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Merck
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主要文件

SML0583

Sigma-Aldrich

铁抑制剂-1

≥95% (HPLC), powder, non-apoptotic cell death inhibitor

别名:

3-氨基-4-环己基氨基苯甲酸乙酯;

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About This Item

经验公式(希尔记法):
C15H22N2O2
分子量:
262.35
UNSPSC代码:
12352200
NACRES:
NA.77

产品名称

铁抑制剂-1, ≥95% (HPLC)

质量水平

方案

≥95% (HPLC)

表单

powder

颜色

, faint purple to brown

溶解性

DMSO: 10 mg/mL, clear

储存温度

2-8°C

SMILES字符串

N(C2CCCCC2)c1c(cc(cc1)C(=O)OCC)N

InChI

1S/C15H22N2O2/c1-2-19-15(18)11-8-9-14(13(16)10-11)17-12-6-4-3-5-7-12/h8-10,12,17H,2-7,16H2,1H3

InChI key

UJHBVMHOBZBWMX-UHFFFAOYSA-N

应用

已经确定了铁抑制剂-1在细胞死亡上的抑制效果。

生化/生理作用

铁抑制剂-1是一种活性自由基捕获抗氧化剂,能够捕获过氧自由基,可用作铁死亡的潜在抑制剂。铁死亡被认为是调节性坏死,和细胞凋亡和自吞噬不同。铁抑制剂-1能够保护人们免于亨廷顿病,还能在细胞模型中防止谷氨酸诱导的神经毒性。
铁抑制剂-1是一种高效的非凋亡的,erastin诱导铁死亡细胞死亡抑制剂。铁抑制剂-1能够防止癌症细胞中铁死亡细胞死亡和器官型大鼠脑切片中谷氨酸诱导毒性。铁抑制剂-1控制脂溶解ROS。

象形图

Exclamation mark

警示用语:

Warning

危险声明

危险分类

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

靶器官

Respiratory system

储存分类代码

11 - Combustible Solids

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable


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分析证书(COA)

Lot/Batch Number

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访问文档库

The neuroprotective role of ferrostatin-1 under rotenone-induced oxidative stress in dopaminergic neuroblastoma cells.
Kabiraj P, et al.
The Protein Journal, 34(5), 349-358 (2015)
On the mechanism of cytoprotection by ferrostatin-1 and liproxstatin-1 and the role of lipid peroxidation in ferroptotic cell death.
Zilka O, et al.
ACS central science, 3(3), 232-243 (2017)
Salinomycin kills cancer stem cells by sequestering iron in lysosomes.
Mai T T, et al.
Nature Chemistry, 9(10), 1025-1025 (2017)
Miao Sui et al.
Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie, 106, 125-133 (2018-06-30)
Ferroptosis is recently reported as a new mode of regulated cell death. It is triggered by disturbed redox homeostasis, overloaded iron and increased lipid peroxidation. Howerver, the role of ferroptosis in hepatic fibrosis remains obscure. In the current study, we
Yimeng Xia et al.
Frontiers in molecular neuroscience, 11, 486-486 (2019-01-29)
The underlying mechanisms of isoflurane neurotoxicity in the developing brain remain unclear. Ferroptosis is a recently characterized form of programmed cell death distinct from apoptosis or autophagy, characterized by iron-dependent reactive oxygen species (ROS) generation secondary to failure of glutathione-dependent

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