Found 92 hits of Enzyme Inhibition Constant Data 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 |
|---|
Hepatocyte growth factor receptor
(Homo sapiens (Human)) | BDBM50306682
((R)-3-(1-(2,6-dichloro-3-fluorophenyl)ethoxy)-5-(1...)Show SMILES C[C@@H](Oc1cc(cnc1N)-c1cnn(c1)C1CCNCC1)c1c(Cl)ccc(F)c1Cl |r| Show InChI InChI=1S/C21H22Cl2FN5O/c1-12(19-16(22)2-3-17(24)20(19)23)30-18-8-13(9-27-21(18)25)14-10-28-29(11-14)15-4-6-26-7-5-15/h2-3,8-12,15,26H,4-7H2,1H3,(H2,25,27)/t12-/m1/s1 | PDB
MMDB
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
| Purchase
CHEMBL
DrugBank
MCE
MMDB
PC cid
PC sid
PDB
UniChem
Patents
Similars
| PDB
Article
PubMed
| n/a | n/a | 8 | n/a | n/a | n/a | n/a | n/a | n/a |
Chugai Pharmaceutical Co, Ltd
Curated by ChEMBL
| Assay Description
Inhibition of recombinant c-Met by TR-FRET assay |
Bioorg Med Chem Lett 20: 1405-9 (2010)
Article DOI: 10.1016/j.bmcl.2009.12.109
BindingDB Entry DOI: 10.7270/Q2HQ401G |
More data for this
Ligand-Target Pair | 
3D Structure (crystal) |
Hepatocyte growth factor receptor
(Homo sapiens (Human)) | BDBM50306684
(2-(6-((R)-1-(2,6-dichloro-3-fluorophenyl)ethoxy)qu...)Show SMILES C[C@@H](Oc1ccc2ncc(cc2c1)C1CC1C(N)=O)c1c(Cl)ccc(F)c1Cl |r| Show InChI InChI=1S/C21H17Cl2FN2O2/c1-10(19-16(22)3-4-17(24)20(19)23)28-13-2-5-18-11(7-13)6-12(9-26-18)14-8-15(14)21(25)27/h2-7,9-10,14-15H,8H2,1H3,(H2,25,27)/t10-,14?,15?/m1/s1 | PDB
MMDB
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | 9.30 | n/a | n/a | n/a | n/a | n/a | n/a |
Chugai Pharmaceutical Co, Ltd
Curated by ChEMBL
| Assay Description
Inhibition of recombinant c-Met by TR-FRET assay |
Bioorg Med Chem Lett 20: 1405-9 (2010)
Article DOI: 10.1016/j.bmcl.2009.12.109
BindingDB Entry DOI: 10.7270/Q2HQ401G |
More data for this
Ligand-Target Pair | |
Hepatocyte growth factor receptor
(Homo sapiens (Human)) | BDBM50306677
((R)-3-(6-(1-(2,6-dichloro-3-fluorophenyl)ethoxy)qu...)Show SMILES C[C@@H](Oc1ccc2ncc(\C=C\C(N)=O)cc2c1)c1c(Cl)ccc(F)c1Cl |r| Show InChI InChI=1S/C20H15Cl2FN2O2/c1-11(19-15(21)4-5-16(23)20(19)22)27-14-3-6-17-13(9-14)8-12(10-25-17)2-7-18(24)26/h2-11H,1H3,(H2,24,26)/b7-2+/t11-/m1/s1 | PDB
MMDB
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | 20 | n/a | n/a | n/a | n/a | n/a | n/a |
Chugai Pharmaceutical Co, Ltd
Curated by ChEMBL
| Assay Description
Inhibition of recombinant c-Met by TR-FRET assay |
Bioorg Med Chem Lett 20: 1405-9 (2010)
Article DOI: 10.1016/j.bmcl.2009.12.109
BindingDB Entry DOI: 10.7270/Q2HQ401G |
More data for this
Ligand-Target Pair | |
Hepatocyte growth factor receptor
(Homo sapiens (Human)) | BDBM50306677
((R)-3-(6-(1-(2,6-dichloro-3-fluorophenyl)ethoxy)qu...)Show SMILES C[C@@H](Oc1ccc2ncc(\C=C\C(N)=O)cc2c1)c1c(Cl)ccc(F)c1Cl |r| Show InChI InChI=1S/C20H15Cl2FN2O2/c1-11(19-15(21)4-5-16(23)20(19)22)27-14-3-6-17-13(9-14)8-12(10-25-17)2-7-18(24)26/h2-11H,1H3,(H2,24,26)/b7-2+/t11-/m1/s1 | PDB
MMDB
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | 23 | n/a | n/a | n/a | n/a | n/a | n/a |
Chugai Pharmaceutical Co, Ltd
Curated by ChEMBL
| Assay Description
Inhibition of recombinant c-Met by TR-FRET assay |
Bioorg Med Chem Lett 20: 1405-9 (2010)
Article DOI: 10.1016/j.bmcl.2009.12.109
BindingDB Entry DOI: 10.7270/Q2HQ401G |
More data for this
Ligand-Target Pair | |
Hepatocyte growth factor receptor
(Homo sapiens (Human)) | BDBM50306680
(CHEMBL598912 | rac-3-(6-(1-(2,6-dichloro-3-fluorop...)Show SMILES CNC(=O)\C=C\c1cnc2ccc(OC(C)c3c(Cl)ccc(F)c3Cl)cc2c1 Show InChI InChI=1S/C21H17Cl2FN2O2/c1-12(20-16(22)5-6-17(24)21(20)23)28-15-4-7-18-14(10-15)9-13(11-26-18)3-8-19(27)25-2/h3-12H,1-2H3,(H,25,27)/b8-3+ | PDB
MMDB
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
PDB
UniChem
Similars
| PDB
Article
PubMed
| n/a | n/a | 28 | n/a | n/a | n/a | n/a | n/a | n/a |
Chugai Pharmaceutical Co, Ltd
Curated by ChEMBL
| Assay Description
Inhibition of recombinant c-Met by TR-FRET assay |
Bioorg Med Chem Lett 20: 1405-9 (2010)
Article DOI: 10.1016/j.bmcl.2009.12.109
BindingDB Entry DOI: 10.7270/Q2HQ401G |
More data for this
Ligand-Target Pair |
3D Structure (crystal) |
Hepatocyte growth factor receptor
(Homo sapiens (Human)) | BDBM50306679
(CHEMBL608738 | rac-3-(6-(1-(2,6-dichloro-3-fluorop...)Show SMILES CC(Oc1ccc2ncc(\C=C\C(=O)N(C)C)cc2c1)c1c(Cl)ccc(F)c1Cl Show InChI InChI=1S/C22H19Cl2FN2O2/c1-13(21-17(23)6-7-18(25)22(21)24)29-16-5-8-19-15(11-16)10-14(12-26-19)4-9-20(28)27(2)3/h4-13H,1-3H3/b9-4+ | PDB
MMDB
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | 59 | n/a | n/a | n/a | n/a | n/a | n/a |
Chugai Pharmaceutical Co, Ltd
Curated by ChEMBL
| Assay Description
Inhibition of recombinant c-Met by TR-FRET assay |
Bioorg Med Chem Lett 20: 1405-9 (2010)
Article DOI: 10.1016/j.bmcl.2009.12.109
BindingDB Entry DOI: 10.7270/Q2HQ401G |
More data for this
Ligand-Target Pair | |
Hepatocyte growth factor receptor
(Homo sapiens (Human)) | BDBM50306685
(CHEMBL602470 | rac-3-(6-(1-(2,6-dichloro-3-fluorop...)Show SMILES CC(Oc1ccc2ncc(\C=C\C(O)=O)cc2c1)c1c(Cl)ccc(F)c1Cl Show InChI InChI=1S/C20H14Cl2FNO3/c1-11(19-15(21)4-5-16(23)20(19)22)27-14-3-6-17-13(9-14)8-12(10-24-17)2-7-18(25)26/h2-11H,1H3,(H,25,26)/b7-2+ | PDB
MMDB
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | 94 | n/a | n/a | n/a | n/a | n/a | n/a |
Chugai Pharmaceutical Co, Ltd
Curated by ChEMBL
| Assay Description
Inhibition of recombinant c-Met by TR-FRET assay |
Bioorg Med Chem Lett 20: 1405-9 (2010)
Article DOI: 10.1016/j.bmcl.2009.12.109
BindingDB Entry DOI: 10.7270/Q2HQ401G |
More data for this
Ligand-Target Pair | |
Hepatocyte growth factor receptor
(Homo sapiens (Human)) | BDBM50306683
((R)-6-(1-(2,6-dichloro-3-fluorophenyl)ethoxy)quino...)Show SMILES C[C@@H](Oc1ccc2ncccc2c1)c1c(Cl)ccc(F)c1Cl |r| Show InChI InChI=1S/C17H12Cl2FNO/c1-10(16-13(18)5-6-14(20)17(16)19)22-12-4-7-15-11(9-12)3-2-8-21-15/h2-10H,1H3/t10-/m1/s1 | PDB
MMDB
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | 130 | n/a | n/a | n/a | n/a | n/a | n/a |
Chugai Pharmaceutical Co, Ltd
Curated by ChEMBL
| Assay Description
Inhibition of recombinant c-Met by TR-FRET assay |
Bioorg Med Chem Lett 20: 1405-9 (2010)
Article DOI: 10.1016/j.bmcl.2009.12.109
BindingDB Entry DOI: 10.7270/Q2HQ401G |
More data for this
Ligand-Target Pair | |
Hepatocyte growth factor receptor
(Homo sapiens (Human)) | BDBM50306678
(CHEMBL591457 | rac-3-(6-(1-(2,6-dichloro-3-fluorop...)Show SMILES CC(Oc1ccc2ncc(CCC(N)=O)cc2c1)c1c(Cl)ccc(F)c1Cl Show InChI InChI=1S/C20H17Cl2FN2O2/c1-11(19-15(21)4-5-16(23)20(19)22)27-14-3-6-17-13(9-14)8-12(10-25-17)2-7-18(24)26/h3-6,8-11H,2,7H2,1H3,(H2,24,26) | PDB
MMDB
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | 205 | n/a | n/a | n/a | n/a | n/a | n/a |
Chugai Pharmaceutical Co, Ltd
Curated by ChEMBL
| Assay Description
Inhibition of recombinant c-Met by TR-FRET assay |
Bioorg Med Chem Lett 20: 1405-9 (2010)
Article DOI: 10.1016/j.bmcl.2009.12.109
BindingDB Entry DOI: 10.7270/Q2HQ401G |
More data for this
Ligand-Target Pair | |
Macrophage-stimulating protein receptor
(Homo sapiens (Human)) | BDBM50306684
(2-(6-((R)-1-(2,6-dichloro-3-fluorophenyl)ethoxy)qu...)Show SMILES C[C@@H](Oc1ccc2ncc(cc2c1)C1CC1C(N)=O)c1c(Cl)ccc(F)c1Cl |r| Show InChI InChI=1S/C21H17Cl2FN2O2/c1-10(19-16(22)3-4-17(24)20(19)23)28-13-2-5-18-11(7-13)6-12(9-26-18)14-8-15(14)21(25)27/h2-7,9-10,14-15H,8H2,1H3,(H2,25,27)/t10-,14?,15?/m1/s1 | PDB
KEGG
UniProtKB/SwissProt
B.MOAD
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | 230 | n/a | n/a | n/a | n/a | n/a | n/a |
Chugai Pharmaceutical Co, Ltd
Curated by ChEMBL
| Assay Description
Inhibition of recombinant RON by TR-FRET assay |
Bioorg Med Chem Lett 20: 1405-9 (2010)
Article DOI: 10.1016/j.bmcl.2009.12.109
BindingDB Entry DOI: 10.7270/Q2HQ401G |
More data for this
Ligand-Target Pair | |
Hepatocyte growth factor receptor
(Homo sapiens (Human)) | BDBM50306686
(CHEMBL599993 | rac-3-(6-(1-(2,6-dichloro-3-fluorop...)Show SMILES CC(Oc1ccc2ncc(\C=C\CN)cc2c1)c1c(Cl)ccc(F)c1Cl Show InChI InChI=1S/C20H17Cl2FN2O/c1-12(19-16(21)5-6-17(23)20(19)22)26-15-4-7-18-14(10-15)9-13(11-25-18)3-2-8-24/h2-7,9-12H,8,24H2,1H3/b3-2+ | PDB
MMDB
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | 368 | n/a | n/a | n/a | n/a | n/a | n/a |
Chugai Pharmaceutical Co, Ltd
Curated by ChEMBL
| Assay Description
Inhibition of recombinant c-Met by TR-FRET assay |
Bioorg Med Chem Lett 20: 1405-9 (2010)
Article DOI: 10.1016/j.bmcl.2009.12.109
BindingDB Entry DOI: 10.7270/Q2HQ401G |
More data for this
Ligand-Target Pair | |
Tyrosine-protein kinase receptor UFO
(Homo sapiens (Human)) | BDBM50306684
(2-(6-((R)-1-(2,6-dichloro-3-fluorophenyl)ethoxy)qu...)Show SMILES C[C@@H](Oc1ccc2ncc(cc2c1)C1CC1C(N)=O)c1c(Cl)ccc(F)c1Cl |r| Show InChI InChI=1S/C21H17Cl2FN2O2/c1-10(19-16(22)3-4-17(24)20(19)23)28-13-2-5-18-11(7-13)6-12(9-26-18)14-8-15(14)21(25)27/h2-7,9-10,14-15H,8H2,1H3,(H2,25,27)/t10-,14?,15?/m1/s1 | PDB
KEGG
UniProtKB/SwissProt
B.MOAD
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | 430 | n/a | n/a | n/a | n/a | n/a | n/a |
Chugai Pharmaceutical Co, Ltd
Curated by ChEMBL
| Assay Description
Inhibition of recombinant AXL by TR-FRET assay |
Bioorg Med Chem Lett 20: 1405-9 (2010)
Article DOI: 10.1016/j.bmcl.2009.12.109
BindingDB Entry DOI: 10.7270/Q2HQ401G |
More data for this
Ligand-Target Pair | |
Macrophage-stimulating protein receptor
(Homo sapiens (Human)) | BDBM50306677
((R)-3-(6-(1-(2,6-dichloro-3-fluorophenyl)ethoxy)qu...)Show SMILES C[C@@H](Oc1ccc2ncc(\C=C\C(N)=O)cc2c1)c1c(Cl)ccc(F)c1Cl |r| Show InChI InChI=1S/C20H15Cl2FN2O2/c1-11(19-15(21)4-5-16(23)20(19)22)27-14-3-6-17-13(9-14)8-12(10-25-17)2-7-18(24)26/h2-11H,1H3,(H2,24,26)/b7-2+/t11-/m1/s1 | PDB
KEGG
UniProtKB/SwissProt
B.MOAD
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | 450 | n/a | n/a | n/a | n/a | n/a | n/a |
Chugai Pharmaceutical Co, Ltd
Curated by ChEMBL
| Assay Description
Inhibition of recombinant RON by TR-FRET assay |
Bioorg Med Chem Lett 20: 1405-9 (2010)
Article DOI: 10.1016/j.bmcl.2009.12.109
BindingDB Entry DOI: 10.7270/Q2HQ401G |
More data for this
Ligand-Target Pair | |
Hepatocyte growth factor receptor
(Homo sapiens (Human)) | BDBM50306681
((S)-6-(1-(2,6-dichloro-3-fluorophenyl)ethoxy)quino...)Show SMILES C[C@H](Oc1ccc2ncccc2c1)c1c(Cl)ccc(F)c1Cl |r| Show InChI InChI=1S/C17H12Cl2FNO/c1-10(16-13(18)5-6-14(20)17(16)19)22-12-4-7-15-11(9-12)3-2-8-21-15/h2-10H,1H3/t10-/m0/s1 | PDB
MMDB
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | 453 | n/a | n/a | n/a | n/a | n/a | n/a |
Chugai Pharmaceutical Co, Ltd
Curated by ChEMBL
| Assay Description
Inhibition of recombinant c-Met by TR-FRET assay |
Bioorg Med Chem Lett 20: 1405-9 (2010)
Article DOI: 10.1016/j.bmcl.2009.12.109
BindingDB Entry DOI: 10.7270/Q2HQ401G |
More data for this
Ligand-Target Pair | |
Tyrosine-protein kinase receptor UFO
(Homo sapiens (Human)) | BDBM50306677
((R)-3-(6-(1-(2,6-dichloro-3-fluorophenyl)ethoxy)qu...)Show SMILES C[C@@H](Oc1ccc2ncc(\C=C\C(N)=O)cc2c1)c1c(Cl)ccc(F)c1Cl |r| Show InChI InChI=1S/C20H15Cl2FN2O2/c1-11(19-15(21)4-5-16(23)20(19)22)27-14-3-6-17-13(9-14)8-12(10-25-17)2-7-18(24)26/h2-11H,1H3,(H2,24,26)/b7-2+/t11-/m1/s1 | PDB
KEGG
UniProtKB/SwissProt
B.MOAD
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | 570 | n/a | n/a | n/a | n/a | n/a | n/a |
Chugai Pharmaceutical Co, Ltd
Curated by ChEMBL
| Assay Description
Inhibition of recombinant AXL by TR-FRET assay |
Bioorg Med Chem Lett 20: 1405-9 (2010)
Article DOI: 10.1016/j.bmcl.2009.12.109
BindingDB Entry DOI: 10.7270/Q2HQ401G |
More data for this
Ligand-Target Pair | |
Hepatocyte growth factor receptor
(Homo sapiens (Human)) | BDBM50306681
((S)-6-(1-(2,6-dichloro-3-fluorophenyl)ethoxy)quino...)Show SMILES C[C@H](Oc1ccc2ncccc2c1)c1c(Cl)ccc(F)c1Cl |r| Show InChI InChI=1S/C17H12Cl2FNO/c1-10(16-13(18)5-6-14(20)17(16)19)22-12-4-7-15-11(9-12)3-2-8-21-15/h2-10H,1H3/t10-/m0/s1 | PDB
MMDB
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | 1.20E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Chugai Pharmaceutical Co, Ltd
Curated by ChEMBL
| Assay Description
Inhibition of recombinant c-Met by TR-FRET assay |
Bioorg Med Chem Lett 20: 1405-9 (2010)
Article DOI: 10.1016/j.bmcl.2009.12.109
BindingDB Entry DOI: 10.7270/Q2HQ401G |
More data for this
Ligand-Target Pair | |
Macrophage-stimulating protein receptor
(Homo sapiens (Human)) | BDBM50306683
((R)-6-(1-(2,6-dichloro-3-fluorophenyl)ethoxy)quino...)Show SMILES C[C@@H](Oc1ccc2ncccc2c1)c1c(Cl)ccc(F)c1Cl |r| Show InChI InChI=1S/C17H12Cl2FNO/c1-10(16-13(18)5-6-14(20)17(16)19)22-12-4-7-15-11(9-12)3-2-8-21-15/h2-10H,1H3/t10-/m1/s1 | PDB
KEGG
UniProtKB/SwissProt
B.MOAD
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | 3.60E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Chugai Pharmaceutical Co, Ltd
Curated by ChEMBL
| Assay Description
Inhibition of recombinant RON by TR-FRET assay |
Bioorg Med Chem Lett 20: 1405-9 (2010)
Article DOI: 10.1016/j.bmcl.2009.12.109
BindingDB Entry DOI: 10.7270/Q2HQ401G |
More data for this
Ligand-Target Pair | |
Ephrin type-A receptor 2
(Homo sapiens (Human)) | BDBM50306677
((R)-3-(6-(1-(2,6-dichloro-3-fluorophenyl)ethoxy)qu...)Show SMILES C[C@@H](Oc1ccc2ncc(\C=C\C(N)=O)cc2c1)c1c(Cl)ccc(F)c1Cl |r| Show InChI InChI=1S/C20H15Cl2FN2O2/c1-11(19-15(21)4-5-16(23)20(19)22)27-14-3-6-17-13(9-14)8-12(10-25-17)2-7-18(24)26/h2-11H,1H3,(H2,24,26)/b7-2+/t11-/m1/s1 | PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | 4.40E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Chugai Pharmaceutical Co, Ltd
Curated by ChEMBL
| Assay Description
Inhibition of recombinant EphA2 by TR-FRET assay |
Bioorg Med Chem Lett 20: 1405-9 (2010)
Article DOI: 10.1016/j.bmcl.2009.12.109
BindingDB Entry DOI: 10.7270/Q2HQ401G |
More data for this
Ligand-Target Pair | |
Ephrin type-A receptor 2
(Homo sapiens (Human)) | BDBM50306684
(2-(6-((R)-1-(2,6-dichloro-3-fluorophenyl)ethoxy)qu...)Show SMILES C[C@@H](Oc1ccc2ncc(cc2c1)C1CC1C(N)=O)c1c(Cl)ccc(F)c1Cl |r| Show InChI InChI=1S/C21H17Cl2FN2O2/c1-10(19-16(22)3-4-17(24)20(19)23)28-13-2-5-18-11(7-13)6-12(9-26-18)14-8-15(14)21(25)27/h2-7,9-10,14-15H,8H2,1H3,(H2,25,27)/t10-,14?,15?/m1/s1 | PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | 5.20E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Chugai Pharmaceutical Co, Ltd
Curated by ChEMBL
| Assay Description
Inhibition of recombinant EphA2 by TR-FRET assay |
Bioorg Med Chem Lett 20: 1405-9 (2010)
Article DOI: 10.1016/j.bmcl.2009.12.109
BindingDB Entry DOI: 10.7270/Q2HQ401G |
More data for this
Ligand-Target Pair | |
Aurora kinase A
(Homo sapiens (Human)) | BDBM50306677
((R)-3-(6-(1-(2,6-dichloro-3-fluorophenyl)ethoxy)qu...)Show SMILES C[C@@H](Oc1ccc2ncc(\C=C\C(N)=O)cc2c1)c1c(Cl)ccc(F)c1Cl |r| Show InChI InChI=1S/C20H15Cl2FN2O2/c1-11(19-15(21)4-5-16(23)20(19)22)27-14-3-6-17-13(9-14)8-12(10-25-17)2-7-18(24)26/h2-11H,1H3,(H2,24,26)/b7-2+/t11-/m1/s1 | PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | 6.40E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Chugai Pharmaceutical Co, Ltd
Curated by ChEMBL
| Assay Description
Inhibition of recombinant Aurora A by IMAP assay |
Bioorg Med Chem Lett 20: 1405-9 (2010)
Article DOI: 10.1016/j.bmcl.2009.12.109
BindingDB Entry DOI: 10.7270/Q2HQ401G |
More data for this
Ligand-Target Pair | |
Fibroblast growth factor receptor 2
(Homo sapiens (Human)) | BDBM50306677
((R)-3-(6-(1-(2,6-dichloro-3-fluorophenyl)ethoxy)qu...)Show SMILES C[C@@H](Oc1ccc2ncc(\C=C\C(N)=O)cc2c1)c1c(Cl)ccc(F)c1Cl |r| Show InChI InChI=1S/C20H15Cl2FN2O2/c1-11(19-15(21)4-5-16(23)20(19)22)27-14-3-6-17-13(9-14)8-12(10-25-17)2-7-18(24)26/h2-11H,1H3,(H2,24,26)/b7-2+/t11-/m1/s1 | PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | 6.90E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Chugai Pharmaceutical Co, Ltd
Curated by ChEMBL
| Assay Description
Inhibition of recombinant FGFR2 by TR-FRET assay |
Bioorg Med Chem Lett 20: 1405-9 (2010)
Article DOI: 10.1016/j.bmcl.2009.12.109
BindingDB Entry DOI: 10.7270/Q2HQ401G |
More data for this
Ligand-Target Pair | |
Leukocyte tyrosine kinase receptor
(Homo sapiens (Human)) | BDBM50306684
(2-(6-((R)-1-(2,6-dichloro-3-fluorophenyl)ethoxy)qu...)Show SMILES C[C@@H](Oc1ccc2ncc(cc2c1)C1CC1C(N)=O)c1c(Cl)ccc(F)c1Cl |r| Show InChI InChI=1S/C21H17Cl2FN2O2/c1-10(19-16(22)3-4-17(24)20(19)23)28-13-2-5-18-11(7-13)6-12(9-26-18)14-8-15(14)21(25)27/h2-7,9-10,14-15H,8H2,1H3,(H2,25,27)/t10-,14?,15?/m1/s1 | PDB
KEGG
UniProtKB/SwissProt
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | 1.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Chugai Pharmaceutical Co, Ltd
Curated by ChEMBL
| Assay Description
Inhibition of recombinant LTK by TR-FRET assay |
Bioorg Med Chem Lett 20: 1405-9 (2010)
Article DOI: 10.1016/j.bmcl.2009.12.109
BindingDB Entry DOI: 10.7270/Q2HQ401G |
More data for this
Ligand-Target Pair | |
Tyrosine-protein kinase ABL1
(Homo sapiens (Human)) | BDBM50306677
((R)-3-(6-(1-(2,6-dichloro-3-fluorophenyl)ethoxy)qu...)Show SMILES C[C@@H](Oc1ccc2ncc(\C=C\C(N)=O)cc2c1)c1c(Cl)ccc(F)c1Cl |r| Show InChI InChI=1S/C20H15Cl2FN2O2/c1-11(19-15(21)4-5-16(23)20(19)22)27-14-3-6-17-13(9-14)8-12(10-25-17)2-7-18(24)26/h2-11H,1H3,(H2,24,26)/b7-2+/t11-/m1/s1 | PDB
MMDB
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | 1.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Chugai Pharmaceutical Co, Ltd
Curated by ChEMBL
| Assay Description
Inhibition of recombinant Abl by TR-FRET assay |
Bioorg Med Chem Lett 20: 1405-9 (2010)
Article DOI: 10.1016/j.bmcl.2009.12.109
BindingDB Entry DOI: 10.7270/Q2HQ401G |
More data for this
Ligand-Target Pair | |
Vascular endothelial growth factor receptor 2
(Homo sapiens (Human)) | BDBM50306682
((R)-3-(1-(2,6-dichloro-3-fluorophenyl)ethoxy)-5-(1...)Show SMILES C[C@@H](Oc1cc(cnc1N)-c1cnn(c1)C1CCNCC1)c1c(Cl)ccc(F)c1Cl |r| Show InChI InChI=1S/C21H22Cl2FN5O/c1-12(19-16(22)2-3-17(24)20(19)23)30-18-8-13(9-27-21(18)25)14-10-28-29(11-14)15-4-6-26-7-5-15/h2-3,8-12,15,26H,4-7H2,1H3,(H2,25,27)/t12-/m1/s1 | PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| Purchase
CHEMBL
DrugBank
MCE
MMDB
PC cid
PC sid
PDB
UniChem
Patents
Similars
| Article
PubMed
| n/a | n/a | >1.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Chugai Pharmaceutical Co, Ltd
Curated by ChEMBL
| Assay Description
Inhibition of recombinant KDR by TR-FRET assay |
Bioorg Med Chem Lett 20: 1405-9 (2010)
Article DOI: 10.1016/j.bmcl.2009.12.109
BindingDB Entry DOI: 10.7270/Q2HQ401G |
More data for this
Ligand-Target Pair | |
Vascular endothelial growth factor receptor 2
(Homo sapiens (Human)) | BDBM50306677
((R)-3-(6-(1-(2,6-dichloro-3-fluorophenyl)ethoxy)qu...)Show SMILES C[C@@H](Oc1ccc2ncc(\C=C\C(N)=O)cc2c1)c1c(Cl)ccc(F)c1Cl |r| Show InChI InChI=1S/C20H15Cl2FN2O2/c1-11(19-15(21)4-5-16(23)20(19)22)27-14-3-6-17-13(9-14)8-12(10-25-17)2-7-18(24)26/h2-11H,1H3,(H2,24,26)/b7-2+/t11-/m1/s1 | PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | 1.10E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Chugai Pharmaceutical Co, Ltd
Curated by ChEMBL
| Assay Description
Inhibition of recombinant KDR by TR-FRET assay |
Bioorg Med Chem Lett 20: 1405-9 (2010)
Article DOI: 10.1016/j.bmcl.2009.12.109
BindingDB Entry DOI: 10.7270/Q2HQ401G |
More data for this
Ligand-Target Pair | |
Fibroblast growth factor receptor 2
(Homo sapiens (Human)) | BDBM50306684
(2-(6-((R)-1-(2,6-dichloro-3-fluorophenyl)ethoxy)qu...)Show SMILES C[C@@H](Oc1ccc2ncc(cc2c1)C1CC1C(N)=O)c1c(Cl)ccc(F)c1Cl |r| Show InChI InChI=1S/C21H17Cl2FN2O2/c1-10(19-16(22)3-4-17(24)20(19)23)28-13-2-5-18-11(7-13)6-12(9-26-18)14-8-15(14)21(25)27/h2-7,9-10,14-15H,8H2,1H3,(H2,25,27)/t10-,14?,15?/m1/s1 | PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | 1.20E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Chugai Pharmaceutical Co, Ltd
Curated by ChEMBL
| Assay Description
Inhibition of recombinant FGFR2 by TR-FRET assay |
Bioorg Med Chem Lett 20: 1405-9 (2010)
Article DOI: 10.1016/j.bmcl.2009.12.109
BindingDB Entry DOI: 10.7270/Q2HQ401G |
More data for this
Ligand-Target Pair | |
Tyrosine-protein kinase Lck
(Homo sapiens (Human)) | BDBM50306677
((R)-3-(6-(1-(2,6-dichloro-3-fluorophenyl)ethoxy)qu...)Show SMILES C[C@@H](Oc1ccc2ncc(\C=C\C(N)=O)cc2c1)c1c(Cl)ccc(F)c1Cl |r| Show InChI InChI=1S/C20H15Cl2FN2O2/c1-11(19-15(21)4-5-16(23)20(19)22)27-14-3-6-17-13(9-14)8-12(10-25-17)2-7-18(24)26/h2-11H,1H3,(H2,24,26)/b7-2+/t11-/m1/s1 | PDB
UniProtKB/SwissProt
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | 1.40E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Chugai Pharmaceutical Co, Ltd
Curated by ChEMBL
| Assay Description
Inhibition of recombinant LCK by TR-FRET assay |
Bioorg Med Chem Lett 20: 1405-9 (2010)
Article DOI: 10.1016/j.bmcl.2009.12.109
BindingDB Entry DOI: 10.7270/Q2HQ401G |
More data for this
Ligand-Target Pair | |
Tyrosine-protein kinase receptor UFO
(Homo sapiens (Human)) | BDBM50306683
((R)-6-(1-(2,6-dichloro-3-fluorophenyl)ethoxy)quino...)Show SMILES C[C@@H](Oc1ccc2ncccc2c1)c1c(Cl)ccc(F)c1Cl |r| Show InChI InChI=1S/C17H12Cl2FNO/c1-10(16-13(18)5-6-14(20)17(16)19)22-12-4-7-15-11(9-12)3-2-8-21-15/h2-10H,1H3/t10-/m1/s1 | PDB
KEGG
UniProtKB/SwissProt
B.MOAD
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | 1.40E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Chugai Pharmaceutical Co, Ltd
Curated by ChEMBL
| Assay Description
Inhibition of recombinant AXL by TR-FRET assay |
Bioorg Med Chem Lett 20: 1405-9 (2010)
Article DOI: 10.1016/j.bmcl.2009.12.109
BindingDB Entry DOI: 10.7270/Q2HQ401G |
More data for this
Ligand-Target Pair | |
Receptor-type tyrosine-protein kinase FLT3
(Homo sapiens (Human)) | BDBM50306684
(2-(6-((R)-1-(2,6-dichloro-3-fluorophenyl)ethoxy)qu...)Show SMILES C[C@@H](Oc1ccc2ncc(cc2c1)C1CC1C(N)=O)c1c(Cl)ccc(F)c1Cl |r| Show InChI InChI=1S/C21H17Cl2FN2O2/c1-10(19-16(22)3-4-17(24)20(19)23)28-13-2-5-18-11(7-13)6-12(9-26-18)14-8-15(14)21(25)27/h2-7,9-10,14-15H,8H2,1H3,(H2,25,27)/t10-,14?,15?/m1/s1 | PDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | 1.50E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Chugai Pharmaceutical Co, Ltd
Curated by ChEMBL
| Assay Description
Inhibition of recombinant Flt3 by TR-FRET assay |
Bioorg Med Chem Lett 20: 1405-9 (2010)
Article DOI: 10.1016/j.bmcl.2009.12.109
BindingDB Entry DOI: 10.7270/Q2HQ401G |
More data for this
Ligand-Target Pair | |
Leukocyte tyrosine kinase receptor
(Homo sapiens (Human)) | BDBM50306677
((R)-3-(6-(1-(2,6-dichloro-3-fluorophenyl)ethoxy)qu...)Show SMILES C[C@@H](Oc1ccc2ncc(\C=C\C(N)=O)cc2c1)c1c(Cl)ccc(F)c1Cl |r| Show InChI InChI=1S/C20H15Cl2FN2O2/c1-11(19-15(21)4-5-16(23)20(19)22)27-14-3-6-17-13(9-14)8-12(10-25-17)2-7-18(24)26/h2-11H,1H3,(H2,24,26)/b7-2+/t11-/m1/s1 | PDB
KEGG
UniProtKB/SwissProt
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | 1.80E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Chugai Pharmaceutical Co, Ltd
Curated by ChEMBL
| Assay Description
Inhibition of recombinant LTK by TR-FRET assay |
Bioorg Med Chem Lett 20: 1405-9 (2010)
Article DOI: 10.1016/j.bmcl.2009.12.109
BindingDB Entry DOI: 10.7270/Q2HQ401G |
More data for this
Ligand-Target Pair | |
Proto-oncogene tyrosine-protein kinase Src
(Homo sapiens (Human)) | BDBM50306681
((S)-6-(1-(2,6-dichloro-3-fluorophenyl)ethoxy)quino...)Show SMILES C[C@H](Oc1ccc2ncccc2c1)c1c(Cl)ccc(F)c1Cl |r| Show InChI InChI=1S/C17H12Cl2FNO/c1-10(16-13(18)5-6-14(20)17(16)19)22-12-4-7-15-11(9-12)3-2-8-21-15/h2-10H,1H3/t10-/m0/s1 | PDB
MMDB
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | 2.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Chugai Pharmaceutical Co, Ltd
Curated by ChEMBL
| Assay Description
Inhibition of recombinant Src by TR-FRET assay |
Bioorg Med Chem Lett 20: 1405-9 (2010)
Article DOI: 10.1016/j.bmcl.2009.12.109
BindingDB Entry DOI: 10.7270/Q2HQ401G |
More data for this
Ligand-Target Pair | |
Proto-oncogene tyrosine-protein kinase Src
(Homo sapiens (Human)) | BDBM50306683
((R)-6-(1-(2,6-dichloro-3-fluorophenyl)ethoxy)quino...)Show SMILES C[C@@H](Oc1ccc2ncccc2c1)c1c(Cl)ccc(F)c1Cl |r| Show InChI InChI=1S/C17H12Cl2FNO/c1-10(16-13(18)5-6-14(20)17(16)19)22-12-4-7-15-11(9-12)3-2-8-21-15/h2-10H,1H3/t10-/m1/s1 | PDB
MMDB
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | 2.20E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Chugai Pharmaceutical Co, Ltd
Curated by ChEMBL
| Assay Description
Inhibition of recombinant Src by TR-FRET assay |
Bioorg Med Chem Lett 20: 1405-9 (2010)
Article DOI: 10.1016/j.bmcl.2009.12.109
BindingDB Entry DOI: 10.7270/Q2HQ401G |
More data for this
Ligand-Target Pair | |
Aurora kinase A
(Homo sapiens (Human)) | BDBM50306684
(2-(6-((R)-1-(2,6-dichloro-3-fluorophenyl)ethoxy)qu...)Show SMILES C[C@@H](Oc1ccc2ncc(cc2c1)C1CC1C(N)=O)c1c(Cl)ccc(F)c1Cl |r| Show InChI InChI=1S/C21H17Cl2FN2O2/c1-10(19-16(22)3-4-17(24)20(19)23)28-13-2-5-18-11(7-13)6-12(9-26-18)14-8-15(14)21(25)27/h2-7,9-10,14-15H,8H2,1H3,(H2,25,27)/t10-,14?,15?/m1/s1 | PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | 2.20E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Chugai Pharmaceutical Co, Ltd
Curated by ChEMBL
| Assay Description
Inhibition of recombinant Aurora A by IMAP assay |
Bioorg Med Chem Lett 20: 1405-9 (2010)
Article DOI: 10.1016/j.bmcl.2009.12.109
BindingDB Entry DOI: 10.7270/Q2HQ401G |
More data for this
Ligand-Target Pair | |
Vascular endothelial growth factor receptor 2
(Homo sapiens (Human)) | BDBM50306683
((R)-6-(1-(2,6-dichloro-3-fluorophenyl)ethoxy)quino...)Show SMILES C[C@@H](Oc1ccc2ncccc2c1)c1c(Cl)ccc(F)c1Cl |r| Show InChI InChI=1S/C17H12Cl2FNO/c1-10(16-13(18)5-6-14(20)17(16)19)22-12-4-7-15-11(9-12)3-2-8-21-15/h2-10H,1H3/t10-/m1/s1 | PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | 2.30E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Chugai Pharmaceutical Co, Ltd
Curated by ChEMBL
| Assay Description
Inhibition of recombinant KDR by TR-FRET assay |
Bioorg Med Chem Lett 20: 1405-9 (2010)
Article DOI: 10.1016/j.bmcl.2009.12.109
BindingDB Entry DOI: 10.7270/Q2HQ401G |
More data for this
Ligand-Target Pair | |
Fibroblast growth factor receptor 2
(Homo sapiens (Human)) | BDBM50306683
((R)-6-(1-(2,6-dichloro-3-fluorophenyl)ethoxy)quino...)Show SMILES C[C@@H](Oc1ccc2ncccc2c1)c1c(Cl)ccc(F)c1Cl |r| Show InChI InChI=1S/C17H12Cl2FNO/c1-10(16-13(18)5-6-14(20)17(16)19)22-12-4-7-15-11(9-12)3-2-8-21-15/h2-10H,1H3/t10-/m1/s1 | PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | 2.40E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Chugai Pharmaceutical Co, Ltd
Curated by ChEMBL
| Assay Description
Inhibition of recombinant FGFR2 by TR-FRET assay |
Bioorg Med Chem Lett 20: 1405-9 (2010)
Article DOI: 10.1016/j.bmcl.2009.12.109
BindingDB Entry DOI: 10.7270/Q2HQ401G |
More data for this
Ligand-Target Pair | |
Tyrosine-protein kinase Fyn
(Homo sapiens (Human)) | BDBM50306684
(2-(6-((R)-1-(2,6-dichloro-3-fluorophenyl)ethoxy)qu...)Show SMILES C[C@@H](Oc1ccc2ncc(cc2c1)C1CC1C(N)=O)c1c(Cl)ccc(F)c1Cl |r| Show InChI InChI=1S/C21H17Cl2FN2O2/c1-10(19-16(22)3-4-17(24)20(19)23)28-13-2-5-18-11(7-13)6-12(9-26-18)14-8-15(14)21(25)27/h2-7,9-10,14-15H,8H2,1H3,(H2,25,27)/t10-,14?,15?/m1/s1 | PDB
UniProtKB/SwissProt
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | 2.50E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Chugai Pharmaceutical Co, Ltd
Curated by ChEMBL
| Assay Description
Inhibition of recombinant Fyn by TR-FRET assay |
Bioorg Med Chem Lett 20: 1405-9 (2010)
Article DOI: 10.1016/j.bmcl.2009.12.109
BindingDB Entry DOI: 10.7270/Q2HQ401G |
More data for this
Ligand-Target Pair | |
Tyrosine-protein kinase Yes
(Homo sapiens (Human)) | BDBM50306677
((R)-3-(6-(1-(2,6-dichloro-3-fluorophenyl)ethoxy)qu...)Show SMILES C[C@@H](Oc1ccc2ncc(\C=C\C(N)=O)cc2c1)c1c(Cl)ccc(F)c1Cl |r| Show InChI InChI=1S/C20H15Cl2FN2O2/c1-11(19-15(21)4-5-16(23)20(19)22)27-14-3-6-17-13(9-14)8-12(10-25-17)2-7-18(24)26/h2-11H,1H3,(H2,24,26)/b7-2+/t11-/m1/s1 | PDB
MMDB
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | 2.60E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Chugai Pharmaceutical Co, Ltd
Curated by ChEMBL
| Assay Description
Inhibition of recombinant YES by TR-FRET assay |
Bioorg Med Chem Lett 20: 1405-9 (2010)
Article DOI: 10.1016/j.bmcl.2009.12.109
BindingDB Entry DOI: 10.7270/Q2HQ401G |
More data for this
Ligand-Target Pair | |
Vascular endothelial growth factor receptor 2
(Homo sapiens (Human)) | BDBM50306677
((R)-3-(6-(1-(2,6-dichloro-3-fluorophenyl)ethoxy)qu...)Show SMILES C[C@@H](Oc1ccc2ncc(\C=C\C(N)=O)cc2c1)c1c(Cl)ccc(F)c1Cl |r| Show InChI InChI=1S/C20H15Cl2FN2O2/c1-11(19-15(21)4-5-16(23)20(19)22)27-14-3-6-17-13(9-14)8-12(10-25-17)2-7-18(24)26/h2-11H,1H3,(H2,24,26)/b7-2+/t11-/m1/s1 | PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | 2.60E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Chugai Pharmaceutical Co, Ltd
Curated by ChEMBL
| Assay Description
Inhibition of recombinant KDR by TR-FRET assay |
Bioorg Med Chem Lett 20: 1405-9 (2010)
Article DOI: 10.1016/j.bmcl.2009.12.109
BindingDB Entry DOI: 10.7270/Q2HQ401G |
More data for this
Ligand-Target Pair | |
Insulin-like growth factor 1 receptor
(Homo sapiens (Human)) | BDBM50306684
(2-(6-((R)-1-(2,6-dichloro-3-fluorophenyl)ethoxy)qu...)Show SMILES C[C@@H](Oc1ccc2ncc(cc2c1)C1CC1C(N)=O)c1c(Cl)ccc(F)c1Cl |r| Show InChI InChI=1S/C21H17Cl2FN2O2/c1-10(19-16(22)3-4-17(24)20(19)23)28-13-2-5-18-11(7-13)6-12(9-26-18)14-8-15(14)21(25)27/h2-7,9-10,14-15H,8H2,1H3,(H2,25,27)/t10-,14?,15?/m1/s1 | PDB
MMDB
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | 2.70E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Chugai Pharmaceutical Co, Ltd
Curated by ChEMBL
| Assay Description
Inhibition of recombinant IGF1R by TR-FRET assay |
Bioorg Med Chem Lett 20: 1405-9 (2010)
Article DOI: 10.1016/j.bmcl.2009.12.109
BindingDB Entry DOI: 10.7270/Q2HQ401G |
More data for this
Ligand-Target Pair | |
Tyrosine-protein kinase Fyn
(Homo sapiens (Human)) | BDBM50306677
((R)-3-(6-(1-(2,6-dichloro-3-fluorophenyl)ethoxy)qu...)Show SMILES C[C@@H](Oc1ccc2ncc(\C=C\C(N)=O)cc2c1)c1c(Cl)ccc(F)c1Cl |r| Show InChI InChI=1S/C20H15Cl2FN2O2/c1-11(19-15(21)4-5-16(23)20(19)22)27-14-3-6-17-13(9-14)8-12(10-25-17)2-7-18(24)26/h2-11H,1H3,(H2,24,26)/b7-2+/t11-/m1/s1 | PDB
UniProtKB/SwissProt
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | 2.80E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Chugai Pharmaceutical Co, Ltd
Curated by ChEMBL
| Assay Description
Inhibition of recombinant Fyn by TR-FRET assay |
Bioorg Med Chem Lett 20: 1405-9 (2010)
Article DOI: 10.1016/j.bmcl.2009.12.109
BindingDB Entry DOI: 10.7270/Q2HQ401G |
More data for this
Ligand-Target Pair | |
Tyrosine-protein kinase Lck
(Homo sapiens (Human)) | BDBM50306684
(2-(6-((R)-1-(2,6-dichloro-3-fluorophenyl)ethoxy)qu...)Show SMILES C[C@@H](Oc1ccc2ncc(cc2c1)C1CC1C(N)=O)c1c(Cl)ccc(F)c1Cl |r| Show InChI InChI=1S/C21H17Cl2FN2O2/c1-10(19-16(22)3-4-17(24)20(19)23)28-13-2-5-18-11(7-13)6-12(9-26-18)14-8-15(14)21(25)27/h2-7,9-10,14-15H,8H2,1H3,(H2,25,27)/t10-,14?,15?/m1/s1 | PDB
UniProtKB/SwissProt
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | 2.80E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Chugai Pharmaceutical Co, Ltd
Curated by ChEMBL
| Assay Description
Inhibition of recombinant LCK by TR-FRET assay |
Bioorg Med Chem Lett 20: 1405-9 (2010)
Article DOI: 10.1016/j.bmcl.2009.12.109
BindingDB Entry DOI: 10.7270/Q2HQ401G |
More data for this
Ligand-Target Pair | |
Protein-tyrosine kinase 6
(Homo sapiens (Human)) | BDBM50306677
((R)-3-(6-(1-(2,6-dichloro-3-fluorophenyl)ethoxy)qu...)Show SMILES C[C@@H](Oc1ccc2ncc(\C=C\C(N)=O)cc2c1)c1c(Cl)ccc(F)c1Cl |r| Show InChI InChI=1S/C20H15Cl2FN2O2/c1-11(19-15(21)4-5-16(23)20(19)22)27-14-3-6-17-13(9-14)8-12(10-25-17)2-7-18(24)26/h2-11H,1H3,(H2,24,26)/b7-2+/t11-/m1/s1 | PDB
MMDB
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | 3.20E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Chugai Pharmaceutical Co, Ltd
Curated by ChEMBL
| Assay Description
Inhibition of recombinant BRK by TR-FRET assay |
Bioorg Med Chem Lett 20: 1405-9 (2010)
Article DOI: 10.1016/j.bmcl.2009.12.109
BindingDB Entry DOI: 10.7270/Q2HQ401G |
More data for this
Ligand-Target Pair | |
Vascular endothelial growth factor receptor 2
(Homo sapiens (Human)) | BDBM50306681
((S)-6-(1-(2,6-dichloro-3-fluorophenyl)ethoxy)quino...)Show SMILES C[C@H](Oc1ccc2ncccc2c1)c1c(Cl)ccc(F)c1Cl |r| Show InChI InChI=1S/C17H12Cl2FNO/c1-10(16-13(18)5-6-14(20)17(16)19)22-12-4-7-15-11(9-12)3-2-8-21-15/h2-10H,1H3/t10-/m0/s1 | PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | 3.20E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Chugai Pharmaceutical Co, Ltd
Curated by ChEMBL
| Assay Description
Inhibition of recombinant KDR by TR-FRET assay |
Bioorg Med Chem Lett 20: 1405-9 (2010)
Article DOI: 10.1016/j.bmcl.2009.12.109
BindingDB Entry DOI: 10.7270/Q2HQ401G |
More data for this
Ligand-Target Pair | |
Receptor-type tyrosine-protein kinase FLT3
(Homo sapiens (Human)) | BDBM50306677
((R)-3-(6-(1-(2,6-dichloro-3-fluorophenyl)ethoxy)qu...)Show SMILES C[C@@H](Oc1ccc2ncc(\C=C\C(N)=O)cc2c1)c1c(Cl)ccc(F)c1Cl |r| Show InChI InChI=1S/C20H15Cl2FN2O2/c1-11(19-15(21)4-5-16(23)20(19)22)27-14-3-6-17-13(9-14)8-12(10-25-17)2-7-18(24)26/h2-11H,1H3,(H2,24,26)/b7-2+/t11-/m1/s1 | PDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | 3.20E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Chugai Pharmaceutical Co, Ltd
Curated by ChEMBL
| Assay Description
Inhibition of recombinant Flt3 by TR-FRET assay |
Bioorg Med Chem Lett 20: 1405-9 (2010)
Article DOI: 10.1016/j.bmcl.2009.12.109
BindingDB Entry DOI: 10.7270/Q2HQ401G |
More data for this
Ligand-Target Pair | |
Vascular endothelial growth factor receptor 2
(Homo sapiens (Human)) | BDBM50306686
(CHEMBL599993 | rac-3-(6-(1-(2,6-dichloro-3-fluorop...)Show SMILES CC(Oc1ccc2ncc(\C=C\CN)cc2c1)c1c(Cl)ccc(F)c1Cl Show InChI InChI=1S/C20H17Cl2FN2O/c1-12(19-16(21)5-6-17(23)20(19)22)26-15-4-7-18-14(10-15)9-13(11-25-18)3-2-8-24/h2-7,9-12H,8,24H2,1H3/b3-2+ | PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | 3.30E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Chugai Pharmaceutical Co, Ltd
Curated by ChEMBL
| Assay Description
Inhibition of recombinant KDR by TR-FRET assay |
Bioorg Med Chem Lett 20: 1405-9 (2010)
Article DOI: 10.1016/j.bmcl.2009.12.109
BindingDB Entry DOI: 10.7270/Q2HQ401G |
More data for this
Ligand-Target Pair | |
Mast/stem cell growth factor receptor Kit
(Homo sapiens (Human)) | BDBM50306683
((R)-6-(1-(2,6-dichloro-3-fluorophenyl)ethoxy)quino...)Show SMILES C[C@@H](Oc1ccc2ncccc2c1)c1c(Cl)ccc(F)c1Cl |r| Show InChI InChI=1S/C17H12Cl2FNO/c1-10(16-13(18)5-6-14(20)17(16)19)22-12-4-7-15-11(9-12)3-2-8-21-15/h2-10H,1H3/t10-/m1/s1 | PDB
UniProtKB/SwissProt
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | 4.10E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Chugai Pharmaceutical Co, Ltd
Curated by ChEMBL
| Assay Description
Inhibition of recombinant Kit by TR-FRET assay |
Bioorg Med Chem Lett 20: 1405-9 (2010)
Article DOI: 10.1016/j.bmcl.2009.12.109
BindingDB Entry DOI: 10.7270/Q2HQ401G |
More data for this
Ligand-Target Pair | |
Mast/stem cell growth factor receptor Kit
(Homo sapiens (Human)) | BDBM50306684
(2-(6-((R)-1-(2,6-dichloro-3-fluorophenyl)ethoxy)qu...)Show SMILES C[C@@H](Oc1ccc2ncc(cc2c1)C1CC1C(N)=O)c1c(Cl)ccc(F)c1Cl |r| Show InChI InChI=1S/C21H17Cl2FN2O2/c1-10(19-16(22)3-4-17(24)20(19)23)28-13-2-5-18-11(7-13)6-12(9-26-18)14-8-15(14)21(25)27/h2-7,9-10,14-15H,8H2,1H3,(H2,25,27)/t10-,14?,15?/m1/s1 | PDB
UniProtKB/SwissProt
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | 4.10E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Chugai Pharmaceutical Co, Ltd
Curated by ChEMBL
| Assay Description
Inhibition of recombinant Kit by TR-FRET assay |
Bioorg Med Chem Lett 20: 1405-9 (2010)
Article DOI: 10.1016/j.bmcl.2009.12.109
BindingDB Entry DOI: 10.7270/Q2HQ401G |
More data for this
Ligand-Target Pair | |
Proto-oncogene tyrosine-protein kinase Src
(Homo sapiens (Human)) | BDBM50306686
(CHEMBL599993 | rac-3-(6-(1-(2,6-dichloro-3-fluorop...)Show SMILES CC(Oc1ccc2ncc(\C=C\CN)cc2c1)c1c(Cl)ccc(F)c1Cl Show InChI InChI=1S/C20H17Cl2FN2O/c1-12(19-16(21)5-6-17(23)20(19)22)26-15-4-7-18-14(10-15)9-13(11-25-18)3-2-8-24/h2-7,9-12H,8,24H2,1H3/b3-2+ | PDB
MMDB
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | 4.60E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Chugai Pharmaceutical Co, Ltd
Curated by ChEMBL
| Assay Description
Inhibition of recombinant Src by TR-FRET assay |
Bioorg Med Chem Lett 20: 1405-9 (2010)
Article DOI: 10.1016/j.bmcl.2009.12.109
BindingDB Entry DOI: 10.7270/Q2HQ401G |
More data for this
Ligand-Target Pair | |
Receptor-type tyrosine-protein kinase FLT3
(Homo sapiens (Human)) | BDBM50306683
((R)-6-(1-(2,6-dichloro-3-fluorophenyl)ethoxy)quino...)Show SMILES C[C@@H](Oc1ccc2ncccc2c1)c1c(Cl)ccc(F)c1Cl |r| Show InChI InChI=1S/C17H12Cl2FNO/c1-10(16-13(18)5-6-14(20)17(16)19)22-12-4-7-15-11(9-12)3-2-8-21-15/h2-10H,1H3/t10-/m1/s1 | PDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | 4.60E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Chugai Pharmaceutical Co, Ltd
Curated by ChEMBL
| Assay Description
Inhibition of recombinant Flt3 by TR-FRET assay |
Bioorg Med Chem Lett 20: 1405-9 (2010)
Article DOI: 10.1016/j.bmcl.2009.12.109
BindingDB Entry DOI: 10.7270/Q2HQ401G |
More data for this
Ligand-Target Pair | |
Epidermal growth factor receptor
(Homo sapiens (Human)) | BDBM50306684
(2-(6-((R)-1-(2,6-dichloro-3-fluorophenyl)ethoxy)qu...)Show SMILES C[C@@H](Oc1ccc2ncc(cc2c1)C1CC1C(N)=O)c1c(Cl)ccc(F)c1Cl |r| Show InChI InChI=1S/C21H17Cl2FN2O2/c1-10(19-16(22)3-4-17(24)20(19)23)28-13-2-5-18-11(7-13)6-12(9-26-18)14-8-15(14)21(25)27/h2-7,9-10,14-15H,8H2,1H3,(H2,25,27)/t10-,14?,15?/m1/s1 | PDB
MMDB
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | >5.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Chugai Pharmaceutical Co, Ltd
Curated by ChEMBL
| Assay Description
Inhibition of recombinant EGFR by TR-FRET assay |
Bioorg Med Chem Lett 20: 1405-9 (2010)
Article DOI: 10.1016/j.bmcl.2009.12.109
BindingDB Entry DOI: 10.7270/Q2HQ401G |
More data for this
Ligand-Target Pair | |
RAC-alpha serine/threonine-protein kinase
(Homo sapiens (Human)) | BDBM50306683
((R)-6-(1-(2,6-dichloro-3-fluorophenyl)ethoxy)quino...)Show SMILES C[C@@H](Oc1ccc2ncccc2c1)c1c(Cl)ccc(F)c1Cl |r| Show InChI InChI=1S/C17H12Cl2FNO/c1-10(16-13(18)5-6-14(20)17(16)19)22-12-4-7-15-11(9-12)3-2-8-21-15/h2-10H,1H3/t10-/m1/s1 | PDB
UniProtKB/SwissProt
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | >5.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Chugai Pharmaceutical Co, Ltd
Curated by ChEMBL
| Assay Description
Inhibition of recombinant AKT1 by IMAP assay |
Bioorg Med Chem Lett 20: 1405-9 (2010)
Article DOI: 10.1016/j.bmcl.2009.12.109
BindingDB Entry DOI: 10.7270/Q2HQ401G |
More data for this
Ligand-Target Pair | |
Ephrin type-A receptor 2
(Homo sapiens (Human)) | BDBM50306683
((R)-6-(1-(2,6-dichloro-3-fluorophenyl)ethoxy)quino...)Show SMILES C[C@@H](Oc1ccc2ncccc2c1)c1c(Cl)ccc(F)c1Cl |r| Show InChI InChI=1S/C17H12Cl2FNO/c1-10(16-13(18)5-6-14(20)17(16)19)22-12-4-7-15-11(9-12)3-2-8-21-15/h2-10H,1H3/t10-/m1/s1 | PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | >5.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Chugai Pharmaceutical Co, Ltd
Curated by ChEMBL
| Assay Description
Inhibition of recombinant EphA2 by TR-FRET assay |
Bioorg Med Chem Lett 20: 1405-9 (2010)
Article DOI: 10.1016/j.bmcl.2009.12.109
BindingDB Entry DOI: 10.7270/Q2HQ401G |
More data for this
Ligand-Target Pair | |
Cyclin-dependent kinase 2
(Homo sapiens (Human)) | BDBM50306684
(2-(6-((R)-1-(2,6-dichloro-3-fluorophenyl)ethoxy)qu...)Show SMILES C[C@@H](Oc1ccc2ncc(cc2c1)C1CC1C(N)=O)c1c(Cl)ccc(F)c1Cl |r| Show InChI InChI=1S/C21H17Cl2FN2O2/c1-10(19-16(22)3-4-17(24)20(19)23)28-13-2-5-18-11(7-13)6-12(9-26-18)14-8-15(14)21(25)27/h2-7,9-10,14-15H,8H2,1H3,(H2,25,27)/t10-,14?,15?/m1/s1 | PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | >5.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Chugai Pharmaceutical Co, Ltd
Curated by ChEMBL
| Assay Description
Inhibition of recombinant CDK2 by IMAP assay |
Bioorg Med Chem Lett 20: 1405-9 (2010)
Article DOI: 10.1016/j.bmcl.2009.12.109
BindingDB Entry DOI: 10.7270/Q2HQ401G |
More data for this
Ligand-Target Pair | |
Protein-tyrosine kinase 6
(Homo sapiens (Human)) | BDBM50306684
(2-(6-((R)-1-(2,6-dichloro-3-fluorophenyl)ethoxy)qu...)Show SMILES C[C@@H](Oc1ccc2ncc(cc2c1)C1CC1C(N)=O)c1c(Cl)ccc(F)c1Cl |r| Show InChI InChI=1S/C21H17Cl2FN2O2/c1-10(19-16(22)3-4-17(24)20(19)23)28-13-2-5-18-11(7-13)6-12(9-26-18)14-8-15(14)21(25)27/h2-7,9-10,14-15H,8H2,1H3,(H2,25,27)/t10-,14?,15?/m1/s1 | PDB
MMDB
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | >5.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Chugai Pharmaceutical Co, Ltd
Curated by ChEMBL
| Assay Description
Inhibition of recombinant BRK by TR-FRET assay |
Bioorg Med Chem Lett 20: 1405-9 (2010)
Article DOI: 10.1016/j.bmcl.2009.12.109
BindingDB Entry DOI: 10.7270/Q2HQ401G |
More data for this
Ligand-Target Pair | |
Tyrosine-protein kinase Yes
(Homo sapiens (Human)) | BDBM50306684
(2-(6-((R)-1-(2,6-dichloro-3-fluorophenyl)ethoxy)qu...)Show SMILES C[C@@H](Oc1ccc2ncc(cc2c1)C1CC1C(N)=O)c1c(Cl)ccc(F)c1Cl |r| Show InChI InChI=1S/C21H17Cl2FN2O2/c1-10(19-16(22)3-4-17(24)20(19)23)28-13-2-5-18-11(7-13)6-12(9-26-18)14-8-15(14)21(25)27/h2-7,9-10,14-15H,8H2,1H3,(H2,25,27)/t10-,14?,15?/m1/s1 | PDB
MMDB
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | >5.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Chugai Pharmaceutical Co, Ltd
Curated by ChEMBL
| Assay Description
Inhibition of recombinant YES by TR-FRET assay |
Bioorg Med Chem Lett 20: 1405-9 (2010)
Article DOI: 10.1016/j.bmcl.2009.12.109
BindingDB Entry DOI: 10.7270/Q2HQ401G |
More data for this
Ligand-Target Pair | |
Cyclin-dependent kinase 2
(Homo sapiens (Human)) | BDBM50306677
((R)-3-(6-(1-(2,6-dichloro-3-fluorophenyl)ethoxy)qu...)Show SMILES C[C@@H](Oc1ccc2ncc(\C=C\C(N)=O)cc2c1)c1c(Cl)ccc(F)c1Cl |r| Show InChI InChI=1S/C20H15Cl2FN2O2/c1-11(19-15(21)4-5-16(23)20(19)22)27-14-3-6-17-13(9-14)8-12(10-25-17)2-7-18(24)26/h2-11H,1H3,(H2,24,26)/b7-2+/t11-/m1/s1 | PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | >5.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Chugai Pharmaceutical Co, Ltd
Curated by ChEMBL
| Assay Description
Inhibition of recombinant CDK2 by IMAP assay |
Bioorg Med Chem Lett 20: 1405-9 (2010)
Article DOI: 10.1016/j.bmcl.2009.12.109
BindingDB Entry DOI: 10.7270/Q2HQ401G |
More data for this
Ligand-Target Pair | |
Vascular endothelial growth factor receptor 2
(Homo sapiens (Human)) | BDBM50306681
((S)-6-(1-(2,6-dichloro-3-fluorophenyl)ethoxy)quino...)Show SMILES C[C@H](Oc1ccc2ncccc2c1)c1c(Cl)ccc(F)c1Cl |r| Show InChI InChI=1S/C17H12Cl2FNO/c1-10(16-13(18)5-6-14(20)17(16)19)22-12-4-7-15-11(9-12)3-2-8-21-15/h2-10H,1H3/t10-/m0/s1 | PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | >5.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Chugai Pharmaceutical Co, Ltd
Curated by ChEMBL
| Assay Description
Inhibition of recombinant KDR by TR-FRET assay |
Bioorg Med Chem Lett 20: 1405-9 (2010)
Article DOI: 10.1016/j.bmcl.2009.12.109
BindingDB Entry DOI: 10.7270/Q2HQ401G |
More data for this
Ligand-Target Pair | |
Epidermal growth factor receptor
(Homo sapiens (Human)) | BDBM50306677
((R)-3-(6-(1-(2,6-dichloro-3-fluorophenyl)ethoxy)qu...)Show SMILES C[C@@H](Oc1ccc2ncc(\C=C\C(N)=O)cc2c1)c1c(Cl)ccc(F)c1Cl |r| Show InChI InChI=1S/C20H15Cl2FN2O2/c1-11(19-15(21)4-5-16(23)20(19)22)27-14-3-6-17-13(9-14)8-12(10-25-17)2-7-18(24)26/h2-11H,1H3,(H2,24,26)/b7-2+/t11-/m1/s1 | PDB
MMDB
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | >5.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Chugai Pharmaceutical Co, Ltd
Curated by ChEMBL
| Assay Description
Inhibition of recombinant EGFR by TR-FRET assay |
Bioorg Med Chem Lett 20: 1405-9 (2010)
Article DOI: 10.1016/j.bmcl.2009.12.109
BindingDB Entry DOI: 10.7270/Q2HQ401G |
More data for this
Ligand-Target Pair | |
Tyrosine-protein kinase Lck
(Homo sapiens (Human)) | BDBM50306683
((R)-6-(1-(2,6-dichloro-3-fluorophenyl)ethoxy)quino...)Show SMILES C[C@@H](Oc1ccc2ncccc2c1)c1c(Cl)ccc(F)c1Cl |r| Show InChI InChI=1S/C17H12Cl2FNO/c1-10(16-13(18)5-6-14(20)17(16)19)22-12-4-7-15-11(9-12)3-2-8-21-15/h2-10H,1H3/t10-/m1/s1 | PDB
UniProtKB/SwissProt
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | >5.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Chugai Pharmaceutical Co, Ltd
Curated by ChEMBL
| Assay Description
Inhibition of recombinant LCK by TR-FRET assay |
Bioorg Med Chem Lett 20: 1405-9 (2010)
Article DOI: 10.1016/j.bmcl.2009.12.109
BindingDB Entry DOI: 10.7270/Q2HQ401G |
More data for this
Ligand-Target Pair | |
Tyrosine-protein kinase Fyn
(Homo sapiens (Human)) | BDBM50306683
((R)-6-(1-(2,6-dichloro-3-fluorophenyl)ethoxy)quino...)Show SMILES C[C@@H](Oc1ccc2ncccc2c1)c1c(Cl)ccc(F)c1Cl |r| Show InChI InChI=1S/C17H12Cl2FNO/c1-10(16-13(18)5-6-14(20)17(16)19)22-12-4-7-15-11(9-12)3-2-8-21-15/h2-10H,1H3/t10-/m1/s1 | PDB
UniProtKB/SwissProt
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | >5.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Chugai Pharmaceutical Co, Ltd
Curated by ChEMBL
| Assay Description
Inhibition of recombinant Fyn by TR-FRET assay |
Bioorg Med Chem Lett 20: 1405-9 (2010)
Article DOI: 10.1016/j.bmcl.2009.12.109
BindingDB Entry DOI: 10.7270/Q2HQ401G |
More data for this
Ligand-Target Pair | |
Leukocyte tyrosine kinase receptor
(Homo sapiens (Human)) | BDBM50306683
((R)-6-(1-(2,6-dichloro-3-fluorophenyl)ethoxy)quino...)Show SMILES C[C@@H](Oc1ccc2ncccc2c1)c1c(Cl)ccc(F)c1Cl |r| Show InChI InChI=1S/C17H12Cl2FNO/c1-10(16-13(18)5-6-14(20)17(16)19)22-12-4-7-15-11(9-12)3-2-8-21-15/h2-10H,1H3/t10-/m1/s1 | PDB
KEGG
UniProtKB/SwissProt
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | >5.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Chugai Pharmaceutical Co, Ltd
Curated by ChEMBL
| Assay Description
Inhibition of recombinant LTK by TR-FRET assay |
Bioorg Med Chem Lett 20: 1405-9 (2010)
Article DOI: 10.1016/j.bmcl.2009.12.109
BindingDB Entry DOI: 10.7270/Q2HQ401G |
More data for this
Ligand-Target Pair | |
RAC-alpha serine/threonine-protein kinase
(Homo sapiens (Human)) | BDBM50306684
(2-(6-((R)-1-(2,6-dichloro-3-fluorophenyl)ethoxy)qu...)Show SMILES C[C@@H](Oc1ccc2ncc(cc2c1)C1CC1C(N)=O)c1c(Cl)ccc(F)c1Cl |r| Show InChI InChI=1S/C21H17Cl2FN2O2/c1-10(19-16(22)3-4-17(24)20(19)23)28-13-2-5-18-11(7-13)6-12(9-26-18)14-8-15(14)21(25)27/h2-7,9-10,14-15H,8H2,1H3,(H2,25,27)/t10-,14?,15?/m1/s1 | PDB
UniProtKB/SwissProt
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | >5.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Chugai Pharmaceutical Co, Ltd
Curated by ChEMBL
| Assay Description
Inhibition of recombinant AKT1 by IMAP assay |
Bioorg Med Chem Lett 20: 1405-9 (2010)
Article DOI: 10.1016/j.bmcl.2009.12.109
BindingDB Entry DOI: 10.7270/Q2HQ401G |
More data for this
Ligand-Target Pair | |
Insulin receptor
(Homo sapiens (Human)) | BDBM50306684
(2-(6-((R)-1-(2,6-dichloro-3-fluorophenyl)ethoxy)qu...)Show SMILES C[C@@H](Oc1ccc2ncc(cc2c1)C1CC1C(N)=O)c1c(Cl)ccc(F)c1Cl |r| Show InChI InChI=1S/C21H17Cl2FN2O2/c1-10(19-16(22)3-4-17(24)20(19)23)28-13-2-5-18-11(7-13)6-12(9-26-18)14-8-15(14)21(25)27/h2-7,9-10,14-15H,8H2,1H3,(H2,25,27)/t10-,14?,15?/m1/s1 | PDB
MMDB
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | >5.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Chugai Pharmaceutical Co, Ltd
Curated by ChEMBL
| Assay Description
Inhibition of recombinant InsR by TR-FRET assay |
Bioorg Med Chem Lett 20: 1405-9 (2010)
Article DOI: 10.1016/j.bmcl.2009.12.109
BindingDB Entry DOI: 10.7270/Q2HQ401G |
More data for this
Ligand-Target Pair | |
Mast/stem cell growth factor receptor Kit
(Homo sapiens (Human)) | BDBM50306677
((R)-3-(6-(1-(2,6-dichloro-3-fluorophenyl)ethoxy)qu...)Show SMILES C[C@@H](Oc1ccc2ncc(\C=C\C(N)=O)cc2c1)c1c(Cl)ccc(F)c1Cl |r| Show InChI InChI=1S/C20H15Cl2FN2O2/c1-11(19-15(21)4-5-16(23)20(19)22)27-14-3-6-17-13(9-14)8-12(10-25-17)2-7-18(24)26/h2-11H,1H3,(H2,24,26)/b7-2+/t11-/m1/s1 | PDB
UniProtKB/SwissProt
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | >5.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Chugai Pharmaceutical Co, Ltd
Curated by ChEMBL
| Assay Description
Inhibition of recombinant Kit by TR-FRET assay |
Bioorg Med Chem Lett 20: 1405-9 (2010)
Article DOI: 10.1016/j.bmcl.2009.12.109
BindingDB Entry DOI: 10.7270/Q2HQ401G |
More data for this
Ligand-Target Pair | |
Aurora kinase A
(Homo sapiens (Human)) | BDBM50306683
((R)-6-(1-(2,6-dichloro-3-fluorophenyl)ethoxy)quino...)Show SMILES C[C@@H](Oc1ccc2ncccc2c1)c1c(Cl)ccc(F)c1Cl |r| Show InChI InChI=1S/C17H12Cl2FNO/c1-10(16-13(18)5-6-14(20)17(16)19)22-12-4-7-15-11(9-12)3-2-8-21-15/h2-10H,1H3/t10-/m1/s1 | PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | >5.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Chugai Pharmaceutical Co, Ltd
Curated by ChEMBL
| Assay Description
Inhibition of recombinant Aurora A by IMAP assay |
Bioorg Med Chem Lett 20: 1405-9 (2010)
Article DOI: 10.1016/j.bmcl.2009.12.109
BindingDB Entry DOI: 10.7270/Q2HQ401G |
More data for this
Ligand-Target Pair | |
Tyrosine-protein kinase ABL1
(Homo sapiens (Human)) | BDBM50306683
((R)-6-(1-(2,6-dichloro-3-fluorophenyl)ethoxy)quino...)Show SMILES C[C@@H](Oc1ccc2ncccc2c1)c1c(Cl)ccc(F)c1Cl |r| Show InChI InChI=1S/C17H12Cl2FNO/c1-10(16-13(18)5-6-14(20)17(16)19)22-12-4-7-15-11(9-12)3-2-8-21-15/h2-10H,1H3/t10-/m1/s1 | PDB
MMDB
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | >5.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Chugai Pharmaceutical Co, Ltd
Curated by ChEMBL
| Assay Description
Inhibition of recombinant Abl by TR-FRET assay |
Bioorg Med Chem Lett 20: 1405-9 (2010)
Article DOI: 10.1016/j.bmcl.2009.12.109
BindingDB Entry DOI: 10.7270/Q2HQ401G |
More data for this
Ligand-Target Pair | |
Proto-oncogene tyrosine-protein kinase Src
(Homo sapiens (Human)) | BDBM50306680
(CHEMBL598912 | rac-3-(6-(1-(2,6-dichloro-3-fluorop...)Show SMILES CNC(=O)\C=C\c1cnc2ccc(OC(C)c3c(Cl)ccc(F)c3Cl)cc2c1 Show InChI InChI=1S/C21H17Cl2FN2O2/c1-12(20-16(22)5-6-17(24)21(20)23)28-15-4-7-18-14(10-15)9-13(11-26-18)3-8-19(27)25-2/h3-12H,1-2H3,(H,25,27)/b8-3+ | PDB
MMDB
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
PDB
UniChem
Similars
| Article
PubMed
| n/a | n/a | >5.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Chugai Pharmaceutical Co, Ltd
Curated by ChEMBL
| Assay Description
Inhibition of recombinant Src by TR-FRET assay |
Bioorg Med Chem Lett 20: 1405-9 (2010)
Article DOI: 10.1016/j.bmcl.2009.12.109
BindingDB Entry DOI: 10.7270/Q2HQ401G |
More data for this
Ligand-Target Pair | |
Vascular endothelial growth factor receptor 2
(Homo sapiens (Human)) | BDBM50306680
(CHEMBL598912 | rac-3-(6-(1-(2,6-dichloro-3-fluorop...)Show SMILES CNC(=O)\C=C\c1cnc2ccc(OC(C)c3c(Cl)ccc(F)c3Cl)cc2c1 Show InChI InChI=1S/C21H17Cl2FN2O2/c1-12(20-16(22)5-6-17(24)21(20)23)28-15-4-7-18-14(10-15)9-13(11-26-18)3-8-19(27)25-2/h3-12H,1-2H3,(H,25,27)/b8-3+ | PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
PDB
UniChem
Similars
| Article
PubMed
| n/a | n/a | >5.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Chugai Pharmaceutical Co, Ltd
Curated by ChEMBL
| Assay Description
Inhibition of recombinant KDR by TR-FRET assay |
Bioorg Med Chem Lett 20: 1405-9 (2010)
Article DOI: 10.1016/j.bmcl.2009.12.109
BindingDB Entry DOI: 10.7270/Q2HQ401G |
More data for this
Ligand-Target Pair | |
Cyclin-dependent kinase 1
(Homo sapiens (Human)) | BDBM50306677
((R)-3-(6-(1-(2,6-dichloro-3-fluorophenyl)ethoxy)qu...)Show SMILES C[C@@H](Oc1ccc2ncc(\C=C\C(N)=O)cc2c1)c1c(Cl)ccc(F)c1Cl |r| Show InChI InChI=1S/C20H15Cl2FN2O2/c1-11(19-15(21)4-5-16(23)20(19)22)27-14-3-6-17-13(9-14)8-12(10-25-17)2-7-18(24)26/h2-11H,1H3,(H2,24,26)/b7-2+/t11-/m1/s1 | PDB
Reactome pathway
KEGG
UniProtKB/SwissProt
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | >5.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Chugai Pharmaceutical Co, Ltd
Curated by ChEMBL
| Assay Description
Inhibition of recombinant CDK1 by IMAP assay |
Bioorg Med Chem Lett 20: 1405-9 (2010)
Article DOI: 10.1016/j.bmcl.2009.12.109
BindingDB Entry DOI: 10.7270/Q2HQ401G |
More data for this
Ligand-Target Pair | |
Insulin-like growth factor 1 receptor
(Homo sapiens (Human)) | BDBM50306677
((R)-3-(6-(1-(2,6-dichloro-3-fluorophenyl)ethoxy)qu...)Show SMILES C[C@@H](Oc1ccc2ncc(\C=C\C(N)=O)cc2c1)c1c(Cl)ccc(F)c1Cl |r| Show InChI InChI=1S/C20H15Cl2FN2O2/c1-11(19-15(21)4-5-16(23)20(19)22)27-14-3-6-17-13(9-14)8-12(10-25-17)2-7-18(24)26/h2-11H,1H3,(H2,24,26)/b7-2+/t11-/m1/s1 | PDB
MMDB
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | >5.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Chugai Pharmaceutical Co, Ltd
Curated by ChEMBL
| Assay Description
Inhibition of recombinant IGF1R by TR-FRET assay |
Bioorg Med Chem Lett 20: 1405-9 (2010)
Article DOI: 10.1016/j.bmcl.2009.12.109
BindingDB Entry DOI: 10.7270/Q2HQ401G |
More data for this
Ligand-Target Pair | |
Proto-oncogene tyrosine-protein kinase Src
(Homo sapiens (Human)) | BDBM50306678
(CHEMBL591457 | rac-3-(6-(1-(2,6-dichloro-3-fluorop...)Show SMILES CC(Oc1ccc2ncc(CCC(N)=O)cc2c1)c1c(Cl)ccc(F)c1Cl Show InChI InChI=1S/C20H17Cl2FN2O2/c1-11(19-15(21)4-5-16(23)20(19)22)27-14-3-6-17-13(9-14)8-12(10-25-17)2-7-18(24)26/h3-6,8-11H,2,7H2,1H3,(H2,24,26) | PDB
MMDB
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | >5.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Chugai Pharmaceutical Co, Ltd
Curated by ChEMBL
| Assay Description
Inhibition of recombinant Src by TR-FRET assay |
Bioorg Med Chem Lett 20: 1405-9 (2010)
Article DOI: 10.1016/j.bmcl.2009.12.109
BindingDB Entry DOI: 10.7270/Q2HQ401G |
More data for this
Ligand-Target Pair | |
Protein kinase C alpha type
(Homo sapiens (Human)) | BDBM50306677
((R)-3-(6-(1-(2,6-dichloro-3-fluorophenyl)ethoxy)qu...)Show SMILES C[C@@H](Oc1ccc2ncc(\C=C\C(N)=O)cc2c1)c1c(Cl)ccc(F)c1Cl |r| Show InChI InChI=1S/C20H15Cl2FN2O2/c1-11(19-15(21)4-5-16(23)20(19)22)27-14-3-6-17-13(9-14)8-12(10-25-17)2-7-18(24)26/h2-11H,1H3,(H2,24,26)/b7-2+/t11-/m1/s1 | PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | >5.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Chugai Pharmaceutical Co, Ltd
Curated by ChEMBL
| Assay Description
Inhibition of recombinant PKCalpha by IMAP assay |
Bioorg Med Chem Lett 20: 1405-9 (2010)
Article DOI: 10.1016/j.bmcl.2009.12.109
BindingDB Entry DOI: 10.7270/Q2HQ401G |
More data for this
Ligand-Target Pair | |
RAC-alpha serine/threonine-protein kinase
(Homo sapiens (Human)) | BDBM50306677
((R)-3-(6-(1-(2,6-dichloro-3-fluorophenyl)ethoxy)qu...)Show SMILES C[C@@H](Oc1ccc2ncc(\C=C\C(N)=O)cc2c1)c1c(Cl)ccc(F)c1Cl |r| Show InChI InChI=1S/C20H15Cl2FN2O2/c1-11(19-15(21)4-5-16(23)20(19)22)27-14-3-6-17-13(9-14)8-12(10-25-17)2-7-18(24)26/h2-11H,1H3,(H2,24,26)/b7-2+/t11-/m1/s1 | PDB
UniProtKB/SwissProt
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | >5.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Chugai Pharmaceutical Co, Ltd
Curated by ChEMBL
| Assay Description
Inhibition of recombinant AKT1 by IMAP assay |
Bioorg Med Chem Lett 20: 1405-9 (2010)
Article DOI: 10.1016/j.bmcl.2009.12.109
BindingDB Entry DOI: 10.7270/Q2HQ401G |
More data for this
Ligand-Target Pair | |
Proto-oncogene tyrosine-protein kinase Src
(Homo sapiens (Human)) | BDBM50306681
((S)-6-(1-(2,6-dichloro-3-fluorophenyl)ethoxy)quino...)Show SMILES C[C@H](Oc1ccc2ncccc2c1)c1c(Cl)ccc(F)c1Cl |r| Show InChI InChI=1S/C17H12Cl2FNO/c1-10(16-13(18)5-6-14(20)17(16)19)22-12-4-7-15-11(9-12)3-2-8-21-15/h2-10H,1H3/t10-/m0/s1 | PDB
MMDB
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | >5.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Chugai Pharmaceutical Co, Ltd
Curated by ChEMBL
| Assay Description
Inhibition of recombinant Src by TR-FRET assay |
Bioorg Med Chem Lett 20: 1405-9 (2010)
Article DOI: 10.1016/j.bmcl.2009.12.109
BindingDB Entry DOI: 10.7270/Q2HQ401G |
More data for this
Ligand-Target Pair | |
Tyrosine-protein kinase Yes
(Homo sapiens (Human)) | BDBM50306683
((R)-6-(1-(2,6-dichloro-3-fluorophenyl)ethoxy)quino...)Show SMILES C[C@@H](Oc1ccc2ncccc2c1)c1c(Cl)ccc(F)c1Cl |r| Show InChI InChI=1S/C17H12Cl2FNO/c1-10(16-13(18)5-6-14(20)17(16)19)22-12-4-7-15-11(9-12)3-2-8-21-15/h2-10H,1H3/t10-/m1/s1 | PDB
MMDB
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | >5.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Chugai Pharmaceutical Co, Ltd
Curated by ChEMBL
| Assay Description
Inhibition of recombinant YES by TR-FRET assay |
Bioorg Med Chem Lett 20: 1405-9 (2010)
Article DOI: 10.1016/j.bmcl.2009.12.109
BindingDB Entry DOI: 10.7270/Q2HQ401G |
More data for this
Ligand-Target Pair | |
Insulin-like growth factor 1 receptor
(Homo sapiens (Human)) | BDBM50306683
((R)-6-(1-(2,6-dichloro-3-fluorophenyl)ethoxy)quino...)Show SMILES C[C@@H](Oc1ccc2ncccc2c1)c1c(Cl)ccc(F)c1Cl |r| Show InChI InChI=1S/C17H12Cl2FNO/c1-10(16-13(18)5-6-14(20)17(16)19)22-12-4-7-15-11(9-12)3-2-8-21-15/h2-10H,1H3/t10-/m1/s1 | PDB
MMDB
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | >5.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Chugai Pharmaceutical Co, Ltd
Curated by ChEMBL
| Assay Description
Inhibition of recombinant IGF1R by TR-FRET assay |
Bioorg Med Chem Lett 20: 1405-9 (2010)
Article DOI: 10.1016/j.bmcl.2009.12.109
BindingDB Entry DOI: 10.7270/Q2HQ401G |
More data for this
Ligand-Target Pair | |
Cyclin-dependent kinase 1
(Homo sapiens (Human)) | BDBM50306684
(2-(6-((R)-1-(2,6-dichloro-3-fluorophenyl)ethoxy)qu...)Show SMILES C[C@@H](Oc1ccc2ncc(cc2c1)C1CC1C(N)=O)c1c(Cl)ccc(F)c1Cl |r| Show InChI InChI=1S/C21H17Cl2FN2O2/c1-10(19-16(22)3-4-17(24)20(19)23)28-13-2-5-18-11(7-13)6-12(9-26-18)14-8-15(14)21(25)27/h2-7,9-10,14-15H,8H2,1H3,(H2,25,27)/t10-,14?,15?/m1/s1 | PDB
Reactome pathway
KEGG
UniProtKB/SwissProt
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | >5.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Chugai Pharmaceutical Co, Ltd
Curated by ChEMBL
| Assay Description
Inhibition of recombinant CDK1 by IMAP assay |
Bioorg Med Chem Lett 20: 1405-9 (2010)
Article DOI: 10.1016/j.bmcl.2009.12.109
BindingDB Entry DOI: 10.7270/Q2HQ401G |
More data for this
Ligand-Target Pair | |
Protein kinase C alpha type
(Homo sapiens (Human)) | BDBM50306684
(2-(6-((R)-1-(2,6-dichloro-3-fluorophenyl)ethoxy)qu...)Show SMILES C[C@@H](Oc1ccc2ncc(cc2c1)C1CC1C(N)=O)c1c(Cl)ccc(F)c1Cl |r| Show InChI InChI=1S/C21H17Cl2FN2O2/c1-10(19-16(22)3-4-17(24)20(19)23)28-13-2-5-18-11(7-13)6-12(9-26-18)14-8-15(14)21(25)27/h2-7,9-10,14-15H,8H2,1H3,(H2,25,27)/t10-,14?,15?/m1/s1 | PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | >5.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Chugai Pharmaceutical Co, Ltd
Curated by ChEMBL
| Assay Description
Inhibition of recombinant PKCalpha by IMAP assay |
Bioorg Med Chem Lett 20: 1405-9 (2010)
Article DOI: 10.1016/j.bmcl.2009.12.109
BindingDB Entry DOI: 10.7270/Q2HQ401G |
More data for this
Ligand-Target Pair | |
Insulin receptor
(Homo sapiens (Human)) | BDBM50306677
((R)-3-(6-(1-(2,6-dichloro-3-fluorophenyl)ethoxy)qu...)Show SMILES C[C@@H](Oc1ccc2ncc(\C=C\C(N)=O)cc2c1)c1c(Cl)ccc(F)c1Cl |r| Show InChI InChI=1S/C20H15Cl2FN2O2/c1-11(19-15(21)4-5-16(23)20(19)22)27-14-3-6-17-13(9-14)8-12(10-25-17)2-7-18(24)26/h2-11H,1H3,(H2,24,26)/b7-2+/t11-/m1/s1 | PDB
MMDB
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | >5.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Chugai Pharmaceutical Co, Ltd
Curated by ChEMBL
| Assay Description
Inhibition of recombinant InsR by TR-FRET assay |
Bioorg Med Chem Lett 20: 1405-9 (2010)
Article DOI: 10.1016/j.bmcl.2009.12.109
BindingDB Entry DOI: 10.7270/Q2HQ401G |
More data for this
Ligand-Target Pair | |
Vascular endothelial growth factor receptor 2
(Homo sapiens (Human)) | BDBM50306678
(CHEMBL591457 | rac-3-(6-(1-(2,6-dichloro-3-fluorop...)Show SMILES CC(Oc1ccc2ncc(CCC(N)=O)cc2c1)c1c(Cl)ccc(F)c1Cl Show InChI InChI=1S/C20H17Cl2FN2O2/c1-11(19-15(21)4-5-16(23)20(19)22)27-14-3-6-17-13(9-14)8-12(10-25-17)2-7-18(24)26/h3-6,8-11H,2,7H2,1H3,(H2,24,26) | PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | 5.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Chugai Pharmaceutical Co, Ltd
Curated by ChEMBL
| Assay Description
Inhibition of recombinant KDR by TR-FRET assay |
Bioorg Med Chem Lett 20: 1405-9 (2010)
Article DOI: 10.1016/j.bmcl.2009.12.109
BindingDB Entry DOI: 10.7270/Q2HQ401G |
More data for this
Ligand-Target Pair | |
Proto-oncogene tyrosine-protein kinase Src
(Homo sapiens (Human)) | BDBM50306677
((R)-3-(6-(1-(2,6-dichloro-3-fluorophenyl)ethoxy)qu...)Show SMILES C[C@@H](Oc1ccc2ncc(\C=C\C(N)=O)cc2c1)c1c(Cl)ccc(F)c1Cl |r| Show InChI InChI=1S/C20H15Cl2FN2O2/c1-11(19-15(21)4-5-16(23)20(19)22)27-14-3-6-17-13(9-14)8-12(10-25-17)2-7-18(24)26/h2-11H,1H3,(H2,24,26)/b7-2+/t11-/m1/s1 | PDB
MMDB
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | >5.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Chugai Pharmaceutical Co, Ltd
Curated by ChEMBL
| Assay Description
Inhibition of recombinant Src by TR-FRET assay |
Bioorg Med Chem Lett 20: 1405-9 (2010)
Article DOI: 10.1016/j.bmcl.2009.12.109
BindingDB Entry DOI: 10.7270/Q2HQ401G |
More data for this
Ligand-Target Pair | |
Insulin receptor
(Homo sapiens (Human)) | BDBM50306683
((R)-6-(1-(2,6-dichloro-3-fluorophenyl)ethoxy)quino...)Show SMILES C[C@@H](Oc1ccc2ncccc2c1)c1c(Cl)ccc(F)c1Cl |r| Show InChI InChI=1S/C17H12Cl2FNO/c1-10(16-13(18)5-6-14(20)17(16)19)22-12-4-7-15-11(9-12)3-2-8-21-15/h2-10H,1H3/t10-/m1/s1 | PDB
MMDB
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | >5.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Chugai Pharmaceutical Co, Ltd
Curated by ChEMBL
| Assay Description
Inhibition of recombinant InsR by TR-FRET assay |
Bioorg Med Chem Lett 20: 1405-9 (2010)
Article DOI: 10.1016/j.bmcl.2009.12.109
BindingDB Entry DOI: 10.7270/Q2HQ401G |
More data for this
Ligand-Target Pair | |
Vascular endothelial growth factor receptor 2
(Homo sapiens (Human)) | BDBM50306679
(CHEMBL608738 | rac-3-(6-(1-(2,6-dichloro-3-fluorop...)Show SMILES CC(Oc1ccc2ncc(\C=C\C(=O)N(C)C)cc2c1)c1c(Cl)ccc(F)c1Cl Show InChI InChI=1S/C22H19Cl2FN2O2/c1-13(21-17(23)6-7-18(25)22(21)24)29-16-5-8-19-15(11-16)10-14(12-26-19)4-9-20(28)27(2)3/h4-13H,1-3H3/b9-4+ | PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | >5.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Chugai Pharmaceutical Co, Ltd
Curated by ChEMBL
| Assay Description
Inhibition of recombinant KDR by TR-FRET assay |
Bioorg Med Chem Lett 20: 1405-9 (2010)
Article DOI: 10.1016/j.bmcl.2009.12.109
BindingDB Entry DOI: 10.7270/Q2HQ401G |
More data for this
Ligand-Target Pair | |
Cyclin-dependent kinase 2
(Homo sapiens (Human)) | BDBM50306683
((R)-6-(1-(2,6-dichloro-3-fluorophenyl)ethoxy)quino...)Show SMILES C[C@@H](Oc1ccc2ncccc2c1)c1c(Cl)ccc(F)c1Cl |r| Show InChI InChI=1S/C17H12Cl2FNO/c1-10(16-13(18)5-6-14(20)17(16)19)22-12-4-7-15-11(9-12)3-2-8-21-15/h2-10H,1H3/t10-/m1/s1 | PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | >5.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Chugai Pharmaceutical Co, Ltd
Curated by ChEMBL
| Assay Description
Inhibition of recombinant CDK2 by IMAP assay |
Bioorg Med Chem Lett 20: 1405-9 (2010)
Article DOI: 10.1016/j.bmcl.2009.12.109
BindingDB Entry DOI: 10.7270/Q2HQ401G |
More data for this
Ligand-Target Pair | |
Epidermal growth factor receptor
(Homo sapiens (Human)) | BDBM50306683
((R)-6-(1-(2,6-dichloro-3-fluorophenyl)ethoxy)quino...)Show SMILES C[C@@H](Oc1ccc2ncccc2c1)c1c(Cl)ccc(F)c1Cl |r| Show InChI InChI=1S/C17H12Cl2FNO/c1-10(16-13(18)5-6-14(20)17(16)19)22-12-4-7-15-11(9-12)3-2-8-21-15/h2-10H,1H3/t10-/m1/s1 | PDB
MMDB
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | >5.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Chugai Pharmaceutical Co, Ltd
Curated by ChEMBL
| Assay Description
Inhibition of recombinant EGFR by TR-FRET assay |
Bioorg Med Chem Lett 20: 1405-9 (2010)
Article DOI: 10.1016/j.bmcl.2009.12.109
BindingDB Entry DOI: 10.7270/Q2HQ401G |
More data for this
Ligand-Target Pair | |
Tyrosine-protein kinase ABL1
(Homo sapiens (Human)) | BDBM50306684
(2-(6-((R)-1-(2,6-dichloro-3-fluorophenyl)ethoxy)qu...)Show SMILES C[C@@H](Oc1ccc2ncc(cc2c1)C1CC1C(N)=O)c1c(Cl)ccc(F)c1Cl |r| Show InChI InChI=1S/C21H17Cl2FN2O2/c1-10(19-16(22)3-4-17(24)20(19)23)28-13-2-5-18-11(7-13)6-12(9-26-18)14-8-15(14)21(25)27/h2-7,9-10,14-15H,8H2,1H3,(H2,25,27)/t10-,14?,15?/m1/s1 | PDB
MMDB
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | >5.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Chugai Pharmaceutical Co, Ltd
Curated by ChEMBL
| Assay Description
Inhibition of recombinant Abl by TR-FRET assay |
Bioorg Med Chem Lett 20: 1405-9 (2010)
Article DOI: 10.1016/j.bmcl.2009.12.109
BindingDB Entry DOI: 10.7270/Q2HQ401G |
More data for this
Ligand-Target Pair | |
Proto-oncogene tyrosine-protein kinase Src
(Homo sapiens (Human)) | BDBM50306685
(CHEMBL602470 | rac-3-(6-(1-(2,6-dichloro-3-fluorop...)Show SMILES CC(Oc1ccc2ncc(\C=C\C(O)=O)cc2c1)c1c(Cl)ccc(F)c1Cl Show InChI InChI=1S/C20H14Cl2FNO3/c1-11(19-15(21)4-5-16(23)20(19)22)27-14-3-6-17-13(9-14)8-12(10-24-17)2-7-18(25)26/h2-11H,1H3,(H,25,26)/b7-2+ | PDB
MMDB
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | >5.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Chugai Pharmaceutical Co, Ltd
Curated by ChEMBL
| Assay Description
Inhibition of recombinant Src by TR-FRET assay |
Bioorg Med Chem Lett 20: 1405-9 (2010)
Article DOI: 10.1016/j.bmcl.2009.12.109
BindingDB Entry DOI: 10.7270/Q2HQ401G |
More data for this
Ligand-Target Pair | |
Protein-tyrosine kinase 6
(Homo sapiens (Human)) | BDBM50306683
((R)-6-(1-(2,6-dichloro-3-fluorophenyl)ethoxy)quino...)Show SMILES C[C@@H](Oc1ccc2ncccc2c1)c1c(Cl)ccc(F)c1Cl |r| Show InChI InChI=1S/C17H12Cl2FNO/c1-10(16-13(18)5-6-14(20)17(16)19)22-12-4-7-15-11(9-12)3-2-8-21-15/h2-10H,1H3/t10-/m1/s1 | PDB
MMDB
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | >5.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Chugai Pharmaceutical Co, Ltd
Curated by ChEMBL
| Assay Description
Inhibition of recombinant BRK by TR-FRET assay |
Bioorg Med Chem Lett 20: 1405-9 (2010)
Article DOI: 10.1016/j.bmcl.2009.12.109
BindingDB Entry DOI: 10.7270/Q2HQ401G |
More data for this
Ligand-Target Pair | |
Cyclin-dependent kinase 1
(Homo sapiens (Human)) | BDBM50306683
((R)-6-(1-(2,6-dichloro-3-fluorophenyl)ethoxy)quino...)Show SMILES C[C@@H](Oc1ccc2ncccc2c1)c1c(Cl)ccc(F)c1Cl |r| Show InChI InChI=1S/C17H12Cl2FNO/c1-10(16-13(18)5-6-14(20)17(16)19)22-12-4-7-15-11(9-12)3-2-8-21-15/h2-10H,1H3/t10-/m1/s1 | PDB
Reactome pathway
KEGG
UniProtKB/SwissProt
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | >5.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Chugai Pharmaceutical Co, Ltd
Curated by ChEMBL
| Assay Description
Inhibition of recombinant CDK1 by IMAP assay |
Bioorg Med Chem Lett 20: 1405-9 (2010)
Article DOI: 10.1016/j.bmcl.2009.12.109
BindingDB Entry DOI: 10.7270/Q2HQ401G |
More data for this
Ligand-Target Pair | |
Vascular endothelial growth factor receptor 2
(Homo sapiens (Human)) | BDBM50306685
(CHEMBL602470 | rac-3-(6-(1-(2,6-dichloro-3-fluorop...)Show SMILES CC(Oc1ccc2ncc(\C=C\C(O)=O)cc2c1)c1c(Cl)ccc(F)c1Cl Show InChI InChI=1S/C20H14Cl2FNO3/c1-11(19-15(21)4-5-16(23)20(19)22)27-14-3-6-17-13(9-14)8-12(10-24-17)2-7-18(25)26/h2-11H,1H3,(H,25,26)/b7-2+ | PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | >5.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Chugai Pharmaceutical Co, Ltd
Curated by ChEMBL
| Assay Description
Inhibition of recombinant KDR by TR-FRET assay |
Bioorg Med Chem Lett 20: 1405-9 (2010)
Article DOI: 10.1016/j.bmcl.2009.12.109
BindingDB Entry DOI: 10.7270/Q2HQ401G |
More data for this
Ligand-Target Pair | |
Protein kinase C alpha type
(Homo sapiens (Human)) | BDBM50306683
((R)-6-(1-(2,6-dichloro-3-fluorophenyl)ethoxy)quino...)Show SMILES C[C@@H](Oc1ccc2ncccc2c1)c1c(Cl)ccc(F)c1Cl |r| Show InChI InChI=1S/C17H12Cl2FNO/c1-10(16-13(18)5-6-14(20)17(16)19)22-12-4-7-15-11(9-12)3-2-8-21-15/h2-10H,1H3/t10-/m1/s1 | PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | >5.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Chugai Pharmaceutical Co, Ltd
Curated by ChEMBL
| Assay Description
Inhibition of recombinant PKCalpha by IMAP assay |
Bioorg Med Chem Lett 20: 1405-9 (2010)
Article DOI: 10.1016/j.bmcl.2009.12.109
BindingDB Entry DOI: 10.7270/Q2HQ401G |
More data for this
Ligand-Target Pair | |
Proto-oncogene tyrosine-protein kinase Src
(Homo sapiens (Human)) | BDBM50306679
(CHEMBL608738 | rac-3-(6-(1-(2,6-dichloro-3-fluorop...)Show SMILES CC(Oc1ccc2ncc(\C=C\C(=O)N(C)C)cc2c1)c1c(Cl)ccc(F)c1Cl Show InChI InChI=1S/C22H19Cl2FN2O2/c1-13(21-17(23)6-7-18(25)22(21)24)29-16-5-8-19-15(11-16)10-14(12-26-19)4-9-20(28)27(2)3/h4-13H,1-3H3/b9-4+ | PDB
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| n/a | n/a | >5.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Chugai Pharmaceutical Co, Ltd
Curated by ChEMBL
| Assay Description
Inhibition of recombinant Src by TR-FRET assay |
Bioorg Med Chem Lett 20: 1405-9 (2010)
Article DOI: 10.1016/j.bmcl.2009.12.109
BindingDB Entry DOI: 10.7270/Q2HQ401G |
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Ligand-Target Pair | |
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