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BN82002

🥰Excellent
Catalog No. T4671Cas No. 396073-89-5
Alias CDC25 Phosphatase Inhibitor I

BN82002 (CDC25 Phosphatase Inhibitor I) is a synthetic inhibitor of CDC25 phophatases

BN82002

BN82002

🥰Excellent
Purity: 99.91%
Catalog No. T4671Alias CDC25 Phosphatase Inhibitor ICas No. 396073-89-5
BN82002 (CDC25 Phosphatase Inhibitor I) is a synthetic inhibitor of CDC25 phophatases
Pack SizePriceAvailabilityQuantity
1 mg$38In Stock
5 mg$89In Stock
10 mg$122In Stock
25 mg$222In Stock
50 mg$372In Stock
100 mg$556In Stock
1 mL x 10 mM (in DMSO)$98In Stock
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Purity:99.91%
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Product Introduction

Bioactivity
Description
BN82002 (CDC25 Phosphatase Inhibitor I) is a synthetic inhibitor of CDC25 phophatases
Targets&IC50
CDC25B2:3.9 μM, CDC25C:5.4 μM, CDC25B3:6.3 μM, CDC25A:2.4 μM, CDC25C-cat:4.6 μM
In vitro
The in vitro impact of BN82002 on the proliferation of various human tumor cell lines has been assessed, with menadione serving as a control due to its documented proliferation inhibitory properties. All tested cell lines exhibit sensitivity to both BN82002 and menadione, demonstrating concentration-dependent inhibition within the low micromolar range. Among these, the pancreatic cancer cell line MIA PaCa-2 is the most affected by BN82002, showing an IC50 of 7.2 μM, while the colon cancer cell line HT-29 shows the least sensitivity with an IC50 of 32.6 μM. This range of inhibitory concentration for BN82002 closely matches that observed with menadione (5-15 μM). Further findings indicate that a 50 μM concentration of BN82002 completely halts cell proliferation. Although the influence on cell cycle distribution is relatively mild, there is a noted decrease in the S phase and an increase in cells with G1 and G2 DNA content, hinting at cell cycle arrest at various stages due to BN82002 treatment.
AliasCDC25 Phosphatase Inhibitor I
Chemical Properties
Molecular Weight359.42
FormulaC19H25N3O4
Cas No.396073-89-5
SmilesCOc1cc(cc(CN(C)CCc2ccc(cc2)[N+]([O-])=O)c1O)N(C)C
Relative Density.1.216 g/cm3 (Predicted)
Storage & Solubility Information
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice.
Solubility Information
DMSO: 150 mg/mL (417.34 mM)
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM2.7823 mL13.9113 mL27.8226 mL139.1130 mL
5 mM0.5565 mL2.7823 mL5.5645 mL27.8226 mL
10 mM0.2782 mL1.3911 mL2.7823 mL13.9113 mL
20 mM0.1391 mL0.6956 mL1.3911 mL6.9557 mL
50 mM0.0556 mL0.2782 mL0.5565 mL2.7823 mL
100 mM0.0278 mL0.1391 mL0.2782 mL1.3911 mL

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Mother liquor preparation method: 2 mg of drug dissolved in 50 μL DMSOTargetMol | reagent (mother liquor concentration of 40 mg/mL), if you need to configure a concentration that exceeds the solubility of the product, please contact us first.
Preparation method for in vivo formula: Take 50 μL DMSOTargetMol | reagent main solution, add 300 μLPEG300TargetMol | reagent mix well and clarify, then add 50 more μL Tween 80, mix well and clarify, then add 600 more μLddH2OTargetMol | reagent mix well and clarify
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