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BChE-IN-41

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Catalog No. T211031

BChE-IN-41 is a highly selective butyrylcholinesterase (BChE) inhibitor with an IC50 of 12 nM and a Ki of 6.6 nM. It exhibits significant brain permeability, with a brain-to-plasma ratio of 9.0. BChE-IN-41 enhances cognitive function in mice with scopolamine and Aβ1-42-induced symptoms of Alzheimer's disease.

BChE-IN-41

BChE-IN-41

😃Good
Catalog No. T211031
BChE-IN-41 is a highly selective butyrylcholinesterase (BChE) inhibitor with an IC50 of 12 nM and a Ki of 6.6 nM. It exhibits significant brain permeability, with a brain-to-plasma ratio of 9.0. BChE-IN-41 enhances cognitive function in mice with scopolamine and Aβ1-42-induced symptoms of Alzheimer's disease.
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Product Introduction

Bioactivity
Description
BChE-IN-41 is a highly selective butyrylcholinesterase (BChE) inhibitor with an IC50 of 12 nM and a Ki of 6.6 nM. It exhibits significant brain permeability, with a brain-to-plasma ratio of 9.0. BChE-IN-41 enhances cognitive function in mice with scopolamine and Aβ1-42-induced symptoms of Alzheimer's disease.
Targets&IC50
AChE (human):22110 nM
In vitro
BChE-IN-41 (Compound (R)-(−)-3) exhibits neuroprotective activity by reducing SH-SY5Y cell death induced by Aβ 1-42, when used at a concentration of 5 μM for 48 hours.
In vivo
BChE-IN-41 (Compound (R)-(−)-3) demonstrates high efficacy and brain penetration at doses ranging from 10-100 mg/kg (i.g, single dose) in wild-type Balb/c mice, exhibiting low toxicity without histopathological changes. At doses of 1-10 mg/kg (i.p, single dose), it enhances contextual and recognition memory deficits in scopolamine-induced adult male CD-1 mice. Furthermore, daily administration of 10 mg/kg (i.p) for 14 days improves learning and cognitive function in Aβ 1-42 oligomer-induced male ICR mice.
Chemical Properties
Storage & Solubility Information
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature.

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TargetMol | Animal experimentsFor example, your dosage is 10 mg/kg Each animal weighs 20 g, and the dosage volume is 100 μL . TargetMol | Animal experiments A total of 10 animals were administered, and the formula you used is 5% TargetMol | reagent DMSO+30% PEG300+5% Tween 80+60% Saline/PBS/ddH2O. So your working solution concentration is 2 mg/mL。
Mother liquor preparation method: 2 mg of drug dissolved in 50 μL DMSOTargetMol | reagent (mother liquor concentration of 40 mg/mL), if you need to configure a concentration that exceeds the solubility of the product, please contact us first.
Preparation method for in vivo formula: Take 50 μL DMSOTargetMol | reagent main solution, add 300 μLPEG300TargetMol | reagent mix well and clarify, then add 50 more μL Tween 80, mix well and clarify, then add 600 more μLSaline/PBS/ddH2OTargetMol | reagent mix well and clarify
For Reference Only. Please develop an appropriate dissolution method based on your laboratory animals and route of administration.
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