null

SMILES: [O-][N+](=O)c1ccc(Nc2ncc3CC(=O)Nc4ccccc4-c3n2)cc1

InChI Key: InChIKey=FGDNDXCDDSSOBV-UHFFFAOYSA-N

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 3 hits for monomerid = 50308229   

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))	BDBM50308229 (2-(4-Nitroanilino)-5,7-dihydro-6H-pyrimido[5,4-d][...) Show SMILES [O-][N+](=O)c1ccc(Nc2ncc3CC(=O)Nc4ccccc4-c3n2)cc1 Show InChI InChI=1S/C18H13N5O3/c24-16-9-11-10-19-18(20-12-5-7-13(8-6-12)23(25)26)22-17(11)14-3-1-2-4-15(14)21-16/h1-8,10H,9H2,(H,21,24)(H,19,20,22)	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	330	n/a	n/a	n/a	n/a	n/a	n/a
Technische Universitat Braunschweig Curated by ChEMBL					Assay Description Inhibition of VEGFR2 assessed as [33Pi] incorporation by microplate scintillation counting in presence of 1 uM ATP				J Med Chem 53: 2433-42 (2010) Article DOI: 10.1021/jm901388c BindingDB Entry DOI: 10.7270/Q24J0G22
					More data for this Ligand-Target Pair
Insulin receptor (Homo sapiens (Human))	BDBM50308229 (2-(4-Nitroanilino)-5,7-dihydro-6H-pyrimido[5,4-d][...) Show SMILES [O-][N+](=O)c1ccc(Nc2ncc3CC(=O)Nc4ccccc4-c3n2)cc1 Show InChI InChI=1S/C18H13N5O3/c24-16-9-11-10-19-18(20-12-5-7-13(8-6-12)23(25)26)22-17(11)14-3-1-2-4-15(14)21-16/h1-8,10H,9H2,(H,21,24)(H,19,20,22)	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
Technische Universitat Braunschweig Curated by ChEMBL					Assay Description Inhibition of INSR assessed as [33Pi] incorporation by microplate scintillation counting in presence of 1 uM ATP				J Med Chem 53: 2433-42 (2010) Article DOI: 10.1021/jm901388c BindingDB Entry DOI: 10.7270/Q24J0G22
					More data for this Ligand-Target Pair
Serine/threonine-protein kinase PLK1 (Homo sapiens (Human))	BDBM50308229 (2-(4-Nitroanilino)-5,7-dihydro-6H-pyrimido[5,4-d][...) Show SMILES [O-][N+](=O)c1ccc(Nc2ncc3CC(=O)Nc4ccccc4-c3n2)cc1 Show InChI InChI=1S/C18H13N5O3/c24-16-9-11-10-19-18(20-12-5-7-13(8-6-12)23(25)26)22-17(11)14-3-1-2-4-15(14)21-16/h1-8,10H,9H2,(H,21,24)(H,19,20,22)	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	>1.00E+5	n/a	n/a	n/a	n/a	n/a	n/a
Technische Universitat Braunschweig Curated by ChEMBL					Assay Description Inhibition of PLK1 assessed as [33Pi] incorporation by microplate scintillation counting in presence of 1 uM ATP				J Med Chem 53: 2433-42 (2010) Article DOI: 10.1021/jm901388c BindingDB Entry DOI: 10.7270/Q24J0G22
					More data for this Ligand-Target Pair