null

SMILES: CC[C@H](C)[C@@H]1NC(=O)[C@@H](Cc2ccccc2)NC(=O)[C@@H]2CCCN2C(=O)[C@@H](Cc2cnc[nH]2)NC(=O)[C@@H]2CCCCN2C(=O)[C@H]2CCCCN2C1=O

InChI Key: InChIKey=UDNIQKUXSMSUBQ-PIVQSOLLSA-N

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 3 hits for monomerid = 50406691   

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 V2 receptor (Rattus norvegicus (Rat))	BDBM50406691 (CHEMBL2112654) Show SMILES CC[C@H](C)[C@@H]1NC(=O)[C@@H](Cc2ccccc2)NC(=O)[C@@H]2CCCN2C(=O)[C@@H](Cc2cnc[nH]2)NC(=O)[C@@H]2CCCCN2C(=O)[C@H]2CCCCN2C1=O Show InChI InChI=1S/C38H52N8O6/c1-3-24(2)32-38(52)46-18-10-8-15-31(46)37(51)45-17-9-7-14-29(45)35(49)42-28(21-26-22-39-23-40-26)36(50)44-19-11-16-30(44)34(48)41-27(33(47)43-32)20-25-12-5-4-6-13-25/h4-6,12-13,22-24,27-32H,3,7-11,14-21H2,1-2H3,(H,39,40)(H,41,48)(H,42,49)(H,43,47)/t24-,27+,28+,29-,30-,31+,32-/m0/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	1.90E+4	n/a	n/a	n/a	n/a	n/a	n/a
Merck Research Laboratories Curated by ChEMBL					Assay Description Inhibition of [3H]arginine vasopressin binding to AVP-V2 site in rat kidney medulla.				J Med Chem 35: 3905-18 (1992) BindingDB Entry DOI: 10.7270/Q2K64JP2
					More data for this Ligand-Target Pair
Vasopressin V1a receptor (RAT)	BDBM50406691 (CHEMBL2112654) Show SMILES CC[C@H](C)[C@@H]1NC(=O)[C@@H](Cc2ccccc2)NC(=O)[C@@H]2CCCN2C(=O)[C@@H](Cc2cnc[nH]2)NC(=O)[C@@H]2CCCCN2C(=O)[C@H]2CCCCN2C1=O Show InChI InChI=1S/C38H52N8O6/c1-3-24(2)32-38(52)46-18-10-8-15-31(46)37(51)45-17-9-7-14-29(45)35(49)42-28(21-26-22-39-23-40-26)36(50)44-19-11-16-30(44)34(48)41-27(33(47)43-32)20-25-12-5-4-6-13-25/h4-6,12-13,22-24,27-32H,3,7-11,14-21H2,1-2H3,(H,39,40)(H,41,48)(H,42,49)(H,43,47)/t24-,27+,28+,29-,30-,31+,32-/m0/s1	UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	7.30E+3	n/a	n/a	n/a	n/a	n/a	n/a
Merck Research Laboratories Curated by ChEMBL					Assay Description Concentration required to displace 50% of [3H]arginine vasopressin from rat liver arginine vasopressin 1A (AVP-V1a) site.				J Med Chem 35: 3905-18 (1992) BindingDB Entry DOI: 10.7270/Q2K64JP2
					More data for this Ligand-Target Pair
Oxytocin receptor (RAT)	BDBM50406691 (CHEMBL2112654) Show SMILES CC[C@H](C)[C@@H]1NC(=O)[C@@H](Cc2ccccc2)NC(=O)[C@@H]2CCCN2C(=O)[C@@H](Cc2cnc[nH]2)NC(=O)[C@@H]2CCCCN2C(=O)[C@H]2CCCCN2C1=O Show InChI InChI=1S/C38H52N8O6/c1-3-24(2)32-38(52)46-18-10-8-15-31(46)37(51)45-17-9-7-14-29(45)35(49)42-28(21-26-22-39-23-40-26)36(50)44-19-11-16-30(44)34(48)41-27(33(47)43-32)20-25-12-5-4-6-13-25/h4-6,12-13,22-24,27-32H,3,7-11,14-21H2,1-2H3,(H,39,40)(H,41,48)(H,42,49)(H,43,47)/t24-,27+,28+,29-,30-,31+,32-/m0/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	88	n/a	n/a	n/a	n/a	n/a	n/a
Merck Research Laboratories Curated by ChEMBL					Assay Description Concentration required to displace 50% of [3H]oxytocin from rat uterine receptor.				J Med Chem 35: 3905-18 (1992) BindingDB Entry DOI: 10.7270/Q2K64JP2
					More data for this Ligand-Target Pair