Acetaminophen glucuronide

CAT:
804-HY-113083
Size:
5 mg

For Laboratory Research Only. Not for Clinical or Personal Use.

  • Availability: 24/48H Stock Items & 2 to 6 Weeks non Stock Items.
  • Dry Ice Shipment: No
Acetaminophen glucuronide - image 1

Acetaminophen glucuronide

  • Description :

    Acetaminophen glucuronide (APAP-glu) is an inactive glucuronide metabolite of Acetaminophen (HY-66005) [1][2]. Acetaminophen is a selective cyclooxygenase-2 (COX-2) inhibitor and a potent hepatic N-acetyltransferase 2 (NAT2) inhibitor[3][4].
  • Product Name Alternative :

    APAP-glu
  • UNSPSC :

    12352005
  • Hazard Statement :

    H302
  • Target :

    Drug Metabolite; Endogenous Metabolite
  • Type :

    Reference compound
  • Related Pathways :

    Metabolic Enzyme/Protease
  • Applications :

    Metabolism-protein/nucleotide metabolism
  • Field of Research :

    Others
  • Assay Protocol :

    https://www.medchemexpress.com/acetaminophen-glucuronide.html
  • Purity :

    99.9
  • Solubility :

    10 mM in DMSO
  • Smiles :

    OC([C@H]([C@H]([C@@H]([C@H]1O)O)O)O[C@H]1OC2=CC=C(C=C2)NC(C)=O)=O
  • Molecular Formula :

    C14H17NO8
  • Molecular Weight :

    327.29
  • Precautions :

    H302
  • References & Citations :

    [1]Carolina I Ghanem, et al. Shift from biliary to urinary elimination of acetaminophen-glucuronide in acetaminophen-pretreated rats. J Pharmacol Exp Ther. 2005 Dec;315 (3) :987-95.|[2]Liudmila L Mazaleuskaya, et al. PharmGKB summary: pathways of acetaminophen metabolism at the therapeutic versus toxic doses. Pharmacogenet Genomics. 2015 Aug;25 (8) :416-26.|[3]Hinz, B, et al. Acetaminophen (paracetamol) is a selective cyclooxygenase-2 inhibitor in man. FASEB J, 2008. 22 (2) : p. 383-90.|[4]Rothen JP, et al. Acetaminophen is an inhibitor of hepatic N-acetyltransferase 2 in vitro and in vivo. Pharmacogenetics. 1998 Dec;8 (6) :553-9.
  • Shipping Conditions :

    Room Temperature
  • Storage Conditions :

    -20°C, 3 years; 4°C, 2 years (Powder)
  • Scientific Category :

    Reference compound1
  • Clinical Information :

    No Development Reported
  • Isoform :

    Human Endogenous Metabolite
  • CAS Number :

    [16110-10-4]

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