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Bupranolol

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Catalog No. T8580Cas No. 14556-46-8

Bupranolol is an antagonist of β2-adrenergic receptor and has been used for angina pectoris, hypertension, glaucoma, cardiac arrhythmia and as an antithrombotic.

Bupranolol

Bupranolol

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🥰Excellent
Purity: 97.63%
Catalog No. T8580Cas No. 14556-46-8
Bupranolol is an antagonist of β2-adrenergic receptor and has been used for angina pectoris, hypertension, glaucoma, cardiac arrhythmia and as an antithrombotic.
Pack SizePriceUSA WarehouseGlobal WarehouseQuantity
1 mg$37In StockIn Stock
5 mg$85In StockIn Stock
10 mg$135In StockIn Stock
25 mg$263In StockIn Stock
50 mg$396In StockIn Stock
100 mg$579In StockIn Stock
1 mL x 10 mM (in DMSO)$103In StockIn 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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Purity:97.63%
Appearance:Solid
Color:White
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Product Introduction

Bupranolol AI Summary
Bupranolol exhibits beta-blocking activity with an activity level of 5.61. It shows potential antiviral efficacy, including significant activity against the Ebola virus, with AC50 values ranging from 5011.9 nM to 28183.8 nM in various assays. Additionally, compound 100929 demonstrates antiviral activity against SARS-CoV-2, inhibiting virus-induced cytotoxicity of Caco-2 cells by 43.82% at 10 µM after 48 hours and exhibiting moderate inhibition of viral replication in HRCE cells with a hit score of 0.4669. It also inhibits SARS-CoV-2 3CL-Pro protease activity by 12.15% at a 20 µM concentration and shows minimal inhibition of viral cytotoxicity in VERO-6 cells at 10 µM. Furthermore, compound 100929 inhibits human HDAC6 enzyme activity, with inhibition rates of 14.84% and 7.02% with commercial and custom peptide substrates, respectively..
Note: Summary generated by AI. Data source: ChEMBL
Bioactivity
Description
Bupranolol is an antagonist of β2-adrenergic receptor and has been used for angina pectoris, hypertension, glaucoma, cardiac arrhythmia and as an antithrombotic.
Chemical Properties
Molecular Weight271.78
FormulaC14H22ClNO2
Cas No.14556-46-8
SmilesCc1ccc(Cl)c(OCC(O)CNC(C)(C)C)c1
Relative Density.1.098g/cm3
Storage & Solubility Information
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature.
Solubility Information
DMSO: 25 mg/mL (91.99 mM), Sonication is recommended.
In Vivo Formulation
10% DMSO+40% PEG300+5% Tween 80+45% Saline: 2 mg/mL (7.36 mM), Sonication is recommended.
Please add the solvents sequentially, clarifying the solution as much as possible before adding the next one. Dissolve by heating and/or sonication if necessary. Working solution is recommended to be prepared and used immediately. The formulation provided above is for reference purposes only. In vivo formulations may vary and should be modified based on specific experimental conditions.
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM3.6794 mL18.3972 mL36.7945 mL183.9723 mL
5 mM0.7359 mL3.6794 mL7.3589 mL36.7945 mL
10 mM0.3679 mL1.8397 mL3.6794 mL18.3972 mL
20 mM0.1840 mL0.9199 mL1.8397 mL9.1986 mL
50 mM0.0736 mL0.3679 mL0.7359 mL3.6794 mL

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In Vivo Formulation Calculator (Clear solution)

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:
mg/kg
g
μL
2 Enter the in vivo formulation:
% DMSO
%
% Tween 80
% Saline/PBS/ddH2O

Dose Conversion

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Tech Support

Please see Inhibitor Handling Instructions for more frequently ask questions. Topics include: how to prepare stock solutions, how to store products, and cautions on cell-based assays & animal experiments, etc

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