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
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Biochemistry,General Medicine,Analytical Chemistry
Reference14 articles.
1. Attempted affinity-labelling of β-d-galactosidase from Escherichia coli with 2,6:3,4-dianhydro-1-deoxy-d-talo-hept-1-enitol
2. 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
3. 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
4. Untersuchungen zum Wirkungsmechanismus glykosidspaltender Enzyme, III. Markierung des aktiven Zentrums einer β-Glucosidase ausAspergillus wentiimit [14C]Condurit-B-epoxid
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1. β-Galactosidase;Encyclopedia of Industrial Biotechnology;2010-04-15
2. Keratan sulfate disaccharide composition determined by FACE analysis of keratanase II and endo- -galactosidase digestion products;Glycobiology;2001-10-01
3. [47] Sphingolipid photoaffinity labels;Sphingolipid Metabolism and Cell Signaling Part A;2000
4. Inhibition of Escherichia coli β-galactosidase by 2-nitro-1-(4,5-dimethoxy-2-nitrophenyl)ethyl, a photoreversible thiol label;Biochimica et Biophysica Acta (BBA) - Protein Structure and Molecular Enzymology;1996-04
5. Mechanism of enzymic glycoside hydrolysis and of glycosyl transfer by glycosidases and glycosyltransferases;Carbohydrate Research;1993-12
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