64889-81-2 Chemical Name: Glutathione-S-acetaminophen conjugate Synonyms Aa-gsh;Aa-glutathion;3-Gsh-acetaminophen;Acetaminophen glutathion;Acetaminophen Impurity 37;3-(glutathion-S-yl)acetaminophen;Acetaminophen glutathione conjugate;3-GlutathionylacetaMinophen DisodiuM;Glutathione-S-acetaminophen conjugate;Acetaminophen Glutathione Disodium Salt CBNumber: CB01247918 Molecular Formula: C18H24N4O8S Molecular Weight: 456.47 MDL Number: MOL File: 64889-81-2.mol MSDS File: SDS TDS File: TDS Last updated:2026-04-24 14:59:10 Glutathione-S-acetaminophen conjugate price More Price(14) Glutathione-S-acetaminophen conjugate Preparation Products And Raw materials Raw materials Preparation Products 64889-81-2(Glutathione-S-acetaminophen conjugate)Related Search: GLUTATHIONE S-TRANSFERASE Disodium edetate dihydrate Glutathione (reduced) sodium salt 1-FMOC-PIPERAZINE HYDROBROMIDE GSSG 1of4 Acetaminophen glutathion Glycine, N-(S-(5-(acetylamino)-2-hydroxyphenyl)-N-L-gamma-glutamyl-L-cysteinyl)- N-(S-(5-(Acetylamino)-2-hydroxyphenyl)-N-L-gamma-glutamyl-L-cysteinylglycine Glutathione-S-acetaminophen conjugate 3-(glutathion-S-yl)acetaminophen Acetaminophen glutathione conjugate L-Glu-S-[2-Hydroxy-5-(acetylamino)phenyl]-L-Cys-Gly-OH N-[N-L--Glutamyl-S-[2-hydroxy-5-(acetylamino)phenyl]-L-cysteinyl]glycine Glu-S-(5-Acetylamino-2-hydroxyphenyl)-L-Cys-Gly-OH Glu-S-[2-Hydroxy-5-(acetylamino)phenyl]-Cys-Gly-OH 3-Gsh-acetaminophen Aa-glutathion Aa-gsh 3-(Glutathion-S-yl)acetaMinophen DisodiuM Salt 3-GlutathionylacetaMinophen DisodiuM AcetaMinophen-glutathione Adduct DisodiuM L--GlutaMyl-S-[5-(acetylaMino)-2-hydroxyphenyl]-L-cysteinylglycine DisodiuM Salt Acetaminophen Glutathione Disodium Salt Glutathione Acetaminophen Disodium Salt Glycine, L--glutamyl-S-[5-(acetylamino)-2-hydroxyphenyl]-L-cysteinyl- Acetaminophen Impurity 37 64889-81-2 C18H24N4O8S Amino Acids & Derivatives Intermediates & Fine Chemicals Metabolites & Impurities Pharmaceuticals Sulfur & Selenium Compounds
Valproate-induced acute liver failure and liver-related deaths have been reported in patients with hereditary neurometabolic syndromes caused by mutations in the gene for mitochondrial DNA polymerase (POLG) (e.g., Alpers-Huttenlocher Syndrome) at a higher rate than those without these syndromes
The initiation of autophagy depends on the activation of the core signal ULK1 complex (a serine/threonine protein kinase complex composed of ULK1, ATG13, FIP200, and ATG101), which activates the downstream class III phosphatidylinositol 3 kinase (PI3K) complex and promotes the formation of phagophores [66]
Versatile nano-PROTAC-induced epigenetic reader degradation for efficient lung cancer therapy
Extracts from Artemisia argyi (AA) contain various flavonoids and volatile oils and exert cardioprotective effects through anti-inflammatory, antioxidant, and anti-apoptotic mechanisms ( Astragaloside IV (AS-IV), the principal active component of Astragalus membranaceus, exhibits antifibrotic, anti-apoptotic, antioxidant, and energy metabolism-enhancing properties in cardiomyocytes (Wang et al., 2024)
