By using the chain to chain mode of cyclization the title glutathione analogue y-Glu-Cys-Asp-Cys (4), containing the 11-membered disulide ring –Cys-Asp-Cys- replacing the native -Cys-Gly fragment, has been synthesized and characterized together with its reduced dithiol form y-Glu-Cys-Asp-Cys (5). The activity of (4) with y-glutamyl-transferase and glutathione reductase has been evaluated and compared with those of the two conformationally restricted glutathione analogues (2) and (3) previously reported.

Synthesis and biological evaluation of the disulfide form of the glutathione analogue g-(l-glutamyl)-l-cysteinyl-l-aspartyl-l-cysteine?

2003

Abstract

By using the chain to chain mode of cyclization the title glutathione analogue y-Glu-Cys-Asp-Cys (4), containing the 11-membered disulide ring –Cys-Asp-Cys- replacing the native -Cys-Gly fragment, has been synthesized and characterized together with its reduced dithiol form y-Glu-Cys-Asp-Cys (5). The activity of (4) with y-glutamyl-transferase and glutathione reductase has been evaluated and compared with those of the two conformationally restricted glutathione analogues (2) and (3) previously reported.
2003
Istituto di Chimica Biomolecolare - ICB - Sede Pozzuoli
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/20.500.14243/160872
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