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Diphenyleneiodonium Chloride (DPI) 二苯基氯化碘鹽
目錄号 MZ2701-50MG 售價 2988.00元
規格 50mg 運輸溫度 室溫
其他名稱 DPI chloride; Dibenziodolium chloride; 氯化二亞苯基碘鎓;二亞苯基碘鎓氯化物(wù); 保存溫度 -20ºC幹燥保存
CAS号 4673-26-1 有效期 3年(nián)
應用 iNOS/eNOS抑制劑;NADPH氧化酶抑制劑;GPR3激動劑; 訂購數量
産品簡介:

Diphenyleneiodonium Chloride (DPI) 二苯基氯化碘鹽


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産品标簽

DPI 二苯基氯化碘鹽;iNOS/eNOS抑制劑;NADPH氧化酶;GPR3 agonist GPR3激動劑; CAS:4673-26-1;


産品信息

産品名稱

産品編号

CAS NO.         

規格            

價格(元)  

Diphenyleneiodonium Chloride (DPI) 二苯基氯化碘鹽      

MZ2701-10MG    

4673-26-1

10mg

988

Diphenyleneiodonium Chloride (DPI) 二苯基氯化碘鹽

MZ2701-50MG

4673-26-1

50mg

2988


産品描述

二苯基氯化碘鹽(Diphenyleneiodonium Chloride, DPI)是一(yī)種不可逆的iNOS和eNOS抑制劑,IC50分别是50nM和0.3µM,其抑制是有效的、不可逆的,時間和溫度依賴性的。NADPH,NADP+和2'5'-ADP能(néng)夠阻斷DPI的抑制活性。類似的,FAD或FMN能(néng)保護NOS不被DPI抑制[1]。DPI結合并抑制中性粒細胞NADPH氧化酶[2]。DPI是一(yī)種GPR3激動劑(EC50=1μM)。通(tōng)過GPR3(但不是GPR6或GPR12)活化腺苷酸環化酶,能(néng)夠誘導鈣動員(yuán)和β-arrestin受體内在化[3]。DPI抑制IL-1β誘導的NFκB活化[4]。齧齒類模型中預防早期酒精性肝損傷。


産品特性

1)   CAS NO:4673-26-1

2)   化學名:1,1'-Biphenyl]-2,2'-diyliodonium chloride

3)   同義名:DPI chloride; Dibenziodolium chloride; 氯化二亞苯基碘鎓;二亞苯基碘鎓氯化物(wù);

4)   分子式:C12H8I·Cl

5)   分子量:314.55 g/mol

6)   純度:>98%

7)   外觀:白(bái)色至類白(bái)色粉末

8)  溶解性:溶于DMSO(>10 mM,可能(néng)需要加熱和超聲助溶)【“>”:表明溶于标示濃度,但飽和溶解度未知。】

9)  結構式:


保存與運輸方法

保存:-20ºC幹燥保存,3年(nián)有效。

運輸:常溫運輸。


注意事(shì)項

1)   為(wèi)了讓化合物(wù)更好的溶解,可通(tōng)過37℃加熱或(和)超聲波水(shuǐ)浴中震動片刻來處理。若實驗所需濃度過大甚至達産品溶解極限,請添加助溶劑助溶或自(zì)行調整濃度。

2)   本品僅用作科研用途,不得用作臨床診斷或治療,不得用于食品或藥品,絕對禁止用在人身上(shàng)。

3)   為(wèi)了您的安全和健康,請穿實驗服并戴一(yī)次性手套操作。


配制儲存液

         質量          

溶劑體積

濃度

1mg

5mg

10mg

1mM

3.1791 mL        

15.8957 mL     

31.7914 mL    

5mM

0.6358 mL

3.1791 mL

6.3583 mL

10mM

0.3179 mL

0.5403 mL

3.1791 mL


使用方法【源自(zì)文獻,僅作參考】

文獻1,Ye C et al. Identification of a novel small-molecule agonist for human G protein-coupled receptor 3. J Pharmacol Exp Ther. 2014 Jun;349(3):437-43.PMID: 24633425

體外研究(細胞實驗):

細胞類型(Cell type):U2OS cells

藥物(wù)配制(Preparation):DPI was dissolved in DMSO to make stock solution and stored at -20℃.

實驗方法(Assay):U2OS cells were seeded onto glass coverslips in 24-well plates and transfected with plasmids encoding FLAG-GPR3-GFP. Thirty-six hours later, cells were changed into Dulbecco’s modified Eagle’s medium containing 0.5% FBS at 37°C for 2 hours followed by 1-hour incubation in mediacontaining DPI (10 μM) or vehicle [0.1% dimethylsulfoxide (DMSO)].Cells were then washed three times with phosphate-buffered saline and fixed in 4% paraformaldehyde. After counterstaining of nuclei with Hoechst dye 33342, cells were examined using an FV10i confocal microscope.

文獻2,Deng CC et al.Nigericin selectively targets cancer stem cells in nasopharyngeal carcinoma. Int J Biochem Cell Biol. 2013 Sep;45(9):1997-2006. PMID: 23831840

體内研究(動物(wù)模型):

動物(wù)模型(Animal Model):ddy mice (6–7 wk of age)

實驗方法(Assay):The ddy mice (6–7 wk of age) were individually placed in transparent cages for 30 min before experiments.An intraplantar injection of 10 μl DPI (2 mM, solvent: Kolliphor EL with 20% DMSO) was then injected into the right hindpaw with or without intraperitoneal administration with HC030031 (300 mg/kg at 0.5 h prior to injection of DPI; solvent: saline with 0.5% methyl cellulose).The time spent licking or biting the injected paw was recorded for 45 min after injection.


參考文獻

[1] Stuehr DJ et al. Inhibition of macrophage and endothelial cell nitric oxide synthase by diphenyleneiodonium and its analogs. FASEB J. 1991 Jan;5(1):98-103.

[2] Yea CM et al. Purification and some properties of the 45 kDa diphenylene iodonium-binding flavoprotein of neutrophil NADPH oxidase. Biochem J. 1990 Jan 1;265(1):95-100.

[3] Ye C et al. Identification of a novel small-molecule agonist for human G protein-coupled receptor 3. J Pharmacol Exp Ther. 2014 Jun;349(3):437-43.

[4] Mendes AF et al. Diphenyleneiodonium inhibits NF-kappaB activation and iNOS expression induced by IL-1beta: involvement of reactive oxygen species. Mediators Inflamm. 2001 Aug;10(4):209-15.

[5] Kono H et al. Diphenyleneiodonium sulfate, an NADPH oxidase inhibitor, prevents early alcohol-induced liver injury in the rat. Am J Physiol Gastrointest Liver Physiol. 2001 May;280(5):G1005-12.

 

 

 — —Written/Edited by V. Shallan【版權歸MKBio懋康所有】

 

 

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