MAO-B-IN-48
MAO-B-IN-48 is a selective MAO-B inhibitor (IC50 = 0.09 μM, Ki = 0.02 μM). MAO-B-IN-48 exhibits 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 suppresses self-induced aggregation of toxic β-amyloid peptides and exerts antioxidant activity, including DPPH radical scavenging, CUPRAC copper ion reduction, and superoxide anion scavenging. MAO-B-IN-48 can be used for the study of Alzheimer's disease (AD).
For research use only. We do not sell to patients.
- Formula: C21H22N2OS
- Molecular Weight:350.48
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Storage:
Please store the product under the recommended conditions in the Certificate of Analysis.
Biological Activity
Description
IC50 & Target
[1]|
MAO-B 0.09 μM (IC50) |
MAO-B 0.02 μM (Ki) |
MAO-A 30.55 μM (IC50) |
MAO-A 8.33 μM (Ki) |
AChE 0.56 μM (IC50) |
AChE 0.14 μM (Ki) |
hBCHE 1.10 μM (IC50) |
hBCHE 0.43 μM (Ki) |
In Vitro
MAO-B-IN-48 (Compound 1d-R) inhibits self-induced aggregation of Aβ1-40 (IC50 = 31.42 μM) and Aβ1-42 (IC50 = 21.32 μM) in vitro[1].
MAO-B-IN-48 shows DPPH radical scavenging activity (IC50 = 3.40 mM), antioxidant activity in the CUPRAC assay (IC50 = 33.40 μM) and superoxide anion scavenging capacity (IC50 = 28.21 μM)[1].
MAO-B-IN-48 (1-25 μM) does not exhibit cytotoxic effects on HepG2 cells[1].
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only. Further protocols information, click here.
In Vivo
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
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Animal Model:40mg/kg of AlCl3 was administered intraperitoneally to male Balb/c mice for 30 days[1]
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Dosage:20 mg/kg
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Administration:i.g. for 1 week
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Result:Ameliorated the cognitive impairment induced by AlCl3 in mice.
Chemical Information
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Molecular Weight 350.48
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Formula C21H22N2OS
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SMILES
C[C@H](C1=CC=CC2=C1C=CC=C2)NC(OC3=CC(N(C)C)=CC=C3)=S
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Shipping
Room temperature in continental US; may vary elsewhere.
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Storage
Please store the product under the recommended conditions in the Certificate of Analysis.
Protocols
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Cell Cytotoxicity Assay
Cytotoxicity assays are usually based on the assessment of cell membrane damage, which can also be indirectly detected by measuring cell viability. Detection methods include MTT assay, CKK-8 assay, LDH assay and ATP assay, etc.
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Amyloid: Congo Red Amyloid Staining
Congo red amyloid staining is a histochemical method used to detect extracellular amyloid deposits in tissue sections based on the affinity of Congo red dye for β-pleated sheet-rich protein aggregates. When bound to amyloid, Congo red produces characteristic apple-green birefringence under polarized light microscopy, which is widely regarded as a diagnostic feature of amyloid deposition in histopathology. The diagnostic principle relies on the combination of dye binding (congophilia) and optical anisotropy under polarized illumination, which distinguishes amyloid from most non-amyloid eosinophilic extracellular deposits in routine histological evaluation. Amyloid identification by Congo red staining remains a cornerstone in diagnostic pathology despite the availability of adjunct methods such as immunohistochemistry and mass spectrometry, particularly because of its ability to localize deposits directly within tissue architecture. The specificity of Congo red-positive deposits is incre
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Alzheimer’s Disease Modeling
Alzheimer’s Disease (AD) is a neurodegenerative disorder characterized by a progressive decline in cognitive functions and loss of specific types of neurons and synapses. Alzheimer's symptoms can be simulated in mice by injecting drugs (such as Aβ) or genetically modified.
Purity & Documentation
References
[1]. Teke Tuncel S, et al. Multitarget-directed carbamate and carbamothioate derivatives: Cholinesterase and monoamine oxidase inhibition, anti-β-amyloid (Aβ) aggregation, antioxidant and blood-brain barrier permeation properties against Alzheimer's disease. Eur J Med Chem. 2025 Nov 15;298:117986. [Content Brief]
Calculators
Concentration (start) × Volume (start) = Concentration (final) × Volume (final)