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Parent Compound(s)
10904JWH 073 13170JWH 073 (exempt preparation)
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(R)-(−)-JWH 073 N-(3-hydroxybutyl) metabolite

Item No. 10899

Product Insert (PDF)Safety Data Sheet (SDS) (PDF)
Technical Information
Formal Name
(1-(3-hydroxybutyl)-1H-indol-3-yl)(naphthalen-1-yl)methanone
Molecular Formula
C23H21NO2
Formula Weight
343.4
Purity
≥98%
Formulation
A crystalline solid
Solubility(Learn about Variance in Solubility)
DMF: 30 mg/mlDMF:PBS (pH 7.2) (1:9): 0.1 mg/mlDMSO: 30 mg/mlEthanol: 0.5 mg/mlMethanol:PBS (pH 7.2) (1:2): 0.1 mg/ml
λmax
218, 247, 314 nm
SMILES
O=C(C1=CN(CCC(O)C)C2=C1C=CC=C2)C3=CC=CC4=CC=CC=C43
InChi Code
InChI=1S/C23H21NO2/c1-16(25)13-14-24-15-21(19-10-4-5-12-22(19)24)23(26)20-11-6-8-17-7-2-3-9-18(17)20/h2-12,15-16,25H,13-14H2,1H3/t16-/m1/s1
InChi Key
YPRJGJFJMZOUSH-MRXNPFEDSA-N
Shipping & Storage Information
Storage
-20°C
Shipping
Room temperature in continental US; may vary elsewhere
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    Product Description

    (R)-(−)-JWH 073 N-(3-hydroxybutyl) metabolite is a purified single enantiomer of a major metabolite of JWH 073, produced by human liver microsomes in vitro and detected, as a glucuronidated form, in urine.1,2,3 The biological actions of this metabolite are unknown.

    WARNING This product is not for human or veterinary use.

    References & Product Citations
    Product Description References

    1. Wintermeyer, A., Möller, I., Thevis, M., et al. In vitro phase I metabolism of the synthetic cannabimimetic JWH-018. Anal. Bioanal. Chem. 398(5), 2141-2153 (2010).

    2. Zhang, Q., Ma, P., Cole, R.B., et al. Identification of in vitro metabolites of JWH-015, an aminoalkylindole agonist for the peripheral cannabinoid receptor (CB2) by HPLC-MS/MS. Anal. Bioanal. Chem. 386(5), 1345-1355 (2006).

    3. Chimalakonda, K.C., Moran, C.L., Kennedy, P.D., et al. Solid-phase extraction and quantitative measurement of omega and omega-1 metabolites of JWH-018 and JWH-073 in human urine. Anal. Chem. 83(16), 6381-6388 (2011).