BDBM50271916 (3S,6S)-3-Cyclohexyl-6-(4-methoxy-benzyl)-7-(4-methyl-cyclohexylmethyl)-2,5,6,7-tetrahydro-3H-imidazo[1,2-a]imidazol-1-ium

SMILES: COc1ccc(C[C@H]2CN3[C@H](C[NH+]=C3N2CC2CCC(C)CC2)C2CCCCC2)cc1

InChI Key: InChIKey=OPNCBMYHRCYEGA-STIJMGRHSA-O

Data: 2 IC50

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 2 hits for monomerid = 50271916   

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 (Cavia porcellus (domestic guinea pig))	BDBM50271916 ((3S,6S)-3-Cyclohexyl-6-(4-methoxy-benzyl)-7-(4-met...) Show SMILES COc1ccc(C[C@H]2CN3[C@H](C[NH+]=C3N2CC2CCC(C)CC2)C2CCCCC2)cc1 |r,wD:10.25,7.6,c:12,(.94,-35.88,;1.67,-37.25,;.87,-38.56,;1.6,-39.93,;.79,-41.23,;-.75,-41.18,;-1.56,-42.49,;-3.1,-42.46,;-3.97,-41.19,;-5.45,-41.62,;-6.91,-41.11,;-7.84,-42.33,;-6.98,-43.6,;-5.49,-43.17,;-4.04,-43.69,;-3.6,-45.16,;-2.1,-45.52,;-1.66,-46.99,;-.17,-47.35,;.89,-46.24,;2.39,-46.6,;.46,-44.76,;-1.04,-44.39,;-7.34,-39.63,;-6.28,-38.52,;-6.72,-37.05,;-8.21,-36.68,;-9.28,-37.8,;-8.84,-39.28,;-1.49,-39.83,;-.68,-38.52,)| Show InChI InChI=1S/C27H41N3O/c1-20-8-10-22(11-9-20)18-29-24(16-21-12-14-25(31-2)15-13-21)19-30-26(17-28-27(29)30)23-6-4-3-5-7-23/h12-15,20,22-24,26H,3-11,16-19H2,1-2H3/p+1/t20?,22?,24-,26+/m0/s1	PDB UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	336	n/a	n/a	n/a	n/a	n/a	n/a
Torrey Pines Institute for Molecular Studies Curated by ChEMBL					Assay Description Displacement of [3H]U69593 from kappa opioid receptor in guinea pig brain homogenate				Bioorg Med Chem 16: 5932-8 (2008) Article DOI: 10.1016/j.bmc.2008.04.061 BindingDB Entry DOI: 10.7270/Q2BG2PW7
					More data for this Ligand-Target Pair
Kappa-type opioid receptor (Homo sapiens (Human))	BDBM50271916 ((3S,6S)-3-Cyclohexyl-6-(4-methoxy-benzyl)-7-(4-met...) Show SMILES COc1ccc(C[C@H]2CN3[C@H](C[NH+]=C3N2CC2CCC(C)CC2)C2CCCCC2)cc1 |r,wD:10.25,7.6,c:12,(.94,-35.88,;1.67,-37.25,;.87,-38.56,;1.6,-39.93,;.79,-41.23,;-.75,-41.18,;-1.56,-42.49,;-3.1,-42.46,;-3.97,-41.19,;-5.45,-41.62,;-6.91,-41.11,;-7.84,-42.33,;-6.98,-43.6,;-5.49,-43.17,;-4.04,-43.69,;-3.6,-45.16,;-2.1,-45.52,;-1.66,-46.99,;-.17,-47.35,;.89,-46.24,;2.39,-46.6,;.46,-44.76,;-1.04,-44.39,;-7.34,-39.63,;-6.28,-38.52,;-6.72,-37.05,;-8.21,-36.68,;-9.28,-37.8,;-8.84,-39.28,;-1.49,-39.83,;-.68,-38.52,)| Show InChI InChI=1S/C27H41N3O/c1-20-8-10-22(11-9-20)18-29-24(16-21-12-14-25(31-2)15-13-21)19-30-26(17-28-27(29)30)23-6-4-3-5-7-23/h12-15,20,22-24,26H,3-11,16-19H2,1-2H3/p+1/t20?,22?,24-,26+/m0/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem Similars	PubMed	n/a	n/a	336	n/a	n/a	n/a	n/a	n/a	n/a
Torrey Pines Institute for Molecular Studies Curated by ChEMBL					Assay Description Inhibitory activity for kappa opioid receptor				J Med Chem 42: 3743-78 (1999) BindingDB Entry DOI: 10.7270/Q22Z167W
					More data for this Ligand-Target Pair