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首页> 外文期刊>ChemistryOpen >Front Cover: Early‐Stage Incorporation Strategy for Regioselective Labeling of Peptides using the 2‐Cyanobenzothiazole/1,2‐Aminothiol Bioorthogonal Click Reaction (ChemistryOpen 3/2018)
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Front Cover: Early‐Stage Incorporation Strategy for Regioselective Labeling of Peptides using the 2‐Cyanobenzothiazole/1,2‐Aminothiol Bioorthogonal Click Reaction (ChemistryOpen 3/2018)

机译:封面:使用2-氰基苯并噻唑/ 1,2-氨基硫醇生物正交点击反应对肽进行区域选择性标记的早期纳入策略(ChemistryOpen 3/2018)

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The Front Cover shows an innovative methodology for the regioselective labeling of peptides. Early‐stage incorporation of a clickable handle during SPPS provides flexibility for the functionalization of peptide‐based targeting vectors. Once the click handle has been ideally positioned, an imaging probe is conjugated to the targeting vector by 2‐cyanobenzothiazole (CBT)/1,2‐aminothiol cycloaddition. This key reaction is as easy as just “one click”. The labeling reaction is rapid, biocompatible, orthogonal, and highly efficient. It offers a nearly ideal labeling strategy for peptides and a powerful tool for the development of novel imaging agents for biomedical applications. More information can be found in the Communication by K.‐T. Chen et?al. on page?256 in Issue?3, 2018 (DOI: 10.1002/open.201700191 ).
机译:封面显示了一种创新的方法,用于肽的区域选择性标记。 SPPS期间可点击手柄的早期合并为基于肽的靶向载体的功能化提供了灵活性。一旦将点击手柄定位到理想位置,即可通过2-氰基苯并噻唑(CBT)/ 1,2-氨基硫醇环加成将成像探针与靶向载体偶联。这个关键反应就像“一键式”一样简单。标记反应快速,生物相容,正交且高效。它为肽提供了近乎理想的标记策略,并为开发用于生物医学应用的新型显像剂提供了强大的工具。可以在K.‐T的通讯中找到更多信息。陈等人。在2018年第3期第256页上(DOI:10.1002 / open.201700191)。

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