A prodrug form of acetaminophen
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Active Metabolite(s)
10024Acetaminophen
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Propacetamol (hydrochloride)

Item No. 36134

Technical Information
Formal Name
N,N-diethyl-glycine, 4-(acetylamino)phenyl ester, monohydrochloride
CAS Number
66532-86-3
Molecular Formula
C14H20N2O3 • HCl
Formula Weight
Purity
≥90%
Formulation
A solid
DMSO: 1 mg/mlPBS (pH 7.2): 5 mg/ml
λmax
248 nm
SMILES
O=C(CN(CC)CC)OC1=CC=C(NC(C)=O)C=C1.Cl
InChi Code
InChI=1S/C14H20N2O3.ClH/c1-4-16(5-2)10-14(18)19-13-8-6-12(7-9-13)15-11(3)17;/h6-9H,4-5,10H2,1-3H3,(H,15,17);1H
InChi Key
WGTYJNGARJPYKG-UHFFFAOYSA-N
Shipping & Storage Information
Storage
-20°C
Shipping
Room temperature in continental US; may vary elsewhere
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    Product Description

    Propacetamol is a prodrug form of the analgesic and antipyretic agent acetaminophen (Item No. 10024).1 It is converted to acetaminophen by rat liver microsomes. Propacetamol reduces acetic acid-induced writhing in mice and LPS-induced pyresis in rats when administered at doses of 200 and 600 mg/kg, respectively.1,2 Propacetamol (1,200 mg/kg) induces hepatotoxicity, decreases hepatic glutathione (GSH), superoxide dismutase (SOD), and glutathione peroxidase (GPX) levels, increases hepatic malondialdehyde (MDA) and nitrotyrosine levels, and increases mortality in mice.3

    WARNING This product is not for human or veterinary use.

    References & Product Citations
    Product Description References

    1. Murie, V.E., Marques, L.M.M., Souza, G.E.P., et alAcetaminophen prodrug: Microwave-assisted synthesis and in vitro metabolism evaluation by mass spectrometry. J. Braz. Chem. Soc. 27(6), 1121-1128 (2016).

    2. Zhang , Y., Du, L., Pan, H., et alEnhanced analgesic effects of propacetamol and tramadol combination in rats and mice. Biol. Pharm. Bull. 34(3), 349-353 (2011).

    3. Liou, G.-G., Hsieh, C.-C., Lee, Y.-J., et alN-Acetyl cysteine overdose inducing hepatic steatosis and systemic inflammation in both propacetamol-induced hepatotoxic and normal mice. Antioxidants (Basel) 10(3), 442 (2021).