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Huperzine B

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Catalog No. T2S1720Cas No. 103548-82-9

1. Huperzine-B is a efficient inhibitor of human brain AChE. 2. Huperzine-B can enhance ognitive and protect neuro, may be potentially new drug candidates for Alzheimer's disease therapy.

Huperzine B

Huperzine B

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Purity: 99.83%
Catalog No. T2S1720Cas No. 103548-82-9
1. Huperzine-B is a efficient inhibitor of human brain AChE. 2. Huperzine-B can enhance ognitive and protect neuro, may be potentially new drug candidates for Alzheimer's disease therapy.
Pack SizePriceUSA WarehouseGlobal WarehouseQuantity
1 mg$37In StockIn Stock
5 mg$88In StockIn Stock
10 mg$151In StockIn Stock
25 mg$286In StockIn Stock
50 mg$359In StockIn Stock
100 mg$511-In Stock
200 mg$692-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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Purity:99.83%
Appearance:Solid
Color:White
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Product Introduction

Huperzine B AI Summary
Huperzine B exhibits significant inhibitory activity against various forms of acetylcholinesterase (AChE) and butyrylcholinesterase (BuChE), demonstrating a range of bioactivities in different experimental setups. It has a Ki value of 794.0 nM against fetal bovine serum (FBS) AChE and a Ki value of 334.0 nM against Torpedo californica AChE. In vitro, it inhibits human recombinant AChE with an IC50 of 30.0 nM and BuChE with an IC50 of 227,000.0 nM, showing moderate selectivity towards AChE with a selectivity index of 11.8-12. Huperzine B also reverses vecuronium-induced neuromuscular block in guinea pig hemi-diaphragm with an EC50 of 19.0 nM and in vivo in chloralose-anesthetized cats with an ED50 of 0.08 µmol/kg, achieving a maximum reversal of 156.0%. Additionally, it induces a decrease in mean arterial pressure (MAP) by 17.0% and heart rate (HR) by 8.0%, while increasing the response to vagal stimulation by 102.0% in anesthetized cats..
Note: Summary generated by AI. Data source: ChEMBL
Bioactivity
Description
1. Huperzine-B is a efficient inhibitor of human brain AChE. 2. Huperzine-B can enhance ognitive and protect neuro, may be potentially new drug candidates for Alzheimer's disease therapy.
Chemical Properties
Molecular Weight256.34
FormulaC16H20N2O
Cas No.103548-82-9
Smiles[H][C@@]12Cc3[nH]c(=O)ccc3[C@]3(CC(C)=C1)NCCC[C@]23[H]
Relative Density.1.21 g/cm3 (Predicted)
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
Chloroform, Dichloromethane, Ethyl Acetate, Acetone, etc.: Soluble
DMSO: 10 mg/mL (39.01 mM), Sonication is recommended.
In Vivo Formulation
10% DMSO+40% PEG300+5% Tween 80+45% Saline: 1 mg/mL (3.9 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 mM3.9011 mL19.5053 mL39.0107 mL195.0534 mL
5 mM0.7802 mL3.9011 mL7.8021 mL39.0107 mL
10 mM0.3901 mL1.9505 mL3.9011 mL19.5053 mL
20 mM0.1951 mL0.9753 mL1.9505 mL9.7527 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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