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Sotagliflozin

(Synonyms: LX-4211, LP-802034) Copy Product Info
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Synonyms: LX-4211, LP-802034

Catalog No. T3547 Copy Product Info
Purity: 99.86%
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Sotagliflozin (LX-4211, LP-802034) is an oral dual inhibitor of sodium-glucose cotransporter 1/2 (SGLT1/SGLT2) (SGLT2, IC₅₀ ≈ 1.8 nM; SGLT1, IC₅₀ ≈ 36 nM) used as an antidiabetic agent. Sotagliflozin is used in research on cardiovascular disease and diabetes.
Sotagliflozin
Cas No. 1018899-04-1
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Pack SizePriceUSA StockGlobal StockQuantity
1 mg$38In StockIn Stock
2 mg$52In StockIn Stock
5 mg$89In StockIn Stock
10 mg$133In StockIn Stock
25 mg$261In StockIn Stock
50 mg$397In StockIn Stock
100 mg$590In StockIn Stock
500 mg$1,260-In Stock
1 mL x 10 mM (in DMSO)$90In StockIn Stock
For In stock only · Estimated delivery: USA Stock (1-2 days) Global Stock (5-7 days)
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Purity:99.86%
Color:White
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Product Introduction

Bioactivity
Description
Sotagliflozin (LX-4211, LP-802034) is an oral dual inhibitor of sodium-glucose cotransporter 1/2 (SGLT1/SGLT2) (SGLT2, IC₅₀ ≈ 1.8 nM; SGLT1, IC₅₀ ≈ 36 nM) used as an antidiabetic agent. Sotagliflozin is used in research on cardiovascular disease and diabetes.
Targets & IC50
SGLT2:0.6 nM (mouse), SGLT2:1.8 nM (human), SGLT1:62 nM (mouse), SGLT1:36 nM (human)
In vitro
LX4211 inhibits [14C]AMG uptake with IC50 of 62.0 nM for mouse SGLT1 and 0.6 nM for mouse SGLT2, respectively. [2]
In vivo
Methods: After 7 days of acclimatization, mice were randomly assigned to groups. Oral administration of sotagliflozin (30 mg/kg/day) began 7 days prior to surgery using a vehicle solution of 10% DMSO + 90% corn oil at a volume of 10 mL/kg/day. Myocardial infarction (MI) or sham surgery was performed on day 8. Following a 3-day postoperative recovery period, drug administration continued for 25 days, totaling approximately 5 weeks of treatment.
Results: Sotagliflozin treatment significantly improved MI-induced cardiac dysfunction, with recovery of EF, FS, and other parameters, and markedly reduced myocardial fibrosis area and infarct size. [1]
SynonymsLX-4211, LP-802034
Chemical Properties
Molecular Weight424.94
FormulaC21H25ClO5S
Cas No.1018899-04-1
SmilesCCOc1ccc(Cc2cc(ccc2Cl)[C@@H]2O[C@H](SC)[C@@H](O)[C@H](O)[C@H]2O)cc1
Relative Density.1.37 g/cm3 (Predicted)
Storage & Solubility Information
StorageKeep away from moisture,Keep away from direct sunlight Powder: -20°C for 3 years | In solvent: -80°C for 1 year Shipping with blue ice/Shipping at ambient temperature.
Solubility Information
DMSO: 262.5 mg/mL (617.73 mM), Sonication is recommended.
H2O: < 1 mg/mL (insoluble or slightly soluble)
Ethanol: 14 mg/mL (32.95 mM), Sonication is recommended.
Solution Preparation Table
Ethanol/DMSO
1mg5mg10mg50mg
1 mM2.3533 mL11.7664 mL23.5327 mL117.6637 mL
5 mM0.4707 mL2.3533 mL4.7065 mL23.5327 mL
10 mM0.2353 mL1.1766 mL2.3533 mL11.7664 mL
20 mM0.1177 mL0.5883 mL1.1766 mL5.8832 mL
DMSO
1mg5mg10mg50mg
50 mM0.0471 mL0.2353 mL0.4707 mL2.3533 mL
100 mM0.0235 mL0.1177 mL0.2353 mL1.1766 mL
Note : The dilution table applies only to solid products. For liquid products, please calculate the stock solution based on the stated concentration and/or density.

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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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Keywords

Related Tags: Sotagliflozin chemical structure | Sotagliflozin in vivo | Sotagliflozin in vitro | Sotagliflozin formula | Sotagliflozin molecular weight