The first public molecular recognition database, BindingDB supports research, education and practice in drug discovery, pharmacology and related fields.

BindingDB contains 2.8M data for 1.2M Compounds and 9.2K Targets. Of those, 1,346K data for 622K Compounds and 4.5K Targets were curated by BindingDB curators. BindingDB is a FAIRsharing resource.

If BindingDB was of value to your research, please take a moment to donate to this nonprofit project. Your donation will let us provide you with more data and improved service.

Advanced Search

22 articles for thisTarget


The following articles (labelled with PubMed ID or TBD) are for your review

PMID
Data
Article Title
Organization
Synthesis and biological evaluation of N-(2-fluorophenyl)-2ß-deoxyfuconojirimycin acetamide as a potent inhibitor fora-l-fucosidases.EBI
University Of Toyama
Isolation of glycosidase-inhibiting hyacinthacines and related alkaloids from Scilla socialis.EBI
University Of Toyama
Biological properties of D- and L-1-deoxyazasugars.EBI
Toyama Medical And Pharmaceutical University
Homonojirimycin isomers and N-alkylated homonojirimycins: structural and conformational basis of inhibition of glycosidases.EBI
Hokuriku University
Nitrogen-in-the-ring pyranoses and furanoses: structural basis of inhibition of mammalian glycosidases.EBI
Hokuriku University
Convenient synthesis and evaluation of enzyme inhibitory activity of several N-alkyl-, N-phenylalkyl, and cyclic isourea derivatives of 5a-carba-alpha-DL-fucopyranosylamine.EBI
Keio University
New leads for selective inhibitors of alpha-L-fucosidases. Synthesis and glycosidase inhibitory activities of [(2R,3S,4R)-3,4-dihydroxypyrrolidin-2-yl]furan derivatives.EBI
Universidad De Sevilla
 
Synthesis of L-fucopyranosyl-4-thiodisaccharides from levoglucosenone and their inhibitory activity on -L-fucosidaseEBI
TBA
 
Synthesis of and glycosidase inhibition by -l-homofuconojirimycinEBI
TBA
 
Azasugar and glycal inhibitors of -L-fucosidaseEBI
TBA
 
Synthesis of a new inhibitor of α-fucosidaseEBI
TBA
 
p-Nitrophenyl 1,5-dithio-alpha-L-fucopyranoside: a novel sulfur based fucosidase inhibitorEBI
TBA
 
Synthesis of C2-symmetrical polyhydroxyazepanes as inhibitors of glycosidasesEBI
TBA
Synthesis and biological evaluation of glycosidase inhibitors: gem-difluoromethylenated nojirimycin analogues.EBI
Chinese Academy Of Sciences
Fluorescent glycosidase inhibiting 1,5-dideoxy-1,5-iminoalditols.EBI
Technische UniversitäT Graz
Synthesis and glycosidase inhibitory activity of some N-substituted 6-deoxy-5a-carba-beta-DL- and L-galactopyranosylamines.EBI
Keio University
Synthesis of [(2S,3S,4R)-3,4-dihydroxypyrrolidin-2-yl]-5-methylfuran-4-carboxylic acid derivatives: new leads as selective beta-galactosidase inhibitors.EBI
Universidad De Sevilla
Synthesis of an alpha-fucosidase inhibitor, 5a-carba-beta-L-fucopyranosylamine, and fucose-type alpha- and beta-DL-valienamine unsaturated derivatives.EBI
Keio University
Revised structure of a homonojirimycin isomer from Aglaonema treubii: first example of a naturally occurring alpha-homoallonojirimycin.EBI
Institut De Chimie Organique Et Analytique (I.C.O.A.)
Chemoenzymatic synthesis of iminocyclitol derivatives: a useful library strategy for the development of selective fucosyltransfer enzymes inhibitors.EBI
Scripps Research Institute
Thio-sugars. IV: Design and synthesis of S-linked fucoside analogs as a new class of alpha-L-fucosidase inhibitors.EBI
University Of Connecticut
BW 723C86, a 5-HT2B receptor agonist, causes hyperphagia and reduced grooming in rats.BDB
Smithkline Beecham Pharmaceuticals