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AChE-IN-62

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Catalog No. T209564

AChE-IN-62 (Compound 1) is a potent, mixed-type selective inhibitor of acetylcholinesterase (AChE) with an IC50 value of 0.421 μM. It effectively penetrates the blood-brain barrier and offers neuroprotective effects. Additionally, AChE-IN-62 inhibits the aggregation of Aβ1-42 with an IC50 of 44.64 μM. This compound also acts as an effective multi-target-directed ligand (MTDL) and is applicable in Alzheimer's disease research.

AChE-IN-62

AChE-IN-62

🥰Excellent
Catalog No. T209564
AChE-IN-62 (Compound 1) is a potent, mixed-type selective inhibitor of acetylcholinesterase (AChE) with an IC50 value of 0.421 μM. It effectively penetrates the blood-brain barrier and offers neuroprotective effects. Additionally, AChE-IN-62 inhibits the aggregation of Aβ1-42 with an IC50 of 44.64 μM. This compound also acts as an effective multi-target-directed ligand (MTDL) and is applicable in Alzheimer's disease research.
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Product Introduction

Bioactivity
Description
AChE-IN-62 (Compound 1) is a potent, mixed-type selective inhibitor of acetylcholinesterase (AChE) with an IC50 value of 0.421 μM. It effectively penetrates the blood-brain barrier and offers neuroprotective effects. Additionally, AChE-IN-62 inhibits the aggregation of Aβ1-42 with an IC50 of 44.64 μM. This compound also acts as an effective multi-target-directed ligand (MTDL) and is applicable in Alzheimer's disease research.
In vitro
AChE-IN-62 effectively inhibits the aggregation of Aβ 1−42 with an IC50 value of 44.64 μM when used at a concentration of 50 μM for 24-48 hours. Additionally, at concentrations ranging from 5-20 μM over 24 hours, AChE-IN-62 demonstrates neuroprotective properties by mitigating neurotoxicity mediated by H2O2 (200 μM; 24 h) and Okadaic acid (30 nM; 24 h) in SH-SY5Y and Neuro2A cells.
In vivo
AChE-IN-62 (Compound 1) at doses of 10-20 mg/kg, administered intraperitoneally once daily for 7 consecutive days, mitigates scopolamine-induced (3 mg/kg; intraperitoneal; once daily for 7 days) memory impairment and learning deficits in Swiss albino mice by repairing damage to the cerebral cortex and hippocampus, thereby offering neuroprotection against scopolamine-induced injuries.
Chemical Properties
FormulaC19H21N5O3S2
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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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
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