Compile Data Set for Download or QSAR
Report error Found 60 Enz. Inhib. hit(s) with all data for entry = 50034383
TargetLysine-specific histone demethylase 1A(Human)
Kyoto Prefectural University of Medicine

Curated by ChEMBL
LigandPNGBDBM50185388(N-(3,3-diphenylpropyl)-1-3-[3-({7-[(3-{N-[3-(3,3-d...)
Affinity DataIC50: 1.00E+3nMAssay Description:Inhibition of LSD1More data for this Ligand-Target Pair
In Depth
Date in BDB:
7/22/2012
Entry Details Article
PubMed
TargetLysine-specific demethylase 4C(Human)
Kyoto Prefectural University of Medicine

Curated by ChEMBL
LigandPNGBDBM50324535(CHEMBL1215519 | CHEMBL1229308 | 3-{[9-(Dimethylami...)
Affinity DataIC50: 1.00E+3nMAssay Description:Inhibition of KDM4CMore data for this Ligand-Target Pair
In Depth
Date in BDB:
7/22/2012
Entry Details Article
PubMed
TargetLysine-specific demethylase 4A(Human)
Kyoto Prefectural University of Medicine

Curated by ChEMBL
LigandPNGBDBM50361473(CHEMBL1435274)
Affinity DataIC50: 1.70E+3nMAssay Description:Inhibition of KDM4AMore data for this Ligand-Target Pair
In Depth
Date in BDB:
7/22/2012
Entry Details Article
PubMedPDB3D3D Structure (crystal)
TargetProlyl hydroxylase EGLN2(Human)
Kyoto Prefectural University of Medicine

Curated by ChEMBL
LigandPNGBDBM26106(CHEMBL90852 | Oxalylglycine | [(carboxymethyl)carb...)
Affinity DataIC50: 2.10E+3nMAssay Description:Inhibition of PHD1More data for this Ligand-Target Pair
In Depth
Date in BDB:
7/22/2012
Entry Details Article
PubMed
TargetLysine-specific demethylase 4A(Human)
Kyoto Prefectural University of Medicine

Curated by ChEMBL
LigandPNGBDBM50324535(CHEMBL1215519 | CHEMBL1229308 | 3-{[9-(Dimethylami...)
Affinity DataIC50: 3.00E+3nMAssay Description:Inhibition of KDM4AMore data for this Ligand-Target Pair
In Depth
Date in BDB:
7/22/2012
Entry Details Article
PubMed
TargetLysine-specific demethylase 4A(Human)
Kyoto Prefectural University of Medicine

Curated by ChEMBL
LigandPNGBDBM50361476(CHEMBL583959)
Affinity DataIC50: 3.30E+3nMAssay Description:Inhibition of KDM4AMore data for this Ligand-Target Pair
In Depth
Date in BDB:
7/22/2012
Entry Details Article
PubMed
TargetLysine-specific demethylase 4C(Human)
Kyoto Prefectural University of Medicine

Curated by ChEMBL
LigandPNGBDBM50361475(CHEMBL1938900)
Affinity DataIC50: 3.40E+3nMAssay Description:Inhibition of KDM4CMore data for this Ligand-Target Pair
In Depth
Date in BDB:
7/22/2012
Entry Details Article
PubMed
TargetLysine-specific demethylase 4A(Human)
Kyoto Prefectural University of Medicine

Curated by ChEMBL
LigandPNGBDBM50361475(CHEMBL1938900)
Affinity DataIC50: 4.30E+3nMAssay Description:Inhibition of KDM4AMore data for this Ligand-Target Pair
In Depth
Date in BDB:
7/22/2012
Entry Details Article
PubMed
TargetLysine-specific histone demethylase 1A(Human)
Kyoto Prefectural University of Medicine

Curated by ChEMBL
LigandPNGBDBM50361470(CHEMBL226102)
Affinity DataIC50: 5.00E+3nMAssay Description:Inhibition of LSD1More data for this Ligand-Target Pair
In Depth
Date in BDB:
7/22/2012
Entry Details Article
PubMed
TargetEgl nine homolog 1(Human)
Kyoto Prefectural University of Medicine

Curated by ChEMBL
LigandPNGBDBM26106(CHEMBL90852 | Oxalylglycine | [(carboxymethyl)carb...)
Affinity DataIC50: 6.20E+3nMAssay Description:Inhibition of PHD2More data for this Ligand-Target Pair
In Depth
Date in BDB:
7/22/2012
Entry Details Article
PubMedPDB3D3D Structure (crystal)
TargetHistone lysine demethylase PHF8(Human)
Kyoto Prefectural University of Medicine

Curated by ChEMBL
LigandPNGBDBM50361475(CHEMBL1938900)
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of KDM7BMore data for this Ligand-Target Pair
In Depth
Date in BDB:
7/22/2012
Entry Details Article
PubMed
TargetLysine-specific demethylase 4A(Human)
Kyoto Prefectural University of Medicine

Curated by ChEMBL
LigandPNGBDBM50306580((R)-3-(4-(4-bromophenylsulfonyloxy)phenyl)-2-(carb...)
Affinity DataIC50: 1.20E+4nMAssay Description:Inhibition of KDM4AMore data for this Ligand-Target Pair
In Depth
Date in BDB:
7/22/2012
Entry Details Article
PubMed
TargetEgl nine homolog 1(Human)
Kyoto Prefectural University of Medicine

Curated by ChEMBL
LigandPNGBDBM50361473(CHEMBL1435274)
Affinity DataIC50: 1.40E+4nMAssay Description:Inhibition of PHD2More data for this Ligand-Target Pair
In Depth
Date in BDB:
7/22/2012
Entry Details Article
PubMed
TargetHypoxia-inducible factor 1-alpha inhibitor(Human)
Kyoto Prefectural University of Medicine

Curated by ChEMBL
LigandPNGBDBM50361473(CHEMBL1435274)
Affinity DataIC50: 2.10E+4nMAssay Description:Inhibition of FIHMore data for this Ligand-Target Pair
In Depth
Date in BDB:
7/22/2012
Entry Details Article
PubMed
TargetHypoxia-inducible factor 1-alpha inhibitor(Human)
Kyoto Prefectural University of Medicine

Curated by ChEMBL
LigandPNGBDBM50361475(CHEMBL1938900)
Affinity DataIC50: 2.20E+4nMAssay Description:Inhibition of FIHMore data for this Ligand-Target Pair
In Depth
Date in BDB:
7/22/2012
Entry Details Article
PubMed
TargetLysine-specific demethylase 4A(Human)
Kyoto Prefectural University of Medicine

Curated by ChEMBL
LigandPNGBDBM50361471(CHEMBL1614745)
Affinity DataIC50: 2.40E+4nMAssay Description:Inhibition of KDM4AMore data for this Ligand-Target Pair
In Depth
Date in BDB:
7/22/2012
Entry Details Article
PubMed
TargetLysine-specific demethylase 3A(Human)
Kyoto Prefectural University of Medicine

Curated by ChEMBL
LigandPNGBDBM50361477(CHEMBL56175)
Affinity DataIC50: 2.50E+4nMAssay Description:Inhibition of KDM3AMore data for this Ligand-Target Pair
In Depth
Date in BDB:
7/22/2012
Entry Details Article
PubMed
TargetLysine-specific demethylase 4A(Human)
Kyoto Prefectural University of Medicine

Curated by ChEMBL
LigandPNGBDBM50344962((2S)-2-HYDROXYPENTANEDIOIC ACID | L-2-Hydroxygluta...)
Affinity DataIC50: 2.60E+4nMAssay Description:Inhibition of KDM4AMore data for this Ligand-Target Pair
In Depth
Date in BDB:
7/22/2012
Entry Details Article
PubMed
TargetProlyl hydroxylase EGLN3(Human)
Kyoto Prefectural University of Medicine

Curated by ChEMBL
LigandPNGBDBM50361475(CHEMBL1938900)
Affinity DataIC50: 3.10E+4nMAssay Description:Inhibition of PHD3More data for this Ligand-Target Pair
In Depth
Date in BDB:
7/22/2012
Entry Details Article
PubMed
TargetLysine-specific demethylase 6B(Human)
Kyoto Prefectural University of Medicine

Curated by ChEMBL
LigandPNGBDBM50361475(CHEMBL1938900)
Affinity DataIC50: 4.30E+4nMAssay Description:Inhibition of KDM6BMore data for this Ligand-Target Pair
In Depth
Date in BDB:
7/22/2012
Entry Details Article
PubMed
TargetLysine-specific demethylase 2A(Human)
Kyoto Prefectural University of Medicine

Curated by ChEMBL
LigandPNGBDBM50344962((2S)-2-HYDROXYPENTANEDIOIC ACID | L-2-Hydroxygluta...)
Affinity DataIC50: 4.80E+4nMAssay Description:Inhibition of KDM2AMore data for this Ligand-Target Pair
In Depth
Date in BDB:
7/22/2012
Entry Details Article
PubMed
TargetProlyl hydroxylase EGLN2(Human)
Kyoto Prefectural University of Medicine

Curated by ChEMBL
LigandPNGBDBM50361475(CHEMBL1938900)
Affinity DataIC50: 5.40E+4nMAssay Description:Inhibition of PHD1More data for this Ligand-Target Pair
In Depth
Date in BDB:
7/22/2012
Entry Details Article
PubMed
TargetLysine-specific demethylase 4C(Human)
Kyoto Prefectural University of Medicine

Curated by ChEMBL
LigandPNGBDBM50361471(CHEMBL1614745)
Affinity DataIC50: 7.90E+4nMAssay Description:Inhibition of KDM4CMore data for this Ligand-Target Pair
In Depth
Date in BDB:
7/22/2012
Entry Details Article
PubMed
TargetEgl nine homolog 1(Human)
Kyoto Prefectural University of Medicine

Curated by ChEMBL
LigandPNGBDBM50361475(CHEMBL1938900)
Affinity DataIC50: 8.30E+4nMAssay Description:Inhibition of PHD2More data for this Ligand-Target Pair
In Depth
Date in BDB:
7/22/2012
Entry Details Article
PubMed
TargetLysine-specific demethylase 4C(Human)
Kyoto Prefectural University of Medicine

Curated by ChEMBL
LigandPNGBDBM50344962((2S)-2-HYDROXYPENTANEDIOIC ACID | L-2-Hydroxygluta...)
Affinity DataIC50: 9.70E+4nMAssay Description:Inhibition of KDM4CMore data for this Ligand-Target Pair
In Depth
Date in BDB:
7/22/2012
Entry Details Article
PubMed
TargetEgl nine homolog 1(Human)
Kyoto Prefectural University of Medicine

Curated by ChEMBL
LigandPNGBDBM50324535(CHEMBL1215519 | CHEMBL1229308 | 3-{[9-(Dimethylami...)
Affinity DataIC50: 1.00E+5nMAssay Description:Inhibition of PHD2More data for this Ligand-Target Pair
In Depth
Date in BDB:
7/22/2012
Entry Details Article
PubMed
TargetProlyl hydroxylase EGLN2(Human)
Kyoto Prefectural University of Medicine

Curated by ChEMBL
LigandPNGBDBM50324535(CHEMBL1215519 | CHEMBL1229308 | 3-{[9-(Dimethylami...)
Affinity DataIC50: 1.00E+5nMAssay Description:Inhibition of PHD1More data for this Ligand-Target Pair
In Depth
Date in BDB:
7/22/2012
Entry Details Article
PubMed
TargetLysine-specific demethylase 2A(Human)
Kyoto Prefectural University of Medicine

Curated by ChEMBL
LigandPNGBDBM50361471(CHEMBL1614745)
Affinity DataIC50: 1.06E+5nMAssay Description:Inhibition of KDM2AMore data for this Ligand-Target Pair
In Depth
Date in BDB:
7/22/2012
Entry Details Article
PubMed
TargetLysine-specific demethylase 4A(Human)
Kyoto Prefectural University of Medicine

Curated by ChEMBL
LigandPNGBDBM26106(CHEMBL90852 | Oxalylglycine | [(carboxymethyl)carb...)
Affinity DataIC50: 2.50E+5nMAssay Description:Inhibition of KDM4AMore data for this Ligand-Target Pair
In Depth
Date in BDB:
7/22/2012
Entry Details Article
PubMedPDB3D3D Structure (crystal)
TargetEgl nine homolog 1(Human)
Kyoto Prefectural University of Medicine

Curated by ChEMBL
LigandPNGBDBM50361472(CHEMBL1938896)
Affinity DataIC50: 4.00E+5nMAssay Description:Inhibition of PHD2More data for this Ligand-Target Pair
In Depth
Date in BDB:
7/22/2012
Entry Details Article
PubMed
TargetLysine-specific demethylase 4C(Human)
Kyoto Prefectural University of Medicine

Curated by ChEMBL
LigandPNGBDBM26106(CHEMBL90852 | Oxalylglycine | [(carboxymethyl)carb...)
Affinity DataIC50: 5.00E+5nMAssay Description:Inhibition of KDM4CMore data for this Ligand-Target Pair
In Depth
Date in BDB:
7/22/2012
Entry Details Article
PubMedPDB3D3D Structure (crystal)
TargetLysine-specific histone demethylase 1A(Human)
Kyoto Prefectural University of Medicine

Curated by ChEMBL
LigandPNGBDBM50346873(CHEMBL1797652)
Affinity DataKi:  4.40nMAssay Description:Inhibition of LSD1More data for this Ligand-Target Pair
In Depth
Date in BDB:
7/22/2012
Entry Details Article
PubMed
TargetLysine-specific histone demethylase 1A(Human)
Kyoto Prefectural University of Medicine

Curated by ChEMBL
LigandPNGBDBM50361478(CHEMBL1938897)
Affinity DataKi:  5nMAssay Description:Inhibition of LSD1More data for this Ligand-Target Pair
In Depth
Date in BDB:
7/22/2012
Entry Details Article
PubMed
TargetLysine-specific histone demethylase 1A(Human)
Kyoto Prefectural University of Medicine

Curated by ChEMBL
LigandPNGBDBM50361481(CHEMBL1938898)
Affinity DataKi:  9nMAssay Description:Inhibition of LSD1More data for this Ligand-Target Pair
In Depth
Date in BDB:
7/22/2012
Entry Details Article
PubMed
TargetLysine-specific histone demethylase 1A(Human)
Kyoto Prefectural University of Medicine

Curated by ChEMBL
LigandPNGBDBM50346875(CHEMBL1797648)
Affinity DataKi:  107nMAssay Description:Inhibition of LSD1More data for this Ligand-Target Pair
In Depth
Date in BDB:
7/22/2012
Entry Details Article
PubMed
TargetLysine-specific histone demethylase 1A(Human)
Kyoto Prefectural University of Medicine

Curated by ChEMBL
LigandPNGBDBM50346585(CHEMBL1795980 | S2101)
Affinity DataKi:  610nMAssay Description:Inhibition of LSD1More data for this Ligand-Target Pair
In Depth
Date in BDB:
7/22/2012
Entry Details Article
PubMed
TargetAmine oxidase [flavin-containing] A(Human)
Kyoto Prefectural University of Medicine

Curated by ChEMBL
LigandPNGBDBM50346864(CHEMBL1797641 | CHEMBL3104337 | US8765820, 8)
Affinity DataKi:  1.20E+3nMAssay Description:Inhibition of MAO AMore data for this Ligand-Target Pair
In Depth
Date in BDB:
7/22/2012
Entry Details Article
PubMed
TargetLysine-specific histone demethylase 1A(Human)
Kyoto Prefectural University of Medicine

Curated by ChEMBL
LigandPNGBDBM50346864(CHEMBL1797641 | CHEMBL3104337 | US8765820, 8)
Affinity DataKi:  1.30E+3nMAssay Description:Inhibition of LSD1More data for this Ligand-Target Pair
In Depth
Date in BDB:
7/22/2012
Entry Details Article
PubMed
TargetLysine-specific histone demethylase 1A(Human)
Kyoto Prefectural University of Medicine

Curated by ChEMBL
LigandPNGBDBM50346862(CHEMBL1215658)
Affinity DataKi:  3.10E+3nMAssay Description:Inhibition of LSD1More data for this Ligand-Target Pair
In Depth
Date in BDB:
7/22/2012
Entry Details Article
PubMed
TargetLysine-specific histone demethylase 1A(Human)
Kyoto Prefectural University of Medicine

Curated by ChEMBL
LigandPNGBDBM50346589(CHEMBL255520 | CHEMBL1795974)
Affinity DataKi:  3.70E+3nMAssay Description:Inhibition of LSD1More data for this Ligand-Target Pair
In Depth
Date in BDB:
7/22/2012
Entry Details Article
PubMed
TargetLysine-specific histone demethylase 1A(Human)
Kyoto Prefectural University of Medicine

Curated by ChEMBL
LigandPNGBDBM50346534(CHEMBL1797705)
Affinity DataKi:  5.70E+3nMAssay Description:Inhibition of LSD1More data for this Ligand-Target Pair
In Depth
Date in BDB:
7/22/2012
Entry Details Article
PubMed
TargetAmine oxidase [flavin-containing] B(Human)
Kyoto Prefectural University of Medicine

Curated by ChEMBL
LigandPNGBDBM50361478(CHEMBL1938897)
Affinity DataKi:  7.40E+3nMAssay Description:Inhibition of MAO BMore data for this Ligand-Target Pair
In Depth
Date in BDB:
7/22/2012
Entry Details Article
PubMed
TargetAmine oxidase [flavin-containing] A(Human)
Kyoto Prefectural University of Medicine

Curated by ChEMBL
LigandPNGBDBM50361481(CHEMBL1938898)
Affinity DataKi:  1.50E+4nMAssay Description:Inhibition of MAO AMore data for this Ligand-Target Pair
In Depth
Date in BDB:
7/22/2012
Entry Details Article
PubMed
TargetAmine oxidase [flavin-containing] B(Human)
Kyoto Prefectural University of Medicine

Curated by ChEMBL
LigandPNGBDBM50236898((1S,2R)-(+)-2-phenylcyclopropylamine | trans-2-phe...)
Affinity DataKi:  1.60E+4nMAssay Description:Inhibition of MAO BMore data for this Ligand-Target Pair
In Depth
Date in BDB:
7/22/2012
Entry Details Article
PubMed
TargetAmine oxidase [flavin-containing] A(Human)
Kyoto Prefectural University of Medicine

Curated by ChEMBL
LigandPNGBDBM50361478(CHEMBL1938897)
Affinity DataKi:  1.60E+4nMAssay Description:Inhibition of MAO AMore data for this Ligand-Target Pair
In Depth
Date in BDB:
7/22/2012
Entry Details Article
PubMed
TargetAmine oxidase [flavin-containing] B(Human)
Kyoto Prefectural University of Medicine

Curated by ChEMBL
LigandPNGBDBM50346585(CHEMBL1795980 | S2101)
Affinity DataKi:  1.70E+4nMAssay Description:Inhibition of MAO BMore data for this Ligand-Target Pair
In Depth
Date in BDB:
7/22/2012
Entry Details Article
PubMed
TargetLysine-specific histone demethylase 1A(Human)
Kyoto Prefectural University of Medicine

Curated by ChEMBL
LigandPNGBDBM50105417(CHEMBL1089 | Nardil | Phenethyl-hydrazine | PHENEL...)
Affinity DataKi:  1.80E+4nMAssay Description:Inhibition of LSD1More data for this Ligand-Target Pair
In Depth
Date in BDB:
7/22/2012
Entry Details Article
PubMed
TargetAmine oxidase [flavin-containing] B(Human)
Kyoto Prefectural University of Medicine

Curated by ChEMBL
LigandPNGBDBM50361479(CHEMBL1938899)
Affinity DataKi:  2.10E+4nMAssay Description:Inhibition of MAO BMore data for this Ligand-Target Pair
In Depth
Date in BDB:
7/22/2012
Entry Details Article
PubMed
TargetLysine-specific histone demethylase 2(Human)
Kyoto Prefectural University of Medicine

Curated by ChEMBL
LigandPNGBDBM50346864(CHEMBL1797641 | CHEMBL3104337 | US8765820, 8)
Affinity DataKi:  3.80E+4nMAssay Description:Inhibition of LSD2More data for this Ligand-Target Pair
In Depth
Date in BDB:
7/22/2012
Entry Details Article
PubMed
TargetAmine oxidase [flavin-containing] B(Human)
Kyoto Prefectural University of Medicine

Curated by ChEMBL
LigandPNGBDBM50361481(CHEMBL1938898)
Affinity DataKi: >4.00E+4nMAssay Description:Inhibition of MAO BMore data for this Ligand-Target Pair
In Depth
Date in BDB:
7/22/2012
Entry Details Article
PubMed
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