小分子
核糖核酸
化学
细胞生物学
生物化学
计算生物学
组合化学
生物
立体化学
基因
作者
Elia Ravegnini,Andrea Trabocchi,Elena Lenci
标识
DOI:10.1080/13543776.2025.2492759
摘要
The number of patents that has been released in the last few years demonstrates the relevance of targeting RNA structures for the development of next generation chemotherapeutic agents and antiviral/antibacterial drugs, even though this field is still in its infancy and many issues still need to be resolved, in particular related to selectivity. An emerging approach to considerably limiting side effects is presented by RIBOTAC derivatives, as promoting a selective RNase-L mediated RNA degradation allows to significantly reduce the dose of the compound.
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