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Synthesis and X-ray crystallographic structure of leucine-phenylalanyl succinimide-based pseudopeptides

机译:亮氨酸-苯丙氨酰琥珀酰亚胺基假肽的合成及X射线晶体结构

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摘要

The incorporation of a structural group, represented by X in Figure 1, which is known to inhibit a particular class of enzyme, into a peptide recognition sequence, has been the subject of much research. The aims of this work are to enhance the selectivity of an inhibitor toward a particular subclass of enzyme and also to produce fami- lids of peptide-based inhibitors to act as biological probes.
机译:在肽识别序列中结合已知在图1中由X表示的结构基团以抑制特定种类的酶,已经成为许多研究的主题。这项工作的目的是增强抑制剂对特定的酶亚类的选择性,并生产出基于肽的抑制剂家族以用作生物探针。

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