A metabolite of atomoxetine
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4’-hydroxy Atomoxetine Glucuronide (hydrate)

Item No. 34822

Product Insert (PDF)Safety Data Sheet (SDS) (PDF)
Technical Information
Formal Name
3-methyl-4-[(1R)-3-(methylamino)-1-phenylpropoxy]phenyl β-D-glucopyranosiduronic acid, hydrate
Molecular Formula
C23H29NO8 • XH2O
Formula Weight
447.5
Purity
≥95%
Formulation (Request formulation change)
A solid
Solubility(Learn about Variance in Solubility)
Methanol: slightly, sonicatedWater: slightly soluble
SMILES
OC([C@H]([C@H]([C@@H]([C@H]1O)O)O)O[C@H]1OC2=CC(C)=C(C=C2)O[C@@H](C3=CC=CC=C3)CCNC)=O.O
InChi Code
InChI=1S/C23H29NO8.H2O/c1-13-12-15(30-23-20(27)18(25)19(26)21(32-23)22(28)29)8-9-16(13)31-17(10-11-24-2)14-6-4-3-5-7-14;/h3-9,12,17-21,23-27H,10-11H2,1-2H3,(H,28,29);1H2/t17-,18+,19+,20-,21+,23-;/m1./s1
InChi Key
YMRWALPEIHAZLT-WOLRTSBYSA-N
Shipping & Storage Information
Storage
-20°C
Shipping
Room temperature in continental US; may vary elsewhere
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    1 mg

    $962

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    Product Description

    4’-hydroxy Atomoxetine glucuronide is a metabolite of the norepinephrine transporter (NET) inhibitor atomoxetine (Item No. 22248).1 It is formed from atomoxetine by glucuronidation of the intermediate metabolite 4-hydroxy atomoxetine.2

    WARNING This product is not for human or veterinary use.

    References & Product Citations
    Product Description References

    1. Todor, I., Popa, A., Neag, M., et al. Evaluation of a potential metabolism-mediated drug-drug interaction between atomoxetine and bupropion in healthy volunteers. J. Pharm. Pharm. Sci. 19(2), 198-207 (2016).

    2. Sauer, J.-M., Ring, B.J., and Witcher, J.W. Clinical pharmacokinetics of atomoxetine. Clin. Pharmacokinet. 44(6), 571-590 (2005).