A rigid bicyclic analogue of α-L-fucose, prepared from a monoacetonide of L-gulonolactone in an overall yield of 36% without the need for column chromatography, is a potent inhibitor of fucosidases and a weak inhibitor of a fucosyl transferase
The only protection required in a five-step synthesis of the a-L-fucosidase inhibitor, deoxyfuconoji...
Studies on the synthesis of, and specific α-L-fucosidase inhibition by, some 2,6-imino-2,6,7-trideox...
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The stability of a 2,7-anhydroheptulose, readily available from L-gulonolactone, may provide clues t...
Bioisosteric modification of known fucosidase inhibitors A and B, resulted in three new types of mol...
AbstractGlycosidase inhibitors have shown great medicinal and pharmaceutical values as exemplified b...
Deoxyfuconojirimycin (1,5-dideoxy-1,5-imino-L-fucitol) is a potent, specific and competitive inhibit...
The aim of this work was to synthesize stable analogs of GDP-beta-L-fucose as fucosyltransferase inh...
Multi-valent inhibitors offer promise for the enhancement of therapeutic compounds across a range of...
International audienceEnhanced metabolism of fucose through fucosidase overexpression is a signature...
L'objectif de ce travail a été de synthétiser des analogues stables du GDP-béta-L-fucose en tant qu'...
1,5-Dideoxy-1,5-imino-L-fucitol (1), synthesised from methyl α-D-glucopyranoside, is a potent compet...
[[sponsorship]]基因體研究中心[[note]]已出版;[SCI];有審查制度;不具代表性[[note]]http://gateway.isiknowledge.com/gateway/G...
Photobromination of the rigid, aza-bicyclic fucose mimic 3 gave a reactive glycosyl type bromide 7 a...
The only protection required in a five-step synthesis of the α-L-fucosidase inhibitor, deoxyfuconoji...
The only protection required in a five-step synthesis of the a-L-fucosidase inhibitor, deoxyfuconoji...
Studies on the synthesis of, and specific α-L-fucosidase inhibition by, some 2,6-imino-2,6,7-trideox...
[[sponsorship]]基因體研究中心[[note]]已出版;[SCI];有審查制度;不具代表性[[note]]http://gateway.isiknowledge.com/gateway/G...
The stability of a 2,7-anhydroheptulose, readily available from L-gulonolactone, may provide clues t...
Bioisosteric modification of known fucosidase inhibitors A and B, resulted in three new types of mol...
AbstractGlycosidase inhibitors have shown great medicinal and pharmaceutical values as exemplified b...
Deoxyfuconojirimycin (1,5-dideoxy-1,5-imino-L-fucitol) is a potent, specific and competitive inhibit...
The aim of this work was to synthesize stable analogs of GDP-beta-L-fucose as fucosyltransferase inh...
Multi-valent inhibitors offer promise for the enhancement of therapeutic compounds across a range of...
International audienceEnhanced metabolism of fucose through fucosidase overexpression is a signature...
L'objectif de ce travail a été de synthétiser des analogues stables du GDP-béta-L-fucose en tant qu'...
1,5-Dideoxy-1,5-imino-L-fucitol (1), synthesised from methyl α-D-glucopyranoside, is a potent compet...
[[sponsorship]]基因體研究中心[[note]]已出版;[SCI];有審查制度;不具代表性[[note]]http://gateway.isiknowledge.com/gateway/G...
Photobromination of the rigid, aza-bicyclic fucose mimic 3 gave a reactive glycosyl type bromide 7 a...
The only protection required in a five-step synthesis of the α-L-fucosidase inhibitor, deoxyfuconoji...
The only protection required in a five-step synthesis of the a-L-fucosidase inhibitor, deoxyfuconoji...
Studies on the synthesis of, and specific α-L-fucosidase inhibition by, some 2,6-imino-2,6,7-trideox...
[[sponsorship]]基因體研究中心[[note]]已出版;[SCI];有審查制度;不具代表性[[note]]http://gateway.isiknowledge.com/gateway/G...