BDBM50166886 CHEMBL195368::methyl alpha-D-mannoside

SMILES CO[C@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@@H]1O

InChI Key InChIKey=HOVAGTYPODGVJG-VEIUFWFVSA-N

Data  6 IC50

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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 6 hits for monomerid = 50166886   

TargetConcanavalin-A(Canavalia ensiformis)
Georgia Southern University

Curated by ChEMBL
LigandPNGBDBM50166886(CHEMBL195368 | methyl alpha-D-mannoside)
Show SMILES CO[C@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@@H]1O
Show InChI InChI=1S/C7H14O6/c1-12-7-6(11)5(10)4(9)3(2-8)13-7/h3-11H,2H2,1H3/t3-,4-,5+,6+,7+/m1/s1
Affinity DataIC50: 3.50E+5nMAssay Description:Inhibition of Canavalia ensiformis concanavalin A binding to yeast mannan by ELLAMore data for this Ligand-Target Pair
TargetType 1 fimbrin D-mannose specific adhesin(Escherichia coli (strain K12))
University of Basel

Curated by ChEMBL
LigandPNGBDBM50166886(CHEMBL195368 | methyl alpha-D-mannoside)
Show SMILES CO[C@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@@H]1O
Show InChI InChI=1S/C7H14O6/c1-12-7-6(11)5(10)4(9)3(2-8)13-7/h3-11H,2H2,1H3/t3-,4-,5+,6+,7+/m1/s1
Affinity DataIC50: 1.90E+3nMAssay Description:Antagonist activity at Escherichia coli recombinant C-terminal 6His-tagged FimH-CRD with a C-terminal thrombin cleavage site expressed in Escherichia...More data for this Ligand-Target Pair
TargetC-type lectin domain family 4 member M(Homo sapiens)
Universit£ de Picardie Jules Verne

Curated by ChEMBL
LigandPNGBDBM50166886(CHEMBL195368 | methyl alpha-D-mannoside)
Show SMILES CO[C@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@@H]1O
Show InChI InChI=1S/C7H14O6/c1-12-7-6(11)5(10)4(9)3(2-8)13-7/h3-11H,2H2,1H3/t3-,4-,5+,6+,7+/m1/s1
Affinity DataIC50: 1.30nMAssay Description:Inhibition of DC-SIGN (unknown origin) expressed in human Jurkat cells assessed as inhibition of EBOV-pseudotyped virus infection measured after 48 h...More data for this Ligand-Target Pair
TargetFucose-binding lectin PA-IIL(Pseudomonas aeruginosa)
Helmholtz Institute for Pharmaceutical Research Saarland (HIPS)

Curated by ChEMBL
LigandPNGBDBM50166886(CHEMBL195368 | methyl alpha-D-mannoside)
Show SMILES CO[C@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@@H]1O
Show InChI InChI=1S/C7H14O6/c1-12-7-6(11)5(10)4(9)3(2-8)13-7/h3-11H,2H2,1H3/t3-,4-,5+,6+,7+/m1/s1
Affinity DataIC50: 3.70E+4nMAssay Description:Competitive inhibition of N-(fluorescein-5-yl)-N'-(alpha-L-fucopyranosyl ethylen)-thiocarbamide binding to Pseudomonas aeruginosa PA14 LecB after 8 t...More data for this Ligand-Target Pair
TargetFucose-binding lectin PA-IIL(Pseudomonas aeruginosa)
Helmholtz Institute for Pharmaceutical Research Saarland (HIPS)

Curated by ChEMBL
LigandPNGBDBM50166886(CHEMBL195368 | methyl alpha-D-mannoside)
Show SMILES CO[C@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@@H]1O
Show InChI InChI=1S/C7H14O6/c1-12-7-6(11)5(10)4(9)3(2-8)13-7/h3-11H,2H2,1H3/t3-,4-,5+,6+,7+/m1/s1
Affinity DataIC50: 1.57E+5nMAssay Description:Inhibition of Pseudomonas aeruginosa LecB by fluorescence polarization assayMore data for this Ligand-Target Pair
TargetFucose-binding lectin PA-IIL(Pseudomonas aeruginosa)
Helmholtz Institute for Pharmaceutical Research Saarland (HIPS)

Curated by ChEMBL
LigandPNGBDBM50166886(CHEMBL195368 | methyl alpha-D-mannoside)
Show SMILES CO[C@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@@H]1O
Show InChI InChI=1S/C7H14O6/c1-12-7-6(11)5(10)4(9)3(2-8)13-7/h3-11H,2H2,1H3/t3-,4-,5+,6+,7+/m1/s1
Affinity DataIC50: 1.57E+5nMAssay Description:Inhibition of Pseudomonas aeruginosa PAO1 LecB after 6 hrs by fluorescence polarization assayMore data for this Ligand-Target Pair