null

SMILES: CCC[C@H](CN[C@H](CNC)Cc1ccc(O)cc1)NCC1CCC(C)CC1

InChI Key: InChIKey=IWCQTTZIUAHSAM-HRAFCDAUSA-N

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 3 hits for monomerid = 50298862   

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 (Rattus norvegicus (rat))	BDBM50298862 (4-((S)-3-(methylamino)-2-((R)-2-((4-methylcyclohex...) Show SMILES CCC[C@H](CN[C@H](CNC)Cc1ccc(O)cc1)NCC1CCC(C)CC1 |r,wD:3.18,6.5,(27.78,-34.64,;26.45,-35.41,;25.12,-34.65,;23.78,-35.42,;23.79,-36.97,;22.46,-37.74,;22.47,-39.28,;23.81,-40.05,;23.82,-41.59,;25.15,-42.35,;21.14,-40.06,;19.8,-39.3,;19.8,-37.75,;18.47,-37,;17.14,-37.77,;15.79,-37.01,;17.14,-39.32,;18.48,-40.08,;22.45,-34.66,;22.45,-33.11,;21.1,-32.36,;21.08,-30.81,;19.74,-30.06,;18.4,-30.84,;17.07,-30.09,;18.42,-32.39,;19.77,-33.16,)| Show InChI InChI=1S/C23H41N3O/c1-4-5-21(25-15-20-8-6-18(2)7-9-20)17-26-22(16-24-3)14-19-10-12-23(27)13-11-19/h10-13,18,20-22,24-27H,4-9,14-17H2,1-3H3/t18?,20?,21-,22+/m1/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	>1.00E+3	n/a	n/a	n/a	n/a	n/a	n/a
Institute for Molecular Studies Curated by ChEMBL					Assay Description Displacement of [3H]DAMGO from mu opioid receptor in rat brain by liquid scintillation counting				Bioorg Med Chem 17: 5583-97 (2009) Article DOI: 10.1016/j.bmc.2009.06.026 BindingDB Entry DOI: 10.7270/Q2DZ08C7
					More data for this Ligand-Target Pair
Delta-type opioid receptor (Rattus norvegicus (rat))	BDBM50298862 (4-((S)-3-(methylamino)-2-((R)-2-((4-methylcyclohex...) Show SMILES CCC[C@H](CN[C@H](CNC)Cc1ccc(O)cc1)NCC1CCC(C)CC1 |r,wD:3.18,6.5,(27.78,-34.64,;26.45,-35.41,;25.12,-34.65,;23.78,-35.42,;23.79,-36.97,;22.46,-37.74,;22.47,-39.28,;23.81,-40.05,;23.82,-41.59,;25.15,-42.35,;21.14,-40.06,;19.8,-39.3,;19.8,-37.75,;18.47,-37,;17.14,-37.77,;15.79,-37.01,;17.14,-39.32,;18.48,-40.08,;22.45,-34.66,;22.45,-33.11,;21.1,-32.36,;21.08,-30.81,;19.74,-30.06,;18.4,-30.84,;17.07,-30.09,;18.42,-32.39,;19.77,-33.16,)| Show InChI InChI=1S/C23H41N3O/c1-4-5-21(25-15-20-8-6-18(2)7-9-20)17-26-22(16-24-3)14-19-10-12-23(27)13-11-19/h10-13,18,20-22,24-27H,4-9,14-17H2,1-3H3/t18?,20?,21-,22+/m1/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	>1.00E+4	n/a	n/a	n/a	n/a	n/a	n/a
Institute for Molecular Studies Curated by ChEMBL					Assay Description Displacement of [3H]DSLET from delta opioid receptor in rat brain by liquid scintillation counting				Bioorg Med Chem 17: 5583-97 (2009) Article DOI: 10.1016/j.bmc.2009.06.026 BindingDB Entry DOI: 10.7270/Q2DZ08C7
					More data for this Ligand-Target Pair
Kappa-type opioid receptor (Cavia porcellus (domestic guinea pig))	BDBM50298862 (4-((S)-3-(methylamino)-2-((R)-2-((4-methylcyclohex...) Show SMILES CCC[C@H](CN[C@H](CNC)Cc1ccc(O)cc1)NCC1CCC(C)CC1 |r,wD:3.18,6.5,(27.78,-34.64,;26.45,-35.41,;25.12,-34.65,;23.78,-35.42,;23.79,-36.97,;22.46,-37.74,;22.47,-39.28,;23.81,-40.05,;23.82,-41.59,;25.15,-42.35,;21.14,-40.06,;19.8,-39.3,;19.8,-37.75,;18.47,-37,;17.14,-37.77,;15.79,-37.01,;17.14,-39.32,;18.48,-40.08,;22.45,-34.66,;22.45,-33.11,;21.1,-32.36,;21.08,-30.81,;19.74,-30.06,;18.4,-30.84,;17.07,-30.09,;18.42,-32.39,;19.77,-33.16,)| Show InChI InChI=1S/C23H41N3O/c1-4-5-21(25-15-20-8-6-18(2)7-9-20)17-26-22(16-24-3)14-19-10-12-23(27)13-11-19/h10-13,18,20-22,24-27H,4-9,14-17H2,1-3H3/t18?,20?,21-,22+/m1/s1	PDB UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	14	n/a	n/a	n/a	n/a	n/a	n/a
Institute for Molecular Studies Curated by ChEMBL					Assay Description Displacement of [3H]U69593 from guinea pig kappa opioid receptor by liquid scintillation counting				Bioorg Med Chem 17: 5583-97 (2009) Article DOI: 10.1016/j.bmc.2009.06.026 BindingDB Entry DOI: 10.7270/Q2DZ08C7
					More data for this Ligand-Target Pair