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AChE-IN-59

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Catalog No. T85554Cas No. 2957916-86-6

AChE-IN-59 (compound 3b) is an AChE inhibitor with an IC₅₀ value of 0.05 μM. It effectively inhibits Aβ1-42 aggregation, protects nerve cells, and penetrates the blood-brain barrier efficiently. AChE-IN-59 is suitable for Alzheimer's disease (AD) research [1].

AChE-IN-59

AChE-IN-59

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Catalog No. T85554Cas No. 2957916-86-6
AChE-IN-59 (compound 3b) is an AChE inhibitor with an IC₅₀ value of 0.05 μM. It effectively inhibits Aβ1-42 aggregation, protects nerve cells, and penetrates the blood-brain barrier efficiently. AChE-IN-59 is suitable for Alzheimer's disease (AD) research [1].
Pack SizePriceUSA WarehouseGlobal WarehouseQuantity
10 mgInquiry10-14 weeks10-14 weeks
50 mgInquiry10-14 weeks10-14 weeks
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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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Product Introduction

Bioactivity
Description
AChE-IN-59 (compound 3b) is an AChE inhibitor with an IC₅₀ value of 0.05 μM. It effectively inhibits Aβ1-42 aggregation, protects nerve cells, and penetrates the blood-brain barrier efficiently. AChE-IN-59 is suitable for Alzheimer's disease (AD) research [1].
Targets&IC50
BChE:4.68 μM, AChE:0.05 μM
In vitro
AChE-IN-59 (compound 3b) inhibits ChEs activity at concentrations of 50/100/500/1000 μg/mL over 5 minutes, with IC50 values of 0.05 μM for AChE and 4.68 μM for BuChE, demonstrating selective inhibition of the AChE subtype [1]. Additionally, AChE-IN-59 exhibits strong in vitro antioxidant activity as indicated by FRAP and DPPH radical scavenging assays [1]. At 25 µM for 5 minutes, AChE-IN-59 shows no cytotoxic effects on SH-SY5Y cells [1]. In cell viability assays using SH-SY5Y cells at concentrations of 0/6.25/12.5/25/50/100 µM over 5 hours, the compound displays notable neuroprotective effects within the 6.25-25 µM range and does not compromise cell viability below 25 µM.
In vivo
AChE-IN-59 (compound 3b) (25 μM, 3 day) has been shown to mitigate the locomotor retardation in zebrafish larvae induced by AlCl3 (5 mg/L) [1]. In this study, zebrafish larvae were utilized as the experimental animal model, with the compound administered through immersion at dosages of 5/10/25/50/100 μg/mL. The findings indicate that AChE-IN-59 offers therapeutic benefits against AlCl3-induced behavioral inhibition in zebrafish, with its efficacy enhancing progressively as the drug concentration increases, as evidenced by the gradual increase in the total distance moved by the larvae.
Chemical Properties
Molecular Weight452.50
FormulaC25H28N2O6
Cas No.2957916-86-6
SmilesO=C1OC=2C=C(OC)C=CC2C=C1NC(=O)C3CCN(CC=4C=C(OC)C=C(OC)C4)CC3
Storage & Solubility Information
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice.

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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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