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

被引:0
作者
Martinez-Gzegozewska, Yohanka [1 ]
Rasmussen, Lynn [1 ]
Nebane, N. Miranda [1 ]
McKellip, Sara [1 ]
Radzieta, Dee [1 ]
Manuvakhova, Anna [1 ]
Reece, Andrew J. [1 ]
Ruiz, Pedro [1 ]
Zhang, Sixue [2 ]
Moukha-Chafiq, Omar [1 ]
Sosa, Melinda [1 ]
Augelli-Szafran, Corinne [1 ]
Whitley, Richard [2 ]
Bostwick, Robert [1 ]
Vinson, Paige [1 ]
机构
[1] Southern Res, Sci Platforms Div, 2000 9th Ave South, Birmingham, AL 35205 USA
[2] Univ Alabama Birmingham, 1720 2nd Ave South, Birmingham, AL 35294 USA
关键词
Influenza; High-throughput; Immunofluorescence; Cell-based; Duplex; Cluster; INTERFERENCE COMPOUNDS PAINS; IN-VITRO; DISCOVERY; VIRUSES;
D O I
10.1016/j.antiviral.2025.106209
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
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 mu M 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 SRI44221 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.
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页数:9
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