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Volumn 19, Issue 11, 2009, Pages 2938-2940

Synthesis and in vivo influenza virus-inhibitory effect of ester prodrug of 4-guanidino-7-O-methyl-Neu5Ac2en

Author keywords

CS 8958; Ester prodrug; Influenza; Long acting NA inhibitor; Zanamivir

Indexed keywords

ANTIVIRUS AGENT; CARBOXYLIC ACID; CS 8958; ESTER DERIVATIVE; SIALIDASE INHIBITOR; UNCLASSIFIED DRUG; ZANAMIVIR;

EID: 65149099661     PISSN: 0960894X     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.bmcl.2009.04.067     Document Type: Article
Times cited : (44)

References (29)
  • 4
    • 65149097746 scopus 로고    scopus 로고
    • Babu, Y.S.; Chand, P.; Montgomery, J.A. PCT Int. Appl., WO9747194.
    • Babu, Y.S.; Chand, P.; Montgomery, J.A. PCT Int. Appl., WO9747194.
  • 6
    • 65149087738 scopus 로고    scopus 로고
    • Maring, C. J; Giranda, V.L.; Kempf, D.J.; Stoll, V.S.; Sun, M.; Zhao, C; Gu, Y.C.; Hanessian, S.; Wang, G.T. PCT Int. Appl., WO0128996.
    • Maring, C. J; Giranda, V.L.; Kempf, D.J.; Stoll, V.S.; Sun, M.; Zhao, C; Gu, Y.C.; Hanessian, S.; Wang, G.T. PCT Int. Appl., WO0128996.
  • 22
    • 65149099974 scopus 로고    scopus 로고
    • note
    • 50 (nM) sialidase inhibitory and plaque reduction activities of compounds were determined by previously reported methods. {A table is presented}
  • 23
    • 65149106044 scopus 로고    scopus 로고
    • note
    • 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).
  • 26
    • 65149100865 scopus 로고    scopus 로고
    • note
    • {A table is presented}
  • 27
    • 65149104495 scopus 로고    scopus 로고
    • note
    • 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.
  • 28
    • 65149085492 scopus 로고    scopus 로고
    • note
    • 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).


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.