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Remogliflozin etabonate

Remogliflozin etabonate
Remogliflozin etabonate (GSK189075A) is a prodrug of regaliflozin and an inhibitor SGLT2 with Ki values of 1.95, 2.14, 8.57, and 43.1μM for hSGLT2, rSGLT2, rSGLT1, and hSGLT1, respectively.
Catalog No. T34286Cas No. 442201-24-3
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Purity:99%
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Remogliflozin etabonate

Catalog No. T34286Cas No. 442201-24-3
Remogliflozin etabonate (GSK189075A) is a prodrug of regaliflozin and an inhibitor SGLT2 with Ki values of 1.95, 2.14, 8.57, and 43.1μM for hSGLT2, rSGLT2, rSGLT1, and hSGLT1, respectively.
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Pack SizePriceAvailabilityQuantity
1 mg$31In Stock
2 mg$46In Stock
5 mg$81In Stock
10 mg$147In Stock
25 mg$278In Stock
50 mg$428In Stock
100 mg$596In Stock
1 mL x 10 mM (in DMSO)$93In Stock
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Product Introduction

Bioactivity
Description
Remogliflozin etabonate (GSK189075A) is a prodrug of regaliflozin and an inhibitor SGLT2 with Ki values of 1.95, 2.14, 8.57, and 43.1μM for hSGLT2, rSGLT2, rSGLT1, and hSGLT1, respectively.
Targets&IC50
SGLT2 (human):1.95 μM (Ki), SGLT2 (rat):2.14 μM (Ki), SGLT1 (human):43.1 μM (Ki), SGLT1 (rat):8.57 μM (Ki)
In vivo
Oral administration of Remogliflozin etabonate (10-30 mg/kg) dose-dependently reduces the levels of FPG and GHb. Oral administration of Remogliflozin etabonate (3-30 mg/kg) dose-dependently increases urine volume and urinary glucose excretion[2].
AliasGSK189075, GSK 189075, GSK-189075A, GSK189075A, GSK-189075, GSK 189075A
Chemical Properties
Molecular Weight522.59
FormulaC26H38N2O9
Cas No.442201-24-3
Storage & Solubility Information
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice.
Solubility Information
DMSO: 90.0 mg/mL (172.2 mM), Sonication is recommended.
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM1.9135 mL9.5677 mL19.1355 mL95.6773 mL
5 mM0.3827 mL1.9135 mL3.8271 mL19.1355 mL
10 mM0.1914 mL0.9568 mL1.9135 mL9.5677 mL
20 mM0.0957 mL0.4784 mL0.9568 mL4.7839 mL
50 mM0.0383 mL0.1914 mL0.3827 mL1.9135 mL
100 mM0.0191 mL0.0957 mL0.1914 mL0.9568 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 mother liquor preparation method and in vivo formula preparation method:
TargetMol | Animal experimentsFor example, your dosage is 10 mg/kg Each animal weighs 20 g, and the dosage volume is 100 μL . TargetMol | Animal experiments A total of 10 animals were administered, and the formula you used is 5% TargetMol | reagent DMSO+30% PEG300+5% Tween 80+60% ddH2O. So your working solution concentration is 2 mg/mL。
Mother liquor preparation method: 2 mg of drug dissolved in 50 μL DMSOTargetMol | reagent (mother liquor concentration of 40 mg/mL), if you need to configure a concentration that exceeds the solubility of the product, please contact us first.
Preparation method for in vivo formula: Take 50 μL DMSOTargetMol | reagent main solution, add 300 μLPEG300TargetMol | reagent mix well and clarify, then add 50 more μL Tween 80, mix well and clarify, then add 600 more μLddH2OTargetMol | reagent mix well and clarify
For Reference Only. Please develop an appropriate dissolution method based on your laboratory animals and route of administration.
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