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Merck
CN

SML2007

Sigma-Aldrich

PMI

≥98% (HPLC)

别名:

1-(3-Iodophenyl)-4-(3-nitrophenyl)-1H-1,2,3-triazole, HB229, P62-Mediated mitophagy inducer

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关于此项目

经验公式(希尔记法):
C14H9IN4O2
化学文摘社编号:
分子量:
392.15
UNSPSC代码:
12352200
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方案

≥98% (HPLC)

表单

powder

颜色

white to beige

溶解性

DMSO: 2 mg/mL, clear (warmed)

储存温度

2-8°C

SMILES字符串

Ic1cc(ccc1)[n]2nnc(c2)c3cc(ccc3)[N+](=O)[O-]

InChI key

LSVWEYNSNZJEGB-UHFFFAOYSA-N

生化/生理作用

P62-mediated mitophagy inducer
PMI is a p62-mediated mitophagy inducer. It is believed to upregulate the major autophagy receptor ubiquitin-binding protein p62 (also named sequestosome 1/SQSTM1) via stabilization of Nrf2. PMI was shown to induce Nrf2 dependent gene products and inhibit the Keap1?Nrf2 protein?protein interaction while being partially dependent upon Parkin and PINK1.

象形图

Flame

警示用语:

Danger

危险声明

危险分类

Self-react. C

储存分类代码

5.2 - Organic peroxides and self-reacting hazardous materials

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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Hélène C Bertrand et al.
Journal of medicinal chemistry, 58(18), 7186-7194 (2015-09-09)
The transcription factor Nrf2 regulates the expression of a large network of cytoprotective and metabolic enzymes and proteins. Compounds that directly and reversibly inhibit the interaction between Nrf2 and its main negative regulator Keap1 are potential pharmacological agents for a
Nikolaos D Georgakopoulos et al.
Nature chemical biology, 13(2), 136-146 (2017-01-20)
Small molecules are pharmacological tools of considerable value for dissecting complex biological processes and identifying potential therapeutic interventions. Recently, the cellular quality-control process of mitophagy has attracted considerable research interest; however, the limited availability of suitable chemical probes has restricted
Daniel A East et al.
Chemistry & biology, 21(11), 1585-1596 (2014-12-03)
Mitophagy is central to mitochondrial and cellular homeostasis and operates via the PINK1/Parkin pathway targeting mitochondria devoid of membrane potential (ΔΨm) to autophagosomes. Although mitophagy is recognized as a fundamental cellular process, selective pharmacologic modulators of mitophagy are almost nonexistent.

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