1. Membrane Transporter/Ion Channel
  2. URAT1
  3. Verinurad

Verinurad (Synonyms: RDEA3170)

Cat. No.: HY-16733 Purity: >98.0%
Handling Instructions

Verinurad (RDEA3170) is a highly potent and specific URAT1 inhibitor with an IC50 of 25 nM.

For research use only. We do not sell to patients.

Verinurad Chemical Structure

Verinurad Chemical Structure

CAS No. : 1352792-74-5

Size Price Stock Quantity
Free Sample (0.5-1 mg)   Apply now  
10 mM * 1 mL in DMSO USD 99 In-stock
Estimated Time of Arrival: December 31
5 mg USD 90 In-stock
Estimated Time of Arrival: December 31
10 mg USD 120 In-stock
Estimated Time of Arrival: December 31
50 mg USD 250 In-stock
Estimated Time of Arrival: December 31
100 mg   Get quote  
200 mg   Get quote  

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Description

Verinurad (RDEA3170) is a highly potent and specific URAT1 inhibitor with an IC50 of 25 nM[1].

IC50 & Target

IC50: 25 nM (URAT1)[1]

In Vitro

Verinurad inhibits the transport activity of human URAT1 in a dose-dependent manner, at high potency with an IC50 of 25 nM [1].

Storage
Powder -20°C 3 years
  4°C 2 years
In solvent -80°C 6 months
  -20°C 1 month
Solvent & Solubility
In Vitro: 

DMSO : ≥ 30 mg/mL (86.10 mM)

*"≥" means soluble, but saturation unknown.

Preparing
Stock Solutions
Concentration Solvent Mass 1 mg 5 mg 10 mg
1 mM 2.8701 mL 14.3505 mL 28.7010 mL
5 mM 0.5740 mL 2.8701 mL 5.7402 mL
10 mM 0.2870 mL 1.4350 mL 2.8701 mL
*Please refer to the solubility information to select the appropriate solvent.
References
Molecular Weight

348.42

Formula

C₂₀H₁₆N₂O₂S

CAS No.

1352792-74-5

SMILES

CC(C)(SC1=C(C2=C3C=CC=CC3=C(C#N)C=C2)C=NC=C1)C(O)=O

Shipping

Room temperature in continental US; may vary elsewhere

Purity: >98.0%

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The dilution calculator equation

Concentration (start) × Volume (start) = Concentration (final) × Volume (final)

This equation is commonly abbreviated as: C1V1 = C2V2

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× = ×
C1   V1   C2   V2

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Product Name:
Verinurad
Cat. No.:
HY-16733
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Verinurad

Cat. No.: HY-16733