Stereoselective fluorination is investigated as a method for modulating the properties of a cyclic RGD-containing tetrapeptide. Three key outcomes of fluorination are assessed: (i) the effect on peptide cyclisation efficiency; (ii) the ability to fine-tune the molecular conformation; and (iii) the effect on the cyclic peptides’ biological activity. Fluorination is found to exert pronounced effects against all
研究了立体选择性
氟化作为调节含环状RGD的四肽性质的方法。评估了
氟化的三个关键结果:(i)对肽环化效率的影响;(ii)微调分子构象的能力;(iii)对环肽
生物活性的影响。发现
氟化作用对所有三个标准都具有明显的作用。