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Synthesis of Esterase‐resistant 9‐O‐Acetylated Polysialoside as Inhibitor of Influenza C Virus Hemagglutinin

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This article is published in Angewandte Chemie.The article was published on 1992-11-01. It has received 76 citations till now. The article focuses on the topics: Orthomyxoviridae & Influenza C Virus.

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Chitosan chemistry and pharmaceutical perspectives.

TL;DR: Department of Pharmaceutics, National Institute of Pharmaceutical Education and Research (NIPER), Sector 67, S. S. Nagar, Punjab-160 062, India, Institute of Biochemistry, Faculty of Medicine, Polytechnic University, Via Ranieri 67, IT-60100 Ancona, Italy, and Department of Medicinal Chemistry & Natural Products,The Hebrew University of Jerusalem, School of Pharmacy-Faculty of medicine, Jerusalem 91120, Israel.
Journal ArticleDOI

Chemically modified chitin and chitosan as biomaterials

TL;DR: The modifications discussed here include chitosan attached to sugars, dendrimers, cyclodextrins, crown ethers, and glass beads, which are excellent candidates for drug delivery systems or cell culture owing to their specificity.
Journal ArticleDOI

Strength in numbers: non-natural polyvalent carbohydrate derivatives

TL;DR: New structural templates for the generation of multivalent carbohydrate displays have recently been developed, and tailored multivalent saccharide derivatives can now be used to study and modulate a wide variety of biological recognition events.
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Solid-phase synthesis of dendritic sialoside inhibitors of influenza A virus haemagglutinin

TL;DR: Efficient solid-phase synthesis of dendritic α-thiosialoside inhibitors of influenza A virus haemagglutinin are described using hyperbranched L-lysine core structures.
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