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Topiroxostat

Cat. No. M5203

All AbMole products are for research use only, cannot be used for human consumption.

Topiroxostat Structure
Synonym:

FYX-051

Size Price Availability Quantity
10mg USD 55 In stock
25mg USD 80 In stock
50mg USD 130 In stock
100mg USD 220 In stock
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Quality Control & Documentation
Biological Activity

Topiroxostat (FYX-051) is a novel and potent xanthine oxidoreductase (XOR) inhibitor with IC50 value of 5.3 nM. Topiroxostat (FYX-051) exhibited competitive-type inhibition with a Ki value of 5.7 × 10-9 M of native XO.

In vivo: In this hyperuricemic model, Topiroxostat in the dose range of 0.03 to 1 mg/kg caused a dose-dependent decrease in serum urate levels with an extremely low ED50 of 0.15 mg/kg, evaluated at 1 h after oral administration.

Chemical Information
Molecular Weight 248.24
Formula C13H8N6
CAS Number 577778-58-6
Form Solid
Solubility (25°C) DMSO 20 mg/mL
Storage Powder          -20°C   3 years ;  4°C   2 years
In solvent       -80°C   6 months ;  -20°C   1 month
References

[1] Shimo T, et al. Arch Toxicol. Xanthine crystals induced by topiroxostat, a xanthine oxidoreductase inhibitor, in rats, cause transitional cell tumors.

[2] Matsumoto K, et al. J Pharmacol Exp Ther. FYX-051: a novel and potent hybrid-type inhibitor of xanthine oxidoreductase.

[3] Sato T, et al. Bioorg Med Chem Lett. Discovery of 3-(2-cyano-4-pyridyl)-5-(4-pyridyl)-1,2,4-triazole, FYX-051 - a xanthine oxidoreductase inhibitor for the treatment of hyperuricemia [corrected].

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Keywords: Topiroxostat, FYX-051 supplier, Xanthine Oxidase, inhibitors, activators

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