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首页> 外文期刊>Heterocycles: An International Journal for Reviews and Communications in Heterocyclic Chemistry >SYNTHESIS OF SUBSTITUTED PYRIMIDINE HYDRAZINE ACIDS(PHA)AND THEIR USE IN PEPTIDE RECOGNITION
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SYNTHESIS OF SUBSTITUTED PYRIMIDINE HYDRAZINE ACIDS(PHA)AND THEIR USE IN PEPTIDE RECOGNITION

机译:取代的嘧啶肼(PHA)的合成及其在肽识别中的用途

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摘要

Substituted pyrimidine-hydrazine-acids(PHA)were prepared from orotic acid in five synthetic steps and high yields.Their geometry of hydrogen bond acceptor and donor sites make them suitable for the molecular recognition of peptide P-sheets.In non-protic solvents the PHA unit emits at around 420 nm after irradiation at 281 nm.The emission intensity decreases upon peptide binding and signals the binding event.Peptides consisting of PHAs and natural amino acids or a turn structure motif were prepared.The investigation of the intramolecular binding pattern by NMR spectroscopy revealed the expected interaction of the PHA and peptide beta-sheet.
机译:由乳清酸经五个合成步骤高产率地制备了取代的嘧啶-肼基酸(PHA),它们的氢键受体和供体位点的几何形状使其适合于肽P-折叠的分子识别。 PHA单元在281 nm照射后在420 nm附近发射,发射强度在肽结合后降低,并发出结合事件信号,制备了由PHA和天然氨基酸组成的肽或具有转向结构的基序。 NMR光谱揭示了PHA和肽β-折叠的预期相互作用。

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