null

SMILES: CN(C(=O)c1cc(c[nH]c1=O)-c1ccc2OCOc2c1)c1ccc(CN2CCN(C)CC2)cc1

InChI Key: InChIKey=CIODCVKOSCDFBC-UHFFFAOYSA-N

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50181671   

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
ALK tyrosine kinase receptor (Homo sapiens (Human))	BDBM50181671 (5-benzo[1,3]dioxol-5-yl-2-oxo-1,2-dihydro-pyridine...) Show SMILES CN(C(=O)c1cc(c[nH]c1=O)-c1ccc2OCOc2c1)c1ccc(CN2CCN(C)CC2)cc1 Show InChI InChI=1S/C26H28N4O4/c1-28-9-11-30(12-10-28)16-18-3-6-21(7-4-18)29(2)26(32)22-13-20(15-27-25(22)31)19-5-8-23-24(14-19)34-17-33-23/h3-8,13-15H,9-12,16-17H2,1-2H3,(H,27,31)	PDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	3.70E+3	n/a	n/a	n/a	n/a	n/a	n/a
ChemBridge Research Laboratories and ChemBridge Corporation Curated by ChEMBL					Assay Description Inhibitory activity against ALK				J Med Chem 49: 1006-15 (2006) Article DOI: 10.1021/jm050824x BindingDB Entry DOI: 10.7270/Q2H994T6
					More data for this Ligand-Target Pair
Insulin receptor (Homo sapiens (Human))	BDBM50181671 (5-benzo[1,3]dioxol-5-yl-2-oxo-1,2-dihydro-pyridine...) Show SMILES CN(C(=O)c1cc(c[nH]c1=O)-c1ccc2OCOc2c1)c1ccc(CN2CCN(C)CC2)cc1 Show InChI InChI=1S/C26H28N4O4/c1-28-9-11-30(12-10-28)16-18-3-6-21(7-4-18)29(2)26(32)22-13-20(15-27-25(22)31)19-5-8-23-24(14-19)34-17-33-23/h3-8,13-15H,9-12,16-17H2,1-2H3,(H,27,31)	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	3.25E+4	n/a	n/a	n/a	n/a	n/a	n/a
ChemBridge Research Laboratories and ChemBridge Corporation Curated by ChEMBL					Assay Description Inhibitory activity against IRK				J Med Chem 49: 1006-15 (2006) Article DOI: 10.1021/jm050824x BindingDB Entry DOI: 10.7270/Q2H994T6
					More data for this Ligand-Target Pair