null

SMILES: CN(C1CCCCC1)C(=O)Cc1c(OCCN2CCCC2)ccc2ccccc12

InChI Key: InChIKey=BYITXUHTWHZPHI-UHFFFAOYSA-N

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50281660   

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))	BDBM50281660 (CHEMBL353654 | N-Cyclohexyl-N-methyl-2-[2-(2-pyrro...) Show SMILES CN(C1CCCCC1)C(=O)Cc1c(OCCN2CCCC2)ccc2ccccc12 Show InChI InChI=1S/C25H34N2O2/c1-26(21-10-3-2-4-11-21)25(28)19-23-22-12-6-5-9-20(22)13-14-24(23)29-18-17-27-15-7-8-16-27/h5-6,9,12-14,21H,2-4,7-8,10-11,15-19H2,1H3	PDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article	160	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Tested in vitro for binding affinity against Opioid receptor kappa 1				Bioorg Med Chem Lett 3: 841-846 (1993) Article DOI: 10.1016/S0960-894X(00)80677-0 BindingDB Entry DOI: 10.7270/Q2ST7PS8
					More data for this Ligand-Target Pair
Mu-type opioid receptor (Homo sapiens (Human))	BDBM50281660 (CHEMBL353654 | N-Cyclohexyl-N-methyl-2-[2-(2-pyrro...) Show SMILES CN(C1CCCCC1)C(=O)Cc1c(OCCN2CCCC2)ccc2ccccc12 Show InChI InChI=1S/C25H34N2O2/c1-26(21-10-3-2-4-11-21)25(28)19-23-22-12-6-5-9-20(22)13-14-24(23)29-18-17-27-15-7-8-16-27/h5-6,9,12-14,21H,2-4,7-8,10-11,15-19H2,1H3	PDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article	>1.00E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Tested in vitro for binding affinity against mu opioid receptor				Bioorg Med Chem Lett 3: 841-846 (1993) Article DOI: 10.1016/S0960-894X(00)80677-0 BindingDB Entry DOI: 10.7270/Q2ST7PS8
					More data for this Ligand-Target Pair