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Diphenyleneiodonium chloride {[allProObj[0].p_purity_real_show]}

货号:A246246 同义名: 二苯基氯化碘盐 / DPI;Diphenyleneiodonium (chloride)

Diphenyleneiodonium chloride是一种 NADPH 氧化酶 (NOX) 抑制剂,同时作为 TRPA1 激活剂,EC50 为 1 至 3 μM,选择性抑制细胞内活性氧

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Accessible (Haz class 3, 4, 5 or 8), Domestic USD 100+
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Diphenyleneiodonium chloride 化学结构 CAS号:4673-26-1
Diphenyleneiodonium chloride 化学结构
CAS号:4673-26-1
Diphenyleneiodonium chloride 3D分子结构
CAS号:4673-26-1
Diphenyleneiodonium chloride 化学结构 CAS号:4673-26-1
Diphenyleneiodonium chloride 3D分子结构 CAS号:4673-26-1
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Diphenyleneiodonium chloride 纯度/质量文件 产品仅供科研

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Diphenyleneiodonium chloride 生物活性

描述 Transient receptor potential ankyrin 1 (TRPA1) is a Ca2+-permeable nonselective cation channel expressed in neuronal and nonneuronal cells and plays an important role in acute and inflammatory pain. Diphenyleneiodonium chloride (DPI), a NADPH oxidase (NOX) inhibitor, also functions as a TRPA1 activator with an EC50 of 1 to 3 μM. Application of DPI at 0.03-10 μM induced a Ca2+ response in HEK-TRPA1 cells in a concentration-dependent manner. In inflammatory human synoviocytes where TRPA1 is functionally expressed, 3 μM DPI evoked a Ca2+ response when cells were treated with IL1α suggesting that DPI activates endogenous TRPA1 expressed in human synoviocytes[3]. In human RPE cell line ARPE-19 cells, DPI (0.1, 1, and 10 μM) resulted in a significant decrease of cell proliferation, without vacuolation and detachment of the cells from the dish. Significantly increased level of p53 was detected at 4 h after treatment of DPI[4]. In mice, intraplantar injection of 2 mM DPI caused a pain-related response which was inhibited by preadministration with HC (a selective TRPA1 antagonist, HC-030031)[3].

Diphenyleneiodonium chloride 参考文献

[1]Pandey M, Singh AK, et al. Diphenyleneiodonium chloride (DPIC) displays broad-spectrum bactericidal activity. Sci Rep. 2017 Sep 14;7(1):11521.

[2]Osaki T, Uchida Y, et al. Diphenyleneiodonium chloride, an inhibitor of reduced nicotinamide adenine dinucleotide phosphate oxidase, suppresses light-dependent induction of clock and DNA repair genes in zebrafish. Biol Pharm Bull. 2011;34(8):1343-7.

[3]Suzuki H, Hatano N, Muraki Y, Itoh Y, Kimura S, Hayashi H, Onozaki K, Ohi Y, Haji A, Muraki K. The NADPH oxidase inhibitor diphenyleneiodonium activates the human TRPA1 nociceptor. Am J Physiol Cell Physiol. 2014 Aug 15;307(4):C384-94.

[4]Park SE, Song JD, Kim KM, Park YM, Kim ND, Yoo YH, Park YC. Diphenyleneiodonium induces ROS-independent p53 expression and apoptosis in human RPE cells. FEBS Lett. 2007 Jan 23;581(2):180-6.

Diphenyleneiodonium chloride 实验方案

计算器
存储液制备 1mg 5mg 10mg

1 mM

5 mM

10 mM

3.18mL

0.64mL

0.32mL

15.90mL

3.18mL

1.59mL

31.79mL

6.36mL

3.18mL

Diphenyleneiodonium chloride 技术信息

CAS号4673-26-1
分子式C12H8ClI
分子量 314.549
别名 二苯基氯化碘盐 ;DPI;Diphenyleneiodonium (chloride)
运输蓝冰
存储条件

液体 -20°C:3-6个月-80°C:12个月

粉末 Keep in dark place,Inert atmosphere,Store in freezer, under -20°C

溶解度

DMSO: 5 mg/mL(15.9 mM),配合低频超声,并水浴加热至45℃助溶,注意:DMSO长时间开封后,会吸水并导致溶解能力下降,请避免使用长期开封的DMSO

动物实验配方

3% DMSO+40% PEG 300+2% Tween 80+water 0.5 mg/mL

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