For research use only. Not for therapeutic Use.
Acetaminophen glucuronide (CAS 16110-10-4), <span style="font-family:arial,helvetica,sans-serif;"><span style="font-size:12px;"><span style="font-variant-ligatures: normal; orphans: 2; widows: 2;">also known as 4-glucuronosidoacetanilide or deethylphenacetin glucuronide, belongs to the class of organic compounds known as phenolic glycosides. These are organic compounds containing a phenolic structure attached to a glycosyl moiety. </span><span style="font-variant-ligatures: normal; orphans: 2; widows: 2;">In humans, acetaminophen glucuronide is involved in acetaminophen metabolism pathway. Acetaminophen glucuronide, with regard to humans, has been linked to the inborn metabolic disorder beta-thalassemia.</span></span></span>
Catalog Number | M074820 |
CAS Number | 16110-10-4 |
Synonyms | Paracetamol glucuronide |
Molecular Formula | C14H17NO8 |
Purity | ≥95% |
Target | Drug Metabolite |
Storage | -20°C |
IUPAC Name | (2S,3S,4S,5R,6S)-6-(4-acetamidophenoxy)-3,4,5-trihydroxyoxane-2-carboxylic acid |
InChI | InChI=1S/C14H17NO8/c1-6(16)15-7-2-4-8(5-3-7)22-14-11(19)9(17)10(18)12(23-14)13(20)21/h2-5,9-12,14,17-19H,1H3,(H,15,16)(H,20,21)/t9-,10-,11+,12-,14+/m0/s1 |
InChIKey | IPROLSVTVHAQLE-BYNIDDHOSA-N |
SMILES | CC(=O)NC1=CC=C(C=C1)OC2C(C(C(C(O2)C(=O)O)O)O)O |
Reference | <span style="font-family:arial,helvetica,sans-serif;"><span style="font-size:12px;">1.<span style="font-variant-ligatures: normal; orphans: 2; widows: 2;">Aw TY, Jones DP: Intracellular inhibition of UDP-glucose dehydrogenase during ethanol oxidation. Chem Biol Interact. 1983 Mar;43(3):283-8.<br /> |