null

SMILES: Oc1cccc(c1)[C@]12CCC[C@H](C1)N(C[C@H]1C[C@H]1c1ccccc1)CC2

InChI Key: InChIKey=BJIZSNKTBYAOCG-ZXMXYHOLSA-N

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 3 hits for monomerid = 50336612   

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))	BDBM50336612 (3-((1S,5R)-2-(((1'S,2'R)-2-Phenylcyclopropyl)methy...) Show SMILES Oc1cccc(c1)[C@]12CCC[C@H](C1)N(C[C@H]1C[C@H]1c1ccccc1)CC2 |r| Show InChI InChI=1S/C24H29NO/c26-22-10-4-8-20(15-22)24-11-5-9-21(16-24)25(13-12-24)17-19-14-23(19)18-6-2-1-3-7-18/h1-4,6-8,10,15,19,21,23,26H,5,9,11-14,16-17H2/t19-,21-,23+,24+/m1/s1	PDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	76	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
National Institute on Drug Abuse Curated by ChEMBL					Assay Description Displacement of [125I]IOXY from human recombinant mu opioid receptor expressed in CHO cells				J Med Chem 54: 957-69 (2011) Article DOI: 10.1021/jm1011676 BindingDB Entry DOI: 10.7270/Q2GX4BV4
					More data for this Ligand-Target Pair
Kappa-type opioid receptor (Homo sapiens (Human))	BDBM50336612 (3-((1S,5R)-2-(((1'S,2'R)-2-Phenylcyclopropyl)methy...) Show SMILES Oc1cccc(c1)[C@]12CCC[C@H](C1)N(C[C@H]1C[C@H]1c1ccccc1)CC2 |r| Show InChI InChI=1S/C24H29NO/c26-22-10-4-8-20(15-22)24-11-5-9-21(16-24)25(13-12-24)17-19-14-23(19)18-6-2-1-3-7-18/h1-4,6-8,10,15,19,21,23,26H,5,9,11-14,16-17H2/t19-,21-,23+,24+/m1/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	174	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
National Institute on Drug Abuse Curated by ChEMBL					Assay Description Displacement of [125I]IOXY from human recombinant kappa opioid receptor expressed in CHO cells				J Med Chem 54: 957-69 (2011) Article DOI: 10.1021/jm1011676 BindingDB Entry DOI: 10.7270/Q2GX4BV4
					More data for this Ligand-Target Pair
Delta-type opioid receptor (Homo sapiens (Human))	BDBM50336612 (3-((1S,5R)-2-(((1'S,2'R)-2-Phenylcyclopropyl)methy...) Show SMILES Oc1cccc(c1)[C@]12CCC[C@H](C1)N(C[C@H]1C[C@H]1c1ccccc1)CC2 |r| Show InChI InChI=1S/C24H29NO/c26-22-10-4-8-20(15-22)24-11-5-9-21(16-24)25(13-12-24)17-19-14-23(19)18-6-2-1-3-7-18/h1-4,6-8,10,15,19,21,23,26H,5,9,11-14,16-17H2/t19-,21-,23+,24+/m1/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	547	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
National Institute on Drug Abuse Curated by ChEMBL					Assay Description Displacement of [125I]IOXY from human recombinant delta opioid receptor expressed in CHO cells				J Med Chem 54: 957-69 (2011) Article DOI: 10.1021/jm1011676 BindingDB Entry DOI: 10.7270/Q2GX4BV4
					More data for this Ligand-Target Pair