Syntheses of C??3??Modified Sialylglycosides as Selective Inhibitors of Influenza Hemagglutinin and Neuraminidase

…, Y Kanie, CT Guo, O Kanie, Y Suzuki…

Index: Sun, Xue-Long; Kanie, Yoshimi; Guo, Chao-Tan; Kanie, Osamu; Suzuki, Yasuo; Wong, Chi-Huey European Journal of Organic Chemistry, 2000 , # 14 p. 2643 - 2653

Full Text: HTML

Citation Number: 45

Abstract

Abstract In an effort to develop new structures as inhibitors of both influenza virus proteins hemagglutinin and neuraminidase, a series of sialic acid derivatives, including those with one of the hydrogen atoms at the C-3 position replaced by either OH or F, were ...

Related Articles:

… acid, 2-methyl-6-(5-acetamido-3, 5-dideoxy-α-d-glycero-d-galacto-nonulopyranosyl-onic acid) xanthene-9-spiro-1′-isobenzofuran-3′-one, a new substrate for …

[Rothermel, Joerg; Faillard, Hans Carbohydrate Research, 1990 , vol. 196, # 1 p. 29 - 40]

… acid, 2-methyl-6-(5-acetamido-3, 5-dideoxy-α-d-glycero-d-galacto-nonulopyranosyl-onic acid) xanthene-9-spiro-1′-isobenzofuran-3′-one, a new substrate for …

[Rothermel, Joerg; Faillard, Hans Carbohydrate Research, 1990 , vol. 196, # 1 p. 29 - 40]

More Articles...