A phase II metabolite of chlorzoxazone
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Parent Compound(s)
18869Chlorzoxazone
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Chlorzoxazone N-Glucuronide

Item No. 19879

Product Insert (PDF)Safety Data Sheet (SDS) (PDF)
Technical Information
Formal Name
(2S,3S,4S,5R)-6-(5-chloro-2-oxobenzo[d]oxazol-3(2H)-yl)-3,4,5-trihydroxytetrahydro-2H-pyran-2-carboxylic acid
Molecular Formula
C13H12ClNO8
Formula Weight
345.7
Purity
≥95%
Formulation (Request formulation change)
A solid
Solubility(Learn about Variance in Solubility)
DMF: 16 mg/mlDMSO: 10 mg/mlEthanol: 20 mg/ml
SMILES
O=C1N(C2[C@H](O)[C@@H](O)[C@H](O)[C@@H](C(O)=O)O2)C3=CC(Cl)=CC=C3O1
InChi Code
InChI=1S/C13H12ClNO8/c14-4-1-2-6-5(3-4)15(13(21)22-6)11-9(18)7(16)8(17)10(23-11)12(19)20/h1-3,7-11,16-18H,(H,19,20)/t7-,8-,9+,10-,11?/m0/s1
InChi Key
FRPKGYRFYSEXSL-GEPHSGDCSA-N
Shipping & Storage Information
Storage
-20°C
Shipping
Wet ice in continental US; may vary elsewhere
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Certificates of Analysis & Batch Specific Data

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    500 µg

    $98

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    1 mg

    $186

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    5 mg

    $686

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    10 mg

    $906

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    Product Description

    Chlorzoxazone N-glucuronide is a phase II metabolite of the skeletal muscle relaxant chlorzoxazone (Item No. 18869).1 Chlorzoxazone N-glucuronide is formed via glucuronidation of chlorzoxazone by the UDP-glucuronosyltransferase (UGT) isoform UGT1A9.

    WARNING This product is not for human or veterinary use.

    References & Product Citations
    Product Description References

    1. Quesnot, N., Bucher, S., Gade, C., et al. Production of chlorzoxazone glucuronides via cytochrome P4502E1 dependent and independent pathways in human hepatocytes. Arch. Toxicol. 92(10), 3077-3091 (2018).