Abstract
In this work, we report a technological approach to a novel Fmoc-protected nucleoamino acid, based on l-tyrosine, carrying the DNA nucleobase on the hydroxyl group by means of an ester bond, suitable for the solid-phase synthesis of novel aromatic nucleopeptides of potential interest in biomedicine. After ESI-MS and NMR characterization this building block was used for the assembly of a thymine-functionalized tetrapeptide, composed of nucleobase-containing and underivatized l-tyrosine moieties alternated in the backbone.
Copyright © 2011 Elsevier B.V. All rights reserved.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Amino Acids / chemical synthesis
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Amino Acids / chemistry
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Amino Acids, Aromatic / chemical synthesis*
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Amino Acids, Aromatic / chemistry
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Chromatography, Liquid
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Esters
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Fluorenes / chemical synthesis
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Fluorenes / chemistry
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Molecular Conformation
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Nuclear Magnetic Resonance, Biomolecular
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Oligopeptides / chemical synthesis*
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Oligopeptides / chemistry
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Peptide Nucleic Acids / chemical synthesis*
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Peptide Nucleic Acids / chemistry
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Spectrometry, Mass, Electrospray Ionization
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Tyrosine / chemistry
Substances
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Amino Acids
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Amino Acids, Aromatic
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Esters
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Fluorenes
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N(alpha)-fluorenylmethyloxycarbonylamino acids
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Oligopeptides
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Peptide Nucleic Acids
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Tyrosine