URAT1-IN-14
URAT1-IN-14 is a potent and orally active Urate transporter 1 (URAT1) inhibitor. URAT1-IN-14 inhibits the human URAT1 in HEK293 cells with an IC50 of 0.72 μM. URAT1-IN-14 exhibits low cytotoxic in Hep-G2 cells. URAT1-IN-14 shows urate-lowering effect in hyperuricemia mouse models. URAT1-IN-14 can be used for the study of hyperuricemia and gout.
For research use only. We do not sell to patients.
- CAS No.: 2516232-89-4
- Formula: C19H19NO3S
- Molecular Weight:341.42
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Storage:
Please store the product under the recommended conditions in the Certificate of Analysis.
Biological Activity
URAT1-IN-14 (Compound 7) (IC50 = 326.5 μM) was less cytotoxic than Benzbromarone (HY-B1135) (IC50 = 67.21 μM) in Hep-G2 cells[1].
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
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Animal Model:Sub-HUA model induced by uric acid and OP in mice[1]
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Dosage:25, 50 and 100 mg/kg
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Administration:Oral administration (p.o.), single dose
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Result:Significantly lowers the blood uric acid level within 24 hours at the dosage of 100 mg/kg.
Decreased the AUC0-24h values treated groups in a dose-dependent manner 6%, 17%, 34%, at the doses of 25, 50 and 100 mg/kg, respectively.
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Animal Model:Ch-HUA model induced by purine-rich yeast extraction and OP in mice[1]
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Dosage:25, 50 and 100 mg/kg
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Administration:Oral administration (p.o.), for 9 days
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Result:Drastically decreased blood uric acid level at the dosage of 50 mg/kg.
Chemical Information
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CAS No. 2516232-89-4
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Molecular Weight 341.42
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Formula C19H19NO3S
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SMILES
O=C(C1(SC2=CC=CC=C2N3CCOC4=CC=CC=C34)CCC1)O
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Shipping
Room temperature in continental US; may vary elsewhere.
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Storage
Please store the product under the recommended conditions in the Certificate of Analysis.
Purity & Documentation
References
Calculators
Concentration (start) × Volume (start) = Concentration (final) × Volume (final)