S-Lactoylglutathione

General

Type : Peptide

Chemical_Nomenclature : (2S)-2-amino-5-[[(2R)-1-(carboxymethylamino)-3-(2-hydroxypropanoylsulfanyl)-1-oxopropan-2-yl]amino]-5-oxopentanoic acid

Canonical SMILES : CC(C(=O)SCC(C(=O)NCC(=O)O)NC(=O)CCC(C(=O)O)N)O

InChI : InChI=1S\/C13H21N3O8S\/c1-6(17)13(24)25-5-8(11(21)15-4-10(19)20)16-9(18)3-2-7(14)12(22)23\/h6-8,17H,2-5,14H2,1H3,(H,15,21)(H,16,18)(H,19,20)(H,22,23)\/t6?,7-,8-\/m0\/s1

InChIKey : VDYDCVUWILIYQF-ALKRTJFJSA-N

Other name(s) : S-Lactylglutathione,     Glutathione, S-lactate (6CI,7CI),     S-D-lactoylglutathione,     Glycine, N-(N-L-gamma-glutamyl-S-(2-hydroxy-1-oxopropyl)-L-cysteinyl)-,     Glycine, l-|A-glutamyl-s-(2-hydroxy-1-oxopropyl)-l-cysteinyl-


MW : 379.38

Formula : C13H21N3O8S

CAS_number :

PubChem :

UniChem :

Iuphar :

Target

Families : A85-EsteraseD-FGH

References (1)

Title : A role for His-160 in peroxide inhibition of S. cerevisiae S-formylglutathione hydrolase: evidence for an oxidation sensitive motif - Legler_2012_Arch.Biochem.Biophys_528_7
Author(s) : Legler PM , Leary DH , Hervey WJt , Millard CB
Ref : Archives of Biochemistry & Biophysics , 528 :7 , 2012
Abstract : Legler_2012_Arch.Biochem.Biophys_528_7
ESTHER : Legler_2012_Arch.Biochem.Biophys_528_7
PubMedSearch : Legler_2012_Arch.Biochem.Biophys_528_7
PubMedID: 22906720
Gene_locus related to this paper: yeast-yjg8