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Epaminurad HCl

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TargetMol
Catalog No. T27275LCas No. 1198153-46-6
Alias URC-102 HCl, UR-1102 HCl, Epaminurad HCl(1198153-15-9 Free base)

Epaminurad HCl is a URAT1 inhibitor with partial inhibition of OAT1 and OAT3 (organic anion transporters).Epaminurad HCl is a pro-uric acid excretory agent used for the prevention and treatment of gout and hyperuricemia.

Epaminurad HCl

Epaminurad HCl

🥰Excellent
TargetMol
Purity: 100%
Catalog No. T27275LAlias URC-102 HCl, UR-1102 HCl, Epaminurad HCl(1198153-15-9 Free base)Cas No. 1198153-46-6
Epaminurad HCl is a URAT1 inhibitor with partial inhibition of OAT1 and OAT3 (organic anion transporters).Epaminurad HCl is a pro-uric acid excretory agent used for the prevention and treatment of gout and hyperuricemia.
Pack SizePriceAvailabilityQuantity
1 mg$126In Stock
5 mg$313In Stock
10 mg$513In Stock
25 mg$819In Stock
50 mg$1,080In Stock
100 mg$1,490In Stock
1 mL x 10 mM (in DMSO)$345In Stock
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Purity:100%
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Product Introduction

Bioactivity
Description
Epaminurad HCl is a URAT1 inhibitor with partial inhibition of OAT1 and OAT3 (organic anion transporters).Epaminurad HCl is a pro-uric acid excretory agent used for the prevention and treatment of gout and hyperuricemia.
In vivo
In tufted capuchin monkeys, Epaminurad HCl (0, 3, 10, and 30 mg/kg; orally, once a day, for 3 consecutive days) showed good uricosuric and urate-lowering effects at the lowest dose of 3 mg/kg[1].
AliasURC-102 HCl, UR-1102 HCl, Epaminurad HCl(1198153-15-9 Free base)
Chemical Properties
Molecular Weight450.51
FormulaC14H11Br2ClN2O3
Cas No.1198153-46-6
SmilesCl.O=C(C1=CC(Br)=C(O)C(Br)=C1)N2C=3C=NC=CC3OCC2
Relative Density.no data available
Storage & Solubility Information
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice.

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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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