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| Cat. No. : | HY-117503 |
| M.Wt: | 314.45 |
| Formula: | C18H22N2OS |
| Purity: | >98 % |
| Solubility: |
M2WJ332 is an inhibitor of the M2 proton channel of the influenza A virus M2S31N mutant M2. M2WJ332 potently inhibits the influenza A virus A/M2-S31N proton channel in Xenopus laevis oocytes, with an IC50 of 16 μM. M2WJ332 completely inhibits plaque formation by the influenza A virus carrying the M2S31N mutant. M2WJ332 is applicable to research related to influenza A virus infection[1][2].
In Vitro:M2WJ332 (Compound 11) (100 μM; 2 min) potently inhibits the activity of the AM2-S31N proton channel in Xenopus laevis oocytes, while exerts extremely weak inhibitory effect on the activity of AM2-WT[1].
M2WJ332 potently inhibits the replication of AM2-S31N-containing influenza A virus A/California/07/2009 (H1N1) in MDCK cells expressing ST6Gal I, with an EC50 of 0.3 μM[1].
M2WJ332 (48 h) exhibits cytotoxicity against MDCK cells with a CC50 of 100 μM, and shows a CC50 of 177.5 μM against A549 cells[1].
M2WJ332 potently inhibits the replication of amantadine (HY-B0402)-resistant influenza A virus strain A/WSN/33 in MDCK cells, with an EC50 of 153 nM, and completely suppresses plaque formation at 10 μM[2].
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