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Synthetic small-molecule RNA ligands: future prospects as therapeutic agents

机译:合成小分子RNA配体:未来前景作为治疗剂

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摘要

RNA is one of the most intriguing and promising biological targets for the discovery of innovative drugs in many pathologies and various biologically relevant RNAs that could serve as drug targets have already been identified. Among the most important ones, one can mention prokaryotic ribosomal RNA which is the target of several marketed antibiotics, viral RNAs or oncogenic microRNAs that are tightly involved in the development and progression of various cancers. Oligonucleotides are efficient and specific RNA targeting agents but suffer from poor pharmacodynamic and pharmacokinetic properties. For this reason, a number of synthetic small-molecule ligands have been identified and studied upon screening of chemical libraries or focused design of RNA binders. In this review, we report the most relevant examples of synthetic compounds bearing sufficient selectivity to envisage clinical studies and future therapeutic applications with a particular attention for the main strategies that can be undertaken toward the improvement of selectivity and biological activity.
机译:RNA是在许多病理中发现创新药物的最有趣和有前途的生物学目标之一,以及可以作为药物目标的各种生物学相关的RNA。在最重要的中,人们可以提到原核核糖体RNA,其是几种销售抗生素,病毒RNA或致癌细微瘤的靶标,这些抗生素是各种癌症的发育和进展的致癌。寡核苷酸是有效的,特异性的RNA靶向剂,但患有差的药物动力学和药代动力学性质。因此,已经鉴定了许多合成的小分子配体并在筛选化学文库或RNA粘合剂的聚焦设计时研究。在本综述中,我们报告了合成化合物的最相关的实施例,其具有足够的选择性来设想临床研究和未来的治疗应用,特别是可以对改善选择性和生物活性进行的主要策略。

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