Compile Data Set for Download or QSAR
Found 329 Enz. Inhib. hit(s) with all data for entry = 2604
TargetLysine-specific demethylase 2B(Homo sapiens (Human))
GSK

LigandPNGBDBM276093(2-(5-bromo-1-(2-chlorobenzyl)-1H-imidazol-4-yl)-4-...)copy SMILEScopy InChI
Affinity DataIC50: 100nMAssay Description:The ability of test compounds to inhibit the activity of FBXL10 was determined in 384-well plate format under the following reaction conditions: 0.3 ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2FT8PBQUS Patent
TargetLysine-specific demethylase 2B(Homo sapiens (Human))
GSK

LigandPNGBDBM319638(2-{1-[2-(2-chlorophenyl)ethyl]-1H-imidazol-4-yl}-4...)copy SMILEScopy InChI
Affinity DataIC50: 100nMAssay Description:The ability of test compounds to inhibit the activity of FBXL10 was determined in 384-well plate format under the following reaction conditions: 0.3 ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2FT8PBQUS Patent
TargetLysine-specific demethylase 5B(Homo sapiens (Human))
GSK

LigandPNGBDBM319638(2-{1-[2-(2-chlorophenyl)ethyl]-1H-imidazol-4-yl}-4...)copy SMILEScopy InChI
Affinity DataIC50: 100nMAssay Description:The ability of test compounds to inhibit the activity of Jarid1B was determined in 384-well plate format under the following reaction conditions: 0.8...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2FT8PBQUS Patent
TargetLysine-specific demethylase 2B(Homo sapiens (Human))
GSK

LigandPNGBDBM319639(2-{1-[(1,2,3,4-tetrahydronaphthalen-1-yl)methyl]- ...)copy SMILES
Affinity DataIC50: 100nMAssay Description:The ability of test compounds to inhibit the activity of FBXL10 was determined in 384-well plate format under the following reaction conditions: 0.3 ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2FT8PBQUS Patent
TargetLysine-specific demethylase 5B(Homo sapiens (Human))
GSK

LigandPNGBDBM319639(2-{1-[(1,2,3,4-tetrahydronaphthalen-1-yl)methyl]- ...)copy SMILES
Affinity DataIC50: 100nMAssay Description:The ability of test compounds to inhibit the activity of Jarid1B was determined in 384-well plate format under the following reaction conditions: 0.8...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2FT8PBQUS Patent
TargetLysine-specific demethylase 5B(Homo sapiens (Human))
GSK

LigandPNGBDBM319640(2-{1-[2-(2-ethoxyphenyl)ethyl]-1H-imidazol-4-yl}-4...)copy SMILEScopy InChI
Affinity DataIC50: 100nMAssay Description:The ability of test compounds to inhibit the activity of Jarid1B was determined in 384-well plate format under the following reaction conditions: 0.8...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2FT8PBQUS Patent
TargetLysine-specific demethylase 5B(Homo sapiens (Human))
GSK

LigandPNGBDBM319641(4-[5-(trifluoromethyl)-1H-1,2,3-triazol-4-yl]-2- (...)copy SMILEScopy InChI
Affinity DataIC50: 100nMAssay Description:The ability of test compounds to inhibit the activity of Jarid1B was determined in 384-well plate format under the following reaction conditions: 0.8...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2FT8PBQUS Patent
TargetLysine-specific demethylase 2B(Homo sapiens (Human))
GSK

LigandPNGBDBM319642(2-{1-[(4-fluorophenyl)methyl]-1H-imidazol-4-yl}-4-...)copy SMILEScopy InChI
Affinity DataIC50: 100nMAssay Description:The ability of test compounds to inhibit the activity of FBXL10 was determined in 384-well plate format under the following reaction conditions: 0.3 ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2FT8PBQUS Patent
TargetLysine-specific demethylase 2B(Homo sapiens (Human))
GSK

LigandPNGBDBM319643(2-{1-[(4-fluorophenyl)methyl]-1H-imidazol-4-yl}-4-...)copy SMILEScopy InChI
Affinity DataIC50: 100nMAssay Description:The ability of test compounds to inhibit the activity of FBXL10 was determined in 384-well plate format under the following reaction conditions: 0.3 ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2FT8PBQUS Patent
TargetLysine-specific demethylase 2B(Homo sapiens (Human))
GSK

LigandPNGBDBM319644(2-{1-[(4-chlorophenyl)methyl]-1H-imidazol-4-yl}-4-...)copy SMILEScopy InChI
Affinity DataIC50: 100nMAssay Description:The ability of test compounds to inhibit the activity of FBXL10 was determined in 384-well plate format under the following reaction conditions: 0.3 ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2FT8PBQUS Patent
TargetLysine-specific demethylase 2B(Homo sapiens (Human))
GSK

LigandPNGBDBM319645(2-{1-[(2-chlorophenyl)methyl]-1H-imidazol-4-yl}-4-...)copy SMILEScopy InChI
Affinity DataIC50: 100nMAssay Description:The ability of test compounds to inhibit the activity of FBXL10 was determined in 384-well plate format under the following reaction conditions: 0.3 ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2FT8PBQUS Patent
TargetLysine-specific demethylase 2B(Homo sapiens (Human))
GSK

LigandPNGBDBM319646(2-{1-[(4-methylphenyl)methyl]-1H-imidazol-4-yl}-4-...)copy SMILEScopy InChI
Affinity DataIC50: 100nMAssay Description:The ability of test compounds to inhibit the activity of FBXL10 was determined in 384-well plate format under the following reaction conditions: 0.3 ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2FT8PBQUS Patent
TargetLysine-specific demethylase 2B(Homo sapiens (Human))
GSK

LigandPNGBDBM319647(2-{1-[(2-methylphenyl)methyl]-1H-imidazol-4-yl}-4-...)copy SMILEScopy InChI
Affinity DataIC50: 100nMAssay Description:The ability of test compounds to inhibit the activity of FBXL10 was determined in 384-well plate format under the following reaction conditions: 0.3 ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2FT8PBQUS Patent
TargetLysine-specific demethylase 2B(Homo sapiens (Human))
GSK

LigandPNGBDBM319648(2-{1-[(4-methoxyphenyl)methyl]-1H-imidazol-4-yl}- ...)copy SMILEScopy InChI
Affinity DataIC50: 100nMAssay Description:The ability of test compounds to inhibit the activity of FBXL10 was determined in 384-well plate format under the following reaction conditions: 0.3 ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2FT8PBQUS Patent
TargetLysine-specific demethylase 2B(Homo sapiens (Human))
GSK

LigandPNGBDBM319649(2-{1-[(2,4-difluorophenyl)methyl]-1H-imidazol-4- y...)copy SMILEScopy InChI
Affinity DataIC50: 100nMAssay Description:The ability of test compounds to inhibit the activity of FBXL10 was determined in 384-well plate format under the following reaction conditions: 0.3 ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2FT8PBQUS Patent
TargetLysine-specific demethylase 2B(Homo sapiens (Human))
GSK

LigandPNGBDBM319650(2-{1-[(2,6-difluorophenyl)methyl]-1H-imidazol-4- y...)copy SMILEScopy InChI
Affinity DataIC50: 100nMAssay Description:The ability of test compounds to inhibit the activity of FBXL10 was determined in 384-well plate format under the following reaction conditions: 0.3 ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2FT8PBQUS Patent
TargetLysine-specific demethylase 2B(Homo sapiens (Human))
GSK

LigandPNGBDBM319651(2-{1-[(4-fluoro-2-methylphenyl)methyl]-1H- imidazo...)copy SMILEScopy InChI
Affinity DataIC50: 100nMAssay Description:The ability of test compounds to inhibit the activity of FBXL10 was determined in 384-well plate format under the following reaction conditions: 0.3 ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2FT8PBQUS Patent
TargetLysine-specific demethylase 2B(Homo sapiens (Human))
GSK

LigandPNGBDBM319652(2-{1-[(2-fluoro-4-methylphenyl)methyl]-1H- imidazo...)copy SMILEScopy InChI
Affinity DataIC50: 100nMAssay Description:The ability of test compounds to inhibit the activity of FBXL10 was determined in 384-well plate format under the following reaction conditions: 0.3 ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2FT8PBQUS Patent
TargetLysine-specific demethylase 2B(Homo sapiens (Human))
GSK

LigandPNGBDBM319653(2-(1-benzyl-1H-imidazol-4-yl)-4-[5- (trifluorometh...)copy SMILEScopy InChI
Affinity DataIC50: 100nMAssay Description:The ability of test compounds to inhibit the activity of FBXL10 was determined in 384-well plate format under the following reaction conditions: 0.3 ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2FT8PBQUS Patent
TargetLysine-specific demethylase 2B(Homo sapiens (Human))
GSK

LigandPNGBDBM319654(2-[1-(1-phenylethyl)-1H-imidazol-4-yl]-4-[5- (trif...)copy SMILES
Affinity DataIC50: 100nMAssay Description:The ability of test compounds to inhibit the activity of FBXL10 was determined in 384-well plate format under the following reaction conditions: 0.3 ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2FT8PBQUS Patent
TargetLysine-specific demethylase 2B(Homo sapiens (Human))
GSK

LigandPNGBDBM319655(2-[1-(1-phenylpropyl)-1H-imidazol-4-yl]-4-[5- (tri...)copy SMILES
Affinity DataIC50: 100nMAssay Description:The ability of test compounds to inhibit the activity of FBXL10 was determined in 384-well plate format under the following reaction conditions: 0.3 ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2FT8PBQUS Patent
TargetLysine-specific demethylase 2B(Homo sapiens (Human))
GSK

LigandPNGBDBM373163(2-{1-[2-(4-fluorophenyl)ethyl]-1H-imidazol- 4-yl}-...)copy SMILEScopy InChI
Affinity DataIC50: 100nMAssay Description:The ability of test compounds to inhibit the activity of FBXL10 was determined in 384-well plate format under the following reaction conditions: 0.3 ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2FT8PBQUS Patent
TargetLysine-specific demethylase 5B(Homo sapiens (Human))
GSK

LigandPNGBDBM373163(2-{1-[2-(4-fluorophenyl)ethyl]-1H-imidazol- 4-yl}-...)copy SMILEScopy InChI
Affinity DataIC50: 100nMAssay Description:The ability of test compounds to inhibit the activity of Jarid1B was determined in 384-well plate format under the following reaction conditions: 0.8...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2FT8PBQUS Patent
TargetLysine-specific demethylase 2B(Homo sapiens (Human))
GSK

LigandPNGBDBM319659(2-{1-[2-(3-fluorophenyl)ethyl]-1H-imidazol-4-yl}-4...)copy SMILEScopy InChI
Affinity DataIC50: 100nMAssay Description:The ability of test compounds to inhibit the activity of FBXL10 was determined in 384-well plate format under the following reaction conditions: 0.3 ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2FT8PBQUS Patent
TargetLysine-specific demethylase 5B(Homo sapiens (Human))
GSK

LigandPNGBDBM319659(2-{1-[2-(3-fluorophenyl)ethyl]-1H-imidazol-4-yl}-4...)copy SMILEScopy InChI
Affinity DataIC50: 100nMAssay Description:The ability of test compounds to inhibit the activity of Jarid1B was determined in 384-well plate format under the following reaction conditions: 0.8...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2FT8PBQUS Patent
TargetLysine-specific demethylase 2B(Homo sapiens (Human))
GSK

LigandPNGBDBM319660(2-{1-[2-(2,3-difluorophenyl)ethyl]-1H-imidazol- 4-...)copy SMILEScopy InChI
Affinity DataIC50: 100nMAssay Description:The ability of test compounds to inhibit the activity of FBXL10 was determined in 384-well plate format under the following reaction conditions: 0.3 ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2FT8PBQUS Patent
TargetLysine-specific demethylase 5B(Homo sapiens (Human))
GSK

LigandPNGBDBM319660(2-{1-[2-(2,3-difluorophenyl)ethyl]-1H-imidazol- 4-...)copy SMILEScopy InChI
Affinity DataIC50: 100nMAssay Description:The ability of test compounds to inhibit the activity of Jarid1B was determined in 384-well plate format under the following reaction conditions: 0.8...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2FT8PBQUS Patent
TargetLysine-specific demethylase 2B(Homo sapiens (Human))
GSK

LigandPNGBDBM319662(4-[5-(trifluoromethyl)-1H-1,2,3-triazol-4-yl]-2-{1...)copy SMILEScopy InChI
Affinity DataIC50: 100nMAssay Description:The ability of test compounds to inhibit the activity of FBXL10 was determined in 384-well plate format under the following reaction conditions: 0.3 ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2FT8PBQUS Patent
TargetLysine-specific demethylase 5B(Homo sapiens (Human))
GSK

LigandPNGBDBM319662(4-[5-(trifluoromethyl)-1H-1,2,3-triazol-4-yl]-2-{1...)copy SMILEScopy InChI
Affinity DataIC50: 100nMAssay Description:The ability of test compounds to inhibit the activity of Jarid1B was determined in 384-well plate format under the following reaction conditions: 0.8...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2FT8PBQUS Patent
TargetLysine-specific demethylase 2B(Homo sapiens (Human))
GSK

LigandPNGBDBM319663(4-[5-(trifluoromethyl)-1H-1,2,3-triazol-4-yl]-2- {...)copy SMILEScopy InChI
Affinity DataIC50: 100nMAssay Description:The ability of test compounds to inhibit the activity of FBXL10 was determined in 384-well plate format under the following reaction conditions: 0.3 ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2FT8PBQUS Patent
TargetLysine-specific demethylase 5B(Homo sapiens (Human))
GSK

LigandPNGBDBM319664(2-{1-[(2,3-dihydro-1H-inden-1-yl)methyl]-1H- imida...)copy SMILES
Affinity DataIC50: 100nMAssay Description:The ability of test compounds to inhibit the activity of Jarid1B was determined in 384-well plate format under the following reaction conditions: 0.8...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2FT8PBQUS Patent
TargetLysine-specific demethylase 2B(Homo sapiens (Human))
GSK

LigandPNGBDBM319665(2-{1-[2-(2-fluorophenyl)ethyl]-1H-imidazol-4-yl}-4...)copy SMILEScopy InChI
Affinity DataIC50: 100nMAssay Description:The ability of test compounds to inhibit the activity of FBXL10 was determined in 384-well plate format under the following reaction conditions: 0.3 ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2FT8PBQUS Patent
TargetLysine-specific demethylase 5B(Homo sapiens (Human))
GSK

LigandPNGBDBM319665(2-{1-[2-(2-fluorophenyl)ethyl]-1H-imidazol-4-yl}-4...)copy SMILEScopy InChI
Affinity DataIC50: 100nMAssay Description:The ability of test compounds to inhibit the activity of Jarid1B was determined in 384-well plate format under the following reaction conditions: 0.8...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2FT8PBQUS Patent
TargetLysine-specific demethylase 2B(Homo sapiens (Human))
GSK

LigandPNGBDBM319666(2-[1-(6-fluoro-2,3-dihydro-1H-inden-1-yl)-1H- imid...)copy SMILES
Affinity DataIC50: 100nMAssay Description:The ability of test compounds to inhibit the activity of FBXL10 was determined in 384-well plate format under the following reaction conditions: 0.3 ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2FT8PBQUS Patent
TargetLysine-specific demethylase 5B(Homo sapiens (Human))
GSK

LigandPNGBDBM319666(2-[1-(6-fluoro-2,3-dihydro-1H-inden-1-yl)-1H- imid...)copy SMILES
Affinity DataIC50: 100nMAssay Description:The ability of test compounds to inhibit the activity of Jarid1B was determined in 384-well plate format under the following reaction conditions: 0.8...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2FT8PBQUS Patent
TargetLysine-specific demethylase 2B(Homo sapiens (Human))
GSK

LigandPNGBDBM319667(2-{1-[2-(2,4-difluorophenyl)ethyl]-1H-imidazol-4- ...)copy SMILEScopy InChI
Affinity DataIC50: 100nMAssay Description:The ability of test compounds to inhibit the activity of FBXL10 was determined in 384-well plate format under the following reaction conditions: 0.3 ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2FT8PBQUS Patent
TargetLysine-specific demethylase 5B(Homo sapiens (Human))
GSK

LigandPNGBDBM319667(2-{1-[2-(2,4-difluorophenyl)ethyl]-1H-imidazol-4- ...)copy SMILEScopy InChI
Affinity DataIC50: 100nMAssay Description:The ability of test compounds to inhibit the activity of Jarid1B was determined in 384-well plate format under the following reaction conditions: 0.8...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2FT8PBQUS Patent
TargetLysine-specific demethylase 2B(Homo sapiens (Human))
GSK

LigandPNGBDBM319668(2-{1-[2-(2,6-difluorophenyl)ethyl]-1H-imidazol-4- ...)copy SMILEScopy InChI
Affinity DataIC50: 100nMAssay Description:The ability of test compounds to inhibit the activity of FBXL10 was determined in 384-well plate format under the following reaction conditions: 0.3 ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2FT8PBQUS Patent
TargetLysine-specific demethylase 2B(Homo sapiens (Human))
GSK

LigandPNGBDBM319669(2-{1-[2-(2,5-difluorophenyl)ethyl]-1H-imidazol-4- ...)copy SMILEScopy InChI
Affinity DataIC50: 100nMAssay Description:The ability of test compounds to inhibit the activity of FBXL10 was determined in 384-well plate format under the following reaction conditions: 0.3 ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2FT8PBQUS Patent
TargetLysine-specific demethylase 5B(Homo sapiens (Human))
GSK

LigandPNGBDBM319669(2-{1-[2-(2,5-difluorophenyl)ethyl]-1H-imidazol-4- ...)copy SMILEScopy InChI
Affinity DataIC50: 100nMAssay Description:The ability of test compounds to inhibit the activity of Jarid1B was determined in 384-well plate format under the following reaction conditions: 0.8...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2FT8PBQUS Patent
TargetLysine-specific demethylase 2B(Homo sapiens (Human))
GSK

LigandPNGBDBM319670(2-{1-[(3R)-1-benzoylpiperidin-3-yl]-1H-imidazol-4-...)copy SMILES
Affinity DataIC50: 100nMAssay Description:The ability of test compounds to inhibit the activity of FBXL10 was determined in 384-well plate format under the following reaction conditions: 0.3 ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2FT8PBQUS Patent
TargetLysine-specific demethylase 5B(Homo sapiens (Human))
GSK

LigandPNGBDBM319670(2-{1-[(3R)-1-benzoylpiperidin-3-yl]-1H-imidazol-4-...)copy SMILES
Affinity DataIC50: 100nMAssay Description:The ability of test compounds to inhibit the activity of Jarid1B was determined in 384-well plate format under the following reaction conditions: 0.8...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2FT8PBQUS Patent
TargetLysine-specific demethylase 2B(Homo sapiens (Human))
GSK

LigandPNGBDBM319671(2-{1-[(3S)-1-benzoylpiperidin-3-yl]-1H-imidazol-4-...)copy SMILES
Affinity DataIC50: 100nMAssay Description:The ability of test compounds to inhibit the activity of FBXL10 was determined in 384-well plate format under the following reaction conditions: 0.3 ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2FT8PBQUS Patent
TargetLysine-specific demethylase 5B(Homo sapiens (Human))
GSK

LigandPNGBDBM319671(2-{1-[(3S)-1-benzoylpiperidin-3-yl]-1H-imidazol-4-...)copy SMILES
Affinity DataIC50: 100nMAssay Description:The ability of test compounds to inhibit the activity of Jarid1B was determined in 384-well plate format under the following reaction conditions: 0.8...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2FT8PBQUS Patent
TargetLysine-specific demethylase 2B(Homo sapiens (Human))
GSK

LigandPNGBDBM319672(2-{1-[2-(4-methylphenyl)ethyl]-1H-imidazol-4-yl}- ...)copy SMILEScopy InChI
Affinity DataIC50: 100nMAssay Description:The ability of test compounds to inhibit the activity of FBXL10 was determined in 384-well plate format under the following reaction conditions: 0.3 ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2FT8PBQUS Patent
TargetLysine-specific demethylase 2B(Homo sapiens (Human))
GSK

LigandPNGBDBM319673(2-{1-[2-(4-chlorophenyl)ethyl]-1H-imidazol-4-yl}-4...)copy SMILEScopy InChI
Affinity DataIC50: 100nMAssay Description:The ability of test compounds to inhibit the activity of FBXL10 was determined in 384-well plate format under the following reaction conditions: 0.3 ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2FT8PBQUS Patent
TargetLysine-specific demethylase 2B(Homo sapiens (Human))
GSK

LigandPNGBDBM319674(2-{1-[2-(4-methoxyphenyl)ethyl]-1H-imidazol-4-yl}-...)copy SMILEScopy InChI
Affinity DataIC50: 100nMAssay Description:The ability of test compounds to inhibit the activity of FBXL10 was determined in 384-well plate format under the following reaction conditions: 0.3 ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2FT8PBQUS Patent
TargetLysine-specific demethylase 5B(Homo sapiens (Human))
GSK

LigandPNGBDBM319674(2-{1-[2-(4-methoxyphenyl)ethyl]-1H-imidazol-4-yl}-...)copy SMILEScopy InChI
Affinity DataIC50: 100nMAssay Description:The ability of test compounds to inhibit the activity of Jarid1B was determined in 384-well plate format under the following reaction conditions: 0.8...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2FT8PBQUS Patent
TargetLysine-specific demethylase 2B(Homo sapiens (Human))
GSK

LigandPNGBDBM319678(2-[5-(4-fluorophenyl)-1-methyl-1H-imidazol-4-yl]-4...)copy SMILEScopy InChI
Affinity DataIC50: 100nMAssay Description:The ability of test compounds to inhibit the activity of FBXL10 was determined in 384-well plate format under the following reaction conditions: 0.3 ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2FT8PBQUS Patent
TargetLysine-specific demethylase 5B(Homo sapiens (Human))
GSK

LigandPNGBDBM319678(2-[5-(4-fluorophenyl)-1-methyl-1H-imidazol-4-yl]-4...)copy SMILEScopy InChI
Affinity DataIC50: 100nMAssay Description:The ability of test compounds to inhibit the activity of Jarid1B was determined in 384-well plate format under the following reaction conditions: 0.8...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2FT8PBQUS Patent
Displayed 1 to 50 (of 329 total ) | Next | Last >>
Jump to: