AbstractAnomeric aminobenzylglycosides of Neu5Ac were coupled with the polyacrylate carrier and a number of synthetic polyvalent sialosides obtained were investigated as inhibitors of influenza virus attachment. The inhibitory activity of polymeric sialosides is highly dependent upon the Neu5Ac residue content and the nature of the carrier. The polyacrylic acid based polymer bearing 10 mol% of Neu5Ac is 3 orders of magnitude more potent inhibitor than the corresponding monovalent benzylsialoside and considerably more active than fetuin
Current treatment options for influenza virus infections in humans are limited and therefore the dev...
AbstractThe binding of influenza A virus hemagglutinin to its cell surface receptor, α-linked 5-N-ac...
Several unnatural N-acyl neuraminic acids (N-propionyl, N-hexanoyl, N-benzoyl, N-trifluoroacetyl, N-...
AbstractAnomeric aminobenzylglycosides of Neu5Ac were coupled with the polyacrylate carrier and a nu...
AbstractBackground: Influenza viruses use hemagglutinin (HA) arrays to bind to sialic acid moieties ...
AbstractBackground: Influenza viruses use hemagglutinin (HA) arrays to bind to sialic acid moieties ...
AbstractWe have previously shown that α-2-O-methyl-5-N-thioacetylneuraminic acid (α-Neu5thioAc2Me) h...
AbstractWe have previously shown that α-2-O-methyl-5-N-thioacetylneuraminic acid (α-Neu5thioAc2Me) h...
Inhibition of influenza A virus infection by multivalent sialic acid inhibitors preventing viral hem...
Purpose: New antiviral agents were prepared by attaching derivatives of sialic acid (1) and of th...
Sialic acid-containing oligosaccharides expressed on the respiratory tract epithelial cell surface a...
The work described in this thesis focuses on the development of inhibitors for the Influenza A virus...
Sialic acid-containing oligosaccharides expressed on the respiratory tract epithelial cell surface a...
The work described in this thesis focuses on the development of inhibitors for the Influenza A virus...
Auf der Zelloberfläche modulieren Sialinsäuren Zell-Zell- und Zell-Molekül-Interaktionen. In der end...
Current treatment options for influenza virus infections in humans are limited and therefore the dev...
AbstractThe binding of influenza A virus hemagglutinin to its cell surface receptor, α-linked 5-N-ac...
Several unnatural N-acyl neuraminic acids (N-propionyl, N-hexanoyl, N-benzoyl, N-trifluoroacetyl, N-...
AbstractAnomeric aminobenzylglycosides of Neu5Ac were coupled with the polyacrylate carrier and a nu...
AbstractBackground: Influenza viruses use hemagglutinin (HA) arrays to bind to sialic acid moieties ...
AbstractBackground: Influenza viruses use hemagglutinin (HA) arrays to bind to sialic acid moieties ...
AbstractWe have previously shown that α-2-O-methyl-5-N-thioacetylneuraminic acid (α-Neu5thioAc2Me) h...
AbstractWe have previously shown that α-2-O-methyl-5-N-thioacetylneuraminic acid (α-Neu5thioAc2Me) h...
Inhibition of influenza A virus infection by multivalent sialic acid inhibitors preventing viral hem...
Purpose: New antiviral agents were prepared by attaching derivatives of sialic acid (1) and of th...
Sialic acid-containing oligosaccharides expressed on the respiratory tract epithelial cell surface a...
The work described in this thesis focuses on the development of inhibitors for the Influenza A virus...
Sialic acid-containing oligosaccharides expressed on the respiratory tract epithelial cell surface a...
The work described in this thesis focuses on the development of inhibitors for the Influenza A virus...
Auf der Zelloberfläche modulieren Sialinsäuren Zell-Zell- und Zell-Molekül-Interaktionen. In der end...
Current treatment options for influenza virus infections in humans are limited and therefore the dev...
AbstractThe binding of influenza A virus hemagglutinin to its cell surface receptor, α-linked 5-N-ac...
Several unnatural N-acyl neuraminic acids (N-propionyl, N-hexanoyl, N-benzoyl, N-trifluoroacetyl, N-...