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Substrate Report for: 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|119450
UniChem|VDYDCVUWILIYQF-ALKRTJFJSA-N
IUPHAR|
Wikipedia|

Target
Families | S-Lactoylglutathione ligand of proteins in family: A85-EsteraseD-FGH

References:
Search PubMed for references concerning: S-Lactoylglutathione
    Title: A role for His-160 in peroxide inhibition of S. cerevisiae S-formylglutathione hydrolase: evidence for an oxidation sensitive motif
    Legler PM, Leary DH, Hervey WJt, Millard CB
    Ref: Archives of Biochemistry & Biophysics, 528:7, 2012 : PubMed