Acetaminophen glucuronide
For Laboratory Research Only. Not for Clinical or Personal Use.
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- Dry Ice Shipment: No


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-gluUNSPSC :
12352005Hazard Statement :
H302Target :
Drug Metabolite; Endogenous MetaboliteType :
Reference compoundRelated Pathways :
Metabolic Enzyme/ProteaseApplications :
Metabolism-protein/nucleotide metabolismField of Research :
OthersAssay Protocol :
https://www.medchemexpress.com/acetaminophen-glucuronide.htmlPurity :
99.9Solubility :
10 mM in DMSOSmiles :
OC([C@H]([C@H]([C@@H]([C@H]1O)O)O)O[C@H]1OC2=CC=C(C=C2)NC(C)=O)=OMolecular Formula :
C14H17NO8Molecular Weight :
327.29Precautions :
H302References & 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 TemperatureStorage Conditions :
-20°C, 3 years; 4°C, 2 years (Powder)Scientific Category :
Reference compound1Clinical Information :
No Development ReportedIsoform :
Human Endogenous MetaboliteCAS Number :
[16110-10-4]

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