Bartolucci Silvia, Retini Michele, Fanini Fabiola, Paderni Daniele, Piersanti Giovanni
Department of Biomolecular Sciences, University of Urbino Carlo Bo, Piazza del Rinascimento 6, 61029 Urbino, Pesaro and Urbino, Italy.
Department of Pure and Applied Sciences, University of Urbino Carlo Bo, Via della Stazione 4, 61029 Urbino, Pesaro and Urbino, Italy.
ACS Omega. 2023 Jun 8;8(24):22190-22194. doi: 10.1021/acsomega.3c02518. eCollection 2023 Jun 20.
Fluorescent ligands are imperative to many facets of chemical biology and medicinal chemistry. Herein, we report the syntheses of two fluorescent melatonin-based derivatives as potential ligands of melatonin receptors. The two compounds, namely, 4-cyano and 4-formyl melatonin (4CN-MLT and 4CHO-MLT, respectively), which differ from melatonin by only two/three atoms that are very compact in size, were prepared using the selective C3-alkylation of indoles with -acetyl ethanolamines involving the "borrowing hydrogen" strategy. These compounds exhibit absorption/emission spectra that are red-shifted from those of melatonin. Binding studies on two melatonin receptor subtypes showed that these derivatives have a modest affinity and selectivity ratio.
荧光配体对化学生物学和药物化学的许多方面都至关重要。在此,我们报告了两种基于褪黑素的荧光衍生物的合成,它们作为褪黑素受体的潜在配体。这两种化合物,即4-氰基和4-甲酰基褪黑素(分别为4CN-MLT和4CHO-MLT),与褪黑素仅相差两/三个原子,且这些原子体积非常紧凑,是通过吲哚与α-乙酰乙醇胺的选择性C3-烷基化反应,采用“借氢”策略制备的。这些化合物的吸收/发射光谱相对于褪黑素发生了红移。对两种褪黑素受体亚型的结合研究表明,这些衍生物具有适度的亲和力和选择性比率。