Found 69 hits Enz. Inhib. hit(s) with all data for entry = 50010231 Target/Host (Institution) | Ligand | Target/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 | pH | Temp °C |
Tyrosine-protein kinase Lck
(Homo sapiens (Human)) | BDBM50092224
(3-[4-Amino-5-(4-phenoxy-phenyl)-pyrrolo[2,3-d]pyri...)Show SMILES Nc1ncnc2n(cc(-c3ccc(Oc4ccccc4)cc3)c12)C1CCC(O)C1 Show InChI InChI=1S/C23H22N4O2/c24-22-21-20(13-27(23(21)26-14-25-22)16-8-9-17(28)12-16)15-6-10-19(11-7-15)29-18-4-2-1-3-5-18/h1-7,10-11,13-14,16-17,28H,8-9,12H2,(H2,24,25,26) | PDB
UniProtKB/SwissProt
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| n/a | n/a | <1 | n/a | n/a | n/a | n/a | n/a | n/a |
BASF Bioresearch Corporation
Curated by ChEMBL
| Assay Description Inhibition of p56 Lck tyrosine kinase at 5 uM ATP |
Bioorg Med Chem Lett 10: 2167-70 (2001)
BindingDB Entry DOI: 10.7270/Q2J38RTH |
More data for this Ligand-Target Pair | |
Tyrosine-protein kinase Lck
(Homo sapiens (Human)) | BDBM50092232
(2-[4-Amino-5-(4-phenoxy-phenyl)-pyrrolo[2,3-d]pyri...)Show SMILES Nc1ncnc2n(cc(-c3ccc(Oc4ccccc4)cc3)c12)C1CCCC1O Show InChI InChI=1S/C23H22N4O2/c24-22-21-18(13-27(23(21)26-14-25-22)19-7-4-8-20(19)28)15-9-11-17(12-10-15)29-16-5-2-1-3-6-16/h1-3,5-6,9-14,19-20,28H,4,7-8H2,(H2,24,25,26) | PDB
UniProtKB/SwissProt
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| n/a | n/a | <1 | n/a | n/a | n/a | n/a | n/a | n/a |
BASF Bioresearch Corporation
Curated by ChEMBL
| Assay Description Inhibition of p56 Lck tyrosine kinase at 5 uM ATP |
Bioorg Med Chem Lett 10: 2167-70 (2001)
BindingDB Entry DOI: 10.7270/Q2J38RTH |
More data for this Ligand-Target Pair | |
Tyrosine-protein kinase Lck
(Homo sapiens (Human)) | BDBM50092233
(7-Isopropyl-5-(4-phenoxy-phenyl)-7H-pyrrolo[2,3-d]...)Show SMILES CC(C)n1cc(-c2ccc(Oc3ccccc3)cc2)c2c(N)ncnc12 Show InChI InChI=1S/C21H20N4O/c1-14(2)25-12-18(19-20(22)23-13-24-21(19)25)15-8-10-17(11-9-15)26-16-6-4-3-5-7-16/h3-14H,1-2H3,(H2,22,23,24) | PDB
UniProtKB/SwissProt
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| n/a | n/a | <1 | n/a | n/a | n/a | n/a | n/a | n/a |
BASF Bioresearch Corporation
Curated by ChEMBL
| Assay Description Inhibition of p56 Lck tyrosine kinase at 5 uM ATP |
Bioorg Med Chem Lett 10: 2167-70 (2001)
BindingDB Entry DOI: 10.7270/Q2J38RTH |
More data for this Ligand-Target Pair | |
Tyrosine-protein kinase Lck
(Homo sapiens (Human)) | BDBM50092228
(4-Amino-5-(4-phenoxyphenyl)-7H-pyrrolo[2,3-d]pyrim...)Show SMILES Nc1ncnc2n(cc(-c3ccc(Oc4ccccc4)cc3)c12)C1CCCC1 Show InChI InChI=1S/C23H22N4O/c24-22-21-20(14-27(17-6-4-5-7-17)23(21)26-15-25-22)16-10-12-19(13-11-16)28-18-8-2-1-3-9-18/h1-3,8-15,17H,4-7H2,(H2,24,25,26) | PDB
UniProtKB/SwissProt
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| n/a | n/a | <1 | n/a | n/a | n/a | n/a | n/a | n/a |
BASF Bioresearch Corporation
Curated by ChEMBL
| Assay Description Inhibition of p56 Lck tyrosine kinase at 5 uM ATP |
Bioorg Med Chem Lett 10: 2167-70 (2001)
BindingDB Entry DOI: 10.7270/Q2J38RTH |
More data for this Ligand-Target Pair | |
Tyrosine-protein kinase Lck
(Homo sapiens (Human)) | BDBM50092224
(3-[4-Amino-5-(4-phenoxy-phenyl)-pyrrolo[2,3-d]pyri...)Show SMILES Nc1ncnc2n(cc(-c3ccc(Oc4ccccc4)cc3)c12)C1CCC(O)C1 Show InChI InChI=1S/C23H22N4O2/c24-22-21-20(13-27(23(21)26-14-25-22)16-8-9-17(28)12-16)15-6-10-19(11-7-15)29-18-4-2-1-3-5-18/h1-7,10-11,13-14,16-17,28H,8-9,12H2,(H2,24,25,26) | PDB
UniProtKB/SwissProt
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| n/a | n/a | <1 | n/a | n/a | n/a | n/a | n/a | n/a |
BASF Bioresearch Corporation
Curated by ChEMBL
| Assay Description Inhibition of p56 Lck tyrosine kinase at 5 uM ATP |
Bioorg Med Chem Lett 10: 2167-70 (2001)
BindingDB Entry DOI: 10.7270/Q2J38RTH |
More data for this Ligand-Target Pair | |
Tyrosine-protein kinase Lck
(Homo sapiens (Human)) | BDBM50092226
(4-[4-Amino-5-(4-phenoxy-phenyl)-pyrrolo[2,3-d]pyri...)Show SMILES Nc1ncnc2n(cc(-c3ccc(Oc4ccccc4)cc3)c12)C1CC(O)C(O)C1 Show InChI InChI=1S/C23H22N4O3/c24-22-21-18(14-6-8-17(9-7-14)30-16-4-2-1-3-5-16)12-27(23(21)26-13-25-22)15-10-19(28)20(29)11-15/h1-9,12-13,15,19-20,28-29H,10-11H2,(H2,24,25,26) | PDB
UniProtKB/SwissProt
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| n/a | n/a | <2 | n/a | n/a | n/a | n/a | n/a | n/a |
BASF Bioresearch Corporation
Curated by ChEMBL
| Assay Description Inhibition of p56 Lck tyrosine kinase catalytic domain at 5 uM ATP |
Bioorg Med Chem Lett 10: 2167-70 (2001)
BindingDB Entry DOI: 10.7270/Q2J38RTH |
More data for this Ligand-Target Pair | |
Tyrosine-protein kinase Lck
(Homo sapiens (Human)) | BDBM50092225
(7-tert-Butyl-5-(4-phenoxy-phenyl)-7H-pyrrolo[2,3-d...)Show SMILES CC(C)(C)n1cc(-c2ccc(Oc3ccccc3)cc2)c2c(N)ncnc12 Show InChI InChI=1S/C22H22N4O/c1-22(2,3)26-13-18(19-20(23)24-14-25-21(19)26)15-9-11-17(12-10-15)27-16-7-5-4-6-8-16/h4-14H,1-3H3,(H2,23,24,25) | PDB
UniProtKB/SwissProt
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| n/a | n/a | 2 | n/a | n/a | n/a | n/a | n/a | n/a |
BASF Bioresearch Corporation
Curated by ChEMBL
| Assay Description Inhibition of p56 Lck tyrosine kinase catalytic domain at 5 uM ATP |
Bioorg Med Chem Lett 10: 2167-70 (2001)
BindingDB Entry DOI: 10.7270/Q2J38RTH |
More data for this Ligand-Target Pair | |
Tyrosine-protein kinase Lck
(Homo sapiens (Human)) | BDBM50092228
(4-Amino-5-(4-phenoxyphenyl)-7H-pyrrolo[2,3-d]pyrim...)Show SMILES Nc1ncnc2n(cc(-c3ccc(Oc4ccccc4)cc3)c12)C1CCCC1 Show InChI InChI=1S/C23H22N4O/c24-22-21-20(14-27(17-6-4-5-7-17)23(21)26-15-25-22)16-10-12-19(13-11-16)28-18-8-2-1-3-9-18/h1-3,8-15,17H,4-7H2,(H2,24,25,26) | PDB
UniProtKB/SwissProt
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| n/a | n/a | 2 | n/a | n/a | n/a | n/a | n/a | n/a |
BASF Bioresearch Corporation
Curated by ChEMBL
| Assay Description Inhibition of p56 Lck tyrosine kinase catalytic domain at 1 mM ATP |
Bioorg Med Chem Lett 10: 2167-70 (2001)
BindingDB Entry DOI: 10.7270/Q2J38RTH |
More data for this Ligand-Target Pair | |
Tyrosine-protein kinase Lck
(Homo sapiens (Human)) | BDBM50092224
(3-[4-Amino-5-(4-phenoxy-phenyl)-pyrrolo[2,3-d]pyri...)Show SMILES Nc1ncnc2n(cc(-c3ccc(Oc4ccccc4)cc3)c12)C1CCC(O)C1 Show InChI InChI=1S/C23H22N4O2/c24-22-21-20(13-27(23(21)26-14-25-22)16-8-9-17(28)12-16)15-6-10-19(11-7-15)29-18-4-2-1-3-5-18/h1-7,10-11,13-14,16-17,28H,8-9,12H2,(H2,24,25,26) | PDB
UniProtKB/SwissProt
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| CHEMBL PC cid PC sid UniChem
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| n/a | n/a | 5 | n/a | n/a | n/a | n/a | n/a | n/a |
BASF Bioresearch Corporation
Curated by ChEMBL
| Assay Description Inhibition of p56 Lck tyrosine kinase at 1 mM ATP |
Bioorg Med Chem Lett 10: 2167-70 (2001)
BindingDB Entry DOI: 10.7270/Q2J38RTH |
More data for this Ligand-Target Pair | |
Tyrosine-protein kinase Lck
(Homo sapiens (Human)) | BDBM50092226
(4-[4-Amino-5-(4-phenoxy-phenyl)-pyrrolo[2,3-d]pyri...)Show SMILES Nc1ncnc2n(cc(-c3ccc(Oc4ccccc4)cc3)c12)C1CC(O)C(O)C1 Show InChI InChI=1S/C23H22N4O3/c24-22-21-18(14-6-8-17(9-7-14)30-16-4-2-1-3-5-16)12-27(23(21)26-13-25-22)15-10-19(28)20(29)11-15/h1-9,12-13,15,19-20,28-29H,10-11H2,(H2,24,25,26) | PDB
UniProtKB/SwissProt
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| n/a | n/a | 5 | n/a | n/a | n/a | n/a | n/a | n/a |
BASF Bioresearch Corporation
Curated by ChEMBL
| Assay Description Inhibition of p56 Lck tyrosine kinase catalytic domain at 5 uM ATP |
Bioorg Med Chem Lett 10: 2167-70 (2001)
BindingDB Entry DOI: 10.7270/Q2J38RTH |
More data for this Ligand-Target Pair | |
Tyrosine-protein kinase Lck
(Homo sapiens (Human)) | BDBM50092231
((4-Phenoxy-phenyl)-quinazolin-4-yl-amine | CHEMBL3...)Show InChI InChI=1S/C20H15N3O/c1-2-6-16(7-3-1)24-17-12-10-15(11-13-17)23-20-18-8-4-5-9-19(18)21-14-22-20/h1-14H,(H,21,22,23) | PDB
UniProtKB/SwissProt
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| n/a | n/a | <8 | n/a | n/a | n/a | n/a | n/a | n/a |
BASF Bioresearch Corporation
Curated by ChEMBL
| Assay Description Inhibition of p56 Lck tyrosine kinase at 1 mM ATP |
Bioorg Med Chem Lett 10: 2167-70 (2001)
BindingDB Entry DOI: 10.7270/Q2J38RTH |
More data for this Ligand-Target Pair | |
Tyrosine-protein kinase Lck
(Homo sapiens (Human)) | BDBM50092232
(2-[4-Amino-5-(4-phenoxy-phenyl)-pyrrolo[2,3-d]pyri...)Show SMILES Nc1ncnc2n(cc(-c3ccc(Oc4ccccc4)cc3)c12)C1CCCC1O Show InChI InChI=1S/C23H22N4O2/c24-22-21-18(13-27(23(21)26-14-25-22)19-7-4-8-20(19)28)15-9-11-17(12-10-15)29-16-5-2-1-3-6-16/h1-3,5-6,9-14,19-20,28H,4,7-8H2,(H2,24,25,26) | PDB
UniProtKB/SwissProt
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| n/a | n/a | <8 | n/a | n/a | n/a | n/a | n/a | n/a |
BASF Bioresearch Corporation
Curated by ChEMBL
| Assay Description Inhibition of p56 Lck tyrosine kinase catalytic domain at 5 uM ATP |
Bioorg Med Chem Lett 10: 2167-70 (2001)
BindingDB Entry DOI: 10.7270/Q2J38RTH |
More data for this Ligand-Target Pair | |
Tyrosine-protein kinase Lck
(Homo sapiens (Human)) | BDBM50092233
(7-Isopropyl-5-(4-phenoxy-phenyl)-7H-pyrrolo[2,3-d]...)Show SMILES CC(C)n1cc(-c2ccc(Oc3ccccc3)cc2)c2c(N)ncnc12 Show InChI InChI=1S/C21H20N4O/c1-14(2)25-12-18(19-20(22)23-13-24-21(19)25)15-8-10-17(11-9-15)26-16-6-4-3-5-7-16/h3-14H,1-2H3,(H2,22,23,24) | PDB
UniProtKB/SwissProt
antibodypedia GoogleScholar AffyNet
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| n/a | n/a | 10 | n/a | n/a | n/a | n/a | n/a | n/a |
BASF Bioresearch Corporation
Curated by ChEMBL
| Assay Description Inhibition of p56 Lck tyrosine kinase at 5 uM ATP |
Bioorg Med Chem Lett 10: 2167-70 (2001)
BindingDB Entry DOI: 10.7270/Q2J38RTH |
More data for this Ligand-Target Pair | |
Tyrosine-protein kinase Lck
(Homo sapiens (Human)) | BDBM50092233
(7-Isopropyl-5-(4-phenoxy-phenyl)-7H-pyrrolo[2,3-d]...)Show SMILES CC(C)n1cc(-c2ccc(Oc3ccccc3)cc2)c2c(N)ncnc12 Show InChI InChI=1S/C21H20N4O/c1-14(2)25-12-18(19-20(22)23-13-24-21(19)25)15-8-10-17(11-9-15)26-16-6-4-3-5-7-16/h3-14H,1-2H3,(H2,22,23,24) | PDB
UniProtKB/SwissProt
antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
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| n/a | n/a | 11 | n/a | n/a | n/a | n/a | n/a | n/a |
BASF Bioresearch Corporation
Curated by ChEMBL
| Assay Description Inhibition of p56 Lck tyrosine kinase at 1 mM ATP |
Bioorg Med Chem Lett 10: 2167-70 (2001)
BindingDB Entry DOI: 10.7270/Q2J38RTH |
More data for this Ligand-Target Pair | |
Tyrosine-protein kinase Lck
(Homo sapiens (Human)) | BDBM50092225
(7-tert-Butyl-5-(4-phenoxy-phenyl)-7H-pyrrolo[2,3-d...)Show SMILES CC(C)(C)n1cc(-c2ccc(Oc3ccccc3)cc2)c2c(N)ncnc12 Show InChI InChI=1S/C22H22N4O/c1-22(2,3)26-13-18(19-20(23)24-14-25-21(19)26)15-9-11-17(12-10-15)27-16-7-5-4-6-8-16/h4-14H,1-3H3,(H2,23,24,25) | PDB
UniProtKB/SwissProt
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| n/a | n/a | 14 | n/a | n/a | n/a | n/a | n/a | n/a |
BASF Bioresearch Corporation
Curated by ChEMBL
| Assay Description Inhibition of p56 Lck tyrosine kinase catalytic domain at 5 uM ATP |
Bioorg Med Chem Lett 10: 2167-70 (2001)
BindingDB Entry DOI: 10.7270/Q2J38RTH |
More data for this Ligand-Target Pair | |
Tyrosine-protein kinase Lck
(Homo sapiens (Human)) | BDBM50092228
(4-Amino-5-(4-phenoxyphenyl)-7H-pyrrolo[2,3-d]pyrim...)Show SMILES Nc1ncnc2n(cc(-c3ccc(Oc4ccccc4)cc3)c12)C1CCCC1 Show InChI InChI=1S/C23H22N4O/c24-22-21-20(14-27(17-6-4-5-7-17)23(21)26-15-25-22)16-10-12-19(13-11-16)28-18-8-2-1-3-9-18/h1-3,8-15,17H,4-7H2,(H2,24,25,26) | PDB
UniProtKB/SwissProt
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| n/a | n/a | 16 | n/a | n/a | n/a | n/a | n/a | n/a |
BASF Bioresearch Corporation
Curated by ChEMBL
| Assay Description Inhibition of p56 Lck tyrosine kinase at 5 uM ATP |
Bioorg Med Chem Lett 10: 2167-70 (2001)
BindingDB Entry DOI: 10.7270/Q2J38RTH |
More data for this Ligand-Target Pair | |
Tyrosine-protein kinase Lck
(Homo sapiens (Human)) | BDBM50092226
(4-[4-Amino-5-(4-phenoxy-phenyl)-pyrrolo[2,3-d]pyri...)Show SMILES Nc1ncnc2n(cc(-c3ccc(Oc4ccccc4)cc3)c12)C1CC(O)C(O)C1 Show InChI InChI=1S/C23H22N4O3/c24-22-21-18(14-6-8-17(9-7-14)30-16-4-2-1-3-5-16)12-27(23(21)26-13-25-22)15-10-19(28)20(29)11-15/h1-9,12-13,15,19-20,28-29H,10-11H2,(H2,24,25,26) | PDB
UniProtKB/SwissProt
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Similars
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| n/a | n/a | 23 | n/a | n/a | n/a | n/a | n/a | n/a |
BASF Bioresearch Corporation
Curated by ChEMBL
| Assay Description Inhibition of p56 Lck tyrosine kinase at 1 mM ATP |
Bioorg Med Chem Lett 10: 2167-70 (2001)
BindingDB Entry DOI: 10.7270/Q2J38RTH |
More data for this Ligand-Target Pair | |
Proto-oncogene tyrosine-protein kinase Src
(Homo sapiens (Human)) | BDBM50092232
(2-[4-Amino-5-(4-phenoxy-phenyl)-pyrrolo[2,3-d]pyri...)Show SMILES Nc1ncnc2n(cc(-c3ccc(Oc4ccccc4)cc3)c12)C1CCCC1O Show InChI InChI=1S/C23H22N4O2/c24-22-21-18(13-27(23(21)26-14-25-22)19-7-4-8-20(19)28)15-9-11-17(12-10-15)29-16-5-2-1-3-6-16/h1-3,5-6,9-14,19-20,28H,4,7-8H2,(H2,24,25,26) | PDB MMDB
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UniProtKB/SwissProt
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| CHEMBL PC cid PC sid UniChem
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| n/a | n/a | 40 | n/a | n/a | n/a | n/a | n/a | n/a |
BASF Bioresearch Corporation
Curated by ChEMBL
| Assay Description Inhibition of src at 5 mM ATP |
Bioorg Med Chem Lett 10: 2167-70 (2001)
BindingDB Entry DOI: 10.7270/Q2J38RTH |
More data for this Ligand-Target Pair | |
Proto-oncogene tyrosine-protein kinase Src
(Homo sapiens (Human)) | BDBM50092233
(7-Isopropyl-5-(4-phenoxy-phenyl)-7H-pyrrolo[2,3-d]...)Show SMILES CC(C)n1cc(-c2ccc(Oc3ccccc3)cc2)c2c(N)ncnc12 Show InChI InChI=1S/C21H20N4O/c1-14(2)25-12-18(19-20(22)23-13-24-21(19)25)15-8-10-17(11-9-15)26-16-6-4-3-5-7-16/h3-14H,1-2H3,(H2,22,23,24) | PDB MMDB
KEGG
UniProtKB/SwissProt
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| CHEMBL PC cid PC sid UniChem
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| n/a | n/a | 48 | n/a | n/a | n/a | n/a | n/a | n/a |
BASF Bioresearch Corporation
Curated by ChEMBL
| Assay Description Inhibition of src at 5 mM ATP |
Bioorg Med Chem Lett 10: 2167-70 (2001)
BindingDB Entry DOI: 10.7270/Q2J38RTH |
More data for this Ligand-Target Pair | |
Angiopoietin-1 receptor
(Homo sapiens (Human)) | BDBM50092224
(3-[4-Amino-5-(4-phenoxy-phenyl)-pyrrolo[2,3-d]pyri...)Show SMILES Nc1ncnc2n(cc(-c3ccc(Oc4ccccc4)cc3)c12)C1CCC(O)C1 Show InChI InChI=1S/C23H22N4O2/c24-22-21-20(13-27(23(21)26-14-25-22)16-8-9-17(28)12-16)15-6-10-19(11-7-15)29-18-4-2-1-3-5-18/h1-7,10-11,13-14,16-17,28H,8-9,12H2,(H2,24,25,26) | PDB MMDB
KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
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| PubMed
| n/a | n/a | 58 | n/a | n/a | n/a | n/a | n/a | n/a |
BASF Bioresearch Corporation
Curated by ChEMBL
| Assay Description Inhibition of tie-2 at 5 uM ATP |
Bioorg Med Chem Lett 10: 2167-70 (2001)
BindingDB Entry DOI: 10.7270/Q2J38RTH |
More data for this Ligand-Target Pair | |
Proto-oncogene tyrosine-protein kinase Src
(Homo sapiens (Human)) | BDBM50092228
(4-Amino-5-(4-phenoxyphenyl)-7H-pyrrolo[2,3-d]pyrim...)Show SMILES Nc1ncnc2n(cc(-c3ccc(Oc4ccccc4)cc3)c12)C1CCCC1 Show InChI InChI=1S/C23H22N4O/c24-22-21-20(14-27(17-6-4-5-7-17)23(21)26-15-25-22)16-10-12-19(13-11-16)28-18-8-2-1-3-9-18/h1-3,8-15,17H,4-7H2,(H2,24,25,26) | PDB MMDB
KEGG
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B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
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| n/a | n/a | 70 | n/a | n/a | n/a | n/a | n/a | n/a |
BASF Bioresearch Corporation
Curated by ChEMBL
| Assay Description Inhibition of src at 5 mM ATP |
Bioorg Med Chem Lett 10: 2167-70 (2001)
BindingDB Entry DOI: 10.7270/Q2J38RTH |
More data for this Ligand-Target Pair | |
Tyrosine-protein kinase Lck
(Homo sapiens (Human)) | BDBM50092225
(7-tert-Butyl-5-(4-phenoxy-phenyl)-7H-pyrrolo[2,3-d...)Show SMILES CC(C)(C)n1cc(-c2ccc(Oc3ccccc3)cc2)c2c(N)ncnc12 Show InChI InChI=1S/C22H22N4O/c1-22(2,3)26-13-18(19-20(23)24-14-25-21(19)26)15-9-11-17(12-10-15)27-16-7-5-4-6-8-16/h4-14H,1-3H3,(H2,23,24,25) | PDB
UniProtKB/SwissProt
antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Patents
Similars
| PubMed
| n/a | n/a | 75 | n/a | n/a | n/a | n/a | n/a | n/a |
BASF Bioresearch Corporation
Curated by ChEMBL
| Assay Description Inhibition of p56 Lck tyrosine kinase at 1 mM ATP |
Bioorg Med Chem Lett 10: 2167-70 (2001)
BindingDB Entry DOI: 10.7270/Q2J38RTH |
More data for this Ligand-Target Pair | |
Proto-oncogene tyrosine-protein kinase Src
(Homo sapiens (Human)) | BDBM50092226
(4-[4-Amino-5-(4-phenoxy-phenyl)-pyrrolo[2,3-d]pyri...)Show SMILES Nc1ncnc2n(cc(-c3ccc(Oc4ccccc4)cc3)c12)C1CC(O)C(O)C1 Show InChI InChI=1S/C23H22N4O3/c24-22-21-18(14-6-8-17(9-7-14)30-16-4-2-1-3-5-16)12-27(23(21)26-13-25-22)15-10-19(28)20(29)11-15/h1-9,12-13,15,19-20,28-29H,10-11H2,(H2,24,25,26) | PDB MMDB
KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| PubMed
| n/a | n/a | 84 | n/a | n/a | n/a | n/a | n/a | n/a |
BASF Bioresearch Corporation
Curated by ChEMBL
| Assay Description Inhibition of src at 5 mM ATP |
Bioorg Med Chem Lett 10: 2167-70 (2001)
BindingDB Entry DOI: 10.7270/Q2J38RTH |
More data for this Ligand-Target Pair | |
Vascular endothelial growth factor receptor 2
(Homo sapiens (Human)) | BDBM50092224
(3-[4-Amino-5-(4-phenoxy-phenyl)-pyrrolo[2,3-d]pyri...)Show SMILES Nc1ncnc2n(cc(-c3ccc(Oc4ccccc4)cc3)c12)C1CCC(O)C1 Show InChI InChI=1S/C23H22N4O2/c24-22-21-20(13-27(23(21)26-14-25-22)16-8-9-17(28)12-16)15-6-10-19(11-7-15)29-18-4-2-1-3-5-18/h1-7,10-11,13-14,16-17,28H,8-9,12H2,(H2,24,25,26) | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Patents
Similars
| PubMed
| n/a | n/a | 85 | n/a | n/a | n/a | n/a | n/a | n/a |
BASF Bioresearch Corporation
Curated by ChEMBL
| Assay Description Inhibition of Vascular endothelial growth factor receptor 2 at 5 uM ATP |
Bioorg Med Chem Lett 10: 2167-70 (2001)
BindingDB Entry DOI: 10.7270/Q2J38RTH |
More data for this Ligand-Target Pair | |
Proto-oncogene tyrosine-protein kinase Src
(Homo sapiens (Human)) | BDBM50092224
(3-[4-Amino-5-(4-phenoxy-phenyl)-pyrrolo[2,3-d]pyri...)Show SMILES Nc1ncnc2n(cc(-c3ccc(Oc4ccccc4)cc3)c12)C1CCC(O)C1 Show InChI InChI=1S/C23H22N4O2/c24-22-21-20(13-27(23(21)26-14-25-22)16-8-9-17(28)12-16)15-6-10-19(11-7-15)29-18-4-2-1-3-5-18/h1-7,10-11,13-14,16-17,28H,8-9,12H2,(H2,24,25,26) | PDB MMDB
KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Patents
Similars
| PubMed
| n/a | n/a | 88 | n/a | n/a | n/a | n/a | n/a | n/a |
BASF Bioresearch Corporation
Curated by ChEMBL
| Assay Description Inhibition of src at 5 mM ATP |
Bioorg Med Chem Lett 10: 2167-70 (2001)
BindingDB Entry DOI: 10.7270/Q2J38RTH |
More data for this Ligand-Target Pair | |
Tyrosine-protein kinase Lck
(Homo sapiens (Human)) | BDBM50092227
(7-Cyclopentyl-5-(3-phenoxy-phenyl)-7H-pyrrolo[2,3-...)Show SMILES Nc1ncnc2n(cc(-c3cccc(Oc4ccccc4)c3)c12)C1CCCC1 Show InChI InChI=1S/C23H22N4O/c24-22-21-20(14-27(17-8-4-5-9-17)23(21)26-15-25-22)16-7-6-12-19(13-16)28-18-10-2-1-3-11-18/h1-3,6-7,10-15,17H,4-5,8-9H2,(H2,24,25,26) | PDB
UniProtKB/SwissProt
antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Patents
Similars
| PubMed
| n/a | n/a | 140 | n/a | n/a | n/a | n/a | n/a | n/a |
BASF Bioresearch Corporation
Curated by ChEMBL
| Assay Description Inhibition of p56 Lck tyrosine kinase catalytic domain at 5 uM ATP |
Bioorg Med Chem Lett 10: 2167-70 (2001)
BindingDB Entry DOI: 10.7270/Q2J38RTH |
More data for this Ligand-Target Pair | |
Proto-oncogene tyrosine-protein kinase Src
(Homo sapiens (Human)) | BDBM50092229
(7-tert-Butyl-5-(4-chloro-phenyl)-7H-pyrrolo[2,3-d]...)Show InChI InChI=1S/C16H17ClN4/c1-16(2,3)21-8-12(10-4-6-11(17)7-5-10)13-14(18)19-9-20-15(13)21/h4-9H,1-3H3,(H2,18,19,20) | PDB MMDB
KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| Purchase
CHEMBL PC cid PC sid UniChem
Patents
Similars
| PubMed
| n/a | n/a | 150 | n/a | n/a | n/a | n/a | n/a | n/a |
BASF Bioresearch Corporation
Curated by ChEMBL
| Assay Description Inhibition of src at 5 mM ATP |
Bioorg Med Chem Lett 10: 2167-70 (2001)
BindingDB Entry DOI: 10.7270/Q2J38RTH |
More data for this Ligand-Target Pair | |
Angiopoietin-1 receptor
(Homo sapiens (Human)) | BDBM50092226
(4-[4-Amino-5-(4-phenoxy-phenyl)-pyrrolo[2,3-d]pyri...)Show SMILES Nc1ncnc2n(cc(-c3ccc(Oc4ccccc4)cc3)c12)C1CC(O)C(O)C1 Show InChI InChI=1S/C23H22N4O3/c24-22-21-18(14-6-8-17(9-7-14)30-16-4-2-1-3-5-16)12-27(23(21)26-13-25-22)15-10-19(28)20(29)11-15/h1-9,12-13,15,19-20,28-29H,10-11H2,(H2,24,25,26) | PDB MMDB
KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| PubMed
| n/a | n/a | 150 | n/a | n/a | n/a | n/a | n/a | n/a |
BASF Bioresearch Corporation
Curated by ChEMBL
| Assay Description Inhibition of tie-2 at 5 uM ATP |
Bioorg Med Chem Lett 10: 2167-70 (2001)
BindingDB Entry DOI: 10.7270/Q2J38RTH |
More data for this Ligand-Target Pair | |
Tyrosine-protein kinase Lck
(Homo sapiens (Human)) | BDBM25116
(1-tert-butyl-3-(4-methylphenyl)-1H-pyrazolo[3,4-d]...)Show InChI InChI=1S/C16H19N5/c1-10-5-7-11(8-6-10)13-12-14(17)18-9-19-15(12)21(20-13)16(2,3)4/h5-9H,1-4H3,(H2,17,18,19) | PDB
UniProtKB/SwissProt
antibodypedia GoogleScholar AffyNet
| Purchase
CHEMBL DrugBank MCE MMDB PC cid PC sid PDB UniChem
Patents
Similars
| PubMed
| n/a | n/a | 151 | n/a | n/a | n/a | n/a | n/a | n/a |
BASF Bioresearch Corporation
Curated by ChEMBL
| Assay Description Inhibition of p56 Lck tyrosine kinase at 5 uM ATP |
Bioorg Med Chem Lett 10: 2167-70 (2001)
BindingDB Entry DOI: 10.7270/Q2J38RTH |
More data for this Ligand-Target Pair | |
Proto-oncogene tyrosine-protein kinase Src
(Homo sapiens (Human)) | BDBM25116
(1-tert-butyl-3-(4-methylphenyl)-1H-pyrazolo[3,4-d]...)Show InChI InChI=1S/C16H19N5/c1-10-5-7-11(8-6-10)13-12-14(17)18-9-19-15(12)21(20-13)16(2,3)4/h5-9H,1-4H3,(H2,17,18,19) | PDB MMDB
KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| Purchase
CHEMBL DrugBank MCE MMDB PC cid PC sid PDB UniChem
Patents
Similars
| PubMed
| n/a | n/a | 170 | n/a | n/a | n/a | n/a | n/a | n/a |
BASF Bioresearch Corporation
Curated by ChEMBL
| Assay Description Inhibition of src at 5 mM ATP |
Bioorg Med Chem Lett 10: 2167-70 (2001)
BindingDB Entry DOI: 10.7270/Q2J38RTH |
More data for this Ligand-Target Pair | |
Tyrosine-protein kinase Lck
(Homo sapiens (Human)) | BDBM50092229
(7-tert-Butyl-5-(4-chloro-phenyl)-7H-pyrrolo[2,3-d]...)Show InChI InChI=1S/C16H17ClN4/c1-16(2,3)21-8-12(10-4-6-11(17)7-5-10)13-14(18)19-9-20-15(13)21/h4-9H,1-3H3,(H2,18,19,20) | PDB
UniProtKB/SwissProt
antibodypedia GoogleScholar AffyNet
| Purchase
CHEMBL PC cid PC sid UniChem
Patents
Similars
| PubMed
| n/a | n/a | 220 | n/a | n/a | n/a | n/a | n/a | n/a |
BASF Bioresearch Corporation
Curated by ChEMBL
| Assay Description Inhibition of p56 Lck tyrosine kinase at 5 uM ATP |
Bioorg Med Chem Lett 10: 2167-70 (2001)
BindingDB Entry DOI: 10.7270/Q2J38RTH |
More data for this Ligand-Target Pair | |
Tyrosine-protein kinase Lck
(Homo sapiens (Human)) | BDBM25116
(1-tert-butyl-3-(4-methylphenyl)-1H-pyrazolo[3,4-d]...)Show InChI InChI=1S/C16H19N5/c1-10-5-7-11(8-6-10)13-12-14(17)18-9-19-15(12)21(20-13)16(2,3)4/h5-9H,1-4H3,(H2,17,18,19) | PDB
UniProtKB/SwissProt
antibodypedia GoogleScholar AffyNet
| Purchase
CHEMBL DrugBank MCE MMDB PC cid PC sid PDB UniChem
Patents
Similars
| PubMed
| n/a | n/a | 250 | n/a | n/a | n/a | n/a | n/a | n/a |
BASF Bioresearch Corporation
Curated by ChEMBL
| Assay Description Inhibition of p56 Lck tyrosine kinase catalytic domain at 5 uM ATP |
Bioorg Med Chem Lett 10: 2167-70 (2001)
BindingDB Entry DOI: 10.7270/Q2J38RTH |
More data for this Ligand-Target Pair | |
Vascular endothelial growth factor receptor 2
(Homo sapiens (Human)) | BDBM50092226
(4-[4-Amino-5-(4-phenoxy-phenyl)-pyrrolo[2,3-d]pyri...)Show SMILES Nc1ncnc2n(cc(-c3ccc(Oc4ccccc4)cc3)c12)C1CC(O)C(O)C1 Show InChI InChI=1S/C23H22N4O3/c24-22-21-18(14-6-8-17(9-7-14)30-16-4-2-1-3-5-16)12-27(23(21)26-13-25-22)15-10-19(28)20(29)11-15/h1-9,12-13,15,19-20,28-29H,10-11H2,(H2,24,25,26) | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| PubMed
| n/a | n/a | 270 | n/a | n/a | n/a | n/a | n/a | n/a |
BASF Bioresearch Corporation
Curated by ChEMBL
| Assay Description Inhibition of Vascular endothelial growth factor receptor 2 at 5 uM ATP |
Bioorg Med Chem Lett 10: 2167-70 (2001)
BindingDB Entry DOI: 10.7270/Q2J38RTH |
More data for this Ligand-Target Pair | |
Tyrosine-protein kinase Lck
(Homo sapiens (Human)) | BDBM50092226
(4-[4-Amino-5-(4-phenoxy-phenyl)-pyrrolo[2,3-d]pyri...)Show SMILES Nc1ncnc2n(cc(-c3ccc(Oc4ccccc4)cc3)c12)C1CC(O)C(O)C1 Show InChI InChI=1S/C23H22N4O3/c24-22-21-18(14-6-8-17(9-7-14)30-16-4-2-1-3-5-16)12-27(23(21)26-13-25-22)15-10-19(28)20(29)11-15/h1-9,12-13,15,19-20,28-29H,10-11H2,(H2,24,25,26) | PDB
UniProtKB/SwissProt
antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| PubMed
| n/a | n/a | 317 | n/a | n/a | n/a | n/a | n/a | n/a |
BASF Bioresearch Corporation
Curated by ChEMBL
| Assay Description Inhibition of p56 Lck tyrosine kinase catalytic domain at 1 mM ATP |
Bioorg Med Chem Lett 10: 2167-70 (2001)
BindingDB Entry DOI: 10.7270/Q2J38RTH |
More data for this Ligand-Target Pair | |
Tyrosine-protein kinase Lck
(Homo sapiens (Human)) | BDBM50092230
(7-Cyclopentyl-5-(2-phenoxy-phenyl)-7H-pyrrolo[2,3-...)Show SMILES Nc1ncnc2n(cc(-c3ccccc3Oc3ccccc3)c12)C1CCCC1 Show InChI InChI=1S/C23H22N4O/c24-22-21-19(14-27(16-8-4-5-9-16)23(21)26-15-25-22)18-12-6-7-13-20(18)28-17-10-2-1-3-11-17/h1-3,6-7,10-16H,4-5,8-9H2,(H2,24,25,26) | PDB
UniProtKB/SwissProt
antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Patents
Similars
| PubMed
| n/a | n/a | 390 | n/a | n/a | n/a | n/a | n/a | n/a |
BASF Bioresearch Corporation
Curated by ChEMBL
| Assay Description Inhibition of p56 Lck tyrosine kinase at 5 uM ATP |
Bioorg Med Chem Lett 10: 2167-70 (2001)
BindingDB Entry DOI: 10.7270/Q2J38RTH |
More data for this Ligand-Target Pair | |
Angiopoietin-1 receptor
(Homo sapiens (Human)) | BDBM50092233
(7-Isopropyl-5-(4-phenoxy-phenyl)-7H-pyrrolo[2,3-d]...)Show SMILES CC(C)n1cc(-c2ccc(Oc3ccccc3)cc2)c2c(N)ncnc12 Show InChI InChI=1S/C21H20N4O/c1-14(2)25-12-18(19-20(22)23-13-24-21(19)25)15-8-10-17(11-9-15)26-16-6-4-3-5-7-16/h3-14H,1-2H3,(H2,22,23,24) | PDB MMDB
KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Patents
Similars
| PubMed
| n/a | n/a | 430 | n/a | n/a | n/a | n/a | n/a | n/a |
BASF Bioresearch Corporation
Curated by ChEMBL
| Assay Description Inhibition of tie-2 at 5 uM ATP |
Bioorg Med Chem Lett 10: 2167-70 (2001)
BindingDB Entry DOI: 10.7270/Q2J38RTH |
More data for this Ligand-Target Pair | |
Vascular endothelial growth factor receptor 2
(Homo sapiens (Human)) | BDBM50092233
(7-Isopropyl-5-(4-phenoxy-phenyl)-7H-pyrrolo[2,3-d]...)Show SMILES CC(C)n1cc(-c2ccc(Oc3ccccc3)cc2)c2c(N)ncnc12 Show InChI InChI=1S/C21H20N4O/c1-14(2)25-12-18(19-20(22)23-13-24-21(19)25)15-8-10-17(11-9-15)26-16-6-4-3-5-7-16/h3-14H,1-2H3,(H2,22,23,24) | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Patents
Similars
| PubMed
| n/a | n/a | 430 | n/a | n/a | n/a | n/a | n/a | n/a |
BASF Bioresearch Corporation
Curated by ChEMBL
| Assay Description Inhibition of Vascular endothelial growth factor receptor 2 at 5 uM ATP |
Bioorg Med Chem Lett 10: 2167-70 (2001)
BindingDB Entry DOI: 10.7270/Q2J38RTH |
More data for this Ligand-Target Pair | |
Tyrosine-protein kinase Lck
(Homo sapiens (Human)) | BDBM50092224
(3-[4-Amino-5-(4-phenoxy-phenyl)-pyrrolo[2,3-d]pyri...)Show SMILES Nc1ncnc2n(cc(-c3ccc(Oc4ccccc4)cc3)c12)C1CCC(O)C1 Show InChI InChI=1S/C23H22N4O2/c24-22-21-20(13-27(23(21)26-14-25-22)16-8-9-17(28)12-16)15-6-10-19(11-7-15)29-18-4-2-1-3-5-18/h1-7,10-11,13-14,16-17,28H,8-9,12H2,(H2,24,25,26) | PDB
UniProtKB/SwissProt
antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Patents
Similars
| PubMed
| n/a | n/a | 544 | n/a | n/a | n/a | n/a | n/a | n/a |
BASF Bioresearch Corporation
Curated by ChEMBL
| Assay Description Inhibition of p56 Lck tyrosine kinase catalytic domain at 1 mM ATP |
Bioorg Med Chem Lett 10: 2167-70 (2001)
BindingDB Entry DOI: 10.7270/Q2J38RTH |
More data for this Ligand-Target Pair | |
Angiopoietin-1 receptor
(Homo sapiens (Human)) | BDBM50092232
(2-[4-Amino-5-(4-phenoxy-phenyl)-pyrrolo[2,3-d]pyri...)Show SMILES Nc1ncnc2n(cc(-c3ccc(Oc4ccccc4)cc3)c12)C1CCCC1O Show InChI InChI=1S/C23H22N4O2/c24-22-21-18(13-27(23(21)26-14-25-22)19-7-4-8-20(19)28)15-9-11-17(12-10-15)29-16-5-2-1-3-6-16/h1-3,5-6,9-14,19-20,28H,4,7-8H2,(H2,24,25,26) | PDB MMDB
KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Patents
Similars
| PubMed
| n/a | n/a | 600 | n/a | n/a | n/a | n/a | n/a | n/a |
BASF Bioresearch Corporation
Curated by ChEMBL
| Assay Description Inhibition of tie-2 at 5 uM ATP |
Bioorg Med Chem Lett 10: 2167-70 (2001)
BindingDB Entry DOI: 10.7270/Q2J38RTH |
More data for this Ligand-Target Pair | |
Proto-oncogene tyrosine-protein kinase Src
(Homo sapiens (Human)) | BDBM50092225
(7-tert-Butyl-5-(4-phenoxy-phenyl)-7H-pyrrolo[2,3-d...)Show SMILES CC(C)(C)n1cc(-c2ccc(Oc3ccccc3)cc2)c2c(N)ncnc12 Show InChI InChI=1S/C22H22N4O/c1-22(2,3)26-13-18(19-20(23)24-14-25-21(19)26)15-9-11-17(12-10-15)27-16-7-5-4-6-8-16/h4-14H,1-3H3,(H2,23,24,25) | PDB MMDB
KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Patents
Similars
| PubMed
| n/a | n/a | 610 | n/a | n/a | n/a | n/a | n/a | n/a |
BASF Bioresearch Corporation
Curated by ChEMBL
| Assay Description Inhibition of src at 5 mM ATP |
Bioorg Med Chem Lett 10: 2167-70 (2001)
BindingDB Entry DOI: 10.7270/Q2J38RTH |
More data for this Ligand-Target Pair | |
Vascular endothelial growth factor receptor 2
(Homo sapiens (Human)) | BDBM50092232
(2-[4-Amino-5-(4-phenoxy-phenyl)-pyrrolo[2,3-d]pyri...)Show SMILES Nc1ncnc2n(cc(-c3ccc(Oc4ccccc4)cc3)c12)C1CCCC1O Show InChI InChI=1S/C23H22N4O2/c24-22-21-18(13-27(23(21)26-14-25-22)19-7-4-8-20(19)28)15-9-11-17(12-10-15)29-16-5-2-1-3-6-16/h1-3,5-6,9-14,19-20,28H,4,7-8H2,(H2,24,25,26) | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Patents
Similars
| PubMed
| n/a | n/a | 1.00E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
BASF Bioresearch Corporation
Curated by ChEMBL
| Assay Description Inhibition of Vascular endothelial growth factor receptor 2 at 5 uM ATP |
Bioorg Med Chem Lett 10: 2167-70 (2001)
BindingDB Entry DOI: 10.7270/Q2J38RTH |
More data for this Ligand-Target Pair | |
Proto-oncogene tyrosine-protein kinase Src
(Homo sapiens (Human)) | BDBM50092227
(7-Cyclopentyl-5-(3-phenoxy-phenyl)-7H-pyrrolo[2,3-...)Show SMILES Nc1ncnc2n(cc(-c3cccc(Oc4ccccc4)c3)c12)C1CCCC1 Show InChI InChI=1S/C23H22N4O/c24-22-21-20(14-27(17-8-4-5-9-17)23(21)26-15-25-22)16-7-6-12-19(13-16)28-18-10-2-1-3-11-18/h1-3,6-7,10-15,17H,4-5,8-9H2,(H2,24,25,26) | PDB MMDB
KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Patents
Similars
| PubMed
| n/a | n/a | >1.00E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
BASF Bioresearch Corporation
Curated by ChEMBL
| Assay Description Inhibition of src at 5 mM ATP |
Bioorg Med Chem Lett 10: 2167-70 (2001)
BindingDB Entry DOI: 10.7270/Q2J38RTH |
More data for this Ligand-Target Pair | |
Tyrosine-protein kinase Lck
(Homo sapiens (Human)) | BDBM50092228
(4-Amino-5-(4-phenoxyphenyl)-7H-pyrrolo[2,3-d]pyrim...)Show SMILES Nc1ncnc2n(cc(-c3ccc(Oc4ccccc4)cc3)c12)C1CCCC1 Show InChI InChI=1S/C23H22N4O/c24-22-21-20(14-27(17-6-4-5-7-17)23(21)26-15-25-22)16-10-12-19(13-11-16)28-18-8-2-1-3-9-18/h1-3,8-15,17H,4-7H2,(H2,24,25,26) | PDB
UniProtKB/SwissProt
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| n/a | n/a | 1.07E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
BASF Bioresearch Corporation
Curated by ChEMBL
| Assay Description Inhibition of p56 Lck tyrosine kinase catalytic domain at 1 mM ATP |
Bioorg Med Chem Lett 10: 2167-70 (2001)
BindingDB Entry DOI: 10.7270/Q2J38RTH |
More data for this Ligand-Target Pair | |
Tyrosine-protein kinase Lck
(Homo sapiens (Human)) | BDBM50092227
(7-Cyclopentyl-5-(3-phenoxy-phenyl)-7H-pyrrolo[2,3-...)Show SMILES Nc1ncnc2n(cc(-c3cccc(Oc4ccccc4)c3)c12)C1CCCC1 Show InChI InChI=1S/C23H22N4O/c24-22-21-20(14-27(17-8-4-5-9-17)23(21)26-15-25-22)16-7-6-12-19(13-16)28-18-10-2-1-3-11-18/h1-3,6-7,10-15,17H,4-5,8-9H2,(H2,24,25,26) | PDB
UniProtKB/SwissProt
antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Patents
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| PubMed
| n/a | n/a | 1.18E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
BASF Bioresearch Corporation
Curated by ChEMBL
| Assay Description Inhibition of p56 Lck tyrosine kinase at 1 mM ATP |
Bioorg Med Chem Lett 10: 2167-70 (2001)
BindingDB Entry DOI: 10.7270/Q2J38RTH |
More data for this Ligand-Target Pair | |
Tyrosine-protein kinase Lck
(Homo sapiens (Human)) | BDBM50092227
(7-Cyclopentyl-5-(3-phenoxy-phenyl)-7H-pyrrolo[2,3-...)Show SMILES Nc1ncnc2n(cc(-c3cccc(Oc4ccccc4)c3)c12)C1CCCC1 Show InChI InChI=1S/C23H22N4O/c24-22-21-20(14-27(17-8-4-5-9-17)23(21)26-15-25-22)16-7-6-12-19(13-16)28-18-10-2-1-3-11-18/h1-3,6-7,10-15,17H,4-5,8-9H2,(H2,24,25,26) | PDB
UniProtKB/SwissProt
antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Patents
Similars
| PubMed
| n/a | n/a | 1.20E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
BASF Bioresearch Corporation
Curated by ChEMBL
| Assay Description Inhibition of p56 Lck tyrosine kinase catalytic domain at 5 uM ATP |
Bioorg Med Chem Lett 10: 2167-70 (2001)
BindingDB Entry DOI: 10.7270/Q2J38RTH |
More data for this Ligand-Target Pair | |
Tyrosine-protein kinase Lck
(Homo sapiens (Human)) | BDBM50092232
(2-[4-Amino-5-(4-phenoxy-phenyl)-pyrrolo[2,3-d]pyri...)Show SMILES Nc1ncnc2n(cc(-c3ccc(Oc4ccccc4)cc3)c12)C1CCCC1O Show InChI InChI=1S/C23H22N4O2/c24-22-21-18(13-27(23(21)26-14-25-22)19-7-4-8-20(19)28)15-9-11-17(12-10-15)29-16-5-2-1-3-6-16/h1-3,5-6,9-14,19-20,28H,4,7-8H2,(H2,24,25,26) | PDB
UniProtKB/SwissProt
antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Patents
Similars
| PubMed
| n/a | n/a | 1.32E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
BASF Bioresearch Corporation
Curated by ChEMBL
| Assay Description Inhibition of p56 Lck tyrosine kinase catalytic domain at 1 mM ATP |
Bioorg Med Chem Lett 10: 2167-70 (2001)
BindingDB Entry DOI: 10.7270/Q2J38RTH |
More data for this Ligand-Target Pair | |
Tyrosine-protein kinase Lck
(Homo sapiens (Human)) | BDBM50092232
(2-[4-Amino-5-(4-phenoxy-phenyl)-pyrrolo[2,3-d]pyri...)Show SMILES Nc1ncnc2n(cc(-c3ccc(Oc4ccccc4)cc3)c12)C1CCCC1O Show InChI InChI=1S/C23H22N4O2/c24-22-21-18(13-27(23(21)26-14-25-22)19-7-4-8-20(19)28)15-9-11-17(12-10-15)29-16-5-2-1-3-6-16/h1-3,5-6,9-14,19-20,28H,4,7-8H2,(H2,24,25,26) | PDB
UniProtKB/SwissProt
antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Patents
Similars
| PubMed
| n/a | n/a | 1.32E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
BASF Bioresearch Corporation
Curated by ChEMBL
| Assay Description Inhibition of p56 Lck tyrosine kinase catalytic domain at 1 mM ATP |
Bioorg Med Chem Lett 10: 2167-70 (2001)
BindingDB Entry DOI: 10.7270/Q2J38RTH |
More data for this Ligand-Target Pair | |
Vascular endothelial growth factor receptor 2
(Homo sapiens (Human)) | BDBM50092228
(4-Amino-5-(4-phenoxyphenyl)-7H-pyrrolo[2,3-d]pyrim...)Show SMILES Nc1ncnc2n(cc(-c3ccc(Oc4ccccc4)cc3)c12)C1CCCC1 Show InChI InChI=1S/C23H22N4O/c24-22-21-20(14-27(17-6-4-5-7-17)23(21)26-15-25-22)16-10-12-19(13-11-16)28-18-8-2-1-3-9-18/h1-3,8-15,17H,4-7H2,(H2,24,25,26) | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
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CHEMBL MCE MMDB PC cid PC sid PDB UniChem
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| n/a | n/a | 1.57E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
BASF Bioresearch Corporation
Curated by ChEMBL
| Assay Description Inhibition of Vascular endothelial growth factor receptor 2 at 5 uM ATP |
Bioorg Med Chem Lett 10: 2167-70 (2001)
BindingDB Entry DOI: 10.7270/Q2J38RTH |
More data for this Ligand-Target Pair | |
Vascular endothelial growth factor receptor 2
(Homo sapiens (Human)) | BDBM25116
(1-tert-butyl-3-(4-methylphenyl)-1H-pyrazolo[3,4-d]...)Show InChI InChI=1S/C16H19N5/c1-10-5-7-11(8-6-10)13-12-14(17)18-9-19-15(12)21(20-13)16(2,3)4/h5-9H,1-4H3,(H2,17,18,19) | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
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CHEMBL DrugBank MCE MMDB PC cid PC sid PDB UniChem
Patents
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| PubMed
| n/a | n/a | 1.60E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
BASF Bioresearch Corporation
Curated by ChEMBL
| Assay Description Inhibition of Vascular endothelial growth factor receptor 2 at 5 uM ATP |
Bioorg Med Chem Lett 10: 2167-70 (2001)
BindingDB Entry DOI: 10.7270/Q2J38RTH |
More data for this Ligand-Target Pair | |
Angiopoietin-1 receptor
(Homo sapiens (Human)) | BDBM50092228
(4-Amino-5-(4-phenoxyphenyl)-7H-pyrrolo[2,3-d]pyrim...)Show SMILES Nc1ncnc2n(cc(-c3ccc(Oc4ccccc4)cc3)c12)C1CCCC1 Show InChI InChI=1S/C23H22N4O/c24-22-21-20(14-27(17-6-4-5-7-17)23(21)26-15-25-22)16-10-12-19(13-11-16)28-18-8-2-1-3-9-18/h1-3,8-15,17H,4-7H2,(H2,24,25,26) | PDB MMDB
KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| Purchase
CHEMBL MCE MMDB PC cid PC sid PDB UniChem
Patents
Similars
| PubMed
| n/a | n/a | 1.98E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
BASF Bioresearch Corporation
Curated by ChEMBL
| Assay Description Inhibition of tie-2 at 5 uM ATP |
Bioorg Med Chem Lett 10: 2167-70 (2001)
BindingDB Entry DOI: 10.7270/Q2J38RTH |
More data for this Ligand-Target Pair | |