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Mosapride

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Catalog No. T8128Cas No. 112885-41-3
Alias TAK-370, AS-4370

Mosapride (AS-4370) is a selective 5HT4 agonist

Mosapride

Mosapride

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Purity: 99.56%
Catalog No. T8128Alias TAK-370, AS-4370Cas No. 112885-41-3
Mosapride (AS-4370) is a selective 5HT4 agonist
Pack SizePriceUSA WarehouseGlobal WarehouseQuantity
10 mg$44In StockIn Stock
25 mg$71In StockIn Stock
50 mg$101-In Stock
100 mg$147-In Stock
1 mL x 10 mM (in DMSO)$30In 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:99.56%
Appearance:Solid
Color:White
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Product Introduction

Mosapride AI Summary
Mosapride exhibits diverse bioactivities across various biological targets and assays. Demonstrating antiemetic activity, it suppresses apomorphine-induced emesis in dogs at 1.0 mg/kg with an efficacy of 8.0% and affects gastric emptying rates in rats ranging from 37.0% to 79.0% depending on dose and meal type. It shows significant affinity for the 5-hydroxytryptamine 4 receptor (Ki = 69.9 nM) and moderate inhibition of the 5-hydroxytryptamine 3 receptor (Ki = 1189.0 nM), with no significant affinity for the Dopamine receptor D2. Additionally, it affects gastrointestinal motility and increases stomach motility by 188.0% in dogs. Mosapride inhibits human ERG channels and displays inhibitory effects on serotonin, adrenergic receptors, and CYP450 enzymes, suggesting potential drug-drug interaction risks. It impacts various physiological parameters including liver and kidney functions, glucose metabolism, and blood cell counts, and has shown moderate antiviral activity against SARS-CoV-2. While it also exhibits HDAC6 inhibitory activities, its overall enzyme and receptor binding at relevant concentrations often is weak, with many AC50 values above 30000.0 nM. The compound's multifaceted pharmacological profile indicates potential applications across various therapeutic areas..
Note: Summary generated by AI. Data source: ChEMBL
Bioactivity
Description
Mosapride (AS-4370) is a selective 5HT4 agonist
SynonymsTAK-370, AS-4370
Chemical Properties
Molecular Weight421.89
FormulaC21H25ClFN3O3
Cas No.112885-41-3
SmilesC(NCC1CN(CC2=CC=C(F)C=C2)CCO1)(=O)C3=C(OCC)C=C(N)C(Cl)=C3
Relative Density.1.272 g/cm3
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: 37.04 mg/mL (87.8 mM), Sonication is recommended.
In Vivo Formulation
10% DMSO+90% Corn Oil: 5 mg/mL (11.85 mM), Sonication is recommended.
Please add the solvents sequentially, clarifying the solution as much as possible before adding the next one. Dissolve by heating and/or sonication if necessary. Working solution is recommended to be prepared and used immediately. The formulation provided above is for reference purposes only. In vivo formulations may vary and should be modified based on specific experimental conditions.
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM2.3703 mL11.8514 mL23.7029 mL118.5143 mL
5 mM0.4741 mL2.3703 mL4.7406 mL23.7029 mL
10 mM0.2370 mL1.1851 mL2.3703 mL11.8514 mL
20 mM0.1185 mL0.5926 mL1.1851 mL5.9257 mL
50 mM0.0474 mL0.2370 mL0.4741 mL2.3703 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:
mg/kg
g
μL
2 Enter the in vivo formulation:
% DMSO
%
% Tween 80
% Saline/PBS/ddH2O

Dose Conversion

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Tech Support

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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