40055-99-0

Upstream product

• 58-15-1 aminopyrine 
• 40055-99-0 glutathione radical 

Downstream Products

• 63983-50-6 ascorbic acid radical anion 
• 52993-47-2 (R)-2-((S)-4-Amino-4-carboxy-butyrylamino)-2-(carboxymethyl-carbamoyl)-ethanethiol anion 
• 27025-41-8 Oxidized glutathione 
• 40055-98-9 oxidized glutathione 
• 18430-02-9 3-carboxy-4-nitrobenzenethiolate 
• 58-15-1 aminopyrine radical cation 
• 40055-99-0 glutathionate 
• 1175-88-8 2C₁₈H₂₂N₂S*C₄H₆O₆*2H⁽¹⁺⁾ 
• 299-36-5 C₆H₈O₆^(1-) 
• 70-18-8 GLUTATHIONE 
• 50-53-3 chloropromazine cation radical 

Relevant academic research and scientific papers

Reversible reactions of thiols and thiyl radicals with nitrone spin traps

The reactions of the reversible addition of thiols and thiyl radicals to the nitrone spin traps DMPO (5,5dimethyl-1-pyrroline N-oxide) and DEPMPO (5-diethoxyphosphoryl-5-methyl-l-pyrroline N-oxide) are described. Addition of the thiols to the double C=N b

Aminopyrine and Antipyrine Free Radical-cations: Pulse Radiolysis Studies of One-electron Transfer Reactions

Absolute rate constants for the reaction of a variety of electrophilic free radicals with the pyrazoline derivatives aminopyrine and antipyrine have been measured by pulse radiolysis.In the case of aminopyrine the resulting radical cation is a particularly stable species ε325 5.35*103 dm3 mol-1 cm-1).Both compounds are readily oxidised to their respective radical-cations with the one-electron oxidation potential of antipyrine (E0 1.1-1.6 V) being higher than that of aminopyrine (E0 0.26-0.5 V).Studies of the reaction of the radical-cations with reducing agents suggest that aminopyrine in particular may prove to be a useful reference compound in studies of free radical one-electron oxidations.