Acetaminophen glucuronide
CAT:
804-HY-113083
Size:
5 mg
For Laboratory Research Only. Not for Clinical or Personal Use.
Price:
Ask
- Availability: 24/48H Stock Items & 2 to 6 Weeks non Stock Items.
- 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
