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.
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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。 |
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]. |
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 | ||
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]. |
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 |
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 |