Laboratorio de Biotecnología Farmacéutica, Dept. of Biotechnologia Farmaceutica, Centro de Biotecnología Genómica, Instituto Politécnico Nacional, 88710 Reynosa, México.
Mini Rev Med Chem. 2024;24(22):1972-1982. doi: 10.2174/0113895575301735240607055839.
Chikungunya is a re-emerging viral infection of worldwide concern, and new antiviral therapeutics are necessary to combat this disease. Inhibitors of the non-structural protein 1 (NsP1), which shows Methyltransferase (MTase) activity and plays a crucial in the Chikungunya virus (ChikV) replication, are exhibiting promising results. This review aimed to describe recent advances in the development of NsP1 inhibitors for the treatment of Chikungunya disease. High-throughput screening of novel ChikV NsP1 inhibitors has been widely performed for the identification of new molecule hits through fluorescence polarization, Western blotting, ELISA-based assay, and capillary electrophoresis assays. Additionally, cell-based assays confirmed that the inhibition of ChikV NsP1 abolishes viral replication. In summary, pyrimidine and pyrimidin-7(6H)-one derivatives, GTP and nucleoside analogs have been demonstrated to show inhibitory activity and are considered promising scaffolds that provide useful knowledge for the research and development of new NsP1 inhibitors as potential treatment of Chikungunya re-emerging disease.
基孔肯雅热是一种具有全球关注度的重新出现的病毒性感染,需要新的抗病毒疗法来对抗这种疾病。非结构蛋白 1(NsP1)抑制剂具有甲基转移酶(MTase)活性,在基孔肯雅病毒(ChikV)复制中发挥关键作用,显示出有希望的结果。本综述旨在描述 NsP1 抑制剂在治疗基孔肯雅病方面的最新进展。已经广泛进行了新型 ChikV NsP1 抑制剂的高通量筛选,以通过荧光偏振、Western blot、基于 ELISA 的测定和毛细管电泳测定来鉴定新的分子命中。此外,细胞测定证实抑制 ChikV NsP1 可消除病毒复制。总之,嘧啶和嘧啶-7(6H)-酮衍生物、GTP 和核苷类似物已被证明具有抑制活性,被认为是有前途的支架,为研究和开发新的 NsP1 抑制剂作为基孔肯雅热新兴疾病的潜在治疗方法提供了有用的知识。