
Erastin/爱拉斯汀 化学结构 CAS号:571203-78-6
Erastin/爱拉斯汀 3D分子结构 CAS号:571203-78-6
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Erastin/爱拉斯汀 纯度/质量文件 产品仅供科研

货号:A145112 标准纯度: {[allProObj[0].p_purity_real_show]}
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全球学术期刊中引用的产品

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产品名称 Ferroptosis 其他靶点 纯度
Ferrostatin-1 ++

Ferroptosis, EC50: 60 nM

98%
Liproxstatin-1 +++

ferroptosis, IC50: 22 nM

99%+
1. 鼠标悬停在“+”上可以显示相关IC50的具体数值。"+"越多,抑制作用越强。2. "✔"表示该化合物对相应的亚型有抑制作用,但抑制强度暂时没有相关数据。

Erastin/爱拉斯汀 生物活性

描述 Erastin is an inducer of ferroptosis, initiating cell death through mechanisms involving reactive oxygen species (ROS) and iron-dependent pathways. It targets and inhibits the voltage-dependent anion channels (VDAC2/VDAC3), which leads to an increase in oxidation and subsequently, a buildup of ROS within cells. Furthermore, Erastin interferes with the mitochondrial permeability transition pore (mPTP), displaying anti-tumor properties[1].[2].[3].

Erastin/爱拉斯汀 细胞研究

细胞系 浓度 检测类型 检测时间 活性说明 数据源
human A673 cells Function assay Induction of cell death in human A673 cells, EC50=30 μM. 17568748
human BJ cells Function assay Induction of cell death in human BJ cells expressing TERT, LT, ST and RAS G12V mutant genes cells in presence of PD-98059 by trypan blue exclusion method, IC50=0.9 μM. 17568748
human BJ cells Function assay Induction of cell death in TERT expressing human BJ cells, EC50=10 μM. 17568748
human BJ cells Function assay Induction of cell death in human BJ cells expressing TERT, LT, ST and RAS G12V mutant genes in presence of U0126 by trypan blue exclusion method, IC50=31.2 μM. 17568748

Erastin/爱拉斯汀 动物研究

Animal study For animal studies, Erastin is utilized to create models demonstrating ferroptosis. Administered intraperitoneally at 40 mg/kg every three days for a duration of two weeks, Erastin reduces endometriotic lesions in mice with endometriosis, suggesting it alleviates ectopic lesions by inducing ferroptosis[1]. At dosages of 10 mg/kg and 30 mg/kg, given intraperitoneally once daily for four weeks, Erastin curbs the growth of HT-29 xenografts in SCID mice, with the higher dosage displaying greater effectiveness[2].

Erastin/爱拉斯汀 参考文献

[1]Li Y, et al. Erastin induces ferroptosis via ferroportin-mediated iron accumulation in endometriosis. Hum Reprod. 2021 Mar 18;36(4):951-964.

[2]Huo H, et al. Erastin Disrupts Mitochondrial Permeability Transition Pore (mPTP) and Induces Apoptotic Death of Colorectal Cancer Cells. PLoS One. 2016 May 12;11(5):e0154605.

[3]Xie Y, et al. Ferroptosis: process and function. Cell Death Differ. 2016 Mar;23(3):369-79.

Erastin/爱拉斯汀 实验方案

计算器
存储液制备 1mg 5mg 10mg

1 mM

5 mM

10 mM

1.83mL

0.37mL

0.18mL

9.14mL

1.83mL

0.91mL

18.28mL

3.66mL

1.83mL

Erastin/爱拉斯汀 技术信息

CAS号571203-78-6
分子式C30H31ClN4O4
分子量 547.04
SMILES Code O=C1N(C2=CC=CC=C2OCC)C(C(N3CCN(C(COC4=CC=C(Cl)C=C4)=O)CC3)C)=NC5=C1C=CC=C5
MDL No. MFCD09837984
别名
运输蓝冰
InChI Key BKQFRNYHFIQEKN-UHFFFAOYSA-N
Pubchem ID 11214940
存储条件

In solvent -20°C:3-6个月-80°C:12个月

Pure form Keep in dark place, inert atmosphere, room temperature

动物实验配方

5%DMSO+40%PEG 300+5%Tween80+water 1.75 mg/mL

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