High-Affinity "Click" RGD Peptidomimetics as Radiolabeled Probes for Imaging alpha(v)beta(3) Integrin

作者：Piras Monica^*; Testa Andrea; Fleming Ian N; Dall'Angelo Sergio; Andriu Alexandra; Menta Sergio; Mori Mattia; Brown Gavin D; Forster Duncan; Williams Kaye J; Zanda Matteo^*

来源：ChemMedChem, 2017, 12(14): 1142-1151.

DOI：10.1002/cmdc.201700328

• angiogenesis
• click chemistry
• peptidomimetics
• PET imaging
• RGD

Nonpeptidic Arg-Gly-Asp (RGD)-mimic ligands were designed and synthesized by click chemistry between an arginine-azide mimic and an aspartic acid-alkyne mimic. Some of these molecules combine excellent in vitro properties (high alpha(v)beta(3) affinity, selectivity, drug-like logD, high metabolic stability) with a variety of radiolabeling options (e.g., tritium and fluorine-18, plus compatibility with radio-iodination), not requiring the use of chelators or prosthetic groups. The binding mode of the resulting triazole RGD mimics to alpha(v)beta(3) or beta(11b)beta(3) receptors was investigated by molecular modeling simulations. Lead compound 12 was successfully radiofluorinated and used for in vivo positron emission tomography/computed tomography (PET/CT) studies in U87 tumor models, which showed only modest tumor uptake and retention, owing to rapid excretion. These results demonstrate that the novel click RGD mimics are excellent radiolabeled probes for in vitro and cell-based studies on alpha(v)beta(3) integrin, whereas further optimization of their pharmacokinetic and dynamic profiles is necessary for successful use in in vivo imaging.

• 出版日期2017-7-20
• 单位河北医科大学