A metabolite of febuxostat
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Parent Compound(s)
14127Febuxostat
Technical Support & Resources

Information provided in the product description is from published literature. Due to the nature of scientific experimentation, your results (e.g., selectivity and effective concentrations) or specific application for this product may differ. If you have questions about how this product fits your application, please contact our technical support staff.

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Febuxostat Acyl Glucuronide

Item No. 26599

Technical Information
Formal Name
1-[2-[3-cyano-4-(2-methylpropoxy)phenyl]-4-methyl-5-thiazolecarboxylate], β-D-glucopyranuronic acid
CAS Number
1351692-92-6
Molecular Formula
C22H24N2O9S
Formula Weight
Purity
≥98%
A solid
DMSO: slightly solubleMethanol: slightly soluble
SMILES
CC(C)COC1=C(C#N)C=C(C2=NC(C)=C(C(O[C@@H]3O[C@H](C(O)=O)[C@@H](O)[C@H](O)[C@H]3O)=O)S2)C=C1
InChi Code
InChI=1S/C22H24N2O9S/c1-9(2)8-31-13-5-4-11(6-12(13)7-23)19-24-10(3)18(34-19)21(30)33-22-16(27)14(25)15(26)17(32-22)20(28)29/h4-6,9,14-17,22,25-27H,8H2,1-3H3,(H,28,29)/t14-,15-,16+,17-,22-/m0/s1
InChi Key
ZRXRMGPMLDOOKN-FVMGUFKOSA-N
Shipping & Storage Information
Storage
-20°C
Shipping
Room temperature in continental US; may vary elsewhere
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Certificates of Analysis & Batch Specific Data

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    Product Description

    Febuxostat acyl glucuronide is a metabolite of the xanthine oxidoreductase inhibitor febuxostat (Item No. 14127).1,2 Febuxostat acyl glucuronide is formed via glucuronidation of febuxostat by uridine diphosphate-glucuronosyltransferases (UGTs).2

    WARNING This product is not for human or veterinary use.

    References & Product Citations
    Product Description References

    1. Grabowski, B.A., Khosravan, R., Vernillet, L., et alMetabolism and excretion of [14C] febuxostat, a novel nonpurine selective inhibitor of xanthine oxidase, in healthy male subjects. J. Clin. Pharmacol. 51(2), 189-201 (2011).

    2. Kamel, B., Graham, G.G., Williams, K.M., et alClinical pharmacokinetics and pharmacodynamics of febuxostat. Clin. Pharmacokinet. 56(5), 459-475 (2017).