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50 (nM) sialidase inhibitory and plaque reduction activities of compounds were determined by previously reported methods. {A table is presented}
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23
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65149106044
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note
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Compound 3 and Zanamivir were administered intranasally at doses of. 0.2 μmol/kg 4 h before and 4 h, 17 h after the infection in mice. Compound3 was more effective than Zanamivir (2/10 survived in the 3 treated infected group while there was no survivor in the case of Zanamivir at 20 days after infection).
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note
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{A table is presented}
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27
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65149104495
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note
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Compounds 10a-10c were administered intranasally at doses of 0.3 μmol/kg 4 h before and 4 h, 17 h after the infection in mice. There was no survivor in the 10a, 10b, and 10c-treated infected groups at 20 days after infection.
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28
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65149085492
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note
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Compounds 12d, 12e,12f, and Zanamivir were administered intranasally at doses of 0.3 μmol/kg 4 h before and 4 h, 17 h after the infection in mice. Their efficacies were found to be almost same as that of Zanamivir (there were no survivors in the 12d, 12e, 12f, and Zanamivir-treated infected groups at 9 days after infection).
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