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. 2022 Nov 2;12:18500. doi: 10.1038/s41598-022-22576-4

Table 1.

List of the 44 confirmed hit molecules retrieved from the HTS campaign as potential N-protein ligands.

Compound IC50 (µM) + Error* − Error*
Chebulinic acid 0.2 0.0 0.0
L-Chicoric acid 0.5 0.1 0.1
Punicalagin 0.7 0.1 0.0
Punicalin 0.7 0.1 0.1
Suramin 0.8 0.1 0.1
Tannic acid 1.4 0.2 0.2
Chlorophyllin B 2.2 0.2 0.3
Corilagin 2.4 0.5 0.4
4,5-Dicaffeoylquinic acid 3.0 0.5 0.3
Methyl Blue 4.2 0.3 0.3
Embelin 5.0 0.9 0.7
Linaclotide 5.5 0.6 0.5
Isochlorogenic acid A 5.5 1.0 0.8
Sennoside A 5.7 0.8 0.7
Lusutrombopag 6.0 0.6 0.5
(R)-(-)-Gossypol acetic acid 6.4 0.4 0.4
Idasanutlin 6.5 0.7 0.6
Sulfamerazine 6.5 0.9 0.8
Eltrombopag 7.1 0.9 0.9
Gossypol acetic acid 7.1 0.5 0.4
IOWH-032 7.7 0.9 0.8
Anacardic Acid 7.7 0.9 0.7
Pranlukast (hemihydrate) 7.8 1.1 1.0
Eltrombopag 8.1 1.0 0.9
Succinobucol 8.1 0.6 0.5
RNPA1000 9.6 1.8 1.4
TMC647055 10.0 1.2 1.0
Montelukast 10.3 1.1 1.0
Micafungin 10.4 0.9 0.8
Zafirlukast 10.4 1.6 1.4
Resazurin 10.5 1.7 1.4
Verteporfin 10.8 3.4 2.6
Chlorophyllin A 10.8 1.2 1.0
Surfactin 11.1 1.5 1.3
Pentagalloylglucose 11.6 1.9 1.7
Hexachlorophene 13.0 1.6 1.3
Ertapenem sodium 13.8 1.4 1.3
MK 0893 14.4 1.1 0,9
Butenafine 15.7 1.3 1.2
Oleic acid 15.7 0.9 0.8
Simeprevir 16.5 0.9 0.9
Sofalcone 18.5 1.6 1.5
Bithionol 23.0 5.6 4.6
Gallic acid 23.3 3.3 2.9

Compounds are ranked by their IC50 values for blocking the N protein-RNA1 interaction. Phenyl propanoids with dicaffeoyl motif are highlighted in bold.

*Reported errors are deviation from mean value for upper (+ Error) and lower (− Error) limits of 95% confidence intervals.