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7-Glutamyl-cysteinylglycine,

Glutathione disulfide /.-y-Glutamyl-/.-cysteinylglycine disulfide C20H32N6O12S2 27025-41-8 612.631 cry (EtOH aq) 179 ... [Pg.427]

Ethyl propenoate 4878 3-FluorO 4-nitrotoluene 5401 -y-Glutamyl- -cysteinylglycine ... [Pg.706]

Glutathione + amino acid —> y-glutamyl-amino acid + cysteinylglycine... [Pg.681]

The reactivity of mechlorethamine was also examined in the presence of reduced glutathione (L-glutamyl-L-cysteinylglycine), a major cytoprotective compound present throughout the body in physiologically high concentra-... [Pg.697]

Fig. 11.5. Mechanism of hydrolytic dechlorination of mechlorethamine (11.31, R = Me) and other antitumor nitrogen mustards [65] [66]. Also shown is the mechanism of the nonenzymat-ic conjugation with reduced glutathione (GSH, L-glutamyl-L-cysteinylglycine). Fig. 11.5. Mechanism of hydrolytic dechlorination of mechlorethamine (11.31, R = Me) and other antitumor nitrogen mustards [65] [66]. Also shown is the mechanism of the nonenzymat-ic conjugation with reduced glutathione (GSH, L-glutamyl-L-cysteinylglycine).
The glutathione (L-y-glutamyl-L-cysteinylglycine GSH) S-transferases (GSTs) are a multigene family of dimeric... [Pg.307]

See other pages where 7-Glutamyl-cysteinylglycine, is mentioned: [Pg.661]    [Pg.629]    [Pg.251]    [Pg.661]    [Pg.427]    [Pg.415]    [Pg.426]    [Pg.706]    [Pg.7]    [Pg.629]    [Pg.356]    [Pg.322]    [Pg.55]    [Pg.274]    [Pg.1009]    [Pg.612]    [Pg.252]    [Pg.316]    [Pg.317]    [Pg.209]    [Pg.552]    [Pg.143]    [Pg.528]    [Pg.529]    [Pg.530]    [Pg.340]    [Pg.184]    [Pg.67]    [Pg.291]    [Pg.243]    [Pg.1291]    [Pg.159]    [Pg.550]    [Pg.552]    [Pg.277]    [Pg.501]    [Pg.1496]    [Pg.335]    [Pg.1291]    [Pg.126]    [Pg.462]    [Pg.506]    [Pg.390]   
See also in sourсe #XX -- [ Pg.264 ]



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Cysteinylglycine

Glutamyl

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