null

SMILES: CCc1ccc(C[C@@H]2NC(=O)CCCSC[C@H](NC(=O)[C@H](CC(N)=O)NC(=O)[C@@H](NC(=O)[C@H](Cc3cccs3)NC2=O)C(C)C)C(=O)N2CCC[C@H]2C(=O)N[C@@H](CO)CCCNC(N)=N)cc1

InChI Key: InChIKey=IRMOCXVCKHHREX-USVUHUQMSA-N

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 3 hits for monomerid = 50525080   

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 (Homo sapiens (Human))	BDBM50525080 (CHEMBL4521602) Show SMILES CCc1ccc(C[C@@H]2NC(=O)CCCSC[C@H](NC(=O)[C@H](CC(N)=O)NC(=O)[C@@H](NC(=O)[C@H](Cc3cccs3)NC2=O)C(C)C)C(=O)N2CCC[C@H]2C(=O)N[C@@H](CO)CCCNC(N)=N)cc1 |r| Show InChI InChI=1S/C45H67N11O9S2/c1-4-27-13-15-28(16-14-27)21-31-39(60)52-32(22-30-10-7-20-67-30)41(62)55-38(26(2)3)43(64)53-33(23-36(46)58)40(61)54-34(25-66-19-8-12-37(59)51-31)44(65)56-18-6-11-35(56)42(63)50-29(24-57)9-5-17-49-45(47)48/h7,10,13-16,20,26,29,31-35,38,57H,4-6,8-9,11-12,17-19,21-25H2,1-3H3,(H2,46,58)(H,50,63)(H,51,59)(H,52,60)(H,53,64)(H,54,61)(H,55,62)(H4,47,48,49)/t29-,31+,32+,33+,34+,35+,38+/m1/s1	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	n/a	n/a	0.350	n/a	n/a	n/a	n/a
Ferring Research Institute Inc. Curated by ChEMBL					Assay Description Agonist activity at recombinant human V2 receptor expressed in HEK293 cells measured after 5 hrs by cAMP response element driven luciferase reporter ...				J Med Chem 62: 4991-5005 (2019) Article DOI: 10.1021/acs.jmedchem.9b00132
					More data for this Ligand-Target Pair
Oxytocin receptor (Homo sapiens (Human))	BDBM50525080 (CHEMBL4521602) Show SMILES CCc1ccc(C[C@@H]2NC(=O)CCCSC[C@H](NC(=O)[C@H](CC(N)=O)NC(=O)[C@@H](NC(=O)[C@H](Cc3cccs3)NC2=O)C(C)C)C(=O)N2CCC[C@H]2C(=O)N[C@@H](CO)CCCNC(N)=N)cc1 |r| Show InChI InChI=1S/C45H67N11O9S2/c1-4-27-13-15-28(16-14-27)21-31-39(60)52-32(22-30-10-7-20-67-30)41(62)55-38(26(2)3)43(64)53-33(23-36(46)58)40(61)54-34(25-66-19-8-12-37(59)51-31)44(65)56-18-6-11-35(56)42(63)50-29(24-57)9-5-17-49-45(47)48/h7,10,13-16,20,26,29,31-35,38,57H,4-6,8-9,11-12,17-19,21-25H2,1-3H3,(H2,46,58)(H,50,63)(H,51,59)(H,52,60)(H,53,64)(H,54,61)(H,55,62)(H4,47,48,49)/t29-,31+,32+,33+,34+,35+,38+/m1/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	n/a	n/a	>1.00E+4	n/a	n/a	n/a	n/a
Ferring Research Institute Inc. Curated by ChEMBL					Assay Description Agonist activity at human OTR stably expressed in CHOK1 cells by NFAT-luciferase reporter gene assay				J Med Chem 62: 4991-5005 (2019) Article DOI: 10.1021/acs.jmedchem.9b00132
					More data for this Ligand-Target Pair
Vasopressin V1b receptor (Homo sapiens (Human))	BDBM50525080 (CHEMBL4521602) Show SMILES CCc1ccc(C[C@@H]2NC(=O)CCCSC[C@H](NC(=O)[C@H](CC(N)=O)NC(=O)[C@@H](NC(=O)[C@H](Cc3cccs3)NC2=O)C(C)C)C(=O)N2CCC[C@H]2C(=O)N[C@@H](CO)CCCNC(N)=N)cc1 |r| Show InChI InChI=1S/C45H67N11O9S2/c1-4-27-13-15-28(16-14-27)21-31-39(60)52-32(22-30-10-7-20-67-30)41(62)55-38(26(2)3)43(64)53-33(23-36(46)58)40(61)54-34(25-66-19-8-12-37(59)51-31)44(65)56-18-6-11-35(56)42(63)50-29(24-57)9-5-17-49-45(47)48/h7,10,13-16,20,26,29,31-35,38,57H,4-6,8-9,11-12,17-19,21-25H2,1-3H3,(H2,46,58)(H,50,63)(H,51,59)(H,52,60)(H,53,64)(H,54,61)(H,55,62)(H4,47,48,49)/t29-,31+,32+,33+,34+,35+,38+/m1/s1	UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	n/a	n/a	>1.00E+4	n/a	n/a	n/a	n/a
Ferring Research Institute Inc. Curated by ChEMBL					Assay Description Agonist activity at recombinant human V1B receptor expressed in HEK293 cells measured after 5 hrs by luciferase reporter gene assay				J Med Chem 62: 4991-5005 (2019) Article DOI: 10.1021/acs.jmedchem.9b00132
					More data for this Ligand-Target Pair