Compile Data Set for Download or QSAR

Found 2 hits of ki for monomerid = 50178184   

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
Vasopressin V1a receptor (Homo sapiens (Human))	BDBM50178184 (CHEMBL200682 | N-(4-chloro-2-methylphenyl)-2-(N-(4...) Show SMILES COc1ccc(cc1)N(CC(=O)Nc1ccc(Cl)cc1C)S(=O)(=O)c1ccccc1 Show InChI InChI=1S/C22H21ClN2O4S/c1-16-14-17(23)8-13-21(16)24-22(26)15-25(18-9-11-19(29-2)12-10-18)30(27,28)20-6-4-3-5-7-20/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	70	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
Oxytocin receptor (Homo sapiens (Human))	BDBM50178184 (CHEMBL200682 | N-(4-chloro-2-methylphenyl)-2-(N-(4...) Show SMILES COc1ccc(cc1)N(CC(=O)Nc1ccc(Cl)cc1C)S(=O)(=O)c1ccccc1 Show InChI InChI=1S/C22H21ClN2O4S/c1-16-14-17(23)8-13-21(16)24-22(26)15-25(18-9-11-19(29-2)12-10-18)30(27,28)20-6-4-3-5-7-20/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	800	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