null

SMILES: C[C@H]1C2Cc3ccc4c(nc[nH]c4=O)c3[C@@]1(C)CCN2CC1CC1

InChI Key: InChIKey=TUTNDJCURTYMCS-DPZUSKQMSA-N

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 3 hits for monomerid = 50261627   

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))	BDBM50261627 ((1S,17R)-14-(cyclopropylmethyl)-1,17-dimethyl-4,6,...) Show SMILES C[C@H]1C2Cc3ccc4c(nc[nH]c4=O)c3[C@@]1(C)CCN2CC1CC1 |r,TLB:8:14:1:19.17.18,20:19:1:4.14.3| Show InChI InChI=1S/C20H25N3O/c1-12-16-9-14-5-6-15-18(21-11-22-19(15)24)17(14)20(12,2)7-8-23(16)10-13-3-4-13/h5-6,11-13,16H,3-4,7-10H2,1-2H3,(H,21,22,24)/t12-,16?,20-/m0/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	160	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Rensselaer Polytechnic Institute Curated by ChEMBL					Assay Description Displacement of [3H]U69,593 from human kappa opioid receptor expressed in CHO cells				Bioorg Med Chem 16: 5653-64 (2008) Article DOI: 10.1016/j.bmc.2008.03.066 BindingDB Entry DOI: 10.7270/Q23X87JZ
					More data for this Ligand-Target Pair
Mu-type opioid receptor (Homo sapiens (Human))	BDBM50261627 ((1S,17R)-14-(cyclopropylmethyl)-1,17-dimethyl-4,6,...) Show SMILES C[C@H]1C2Cc3ccc4c(nc[nH]c4=O)c3[C@@]1(C)CCN2CC1CC1 |r,TLB:8:14:1:19.17.18,20:19:1:4.14.3| Show InChI InChI=1S/C20H25N3O/c1-12-16-9-14-5-6-15-18(21-11-22-19(15)24)17(14)20(12,2)7-8-23(16)10-13-3-4-13/h5-6,11-13,16H,3-4,7-10H2,1-2H3,(H,21,22,24)/t12-,16?,20-/m0/s1	PDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	270	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Rensselaer Polytechnic Institute Curated by ChEMBL					Assay Description Displacement of [3H]DAMGO from human mu opioid receptor expressed in CHO cells				Bioorg Med Chem 16: 5653-64 (2008) Article DOI: 10.1016/j.bmc.2008.03.066 BindingDB Entry DOI: 10.7270/Q23X87JZ
					More data for this Ligand-Target Pair
Delta-type opioid receptor (Homo sapiens (Human))	BDBM50261627 ((1S,17R)-14-(cyclopropylmethyl)-1,17-dimethyl-4,6,...) Show SMILES C[C@H]1C2Cc3ccc4c(nc[nH]c4=O)c3[C@@]1(C)CCN2CC1CC1 |r,TLB:8:14:1:19.17.18,20:19:1:4.14.3| Show InChI InChI=1S/C20H25N3O/c1-12-16-9-14-5-6-15-18(21-11-22-19(15)24)17(14)20(12,2)7-8-23(16)10-13-3-4-13/h5-6,11-13,16H,3-4,7-10H2,1-2H3,(H,21,22,24)/t12-,16?,20-/m0/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	2.00E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Rensselaer Polytechnic Institute Curated by ChEMBL					Assay Description Displacement of [3H]naltrindole from human delta opioid receptor expressed in CHO cells				Bioorg Med Chem 16: 5653-64 (2008) Article DOI: 10.1016/j.bmc.2008.03.066 BindingDB Entry DOI: 10.7270/Q23X87JZ
					More data for this Ligand-Target Pair