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FCE 28073

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Catalog No. T67850Cas No. 174756-44-6

FCE 28073 is a Monoamine oxidase B inibitor with IC50 of 0.45 uM.

FCE 28073

FCE 28073

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Purity: 99.92%
Catalog No. T67850Cas No. 174756-44-6
FCE 28073 is a Monoamine oxidase B inibitor with IC50 of 0.45 uM.
Pack SizePriceUSA WarehouseGlobal WarehouseQuantity
10 mg$31In StockIn Stock
25 mg$54In StockIn Stock
50 mg$79In StockIn Stock
1 mL x 10 mM (in DMSO)$29In 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:99.92%
Appearance:Solid
Color:White
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Product Introduction

FCE 28073 AI Summary
FCE 28073 exhibits potent anticonvulsant activities, indicated by its effectiveness in various seizure tests in mice: an ED50 of 26.9 mg/kg in the intravenous BIC test, 8.0 mg/kg in the maximal electroshock (MES) test, 60.6 mg/kg in the PTX test, 21.5 mg/kg in the 3-MPA test, and 104.1 mg/kg in the STRY test. When administered orally, it demonstrates significant anticonvulsant activity with an ED50 of 7.2 mg/kg before MES induction. The compound also shows bioactivity in inhibiting neurotransmitter binding. It inhibits [3H]batrachotoxin binding to rat brain sodium channels (IC50 of 8500.0 nM) but does not significantly affect [3H]saxitoxin binding (IC50 > 300,000.0 nM). It inhibits [3H]pentazocine binding to the sigma-1 opioid receptor with an IC50 of 280.0 nM. For the inhibition of rat brain mitochondria, it indicates IC50 values of 450.0 nM for MAOB and 42,000.0 nM for MAOA, showing a selectivity index of 93.0 for MAOB over MAOA. In terms of toxicity, FCE 28073 has a TD50 of 626.0 mg/kg in the rotarod neurological impairment test, though another source mentions a slightly different TD50 value of 584.0 mg/kg. The protective index, based on the ratio of TD50 to the anticonvulsant ED50, is calculated to be around 87.8 to 88.0, suggesting a relatively favorable safety profile..
Note: Summary generated by AI. Data source: ChEMBL
Bioactivity
Description
FCE 28073 is a Monoamine oxidase B inibitor with IC50 of 0.45 uM.
Targets&IC50
MAO-B:0.45 μM
Chemical Properties
Molecular Weight302.34
FormulaC17H19FN2O2
Cas No.174756-44-6
SmilesO(CC1=CC(F)=CC=C1)C2=CC=C(CN[C@@H](C(N)=O)C)C=C2
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: 25 mg/mL (82.69 mM), Sonication is recommended.
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM3.3075 mL16.5377 mL33.0753 mL165.3767 mL
5 mM0.6615 mL3.3075 mL6.6151 mL33.0753 mL
10 mM0.3308 mL1.6538 mL3.3075 mL16.5377 mL
20 mM0.1654 mL0.8269 mL1.6538 mL8.2688 mL
50 mM0.0662 mL0.3308 mL0.6615 mL3.3075 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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%
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Please see Inhibitor Handling Instructions for more frequently ask questions. Topics include: how to prepare stock solutions, how to store products, and cautions on cell-based assays & animal experiments, etc

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