期刊
AMINO ACIDS
卷 43, 期 2, 页码 857-874出版社
SPRINGER WIEN
DOI: 10.1007/s00726-011-1145-2
关键词
Phosphohistidine; Azide-alkyne cycloaddition; Triazolylalanine; Stable analogues; Synthesis; Haptens
资金
- UWA
Histidine-phosphorylated proteins and the corresponding kinases are important components of bacterial and eukaryotic cell-signalling pathways, and are therefore potential drug targets. The study of these biomolecules has been hampered by the lability of the phosphoramidate functional group in the phosphohistidines and the lack of generic antibodies. Herein, the design and concise synthesis of stable triazolylphosphonate analogues of N1- and N3-phosphohistidine, and derivatives suitable for bioconjugation, are described.
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