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Sulamserod
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Catalog No. T13021Cas No. 219757-90-1
Alias RS-100302
Sulamserod (RS 100302) is a potent 5-HT4 receptor antagonist with antiarrhythmic activity for the study of atrial fibrillation and cardiovascular related diseases.
Sulamserod
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Purity: 98.76%
Catalog No. T13021Alias RS-100302Cas No. 219757-90-1
Sulamserod (RS 100302) is a potent 5-HT4 receptor antagonist with antiarrhythmic activity for the study of atrial fibrillation and cardiovascular related diseases.
| Pack Size | Price | USA Warehouse | Global Warehouse | Quantity |
|---|---|---|---|---|
| 1 mg | $545 | - | In Stock | |
| 5 mg | $1,190 | - | In Stock |
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In Stock Estimated shipping dateUSA Warehouse[1-2 days] Global Warehouse[5-7 days]
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Purity:98.76%
Appearance:Solid
Color:Yellow
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Product Introduction
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Chemical Properties
Storage & Solubility Information
| Description | Sulamserod (RS 100302) is a potent 5-HT4 receptor antagonist with antiarrhythmic activity for the study of atrial fibrillation and cardiovascular related diseases. |
| In vivo | In pigs, the administration of Sulamserod at a dose of 30 mg/kg results in significant effects on electrophysiological parameters. Specifically, Sulamserod prolongs the mean effective refractory period (ERP) (14667 ms versus 11568 ms, P < 0.01) and wavelength (9.960.8 cm versus 8.360.9 cm, P < 0.01). Additionally, it reduces the dispersion of ERP (861 ms versus 1565 ms, P < 0.01) and causes a minimal slowing of conduction velocity (6765 cm/s versus 7264 cm/s, P < 0.01). Notably, Sulamserod does not induce any ventricular electrophysiological effects. Moreover, its administration leads to the termination of atrial flutter in 6 out of 8 animals and atrial fibrillation in 8 out of 9 animals. Furthermore, Sulamserod effectively prevents the reinduction of sustained tachycardia in all animals[1]. |
| Synonyms | RS-100302 |
| Molecular Weight | 445.96 |
| Formula | C19H28ClN3O5S |
| Cas No. | 219757-90-1 |
| Smiles | O=C(C1=CC(Cl)=C(N)C=2OCCOC21)CCC3CCN(CCNS(=O)(=O)C)CC3 |
| Relative Density. | 1.319 g/cm3 (Predicted) |
| Storage | store at low temperature | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature. |
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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:
For example, if the intended dosage is 10 mg/kg for animals weighing 20 g , with a dosing volume of 100 μL per animal, and a total of 10 animals are to be administered, using a formulation of 
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 DMSO 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 DMSO stock solution to 400 μL PEG300 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 ddH2O 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.
Dose Conversion
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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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