Awad Laila Fathy, Ayoup Mohammed Salah
Chemistry Department, Faculty of Science, Alexandria University, P.O. Box 426, Alexandria, 21321, Egypt.
Beilstein J Org Chem. 2020 May 15;16:1022-1050. doi: 10.3762/bjoc.16.91. eCollection 2020.
Recent advances in the chemistry of peptides containing fluorinated phenylalanines (Phe) represents a hot topic in drug research over the last few decades. ᴅ- or ʟ-fluorinated phenylalanines have had considerable industrial and pharmaceutical applications and they have been expanded also to play an important role as potential enzyme inhibitors as well as therapeutic agents and topography imaging of tumor ecosystems using PET. Incorporation of fluorinated aromatic amino acids into proteins increases their catabolic stability especially in therapeutic proteins and peptide-based vaccines. This review seeks to summarize the different synthetic approaches in the literature to prepare ᴅ- or ʟ-fluorinated phenylalanines and their pharmaceutical applications with a focus on published synthetic methods that introduce fluorine into the phenyl, the β-carbon or the α-carbon of ᴅ-or ʟ-phenylalanines.
含氟化苯丙氨酸(Phe)肽类化学的最新进展是过去几十年来药物研究中的一个热门话题。D-或L-氟化苯丙氨酸已在工业和制药领域有相当广泛的应用,并且它们还被扩展用于作为潜在的酶抑制剂、治疗剂以及利用正电子发射断层扫描(PET)对肿瘤生态系统进行拓扑成像。将氟化芳香族氨基酸掺入蛋白质中可提高其分解代谢稳定性,特别是在治疗性蛋白质和基于肽的疫苗中。本综述旨在总结文献中制备D-或L-氟化苯丙氨酸的不同合成方法及其药物应用,重点关注已发表的将氟引入D-或L-苯丙氨酸的苯环、β-碳或α-碳的合成方法。