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Small Molecule Inhibitors of Middle East Respiratory Syndrome Coronavirus Fusion by Targeting Cavities on Heptad Repeat Trimers

机译:中东呼吸道综合征冠状病毒辅助胚胎呼吸综合征的小分子抑制剂通过靶向孔隙重复三聚体

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Middle East Respiratory Syndrome Coronavirus (MERS-CoV) is a newly emerging viral disease with fatal outcomes. However, no MERS-CoV-specific treatment is commercially available. Given the absence of previous structure-based drug discovery studies targeting MERS-CoV fusion proteins, this set of compounds is considered the first generation of MERS-CoV small molecule fusion inhibitors. After a virtual screening campaign of 1.56 million compounds followed by cell-cell fusion assay and MERS-CoV plaques inhibition assay, three new compounds were identified. Compound numbers 22, 73, and 74 showed IC50 values of 12.6, 21.8, and 11.12 mu M, respectively, and were most effective at the onset of spike-receptor interactions. The compounds exhibited safe profiles against Human embryonic kidney cells 293 at a concentration of 20 mu M with no observed toxicity in Vero cells at 10 mu M. The experimental results are accompanied with predicted favorable pharmacokinetic descriptors and drug-likeness parameters. In conclusion, this study provides the first generation of MERS-CoV fusion inhibitors with potencies in the low micromolar range.
机译:中东呼吸综合征冠状病毒(MERS-COV)是一种新兴的病毒疾病,具有致命的结果。但是,没有MERS-COV特异性处理是可商购的。鉴于靶向MERS-COV融合蛋白的先前结构的药物发现研究,这套化合物被认为是第一代MERS-COV小分子融合剂。在虚拟筛选活动中为156万化合物,然后进行细胞 - 细胞融合测定和MERS-COV斑块抑制测定,鉴定了三种新化合物。化合物数22,73和74分别显示IC 50值为12.6,21.8和11.12μm,并且在穗受体相互作用的发作中最有效。该化合物以20μm的浓度向人胚胎肾细胞293表现出安全的曲线,在10μmm的Vero细胞中没有观察到的毒性。实验结果伴随着预测有利的药代动力学描述符和药物肖像参数。总之,本研究提供了第一代MERS-COV融合抑制剂,具有低微摩尔范围内的抗体。

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