null

SMILES: CN(C)[C@H]1CC[C@@H](CC1)NC(=O)[C@@H](Cc1ccc(Cl)cc1)NC(=O)Cc1ccc(F)cc1

InChI Key: InChIKey=OUKGXVIBVLCUHQ-DNVJHFABSA-N

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50418911   

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 V1a receptor (Homo sapiens (Human))	BDBM50418911 (CHEMBL1807274) Show SMILES CN(C)[C@H]1CC[C@@H](CC1)NC(=O)[C@@H](Cc1ccc(Cl)cc1)NC(=O)Cc1ccc(F)cc1 |r,wU:6.9,12.22,wD:3.2,(27.69,-10,;26.33,-9.22,;26.33,-7.67,;24.98,-10.01,;23.65,-9.25,;22.32,-10.02,;22.35,-11.55,;23.67,-12.31,;24.99,-11.54,;21.03,-12.32,;19.69,-11.56,;19.69,-10.02,;18.36,-12.33,;18.36,-13.87,;17.04,-14.65,;15.7,-13.88,;14.37,-14.65,;14.38,-16.2,;13.03,-16.98,;15.72,-16.97,;17.05,-16.18,;17.02,-11.57,;17.02,-10.03,;18.35,-9.25,;15.68,-9.26,;14.35,-10.04,;13.01,-9.27,;11.68,-10.04,;11.68,-11.59,;10.35,-12.35,;13.01,-12.36,;14.35,-11.59,)| Show InChI InChI=1S/C25H31ClFN3O2/c1-30(2)22-13-11-21(12-14-22)28-25(32)23(15-17-3-7-19(26)8-4-17)29-24(31)16-18-5-9-20(27)10-6-18/h3-10,21-23H,11-16H2,1-2H3,(H,28,32)(H,29,31)/t21-,22-,23-/m1/s1	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	1.12	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
MSD Curated by ChEMBL					Assay Description Displacement of [3H]AVP from human V1A receptor expressed in CHO cells				Bioorg Med Chem Lett 21: 4622-8 (2011) Article DOI: 10.1016/j.bmcl.2011.05.092 BindingDB Entry DOI: 10.7270/Q20866KR
					More data for this Ligand-Target Pair
Vasopressin V1a receptor (RAT)	BDBM50418911 (CHEMBL1807274) Show SMILES CN(C)[C@H]1CC[C@@H](CC1)NC(=O)[C@@H](Cc1ccc(Cl)cc1)NC(=O)Cc1ccc(F)cc1 |r,wU:6.9,12.22,wD:3.2,(27.69,-10,;26.33,-9.22,;26.33,-7.67,;24.98,-10.01,;23.65,-9.25,;22.32,-10.02,;22.35,-11.55,;23.67,-12.31,;24.99,-11.54,;21.03,-12.32,;19.69,-11.56,;19.69,-10.02,;18.36,-12.33,;18.36,-13.87,;17.04,-14.65,;15.7,-13.88,;14.37,-14.65,;14.38,-16.2,;13.03,-16.98,;15.72,-16.97,;17.05,-16.18,;17.02,-11.57,;17.02,-10.03,;18.35,-9.25,;15.68,-9.26,;14.35,-10.04,;13.01,-9.27,;11.68,-10.04,;11.68,-11.59,;10.35,-12.35,;13.01,-12.36,;14.35,-11.59,)| Show InChI InChI=1S/C25H31ClFN3O2/c1-30(2)22-13-11-21(12-14-22)28-25(32)23(15-17-3-7-19(26)8-4-17)29-24(31)16-18-5-9-20(27)10-6-18/h3-10,21-23H,11-16H2,1-2H3,(H,28,32)(H,29,31)/t21-,22-,23-/m1/s1	UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	69.2	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
MSD Curated by ChEMBL					Assay Description Displacement of [3H]AVP from rat V1A receptor expressed in CHO cells				Bioorg Med Chem Lett 21: 4622-8 (2011) Article DOI: 10.1016/j.bmcl.2011.05.092 BindingDB Entry DOI: 10.7270/Q20866KR
					More data for this Ligand-Target Pair