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PubMed code 1995903

Compile data set for download or QSAR
Found 49 hits of Enzyme Inhibition Constant Data   
Target/Host
(Institution)
LigandTarget/Host
Links
Ligand
Links
Trg + Lig
Links
Ki
nM
ΔG°
kJ/mole
IC50
nM
Kd
nM
EC50/IC50
nM
koff
s-1
kon
M-1s-1
pHTemp
°C
Tyrosine-protein kinase Lck


(Homo sapiens (Human))
BDBM50011418
PNG
(2-(4-Amino-phenyl)-6-hydroxy-chromen-4-one | 2-(4-...)
Show SMILES Nc1ccc(cc1)-c1cc(=O)c2cc(O)ccc2o1
Show InChI InChI=1S/C15H11NO3/c16-10-3-1-9(2-4-10)15-8-13(18)12-7-11(17)5-6-14(12)19-15/h1-8,17H,16H2
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n/an/a 1.20E+3n/an/an/an/an/an/a



Purdue University

Curated by ChEMBL


Assay Description
Ability to inhibit protein-tyrosine kinase activity of p56lck (isolated from bovine thymus) in vitro.


J Med Chem 34: 798-806 (1991)


Article DOI: 10.1021/jm00106a047
BindingDB Entry DOI: 10.7270/Q2CF9P3J
More data for this
Ligand-Target Pair
Tyrosine-protein kinase Lck


(Homo sapiens (Human))
BDBM50011429
PNG
(2-(4-Amino-phenyl)-5,7-dihydroxy-chromen-4-one | 2...)
Show SMILES Nc1ccc(cc1)-c1cc(=O)c2c(O)cc(O)cc2o1
Show InChI InChI=1S/C15H11NO4/c16-9-3-1-8(2-4-9)13-7-12(19)15-11(18)5-10(17)6-14(15)20-13/h1-7,17-18H,16H2
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n/an/a 7.40E+3n/an/an/an/an/an/a



Purdue University

Curated by ChEMBL


Assay Description
Ability to inhibit protein-tyrosine kinase activity of p56lck (isolated from bovine thymus) in vitro.


J Med Chem 34: 798-806 (1991)


Article DOI: 10.1021/jm00106a047
BindingDB Entry DOI: 10.7270/Q2CF9P3J
More data for this
Ligand-Target Pair
Tyrosine-protein kinase Lck


(Homo sapiens (Human))
BDBM7460
PNG
(2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-4H-chrome...)
Show SMILES Oc1cc(O)c2c(c1)oc(-c1ccc(O)c(O)c1)c(O)c2=O
Show InChI InChI=1S/C15H10O7/c16-7-4-10(19)12-11(5-7)22-15(14(21)13(12)20)6-1-2-8(17)9(18)3-6/h1-5,16-19,21H
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n/an/a 1.30E+4n/an/an/an/an/an/a



Purdue University

Curated by ChEMBL


Assay Description
Ability to inhibit protein-tyrosine kinase activity of p56lck (isolated from bovine thymus) in vitro.


J Med Chem 34: 798-806 (1991)


Article DOI: 10.1021/jm00106a047
BindingDB Entry DOI: 10.7270/Q2CF9P3J
More data for this
Ligand-Target Pair
Tyrosine-protein kinase Lck


(Homo sapiens (Human))
BDBM50011424
PNG
(2-(4-Hydroxy-3,5-dimethoxy-phenyl)-chromen-4-one |...)
Show SMILES COc1cc(cc(OC)c1O)-c1cc(=O)c2ccccc2o1
Show InChI InChI=1S/C17H14O5/c1-20-15-7-10(8-16(21-2)17(15)19)14-9-12(18)11-5-3-4-6-13(11)22-14/h3-9,19H,1-2H3
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n/an/a 2.60E+4n/an/an/an/an/an/a



Purdue University

Curated by ChEMBL


Assay Description
Ability to inhibit protein-tyrosine kinase activity of p56lck (isolated from bovine thymus) in vitro.


J Med Chem 34: 798-806 (1991)


Article DOI: 10.1021/jm00106a047
BindingDB Entry DOI: 10.7270/Q2CF9P3J
More data for this
Ligand-Target Pair
Tyrosine-protein kinase Lck


(Homo sapiens (Human))
BDBM50011438
PNG
(2-(4-Amino-phenyl)-7-hydroxy-chromen-4-one | 2-(4-...)
Show SMILES Nc1ccc(cc1)-c1cc(=O)c2ccc(O)cc2o1
Show InChI InChI=1S/C15H11NO3/c16-10-3-1-9(2-4-10)14-8-13(18)12-6-5-11(17)7-15(12)19-14/h1-8,17H,16H2
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n/an/a 1.38E+5n/an/an/an/an/an/a



Purdue University

Curated by ChEMBL


Assay Description
Ability to inhibit protein-tyrosine kinase activity of p56lck (isolated from bovine thymus) in vitro.


J Med Chem 34: 798-806 (1991)


Article DOI: 10.1021/jm00106a047
BindingDB Entry DOI: 10.7270/Q2CF9P3J
More data for this
Ligand-Target Pair
Tyrosine-protein kinase Lck


(Homo sapiens (Human))
BDBM50011437
PNG
(2-(4-Amino-phenyl)-chromen-4-one | 2-(4-aminopheny...)
Show SMILES Nc1ccc(cc1)-c1cc(=O)c2ccccc2o1
Show InChI InChI=1S/C15H11NO2/c16-11-7-5-10(6-8-11)15-9-13(17)12-3-1-2-4-14(12)18-15/h1-9H,16H2
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n/an/a 2.10E+5n/an/an/an/an/an/a



Purdue University

Curated by ChEMBL


Assay Description
Ability to inhibit protein-tyrosine kinase activity of p56lck (isolated from bovine thymus) in vitro.


J Med Chem 34: 798-806 (1991)


Article DOI: 10.1021/jm00106a047
BindingDB Entry DOI: 10.7270/Q2CF9P3J
More data for this
Ligand-Target Pair
Tyrosine-protein kinase Lck


(Homo sapiens (Human))
BDBM50011455
PNG
(2-(4-Hydroxy-phenyl)-4-oxo-4H-chromene-3-carboxyli...)
Show SMILES COC(=O)c1c(oc2ccccc2c1=O)-c1ccc(O)cc1
Show InChI InChI=1S/C17H12O5/c1-21-17(20)14-15(19)12-4-2-3-5-13(12)22-16(14)10-6-8-11(18)9-7-10/h2-9,18H,1H3
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n/an/a 4.39E+5n/an/an/an/an/an/a



Purdue University

Curated by ChEMBL


Assay Description
Ability to inhibit protein-tyrosine kinase activity of p56lck (isolated from bovine thymus) in vitro.


J Med Chem 34: 798-806 (1991)


Article DOI: 10.1021/jm00106a047
BindingDB Entry DOI: 10.7270/Q2CF9P3J
More data for this
Ligand-Target Pair
Tyrosine-protein kinase Lck


(Homo sapiens (Human))
BDBM50011446
PNG
(2-(4-Hydroxy-phenyl)-chromen-4-one | 2-(4-hydroxyp...)
Show SMILES Oc1ccc(cc1)-c1cc(=O)c2ccccc2o1
Show InChI InChI=1S/C15H10O3/c16-11-7-5-10(6-8-11)15-9-13(17)12-3-1-2-4-14(12)18-15/h1-9,16H
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n/an/a 5.04E+5n/an/an/an/an/an/a



Purdue University

Curated by ChEMBL


Assay Description
Ability to inhibit protein-tyrosine kinase activity of p56lck (isolated from bovine thymus) in vitro.


J Med Chem 34: 798-806 (1991)


Article DOI: 10.1021/jm00106a047
BindingDB Entry DOI: 10.7270/Q2CF9P3J
More data for this
Ligand-Target Pair
Tyrosine-protein kinase Lck


(Homo sapiens (Human))
BDBM50011416
PNG
(2-(4-Amino-phenyl)-4-oxo-4H-chromene-3-carboxylic ...)
Show SMILES COC(=O)c1c(oc2ccccc2c1=O)-c1ccc(N)cc1
Show InChI InChI=1S/C17H13NO4/c1-21-17(20)14-15(19)12-4-2-3-5-13(12)22-16(14)10-6-8-11(18)9-7-10/h2-9H,18H2,1H3
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n/an/a 8.10E+5n/an/an/an/an/an/a



Purdue University

Curated by ChEMBL


Assay Description
Ability to inhibit protein-tyrosine kinase activity of p56lck (isolated from bovine thymus) in vitro.


J Med Chem 34: 798-806 (1991)


Article DOI: 10.1021/jm00106a047
BindingDB Entry DOI: 10.7270/Q2CF9P3J
More data for this
Ligand-Target Pair
Tyrosine-protein kinase Lck


(Homo sapiens (Human))
BDBM50011422
PNG
(2-(4-Hydroxy-phenyl)-7-methoxy-4-oxo-4H-chromene-3...)
Show SMILES COc1ccc2c(c1)oc(-c1ccc(O)cc1)c(C(O)=O)c2=O
Show InChI InChI=1S/C17H12O6/c1-22-11-6-7-12-13(8-11)23-16(14(15(12)19)17(20)21)9-2-4-10(18)5-3-9/h2-8,18H,1H3,(H,20,21)
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n/an/a 1.03E+6n/an/an/an/an/an/a



Purdue University

Curated by ChEMBL


Assay Description
Ability to inhibit protein-tyrosine kinase activity of p56lck (isolated from bovine thymus) in vitro.


J Med Chem 34: 798-806 (1991)


Article DOI: 10.1021/jm00106a047
BindingDB Entry DOI: 10.7270/Q2CF9P3J
More data for this
Ligand-Target Pair
Tyrosine-protein kinase Lck


(Homo sapiens (Human))
BDBM50011451
PNG
(3-(2-Hydroxy-4-methoxy-phenyl)-3-oxo-propionic aci...)
Show SMILES COC(=O)CC(=O)c1ccc(OC)cc1O
Show InChI InChI=1S/C11H12O5/c1-15-7-3-4-8(9(12)5-7)10(13)6-11(14)16-2/h3-5,12H,6H2,1-2H3
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n/an/a 1.16E+6n/an/an/an/an/an/a



Purdue University

Curated by ChEMBL


Assay Description
Ability to inhibit protein-tyrosine kinase activity of p56lck (isolated from bovine thymus) in vitro.


J Med Chem 34: 798-806 (1991)


Article DOI: 10.1021/jm00106a047
BindingDB Entry DOI: 10.7270/Q2CF9P3J
More data for this
Ligand-Target Pair
Tyrosine-protein kinase Lck


(Homo sapiens (Human))
BDBM50011458
PNG
(2-(4-Hydroxy-phenyl)-4-oxo-4H-chromene-3-carboxyli...)
Show SMILES OC(=O)c1c(oc2ccccc2c1=O)-c1ccc(O)cc1
Show InChI InChI=1S/C16H10O5/c17-10-7-5-9(6-8-10)15-13(16(19)20)14(18)11-3-1-2-4-12(11)21-15/h1-8,17H,(H,19,20)
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n/an/a 1.60E+6n/an/an/an/an/an/a



Purdue University

Curated by ChEMBL


Assay Description
Ability to inhibit protein-tyrosine kinase activity of p56lck (isolated from bovine thymus) in vitro.


J Med Chem 34: 798-806 (1991)


Article DOI: 10.1021/jm00106a047
BindingDB Entry DOI: 10.7270/Q2CF9P3J
More data for this
Ligand-Target Pair
Tyrosine-protein kinase Lck


(Homo sapiens (Human))
BDBM50011447
PNG
(4-Oxo-2-(3,4,5-trimethoxy-phenyl)-4H-chromene-3-ca...)
Show SMILES COC(=O)c1c(oc2ccccc2c1=O)-c1cc(OC)c(OC)c(OC)c1
Show InChI InChI=1S/C20H18O7/c1-23-14-9-11(10-15(24-2)19(14)25-3)18-16(20(22)26-4)17(21)12-7-5-6-8-13(12)27-18/h5-10H,1-4H3
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n/an/a>2.00E+6n/an/an/an/an/an/a



Purdue University

Curated by ChEMBL


Assay Description
Ability to inhibit protein-tyrosine kinase activity of p56lck (isolated from bovine thymus) in vitro.


J Med Chem 34: 798-806 (1991)


Article DOI: 10.1021/jm00106a047
BindingDB Entry DOI: 10.7270/Q2CF9P3J
More data for this
Ligand-Target Pair
Tyrosine-protein kinase Lck


(Homo sapiens (Human))
BDBM50011448
PNG
(4-Oxo-2-[4-(3,4,5-trimethoxy-benzoylamino)-phenyl]...)
Show SMILES COC(=O)c1c(oc2ccccc2c1=O)-c1ccc(NC(=O)c2cc(OC)c(OC)c(OC)c2)cc1
Show InChI InChI=1S/C27H23NO8/c1-32-20-13-16(14-21(33-2)25(20)34-3)26(30)28-17-11-9-15(10-12-17)24-22(27(31)35-4)23(29)18-7-5-6-8-19(18)36-24/h5-14H,1-4H3,(H,28,30)
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n/an/a>2.00E+6n/an/an/an/an/an/a



Purdue University

Curated by ChEMBL


Assay Description
Ability to inhibit protein-tyrosine kinase activity of p56lck (isolated from bovine thymus) in vitro.


J Med Chem 34: 798-806 (1991)


Article DOI: 10.1021/jm00106a047
BindingDB Entry DOI: 10.7270/Q2CF9P3J
More data for this
Ligand-Target Pair
Tyrosine-protein kinase Lck


(Homo sapiens (Human))
BDBM50011462
PNG
(3-(2,4-Bis-benzyloxy-6-hydroxy-phenyl)-3-oxo-propi...)
Show SMILES CCOC(=O)CC(=O)c1c(O)cc(OCc2ccccc2)cc1OCc1ccccc1
Show InChI InChI=1S/C25H24O6/c1-2-29-24(28)15-22(27)25-21(26)13-20(30-16-18-9-5-3-6-10-18)14-23(25)31-17-19-11-7-4-8-12-19/h3-14,26H,2,15-17H2,1H3
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Purdue University

Curated by ChEMBL


Assay Description
Ability to inhibit protein-tyrosine kinase activity of p56lck (isolated from bovine thymus) in vitro.


J Med Chem 34: 798-806 (1991)


Article DOI: 10.1021/jm00106a047
BindingDB Entry DOI: 10.7270/Q2CF9P3J
More data for this
Ligand-Target Pair
Tyrosine-protein kinase Lck


(Homo sapiens (Human))
BDBM50011417
PNG
(5,7-Dihydroxy-2-(4-nitro-phenyl)-chromen-4-one | 5...)
Show SMILES Oc1cc(O)c2c(c1)oc(cc2=O)-c1ccc(cc1)[N+]([O-])=O
Show InChI InChI=1S/C15H9NO6/c17-10-5-11(18)15-12(19)7-13(22-14(15)6-10)8-1-3-9(4-2-8)16(20)21/h1-7,17-18H
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Purdue University

Curated by ChEMBL


Assay Description
Ability to inhibit protein-tyrosine kinase activity of p56lck (isolated from bovine thymus) in vitro.


J Med Chem 34: 798-806 (1991)


Article DOI: 10.1021/jm00106a047
BindingDB Entry DOI: 10.7270/Q2CF9P3J
More data for this
Ligand-Target Pair
Tyrosine-protein kinase Lck


(Homo sapiens (Human))
BDBM50011426
PNG
(2-(4-Hydroxy-phenyl)-7-methoxy-4-oxo-4H-chromene-3...)
Show SMILES COC(=O)c1c(oc2cc(OC)ccc2c1=O)-c1ccc(O)cc1
Show InChI InChI=1S/C18H14O6/c1-22-12-7-8-13-14(9-12)24-17(10-3-5-11(19)6-4-10)15(16(13)20)18(21)23-2/h3-9,19H,1-2H3
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Purdue University

Curated by ChEMBL


Assay Description
Ability to inhibit protein-tyrosine kinase activity of p56lck (isolated from bovine thymus) in vitro.


J Med Chem 34: 798-806 (1991)


Article DOI: 10.1021/jm00106a047
BindingDB Entry DOI: 10.7270/Q2CF9P3J
More data for this
Ligand-Target Pair
Tyrosine-protein kinase Lck


(Homo sapiens (Human))
BDBM50011428
PNG
(2-(3,4,5-Trimethoxy-phenyl)-chromen-4-one | 2-(3,4...)
Show SMILES COc1cc(cc(OC)c1OC)-c1cc(=O)c2ccccc2o1
Show InChI InChI=1S/C18H16O5/c1-20-16-8-11(9-17(21-2)18(16)22-3)15-10-13(19)12-6-4-5-7-14(12)23-15/h4-10H,1-3H3
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Purdue University

Curated by ChEMBL


Assay Description
Ability to inhibit protein-tyrosine kinase activity of p56lck (isolated from bovine thymus) in vitro.


J Med Chem 34: 798-806 (1991)


Article DOI: 10.1021/jm00106a047
BindingDB Entry DOI: 10.7270/Q2CF9P3J
More data for this
Ligand-Target Pair
Tyrosine-protein kinase Lck


(Homo sapiens (Human))
BDBM50011444
PNG
(7-Methoxy-2-(4-nitro-phenyl)-4-oxo-4H-chromene-3-c...)
Show SMILES COC(=O)c1c(oc2cc(OC)ccc2c1=O)-c1ccc(cc1)[N+]([O-])=O
Show InChI InChI=1S/C18H13NO7/c1-24-12-7-8-13-14(9-12)26-17(15(16(13)20)18(21)25-2)10-3-5-11(6-4-10)19(22)23/h3-9H,1-2H3
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Purdue University

Curated by ChEMBL


Assay Description
Ability to inhibit protein-tyrosine kinase activity of p56lck (isolated from bovine thymus) in vitro.


J Med Chem 34: 798-806 (1991)


Article DOI: 10.1021/jm00106a047
BindingDB Entry DOI: 10.7270/Q2CF9P3J
More data for this
Ligand-Target Pair
Tyrosine-protein kinase Lck


(Homo sapiens (Human))
BDBM50011420
PNG
(7-Methoxy-2-(4-nitro-phenyl)-4-oxo-4H-chromene-3-c...)
Show SMILES COc1ccc2c(c1)oc(-c1ccc(cc1)[N+]([O-])=O)c(C(O)=O)c2=O
Show InChI InChI=1S/C17H11NO7/c1-24-11-6-7-12-13(8-11)25-16(14(15(12)19)17(20)21)9-2-4-10(5-3-9)18(22)23/h2-8H,1H3,(H,20,21)
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n/an/a>2.00E+6n/an/an/an/an/an/a



Purdue University

Curated by ChEMBL


Assay Description
Ability to inhibit protein-tyrosine kinase activity of p56lck (isolated from bovine thymus) in vitro.


J Med Chem 34: 798-806 (1991)


Article DOI: 10.1021/jm00106a047
BindingDB Entry DOI: 10.7270/Q2CF9P3J
More data for this
Ligand-Target Pair
Tyrosine-protein kinase Lck


(Homo sapiens (Human))
BDBM50011450
PNG
(2-(4-Bromo-phenyl)-4-oxo-4H-chromene-3-carboxylic ...)
Show SMILES OC(=O)c1c(oc2ccccc2c1=O)-c1ccc(Br)cc1
Show InChI InChI=1S/C16H9BrO4/c17-10-7-5-9(6-8-10)15-13(16(19)20)14(18)11-3-1-2-4-12(11)21-15/h1-8H,(H,19,20)
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Purdue University

Curated by ChEMBL


Assay Description
Ability to inhibit protein-tyrosine kinase activity of p56lck (isolated from bovine thymus) in vitro.


J Med Chem 34: 798-806 (1991)


Article DOI: 10.1021/jm00106a047
BindingDB Entry DOI: 10.7270/Q2CF9P3J
More data for this
Ligand-Target Pair
Tyrosine-protein kinase Lck


(Homo sapiens (Human))
BDBM50011460
PNG
(2-(4-Acetylamino-phenyl)-7-methoxy-4-oxo-4H-chrome...)
Show SMILES COC(=O)c1c(oc2cc(OC)ccc2c1=O)-c1ccc(NC(C)=O)cc1
Show InChI InChI=1S/C20H17NO6/c1-11(22)21-13-6-4-12(5-7-13)19-17(20(24)26-3)18(23)15-9-8-14(25-2)10-16(15)27-19/h4-10H,1-3H3,(H,21,22)
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Purdue University

Curated by ChEMBL


Assay Description
Ability to inhibit protein-tyrosine kinase activity of p56lck (isolated from bovine thymus) in vitro.


J Med Chem 34: 798-806 (1991)


Article DOI: 10.1021/jm00106a047
BindingDB Entry DOI: 10.7270/Q2CF9P3J
More data for this
Ligand-Target Pair
Tyrosine-protein kinase Lck


(Homo sapiens (Human))
BDBM50011431
PNG
(2-(4-Acetylamino-phenyl)-6-methoxy-4-oxo-4H-chrome...)
Show SMILES COC(=O)c1c(oc2ccc(OC)cc2c1=O)-c1ccc(NC(C)=O)cc1
Show InChI InChI=1S/C20H17NO6/c1-11(22)21-13-6-4-12(5-7-13)19-17(20(24)26-3)18(23)15-10-14(25-2)8-9-16(15)27-19/h4-10H,1-3H3,(H,21,22)
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n/an/a>2.00E+6n/an/an/an/an/an/a



Purdue University

Curated by ChEMBL


Assay Description
Ability to inhibit protein-tyrosine kinase activity of p56lck (isolated from bovine thymus) in vitro.


J Med Chem 34: 798-806 (1991)


Article DOI: 10.1021/jm00106a047
BindingDB Entry DOI: 10.7270/Q2CF9P3J
More data for this
Ligand-Target Pair
Tyrosine-protein kinase Lck


(Homo sapiens (Human))
BDBM50011432
PNG
(2-(3,4-Dimethoxy-phenyl)-4-oxo-4H-chromene-3-carbo...)
Show SMILES COc1ccc(cc1OC)-c1oc2ccccc2c(=O)c1C(O)=O
Show InChI InChI=1S/C18H14O6/c1-22-13-8-7-10(9-14(13)23-2)17-15(18(20)21)16(19)11-5-3-4-6-12(11)24-17/h3-9H,1-2H3,(H,20,21)
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n/an/a>2.00E+6n/an/an/an/an/an/a



Purdue University

Curated by ChEMBL


Assay Description
Ability to inhibit protein-tyrosine kinase activity of p56lck (isolated from bovine thymus) in vitro.


J Med Chem 34: 798-806 (1991)


Article DOI: 10.1021/jm00106a047
BindingDB Entry DOI: 10.7270/Q2CF9P3J
More data for this
Ligand-Target Pair
Tyrosine-protein kinase Lck


(Homo sapiens (Human))
BDBM50011436
PNG
(5,7-Dihydroxy-2-(4-nitro-phenyl)-4-oxo-4H-chromene...)
Show SMILES OC(=O)c1c([O-])c2c(cc(O)cc2=[OH+])oc1-c1ccc(cc1)[N+]([O-])=O
Show InChI InChI=1S/C16H9NO8/c18-9-5-10(19)12-11(6-9)25-15(13(14(12)20)16(21)22)7-1-3-8(4-2-7)17(23)24/h1-6,18,20H,(H,21,22)
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n/an/a>2.00E+6n/an/an/an/an/an/a



Purdue University

Curated by ChEMBL


Assay Description
Ability to inhibit protein-tyrosine kinase activity of p56lck (isolated from bovine thymus) in vitro.


J Med Chem 34: 798-806 (1991)


Article DOI: 10.1021/jm00106a047
BindingDB Entry DOI: 10.7270/Q2CF9P3J
More data for this
Ligand-Target Pair
Tyrosine-protein kinase Lck


(Homo sapiens (Human))
BDBM50011435
PNG
(3-(2-Hydroxy-5-methoxy-phenyl)-3-oxo-propionic aci...)
Show SMILES COC(=O)CC(=O)c1cc(OC)ccc1O
Show InChI InChI=1S/C11H12O5/c1-15-7-3-4-9(12)8(5-7)10(13)6-11(14)16-2/h3-5,12H,6H2,1-2H3
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n/an/a>2.00E+6n/an/an/an/an/an/a



Purdue University

Curated by ChEMBL


Assay Description
Ability to inhibit protein-tyrosine kinase activity of p56lck (isolated from bovine thymus) in vitro.


J Med Chem 34: 798-806 (1991)


Article DOI: 10.1021/jm00106a047
BindingDB Entry DOI: 10.7270/Q2CF9P3J
More data for this
Ligand-Target Pair
Tyrosine-protein kinase Lck


(Homo sapiens (Human))
BDBM50011442
PNG
(6-Hydroxy-2-(4-nitro-phenyl)-chromen-4-one | 6-hyd...)
Show SMILES Oc1ccc2oc(cc(=O)c2c1)-c1ccc(cc1)[N+]([O-])=O
Show InChI InChI=1S/C15H9NO5/c17-11-5-6-14-12(7-11)13(18)8-15(21-14)9-1-3-10(4-2-9)16(19)20/h1-8,17H
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n/an/a>2.00E+6n/an/an/an/an/an/a



Purdue University

Curated by ChEMBL


Assay Description
Ability to inhibit protein-tyrosine kinase activity of p56lck (isolated from bovine thymus) in vitro.


J Med Chem 34: 798-806 (1991)


Article DOI: 10.1021/jm00106a047
BindingDB Entry DOI: 10.7270/Q2CF9P3J
More data for this
Ligand-Target Pair
Tyrosine-protein kinase Lck


(Homo sapiens (Human))
BDBM50011443
PNG
(2-(3,5-Dimethoxy-phenyl)-4-oxo-4H-chromene-3-carbo...)
Show SMILES COC(=O)c1c(oc2ccccc2c1=O)-c1cc(OC)cc(OC)c1
Show InChI InChI=1S/C19H16O6/c1-22-12-8-11(9-13(10-12)23-2)18-16(19(21)24-3)17(20)14-6-4-5-7-15(14)25-18/h4-10H,1-3H3
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Purdue University

Curated by ChEMBL


Assay Description
Ability to inhibit protein-tyrosine kinase activity of p56lck (isolated from bovine thymus) in vitro.


J Med Chem 34: 798-806 (1991)


Article DOI: 10.1021/jm00106a047
BindingDB Entry DOI: 10.7270/Q2CF9P3J
More data for this
Ligand-Target Pair
Tyrosine-protein kinase Lck


(Homo sapiens (Human))
BDBM50011453
PNG
(3-Oxo-3-(2,3,4-trihydroxy-phenyl)-propionic acid m...)
Show SMILES COC(=O)CC(=O)c1ccc(O)c(O)c1O
Show InChI InChI=1S/C10H10O6/c1-16-8(13)4-7(12)5-2-3-6(11)10(15)9(5)14/h2-3,11,14-15H,4H2,1H3
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Purdue University

Curated by ChEMBL


Assay Description
Ability to inhibit protein-tyrosine kinase activity of p56lck (isolated from bovine thymus) in vitro.


J Med Chem 34: 798-806 (1991)


Article DOI: 10.1021/jm00106a047
BindingDB Entry DOI: 10.7270/Q2CF9P3J
More data for this
Ligand-Target Pair
Tyrosine-protein kinase Lck


(Homo sapiens (Human))
BDBM50011454
PNG
(2-(4-Benzyloxy-phenyl)-6-methoxy-4-oxo-4H-chromene...)
Show SMILES COC(=O)c1c(oc2ccc(OC)cc2c1=O)-c1ccc(OCc2ccccc2)cc1
Show InChI InChI=1S/C25H20O6/c1-28-19-12-13-21-20(14-19)23(26)22(25(27)29-2)24(31-21)17-8-10-18(11-9-17)30-15-16-6-4-3-5-7-16/h3-14H,15H2,1-2H3
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Purdue University

Curated by ChEMBL


Assay Description
Ability to inhibit protein-tyrosine kinase activity of p56lck (isolated from bovine thymus) in vitro.


J Med Chem 34: 798-806 (1991)


Article DOI: 10.1021/jm00106a047
BindingDB Entry DOI: 10.7270/Q2CF9P3J
More data for this
Ligand-Target Pair
Tyrosine-protein kinase Lck


(Homo sapiens (Human))
BDBM50011457
PNG
(2-(4-Nitro-phenyl)-4-oxo-4H-chromene-3-carboxylic ...)
Show SMILES COC(=O)c1c(oc2ccccc2c1=O)-c1ccc(cc1)[N+]([O-])=O
Show InChI InChI=1S/C17H11NO6/c1-23-17(20)14-15(19)12-4-2-3-5-13(12)24-16(14)10-6-8-11(9-7-10)18(21)22/h2-9H,1H3
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Purdue University

Curated by ChEMBL


Assay Description
Ability to inhibit protein-tyrosine kinase activity of p56lck (isolated from bovine thymus) in vitro.


J Med Chem 34: 798-806 (1991)


Article DOI: 10.1021/jm00106a047
BindingDB Entry DOI: 10.7270/Q2CF9P3J
More data for this
Ligand-Target Pair
Tyrosine-protein kinase Lck


(Homo sapiens (Human))
BDBM50011459
PNG
(6-Methoxy-2-(4-nitro-phenyl)-4-oxo-4H-chromene-3-c...)
Show SMILES COc1ccc2oc(-c3ccc(cc3)[N+]([O-])=O)c(C(O)=O)c(=O)c2c1
Show InChI InChI=1S/C17H11NO7/c1-24-11-6-7-13-12(8-11)15(19)14(17(20)21)16(25-13)9-2-4-10(5-3-9)18(22)23/h2-8H,1H3,(H,20,21)
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Purdue University

Curated by ChEMBL


Assay Description
Ability to inhibit protein-tyrosine kinase activity of p56lck (isolated from bovine thymus) in vitro.


J Med Chem 34: 798-806 (1991)


Article DOI: 10.1021/jm00106a047
BindingDB Entry DOI: 10.7270/Q2CF9P3J
More data for this
Ligand-Target Pair
Tyrosine-protein kinase Lck


(Homo sapiens (Human))
BDBM50011421
PNG
(2-(4-Nitro-phenyl)-chromen-4-one | CHEMBL64780)
Show SMILES [O-][N+](=O)c1ccc(cc1)-c1cc(=O)c2ccccc2o1
Show InChI InChI=1S/C15H9NO4/c17-13-9-15(20-14-4-2-1-3-12(13)14)10-5-7-11(8-6-10)16(18)19/h1-9H
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Purdue University

Curated by ChEMBL


Assay Description
Ability to inhibit protein-tyrosine kinase activity of p56lck (isolated from bovine thymus) in vitro.


J Med Chem 34: 798-806 (1991)


Article DOI: 10.1021/jm00106a047
BindingDB Entry DOI: 10.7270/Q2CF9P3J
More data for this
Ligand-Target Pair
Tyrosine-protein kinase Lck


(Homo sapiens (Human))
BDBM50011433
PNG
(3-(2,4-Bis-benzyloxy-6-hydroxy-phenyl)-3-oxo-propi...)
Show SMILES COC(=O)CC(=O)c1c(O)cc(OCc2ccccc2)cc1OCc1ccccc1
Show InChI InChI=1S/C24H22O6/c1-28-23(27)14-21(26)24-20(25)12-19(29-15-17-8-4-2-5-9-17)13-22(24)30-16-18-10-6-3-7-11-18/h2-13,25H,14-16H2,1H3
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Purdue University

Curated by ChEMBL


Assay Description
Ability to inhibit protein-tyrosine kinase activity of p56lck (isolated from bovine thymus) in vitro.


J Med Chem 34: 798-806 (1991)


Article DOI: 10.1021/jm00106a047
BindingDB Entry DOI: 10.7270/Q2CF9P3J
More data for this
Ligand-Target Pair
Tyrosine-protein kinase Lck


(Homo sapiens (Human))
BDBM50011440
PNG
(2-(4-Nitro-phenyl)-4-oxo-4H-chromene-3-carboxylic ...)
Show SMILES OC(=O)c1c(oc2ccccc2c1=O)-c1ccc(cc1)[N+]([O-])=O
Show InChI InChI=1S/C16H9NO6/c18-14-11-3-1-2-4-12(11)23-15(13(14)16(19)20)9-5-7-10(8-6-9)17(21)22/h1-8H,(H,19,20)
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Purdue University

Curated by ChEMBL


Assay Description
Ability to inhibit protein-tyrosine kinase activity of p56lck (isolated from bovine thymus) in vitro.


J Med Chem 34: 798-806 (1991)


Article DOI: 10.1021/jm00106a047
BindingDB Entry DOI: 10.7270/Q2CF9P3J
More data for this
Ligand-Target Pair
Tyrosine-protein kinase Lck


(Homo sapiens (Human))
BDBM50011456
PNG
(2-(4-Hydroxy-phenyl)-6-methoxy-4-oxo-4H-chromene-3...)
Show SMILES COC(=O)c1c(oc2ccc(OC)cc2c1=O)-c1ccc(O)cc1
Show InChI InChI=1S/C18H14O6/c1-22-12-7-8-14-13(9-12)16(20)15(18(21)23-2)17(24-14)10-3-5-11(19)6-4-10/h3-9,19H,1-2H3
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Purdue University

Curated by ChEMBL


Assay Description
Ability to inhibit protein-tyrosine kinase activity of p56lck (isolated from bovine thymus) in vitro.


J Med Chem 34: 798-806 (1991)


Article DOI: 10.1021/jm00106a047
BindingDB Entry DOI: 10.7270/Q2CF9P3J
More data for this
Ligand-Target Pair
Tyrosine-protein kinase Lck


(Homo sapiens (Human))
BDBM50011441
PNG
(2-(4-Methoxy-phenyl)-4-oxo-4H-chromene-3-carboxyli...)
Show SMILES COc1ccc(cc1)-c1oc2ccccc2c(=O)c1C(O)=O
Show InChI InChI=1S/C17H12O5/c1-21-11-8-6-10(7-9-11)16-14(17(19)20)15(18)12-4-2-3-5-13(12)22-16/h2-9H,1H3,(H,19,20)
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Purdue University

Curated by ChEMBL


Assay Description
Ability to inhibit protein-tyrosine kinase activity of p56lck (isolated from bovine thymus) in vitro.


J Med Chem 34: 798-806 (1991)


Article DOI: 10.1021/jm00106a047
BindingDB Entry DOI: 10.7270/Q2CF9P3J
More data for this
Ligand-Target Pair
Tyrosine-protein kinase Lck


(Homo sapiens (Human))
BDBM50011427
PNG
(7-Hydroxy-2-(4-nitro-phenyl)-chromen-4-one | 7-hyd...)
Show SMILES Oc1ccc2c(c1)oc(cc2=O)-c1ccc(cc1)[N+]([O-])=O
Show InChI InChI=1S/C15H9NO5/c17-11-5-6-12-13(18)8-14(21-15(12)7-11)9-1-3-10(4-2-9)16(19)20/h1-8,17H
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Purdue University

Curated by ChEMBL


Assay Description
Ability to inhibit protein-tyrosine kinase activity of p56lck (isolated from bovine thymus) in vitro.


J Med Chem 34: 798-806 (1991)


Article DOI: 10.1021/jm00106a047
BindingDB Entry DOI: 10.7270/Q2CF9P3J
More data for this
Ligand-Target Pair
Tyrosine-protein kinase Lck


(Homo sapiens (Human))
BDBM50011415
PNG
(3-(2-Hydroxy-phenyl)-3-oxo-propionic acid ethyl es...)
Show SMILES CCOC(=O)CC(=O)c1ccccc1O
Show InChI InChI=1S/C11H12O4/c1-2-15-11(14)7-10(13)8-5-3-4-6-9(8)12/h3-6,12H,2,7H2,1H3
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Purdue University

Curated by ChEMBL


Assay Description
Ability to inhibit protein-tyrosine kinase activity of p56lck (isolated from bovine thymus) in vitro.


J Med Chem 34: 798-806 (1991)


Article DOI: 10.1021/jm00106a047
BindingDB Entry DOI: 10.7270/Q2CF9P3J
More data for this
Ligand-Target Pair
Tyrosine-protein kinase Lck


(Homo sapiens (Human))
BDBM50011461
PNG
(2-(4-Benzyloxy-phenyl)-4-oxo-4H-chromene-3-carboxy...)
Show SMILES COC(=O)c1c(oc2ccccc2c1=O)-c1ccc(OCc2ccccc2)cc1
Show InChI InChI=1S/C24H18O5/c1-27-24(26)21-22(25)19-9-5-6-10-20(19)29-23(21)17-11-13-18(14-12-17)28-15-16-7-3-2-4-8-16/h2-14H,15H2,1H3
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Purdue University

Curated by ChEMBL


Assay Description
Ability to inhibit protein-tyrosine kinase activity of p56lck (isolated from bovine thymus) in vitro.


J Med Chem 34: 798-806 (1991)


Article DOI: 10.1021/jm00106a047
BindingDB Entry DOI: 10.7270/Q2CF9P3J
More data for this
Ligand-Target Pair
Tyrosine-protein kinase Lck


(Homo sapiens (Human))
BDBM50011449
PNG
(3-(2-Hydroxy-phenyl)-3-oxo-propionic acid methyl e...)
Show SMILES COC(=O)CC(=O)c1ccccc1O
Show InChI InChI=1S/C10H10O4/c1-14-10(13)6-9(12)7-4-2-3-5-8(7)11/h2-5,11H,6H2,1H3
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Purdue University

Curated by ChEMBL


Assay Description
Ability to inhibit protein-tyrosine kinase activity of p56lck (isolated from bovine thymus) in vitro.


J Med Chem 34: 798-806 (1991)


Article DOI: 10.1021/jm00106a047
BindingDB Entry DOI: 10.7270/Q2CF9P3J
More data for this
Ligand-Target Pair
Tyrosine-protein kinase Lck


(Homo sapiens (Human))
BDBM50011452
PNG
(2-(4-Methoxy-phenyl)-4-oxo-4H-chromene-3-carboxyli...)
Show SMILES COC(=O)c1c(oc2ccccc2c1=O)-c1ccc(OC)cc1
Show InChI InChI=1S/C18H14O5/c1-21-12-9-7-11(8-10-12)17-15(18(20)22-2)16(19)13-5-3-4-6-14(13)23-17/h3-10H,1-2H3
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Purdue University

Curated by ChEMBL


Assay Description
Ability to inhibit protein-tyrosine kinase activity of p56lck (isolated from bovine thymus) in vitro.


J Med Chem 34: 798-806 (1991)


Article DOI: 10.1021/jm00106a047
BindingDB Entry DOI: 10.7270/Q2CF9P3J
More data for this
Ligand-Target Pair
Tyrosine-protein kinase Lck


(Homo sapiens (Human))
BDBM50011425
PNG
(2-(3,4-Dimethoxy-phenyl)-4-oxo-4H-chromene-3-carbo...)
Show SMILES COC(=O)c1c(oc2ccccc2c1=O)-c1ccc(OC)c(OC)c1
Show InChI InChI=1S/C19H16O6/c1-22-14-9-8-11(10-15(14)23-2)18-16(19(21)24-3)17(20)12-6-4-5-7-13(12)25-18/h4-10H,1-3H3
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Purdue University

Curated by ChEMBL


Assay Description
Ability to inhibit protein-tyrosine kinase activity of p56lck (isolated from bovine thymus) in vitro.


J Med Chem 34: 798-806 (1991)


Article DOI: 10.1021/jm00106a047
BindingDB Entry DOI: 10.7270/Q2CF9P3J
More data for this
Ligand-Target Pair
Tyrosine-protein kinase Lck


(Homo sapiens (Human))
BDBM50011423
PNG
(5,7-Bis-benzyloxy-2-(4-nitro-phenyl)-4-oxo-4H-chro...)
Show SMILES COC(=O)c1c(oc2cc(OCc3ccccc3)cc(OCc3ccccc3)c2c1=O)-c1ccc(cc1)[N+]([O-])=O
Show InChI InChI=1S/C31H23NO8/c1-37-31(34)28-29(33)27-25(39-19-21-10-6-3-7-11-21)16-24(38-18-20-8-4-2-5-9-20)17-26(27)40-30(28)22-12-14-23(15-13-22)32(35)36/h2-17H,18-19H2,1H3
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Purdue University

Curated by ChEMBL


Assay Description
Ability to inhibit protein-tyrosine kinase activity of p56lck (isolated from bovine thymus) in vitro.


J Med Chem 34: 798-806 (1991)


Article DOI: 10.1021/jm00106a047
BindingDB Entry DOI: 10.7270/Q2CF9P3J
More data for this
Ligand-Target Pair
Tyrosine-protein kinase Lck


(Homo sapiens (Human))
BDBM50011439
PNG
(2-(3,5-Dimethoxy-phenyl)-4-oxo-4H-chromene-3-carbo...)
Show SMILES COc1cc(OC)cc(c1)-c1oc2ccccc2c(=O)c1C(O)=O
Show InChI InChI=1S/C18H14O6/c1-22-11-7-10(8-12(9-11)23-2)17-15(18(20)21)16(19)13-5-3-4-6-14(13)24-17/h3-9H,1-2H3,(H,20,21)
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n/an/a>2.00E+6n/an/an/an/an/an/a



Purdue University

Curated by ChEMBL


Assay Description
Ability to inhibit protein-tyrosine kinase activity of p56lck (isolated from bovine thymus) in vitro.


J Med Chem 34: 798-806 (1991)


Article DOI: 10.1021/jm00106a047
BindingDB Entry DOI: 10.7270/Q2CF9P3J
More data for this
Ligand-Target Pair
Tyrosine-protein kinase Lck


(Homo sapiens (Human))
BDBM50011434
PNG
(2-(4-Bromo-phenyl)-4-oxo-4H-chromene-3-carboxylic ...)
Show SMILES COC(=O)c1c(oc2ccccc2c1=O)-c1ccc(Br)cc1
Show InChI InChI=1S/C17H11BrO4/c1-21-17(20)14-15(19)12-4-2-3-5-13(12)22-16(14)10-6-8-11(18)9-7-10/h2-9H,1H3
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n/an/a>2.00E+6n/an/an/an/an/an/a



Purdue University

Curated by ChEMBL


Assay Description
Ability to inhibit protein-tyrosine kinase activity of p56lck (isolated from bovine thymus) in vitro.


J Med Chem 34: 798-806 (1991)


Article DOI: 10.1021/jm00106a047
BindingDB Entry DOI: 10.7270/Q2CF9P3J
More data for this
Ligand-Target Pair
Tyrosine-protein kinase Lck


(Homo sapiens (Human))
BDBM50011445
PNG
(2-(4-Benzyloxy-phenyl)-7-methoxy-4-oxo-4H-chromene...)
Show SMILES COC(=O)c1c(oc2cc(OC)ccc2c1=O)-c1ccc(OCc2ccccc2)cc1
Show InChI InChI=1S/C25H20O6/c1-28-19-12-13-20-21(14-19)31-24(22(23(20)26)25(27)29-2)17-8-10-18(11-9-17)30-15-16-6-4-3-5-7-16/h3-14H,15H2,1-2H3
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n/an/a>2.00E+6n/an/an/an/an/an/a



Purdue University

Curated by ChEMBL


Assay Description
Ability to inhibit protein-tyrosine kinase activity of p56lck (isolated from bovine thymus) in vitro.


J Med Chem 34: 798-806 (1991)


Article DOI: 10.1021/jm00106a047
BindingDB Entry DOI: 10.7270/Q2CF9P3J
More data for this
Ligand-Target Pair
Tyrosine-protein kinase Lck


(Homo sapiens (Human))
BDBM50011419
PNG
(6-Methoxy-2-(4-nitro-phenyl)-4-oxo-4H-chromene-3-c...)
Show SMILES COC(=O)c1c(oc2ccc(OC)cc2c1=O)-c1ccc(cc1)[N+]([O-])=O
Show InChI InChI=1S/C18H13NO7/c1-24-12-7-8-14-13(9-12)16(20)15(18(21)25-2)17(26-14)10-3-5-11(6-4-10)19(22)23/h3-9H,1-2H3
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n/an/a>2.00E+6n/an/an/an/an/an/a



Purdue University

Curated by ChEMBL


Assay Description
Ability to inhibit protein-tyrosine kinase activity of p56lck (isolated from bovine thymus) in vitro.


J Med Chem 34: 798-806 (1991)


Article DOI: 10.1021/jm00106a047
BindingDB Entry DOI: 10.7270/Q2CF9P3J
More data for this
Ligand-Target Pair
Tyrosine-protein kinase Lck


(Homo sapiens (Human))
BDBM50011430
PNG
(4-Oxo-2-(3,4,5-trimethoxy-phenyl)-4H-chromene-3-ca...)
Show SMILES COc1cc(cc(OC)c1OC)-c1oc2ccccc2c(=O)c1C(O)=O
Show InChI InChI=1S/C19H16O7/c1-23-13-8-10(9-14(24-2)18(13)25-3)17-15(19(21)22)16(20)11-6-4-5-7-12(11)26-17/h4-9H,1-3H3,(H,21,22)
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n/an/a>2.00E+6n/an/an/an/an/an/a



Purdue University

Curated by ChEMBL


Assay Description
Ability to inhibit protein-tyrosine kinase activity of p56lck (isolated from bovine thymus) in vitro.


J Med Chem 34: 798-806 (1991)


Article DOI: 10.1021/jm00106a047
BindingDB Entry DOI: 10.7270/Q2CF9P3J
More data for this
Ligand-Target Pair
* indicates data uncertainty>20%