Compile Data Set for Download or QSAR
Report error Found 49 Enz. Inhib. hit(s) with all data for entry = 50000960
TargetTyrosine-protein kinase Lck(Human)
Purdue University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50011418BDBM50011418(2-(4-aminophenyl)-6-hydroxy-4H-chromen-4-one | 2-(...)
Affinity DataIC50: 1.20E+3nMAssay Description:Ability to inhibit protein-tyrosine kinase activity of p56lck (isolated from bovine thymus) in vitro.More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetTyrosine-protein kinase Lck(Human)
Purdue University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50011429BDBM50011429(CHEMBL167154 | 2-(4-Amino-phenyl)-5,7-dihydroxy-ch...)
Affinity DataIC50: 7.40E+3nMAssay Description:Ability to inhibit protein-tyrosine kinase activity of p56lck (isolated from bovine thymus) in vitro.More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetTyrosine-protein kinase Lck(Human)
Purdue University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 7460BDBM7460(2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-chromone;...)
Affinity DataIC50: 1.30E+4nMAssay Description:Ability to inhibit protein-tyrosine kinase activity of p56lck (isolated from bovine thymus) in vitro.More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetTyrosine-protein kinase Lck(Human)
Purdue University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50011424BDBM50011424(3',5'-dimethoxy-4'-hydroxyflavone | 2-(4-Hydroxy-3...)
Affinity DataIC50: 2.60E+4nMAssay Description:Ability to inhibit protein-tyrosine kinase activity of p56lck (isolated from bovine thymus) in vitro.More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetTyrosine-protein kinase Lck(Human)
Purdue University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50011438BDBM50011438(7-Hydroxy-flavone, 6 | 2-(4-aminophenyl)-7-hydroxy...)
Affinity DataIC50: 1.38E+5nMAssay Description:Ability to inhibit protein-tyrosine kinase activity of p56lck (isolated from bovine thymus) in vitro.More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetTyrosine-protein kinase Lck(Human)
Purdue University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50011437BDBM50011437(2-(4-aminophenyl)-4H-chromen-4-one | CHEMBL352730 ...)
Affinity DataIC50: 2.10E+5nMAssay Description:Ability to inhibit protein-tyrosine kinase activity of p56lck (isolated from bovine thymus) in vitro.More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetTyrosine-protein kinase Lck(Human)
Purdue University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50011455BDBM50011455(CHEMBL353803 | 2-(4-Hydroxy-phenyl)-4-oxo-4H-chrom...)
Affinity DataIC50: 4.39E+5nMAssay Description:Ability to inhibit protein-tyrosine kinase activity of p56lck (isolated from bovine thymus) in vitro.More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetTyrosine-protein kinase Lck(Human)
Purdue University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50011446BDBM50011446(NSC-22357 | 4'-hydroxyflavone | 2-(4-hydroxyphenyl...)
Affinity DataIC50: 5.04E+5nMAssay Description:Ability to inhibit protein-tyrosine kinase activity of p56lck (isolated from bovine thymus) in vitro.More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetTyrosine-protein kinase Lck(Human)
Purdue University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50011416BDBM50011416(CHEMBL424196 | methyl 2-(4-aminophenyl)-4-oxo-4H-c...)
Affinity DataIC50: 8.10E+5nMAssay Description:Ability to inhibit protein-tyrosine kinase activity of p56lck (isolated from bovine thymus) in vitro.More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetTyrosine-protein kinase Lck(Human)
Purdue University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50011422BDBM50011422(CHEMBL167536 | 2-(4-Hydroxy-phenyl)-7-methoxy-4-ox...)
Affinity DataIC50: 1.03E+6nMAssay Description:Ability to inhibit protein-tyrosine kinase activity of p56lck (isolated from bovine thymus) in vitro.More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetTyrosine-protein kinase Lck(Human)
Purdue University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50011451BDBM50011451(CHEMBL166051 | 3-(2-Hydroxy-4-methoxy-phenyl)-3-ox...)
Affinity DataIC50: 1.16E+6nMAssay Description:Ability to inhibit protein-tyrosine kinase activity of p56lck (isolated from bovine thymus) in vitro.More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetTyrosine-protein kinase Lck(Human)
Purdue University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50011458BDBM50011458(CHEMBL167555 | 2-(4-Hydroxy-phenyl)-4-oxo-4H-chrom...)
Affinity DataIC50: 1.60E+6nMAssay Description:Ability to inhibit protein-tyrosine kinase activity of p56lck (isolated from bovine thymus) in vitro.More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetTyrosine-protein kinase Lck(Human)
Purdue University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50011439BDBM50011439(CHEMBL351392 | 2-(3,5-dimethoxyphenyl)-4-oxo-4H-ch...)
Affinity DataIC50: 2.00E+6nMAssay Description:Ability to inhibit protein-tyrosine kinase activity of p56lck (isolated from bovine thymus) in vitro.More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetTyrosine-protein kinase Lck(Human)
Purdue University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50011435BDBM50011435(CHEMBL355621 | 3-(2-Hydroxy-5-methoxy-phenyl)-3-ox...)
Affinity DataIC50: 2.00E+6nMAssay Description:Ability to inhibit protein-tyrosine kinase activity of p56lck (isolated from bovine thymus) in vitro.More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetTyrosine-protein kinase Lck(Human)
Purdue University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50011436BDBM50011436(CHEMBL167834 | 5,7-Dihydroxy-2-(4-nitro-phenyl)-4-...)
Affinity DataIC50: 2.00E+6nMAssay Description:Ability to inhibit protein-tyrosine kinase activity of p56lck (isolated from bovine thymus) in vitro.More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetTyrosine-protein kinase Lck(Human)
Purdue University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50011441BDBM50011441(2-(4-methoxyphenyl)-4-oxo-4H-chromene-3-carboxylic...)
Affinity DataIC50: 2.00E+6nMAssay Description:Ability to inhibit protein-tyrosine kinase activity of p56lck (isolated from bovine thymus) in vitro.More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetTyrosine-protein kinase Lck(Human)
Purdue University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50011440BDBM50011440(2-(4-nitrophenyl)-4-oxo-4H-chromene-3-carboxylic a...)
Affinity DataIC50: 2.00E+6nMAssay Description:Ability to inhibit protein-tyrosine kinase activity of p56lck (isolated from bovine thymus) in vitro.More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetTyrosine-protein kinase Lck(Human)
Purdue University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50011431BDBM50011431(CHEMBL167234 | 2-(4-Acetylamino-phenyl)-6-methoxy-...)
Affinity DataIC50: 2.00E+6nMAssay Description:Ability to inhibit protein-tyrosine kinase activity of p56lck (isolated from bovine thymus) in vitro.More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetTyrosine-protein kinase Lck(Human)
Purdue University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50011428BDBM50011428(CHEMBL307856 | 2-(3,4,5-Trimethoxy-phenyl)-chromen...)
Affinity DataIC50: 2.00E+6nMAssay Description:Ability to inhibit protein-tyrosine kinase activity of p56lck (isolated from bovine thymus) in vitro.More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetTyrosine-protein kinase Lck(Human)
Purdue University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50011427BDBM50011427(CHEMBL167787 | 7-Hydroxy-2-(4-nitro-phenyl)-chrome...)
Affinity DataIC50: 2.00E+6nMAssay Description:Ability to inhibit protein-tyrosine kinase activity of p56lck (isolated from bovine thymus) in vitro.More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetTyrosine-protein kinase Lck(Human)
Purdue University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50011434BDBM50011434(CHEMBL166960 | methyl 2-(4-bromophenyl)-4-oxo-4H-c...)
Affinity DataIC50: 2.00E+6nMAssay Description:Ability to inhibit protein-tyrosine kinase activity of p56lck (isolated from bovine thymus) in vitro.More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetTyrosine-protein kinase Lck(Human)
Purdue University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50011433BDBM50011433(CHEMBL166888 | 3-(2,4-Bis-benzyloxy-6-hydroxy-phen...)
Affinity DataIC50: 2.00E+6nMAssay Description:Ability to inhibit protein-tyrosine kinase activity of p56lck (isolated from bovine thymus) in vitro.More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetTyrosine-protein kinase Lck(Human)
Purdue University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50011432BDBM50011432(2-(3,4-Dimethoxy-phenyl)-4-oxo-4H-chromene-3-carbo...)
Affinity DataIC50: 2.00E+6nMAssay Description:Ability to inhibit protein-tyrosine kinase activity of p56lck (isolated from bovine thymus) in vitro.More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetTyrosine-protein kinase Lck(Human)
Purdue University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50011430BDBM50011430(CHEMBL167940 | 4-oxo-2-(3,4,5-trimethoxyphenyl)-4H...)
Affinity DataIC50: 2.00E+6nMAssay Description:Ability to inhibit protein-tyrosine kinase activity of p56lck (isolated from bovine thymus) in vitro.More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetTyrosine-protein kinase Lck(Human)
Purdue University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50011421BDBM50011421(CHEMBL64780 | 2-(4-Nitro-phenyl)-chromen-4-one)
Affinity DataIC50: 2.00E+6nMAssay Description:Ability to inhibit protein-tyrosine kinase activity of p56lck (isolated from bovine thymus) in vitro.More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetTyrosine-protein kinase Lck(Human)
Purdue University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50011417BDBM50011417(5,7-Dihydroxy-2-(4-nitro-phenyl)-chromen-4-one | C...)
Affinity DataIC50: 2.00E+6nMAssay Description:Ability to inhibit protein-tyrosine kinase activity of p56lck (isolated from bovine thymus) in vitro.More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetTyrosine-protein kinase Lck(Human)
Purdue University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50011426BDBM50011426(CHEMBL166523 | 2-(4-Hydroxy-phenyl)-7-methoxy-4-ox...)
Affinity DataIC50: 2.00E+6nMAssay Description:Ability to inhibit protein-tyrosine kinase activity of p56lck (isolated from bovine thymus) in vitro.More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetTyrosine-protein kinase Lck(Human)
Purdue University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50011425BDBM50011425(methyl 2-(3,4-dimethoxyphenyl)-4-oxo-4H-chromene-3...)
Affinity DataIC50: 2.00E+6nMAssay Description:Ability to inhibit protein-tyrosine kinase activity of p56lck (isolated from bovine thymus) in vitro.More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetTyrosine-protein kinase Lck(Human)
Purdue University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50011423BDBM50011423(CHEMBL352269 | 5,7-Bis-benzyloxy-2-(4-nitro-phenyl...)
Affinity DataIC50: 2.00E+6nMAssay Description:Ability to inhibit protein-tyrosine kinase activity of p56lck (isolated from bovine thymus) in vitro.More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetTyrosine-protein kinase Lck(Human)
Purdue University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50011420BDBM50011420(CHEMBL354254 | 7-Methoxy-2-(4-nitro-phenyl)-4-oxo-...)
Affinity DataIC50: 2.00E+6nMAssay Description:Ability to inhibit protein-tyrosine kinase activity of p56lck (isolated from bovine thymus) in vitro.More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetTyrosine-protein kinase Lck(Human)
Purdue University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50011419BDBM50011419(CHEMBL166682 | methyl 6-methoxy-2-(4-nitrophenyl)-...)
Affinity DataIC50: 2.00E+6nMAssay Description:Ability to inhibit protein-tyrosine kinase activity of p56lck (isolated from bovine thymus) in vitro.More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetTyrosine-protein kinase Lck(Human)
Purdue University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50011415BDBM50011415(CHEMBL167152 | 3-(2-Hydroxy-phenyl)-3-oxo-propioni...)
Affinity DataIC50: 2.00E+6nMAssay Description:Ability to inhibit protein-tyrosine kinase activity of p56lck (isolated from bovine thymus) in vitro.More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetTyrosine-protein kinase Lck(Human)
Purdue University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50011459BDBM50011459(CHEMBL167624 | 6-Methoxy-2-(4-nitro-phenyl)-4-oxo-...)
Affinity DataIC50: 2.00E+6nMAssay Description:Ability to inhibit protein-tyrosine kinase activity of p56lck (isolated from bovine thymus) in vitro.More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetTyrosine-protein kinase Lck(Human)
Purdue University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50011457BDBM50011457(CHEMBL166480 | 2-(4-Nitro-phenyl)-4-oxo-4H-chromen...)
Affinity DataIC50: 2.00E+6nMAssay Description:Ability to inhibit protein-tyrosine kinase activity of p56lck (isolated from bovine thymus) in vitro.More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetTyrosine-protein kinase Lck(Human)
Purdue University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50011462BDBM50011462(CHEMBL164977 | 3-(2,4-Bis-benzyloxy-6-hydroxy-phen...)
Affinity DataIC50: 2.00E+6nMAssay Description:Ability to inhibit protein-tyrosine kinase activity of p56lck (isolated from bovine thymus) in vitro.More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetTyrosine-protein kinase Lck(Human)
Purdue University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50011448BDBM50011448(CHEMBL354823 | 4-Oxo-2-[4-(3,4,5-trimethoxy-benzoy...)
Affinity DataIC50: 2.00E+6nMAssay Description:Ability to inhibit protein-tyrosine kinase activity of p56lck (isolated from bovine thymus) in vitro.More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetTyrosine-protein kinase Lck(Human)
Purdue University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50011449BDBM50011449(CHEMBL166749 | 3-(2-Hydroxy-phenyl)-3-oxo-propioni...)
Affinity DataIC50: 2.00E+6nMAssay Description:Ability to inhibit protein-tyrosine kinase activity of p56lck (isolated from bovine thymus) in vitro.More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetTyrosine-protein kinase Lck(Human)
Purdue University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50011447BDBM50011447(CHEMBL166383 | methyl 4-oxo-2-(3,4,5-trimethoxyphe...)
Affinity DataIC50: 2.00E+6nMAssay Description:Ability to inhibit protein-tyrosine kinase activity of p56lck (isolated from bovine thymus) in vitro.More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetTyrosine-protein kinase Lck(Human)
Purdue University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50011461BDBM50011461(CHEMBL168154 | methyl 2-(4-(benzyloxy)phenyl)-4-ox...)
Affinity DataIC50: 2.00E+6nMAssay Description:Ability to inhibit protein-tyrosine kinase activity of p56lck (isolated from bovine thymus) in vitro.More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetTyrosine-protein kinase Lck(Human)
Purdue University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50011460BDBM50011460(CHEMBL352715 | 2-(4-Acetylamino-phenyl)-7-methoxy-...)
Affinity DataIC50: 2.00E+6nMAssay Description:Ability to inhibit protein-tyrosine kinase activity of p56lck (isolated from bovine thymus) in vitro.More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetTyrosine-protein kinase Lck(Human)
Purdue University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50011456BDBM50011456(CHEMBL167298 | 2-(4-Hydroxy-phenyl)-6-methoxy-4-ox...)
Affinity DataIC50: 2.00E+6nMAssay Description:Ability to inhibit protein-tyrosine kinase activity of p56lck (isolated from bovine thymus) in vitro.More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetTyrosine-protein kinase Lck(Human)
Purdue University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50011450BDBM50011450(CHEMBL165482 | 2-(4-Bromo-phenyl)-4-oxo-4H-chromen...)
Affinity DataIC50: 2.00E+6nMAssay Description:Ability to inhibit protein-tyrosine kinase activity of p56lck (isolated from bovine thymus) in vitro.More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetTyrosine-protein kinase Lck(Human)
Purdue University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50011445BDBM50011445(2-(4-Benzyloxy-phenyl)-7-methoxy-4-oxo-4H-chromene...)
Affinity DataIC50: 2.00E+6nMAssay Description:Ability to inhibit protein-tyrosine kinase activity of p56lck (isolated from bovine thymus) in vitro.More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetTyrosine-protein kinase Lck(Human)
Purdue University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50011444BDBM50011444(methyl 7-methoxy-2-(4-nitrophenyl)-4-oxo-4H-chrome...)
Affinity DataIC50: 2.00E+6nMAssay Description:Ability to inhibit protein-tyrosine kinase activity of p56lck (isolated from bovine thymus) in vitro.More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetTyrosine-protein kinase Lck(Human)
Purdue University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50011443BDBM50011443(CHEMBL353865 | 2-(3,5-Dimethoxy-phenyl)-4-oxo-4H-c...)
Affinity DataIC50: 2.00E+6nMAssay Description:Ability to inhibit protein-tyrosine kinase activity of p56lck (isolated from bovine thymus) in vitro.More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetTyrosine-protein kinase Lck(Human)
Purdue University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50011442BDBM50011442(CHEMBL168090 | 6-hydroxy-2-(4-nitrophenyl)-4H-chro...)
Affinity DataIC50: 2.00E+6nMAssay Description:Ability to inhibit protein-tyrosine kinase activity of p56lck (isolated from bovine thymus) in vitro.More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetTyrosine-protein kinase Lck(Human)
Purdue University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50011452BDBM50011452(methyl 2-(4-methoxyphenyl)-4-oxo-4H-chromene-3-car...)
Affinity DataIC50: 2.00E+6nMAssay Description:Ability to inhibit protein-tyrosine kinase activity of p56lck (isolated from bovine thymus) in vitro.More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetTyrosine-protein kinase Lck(Human)
Purdue University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50011454BDBM50011454(2-(4-Benzyloxy-phenyl)-6-methoxy-4-oxo-4H-chromene...)
Affinity DataIC50: 2.00E+6nMAssay Description:Ability to inhibit protein-tyrosine kinase activity of p56lck (isolated from bovine thymus) in vitro.More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetTyrosine-protein kinase Lck(Human)
Purdue University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50011453BDBM50011453(CHEMBL354792 | 3-Oxo-3-(2,3,4-trihydroxy-phenyl)-p...)
Affinity DataIC50: 2.00E+6nMAssay Description:Ability to inhibit protein-tyrosine kinase activity of p56lck (isolated from bovine thymus) in vitro.More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed