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使用基于细胞的免疫荧光测定法进行高通量筛选以鉴定甲型流感病毒抑制剂。

High-throughput screening for identification of influenza a inhibitors using a cell-based immunofluorescence assay.

作者信息

Martinez-Gzegozewska Yohanka, Rasmussen Lynn, Nebane N Miranda, McKellip Sara, Radzieta Dee, Manuvakhova Anna, Reece Andrew J, Ruiz Pedro, Zhang Sixue, Moukha-Chafiq Omar, Sosa Melinda, Augelli-Szafran Corinne, Whitley Richard, Bostwick Robert, Vinson Paige

机构信息

Southern Research, Scientific Platforms Division, 2000 9th Ave South, Birmingham, AL 35205, USA.

Southern Research, Scientific Platforms Division, 2000 9th Ave South, Birmingham, AL 35205, USA.

出版信息

Antiviral Res. 2025 Aug;240:106209. doi: 10.1016/j.antiviral.2025.106209. Epub 2025 Jun 6.

Abstract

A highly sensitive cell-based imaging assay has been used to screen a 200,000 compounds library for potential influenza antivirals. Compounds were screened at a concentration of 10 μM against the influenza strain A/Udorn/72 (H3N2) and the duplex capability of the assay was taken advantage of to select compounds with no or low cytotoxicity. The assay was also used for confirmation in concentration-response of the active compounds. In the set of confirmed hits, three major structural clusters, 23 minor clusters and 86 singletons were identified. Further evaluation of anti-influenza activity was performed for two additional influenza strains of the H1N1 subtype, A/WSN/33 and A/California/07/09. Three compounds from cluster A, SRI-44211, SRI-44215 and SRI-44221 showed selectivity indices for the pandemic strain A/California/07/09 in the range of 54.3-252, providing evidence that the core structure of cluster A could play a relevant role in their inhibitory potency and may serve as a starting point for future hit-to-lead optimization efforts.

摘要

一种高度灵敏的基于细胞的成像分析方法已被用于筛选一个包含200,000种化合物的文库,以寻找潜在的抗流感病毒药物。化合物以10 μM的浓度针对流感病毒A/Udorn/72(H3N2)进行筛选,并利用该分析方法的双重能力来选择无细胞毒性或低细胞毒性的化合物。该分析方法还用于对活性化合物进行浓度响应确认。在一组经确认的活性化合物中,鉴定出了三个主要结构簇、23个次要结构簇和86个单一组分。针对另外两种H1N1亚型流感病毒株A/WSN/33和A/California/07/09进一步评估了抗流感活性。来自簇A的三种化合物SRI-44211、SRI-44215和SRI-44221对大流行株A/California/07/09的选择性指数在54.3至252之间,这表明簇A的核心结构可能在其抑制效力中发挥相关作用,并可能作为未来从活性化合物到先导化合物优化工作的起点。

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