Compile Data Set for Download or QSAR
Found 51 Enz. Inhib. hit(s) with all data for assayid = 5 entry = 2604
TargetLysine-specific demethylase 4C(Homo sapiens (Human))
GSK

LigandPNGBDBM319641(4-[5-(trifluoromethyl)-1H-1,2,3-triazol-4-yl]-2- (...)copy SMILEScopy InChI
Affinity DataIC50: 500nMAssay Description:The ability of test compounds to inhibit the activity of JMJD2C 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 4C(Homo sapiens (Human))
GSK

LigandPNGBDBM319666(2-[1-(6-fluoro-2,3-dihydro-1H-inden-1-yl)-1H- imid...)copy SMILES
Affinity DataIC50: 500nMAssay Description:The ability of test compounds to inhibit the activity of JMJD2C 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 4C(Homo sapiens (Human))
GSK

LigandPNGBDBM319648(2-{1-[(4-methoxyphenyl)methyl]-1H-imidazol-4-yl}- ...)copy SMILEScopy InChI
Affinity DataIC50: 500nMAssay Description:The ability of test compounds to inhibit the activity of JMJD2C 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 4C(Homo sapiens (Human))
GSK

LigandPNGBDBM319664(2-{1-[(2,3-dihydro-1H-inden-1-yl)methyl]-1H- imida...)copy SMILES
Affinity DataIC50: 500nMAssay Description:The ability of test compounds to inhibit the activity of JMJD2C 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 4C(Homo sapiens (Human))
GSK

LigandPNGBDBM319643(2-{1-[(4-fluorophenyl)methyl]-1H-imidazol-4-yl}-4-...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+4nMAssay Description:The ability of test compounds to inhibit the activity of JMJD2C 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 4C(Homo sapiens (Human))
GSK

LigandPNGBDBM319644(2-{1-[(4-chlorophenyl)methyl]-1H-imidazol-4-yl}-4-...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+4nMAssay Description:The ability of test compounds to inhibit the activity of JMJD2C 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 4C(Homo sapiens (Human))
GSK

LigandPNGBDBM319645(2-{1-[(2-chlorophenyl)methyl]-1H-imidazol-4-yl}-4-...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+4nMAssay Description:The ability of test compounds to inhibit the activity of JMJD2C 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 4C(Homo sapiens (Human))
GSK

LigandPNGBDBM319646(2-{1-[(4-methylphenyl)methyl]-1H-imidazol-4-yl}-4-...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+4nMAssay Description:The ability of test compounds to inhibit the activity of JMJD2C 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 4C(Homo sapiens (Human))
GSK

LigandPNGBDBM319647(2-{1-[(2-methylphenyl)methyl]-1H-imidazol-4-yl}-4-...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+4nMAssay Description:The ability of test compounds to inhibit the activity of JMJD2C 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 4C(Homo sapiens (Human))
GSK

LigandPNGBDBM319649(2-{1-[(2,4-difluorophenyl)methyl]-1H-imidazol-4- y...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+4nMAssay Description:The ability of test compounds to inhibit the activity of JMJD2C 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 4C(Homo sapiens (Human))
GSK

LigandPNGBDBM319650(2-{1-[(2,6-difluorophenyl)methyl]-1H-imidazol-4- y...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+4nMAssay Description:The ability of test compounds to inhibit the activity of JMJD2C 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 4C(Homo sapiens (Human))
GSK

LigandPNGBDBM319651(2-{1-[(4-fluoro-2-methylphenyl)methyl]-1H- imidazo...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+4nMAssay Description:The ability of test compounds to inhibit the activity of JMJD2C 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 4C(Homo sapiens (Human))
GSK

LigandPNGBDBM319652(2-{1-[(2-fluoro-4-methylphenyl)methyl]-1H- imidazo...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+4nMAssay Description:The ability of test compounds to inhibit the activity of JMJD2C 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 4C(Homo sapiens (Human))
GSK

LigandPNGBDBM319653(2-(1-benzyl-1H-imidazol-4-yl)-4-[5- (trifluorometh...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+4nMAssay Description:The ability of test compounds to inhibit the activity of JMJD2C 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 4C(Homo sapiens (Human))
GSK

LigandPNGBDBM319654(2-[1-(1-phenylethyl)-1H-imidazol-4-yl]-4-[5- (trif...)copy SMILES
Affinity DataIC50: 1.00E+4nMAssay Description:The ability of test compounds to inhibit the activity of JMJD2C 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 4C(Homo sapiens (Human))
GSK

LigandPNGBDBM319655(2-[1-(1-phenylpropyl)-1H-imidazol-4-yl]-4-[5- (tri...)copy SMILES
Affinity DataIC50: 1.00E+4nMAssay Description:The ability of test compounds to inhibit the activity of JMJD2C 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 4C(Homo sapiens (Human))
GSK

LigandPNGBDBM319656(2-[1-(2-methyl-1-phenylpropyl)-1H-imidazol-4-yl]-4...)copy SMILES
Affinity DataIC50: 1.00E+4nMAssay Description:The ability of test compounds to inhibit the activity of JMJD2C 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 4C(Homo sapiens (Human))
GSK

LigandPNGBDBM373162(2-(1-{[2-(2,2,2- trifluoroethoxy)phenyl]methyl}-1H...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+4nMAssay Description:The ability of test compounds to inhibit the activity of JMJD2C 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 4C(Homo sapiens (Human))
GSK

LigandPNGBDBM373163(2-{1-[2-(4-fluorophenyl)ethyl]-1H-imidazol- 4-yl}-...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+4nMAssay Description:The ability of test compounds to inhibit the activity of JMJD2C 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 4C(Homo sapiens (Human))
GSK

LigandPNGBDBM319659(2-{1-[2-(3-fluorophenyl)ethyl]-1H-imidazol-4-yl}-4...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+4nMAssay Description:The ability of test compounds to inhibit the activity of JMJD2C 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 4C(Homo sapiens (Human))
GSK

LigandPNGBDBM319660(2-{1-[2-(2,3-difluorophenyl)ethyl]-1H-imidazol- 4-...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+4nMAssay Description:The ability of test compounds to inhibit the activity of JMJD2C 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 4C(Homo sapiens (Human))
GSK

LigandPNGBDBM319661(2-{1-[2-(2-chloro-6-fluorophenyl)ethyl]-1H- imidaz...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+4nMAssay Description:The ability of test compounds to inhibit the activity of JMJD2C 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 4C(Homo sapiens (Human))
GSK

LigandPNGBDBM319662(4-[5-(trifluoromethyl)-1H-1,2,3-triazol-4-yl]-2-{1...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+4nMAssay Description:The ability of test compounds to inhibit the activity of JMJD2C 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 4C(Homo sapiens (Human))
GSK

LigandPNGBDBM319663(4-[5-(trifluoromethyl)-1H-1,2,3-triazol-4-yl]-2- {...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+4nMAssay Description:The ability of test compounds to inhibit the activity of JMJD2C 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 4C(Homo sapiens (Human))
GSK

LigandPNGBDBM319665(2-{1-[2-(2-fluorophenyl)ethyl]-1H-imidazol-4-yl}-4...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+4nMAssay Description:The ability of test compounds to inhibit the activity of JMJD2C 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 4C(Homo sapiens (Human))
GSK

LigandPNGBDBM319667(2-{1-[2-(2,4-difluorophenyl)ethyl]-1H-imidazol-4- ...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+4nMAssay Description:The ability of test compounds to inhibit the activity of JMJD2C 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 4C(Homo sapiens (Human))
GSK

LigandPNGBDBM319668(2-{1-[2-(2,6-difluorophenyl)ethyl]-1H-imidazol-4- ...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+4nMAssay Description:The ability of test compounds to inhibit the activity of JMJD2C 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 4C(Homo sapiens (Human))
GSK

LigandPNGBDBM319669(2-{1-[2-(2,5-difluorophenyl)ethyl]-1H-imidazol-4- ...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+4nMAssay Description:The ability of test compounds to inhibit the activity of JMJD2C 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 4C(Homo sapiens (Human))
GSK

LigandPNGBDBM319670(2-{1-[(3R)-1-benzoylpiperidin-3-yl]-1H-imidazol-4-...)copy SMILES
Affinity DataIC50: 1.00E+4nMAssay Description:The ability of test compounds to inhibit the activity of JMJD2C 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 4C(Homo sapiens (Human))
GSK

LigandPNGBDBM319671(2-{1-[(3S)-1-benzoylpiperidin-3-yl]-1H-imidazol-4-...)copy SMILES
Affinity DataIC50: 1.00E+4nMAssay Description:The ability of test compounds to inhibit the activity of JMJD2C 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 4C(Homo sapiens (Human))
GSK

LigandPNGBDBM319672(2-{1-[2-(4-methylphenyl)ethyl]-1H-imidazol-4-yl}- ...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+4nMAssay Description:The ability of test compounds to inhibit the activity of JMJD2C 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 4C(Homo sapiens (Human))
GSK

LigandPNGBDBM319673(2-{1-[2-(4-chlorophenyl)ethyl]-1H-imidazol-4-yl}-4...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+4nMAssay Description:The ability of test compounds to inhibit the activity of JMJD2C 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 4C(Homo sapiens (Human))
GSK

LigandPNGBDBM319674(2-{1-[2-(4-methoxyphenyl)ethyl]-1H-imidazol-4-yl}-...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+4nMAssay Description:The ability of test compounds to inhibit the activity of JMJD2C 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 4C(Homo sapiens (Human))
GSK

LigandPNGBDBM319675(4-[5-(trifluoromethyl)-1H-1,2,3-triazol-4-yl]-2-(1...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+4nMAssay Description:The ability of test compounds to inhibit the activity of JMJD2C 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 4C(Homo sapiens (Human))
GSK

LigandPNGBDBM319676(2-{1-[2-(4-ethylphenyl)ethyl]-1H-imidazol-4-yl}-4-...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+4nMAssay Description:The ability of test compounds to inhibit the activity of JMJD2C 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 4C(Homo sapiens (Human))
GSK

LigandPNGBDBM319677(2-{1-[2-(4-tert-butylphenyl)ethyl]-1H-imidazol-4- ...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+4nMAssay Description:The ability of test compounds to inhibit the activity of JMJD2C 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 4C(Homo sapiens (Human))
GSK

LigandPNGBDBM319678(2-[5-(4-fluorophenyl)-1-methyl-1H-imidazol-4-yl]-4...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+4nMAssay Description:The ability of test compounds to inhibit the activity of JMJD2C 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 4C(Homo sapiens (Human))
GSK

LigandPNGBDBM319679(2-{1-[(3,4-dihydro-2H-1-benzopyran-4-yl)methyl]- 1...)copy SMILES
Affinity DataIC50: 1.00E+4nMAssay Description:The ability of test compounds to inhibit the activity of JMJD2C 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 4C(Homo sapiens (Human))
GSK

LigandPNGBDBM319680(2-{1-[(5-fluoro-1,2,3,4-tetrahydronaphthalen-1- yl...)copy SMILES
Affinity DataIC50: 1.00E+4nMAssay Description:The ability of test compounds to inhibit the activity of JMJD2C 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 4C(Homo sapiens (Human))
GSK

LigandPNGBDBM319681(2-{1-[(6-fluoro-1,2,3,4-tetrahydronaphthalen-1- yl...)copy SMILES
Affinity DataIC50: 1.00E+4nMAssay Description:The ability of test compounds to inhibit the activity of JMJD2C 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 4C(Homo sapiens (Human))
GSK

LigandPNGBDBM319682(2-{1-[(7-fluoro-1,2,3,4-tetrahydronaphthalen-1- yl...)copy SMILES
Affinity DataIC50: 1.00E+4nMAssay Description:The ability of test compounds to inhibit the activity of JMJD2C 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 4C(Homo sapiens (Human))
GSK

LigandPNGBDBM319683(2-{1-[(6-methyl-1,2,3,4-tetrahydronaphthalen-1- yl...)copy SMILES
Affinity DataIC50: 1.00E+4nMAssay Description:The ability of test compounds to inhibit the activity of JMJD2C 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 4C(Homo sapiens (Human))
GSK

LigandPNGBDBM319684(2-{1-[(7-methyl-1,2,3,4-tetrahydronaphthalen-1- yl...)copy SMILES
Affinity DataIC50: 1.00E+4nMAssay Description:The ability of test compounds to inhibit the activity of JMJD2C 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 4C(Homo sapiens (Human))
GSK

LigandPNGBDBM319685(2-{1-[(5-methoxy-1,2,3,4-tetrahydronaphthalen-1- y...)copy SMILES
Affinity DataIC50: 1.00E+4nMAssay Description:The ability of test compounds to inhibit the activity of JMJD2C 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 4C(Homo sapiens (Human))
GSK

LigandPNGBDBM319686(2-{1-[(6-methoxy-1,2,3,4-tetrahydronaphthalen-1- y...)copy SMILES
Affinity DataIC50: 1.00E+4nMAssay Description:The ability of test compounds to inhibit the activity of JMJD2C 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 4C(Homo sapiens (Human))
GSK

LigandPNGBDBM319687(2-{1-[(7-methoxy-1,2,3,4-tetrahydronaphthalen-1- y...)copy SMILES
Affinity DataIC50: 1.00E+4nMAssay Description:The ability of test compounds to inhibit the activity of JMJD2C 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 4C(Homo sapiens (Human))
GSK

LigandPNGBDBM319642(2-{1-[(4-fluorophenyl)methyl]-1H-imidazol-4-yl}-4-...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+4nMAssay Description:The ability of test compounds to inhibit the activity of JMJD2C 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 4C(Homo sapiens (Human))
GSK

LigandPNGBDBM319640(2-{1-[2-(2-ethoxyphenyl)ethyl]-1H-imidazol-4-yl}-4...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+4nMAssay Description:The ability of test compounds to inhibit the activity of JMJD2C 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 4C(Homo sapiens (Human))
GSK

LigandPNGBDBM319688(2-{1-[(8-methoxy-1,2,3,4-tetrahydro-naphthalen-1-y...)copy SMILES
Affinity DataIC50: 1.00E+4nMAssay Description:The ability of test compounds to inhibit the activity of JMJD2C 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 4C(Homo sapiens (Human))
GSK

LigandPNGBDBM319638(2-{1-[2-(2-chlorophenyl)ethyl]-1H-imidazol-4-yl}-4...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+4nMAssay Description:The ability of test compounds to inhibit the activity of JMJD2C 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
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