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BpV(phen) trihydrate

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Catalog No. T41339Cas No. 171202-16-7
Alias Bisperoxovanadium(phen) trihydrate

BpV(phen) trihydrate is an insulin mimic and an effective PTP and PTEN inhibitor, with an IC50 of 38/343/920 nM for PTEN/PTP-β/PTP-1B, and has inhibitory activity against leishmania, can induce apoptosis and promote the secretion of pro-inflammatory factors, activate the Th1 pathway, and has anti-angiogenic and anti-tumor activity.

BpV(phen) trihydrate

BpV(phen) trihydrate

Copy Product Info
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Catalog No. T41339Alias Bisperoxovanadium(phen) trihydrateCas No. 171202-16-7
BpV(phen) trihydrate is an insulin mimic and an effective PTP and PTEN inhibitor, with an IC50 of 38/343/920 nM for PTEN/PTP-β/PTP-1B, and has inhibitory activity against leishmania, can induce apoptosis and promote the secretion of pro-inflammatory factors, activate the Th1 pathway, and has anti-angiogenic and anti-tumor activity.
Pack SizePriceUSA WarehouseGlobal WarehouseQuantity
1 mg$29-In Stock
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In Stock Estimated shipping dateUSA Warehouse[1-2 days] Global Warehouse[5-7 days]
All TargetMol products are for research purposes only and cannot be used for human consumption. We do not provide products or services to individuals. Please comply with the intended use and do not use TargetMol products for any other purpose.
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Appearance:Solid
Color:Yellow
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Product Introduction

Bioactivity
Description
BpV(phen) trihydrate is an insulin mimic and an effective PTP and PTEN inhibitor, with an IC50 of 38/343/920 nM for PTEN/PTP-β/PTP-1B, and has inhibitory activity against leishmania, can induce apoptosis and promote the secretion of pro-inflammatory factors, activate the Th1 pathway, and has anti-angiogenic and anti-tumor activity.
Targets&IC50
PTP-1B:920 nM, PTEN:38 nM, PTPβ:343 nM
In vitro
Bpv(phen) (5 mg/kg; intraperitoneal injection; daily; for 38 days; male BALB/c nude (nu/nu) athymic mice) treatment causes a significant reduction in average tumor volume[1].
In vivo
Bpv(phen) (5 μM; 24.5 hours; H9c2 cells) reduces survival rates and promotes apoptosis in hypoxia/reperfusion-injured H9c2 cells, facilitating the accumulation of cytochrome C in the cytoplasm [1].
Bpv(phen), an insulin-like substance, exerts its effects through hyperphosphorylation and activation of insulin receptor tyrosine kinase [4].
SynonymsBisperoxovanadium(phen) trihydrate
Chemical Properties
Molecular Weight404.29
FormulaC12H14KN2O8V
Cas No.171202-16-7
SmilesO=[V+3]123([O-][O-]2)([N]4=C5C6=[N]3C=CC=C6C=CC5=CC=C4)[O-][O-]1.[K+].O.O.O
Storage & Solubility Information
Storagestore at low temperature | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature.
Solubility Information
H2O: 80 mg/mL (197.88 mM), Sonication is recommended.
Solution Preparation Table
H2O
1mg5mg10mg50mg
1 mM2.4735 mL12.3674 mL24.7347 mL123.6736 mL
5 mM0.4947 mL2.4735 mL4.9469 mL24.7347 mL
10 mM0.2473 mL1.2367 mL2.4735 mL12.3674 mL
20 mM0.1237 mL0.6184 mL1.2367 mL6.1837 mL
50 mM0.0495 mL0.2473 mL0.4947 mL2.4735 mL
100 mM0.0247 mL0.1237 mL0.2473 mL1.2367 mL

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Please enter your animal experiment information in the following box and click Calculate to obtain the stock solution preparation method and in vivo formula preparation method:
TargetMol | Animal experiments For example, if the intended dosage is 10 mg/kg for animals weighing 20 g , with a dosing volume of 100 μL per animal, TargetMol | Animal experiments and a total of 10 animals are to be administered, using a formulation of TargetMol | reagent 10% DMSO+ 40% PEG300+ 5% Tween 80+ 45% Saline/PBS/ddH2O , the resulting working solution concentration would be 2 mg/mL.
Stock Solution Preparation:

Dissolve 2 mg of the compound in 100 μL DMSOTargetMol | reagent to obtain a stock solution at a concentration of 20 mg/mL . If the required concentration exceeds the compound's known solubility, please contact us for technical support before proceeding.

Preparation of the In Vivo Formulation:

1) Add 100 μL of the DMSOTargetMol | reagent stock solution to 400 μL PEG300TargetMol | reagent and mix thoroughly until the solution becomes clear.

2) Add 50 μL Tween 80 and mix well until fully clarified.

3) Add 450 μL Saline,PBS or ddH2OTargetMol | reagent and mix thoroughly until a homogeneous solution is obtained.

This example is provided solely to demonstrate the use of the In Vivo Formulation Calculator and does not constitute a recommended formulation for any specific compound. Please select an appropriate dissolution and formulation strategy based on your experimental model and route of administration.
All co-solvents required for this protocol, includingDMSO, PEG300/PEG400, Tween 80, SBE-β-CD, and Corn oil, are available for purchase on the TargetMol website.
1 Enter information below:
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2 Enter the in vivo formulation:
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