Pratesi Alessandro, Ginanneschi Mauro, Lumini Marco, Papini Anna M, Novellino Ettore, Brancaccio Diego, Carotenuto Alfonso
Department of Chemistry "Ugo Schiff," University of Florence Firenze, Italy.
Department of Chemistry "Ugo Schiff," University of FlorenceFirenze, Italy; Interdepartmental Laboratory of Peptide & Protein Chemistry & Biology, University of FlorenceFirenze, Italy.
Front Chem. 2017 Feb 23;5:8. doi: 10.3389/fchem.2017.00008. eCollection 2017.
somatostatin receptor scintigraphy is a valuable method for the visualization of human endocrine tumors and their metastases. In fact, peptide ligands of somatostatin receptors (sst's) conjugated with chelating agents are in clinical use. We have recently developed octreotide dicarba-analogs, which show interesting binding profiles at sst's. In this context, it was mandatory to explore the possibility that our analogs could maintain their activity also upon conjugation with DOTA. In this paper, we report and discuss the synthesis, binding affinity and conformational preferences of three DOTA-conjugated dicarba-analogs of octreotide. Interestingly, two conjugated analogs exhibited nanomolar affinities on sst and sst somatostatin receptor subtypes.
生长抑素受体闪烁扫描术是一种用于可视化人类内分泌肿瘤及其转移灶的重要方法。事实上,与螯合剂结合的生长抑素受体(sst)的肽配体已在临床中使用。我们最近开发了奥曲肽双环类似物,其在sst上显示出有趣的结合谱。在此背景下,有必要探索我们的类似物与DOTA结合后是否也能保持其活性。在本文中,我们报告并讨论了三种DOTA结合的奥曲肽双环类似物的合成、结合亲和力和构象偏好。有趣的是,两种结合的类似物对sst和sst生长抑素受体亚型表现出纳摩尔亲和力。