Oxalyl thiolesters and N-oxalylcysteine are normal mammalian metabolites

This publication has 16 references indexed in Scilit:

• The nonenzymic hydrolysis of Δ2-thiazoline-2-carboxylate: The product of the suspected physiological reaction catalyzed by d-amino acid oxidase
  Bioorganic Chemistry, 1986
• Inhibition of the catalytic subunit of phosphorylase phosphatase by oxalyl thioesters and its possible relevance to the mechanism of insulin action
  Biochemical and Biophysical Research Communications, 1986
• Equilibrium constants for the formation of glyoxylate thiohemiacetals and kinetic constants for their oxidation by O2 catalyzed by l-hydroxy acid oxidase
  Bioorganic Chemistry, 1985
• Thiazolidine-2-carboxylate derivatives formed from glyoxylate and L-cysteine or L-cysteinylglycine as possible physiological substrates for D-aspartate oxidase
  Biochemical and Biophysical Research Communications, 1984
• The inhibition of mammalian d-amino acid oxidase by metabolites and drugs. Inferences concerning physiological function
  Bioorganic Chemistry, 1982
• Inhibition of dopamine β-hydroxylase by thiazoline-2-carboxylate, a suspected physiological product of D-amino acid oxidase
  Biochemical and Biophysical Research Communications, 1982
• THIOL-GLYOXYLATE ADDUCTS AS SUBSTRATES FOR RAT KIDNEY L-?-HYDROXY ACID OXIDASE
  Annals of the New York Academy of Sciences, 1982
• Thiol-glyoxylate adducts as substrates for rat kidney L-α-hydroxy acid oxidase
  Biochemical and Biophysical Research Communications, 1981
• CARBON ASSIMILATION BY PSEUDOMONAS OXALATICUS (OX 1). 7. DECARBOXYLATION OF OXALYL-COENZYME A TO FORMYL-COENZYME A
  Biochemical Journal, 1963
• Carbon assimilation by Pseudomonas oxalaticus (OX 1). 6. Reactions of oxalyl-coenzyme A
  Biochemical Journal, 1963