Mechanism-based inactivation of E. coli γ-glutamylcysteine synthetase by phosphinic acid- and sulfoximine-based transition-state analogues
- 9 July 1996
- journal article
- Published by Elsevier in Bioorganic & Medicinal Chemistry Letters
- Vol. 6 (13) , 1437-1442
- https://doi.org/10.1016/s0960-894x(96)00247-8
Abstract
No abstract availableKeywords
This publication has 11 references indexed in Scilit:
- Mechanism-Based Inactivation of Glutathione Synthetase by Phosphinic Acid Transition-State AnalogJournal of the American Chemical Society, 1994
- Analytical and preparative separation of the diastereomers of l-buthionine (SR)-sulfoximine, a potent inhibitor of glutathione biosynthesisAnalytical Biochemistry, 1991
- Diethoxymethylphosphonites and phosphinates. Intermediates for thesynthesis of α,β- and X aminoalkylphosphonous acidsTetrahedron, 1989
- A novel and efficient synthesis of L-vinylglycineTetrahedron Letters, 1984
- GLUTATHIONEAnnual Review of Biochemistry, 1983
- Organophosphorus intermediates. VI. The acid-catalysed reaction of trialkyl orthoformates with phosphinic acidAustralian Journal of Chemistry, 1980
- Eine einfache Herstellung von α-Alkylacrylsäure-esternSynthesis, 1979
- Chemistry of sulfoxides and related compounds. XLIV. Nucleophilic alkylidene transfer reagents. Ethylides, isopropylides, and cyclopropylides derived from salts of sulfoximinesJournal of the American Chemical Society, 1973
- Mechanism of inhibition of glutamine synthetase by methionine sulfoximineBiochemistry, 1969
- Phosphorus Derivatives of Fatty Acids. VII.2 Addition of Dialkyl Phosphonates to Unsaturated CompoundsJournal of the American Chemical Society, 1959