Compile Data Set for Download or QSAR
maximum 50k data
Found 72 Enz. Inhib. hit(s) with all data for entry = 10480
TargetLysine-specific histone demethylase 1A(Homo sapiens (Human))
Hanmi Pharm.

US Patent
LigandPNGBDBM539201((R)-4-(3-(3-aminopiperidine-1-carbonyl)- 1-(2-fluo...)
Affinity DataIC50:  20nMAssay Description:The biochemical inhibition activity of the synthesized compounds on LSD1 was measured. The activity measurement was performed using LSD1 fluorescence...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
TargetLysine-specific histone demethylase 1A(Homo sapiens (Human))
Hanmi Pharm.

US Patent
LigandPNGBDBM539151((R)-4-(3-(3-aminopiperidine-1-carbonyl)- 1-(4-cycl...)
Affinity DataIC50:  21nMAssay Description:The biochemical inhibition activity of the synthesized compounds on LSD1 was measured. The activity measurement was performed using LSD1 fluorescence...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
TargetLysine-specific histone demethylase 1A(Homo sapiens (Human))
Hanmi Pharm.

US Patent
LigandPNGBDBM539174((R)-4-(3-(3-aminopiperidine-1-carbonyl)- 1-(4-(ter...)
Affinity DataIC50:  21nMAssay Description:The biochemical inhibition activity of the synthesized compounds on LSD1 was measured. The activity measurement was performed using LSD1 fluorescence...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
TargetLysine-specific histone demethylase 1A(Homo sapiens (Human))
Hanmi Pharm.

US Patent
LigandPNGBDBM539152((R)-4-(1-(4-cyclopropyl-2-fluorophenyl)- 3-(3-(met...)
Affinity DataIC50:  21nMAssay Description:The biochemical inhibition activity of the synthesized compounds on LSD1 was measured. The activity measurement was performed using LSD1 fluorescence...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
TargetLysine-specific histone demethylase 1A(Homo sapiens (Human))
Hanmi Pharm.

US Patent
LigandPNGBDBM539187((R)-4-(3-(3-aminopiperidine-1-carbonyl)- 1-(2-fluo...)
Affinity DataIC50:  21nMAssay Description:The biochemical inhibition activity of the synthesized compounds on LSD1 was measured. The activity measurement was performed using LSD1 fluorescence...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
TargetLysine-specific histone demethylase 1A(Homo sapiens (Human))
Hanmi Pharm.

US Patent
LigandPNGBDBM539197(2-fluoro-4-(1-(2-fluoro-4-((S)-3-methoxy- pyrrolid...)
Affinity DataIC50:  22nMAssay Description:The biochemical inhibition activity of the synthesized compounds on LSD1 was measured. The activity measurement was performed using LSD1 fluorescence...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
TargetLysine-specific histone demethylase 1A(Homo sapiens (Human))
Hanmi Pharm.

US Patent
LigandPNGBDBM539175((R)-4-(3-(3-aminoazepane-1-carbonyl)- 1-(4-(tert-b...)
Affinity DataIC50:  23nMAssay Description:The biochemical inhibition activity of the synthesized compounds on LSD1 was measured. The activity measurement was performed using LSD1 fluorescence...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
TargetLysine-specific histone demethylase 1A(Homo sapiens (Human))
Hanmi Pharm.

US Patent
LigandPNGBDBM539202((R)-4-(3-(3-aminopiperidine-1-carbonyl)- 1-(2-fluo...)
Affinity DataIC50:  26nMAssay Description:The biochemical inhibition activity of the synthesized compounds on LSD1 was measured. The activity measurement was performed using LSD1 fluorescence...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
TargetLysine-specific histone demethylase 1A(Homo sapiens (Human))
Hanmi Pharm.

US Patent
LigandPNGBDBM539198(4-(3-((R)-3-aminopiperidine-1-carbonyl)- 1-(2-fluo...)
Affinity DataIC50:  26nMAssay Description:The biochemical inhibition activity of the synthesized compounds on LSD1 was measured. The activity measurement was performed using LSD1 fluorescence...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
TargetLysine-specific histone demethylase 1A(Homo sapiens (Human))
Hanmi Pharm.

US Patent
LigandPNGBDBM539199(2-fluoro-4-(1-(2-fluoro-4-((R)-3-methoxy- pyrrolid...)
Affinity DataIC50:  28nMAssay Description:The biochemical inhibition activity of the synthesized compounds on LSD1 was measured. The activity measurement was performed using LSD1 fluorescence...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
TargetLysine-specific histone demethylase 1A(Homo sapiens (Human))
Hanmi Pharm.

US Patent
LigandPNGBDBM539188((R)-4-(3-(3-aminopiperidine-1-carbonyl)- 1-(2-fluo...)
Affinity DataIC50:  28nMAssay Description:The biochemical inhibition activity of the synthesized compounds on LSD1 was measured. The activity measurement was performed using LSD1 fluorescence...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
TargetLysine-specific histone demethylase 1A(Homo sapiens (Human))
Hanmi Pharm.

US Patent
LigandPNGBDBM539208((R)-4-(1-(2,3-dihydro-1H-inden-5-yl)-3- (3-(methyl...)
Affinity DataIC50:  28nMAssay Description:The biochemical inhibition activity of the synthesized compounds on LSD1 was measured. The activity measurement was performed using LSD1 fluorescence...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
TargetLysine-specific histone demethylase 1A(Homo sapiens (Human))
Hanmi Pharm.

US Patent
LigandPNGBDBM539154((R)-4-(3-(3-aminoazepane-1-carbonyl)- 1-(4-cyclopr...)
Affinity DataIC50:  28nMAssay Description:The biochemical inhibition activity of the synthesized compounds on LSD1 was measured. The activity measurement was performed using LSD1 fluorescence...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
TargetLysine-specific histone demethylase 1A(Homo sapiens (Human))
Hanmi Pharm.

US Patent
LigandPNGBDBM539148((R)-4-(1-(4-cyclopropylphenyl)-3-(3- methylaminopi...)
Affinity DataIC50:  29nMAssay Description:The biochemical inhibition activity of the synthesized compounds on LSD1 was measured. The activity measurement was performed using LSD1 fluorescence...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
TargetLysine-specific histone demethylase 1A(Homo sapiens (Human))
Hanmi Pharm.

US Patent
LigandPNGBDBM539204((R)-4-(3-(3-aminoazepane-1-carbonyl)- 1-(2-fluoro-...)
Affinity DataIC50:  30nMAssay Description:The biochemical inhibition activity of the synthesized compounds on LSD1 was measured. The activity measurement was performed using LSD1 fluorescence...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
TargetLysine-specific histone demethylase 1A(Homo sapiens (Human))
Hanmi Pharm.

US Patent
LigandPNGBDBM539217(4-(3-(3-amino-8-azabicyclo[3.2.1]octane- 8-carbony...)
Affinity DataIC50:  33nMAssay Description:The biochemical inhibition activity of the synthesized compounds on LSD1 was measured. The activity measurement was performed using LSD1 fluorescence...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
TargetLysine-specific histone demethylase 1A(Homo sapiens (Human))
Hanmi Pharm.

US Patent
LigandPNGBDBM539170((R)-4-(3-(3-aminoazepane-1-carbonyl)- 1-(2-fluoro-...)
Affinity DataIC50:  33nMAssay Description:The biochemical inhibition activity of the synthesized compounds on LSD1 was measured. The activity measurement was performed using LSD1 fluorescence...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
TargetLysine-specific histone demethylase 1A(Homo sapiens (Human))
Hanmi Pharm.

US Patent
LigandPNGBDBM539195(2-fluoro-4-(1-(2-fluoro-4-(3-methoxy- pyrrolidine-...)
Affinity DataIC50:  34nMAssay Description:The biochemical inhibition activity of the synthesized compounds on LSD1 was measured. The activity measurement was performed using LSD1 fluorescence...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
TargetLysine-specific histone demethylase 1A(Homo sapiens (Human))
Hanmi Pharm.

US Patent
LigandPNGBDBM539156((R)-4-(3-(3-aminopiperidine-1-carbonyl)- 1-(4-cycl...)
Affinity DataIC50:  34nMAssay Description:The biochemical inhibition activity of the synthesized compounds on LSD1 was measured. The activity measurement was performed using LSD1 fluorescence...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
TargetLysine-specific histone demethylase 1A(Homo sapiens (Human))
Hanmi Pharm.

US Patent
LigandPNGBDBM539172((R)-4-(1-(4-(tert-butyl)phenyl-3-(3-methyl- aminop...)
Affinity DataIC50:  34nMAssay Description:The biochemical inhibition activity of the synthesized compounds on LSD1 was measured. The activity measurement was performed using LSD1 fluorescence...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
TargetLysine-specific histone demethylase 1A(Homo sapiens (Human))
Hanmi Pharm.

US Patent
LigandPNGBDBM539191(4-(3-((R)-3-aminopiperidine-1-carbonyl)- 1-(2-fluo...)
Affinity DataIC50:  35nMAssay Description:The biochemical inhibition activity of the synthesized compounds on LSD1 was measured. The activity measurement was performed using LSD1 fluorescence...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
TargetLysine-specific histone demethylase 1A(Homo sapiens (Human))
Hanmi Pharm.

US Patent
LigandPNGBDBM539181((R)-4-(1-(4-(dimethylamino)phenyl)-3-(3- (methylam...)
Affinity DataIC50:  35nMAssay Description:The biochemical inhibition activity of the synthesized compounds on LSD1 was measured. The activity measurement was performed using LSD1 fluorescence...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
TargetLysine-specific histone demethylase 1A(Homo sapiens (Human))
Hanmi Pharm.

US Patent
LigandPNGBDBM539173((R)-4-(3-(3-aminopiperidine-1-carbonyl)- 1-(4-(ter...)
Affinity DataIC50:  36nMAssay Description:The biochemical inhibition activity of the synthesized compounds on LSD1 was measured. The activity measurement was performed using LSD1 fluorescence...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
TargetLysine-specific histone demethylase 1A(Homo sapiens (Human))
Hanmi Pharm.

US Patent
LigandPNGBDBM539168((R)-4-(3-(3-aminopiperidine-1-carbonyl)- 1-(2-fluo...)
Affinity DataIC50:  36nMAssay Description:The biochemical inhibition activity of the synthesized compounds on LSD1 was measured. The activity measurement was performed using LSD1 fluorescence...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
TargetLysine-specific histone demethylase 1A(Homo sapiens (Human))
Hanmi Pharm.

US Patent
LigandPNGBDBM539171((R)-4-(3-(3-aminopiperidine-1-carbonyl)- 1-(4-(ter...)
Affinity DataIC50:  36nMAssay Description:The biochemical inhibition activity of the synthesized compounds on LSD1 was measured. The activity measurement was performed using LSD1 fluorescence...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
TargetLysine-specific histone demethylase 1A(Homo sapiens (Human))
Hanmi Pharm.

US Patent
LigandPNGBDBM539150((R)-4-(1-(4-cyclopropyl-2-fluorophenyl)- 3-(3-(met...)
Affinity DataIC50:  38nMAssay Description:The biochemical inhibition activity of the synthesized compounds on LSD1 was measured. The activity measurement was performed using LSD1 fluorescence...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
TargetLysine-specific histone demethylase 1A(Homo sapiens (Human))
Hanmi Pharm.

US Patent
LigandPNGBDBM539203((R)-2-fluoro-4-(1-(2-fluoro-4-(piperidine- 1-yl)ph...)
Affinity DataIC50:  38nMAssay Description:The biochemical inhibition activity of the synthesized compounds on LSD1 was measured. The activity measurement was performed using LSD1 fluorescence...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
TargetLysine-specific histone demethylase 1A(Homo sapiens (Human))
Hanmi Pharm.

US Patent
LigandPNGBDBM539186((R)-4-(3-(3-aminopiperidine-1-carbonyl)- 1-(4-(aze...)
Affinity DataIC50:  40nMAssay Description:The biochemical inhibition activity of the synthesized compounds on LSD1 was measured. The activity measurement was performed using LSD1 fluorescence...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
TargetLysine-specific histone demethylase 1A(Homo sapiens (Human))
Hanmi Pharm.

US Patent
LigandPNGBDBM539196(4-(3-((R)-3-aminopiperidine-1-carbonyl)- 1-(2-fluo...)
Affinity DataIC50:  41nMAssay Description:The biochemical inhibition activity of the synthesized compounds on LSD1 was measured. The activity measurement was performed using LSD1 fluorescence...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
TargetLysine-specific histone demethylase 1A(Homo sapiens (Human))
Hanmi Pharm.

US Patent
LigandPNGBDBM539192(4-(3-((R)-3-aminopiperidine-1-carbonyl)- 1-(2-fluo...)
Affinity DataIC50:  41nMAssay Description:The biochemical inhibition activity of the synthesized compounds on LSD1 was measured. The activity measurement was performed using LSD1 fluorescence...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
TargetLysine-specific histone demethylase 1A(Homo sapiens (Human))
Hanmi Pharm.

US Patent
LigandPNGBDBM539184((R)-4-(3-(3-aminopiperidine-1-carbonyl)- 1-(4-(dim...)
Affinity DataIC50:  42nMAssay Description:The biochemical inhibition activity of the synthesized compounds on LSD1 was measured. The activity measurement was performed using LSD1 fluorescence...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
TargetLysine-specific histone demethylase 1A(Homo sapiens (Human))
Hanmi Pharm.

US Patent
LigandPNGBDBM539183(((R)-4-(3-(3-aminopiperidine-1-carbonyl)- 1-(4-(di...)
Affinity DataIC50:  44nMAssay Description:The biochemical inhibition activity of the synthesized compounds on LSD1 was measured. The activity measurement was performed using LSD1 fluorescence...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
TargetLysine-specific histone demethylase 1A(Homo sapiens (Human))
Hanmi Pharm.

US Patent
LigandPNGBDBM539190((R)-4-(3-(3-aminoazepane-1-carbonyl)- 1-(2-fluoro-...)
Affinity DataIC50:  46nMAssay Description:The biochemical inhibition activity of the synthesized compounds on LSD1 was measured. The activity measurement was performed using LSD1 fluorescence...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
TargetLysine-specific histone demethylase 1A(Homo sapiens (Human))
Hanmi Pharm.

US Patent
LigandPNGBDBM539149((R)-4-(3-(3-aminopiperidine-1-carbonyl)- 1-(4-cycl...)
Affinity DataIC50:  46nMAssay Description:The biochemical inhibition activity of the synthesized compounds on LSD1 was measured. The activity measurement was performed using LSD1 fluorescence...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
TargetLysine-specific histone demethylase 1A(Homo sapiens (Human))
Hanmi Pharm.

US Patent
LigandPNGBDBM539207((R)-4-(3-(3-aminopiperidine-1-carbonyl)- 1-(2,3-di...)
Affinity DataIC50:  46nMAssay Description:The biochemical inhibition activity of the synthesized compounds on LSD1 was measured. The activity measurement was performed using LSD1 fluorescence...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
TargetLysine-specific histone demethylase 1A(Homo sapiens (Human))
Hanmi Pharm.

US Patent
LigandPNGBDBM539165((R)-4-(3-(3-aminopiperidine-1-carbonyl)- 1-(4-ethy...)
Affinity DataIC50:  46nMAssay Description:The biochemical inhibition activity of the synthesized compounds on LSD1 was measured. The activity measurement was performed using LSD1 fluorescence...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
TargetLysine-specific histone demethylase 1A(Homo sapiens (Human))
Hanmi Pharm.

US Patent
LigandPNGBDBM539166((R)-4-(1-(4-ethylphenyl)-3-(3-(methyl- amino)piper...)
Affinity DataIC50:  47nMAssay Description:The biochemical inhibition activity of the synthesized compounds on LSD1 was measured. The activity measurement was performed using LSD1 fluorescence...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
TargetLysine-specific histone demethylase 1A(Homo sapiens (Human))
Hanmi Pharm.

US Patent
LigandPNGBDBM539200((R)-4-(3-(3-aminopiperidine-1-carbonyl)- 1-(2,6-di...)
Affinity DataIC50:  48nMAssay Description:The biochemical inhibition activity of the synthesized compounds on LSD1 was measured. The activity measurement was performed using LSD1 fluorescence...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
TargetLysine-specific histone demethylase 1A(Homo sapiens (Human))
Hanmi Pharm.

US Patent
LigandPNGBDBM539153((R)-4-(3-(3-aminoazepane-1-carbonyl)- 1-(4-(cyclop...)
Affinity DataIC50:  49nMAssay Description:The biochemical inhibition activity of the synthesized compounds on LSD1 was measured. The activity measurement was performed using LSD1 fluorescence...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
TargetLysine-specific histone demethylase 1A(Homo sapiens (Human))
Hanmi Pharm.

US Patent
LigandPNGBDBM539194(4-(3-((R)-3-aminopiperidine-1-carbonyl)- 1-(2-fluo...)
Affinity DataIC50:  53nMAssay Description:The biochemical inhibition activity of the synthesized compounds on LSD1 was measured. The activity measurement was performed using LSD1 fluorescence...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
TargetLysine-specific histone demethylase 1A(Homo sapiens (Human))
Hanmi Pharm.

US Patent
LigandPNGBDBM539193((R)-4-(3-(3-aminopiperidine-1-carbonyl)- 1-(4-(3,3...)
Affinity DataIC50:  55nMAssay Description:The biochemical inhibition activity of the synthesized compounds on LSD1 was measured. The activity measurement was performed using LSD1 fluorescence...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
TargetLysine-specific histone demethylase 1A(Homo sapiens (Human))
Hanmi Pharm.

US Patent
LigandPNGBDBM539189((R)-2-fluoro-4-(1-(2-fluoro-4-(pyrrolidine- 1-yl)p...)
Affinity DataIC50:  56nMAssay Description:The biochemical inhibition activity of the synthesized compounds on LSD1 was measured. The activity measurement was performed using LSD1 fluorescence...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
TargetLysine-specific histone demethylase 1A(Homo sapiens (Human))
Hanmi Pharm.

US Patent
LigandPNGBDBM539185((R)-4-(3-(3-aminopiperidine-1-carbonyl)- 1-(4-(die...)
Affinity DataIC50:  56nMAssay Description:The biochemical inhibition activity of the synthesized compounds on LSD1 was measured. The activity measurement was performed using LSD1 fluorescence...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
TargetLysine-specific histone demethylase 1A(Homo sapiens (Human))
Hanmi Pharm.

US Patent
LigandPNGBDBM539147((R)-4-(3-(3-aminopiperidine-1-carbonyl)- 1-(4-cycl...)
Affinity DataIC50:  57nMAssay Description:The biochemical inhibition activity of the synthesized compounds on LSD1 was measured. The activity measurement was performed using LSD1 fluorescence...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
TargetLysine-specific histone demethylase 1A(Homo sapiens (Human))
Hanmi Pharm.

US Patent
LigandPNGBDBM539169((R)-4-(3-(3-aminopiperidine-1-carbonyl)- 1-(2-fluo...)
Affinity DataIC50:  61nMAssay Description:The biochemical inhibition activity of the synthesized compounds on LSD1 was measured. The activity measurement was performed using LSD1 fluorescence...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
TargetLysine-specific histone demethylase 1A(Homo sapiens (Human))
Hanmi Pharm.

US Patent
LigandPNGBDBM539167((R)-4-(1-(4-isopropylphenyl)-3-(3- (methylamino)pi...)
Affinity DataIC50:  67nMAssay Description:The biochemical inhibition activity of the synthesized compounds on LSD1 was measured. The activity measurement was performed using LSD1 fluorescence...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
TargetLysine-specific histone demethylase 1A(Homo sapiens (Human))
Hanmi Pharm.

US Patent
LigandPNGBDBM539157((R)-4-(3-(3-aminopiperidine-1-carbonyl)- 1-(2-chlo...)
Affinity DataIC50:  70nMAssay Description:The biochemical inhibition activity of the synthesized compounds on LSD1 was measured. The activity measurement was performed using LSD1 fluorescence...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
TargetLysine-specific histone demethylase 1A(Homo sapiens (Human))
Hanmi Pharm.

US Patent
LigandPNGBDBM539216(4-(3-(3-amino-8-azabicyclo[3.2.1]octane- 8-carbony...)
Affinity DataIC50:  87nMAssay Description:The biochemical inhibition activity of the synthesized compounds on LSD1 was measured. The activity measurement was performed using LSD1 fluorescence...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
TargetLysine-specific histone demethylase 1A(Homo sapiens (Human))
Hanmi Pharm.

US Patent
LigandPNGBDBM539161((R)-4-(1-(4-bromophenyl)-3-(3-(methyl- amino)piper...)
Affinity DataIC50:  100nMAssay Description:The biochemical inhibition activity of the synthesized compounds on LSD1 was measured. The activity measurement was performed using LSD1 fluorescence...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
TargetLysine-specific histone demethylase 1A(Homo sapiens (Human))
Hanmi Pharm.

US Patent
LigandPNGBDBM539205((R)-4-(3-(3-aminopiperidine-1-carbonyl)- 1-(1-meth...)
Affinity DataIC50:  125nMAssay Description:The biochemical inhibition activity of the synthesized compounds on LSD1 was measured. The activity measurement was performed using LSD1 fluorescence...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
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