null

SMILES: Fc1cc(Cl)ccc1Nc1ncnc2[nH]c(CCc3ccccc3)cc12

InChI Key: InChIKey=OLTGDTOUJBNHPA-UHFFFAOYSA-N

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 4 hits for monomerid = 50318167   

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
Epidermal growth factor receptor (Homo sapiens (Human))	BDBM50318167 (CHEMBL1096416 | N-(4-chloro-2-fluorophenyl)-6-(2-p...) Show SMILES Fc1cc(Cl)ccc1Nc1ncnc2[nH]c(CCc3ccccc3)cc12 Show InChI InChI=1S/C20H16ClFN4/c21-14-7-9-18(17(22)10-14)26-20-16-11-15(25-19(16)23-12-24-20)8-6-13-4-2-1-3-5-13/h1-5,7,9-12H,6,8H2,(H2,23,24,25,26)	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	>2.00E+5	n/a	n/a	n/a	n/a	n/a	n/a
Duquesne University Curated by ChEMBL					Assay Description Inhibition of EGFR				Bioorg Med Chem Lett 20: 3177-81 (2010) Article DOI: 10.1016/j.bmcl.2010.03.064 BindingDB Entry DOI: 10.7270/Q23R0T2Z
					More data for this Ligand-Target Pair
Platelet-derived growth factor receptor beta (Homo sapiens (Human))	BDBM50318167 (CHEMBL1096416 | N-(4-chloro-2-fluorophenyl)-6-(2-p...) Show SMILES Fc1cc(Cl)ccc1Nc1ncnc2[nH]c(CCc3ccccc3)cc12 Show InChI InChI=1S/C20H16ClFN4/c21-14-7-9-18(17(22)10-14)26-20-16-11-15(25-19(16)23-12-24-20)8-6-13-4-2-1-3-5-13/h1-5,7,9-12H,6,8H2,(H2,23,24,25,26)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	>5.00E+5	n/a	n/a	n/a	n/a	n/a	n/a
Duquesne University Curated by ChEMBL					Assay Description Inhibition of PDGFRbeta				Bioorg Med Chem Lett 20: 3177-81 (2010) Article DOI: 10.1016/j.bmcl.2010.03.064 BindingDB Entry DOI: 10.7270/Q23R0T2Z
					More data for this Ligand-Target Pair
Vascular endothelial growth factor receptor 2 (Homo sapiens (Human))	BDBM50318167 (CHEMBL1096416 | N-(4-chloro-2-fluorophenyl)-6-(2-p...) Show SMILES Fc1cc(Cl)ccc1Nc1ncnc2[nH]c(CCc3ccccc3)cc12 Show InChI InChI=1S/C20H16ClFN4/c21-14-7-9-18(17(22)10-14)26-20-16-11-15(25-19(16)23-12-24-20)8-6-13-4-2-1-3-5-13/h1-5,7,9-12H,6,8H2,(H2,23,24,25,26)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	4.05E+4	n/a	n/a	n/a	n/a	n/a	n/a
Duquesne University Curated by ChEMBL					Assay Description Inhibition of VEGFR2				Bioorg Med Chem Lett 20: 3177-81 (2010) Article DOI: 10.1016/j.bmcl.2010.03.064 BindingDB Entry DOI: 10.7270/Q23R0T2Z
					More data for this Ligand-Target Pair
Vascular endothelial growth factor receptor 1 (Homo sapiens (Human))	BDBM50318167 (CHEMBL1096416 | N-(4-chloro-2-fluorophenyl)-6-(2-p...) Show SMILES Fc1cc(Cl)ccc1Nc1ncnc2[nH]c(CCc3ccccc3)cc12 Show InChI InChI=1S/C20H16ClFN4/c21-14-7-9-18(17(22)10-14)26-20-16-11-15(25-19(16)23-12-24-20)8-6-13-4-2-1-3-5-13/h1-5,7,9-12H,6,8H2,(H2,23,24,25,26)	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	>2.00E+5	n/a	n/a	n/a	n/a	n/a	n/a
Duquesne University Curated by ChEMBL					Assay Description Inhibition of VEGFR1				Bioorg Med Chem Lett 20: 3177-81 (2010) Article DOI: 10.1016/j.bmcl.2010.03.064 BindingDB Entry DOI: 10.7270/Q23R0T2Z
					More data for this Ligand-Target Pair