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(-)-Huperzine A

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Catalog No. T3026Cas No. 102518-79-6
Alias Huperzine A, HupA

(-)-Huperzine A (HupA) , an active Lycopodium alkaloid extracted from the traditional Chinese herb, is a potent, selective and reversible acetylcholinesterase (AChE) inhibitor and has been widely used in China for the treatment of Alzheimer's disease (AD).

(-)-Huperzine A

(-)-Huperzine A

😃Good
Purity: 99.46%
Catalog No. T3026Alias Huperzine A, HupACas No. 102518-79-6
(-)-Huperzine A (HupA) , an active Lycopodium alkaloid extracted from the traditional Chinese herb, is a potent, selective and reversible acetylcholinesterase (AChE) inhibitor and has been widely used in China for the treatment of Alzheimer's disease (AD).
Pack SizePriceUSA WarehouseGlobal WarehouseQuantity
10 mg$43In StockIn Stock
25 mg$82In StockIn Stock
50 mg$148In StockIn Stock
100 mg$263In StockIn Stock
200 mg$490-In Stock
500 mg$785-In Stock
1 mL x 10 mM (in DMSO)$48In StockIn Stock
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In Stock Estimated shipping dateUSA Warehouse[1-2 days] Global Warehouse[5-7 days]
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Purity:99.46%
Appearance:Solid
Color:White
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Product Introduction

Bioactivity
Description
(-)-Huperzine A (HupA) , an active Lycopodium alkaloid extracted from the traditional Chinese herb, is a potent, selective and reversible acetylcholinesterase (AChE) inhibitor and has been widely used in China for the treatment of Alzheimer's disease (AD).
Targets&IC50
AChE (G4 form):7 nM(Ki)
In vitro
In both animal models and patients with Alzheimer's Disease (AD), (-)-Huperzine A has been shown to improve learning and memory impairments. Compared to the control group treated with saline, significant inhibition of acetylcholinesterase (AchE) activity was observed in the cortex, striatum, hippocampus, medulla, septal nuclei, cerebellum, and thalamus of rats 30 minutes post-mortem.
In vivo
Compared to tacrine, strychnine, galantamine, and carbachol, (-)-Huperzine A exhibits stronger inhibition of acetylcholinesterase (AChE) activity but has the least effect on butyrylcholinesterase (BuChE). (-)-Huperzine A protects cells against glutamate, hydrogen peroxide, β-amyloid, ischemia, and astrosporine-induced cytotoxicity and apoptosis. This protective function is achieved through a series of processes including the regulation of apoptotic protein expression (such as Bcl-2, Bax, p53, and caspase-3), alleviation of oxidative stress, mitochondrial protection, upregulation of nerve growth factor and its receptors, and interference with amyloid precursor protein metabolism. Notably, (-)-Huperzine A preferentially inhibits the tetrameric form of AChE (G4 form).
SynonymsHuperzine A, HupA
Chemical Properties
Molecular Weight242.32
FormulaC15H18N2O
Cas No.102518-79-6
Smiles[H][C@@]12Cc3[nH]c(=O)ccc3[C@@](N)(CC(C)=C1)C2=CC
Relative Density.1.20 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
DMSO: 250 mg/mL (1031.69 mM), Sonication is recommended.
In Vivo Formulation
10% DMSO+40% PEG300+5% Tween 80+45% Saline: 5 mg/mL (20.63 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 mM4.1268 mL20.6339 mL41.2677 mL206.3387 mL
5 mM0.8254 mL4.1268 mL8.2535 mL41.2677 mL
10 mM0.4127 mL2.0634 mL4.1268 mL20.6339 mL
20 mM0.2063 mL1.0317 mL2.0634 mL10.3169 mL
50 mM0.0825 mL0.4127 mL0.8254 mL4.1268 mL
100 mM0.0413 mL0.2063 mL0.4127 mL2.0634 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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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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