null

SMILES: [H][C@]12CN(CCc3ccc(F)cc3)CC[C@@]1(CCCCCc1ccccc1)c1cc(O)ccc1O2

InChI Key: InChIKey=UINYCIYEIIVYEA-KYJUHHDHSA-N

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 3 hits for monomerid = 50072333   

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))	BDBM50072333 (CHEMBL3409119) Show SMILES [H][C@]12CN(CCc3ccc(F)cc3)CC[C@@]1(CCCCCc1ccccc1)c1cc(O)ccc1O2 |r| Show InChI InChI=1S/C30H34FNO2/c31-25-12-10-24(11-13-25)16-19-32-20-18-30(17-6-2-5-9-23-7-3-1-4-8-23)27-21-26(33)14-15-28(27)34-29(30)22-32/h1,3-4,7-8,10-15,21,29,33H,2,5-6,9,16-20,22H2/t29-,30-/m0/s1	PDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	4.20	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 [3H]DAMGO from human recombinant opioid mu receptor expressed in CHO cell membranes after 2 hrs by liquid scintillation counting meth...				Eur J Med Chem 92: 531-9 (2015) Article DOI: 10.1016/j.ejmech.2015.01.025 BindingDB Entry DOI: 10.7270/Q2GF0W6W
					More data for this Ligand-Target Pair
Delta-type opioid receptor (Homo sapiens (Human))	BDBM50072333 (CHEMBL3409119) Show SMILES [H][C@]12CN(CCc3ccc(F)cc3)CC[C@@]1(CCCCCc1ccccc1)c1cc(O)ccc1O2 |r| Show InChI InChI=1S/C30H34FNO2/c31-25-12-10-24(11-13-25)16-19-32-20-18-30(17-6-2-5-9-23-7-3-1-4-8-23)27-21-26(33)14-15-28(27)34-29(30)22-32/h1,3-4,7-8,10-15,21,29,33H,2,5-6,9,16-20,22H2/t29-,30-/m0/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	44	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 [3H]DADLE from human recombinant opioid delta receptor expressed in CHO cell membranes after 2 hrs by liquid scintillation counting m...				Eur J Med Chem 92: 531-9 (2015) Article DOI: 10.1016/j.ejmech.2015.01.025 BindingDB Entry DOI: 10.7270/Q2GF0W6W
					More data for this Ligand-Target Pair
Kappa-type opioid receptor (Homo sapiens (Human))	BDBM50072333 (CHEMBL3409119) Show SMILES [H][C@]12CN(CCc3ccc(F)cc3)CC[C@@]1(CCCCCc1ccccc1)c1cc(O)ccc1O2 |r| Show InChI InChI=1S/C30H34FNO2/c31-25-12-10-24(11-13-25)16-19-32-20-18-30(17-6-2-5-9-23-7-3-1-4-8-23)27-21-26(33)14-15-28(27)34-29(30)22-32/h1,3-4,7-8,10-15,21,29,33H,2,5-6,9,16-20,22H2/t29-,30-/m0/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	130	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 [3H]U69,593 from human recombinant opioid kappa receptor expressed in CHO cell membranes after 2 hrs by liquid scintillation counting...				Eur J Med Chem 92: 531-9 (2015) Article DOI: 10.1016/j.ejmech.2015.01.025 BindingDB Entry DOI: 10.7270/Q2GF0W6W
					More data for this Ligand-Target Pair