null

SMILES: Clc1ccc(cc1)S(=O)(=O)N1C(CCC(=O)N2CCC(CC2)NCc2cccs2)CCc2ccccc12

InChI Key: InChIKey=ZKUDYKATSJZZEJ-UHFFFAOYSA-N

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 3 hits for monomerid = 50299336   

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
Vasopressin V1b receptor (Homo sapiens (Human))	BDBM50299336 (3-(1-(4-chlorophenylsulfonyl)-1,2,3,4-tetrahydroqu...) Show SMILES Clc1ccc(cc1)S(=O)(=O)N1C(CCC(=O)N2CCC(CC2)NCc2cccs2)CCc2ccccc12 Show InChI InChI=1S/C28H32ClN3O3S2/c29-22-8-12-26(13-9-22)37(34,35)32-24(10-7-21-4-1-2-6-27(21)32)11-14-28(33)31-17-15-23(16-18-31)30-20-25-5-3-19-36-25/h1-6,8-9,12-13,19,23-24,30H,7,10-11,14-18,20H2	UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	715	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Schering-Plough Research Institute Curated by ChEMBL					Assay Description Displacement of [3H]Arg8-vasopressin from human vasopressin V1b receptor expressed in CHO-K1 cells by Packard Topcount scintillation counter				Bioorg Med Chem Lett 19: 6018-22 (2009) Article DOI: 10.1016/j.bmcl.2009.09.050 BindingDB Entry DOI: 10.7270/Q2J9679W
					More data for this Ligand-Target Pair
Vasopressin V1a receptor (Homo sapiens (Human))	BDBM50299336 (3-(1-(4-chlorophenylsulfonyl)-1,2,3,4-tetrahydroqu...) Show SMILES Clc1ccc(cc1)S(=O)(=O)N1C(CCC(=O)N2CCC(CC2)NCc2cccs2)CCc2ccccc12 Show InChI InChI=1S/C28H32ClN3O3S2/c29-22-8-12-26(13-9-22)37(34,35)32-24(10-7-21-4-1-2-6-27(21)32)11-14-28(33)31-17-15-23(16-18-31)30-20-25-5-3-19-36-25/h1-6,8-9,12-13,19,23-24,30H,7,10-11,14-18,20H2	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	6.89E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Schering-Plough Research Institute Curated by ChEMBL					Assay Description Displacement of [3H]Arg8-vasopressin from human vasopressin V1a receptor expressed in CHO-K1 cells by Packard Topcount scintillation counter				Bioorg Med Chem Lett 19: 6018-22 (2009) Article DOI: 10.1016/j.bmcl.2009.09.050 BindingDB Entry DOI: 10.7270/Q2J9679W
					More data for this Ligand-Target Pair
Vasopressin V1b receptor (RAT)	BDBM50299336 (3-(1-(4-chlorophenylsulfonyl)-1,2,3,4-tetrahydroqu...) Show SMILES Clc1ccc(cc1)S(=O)(=O)N1C(CCC(=O)N2CCC(CC2)NCc2cccs2)CCc2ccccc12 Show InChI InChI=1S/C28H32ClN3O3S2/c29-22-8-12-26(13-9-22)37(34,35)32-24(10-7-21-4-1-2-6-27(21)32)11-14-28(33)31-17-15-23(16-18-31)30-20-25-5-3-19-36-25/h1-6,8-9,12-13,19,23-24,30H,7,10-11,14-18,20H2	UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	>1.00E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Schering-Plough Research Institute Curated by ChEMBL					Assay Description Displacement of [3H]Arg8-vasopressin from rat vasopressin V1b receptor expressed in CHO-K1 cells by Packard Topcount scintillation counter				Bioorg Med Chem Lett 19: 6018-22 (2009) Article DOI: 10.1016/j.bmcl.2009.09.050 BindingDB Entry DOI: 10.7270/Q2J9679W
					More data for this Ligand-Target Pair