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Compile Data Set for Download or QSAR

Marvin 2D Structure

The following similar (0.9) ligands are found in BindingDB

Wt: 180.1 sim=1.00
BDBM34103
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Wt: 180.1 sim=1.00
BDBM50077229
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Wt: 180.1 sim=1.00
BDBM50102882
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Wt: 180.1 sim=1.00
BDBM50147883
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Wt: 210.1 sim=0.96
BDBM50147907
Wt: 292.3 sim=0.86
BDBM50179091
Wt: 306.3 sim=0.86
BDBM50179094
Wt: 432.6 sim=0.86
BDBM50179096
Wt: 180.1 sim=1.00
BDBM50240803
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Wt: 164.1 sim=0.97
BDBM50242419
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Wt: 180.1 sim=1.00
BDBM50351158
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Wt: 210.1 sim=0.96
BDBM50422217
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Wt: 180.1 sim=1.00
BDBM50423644
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Wt: 180.1 sim=1.00
BDBM50448403
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Wt: 180.1 sim=1.00
BDBM228805
Displayed 1 to 15 (of 27 total )  |  Next  |  Last  >>

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB (change energy unit to kcal/mol)

Found 32 hits in this display   
Target
(Institution)
LigandTarget
Links
Ligand
Links
Trg + Lig
Links
Ki
nM
ΔG°
kJ/mole
IC50
nM
Kd
nM
EC50/IC50
nM
koff
s-1
kon
M-1s-1
pHTemp
°C
Hexose transporter 1


(Plasmodium falciparum)
BDBM50179091
PNG
((3R,4S,5R,6R)-6-(hydroxymethyl)-4-(octyloxy)-tetra...)
Show SMILES CCCCCCCCO[C@@H]1[C@@H](O)C(O)O[C@H](CO)[C@H]1O
Show InChI InChI=1S/C14H28O6/c1-2-3-4-5-6-7-8-19-13-11(16)10(9-15)20-14(18)12(13)17/h10-18H,2-9H2,1H3/t10-,11-,12-,13+,14?/m1/s1
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PubMed
3.00E+4n/an/an/an/an/an/an/an/a



Université Joseph Fourier Grenoble 1

Curated by ChEMBL


Assay Description
Inhibition of D-glucose uptake mediated by PfHT expressed in Xenopus oocytes


Bioorg Med Chem Lett 16: 1267-71 (2006)

More data for this
Ligand-Target Pair
Hexose transporter 1


(Plasmodium falciparum)
BDBM50179094
PNG
((3R,4S,5R,6R)-6-(hydroxymethyl)-4-(nonyloxy)-tetra...)
Show SMILES CCCCCCCCCO[C@@H]1[C@@H](O)C(O)O[C@H](CO)[C@H]1O
Show InChI InChI=1S/C15H30O6/c1-2-3-4-5-6-7-8-9-20-14-12(17)11(10-16)21-15(19)13(14)18/h11-19H,2-10H2,1H3/t11-,12-,13-,14+,15?/m1/s1
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3.20E+4n/an/an/an/an/an/an/an/a



Université Joseph Fourier Grenoble 1

Curated by ChEMBL


Assay Description
Inhibition of D-glucose uptake mediated by PfHT expressed in Xenopus oocytes


Bioorg Med Chem Lett 16: 1267-71 (2006)

More data for this
Ligand-Target Pair
Alpha-L-fucosidase I


(Homo sapiens)
BDBM50242419
PNG
(6-Deoxy-L-galactose | 6-deoxy-L-galactopyranoseL-f...)
Show SMILES C[C@@H]1OC(O)[C@@H](O)[C@H](O)[C@@H]1O
Show InChI InChI=1S/C6H12O5/c1-2-3(7)4(8)5(9)6(10)11-2/h2-10H,1H3/t2-,3+,4+,5-,6?/m0/s1
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3.00E+5n/an/an/an/an/an/an/an/a


TBA

Assay Description
Inhibition constant against Alpha-Fucosidase


Citation and Details
More data for this
Ligand-Target Pair
Alpha-L-fucosidase I


(Homo sapiens)
BDBM50242419
PNG
(6-Deoxy-L-galactose | 6-deoxy-L-galactopyranoseL-f...)
Show SMILES C[C@@H]1OC(O)[C@@H](O)[C@H](O)[C@@H]1O
Show InChI InChI=1S/C6H12O5/c1-2-3(7)4(8)5(9)6(10)11-2/h2-10H,1H3/t2-,3+,4+,5-,6?/m0/s1
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3.00E+5n/an/an/an/an/an/an/an/a


TBA

Assay Description
Compound was tested for inhibitory activity (competitive) against alpha-L-fucosidase from bovine kidney


Citation and Details
More data for this
Ligand-Target Pair
Hexose transporter 1


(Plasmodium falciparum)
BDBM50179096
PNG
((3R,4S,5R,6R)-6-(hydroxymethyl)-4-(octadecyloxy)-t...)
Show SMILES CCCCCCCCCCCCCCCCCCO[C@@H]1[C@@H](O)C(O)O[C@H](CO)[C@H]1O
Show InChI InChI=1S/C24H48O6/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-29-23-21(26)20(19-25)30-24(28)22(23)27/h20-28H,2-19H2,1H3/t20-,21-,22-,23+,24?/m1/s1
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>5.00E+5n/an/an/an/an/an/an/an/a



Université Joseph Fourier Grenoble 1

Curated by ChEMBL


Assay Description
Inhibition of D-glucose uptake mediated by PfHT expressed in Xenopus oocytes


Bioorg Med Chem Lett 16: 1267-71 (2006)

More data for this
Ligand-Target Pair
Muscle glycogen phosphorylase


(Homo sapiens)
BDBM34103
PNG
(D-glucose | dextrose | glucose)
Show SMILES OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O
Show InChI InChI=1S/C6H12O6/c7-1-2-3(8)4(9)5(10)6(11)12-2/h2-11H,1H2/t2-,3-,4+,5-,6?/m1/s1
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PubMed
1.70E+6n/an/an/an/an/an/an/an/a



University of Alcala

Curated by ChEMBL


Assay Description
Inhibitory activity against rabbit muscle glycogen phosphorylase


J Med Chem 40: 4089-102 (1998)

Checked by Author
More data for this
Ligand-Target Pair
Glycogen phosphorylase, muscle form


(Oryctolagus cuniculus (rabbit))
BDBM50351158
PNG
(CHEMBL423707)
Show SMILES OC[C@H]1O[C@H](O)[C@H](O)[C@@H](O)[C@@H]1O
Show InChI InChI=1S/C6H12O6/c7-1-2-3(8)4(9)5(10)6(11)12-2/h2-11H,1H2/t2-,3-,4+,5-,6+/m1/s1
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1.70E+6n/an/an/an/an/an/an/an/a



National Hellenic Research Foundation

Curated by ChEMBL


Assay Description
Competitive inhibition of rabbit muscle glycogen phosphorylase b assessed as inorganic phosphate release using alphaD glucose-1-phosphate as substrat...


Bioorg Med Chem 19: 5125-36 (2011)

More data for this
Ligand-Target Pair
3D
3D Structure (docked)
Brain glycogen phosphorylase


(Homo sapiens)
BDBM50102882
PNG
(6-Hydroxymethyl-tetrahydro-pyran-2,3,4,5-tetraol |...)
Show SMILES OCC1O[C@H](O)C(O)[C@@H](O)[C@@H]1O
Show InChI InChI=1S/C6H12O6/c7-1-2-3(8)4(9)5(10)6(11)12-2/h2-11H,1H2/t2?,3-,4+,5?,6+/m1/s1
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PubMed
1.70E+6n/an/an/an/an/an/an/an/a



University of Debrecen

Curated by ChEMBL


Assay Description
Inhibitory activity against muscle Glycogen Phosphorylase b


J Med Chem 44: 2843-8 (2001)

More data for this
Ligand-Target Pair
Muscle glycogen phosphorylase


(Homo sapiens)
BDBM50351158
PNG
(CHEMBL423707)
Show SMILES OC[C@H]1O[C@H](O)[C@H](O)[C@@H](O)[C@@H]1O
Show InChI InChI=1S/C6H12O6/c7-1-2-3(8)4(9)5(10)6(11)12-2/h2-11H,1H2/t2-,3-,4+,5-,6+/m1/s1
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1.70E+6n/an/an/an/an/an/an/an/a



University of Thessaly

Curated by ChEMBL


Assay Description
Inhibition of glycogen phosphorylase b (unknown origin)


Bioorg Med Chem 22: 4810-25 (2014)

More data for this
Ligand-Target Pair
Glycogen phosphorylase, muscle form


(Oryctolagus cuniculus (rabbit))
BDBM50351158
PNG
(CHEMBL423707)
Show SMILES OC[C@H]1O[C@H](O)[C@H](O)[C@@H](O)[C@@H]1O
Show InChI InChI=1S/C6H12O6/c7-1-2-3(8)4(9)5(10)6(11)12-2/h2-11H,1H2/t2-,3-,4+,5-,6+/m1/s1
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1.70E+6n/an/an/an/an/an/an/an/a



National Hellenic Research Foundation

Curated by ChEMBL


Assay Description
Inhibition of rabbit muscle glycogen phosphorylase inactive form b


Bioorg Med Chem 18: 3413-25 (2010)

More data for this
Ligand-Target Pair
3D
3D Structure (docked)
Brain glycogen phosphorylase


(Homo sapiens)
BDBM34103
PNG
(D-glucose | dextrose | glucose)
Show SMILES OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O
Show InChI InChI=1S/C6H12O6/c7-1-2-3(8)4(9)5(10)6(11)12-2/h2-11H,1H2/t2-,3-,4+,5-,6?/m1/s1
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PubMed
1.70E+6n/an/an/an/an/an/an/an/a



University of Perugia

Curated by ChEMBL


Assay Description
Inhibition of rabbit glycogen phosphorylase B enzyme


J Med Chem 40: 1455-64 (1997)

More data for this
Ligand-Target Pair
Brain glycogen phosphorylase


(Homo sapiens)
BDBM50147883
PNG
((S)-6-Hydroxymethyl-tetrahydro-pyran-2,3,4,5-tetra...)
Show SMILES OCC1O[C@H](O)C(O)C(O)C1O
Show InChI InChI=1S/C6H12O6/c7-1-2-3(8)4(9)5(10)6(11)12-2/h2-11H,1H2/t2?,3?,4?,5?,6-/m0/s1
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1.70E+6n/an/an/an/an/an/an/an/a



The University of Illinois at Chicago

Curated by ChEMBL


Assay Description
Inhibitory binding constant against glycogen phosphorylase B


J Med Chem 47: 3075-88 (2004)

More data for this
Ligand-Target Pair
Glycogen phosphorylase, muscle form


(Oryctolagus cuniculus (rabbit))
BDBM50351158
PNG
(CHEMBL423707)
Show SMILES OC[C@H]1O[C@H](O)[C@H](O)[C@@H](O)[C@@H]1O
Show InChI InChI=1S/C6H12O6/c7-1-2-3(8)4(9)5(10)6(11)12-2/h2-11H,1H2/t2-,3-,4+,5-,6+/m1/s1
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1.70E+6n/an/an/an/an/an/an/an/a



University of Thessaly

Curated by ChEMBL


Assay Description
Competitive inhibition of rabbit skeletal muscle glycogen phosphorylase b using Glc-1-P as substrate


Eur J Med Chem 54: 740-9 (2012)

More data for this
Ligand-Target Pair
3D
3D Structure (docked)
beta-Galactosidase (β-Gal)


(Homo sapiens (Human))
BDBM228805
PNG
(Galactose)
Show SMILES OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@H]1O
Show InChI InChI=1S/C6H12O6/c7-1-2-3(8)4(9)5(10)6(11)12-2/h2-11H,1H2/t2-,3+,4+,5-,6?/m1/s1
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4.14E+6 -14.1n/an/an/an/an/a4.537



The University of Tokyo



Assay Description
β-Gal activity was measured by using 4-methylumbelliferyll-β-D-galactopyranoside in buffer B (0.15 M sodium citrate, pH 4.5, and 0.2 M NaCl...


J Biol Chem 289: 14560-8 (2014)

More data for this
Ligand-Target Pair
Glycogen Phosphorylase (PYGL)


(Homo sapiens (human))
BDBM50351158
PNG
(CHEMBL423707)
Show SMILES OC[C@H]1O[C@H](O)[C@H](O)[C@@H](O)[C@@H]1O
Show InChI InChI=1S/C6H12O6/c7-1-2-3(8)4(9)5(10)6(11)12-2/h2-11H,1H2/t2-,3-,4+,5-,6+/m1/s1
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4.90E+6n/an/an/an/an/an/an/an/a



University of Thessaly

Curated by ChEMBL


Assay Description
Inhibition of glycogen phosphorylase a (unknown origin)


Bioorg Med Chem 22: 4810-25 (2014)

More data for this
Ligand-Target Pair
beta-Galactosidase (β-Gal)(I51T)


(Homo sapiens (Human))
BDBM228805
PNG
(Galactose)
Show SMILES OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@H]1O
Show InChI InChI=1S/C6H12O6/c7-1-2-3(8)4(9)5(10)6(11)12-2/h2-11H,1H2/t2-,3+,4+,5-,6?/m1/s1
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4.91E+6 -13.7n/an/an/an/an/a4.537



The University of Tokyo



Assay Description
β-Gal activity was measured by using 4-methylumbelliferyll-β-D-galactopyranoside in buffer B (0.15 M sodium citrate, pH 4.5, and 0.2 M NaCl...


J Biol Chem 289: 14560-8 (2014)

More data for this
Ligand-Target Pair
beta-Galactosidase (β-Gal)(R201C)


(Homo sapiens (Human))
BDBM228805
PNG
(Galactose)
Show SMILES OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@H]1O
Show InChI InChI=1S/C6H12O6/c7-1-2-3(8)4(9)5(10)6(11)12-2/h2-11H,1H2/t2-,3+,4+,5-,6?/m1/s1
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5.61E+6 -13.4n/an/an/an/an/a4.537



The University of Tokyo



Assay Description
β-Gal activity was measured by using 4-methylumbelliferyll-β-D-galactopyranoside in buffer B (0.15 M sodium citrate, pH 4.5, and 0.2 M NaCl...


J Biol Chem 289: 14560-8 (2014)

More data for this
Ligand-Target Pair
CD209 antigen


(Homo sapiens)
BDBM50242419
PNG
(6-Deoxy-L-galactose | 6-deoxy-L-galactopyranoseL-f...)
Show SMILES C[C@@H]1OC(O)[C@@H](O)[C@H](O)[C@@H]1O
Show InChI InChI=1S/C6H12O5/c1-2-3(7)4(8)5(9)6(10)11-2/h2-10H,1H3/t2-,3+,4+,5-,6?/m0/s1
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6.70E+6n/an/an/an/an/an/an/an/a



University of Ljubljana

Curated by ChEMBL


Assay Description
Displacement of [125I]-Man30-BSA from DC-SIGN receptor carbohydrate recognition domain (unknown origin) after 2 hrs by gamma-counting analysis


Eur J Med Chem 75: 308-26 (2014)

More data for this
Ligand-Target Pair
Brain glycogen phosphorylase


(Homo sapiens)
BDBM34103
PNG
(D-glucose | dextrose | glucose)
Show SMILES OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O
Show InChI InChI=1S/C6H12O6/c7-1-2-3(8)4(9)5(10)6(11)12-2/h2-11H,1H2/t2-,3-,4+,5-,6?/m1/s1
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7.40E+6n/an/an/an/an/an/an/an/a



University of Debrecen

Curated by ChEMBL


Assay Description
Inhibitory activity against muscle Glycogen Phosphorylase b


J Med Chem 44: 2843-8 (2001)

More data for this
Ligand-Target Pair
Brain glycogen phosphorylase


(Homo sapiens)
BDBM34103
PNG
(D-glucose | dextrose | glucose)
Show SMILES OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O
Show InChI InChI=1S/C6H12O6/c7-1-2-3(8)4(9)5(10)6(11)12-2/h2-11H,1H2/t2-,3-,4+,5-,6?/m1/s1
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7.40E+6n/an/an/an/an/an/an/an/a



The University of Illinois at Chicago

Curated by ChEMBL


Assay Description
Inhibitory binding constant against glycogen phosphorylase B


J Med Chem 47: 3075-88 (2004)

More data for this
Ligand-Target Pair
Glycogen phosphorylase, muscle form


(Oryctolagus cuniculus (rabbit))
BDBM50240803
PNG
(CHEMBL1614854 | Glucoside | beta-D-glucopyranose |...)
Show SMILES OC[C@H]1O[C@@H](O)[C@H](O)[C@@H](O)[C@@H]1O
Show InChI InChI=1S/C6H12O6/c7-1-2-3(8)4(9)5(10)6(11)12-2/h2-11H,1H2/t2-,3-,4+,5-,6-/m1/s1
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7.40E+6n/an/an/an/an/an/an/an/a



National Hellenic Research Foundation

Curated by ChEMBL


Assay Description
Inhibition of rabbit muscle glycogen phosphorylase inactive form b


Bioorg Med Chem 18: 3413-25 (2010)

More data for this
Ligand-Target Pair
3D
3D Structure (docked)
CD209 antigen


(Homo sapiens)
BDBM50448403
PNG
(CHEBI:4208 | D-MANNOSE | D-Mannose)
Show SMILES OC[C@H]1OC(O)[C@@H](O)[C@@H](O)[C@@H]1O
Show InChI InChI=1S/C6H12O6/c7-1-2-3(8)4(9)5(10)6(11)12-2/h2-11H,1H2/t2-,3-,4+,5+,6?/m1/s1
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1.31E+7n/an/an/an/an/an/an/an/a



University of Ljubljana

Curated by ChEMBL


Assay Description
Displacement of [125I]-Man30-BSA from DC-SIGN receptor carbohydrate recognition domain (unknown origin) after 2 hrs by gamma-counting analysis


Eur J Med Chem 75: 308-26 (2014)

More data for this
Ligand-Target Pair
Brain glycogen phosphorylase


(Homo sapiens)
BDBM50422217
PNG
(CHEMBL2303800)
Show SMILES OC[C@@H]1O[C@@](O)(CO)[C@@H](O)[C@@H](O)[C@@H]1O
Show InChI InChI=1S/C7H14O7/c8-1-3-4(10)5(11)6(12)7(13,2-9)14-3/h3-6,8-13H,1-2H2/t3-,4+,5-,6-,7-/m0/s1
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1.58E+7n/an/an/an/an/an/an/an/a



University of Perugia

Curated by ChEMBL


Assay Description
Inhibition of rabbit glycogen phosphorylase B enzyme


J Med Chem 40: 1455-64 (1997)

More data for this
Ligand-Target Pair
Brain glycogen phosphorylase


(Homo sapiens)
BDBM50147907
PNG
((S)-2,6-Bis-hydroxymethyl-tetrahydro-pyran-2,3,4,5...)
Show SMILES OCC1O[C@@](O)(CO)C(O)C(O)C1O
Show InChI InChI=1S/C7H14O7/c8-1-3-4(10)5(11)6(12)7(13,2-9)14-3/h3-6,8-13H,1-2H2/t3?,4?,5?,6?,7-/m0/s1
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1.58E+7n/an/an/an/an/an/an/an/a



The University of Illinois at Chicago

Curated by ChEMBL


Assay Description
Inhibitory binding constant against glycogen phosphorylase B


J Med Chem 47: 3075-88 (2004)

More data for this
Ligand-Target Pair
Muscle glycogen phosphorylase


(Homo sapiens)
BDBM50422217
PNG
(CHEMBL2303800)
Show SMILES OC[C@@H]1O[C@@](O)(CO)[C@@H](O)[C@@H](O)[C@@H]1O
Show InChI InChI=1S/C7H14O7/c8-1-3-4(10)5(11)6(12)7(13,2-9)14-3/h3-6,8-13H,1-2H2/t3-,4+,5-,6-,7-/m0/s1
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1.58E+7n/an/an/an/an/an/an/an/a



University of Alcala

Curated by ChEMBL


Assay Description
Inhibitory activity against rabbit muscle glycogen phosphorylase


J Med Chem 40: 4089-102 (1998)

Checked by Author
More data for this
Ligand-Target Pair
Asialoglycoprotein receptor 1


(Homo sapiens)
BDBM50077229
PNG
(CHEMBL300520 | beta-D-galactopyranose | beta-D-gal...)
Show SMILES OC[C@H]1O[C@@H](O)[C@H](O)[C@@H](O)[C@H]1O
Show InChI InChI=1S/C6H12O6/c7-1-2-3(8)4(9)5(10)6(11)12-2/h2-11H,1H2/t2-,3+,4+,5-,6-/m1/s1
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n/an/a 1.05E+6n/an/an/an/an/an/a



University of Basel

Curated by ChEMBL


Assay Description
Inhibition of D-GalNAc-PAA binding to human recombinant ASGPR1 carbohydrate recognition domain expressed in Escherichia coli AD494 by competitive sol...


Bioorg Med Chem 17: 7254-64 (2009)

More data for this
Ligand-Target Pair
CD209 antigen


(Homo sapiens)
BDBM50242419
PNG
(6-Deoxy-L-galactose | 6-deoxy-L-galactopyranoseL-f...)
Show SMILES C[C@@H]1OC(O)[C@@H](O)[C@H](O)[C@@H]1O
Show InChI InChI=1S/C6H12O5/c1-2-3(7)4(8)5(9)6(10)11-2/h2-10H,1H3/t2-,3+,4+,5-,6?/m0/s1
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n/an/a 2.95E+6n/an/an/an/an/an/a



University of Ljubljana

Curated by ChEMBL


Assay Description
Displacement of biotinylated HIV1 gp120 from DC-SIGN receptor carbohydrate recognition domain (unknown origin) after 2 hrs by solid-phase competitive...


Eur J Med Chem 75: 308-26 (2014)

More data for this
Ligand-Target Pair
Asialoglycoprotein receptor 1


(Homo sapiens)
BDBM50240803
PNG
(CHEMBL1614854 | Glucoside | beta-D-glucopyranose |...)
Show SMILES OC[C@H]1O[C@@H](O)[C@H](O)[C@@H](O)[C@@H]1O
Show InChI InChI=1S/C6H12O6/c7-1-2-3(8)4(9)5(10)6(11)12-2/h2-11H,1H2/t2-,3-,4+,5-,6-/m1/s1
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n/an/a>3.00E+7n/an/an/an/an/an/a



University of Basel

Curated by ChEMBL


Assay Description
Inhibition of D-GalNAc-PAA binding to human recombinant ASGPR1 carbohydrate recognition domain expressed in Escherichia coli AD494 by competitive sol...


Bioorg Med Chem 17: 7254-64 (2009)

More data for this
Ligand-Target Pair
Galectin-1


(Homo sapiens (human))
BDBM50423644
PNG
(GALACTOSE)
Show SMILES OC[C@H]1O[C@H](O)[C@H](O)[C@@H](O)[C@H]1O
Show InChI InChI=1S/C6H12O6/c7-1-2-3(8)4(9)5(10)6(11)12-2/h2-11H,1H2/t2-,3+,4+,5-,6+/m1/s1
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n/an/a 5.00E+7n/an/an/an/an/an/a



Universit£ du Qu£bec£ Montr£al

Curated by ChEMBL


Assay Description
Inhibition of recombinant galectin 1 in human O type red blood cells by hemagglutination assay


Bioorg Med Chem 16: 7811-23 (2008)

More data for this
Ligand-Target Pair
Galectin-3


(Homo sapiens (Human))
BDBM50423644
PNG
(GALACTOSE)
Show SMILES OC[C@H]1O[C@H](O)[C@H](O)[C@@H](O)[C@H]1O
Show InChI InChI=1S/C6H12O6/c7-1-2-3(8)4(9)5(10)6(11)12-2/h2-11H,1H2/t2-,3+,4+,5-,6+/m1/s1
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n/an/a 5.00E+7n/an/an/an/an/an/a



Universit£ du Qu£bec£ Montr£al

Curated by ChEMBL


Assay Description
Inhibition of recombinant galectin 3 in human O type red blood cells by hemagglutination assay


Bioorg Med Chem 16: 7811-23 (2008)

More data for this
Ligand-Target Pair
Asialoglycoprotein receptor 1


(Homo sapiens)
BDBM50077229
PNG
(CHEMBL300520 | beta-D-galactopyranose | beta-D-gal...)
Show SMILES OC[C@H]1O[C@@H](O)[C@H](O)[C@@H](O)[C@H]1O
Show InChI InChI=1S/C6H12O6/c7-1-2-3(8)4(9)5(10)6(11)12-2/h2-11H,1H2/t2-,3+,4+,5-,6-/m1/s1
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n/an/an/a 1.46E+6n/an/an/an/an/a



University of Basel

Curated by ChEMBL


Assay Description
Binding affinity to human recombinant ASGPR1 carbohydrate recognition domain expressed in Escherichia coli AD494 by surface plasmon resonance spectro...


Bioorg Med Chem 17: 7254-64 (2009)

More data for this
Ligand-Target Pair
Asialoglycoprotein receptor 1


(Homo sapiens)
BDBM50240803
PNG
(CHEMBL1614854 | Glucoside | beta-D-glucopyranose |...)
Show SMILES OC[C@H]1O[C@@H](O)[C@H](O)[C@@H](O)[C@@H]1O
Show InChI InChI=1S/C6H12O6/c7-1-2-3(8)4(9)5(10)6(11)12-2/h2-11H,1H2/t2-,3-,4+,5-,6-/m1/s1
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n/an/an/a>1.00E+7n/an/an/an/an/a



University of Basel

Curated by ChEMBL


Assay Description
Binding affinity to human recombinant ASGPR1 carbohydrate recognition domain expressed in Escherichia coli AD494 by surface plasmon resonance spectro...


Bioorg Med Chem 17: 7254-64 (2009)

More data for this
Ligand-Target Pair