1998Inorganic ChemistryRequires access

Oxovanadium(IV)-Promoted Peptide-Amide Deprotonation in Aqueous Solution

Tivadar Kiss, K. Petrohán, Péter Buglyó, Daniele Sanna, Giovanni Micera, João Costa Pessoa, Catarina Madeira

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Abstract

The speciation and solution structural studies of the complexes formed in the aqueous solution of oxovanadium(IV) and 2-hydroxyhippuric acid (a pseudopeptide, SalGly) revealed that the metal ion-promoted deprotonation and coordination of the peptide-amide occurs at pH as low as 4 and the complex formed is the predominant species at physiological pH.

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What this paper is about

The speciation and solution structural studies of the complexes formed in the aqueous solution of oxovanadium(IV) and 2-hydroxyhippuric acid (a pseudopeptide, SalGly) revealed that the metal ion-promoted deprotonation and coordination of the peptide-amide occurs at pH as low as 4 and the complex formed is the predominant species at physiological pH.

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Available abstract

The speciation and solution structural studies of the complexes formed in the aqueous solution of oxovanadium(IV) and 2-hydroxyhippuric acid (a pseudopeptide, SalGly) revealed that the metal ion-promoted deprotonation and coordination of the peptide-amide occurs at pH as low as 4 and the complex formed is the predominant species at physiological pH.

Key concepts: Deprotonation, Chemistry, Amide, Aqueous solution, Peptide, Metal, Genetic algorithm, Ion

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