A bireactant, irreversible, active-site-directed inhibitor of β-d-galactosidase (Escherichia coli). Synthesis and properties of (1/2,5,6)-2-(3-azibutylthio)-5,6-epoxy-3-cyclohexen-1-ol

This publication has 11 references indexed in Scilit:

• Reactive pseudo-oligosaccharides as potential irreversible inhibitors for sugar-binding proteins: synthesis of the diastereoisomers of (3,4,6/5)-3,4-epoxy-6-(β-d-galactopyranosyl-thio)-5-hydroxycyclohexene
  Carbohydrate Research, 1990
• Binding and reactivity at the “glucose” site of galactosyl-β-galactosidase (Escherichia coli)
  Archives of Biochemistry and Biophysics, 1984
• Identification of an essential carboxylate group at the active site of lacZβ‐galactosidase from Escherichia coli
  European Journal of Biochemistry, 1984
• Radioaffinity labelling of β-d-galactosidase from Escherichia coli with [14C]-glycerol, mediated through covalently bound 2,6-anhydro-1-deoxy-d-galacto-hept-1-enitol
  Carbohydrate Research, 1982
• Inactivation of .beta.-galactosidase by iodination of tyrosine-253
  Biochemistry, 1982
• Attempted affinity-labelling of β-d-galactosidase from Escherichia coli with 2,6:3,4-dianhydro-1-deoxy-d-talo-hept-1-enitol
  Carbohydrate Research, 1982
• The inhibition of β-galactosidase (Escherichia coli) by amino sugars and amino alcohols
  Canadian Journal of Biochemistry, 1982
• Probe of β-galactosidase structure with iodoacetate. Differential reactivity of thiol groups in wild-type and mutant forms of β-galactosidase
  Biochemistry, 1978
• pH Dependence of the Activity of β‐Galactosidase from Escherichia coli
  European Journal of Biochemistry, 1971
• Untersuchungen zum Wirkungsmechanismus glykosidspaltender Enzyme, III. Markierung des aktiven Zentrums einer β-Glucosidase ausAspergillus wentiimit [¹⁴C]Condurit-B-epoxid
  Hoppe-Seyler´s Zeitschrift Für Physiologische Chemie, 1968