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Interactions of oxidative radicals with N‐phosphoryl dipeptide derivatives

Interactions of oxidative radicals with N‐phosphoryl dipeptide derivatives The interactions of oxidative radicals (Br2−‐, HO− etc.) with N‐phosphoryl dipeptide derivatives (NDM‐TrpOMe and NDT‐MetOMe) have been investigated by using pulse radiolysis at different pH values. It has been found that Br2−‐ and HO− radicals oxidize the Met‐site and Trp‐site in the dipeptide derivatives via formation of the three‐electron‐bonded intermediate and indolyl radical simultaneously. Then the intramolecular electron transfer along the peptide backbone occurs. The rate constants of electron transfer, k, have been determined and the reaction mechanism has been deduced. http://www.deepdyve.com/assets/images/DeepDyve-Logo-lg.png Chinese Journal of Chemistry Wiley

Interactions of oxidative radicals with N‐phosphoryl dipeptide derivatives

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References (10)

Publisher
Wiley
Copyright
Copyright © 1999 Wiley Subscription Services, Inc., A Wiley Company
ISSN
1001-604X
eISSN
1614-7065
DOI
10.1002/cjoc.19990170606
Publisher site
See Article on Publisher Site

Abstract

The interactions of oxidative radicals (Br2−‐, HO− etc.) with N‐phosphoryl dipeptide derivatives (NDM‐TrpOMe and NDT‐MetOMe) have been investigated by using pulse radiolysis at different pH values. It has been found that Br2−‐ and HO− radicals oxidize the Met‐site and Trp‐site in the dipeptide derivatives via formation of the three‐electron‐bonded intermediate and indolyl radical simultaneously. Then the intramolecular electron transfer along the peptide backbone occurs. The rate constants of electron transfer, k, have been determined and the reaction mechanism has been deduced.

Journal

Chinese Journal of ChemistryWiley

Published: Nov 1, 1999

Keywords: ; ; ;

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