BDBM50306681 (S)-6-(1-(2,6-dichloro-3-fluorophenyl)ethoxy)quinoline::CHEMBL598523

SMILES: C[C@H](Oc1ccc2ncccc2c1)c1c(Cl)ccc(F)c1Cl

InChI Key: InChIKey=DORFEDMRVQLEQT-JTQLQIEISA-N

Data: 6 IC50

Find this compound or compounds like it in BindingDB or PDB:

Substructure Similarity at least:  must be >=0.5 Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 6 hits for monomerid = 50306681   

Target/Host (Institution)	Ligand	Target/Host Links	Ligand Links	Trg + Lig Links	Ki nM	ΔG° kcal/mole	IC50 nM	Kd nM	EC50/IC50 nM	koff s-1	kon M-1s-1	pH	Temp °C
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
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 UniProtKB/TrEMBL 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
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
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 UniProtKB/TrEMBL 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
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
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