null

SMILES: CN(C)CC1CN(CCc2ccccc2)CCC1(O)c1cccc(c1)C(N)=O

InChI Key: InChIKey=SRGSCTCALJARLU-UHFFFAOYSA-N

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 472721   

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
Beta-arrestin-1 (Homo sapiens (Human))	BDBM472721 (3-(3-((Dimethylamino)methyl)-4-hydroxy-1-phenethyl...) Show SMILES CN(C)CC1CN(CCc2ccccc2)CCC1(O)c1cccc(c1)C(N)=O Show InChI InChI=1S/C23H31N3O2/c1-25(2)16-21-17-26(13-11-18-7-4-3-5-8-18)14-12-23(21,28)20-10-6-9-19(15-20)22(24)27/h3-10,15,21,28H,11-14,16-17H2,1-2H3,(H2,24,27)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	n/a	n/a	830	n/a	n/a	n/a	n/a
Mebias Discovery, Inc. US Patent					Assay Description The DISCOVERX PATHHUNTER® β-Arrestin assay is used to measure β-arrestin-2 activity. The technology is based on Enzyme Fragment Complementa...				US Patent US10836728 (2020)
					More data for this Ligand-Target Pair
Mu-type opioid receptor (Homo sapiens (Human))	BDBM472721 (3-(3-((Dimethylamino)methyl)-4-hydroxy-1-phenethyl...) Show SMILES CN(C)CC1CN(CCc2ccccc2)CCC1(O)c1cccc(c1)C(N)=O Show InChI InChI=1S/C23H31N3O2/c1-25(2)16-21-17-26(13-11-18-7-4-3-5-8-18)14-12-23(21,28)20-10-6-9-19(15-20)22(24)27/h3-10,15,21,28H,11-14,16-17H2,1-2H3,(H2,24,27)	PDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	n/a	n/a	34	n/a	n/a	n/a	n/a
Mebias Discovery, Inc. US Patent					Assay Description G-protein signaling was measured via second messenger cAMP modulation. Detection of cAMP modulation was accomplished in the PathHunter human OPRM1 (&...				US Patent US10836728 (2020)
					More data for this Ligand-Target Pair