Neoglycoconjugates based on cyclodextrins and calixarenes.
about
Multivalent glycoconjugates as anti-pathogenic agentsCharacteristics of protein-carbohydrate interactions as a basis for developing novel carbohydrate-based antirejection therapies.Self-assembled multivalent carbohydrate ligands.Application of click-click chemistry to the synthesis of new multivalent RGD conjugates.Cyclodextrin-based gene delivery systems.Multivalency in heterogeneous glycoenvironments: hetero-glycoclusters, -glycopolymers and -glycoassemblies.Biological applications of functionalized calixarenes.Cyclodextrin-based multivalent glycodisplays: covalent and supramolecular conjugates to assess carbohydrate-protein interactions.The third dimension of reading the sugar code by lectins: design of glycoclusters with cyclic scaffolds as tools with the aim to define correlations between spatial presentation and activity.Glyconanosynthons as powerful scaffolds and building blocks for the rapid construction of multifaceted, dense and chiral dendrimers.Cyclic neoglycodecapeptides: how to increase their inhibitory activity and selectivity on lectin/toxin binding to a glycoprotein and cells.Click multivalent neoglycoconjugates as synthetic activators in cell adhesion and stimulation of monocyte/machrophage cell lines.Icosahedral virus particles as polyvalent carbohydrate display platforms.Thiourea-linked upper rim calix[4]arene neoglycoconjugates: synthesis, conformations and binding properties.Functional evaluation of carbohydrate-centred glycoclusters by enzyme-linked lectin assay: ligands for concanavalin A.Multivalent binding of galactosylated cyclodextrin vesicles to lectin.Heptyl α-D-mannosides grafted on a β-cyclodextrin core to interfere with Escherichia coli adhesion: an in vivo multivalent effect.A new generation of carbohydrate-based therapeutics: recombinant mucin-type fusion proteins as versatile inhibitors of protein-carbohydrate interactions.Combining carbohydrate substitutions at bioinspired positions with multivalent presentation towards optimising lectin inhibitors: case study with calixarenes.Synthesis and conformational studies of chiral macrocyclic [1.1.1]metacyclophanes containing benzofuran rings.Glycodendritic structures: tools to interact with DC-SIGNDendri-RAFTs: a second generation of cyclopeptide-based glycoclusters
P2860
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P2860
Neoglycoconjugates based on cyclodextrins and calixarenes.
description
2001 nî lūn-bûn
@nan
2001 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած
@hyw
2001 թվականի սեպտեմբերին հրատարակված գիտական հոդված
@hy
2001年の論文
@ja
2001年論文
@yue
2001年論文
@zh-hant
2001年論文
@zh-hk
2001年論文
@zh-mo
2001年論文
@zh-tw
2001年论文
@wuu
name
Neoglycoconjugates based on cyclodextrins and calixarenes.
@ast
Neoglycoconjugates based on cyclodextrins and calixarenes.
@en
Neoglycoconjugates based on cyclodextrins and calixarenes.
@nl
type
label
Neoglycoconjugates based on cyclodextrins and calixarenes.
@ast
Neoglycoconjugates based on cyclodextrins and calixarenes.
@en
Neoglycoconjugates based on cyclodextrins and calixarenes.
@nl
prefLabel
Neoglycoconjugates based on cyclodextrins and calixarenes.
@ast
Neoglycoconjugates based on cyclodextrins and calixarenes.
@en
Neoglycoconjugates based on cyclodextrins and calixarenes.
@nl
P356
P1476
Neoglycoconjugates based on cyclodextrins and calixarenes
@en
P2093
J F Stoddart
P304
P356
10.1021/BC0100410
P577
2001-09-01T00:00:00Z