BDBM50320462 AD[CFWKYC]A::CHEMBL1165767

SMILES: C[C@H](N)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@H]1CSSC[C@H](NC(=O)[C@H](Cc2ccc(O)cc2)NC(=O)[C@H](CCCCN)NC(=O)[C@H](Cc2c[nH]c3ccccc23)NC(=O)[C@H](Cc2ccccc2)NC1=O)C(=O)N[C@@H](C)C(O)=O

InChI Key: InChIKey=BLICVBXAQIYYJW-UZXJSEJMSA-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 = 50320462   

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
Urotensin-2 receptor (RAT)	BDBM50320462 (AD[CFWKYC]A | CHEMBL1165767) Show SMILES C[C@H](N)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@H]1CSSC[C@H](NC(=O)[C@H](Cc2ccc(O)cc2)NC(=O)[C@H](CCCCN)NC(=O)[C@H](Cc2c[nH]c3ccccc23)NC(=O)[C@H](Cc2ccccc2)NC1=O)C(=O)N[C@@H](C)C(O)=O |r| Show InChI InChI=1S/C51H66N12O12S2/c1-27(53)43(66)58-39(23-42(54)65)48(71)63-41-26-77-76-25-40(49(72)56-28(2)51(74)75)62-46(69)37(21-30-15-17-32(64)18-16-30)59-44(67)35(14-8-9-19-52)57-47(70)38(22-31-24-55-34-13-7-6-12-33(31)34)61-45(68)36(60-50(41)73)20-29-10-4-3-5-11-29/h3-7,10-13,15-18,24,27-28,35-41,55,64H,8-9,14,19-23,25-26,52-53H2,1-2H3,(H2,54,65)(H,56,72)(H,57,70)(H,58,66)(H,59,67)(H,60,73)(H,61,68)(H,62,69)(H,63,71)(H,74,75)/t27-,28-,35-,36-,37-,38-,39-,40-,41-/m0/s1	Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL KEGG PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	n/a	n/a	0.400	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