BDBM50265786 4-Amino-3-benzimidazol-2-yl-6-(4-methylpiperazinyl)hydroquinolin-2-one::CHEMBL457985

SMILES: CN1CCN(CC1)c1ccc2[nH]c(=O)c(-c3nc4ccccc4[nH]3)c(N)c2c1

InChI Key: InChIKey=NZDKMYJOLQKUML-UHFFFAOYSA-N

Data: 3 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 3 hits for monomerid = 50265786   

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))	BDBM50265786 (4-Amino-3-benzimidazol-2-yl-6-(4-methylpiperazinyl...) Show SMILES CN1CCN(CC1)c1ccc2[nH]c(=O)c(-c3nc4ccccc4[nH]3)c(N)c2c1 Show InChI InChI=1S/C21H22N6O/c1-26-8-10-27(11-9-26)13-6-7-15-14(12-13)19(22)18(21(28)25-15)20-23-16-4-2-3-5-17(16)24-20/h2-7,12H,8-11H2,1H3,(H,23,24)(H3,22,25,28)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	6.50E+3	n/a	n/a	n/a	n/a	n/a	n/a
Novartis Institutes for Biomedical Research Curated by ChEMBL					Assay Description Inhibition of human recombinant VEGFR2				J Med Chem 52: 278-92 (2009) Article DOI: 10.1021/jm800790t BindingDB Entry DOI: 10.7270/Q2TD9X7X
					More data for this Ligand-Target Pair
Platelet-derived growth factor receptor beta (Homo sapiens (Human))	BDBM50265786 (4-Amino-3-benzimidazol-2-yl-6-(4-methylpiperazinyl...) Show SMILES CN1CCN(CC1)c1ccc2[nH]c(=O)c(-c3nc4ccccc4[nH]3)c(N)c2c1 Show InChI InChI=1S/C21H22N6O/c1-26-8-10-27(11-9-26)13-6-7-15-14(12-13)19(22)18(21(28)25-15)20-23-16-4-2-3-5-17(16)24-20/h2-7,12H,8-11H2,1H3,(H,23,24)(H3,22,25,28)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	130	n/a	n/a	n/a	n/a	n/a	n/a
Novartis Institutes for Biomedical Research Curated by ChEMBL					Assay Description Inhibition of human recombinant PDGFRbeta				J Med Chem 52: 278-92 (2009) Article DOI: 10.1021/jm800790t BindingDB Entry DOI: 10.7270/Q2TD9X7X
					More data for this Ligand-Target Pair
Fibroblast growth factor receptor 1 (Homo sapiens (Human))	BDBM50265786 (4-Amino-3-benzimidazol-2-yl-6-(4-methylpiperazinyl...) Show SMILES CN1CCN(CC1)c1ccc2[nH]c(=O)c(-c3nc4ccccc4[nH]3)c(N)c2c1 Show InChI InChI=1S/C21H22N6O/c1-26-8-10-27(11-9-26)13-6-7-15-14(12-13)19(22)18(21(28)25-15)20-23-16-4-2-3-5-17(16)24-20/h2-7,12H,8-11H2,1H3,(H,23,24)(H3,22,25,28)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	4.10E+3	n/a	n/a	n/a	n/a	n/a	n/a
Novartis Institutes for Biomedical Research Curated by ChEMBL					Assay Description Inhibition of human recombinant FGFR1				J Med Chem 52: 278-92 (2009) Article DOI: 10.1021/jm800790t BindingDB Entry DOI: 10.7270/Q2TD9X7X
					More data for this Ligand-Target Pair