null

SMILES: COC1=CC[C@H]2[C@@H]3Cc4ccc(OC)cc4[C@H]([C@@H](C)N3CC3CC3)C2=C1

InChI Key: InChIKey=MKXNFBCGAIGPNB-OGFXBJFLSA-N

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 3 hits for monomerid = 50122556   

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
Delta-type opioid receptor (Homo sapiens (Human))	BDBM50122556 (17-cyclopropylmethyl-4,13-dimethoxy-16-methyl-17-a...) Show SMILES COC1=CC[C@H]2[C@@H]3Cc4ccc(OC)cc4[C@H]([C@@H](C)N3CC3CC3)C2=C1 |wU:16.26,6.20,5.4,17.18,c:28,t:2,TLB:9:8:19.17:24.5,20:19:24.5:15.8.7,THB:18:17:24.5:15.8.7,4:5:19.17:15.8.7,14:15:19.17:24.5,(4.9,4.64,;6.24,3.87,;6.24,2.33,;7.57,1.56,;7.57,.02,;6.24,-.75,;6.45,-4.63,;4.91,-4.63,;3.58,-3.86,;2.25,-4.63,;.91,-3.86,;.91,-2.31,;-.44,-1.52,;-.44,.02,;2.25,-1.54,;3.58,-2.31,;4.91,-1.54,;8.73,-2.8,;9.83,-1.7,;7.89,-4.07,;8.85,-5.28,;8.29,-6.72,;7.09,-7.66,;8.52,-8.24,;4.91,.02,;4.91,1.56,)| Show InChI InChI=1S/C23H29NO2/c1-14-23-20-11-17(25-2)7-6-16(20)10-22(24(14)13-15-4-5-15)19-9-8-18(26-3)12-21(19)23/h6-8,11-12,14-15,19,22-23H,4-5,9-10,13H2,1-3H3/t14-,19-,22+,23+/m1/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	6.63E+3	n/a	n/a	n/a	n/a	n/a	n/a
Universit£ de Montr£al Curated by ChEMBL					Assay Description In vitro binding affinity against cloned human Opioid receptor delta 1 expressed in HEK 293S cells				J Med Chem 46: 34-48 (2002) Article DOI: 10.1021/jm020164l BindingDB Entry DOI: 10.7270/Q2TM7BTT
					More data for this Ligand-Target Pair
Mu-type opioid receptor (Homo sapiens (Human))	BDBM50122556 (17-cyclopropylmethyl-4,13-dimethoxy-16-methyl-17-a...) Show SMILES COC1=CC[C@H]2[C@@H]3Cc4ccc(OC)cc4[C@H]([C@@H](C)N3CC3CC3)C2=C1 |wU:16.26,6.20,5.4,17.18,c:28,t:2,TLB:9:8:19.17:24.5,20:19:24.5:15.8.7,THB:18:17:24.5:15.8.7,4:5:19.17:15.8.7,14:15:19.17:24.5,(4.9,4.64,;6.24,3.87,;6.24,2.33,;7.57,1.56,;7.57,.02,;6.24,-.75,;6.45,-4.63,;4.91,-4.63,;3.58,-3.86,;2.25,-4.63,;.91,-3.86,;.91,-2.31,;-.44,-1.52,;-.44,.02,;2.25,-1.54,;3.58,-2.31,;4.91,-1.54,;8.73,-2.8,;9.83,-1.7,;7.89,-4.07,;8.85,-5.28,;8.29,-6.72,;7.09,-7.66,;8.52,-8.24,;4.91,.02,;4.91,1.56,)| Show InChI InChI=1S/C23H29NO2/c1-14-23-20-11-17(25-2)7-6-16(20)10-22(24(14)13-15-4-5-15)19-9-8-18(26-3)12-21(19)23/h6-8,11-12,14-15,19,22-23H,4-5,9-10,13H2,1-3H3/t14-,19-,22+,23+/m1/s1	PDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	1.03E+3	n/a	n/a	n/a	n/a	n/a	n/a
Universit£ de Montr£al Curated by ChEMBL					Assay Description Tested for effective concentration against cloned human Opioid receptor mu 1				J Med Chem 46: 34-48 (2002) Article DOI: 10.1021/jm020164l BindingDB Entry DOI: 10.7270/Q2TM7BTT
					More data for this Ligand-Target Pair
Kappa-type opioid receptor (Homo sapiens (Human))	BDBM50122556 (17-cyclopropylmethyl-4,13-dimethoxy-16-methyl-17-a...) Show SMILES COC1=CC[C@H]2[C@@H]3Cc4ccc(OC)cc4[C@H]([C@@H](C)N3CC3CC3)C2=C1 |wU:16.26,6.20,5.4,17.18,c:28,t:2,TLB:9:8:19.17:24.5,20:19:24.5:15.8.7,THB:18:17:24.5:15.8.7,4:5:19.17:15.8.7,14:15:19.17:24.5,(4.9,4.64,;6.24,3.87,;6.24,2.33,;7.57,1.56,;7.57,.02,;6.24,-.75,;6.45,-4.63,;4.91,-4.63,;3.58,-3.86,;2.25,-4.63,;.91,-3.86,;.91,-2.31,;-.44,-1.52,;-.44,.02,;2.25,-1.54,;3.58,-2.31,;4.91,-1.54,;8.73,-2.8,;9.83,-1.7,;7.89,-4.07,;8.85,-5.28,;8.29,-6.72,;7.09,-7.66,;8.52,-8.24,;4.91,.02,;4.91,1.56,)| Show InChI InChI=1S/C23H29NO2/c1-14-23-20-11-17(25-2)7-6-16(20)10-22(24(14)13-15-4-5-15)19-9-8-18(26-3)12-21(19)23/h6-8,11-12,14-15,19,22-23H,4-5,9-10,13H2,1-3H3/t14-,19-,22+,23+/m1/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	5.33E+3	n/a	n/a	n/a	n/a	n/a	n/a
Universit£ de Montr£al Curated by ChEMBL					Assay Description In vitro binding affinity against cloned human Opioid receptor kappa 1 expressed in HEK 293S cells				J Med Chem 46: 34-48 (2002) Article DOI: 10.1021/jm020164l BindingDB Entry DOI: 10.7270/Q2TM7BTT
					More data for this Ligand-Target Pair