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BuChE-IN-TM-10

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Catalog No. T10630Cas No. 2313524-95-5
Alias TM-10

BuChE-IN-TM-10 (TM-10) is a potent inhibitor of butyrylcholinesterase (BuChE) with an IC50 of 8.9 nM. It effectively inhibits and disaggregates self-induced Aβ aggregation, exhibits significant antioxidant activity, and demonstrates substantial penetration through the blood-brain barrier (BBB), holding promise as a potential treatment for Alzheimer's disease.

BuChE-IN-TM-10

BuChE-IN-TM-10

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Purity: 99.54%
Catalog No. T10630Alias TM-10Cas No. 2313524-95-5
BuChE-IN-TM-10 (TM-10) is a potent inhibitor of butyrylcholinesterase (BuChE) with an IC50 of 8.9 nM. It effectively inhibits and disaggregates self-induced Aβ aggregation, exhibits significant antioxidant activity, and demonstrates substantial penetration through the blood-brain barrier (BBB), holding promise as a potential treatment for Alzheimer's disease.
Pack SizePriceUSA WarehouseGlobal WarehouseQuantity
1 mg$195In StockIn Stock
2 mg$293In StockIn Stock
5 mg$448In StockIn Stock
10 mg$658In StockIn Stock
25 mg$987In StockIn Stock
50 mg$1,380In StockIn Stock
100 mg$1,890In 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:99.54%
Appearance:Solid
Color:White
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Product Introduction

BuChE-IN-TM-10 AI Summary
BuChE-IN-TM-10 demonstrates a range of bioactivities, including the inhibition of various enzymes and effects on amyloid beta aggregation. Specifically, it inhibits equine serum butyrylcholinesterase (BChE) with an IC50 of 8.9 nM and electric eel acetylcholinesterase (AChE) with an IC50 of 12100.0 nM. Additionally, it inhibits human monoamine oxidase A (MAO-A) and monoamine oxidase B (MAO-B) with IC50 values of 6300.0 nM and 8600.0 nM, respectively. The compound also inhibits an unidentified source of BChE with an IC50 of 8900.0 nM. It exhibits significant activity against amyloid beta aggregation, inhibiting self-induced amyloid beta (1-42) aggregation by 53.9% at a concentration of 25 μM and disaggregating pre-formed amyloid beta aggregates by 43.8% at the same concentration. Furthermore, BuChE-IN-TM-10 has demonstrated antioxidant activity comparable to 0.53 trolox in the ORAC radical scavenging assay..
Note: Summary generated by AI. Data source: ChEMBL
Bioactivity
Description
BuChE-IN-TM-10 (TM-10) is a potent inhibitor of butyrylcholinesterase (BuChE) with an IC50 of 8.9 nM. It effectively inhibits and disaggregates self-induced Aβ aggregation, exhibits significant antioxidant activity, and demonstrates substantial penetration through the blood-brain barrier (BBB), holding promise as a potential treatment for Alzheimer's disease.
Targets&IC50
BuChE:8.9 nM
SynonymsTM-10
Chemical Properties
Molecular Weight498.66
FormulaC32H38N2O3
Cas No.2313524-95-5
SmilesC(/C=C/C1=CC(OC)=C(OCCCCN(CC2=CC=CC=C2)CC)C=C1)(=O)N3CC=4C(CC3)=CC=CC4
Relative Density.1.127 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: 5.48 mg/mL (10.99 mM), Sonication is recommended.
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM2.0054 mL10.0269 mL20.0537 mL100.2687 mL
5 mM0.4011 mL2.0054 mL4.0107 mL20.0537 mL
10 mM0.2005 mL1.0027 mL2.0054 mL10.0269 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:
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2 Enter the in vivo formulation:
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