2019
DOI: 10.1016/j.bmcl.2019.08.009
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Novel amides modified rupestonic acid derivatives as anti-influenza virus reagents

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Cited by 6 publications
(4 citation statements)
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“…They had comparable activity as the reference drug ribavirin in inhibiting influenza B virus. Therefore, compound 25 showed the potential to develop new broad-spectrum anti-influenza compounds(see Table 4 [24] ). Compound TC 50 [a] (μg/ mL) Against influenza A Against influenza B IC 50 [b] (μg/ mL) SI [c] IC 50 [b] (μg/ mL) SI [c] - [e] [a]50 % cytotoxic concentration.…”
Section: -Substituted Rupestonic Acid Derivativesmentioning
confidence: 99%
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“…They had comparable activity as the reference drug ribavirin in inhibiting influenza B virus. Therefore, compound 25 showed the potential to develop new broad-spectrum anti-influenza compounds(see Table 4 [24] ). Compound TC 50 [a] (μg/ mL) Against influenza A Against influenza B IC 50 [b] (μg/ mL) SI [c] IC 50 [b] (μg/ mL) SI [c] - [e] [a]50 % cytotoxic concentration.…”
Section: -Substituted Rupestonic Acid Derivativesmentioning
confidence: 99%
“…In 2019, inspired by the primary research and the indispensable role of the acetamido group in anti-influenza drugs, such as oseltamivir, zanamivir, and peramivir, in binding to active pockets, Li et al [24] introduced several amides to the 2position of rupestonic acid. This improved its anti-viral activity against both influenza A and B.…”
Section: -Substituted Rupestonic Acid Derivativesmentioning
confidence: 99%
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