BDBM50320456 CHEMBL1165734::TAD[CFWKYC]V

SMILES: CC(C)[C@H](NC(=O)[C@@H]1CSSC[C@H](NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](C)NC(=O)[C@@H](N)[C@@H](C)O)C(=O)N[C@@H](Cc2ccccc2)C(=O)N[C@@H](Cc2c[nH]c3ccccc23)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](Cc2ccc(O)cc2)C(=O)N1)C(O)=O

InChI Key: InChIKey=OSAAGHNIQWODAC-MIBPFTBTSA-N

Data: 1 EC50

Find this compound or compounds like it in BindingDB or PDB:

Substructure Similarity at least:  must be >=0.5 Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 1 hit for monomerid = 50320456   

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
UTS2R (RAT)	BDBM50320456 (CHEMBL1165734 | TAD[CFWKYC]V) Show SMILES CC(C)[C@H](NC(=O)[C@@H]1CSSC[C@H](NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](C)NC(=O)[C@@H](N)[C@@H](C)O)C(=O)N[C@@H](Cc2ccccc2)C(=O)N[C@@H](Cc2c[nH]c3ccccc23)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](Cc2ccc(O)cc2)C(=O)N1)C(O)=O |r| Show InChI InChI=1S/C57H76N12O15S2/c1-29(2)47(57(83)84)69-55(81)44-28-86-85-27-43(67-53(79)42(25-45(72)73)63-48(74)30(3)61-56(82)46(59)31(4)70)54(80)65-39(22-32-12-6-5-7-13-32)50(76)66-41(24-34-26-60-37-15-9-8-14-36(34)37)52(78)62-38(16-10-11-21-58)49(75)64-40(51(77)68-44)23-33-17-19-35(71)20-18-33/h5-9,12-15,17-20,26,29-31,38-44,46-47,60,70-71H,10-11,16,21-25,27-28,58-59H2,1-4H3,(H,61,82)(H,62,78)(H,63,74)(H,64,75)(H,65,80)(H,66,76)(H,67,79)(H,68,77)(H,69,81)(H,72,73)(H,83,84)/t30-,31+,38-,39-,40-,41-,42-,43-,44-,46-,47-/m0/s1	Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	n/a	n/a	0.110	n/a	n/a	n/a	n/a
Johnson& Johnson Pharmaceutical Research& Development Curated by ChEMBL					Assay Description Agonist activity at rat urotensin 2 receptor expressed in CHO cells assessed as calcium mobilization by FLIPR				J Med Chem 53: 2695-708 (2010) Article DOI: 10.1021/jm901294u BindingDB Entry DOI: 10.7270/Q20G3K9N
					More data for this Ligand-Target Pair