BDBM50320457 AD[CFWKYC]V::CHEMBL1163460

SMILES: CC(C)[C@H](NC(=O)[C@@H]1CSSC[C@H](NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](C)N)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=MIDDXLODBRIHKS-LUFBBIINSA-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 = 50320457   

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)	BDBM50320457 (AD[CFWKYC]V | CHEMBL1163460) 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)N)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/C53H69N11O13S2/c1-28(2)44(53(76)77)64-52(75)42-27-79-78-26-41(62-50(73)40(24-43(66)67)58-45(68)29(3)55)51(74)60-37(21-30-11-5-4-6-12-30)47(70)61-39(23-32-25-56-35-14-8-7-13-34(32)35)49(72)57-36(15-9-10-20-54)46(69)59-38(48(71)63-42)22-31-16-18-33(65)19-17-31/h4-8,11-14,16-19,25,28-29,36-42,44,56,65H,9-10,15,20-24,26-27,54-55H2,1-3H3,(H,57,72)(H,58,68)(H,59,69)(H,60,74)(H,61,70)(H,62,73)(H,63,71)(H,64,75)(H,66,67)(H,76,77)/t29-,36-,37-,38-,39-,40-,41-,42-,44-/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	0.160	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