null

SMILES: CCCC[C@H](NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CO)NC(=O)C[C@H](Cc1ccc2ccccc2c1)NC(=O)CCCCCN)C(=O)N[C@H](CCCBr)B(O)O

InChI Key: InChIKey=XJPFLQNETXJYGM-QEUNAIBPSA-N

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 1 hit for monomerid = 50434143   

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
Prostate-specific antigen (Homo sapiens (Human))	BDBM50434143 (CHEMBL2381658) Show SMILES CCCC[C@H](NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CO)NC(=O)C[C@H](Cc1ccc2ccccc2c1)NC(=O)CCCCCN)C(=O)N[C@H](CCCBr)B(O)O |r| Show InChI InChI=1S/C38H59BBrN7O9/c1-2-3-12-29(37(53)47-32(39(55)56)13-9-19-40)45-36(52)30(17-18-33(42)49)46-38(54)31(24-48)44-35(51)23-28(43-34(50)14-5-4-8-20-41)22-25-15-16-26-10-6-7-11-27(26)21-25/h6-7,10-11,15-16,21,28-32,48,55-56H,2-5,8-9,12-14,17-20,22-24,41H2,1H3,(H2,42,49)(H,43,50)(H,44,51)(H,45,52)(H,46,54)(H,47,53)/t28-,29-,30-,31-,32+/m0/s1	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	102	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
The Johns Hopkins University Curated by ChEMBL					Assay Description Inhibition of human seminal fluid PSA using Mu-SRKSQQY-AMC as substrate measured for 30 mins by fluorescence assay				J Med Chem 56: 4224-35 (2013) Article DOI: 10.1021/jm301718c BindingDB Entry DOI: 10.7270/Q2V69KZF
					More data for this Ligand-Target Pair