Compile Data Set for Download or QSAR
Report error Found 19 Enz. Inhib. hit(s) with all data for entry = 3074
LigandChemical structure of BindingDB Monomer ID 27642BDBM27642(1-(5-{[(2S)-2-aminopropanamido]methyl}thiophen-3-y...)
Affinity DataIC50: 60nMpH: 9.0 T: 2°CAssay Description:Histone H3 is used as the substrate for CARM-1 enzyme, and the methylation is monitored using tritiated S-Adenosyl-Methionine (SAM) as a methyl donor...More data for this Ligand-Target Pair
In Depth
Date in BDB:
3/25/2009
Entry Details Article
PubMed
LigandChemical structure of BindingDB Monomer ID 27641BDBM27641(1-(3-{[(2S)-2-aminopropanamido]methyl}phenyl)-N-[(...)
Affinity DataIC50: 60nMpH: 9.0 T: 2°CAssay Description:Histone H3 is used as the substrate for CARM-1 enzyme, and the methylation is monitored using tritiated S-Adenosyl-Methionine (SAM) as a methyl donor...More data for this Ligand-Target Pair
In Depth
Date in BDB:
3/25/2009
Entry Details Article
PubMed
LigandChemical structure of BindingDB Monomer ID 27659BDBM27659(CHEMBL466658 | 1-(3-{[(2S)-2-aminopropanamido]meth...)
Affinity DataIC50: 80nMpH: 9.0 T: 2°CAssay Description:Histone H3 is used as the substrate for CARM-1 enzyme, and the methylation is monitored using tritiated S-Adenosyl-Methionine (SAM) as a methyl donor...More data for this Ligand-Target Pair
In Depth
Date in BDB:
3/25/2009
Entry Details Article
PubMed
LigandChemical structure of BindingDB Monomer ID 27650BDBM27650(1-(5-{[(2S)-2-aminopropanamido]methyl}thiophen-3-y...)
Affinity DataIC50: 220nMpH: 9.0 T: 2°CAssay Description:Histone H3 is used as the substrate for CARM-1 enzyme, and the methylation is monitored using tritiated S-Adenosyl-Methionine (SAM) as a methyl donor...More data for this Ligand-Target Pair
In Depth
Date in BDB:
3/25/2009
Entry Details Article
PubMed
LigandChemical structure of BindingDB Monomer ID 27655BDBM27655(1-(5-{[(2S)-2-aminopropanamido]methyl}thiophen-2-y...)
Affinity DataIC50: 230nMpH: 9.0 T: 2°CAssay Description:Histone H3 is used as the substrate for CARM-1 enzyme, and the methylation is monitored using tritiated S-Adenosyl-Methionine (SAM) as a methyl donor...More data for this Ligand-Target Pair
In Depth
Date in BDB:
3/25/2009
Entry Details Article
PubMed
LigandChemical structure of BindingDB Monomer ID 27651BDBM27651(1-(5-{[(2S)-2-aminopropanamido]methyl}thiophen-3-y...)
Affinity DataIC50: 260nMpH: 9.0 T: 2°CAssay Description:Histone H3 is used as the substrate for CARM-1 enzyme, and the methylation is monitored using tritiated S-Adenosyl-Methionine (SAM) as a methyl donor...More data for this Ligand-Target Pair
In Depth
Date in BDB:
3/25/2009
Entry Details Article
PubMed
LigandChemical structure of BindingDB Monomer ID 27643BDBM27643(1-(5-{[(2S)-2-aminopropanamido]methyl}thiophen-2-y...)
Affinity DataIC50: 300nMpH: 9.0 T: 2°CAssay Description:Histone H3 is used as the substrate for CARM-1 enzyme, and the methylation is monitored using tritiated S-Adenosyl-Methionine (SAM) as a methyl donor...More data for this Ligand-Target Pair
In Depth
Date in BDB:
3/25/2009
Entry Details Article
PubMed
LigandChemical structure of BindingDB Monomer ID 27652BDBM27652(1-(5-{[(2S)-2-aminopropanamido]methyl}thiophen-3-y...)
Affinity DataIC50: 370nMpH: 9.0 T: 2°CAssay Description:Histone H3 is used as the substrate for CARM-1 enzyme, and the methylation is monitored using tritiated S-Adenosyl-Methionine (SAM) as a methyl donor...More data for this Ligand-Target Pair
In Depth
Date in BDB:
3/25/2009
Entry Details Article
PubMed
LigandChemical structure of BindingDB Monomer ID 27653BDBM27653(methyl 2-({[1-(5-{[(2S)-2-aminopropanamido]methyl}...)
Affinity DataIC50: 770nMpH: 9.0 T: 2°CAssay Description:Histone H3 is used as the substrate for CARM-1 enzyme, and the methylation is monitored using tritiated S-Adenosyl-Methionine (SAM) as a methyl donor...More data for this Ligand-Target Pair
In Depth
Date in BDB:
3/25/2009
Entry Details Article
PubMed
LigandChemical structure of BindingDB Monomer ID 27649BDBM27649(1-(5-{[(2S)-2-aminopropanamido]methyl}thiophen-3-y...)
Affinity DataIC50: 790nMpH: 9.0 T: 2°CAssay Description:Histone H3 is used as the substrate for CARM-1 enzyme, and the methylation is monitored using tritiated S-Adenosyl-Methionine (SAM) as a methyl donor...More data for this Ligand-Target Pair
In Depth
Date in BDB:
3/25/2009
Entry Details Article
PubMed
LigandChemical structure of BindingDB Monomer ID 27644BDBM27644(1-(4-{[(2S)-2-aminopropanamido]methyl}-1,3-thiazol...)
Affinity DataIC50: 2.20E+3nMpH: 9.0 T: 2°CAssay Description:Histone H3 is used as the substrate for CARM-1 enzyme, and the methylation is monitored using tritiated S-Adenosyl-Methionine (SAM) as a methyl donor...More data for this Ligand-Target Pair
In Depth
Date in BDB:
3/25/2009
Entry Details Article
PubMed
LigandChemical structure of BindingDB Monomer ID 27654BDBM27654(1-(5-{[(2S)-2-aminopropanamido]methyl}thiophen-2-y...)
Affinity DataIC50: 2.31E+3nMpH: 9.0 T: 2°CAssay Description:Histone H3 is used as the substrate for CARM-1 enzyme, and the methylation is monitored using tritiated S-Adenosyl-Methionine (SAM) as a methyl donor...More data for this Ligand-Target Pair
In Depth
Date in BDB:
3/25/2009
Entry Details Article
PubMed
LigandChemical structure of BindingDB Monomer ID 27657BDBM27657(1-(5-{[(2S)-2-aminopropanamido]methyl}thiophen-2-y...)
Affinity DataIC50: 2.92E+3nMpH: 9.0 T: 2°CAssay Description:Histone H3 is used as the substrate for CARM-1 enzyme, and the methylation is monitored using tritiated S-Adenosyl-Methionine (SAM) as a methyl donor...More data for this Ligand-Target Pair
In Depth
Date in BDB:
3/25/2009
Entry Details Article
PubMed
LigandChemical structure of BindingDB Monomer ID 27646BDBM27646(1-(6-{[(2S)-2-aminopropanamido]methyl}pyridin-2-yl...)
Affinity DataIC50: 3.05E+3nMpH: 9.0 T: 2°CAssay Description:Histone H3 is used as the substrate for CARM-1 enzyme, and the methylation is monitored using tritiated S-Adenosyl-Methionine (SAM) as a methyl donor...More data for this Ligand-Target Pair
In Depth
Date in BDB:
3/25/2009
Entry Details Article
PubMed
LigandChemical structure of BindingDB Monomer ID 27658BDBM27658(1-(5-{[(2S)-2-aminopropanamido]methyl}thiophen-3-y...)
Affinity DataIC50: 3.35E+3nMpH: 9.0 T: 2°CAssay Description:Histone H3 is used as the substrate for CARM-1 enzyme, and the methylation is monitored using tritiated S-Adenosyl-Methionine (SAM) as a methyl donor...More data for this Ligand-Target Pair
In Depth
Date in BDB:
3/25/2009
Entry Details Article
PubMed
LigandChemical structure of BindingDB Monomer ID 27645BDBM27645(1-(4-{[(2S)-2-aminopropanamido]methyl}pyridin-2-yl...)
Affinity DataIC50: 4.20E+3nMpH: 9.0 T: 2°CAssay Description:Histone H3 is used as the substrate for CARM-1 enzyme, and the methylation is monitored using tritiated S-Adenosyl-Methionine (SAM) as a methyl donor...More data for this Ligand-Target Pair
In Depth
Date in BDB:
3/25/2009
Entry Details Article
PubMed
LigandChemical structure of BindingDB Monomer ID 27656BDBM27656(1-(5-{[(2S)-2-aminopropanamido]methyl}thiophen-2-y...)
Affinity DataIC50: 4.48E+3nMpH: 9.0 T: 2°CAssay Description:Histone H3 is used as the substrate for CARM-1 enzyme, and the methylation is monitored using tritiated S-Adenosyl-Methionine (SAM) as a methyl donor...More data for this Ligand-Target Pair
In Depth
Date in BDB:
3/25/2009
Entry Details Article
PubMed
LigandChemical structure of BindingDB Monomer ID 27647BDBM27647(1-{2-[(2S)-2-aminopropanoyl]-2,3-dihydro-1H-isoind...)
Affinity DataIC50: 1.00E+4nMpH: 9.0 T: 2°CAssay Description:Histone H3 is used as the substrate for CARM-1 enzyme, and the methylation is monitored using tritiated S-Adenosyl-Methionine (SAM) as a methyl donor...More data for this Ligand-Target Pair
In Depth
Date in BDB:
3/25/2009
Entry Details Article
PubMed
LigandChemical structure of BindingDB Monomer ID 27648BDBM27648(1-(2-{[(2S)-2-aminopropanamido]methyl}-1-benzofura...)
Affinity DataIC50: 1.00E+4nMpH: 9.0 T: 2°CAssay Description:Histone H3 is used as the substrate for CARM-1 enzyme, and the methylation is monitored using tritiated S-Adenosyl-Methionine (SAM) as a methyl donor...More data for this Ligand-Target Pair
In Depth
Date in BDB:
3/25/2009
Entry Details Article
PubMed