Thiol-group reactivity, hydrophilicity and stability of alloxan, its reduction products and its N-methyl derivatives and a comparison with ninhydrin
- 12 September 1991
- journal article
- Published by Elsevier BV in Biochemical Pharmacology
- Vol. 42 (7), 1385-1391
- https://doi.org/10.1016/0006-2952(91)90449-f
Abstract
No abstract availableThis publication has 32 references indexed in Scilit:
- Glutathione-mediated redox cycling of alloxan: Mechanisms of superoxide dismutase inhibition and of metal-catalyzed OH formationBiochemical Pharmacology, 1989
- Free radicals and diabetesFree Radical Biology & Medicine, 1988
- Structural requirements of alloxan and ninhydrin for glucokinase inhibition and of glucose for protection against inhibitionBritish Journal of Pharmacology, 1988
- Alloxan: history and mechanism of actionDiabetologia, 1988
- Signal recognition by pancreatic B-cellsBiochemical Pharmacology, 1988
- Selective uptake of alloxan by pancreatic B-cellsBiochemical Journal, 1982
- Die chemie des ninhydrins und anderer cyclischer 1,2,3-tricarbonylverbindungenTetrahedron, 1978
- Chemistry of vicinal polyketonesChemical Reviews, 1975
- Intermolecular Carbonyl Carbon–oxygen Interactions in Organic Crystal StructuresNature, 1964
- The Chemistry of Ninhydrin.Chemical Reviews, 1960