null

SMILES: Cc1cc(NCC(=O)Nc2ccccc2)c2ccccc2n1

InChI Key: InChIKey=HRXVDSHQRNNGBO-UHFFFAOYSA-N

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50304074   

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
Kappa-type opioid receptor (Homo sapiens (Human))	BDBM50304074 (2-(2-methylquinolin-4-ylamino)-N-phenylacetamide |...) Show SMILES Cc1cc(NCC(=O)Nc2ccccc2)c2ccccc2n1 Show InChI InChI=1S/C18H17N3O/c1-13-11-17(15-9-5-6-10-16(15)20-13)19-12-18(22)21-14-7-3-2-4-8-14/h2-11H,12H2,1H3,(H,19,20)(H,21,22)	PDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	n/a	n/a	1.03	n/a	n/a	n/a	n/a	n/a	n/a
Institute of Chemical Biology Curated by ChEMBL					Assay Description Displacement of [3H]dynorphin from human kappa opioid receptor expressed in C6 giloma cells				Bioorg Med Chem 17: 5782-90 (2009) Article DOI: 10.1016/j.bmc.2009.07.024 BindingDB Entry DOI: 10.7270/Q2VQ32RF
					More data for this Ligand-Target Pair
Mu-type opioid receptor (Rattus norvegicus (rat))	BDBM50304074 (2-(2-methylquinolin-4-ylamino)-N-phenylacetamide |...) Show SMILES Cc1cc(NCC(=O)Nc2ccccc2)c2ccccc2n1 Show InChI InChI=1S/C18H17N3O/c1-13-11-17(15-9-5-6-10-16(15)20-13)19-12-18(22)21-14-7-3-2-4-8-14/h2-11H,12H2,1H3,(H,19,20)(H,21,22)	PDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	n/a	n/a	1.15	n/a	n/a	n/a	n/a	n/a	n/a
Institute of Chemical Biology Curated by ChEMBL					Assay Description Displacement of [3H]DAMGO from mu opioid receptor in rat brain				Bioorg Med Chem 17: 5782-90 (2009) Article DOI: 10.1016/j.bmc.2009.07.024 BindingDB Entry DOI: 10.7270/Q2VQ32RF
					More data for this Ligand-Target Pair