BDBM50493034 CHEMBL2418571

SMILES: [H][C@@]12C[C@@](CC[C@@H]1C)(CCN2C)c1cccc(O)c1

InChI Key: InChIKey=GYMNUWBSTONAJV-APHBMKBZSA-N

Data: 3 KI

Find this compound or compounds like it in BindingDB or PDB:

Substructure Similarity at least:  must be >=0.5 Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 3 hits for monomerid = 50493034   

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
Mu-type opioid receptor (Homo sapiens (Human))	BDBM50493034 (CHEMBL2418571) Show SMILES [H][C@@]12C[C@@](CC[C@@H]1C)(CCN2C)c1cccc(O)c1 |r| Show InChI InChI=1S/C16H23NO/c1-12-6-7-16(8-9-17(2)15(12)11-16)13-4-3-5-14(18)10-13/h3-5,10,12,15,18H,6-9,11H2,1-2H3/t12-,15+,16+/m0/s1	PDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	1.5	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
National Institute on Drug Abuse and the National Institute on Alcohol Abuse and Alcoholism Curated by ChEMBL					Assay Description Displacement of [3H]DAMGO from human mu opioid receptor expressed in CHO cells after 2 hrs by liquid scintillation counting				Eur J Med Chem 67: 335-43 (2013) Article DOI: 10.1016/j.ejmech.2013.06.030 BindingDB Entry DOI: 10.7270/Q2251N40
					More data for this Ligand-Target Pair
Kappa-type opioid receptor (Homo sapiens (Human))	BDBM50493034 (CHEMBL2418571) Show SMILES [H][C@@]12C[C@@](CC[C@@H]1C)(CCN2C)c1cccc(O)c1 |r| Show InChI InChI=1S/C16H23NO/c1-12-6-7-16(8-9-17(2)15(12)11-16)13-4-3-5-14(18)10-13/h3-5,10,12,15,18H,6-9,11H2,1-2H3/t12-,15+,16+/m0/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	39	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
National Institute on Drug Abuse and the National Institute on Alcohol Abuse and Alcoholism Curated by ChEMBL					Assay Description Displacement of [3H]U69,593 from human kappa opioid receptor expressed in CHO cells after 2 hrs by liquid scintillation counting				Eur J Med Chem 67: 335-43 (2013) Article DOI: 10.1016/j.ejmech.2013.06.030 BindingDB Entry DOI: 10.7270/Q2251N40
					More data for this Ligand-Target Pair
Delta-type opioid receptor (Homo sapiens (Human))	BDBM50493034 (CHEMBL2418571) Show SMILES [H][C@@]12C[C@@](CC[C@@H]1C)(CCN2C)c1cccc(O)c1 |r| Show InChI InChI=1S/C16H23NO/c1-12-6-7-16(8-9-17(2)15(12)11-16)13-4-3-5-14(18)10-13/h3-5,10,12,15,18H,6-9,11H2,1-2H3/t12-,15+,16+/m0/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	139	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
National Institute on Drug Abuse and the National Institute on Alcohol Abuse and Alcoholism Curated by ChEMBL					Assay Description Displacement of [3H]DADLE from human delta opioid receptor expressed in CHO cells after 2 hrs by liquid scintillation counting				Eur J Med Chem 67: 335-43 (2013) Article DOI: 10.1016/j.ejmech.2013.06.030 BindingDB Entry DOI: 10.7270/Q2251N40
					More data for this Ligand-Target Pair