BDBM50382929 CHEMBL2029399

SMILES: [#7]-[#6@@H](-[#6]-[#16])-[#6](=O)-[#7]-[#6@@H](-[#6]-[#6]-[#6](-[#7])=O)-[#6](=O)-[#7]-[#6@@H](-[#6]-[#6]-[#6]\[#7]=[#6](/[#7])-[#7])-[#6](=O)-[#7]-[#6@@H](-[#6]-c1ccccc1)-[#6](=O)-[#7]-[#6@@H](-[#6]-[#8])-[#6](=O)-[#7]-[#6@@H](-[#6]-[#6]-[#6]\[#7]=[#6](/[#7])-[#7])-[#6](-[#8])=O

InChI Key: InChIKey=RWSNMTBULLTXOS-LLINQDLYSA-N

Data: 2 IC50

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 2 hits for monomerid = 50382929   

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
Neprilysin (Homo sapiens (Human))	BDBM50382929 (CHEMBL2029399) Show SMILES [#7]-[#6@@H](-[#6]-[#16])-[#6](=O)-[#7]-[#6@@H](-[#6]-[#6]-[#6](-[#7])=O)-[#6](=O)-[#7]-[#6@@H](-[#6]-[#6]-[#6]\[#7]=[#6](/[#7])-[#7])-[#6](=O)-[#7]-[#6@@H](-[#6]-c1ccccc1)-[#6](=O)-[#7]-[#6@@H](-[#6]-[#8])-[#6](=O)-[#7]-[#6@@H](-[#6]-[#6]-[#6]\[#7]=[#6](/[#7])-[#7])-[#6](-[#8])=O |r| Show InChI InChI=1S/C32H53N13O9S/c33-18(16-55)25(48)41-20(10-11-24(34)47)27(50)42-19(8-4-12-39-31(35)36)26(49)44-22(14-17-6-2-1-3-7-17)28(51)45-23(15-46)29(52)43-21(30(53)54)9-5-13-40-32(37)38/h1-3,6-7,18-23,46,55H,4-5,8-16,33H2,(H2,34,47)(H,41,48)(H,42,50)(H,43,52)(H,44,49)(H,45,51)(H,53,54)(H4,35,36,39)(H4,37,38,40)/t18-,19-,20-,21-,22-,23-/m0/s1	PDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	7.00E+3	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibition of human neprilysin				ACS Med Chem Lett 3: 20-24 (2012) Article DOI: 10.1021/ml200182v BindingDB Entry DOI: 10.7270/Q2P84CZ6
					More data for this Ligand-Target Pair
Aminopeptidase N (Homo sapiens (Human))	BDBM50382929 (CHEMBL2029399) Show SMILES [#7]-[#6@@H](-[#6]-[#16])-[#6](=O)-[#7]-[#6@@H](-[#6]-[#6]-[#6](-[#7])=O)-[#6](=O)-[#7]-[#6@@H](-[#6]-[#6]-[#6]\[#7]=[#6](/[#7])-[#7])-[#6](=O)-[#7]-[#6@@H](-[#6]-c1ccccc1)-[#6](=O)-[#7]-[#6@@H](-[#6]-[#8])-[#6](=O)-[#7]-[#6@@H](-[#6]-[#6]-[#6]\[#7]=[#6](/[#7])-[#7])-[#6](-[#8])=O |r| Show InChI InChI=1S/C32H53N13O9S/c33-18(16-55)25(48)41-20(10-11-24(34)47)27(50)42-19(8-4-12-39-31(35)36)26(49)44-22(14-17-6-2-1-3-7-17)28(51)45-23(15-46)29(52)43-21(30(53)54)9-5-13-40-32(37)38/h1-3,6-7,18-23,46,55H,4-5,8-16,33H2,(H2,34,47)(H,41,48)(H,42,50)(H,43,52)(H,44,49)(H,45,51)(H,53,54)(H4,35,36,39)(H4,37,38,40)/t18-,19-,20-,21-,22-,23-/m0/s1	PDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt UniProtKB/TrEMBL B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	800	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibition of human aminopeptidase N				ACS Med Chem Lett 3: 20-24 (2012) Article DOI: 10.1021/ml200182v BindingDB Entry DOI: 10.7270/Q2P84CZ6
					More data for this Ligand-Target Pair