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MAO-B-IN-48

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Catalog No. T212463

MAO-B-IN-48 is a selective inhibitor of MAO-B with an IC50 of 0.09 μM and Ki of 0.02 μM. It also demonstrates inhibitory activity against hBChE (IC50= 1.10 μM, Ki= 0.43 μM) and AChE (IC50= 0.56 μM, Ki= 0.14 μM). MAO-B-IN-48 disrupts the self-induced aggregation of toxic β-amyloid peptides and exhibits antioxidant properties, including DPPH radical scavenging, CUPRAC copper ion reduction, and superoxide anion scavenging. This compound is applicable in Alzheimer’s disease (AD) research.

MAO-B-IN-48

MAO-B-IN-48

😃Good
Catalog No. T212463
MAO-B-IN-48 is a selective inhibitor of MAO-B with an IC50 of 0.09 μM and Ki of 0.02 μM. It also demonstrates inhibitory activity against hBChE (IC50= 1.10 μM, Ki= 0.43 μM) and AChE (IC50= 0.56 μM, Ki= 0.14 μM). MAO-B-IN-48 disrupts the self-induced aggregation of toxic β-amyloid peptides and exhibits antioxidant properties, including DPPH radical scavenging, CUPRAC copper ion reduction, and superoxide anion scavenging. This compound is applicable in Alzheimer’s disease (AD) research.
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Product Introduction

Bioactivity
Description
MAO-B-IN-48 is a selective inhibitor of MAO-B with an IC50 of 0.09 μM and Ki of 0.02 μM. It also demonstrates inhibitory activity against hBChE (IC50= 1.10 μM, Ki= 0.43 μM) and AChE (IC50= 0.56 μM, Ki= 0.14 μM). MAO-B-IN-48 disrupts the self-induced aggregation of toxic β-amyloid peptides and exhibits antioxidant properties, including DPPH radical scavenging, CUPRAC copper ion reduction, and superoxide anion scavenging. This compound is applicable in Alzheimer’s disease (AD) research.
Targets&IC50
MAO-B:0.09 μM
In vitro
MAO-B-IN-48 (Compound 1d-R) effectively inhibits the self-induced aggregation of Aβ 1-40 (IC 50 = 31.42 μM) and Aβ 1-42 (IC 50 = 21.32 μM) in vitro. It demonstrates DPPH radical scavenging activity (IC 50 = 3.40 mM), exhibits antioxidant properties in CUPRAC assays (IC 50 = 33.40 μM), and has superoxide anion scavenging capabilities (IC 50 = 28.21 μM). Additionally, MAO-B-IN-48 (1-25 μM) is non-cytotoxic to HepG2 cells.
In vivo
MAO-B-IN-48 (20 mg/kg, administered orally for one week) can ameliorate cognitive impairment in mice induced by AlCl3.
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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