null

SMILES: CC(=O)N[C@H]1CSSC[C@H](NC(=O)[C@H](Cc2ccc(O)cc2)NC(=O)[C@H](CCCCN)NC(=O)[C@H](Cc2ccc3ccccc3c2)NC(=O)[C@H](Cc2ccccc2)NC1=O)C(N)=O

InChI Key: InChIKey=HDWATWPWJNTOQQ-BGBFCPIGSA-N

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50320470   

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)	BDBM50320470 ((4R,7S,10S,13S,16S,19R)-19-acetamido-10-(4-aminobu...) Show SMILES CC(=O)N[C@H]1CSSC[C@H](NC(=O)[C@H](Cc2ccc(O)cc2)NC(=O)[C@H](CCCCN)NC(=O)[C@H](Cc2ccc3ccccc3c2)NC(=O)[C@H](Cc2ccccc2)NC1=O)C(N)=O |r| Show InChI InChI=1S/C45H54N8O8S2/c1-27(54)48-39-26-63-62-25-38(40(47)56)53-44(60)36(23-29-15-18-33(55)19-16-29)50-41(57)34(13-7-8-20-46)49-42(58)37(24-30-14-17-31-11-5-6-12-32(31)21-30)51-43(59)35(52-45(39)61)22-28-9-3-2-4-10-28/h2-6,9-12,14-19,21,34-39,55H,7-8,13,20,22-26,46H2,1H3,(H2,47,56)(H,48,54)(H,49,58)(H,50,57)(H,51,59)(H,52,61)(H,53,60)/t34-,35-,36-,37-,38-,39-/m0/s1	Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	200	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Johnson& Johnson Pharmaceutical Research& Development Curated by ChEMBL					Assay Description Displacement of [125I]U2 from rat urotensin 2 receptor expressed in CHO cells				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
Urotensin-2 receptor (RAT)	BDBM50320470 ((4R,7S,10S,13S,16S,19R)-19-acetamido-10-(4-aminobu...) Show SMILES CC(=O)N[C@H]1CSSC[C@H](NC(=O)[C@H](Cc2ccc(O)cc2)NC(=O)[C@H](CCCCN)NC(=O)[C@H](Cc2ccc3ccccc3c2)NC(=O)[C@H](Cc2ccccc2)NC1=O)C(N)=O |r| Show InChI InChI=1S/C45H54N8O8S2/c1-27(54)48-39-26-63-62-25-38(40(47)56)53-44(60)36(23-29-15-18-33(55)19-16-29)50-41(57)34(13-7-8-20-46)49-42(58)37(24-30-14-17-31-11-5-6-12-32(31)21-30)51-43(59)35(52-45(39)61)22-28-9-3-2-4-10-28/h2-6,9-12,14-19,21,34-39,55H,7-8,13,20,22-26,46H2,1H3,(H2,47,56)(H,48,54)(H,49,58)(H,50,57)(H,51,59)(H,52,61)(H,53,60)/t34-,35-,36-,37-,38-,39-/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	31	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