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BN82002 hydrochloride

Catalog No.GC63788 Copy One-Click Copy Product Info

Le chlorhydrate de BN82002 est un inhibiteur puissant, sélectif et irréversible de la famille des phosphatases CDC25. Le chlorhydrate de BN82002 inhibe CDC25A, CDC25B2, CDC25B3, CDC25C CDC25A et 25C-cat avec des valeurs IC50 de 2,4, 3,9, 6,3, 5,4 et 4,6 μM, respectivement. Le chlorhydrate de BN82002 affiche une sélectivité environ 20 fois supérieure À celle de la tyrosine phosphatase CD45.

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BN82002 hydrochloride Chemical Structure

Cas No.: 1049740-43-3

Taille Prix Stock Qté
10mM (in 1mL DMSO)
109,00 $US
En stock
1mg
45,00 $US
En stock
5mg
99,00 $US
En stock
10mg
135,00 $US
En stock
25mg
216,00 $US
En stock
50mg
342,00 $US
En stock

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Based on customer reviews.

Sample solution is provided at 25 µL, 10mM.



Description of BN82002 hydrochloride

BN82002 hydrochloride is a potent, selective and irreversible inhibitor of CDC25 phosphatase family. BN82002 hydrochloride inhibits CDC25A, CDC25B2, CDC25B3, CDC25C CDC25A, and 25C-cat with IC50 values of 2.4, 3.9, 6.3, 5.4, and 4.6 µM, respectively. BN82002 hydrochloride displays ~20-fold greater selectivity over CD45 tyrosine phosphatase[1].

The effect of BN82002 on cell proliferation is evaluated in vitro on several human tumor cell lines. Menadione, which has been reported to inhibit cell proliferation, is used as a control. All of the examined cell lines are sensitive to BN82002 and Menadione in a concentration-dependent manner in the low micromolar range. The most sensitive is the pancreatic cancer cell line MIA PaCa-2 with an IC50 of 7.2 μM, and the less sensitive cell line is the colon cancer HT-29 with an IC50 of 32.6 μM. The range of activity is very similar to the one observed with menadione (5-15 μM). It is also showed that 50 μM BN82002 is a concentration that fully inhibits cell proliferation, the cell cycle distribution is only modestly affected with a slight decrease in S phase and an increase in cells containing both a G1 and a G2 DNA content, suggesting that the cells treated with BN82002 are arrested at various stages of the cell cycle[1].

[1]. Brezak MC, et al. A novel synthetic inhibitor of CDC25 phosphatases: BN82002. Cancer Res. 2004 May 1;64(9):3320-5.

Chemical Properties of BN82002 hydrochloride

Cas No. 1049740-43-3 SDF
Formula C19H26ClN3O4 M.Wt 395.88
Solubility DMSO : 220 mg/mL (555.72 mM; Need ultrasonic) Storage 4°C, away from moisture and light
General tips Please select the appropriate solvent to prepare the stock solution according to the solubility of the product in different solvents; once the solution is prepared, please store it in separate packages to avoid product failure caused by repeated freezing and thawing.Storage method and period of the stock solution: When stored at -80°C, please use it within 6 months; when stored at -20°C, please use it within 1 month.
To increase solubility, heat the tube to 37°C and then oscillate in an ultrasonic bath for some time.
Shipping Condition Evaluation sample solution: shipped with blue ice. All other sizes available: with RT, or with Blue Ice upon request.

Complete Stock Solution Preparation Table of BN82002 hydrochloride

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1 mg 5 mg 10 mg
1 mM 2.526 mL 12.6301 mL 25.2602 mL
5 mM 505.2 μL 2.526 mL 5.052 mL
10 mM 252.6 μL 1.263 mL 2.526 mL
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Method for preparing DMSO master liquid: mg drug pre-dissolved in μL DMSO ( Master liquid concentration mg/mL, Please contact us first if the concentration exceeds the DMSO solubility of the batch of drug. )

Method for preparing in vivo formulation: Take μL DMSO master liquid, next addμL PEG300, mix and clarify, next addμL Tween 80, mix and clarify, next add μL saline, mix and clarify.

Method for preparing in vivo formulation: Take μL DMSO master liquid, next add μL Corn oil, mix and clarify.

Note: 1. Please make sure the liquid is clear before adding the next solvent.
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3. All of the above co-solvents are available for purchase on the GlpBio website.

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Review for BN82002 hydrochloride

Average Rating: 5 ★★★★★ (Based on Reviews and 7 reference(s) in Google Scholar.)

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