Compile Data Set for Download or QSAR

Found 2 hits of ki for monomerid = 50178214   

Target/Host (Institution)	Ligand	Target/Host Links	Ligand Links	Trg + Lig Links	Ki nM	ΔG° kJ/mole	IC50 nM	Kd nM	EC50/IC50 nM	koff s-1	kon M-1s-1	pH	Temp °C
Oxytocin receptor (Homo sapiens (Human))	BDBM50178214 (2-[Benzenesulfonyl-(4-methoxy-phenyl)-amino]-N-(3-...) Show SMILES COc1ccc(cc1)N(CC(=O)Nc1cccc(Cl)c1C)S(=O)(=O)c1ccccc1 Show InChI InChI=1S/C22H21ClN2O4S/c1-16-20(23)9-6-10-21(16)24-22(26)15-25(17-11-13-18(29-2)14-12-17)30(27,28)19-7-4-3-5-8-19/h3-14H,15H2,1-2H3,(H,24,26)	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	100	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Serono Pharmaceutical Research Institute Curated by ChEMBL					Assay Description Displacement of [125I]OVTA antagonist from human oxytocin receptor expressed in HEK293-EBNA cells				J Med Chem 48: 7882-905 (2005) Article DOI: 10.1021/jm050645f BindingDB Entry DOI: 10.7270/Q2QF8TN3
					More data for this Ligand-Target Pair
Vasopressin V1a receptor (Homo sapiens (Human))	BDBM50178214 (2-[Benzenesulfonyl-(4-methoxy-phenyl)-amino]-N-(3-...) Show SMILES COc1ccc(cc1)N(CC(=O)Nc1cccc(Cl)c1C)S(=O)(=O)c1ccccc1 Show InChI InChI=1S/C22H21ClN2O4S/c1-16-20(23)9-6-10-21(16)24-22(26)15-25(17-11-13-18(29-2)14-12-17)30(27,28)19-7-4-3-5-8-19/h3-14H,15H2,1-2H3,(H,24,26)	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	300	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Serono Pharmaceutical Research Institute Curated by ChEMBL					Assay Description Displacement of [125I]LVA antagonist from human vasopressin 1a receptor expressed in HEK293-EBNA cells				J Med Chem 48: 7882-905 (2005) Article DOI: 10.1021/jm050645f BindingDB Entry DOI: 10.7270/Q2QF8TN3
					More data for this Ligand-Target Pair