Found 177 hits with Last Name = 'koyano' and Initial = 'h' 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
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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 | |
Lactoylglutathione lyase
(Homo sapiens (Human)) | BDBM50402202
(CHEMBL2203964)Show SMILES COCCCn1ccc2cc(cnc12)-c1cc(cc(=O)n1O)-c1ccccc1 Show InChI InChI=1S/C22H21N3O3/c1-28-11-5-9-24-10-8-17-12-19(15-23-22(17)24)20-13-18(14-21(26)25(20)27)16-6-3-2-4-7-16/h2-4,6-8,10,12-15,27H,5,9,11H2,1H3 | PDB
UniProtKB/SwissProt
antibodypedia GoogleScholar AffyNet
| Purchase
CHEMBL MCE MMDB PC cid PC sid PDB UniChem
Similars
| PDB Article PubMed
| n/a | n/a | 11 | n/a | n/a | n/a | n/a | n/a | n/a |
Chugai Pharmaceutical Co., Ltd
Curated by ChEMBL
| Assay Description Inhibition of human recombinant GLO1 expressed in Escherichia coli BL21 assessed as decrease in reduced glutathione level after 1 hr by Ellman's meth... |
Bioorg Med Chem Lett 22: 7486-9 (2012)
Article DOI: 10.1016/j.bmcl.2012.10.045 BindingDB Entry DOI: 10.7270/Q2RX9D8Q |
More data for this Ligand-Target Pair | 3D Structure (crystal) |
Lactoylglutathione lyase
(Homo sapiens (Human)) | BDBM50402204
(CHEMBL2203978)Show SMILES COCCn1ccc2cc(cnc12)-c1cc(cc(=O)n1O)-c1ccccc1 Show InChI InChI=1S/C21H19N3O3/c1-27-10-9-23-8-7-16-11-18(14-22-21(16)23)19-12-17(13-20(25)24(19)26)15-5-3-2-4-6-15/h2-8,11-14,26H,9-10H2,1H3 | PDB
UniProtKB/SwissProt
antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 14 | n/a | n/a | n/a | n/a | n/a | n/a |
Chugai Pharmaceutical Co., Ltd
Curated by ChEMBL
| Assay Description Inhibition of human recombinant GLO1 expressed in Escherichia coli BL21 assessed as decrease in reduced glutathione level after 1 hr by Ellman's meth... |
Bioorg Med Chem Lett 22: 7486-9 (2012)
Article DOI: 10.1016/j.bmcl.2012.10.045 BindingDB Entry DOI: 10.7270/Q2RX9D8Q |
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) |
Lactoylglutathione lyase
(Homo sapiens (Human)) | BDBM50402206
(CHEMBL2203976)Show SMILES NC(=O)c1cccc(Cn2ccc3cc(cnc23)-c2cc(cc(=O)n2O)-c2ccccc2)c1 Show InChI InChI=1S/C26H20N4O3/c27-25(32)19-8-4-5-17(11-19)16-29-10-9-20-12-22(15-28-26(20)29)23-13-21(14-24(31)30(23)33)18-6-2-1-3-7-18/h1-15,33H,16H2,(H2,27,32) | PDB
UniProtKB/SwissProt
antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 40 | n/a | n/a | n/a | n/a | n/a | n/a |
Chugai Pharmaceutical Co., Ltd
Curated by ChEMBL
| Assay Description Inhibition of human recombinant GLO1 expressed in Escherichia coli BL21 assessed as decrease in reduced glutathione level after 1 hr by Ellman's meth... |
Bioorg Med Chem Lett 22: 7486-9 (2012)
Article DOI: 10.1016/j.bmcl.2012.10.045 BindingDB Entry DOI: 10.7270/Q2RX9D8Q |
More data for this Ligand-Target Pair | |
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 | |
Lactoylglutathione lyase
(Homo sapiens (Human)) | BDBM50402207
(CHEMBL2203975)Show InChI InChI=1S/C19H14N2O2/c22-19-12-16(13-4-2-1-3-5-13)11-18(21(19)23)15-6-7-17-14(10-15)8-9-20-17/h1-12,20,23H | PDB
UniProtKB/SwissProt
antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 250 | n/a | n/a | n/a | n/a | n/a | n/a |
Chugai Pharmaceutical Co., Ltd
Curated by ChEMBL
| Assay Description Inhibition of human recombinant GLO1 expressed in Escherichia coli BL21 assessed as decrease in reduced glutathione level after 1 hr by Ellman's meth... |
Bioorg Med Chem Lett 22: 7486-9 (2012)
Article DOI: 10.1016/j.bmcl.2012.10.045 BindingDB Entry DOI: 10.7270/Q2RX9D8Q |
More data for this Ligand-Target Pair | |
Lactoylglutathione lyase
(Homo sapiens (Human)) | BDBM50402203
(CHEMBL2203963)Show SMILES COCCn1ccc2cc(ccc12)-c1cc(cc(=O)n1O)-c1ccccc1 Show InChI InChI=1S/C22H20N2O3/c1-27-12-11-23-10-9-18-13-17(7-8-20(18)23)21-14-19(15-22(25)24(21)26)16-5-3-2-4-6-16/h2-10,13-15,26H,11-12H2,1H3 | PDB
UniProtKB/SwissProt
antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 260 | n/a | n/a | n/a | n/a | n/a | n/a |
Chugai Pharmaceutical Co., Ltd
Curated by ChEMBL
| Assay Description Inhibition of human recombinant GLO1 expressed in Escherichia coli BL21 assessed as decrease in reduced glutathione level after 1 hr by Ellman's meth... |
Bioorg Med Chem Lett 22: 7486-9 (2012)
Article DOI: 10.1016/j.bmcl.2012.10.045 BindingDB Entry DOI: 10.7270/Q2RX9D8Q |
More data for this Ligand-Target Pair | |
Lactoylglutathione lyase
(Homo sapiens (Human)) | BDBM50402208
(CHEMBL2203974)Show InChI InChI=1S/C18H13N3O2/c22-17-10-14(12-4-2-1-3-5-12)9-16(21(17)23)15-8-13-6-7-19-18(13)20-11-15/h1-11,23H,(H,19,20) | PDB
UniProtKB/SwissProt
antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 280 | n/a | n/a | n/a | n/a | n/a | n/a |
Chugai Pharmaceutical Co., Ltd
Curated by ChEMBL
| Assay Description Inhibition of human recombinant GLO1 expressed in Escherichia coli BL21 assessed as decrease in reduced glutathione level after 1 hr by Ellman's meth... |
Bioorg Med Chem Lett 22: 7486-9 (2012)
Article DOI: 10.1016/j.bmcl.2012.10.045 BindingDB Entry DOI: 10.7270/Q2RX9D8Q |
More data for this Ligand-Target Pair | |
Lactoylglutathione lyase
(Homo sapiens (Human)) | BDBM50402200
(CHEMBL2203966)Show SMILES CCCCn1ccc2cc(cnc12)-c1cc(cc(=O)n1O)-c1ccccc1 Show InChI InChI=1S/C22H21N3O2/c1-2-3-10-24-11-9-17-12-19(15-23-22(17)24)20-13-18(14-21(26)25(20)27)16-7-5-4-6-8-16/h4-9,11-15,27H,2-3,10H2,1H3 | PDB
UniProtKB/SwissProt
antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 300 | n/a | n/a | n/a | n/a | n/a | n/a |
Chugai Pharmaceutical Co., Ltd
Curated by ChEMBL
| Assay Description Inhibition of human recombinant GLO1 expressed in Escherichia coli BL21 assessed as decrease in reduced glutathione level after 1 hr by Ellman's meth... |
Bioorg Med Chem Lett 22: 7486-9 (2012)
Article DOI: 10.1016/j.bmcl.2012.10.045 BindingDB Entry DOI: 10.7270/Q2RX9D8Q |
More data for this Ligand-Target Pair | |
Lactoylglutathione lyase
(Homo sapiens (Human)) | BDBM50402201
(CHEMBL2203965)Show SMILES COCCCn1ccc2cc(ccc12)-c1cc(cc(=O)n1O)-c1ccccc1 Show InChI InChI=1S/C23H22N2O3/c1-28-13-5-11-24-12-10-19-14-18(8-9-21(19)24)22-15-20(16-23(26)25(22)27)17-6-3-2-4-7-17/h2-4,6-10,12,14-16,27H,5,11,13H2,1H3 | PDB
UniProtKB/SwissProt
antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 300 | n/a | n/a | n/a | n/a | n/a | n/a |
Chugai Pharmaceutical Co., Ltd
Curated by ChEMBL
| Assay Description Inhibition of human recombinant GLO1 expressed in Escherichia coli BL21 assessed as decrease in reduced glutathione level after 1 hr by Ellman's meth... |
Bioorg Med Chem Lett 22: 7486-9 (2012)
Article DOI: 10.1016/j.bmcl.2012.10.045 BindingDB Entry DOI: 10.7270/Q2RX9D8Q |
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 | |
Lactoylglutathione lyase
(Homo sapiens (Human)) | BDBM50402205
(CHEMBL2203977)Show SMILES NC(=O)c1cccc(Cn2ccc3cc(ccc23)-c2cc(cc(=O)n2O)-c2ccccc2)c1 Show InChI InChI=1S/C27H21N3O3/c28-27(32)22-8-4-5-18(13-22)17-29-12-11-21-14-20(9-10-24(21)29)25-15-23(16-26(31)30(25)33)19-6-2-1-3-7-19/h1-16,33H,17H2,(H2,28,32) | PDB
UniProtKB/SwissProt
antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 480 | n/a | n/a | n/a | n/a | n/a | n/a |
Chugai Pharmaceutical Co., Ltd
Curated by ChEMBL
| Assay Description Inhibition of human recombinant GLO1 expressed in Escherichia coli BL21 assessed as decrease in reduced glutathione level after 1 hr by Ellman's meth... |
Bioorg Med Chem Lett 22: 7486-9 (2012)
Article DOI: 10.1016/j.bmcl.2012.10.045 BindingDB Entry DOI: 10.7270/Q2RX9D8Q |
More data for this Ligand-Target Pair | |
Lactoylglutathione lyase
(Homo sapiens (Human)) | BDBM50402199
(CHEMBL2203967)Show SMILES CCCCCn1ccc2cc(cnc12)-c1cc(cc(=O)n1O)-c1ccccc1 Show InChI InChI=1S/C23H23N3O2/c1-2-3-7-11-25-12-10-18-13-20(16-24-23(18)25)21-14-19(15-22(27)26(21)28)17-8-5-4-6-9-17/h4-6,8-10,12-16,28H,2-3,7,11H2,1H3 | PDB
UniProtKB/SwissProt
antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 510 | n/a | n/a | n/a | n/a | n/a | n/a |
Chugai Pharmaceutical Co., Ltd
Curated by ChEMBL
| Assay Description Inhibition of human recombinant GLO1 expressed in Escherichia coli BL21 assessed as decrease in reduced glutathione level after 1 hr by Ellman's meth... |
Bioorg Med Chem Lett 22: 7486-9 (2012)
Article DOI: 10.1016/j.bmcl.2012.10.045 BindingDB Entry DOI: 10.7270/Q2RX9D8Q |
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 | |
Lactoylglutathione lyase
(Homo sapiens (Human)) | BDBM50402215
(CHEMBL1624076)Show InChI InChI=1S/C17H13NO2/c19-17-12-15(13-7-3-1-4-8-13)11-16(18(17)20)14-9-5-2-6-10-14/h1-12,20H | PDB
UniProtKB/SwissProt
antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 1.19E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Chugai Pharmaceutical Co., Ltd
Curated by ChEMBL
| Assay Description Inhibition of human recombinant GLO1 expressed in Escherichia coli BL21 assessed as decrease in reduced glutathione level after 1 hr by Ellman's meth... |
Bioorg Med Chem Lett 22: 7486-9 (2012)
Article DOI: 10.1016/j.bmcl.2012.10.045 BindingDB Entry DOI: 10.7270/Q2RX9D8Q |
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 | |
Lactoylglutathione lyase
(Homo sapiens (Human)) | BDBM50241121
((S)-5-((R)-3-(4-bromobenzylthio)-1-(carboxymethyla...)Show SMILES N[C@@H](CCC(=O)N[C@@H](CSCc1ccc(Br)cc1)C(=O)NCC(O)=O)C(O)=O |r| Show InChI InChI=1S/C17H22BrN3O6S/c18-11-3-1-10(2-4-11)8-28-9-13(16(25)20-7-15(23)24)21-14(22)6-5-12(19)17(26)27/h1-4,12-13H,5-9,19H2,(H,20,25)(H,21,22)(H,23,24)(H,26,27)/t12-,13-/m0/s1 | PDB
UniProtKB/SwissProt
antibodypedia GoogleScholar AffyNet
| Purchase
CHEMBL KEGG MMDB 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 human recombinant GLO1 expressed in Escherichia coli BL21 assessed as decrease in reduced glutathione level after 1 hr by Ellman's meth... |
Bioorg Med Chem Lett 22: 7486-9 (2012)
Article DOI: 10.1016/j.bmcl.2012.10.045 BindingDB Entry DOI: 10.7270/Q2RX9D8Q |
More data for this Ligand-Target Pair | |
Lactoylglutathione lyase
(Homo sapiens (Human)) | BDBM50402214
(CHEMBL2203968)Show InChI InChI=1S/C15H11NO2S/c17-15-9-13(12-6-7-19-10-12)8-14(16(15)18)11-4-2-1-3-5-11/h1-10,18H | PDB
UniProtKB/SwissProt
antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | 1.52E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Chugai Pharmaceutical Co., Ltd
Curated by ChEMBL
| Assay Description Inhibition of human recombinant GLO1 expressed in Escherichia coli BL21 assessed as decrease in reduced glutathione level after 1 hr by Ellman's meth... |
Bioorg Med Chem Lett 22: 7486-9 (2012)
Article DOI: 10.1016/j.bmcl.2012.10.045 BindingDB Entry DOI: 10.7270/Q2RX9D8Q |
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 | |
Lactoylglutathione lyase
(Homo sapiens (Human)) | BDBM50402212
(CHEMBL2203970)Show SMILES On1c(cc(cc1=O)-c1ccc(cc1)C(F)(F)F)-c1ccccc1 Show InChI InChI=1S/C18H12F3NO2/c19-18(20,21)15-8-6-12(7-9-15)14-10-16(22(24)17(23)11-14)13-4-2-1-3-5-13/h1-11,24H | PDB
UniProtKB/SwissProt
antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 8.13E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Chugai Pharmaceutical Co., Ltd
Curated by ChEMBL
| Assay Description Inhibition of human recombinant GLO1 expressed in Escherichia coli BL21 assessed as decrease in reduced glutathione level after 1 hr by Ellman's meth... |
Bioorg Med Chem Lett 22: 7486-9 (2012)
Article DOI: 10.1016/j.bmcl.2012.10.045 BindingDB Entry DOI: 10.7270/Q2RX9D8Q |
More data for this Ligand-Target Pair | |
Lactoylglutathione lyase
(Homo sapiens (Human)) | BDBM50402213
(CHEMBL2203969)Show InChI InChI=1S/C16H12N2O2/c19-16-10-14(13-7-4-8-17-11-13)9-15(18(16)20)12-5-2-1-3-6-12/h1-11,20H | PDB
UniProtKB/SwissProt
antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 8.28E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Chugai Pharmaceutical Co., Ltd
Curated by ChEMBL
| Assay Description Inhibition of human recombinant GLO1 expressed in Escherichia coli BL21 assessed as decrease in reduced glutathione level after 1 hr by Ellman's meth... |
Bioorg Med Chem Lett 22: 7486-9 (2012)
Article DOI: 10.1016/j.bmcl.2012.10.045 BindingDB Entry DOI: 10.7270/Q2RX9D8Q |
More data for this Ligand-Target Pair | |
Lactoylglutathione lyase
(Homo sapiens (Human)) | BDBM50402211
(CHEMBL2203971)Show SMILES On1c(cc(cc1=O)-c1ccc(cc1)-c1ccccc1)-c1ccccc1 Show InChI InChI=1S/C23H17NO2/c25-23-16-21(15-22(24(23)26)20-9-5-2-6-10-20)19-13-11-18(12-14-19)17-7-3-1-4-8-17/h1-16,26H | PDB
UniProtKB/SwissProt
antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 8.40E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Chugai Pharmaceutical Co., Ltd
Curated by ChEMBL
| Assay Description Inhibition of human recombinant GLO1 expressed in Escherichia coli BL21 assessed as decrease in reduced glutathione level after 1 hr by Ellman's meth... |
Bioorg Med Chem Lett 22: 7486-9 (2012)
Article DOI: 10.1016/j.bmcl.2012.10.045 BindingDB Entry DOI: 10.7270/Q2RX9D8Q |
More data for this Ligand-Target Pair | |
Lactoylglutathione lyase
(Homo sapiens (Human)) | BDBM50402210
(CHEMBL2203972)Show InChI InChI=1S/C15H13NO2/c1-2-3-7-12-10-14(16(18)15(17)11-12)13-8-5-4-6-9-13/h4-6,8-11,18H,2H2,1H3 | PDB
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 human recombinant GLO1 expressed in Escherichia coli BL21 assessed as decrease in reduced glutathione level after 1 hr by Ellman's meth... |
Bioorg Med Chem Lett 22: 7486-9 (2012)
Article DOI: 10.1016/j.bmcl.2012.10.045 BindingDB Entry DOI: 10.7270/Q2RX9D8Q |
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 | |
Lactoylglutathione lyase
(Homo sapiens (Human)) | BDBM50402209
(CHEMBL2203973)Show InChI InChI=1S/C15H17NO2/c1-2-3-7-12-10-14(16(18)15(17)11-12)13-8-5-4-6-9-13/h4-6,8-11,18H,2-3,7H2,1H3 | PDB
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 human recombinant GLO1 expressed in Escherichia coli BL21 assessed as decrease in reduced glutathione level after 1 hr by Ellman's meth... |
Bioorg Med Chem Lett 22: 7486-9 (2012)
Article DOI: 10.1016/j.bmcl.2012.10.045 BindingDB Entry DOI: 10.7270/Q2RX9D8Q |
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 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 | |
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 | |
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 | |
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 | |