BDBM50403266 CHEMBL415932

SMILES: CC(C)C[C@H](S)C(=O)N[C@H]1CCc2ccccc2N(CC(O)=O)C1=O

InChI Key: InChIKey=LWRWHXRRIHLFGY-ZFWWWQNUSA-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 = 50403266   

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))	BDBM50403266 (CHEMBL415932) Show SMILES CC(C)C[C@H](S)C(=O)N[C@H]1CCc2ccccc2N(CC(O)=O)C1=O Show InChI InChI=1S/C18H24N2O4S/c1-11(2)9-15(25)17(23)19-13-8-7-12-5-3-4-6-14(12)20(18(13)24)10-16(21)22/h3-6,11,13,15,25H,7-10H2,1-2H3,(H,19,23)(H,21,22)/t13-,15-/m0/s1	PDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL KEGG PC cid PC sid UniChem Similars	Article	n/a	n/a	7	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibition of Neutral Endopeptidase (NEP)				Bioorg Med Chem Lett 4: 1795-1800 (1994) Article DOI: 10.1016/S0960-894X(01)80373-5 BindingDB Entry DOI: 10.7270/Q2Z60Q76
					More data for this Ligand-Target Pair
Angiotensin-converting enzyme (Homo sapiens (Human))	BDBM50403266 (CHEMBL415932) Show SMILES CC(C)C[C@H](S)C(=O)N[C@H]1CCc2ccccc2N(CC(O)=O)C1=O Show InChI InChI=1S/C18H24N2O4S/c1-11(2)9-15(25)17(23)19-13-8-7-12-5-3-4-6-14(12)20(18(13)24)10-16(21)22/h3-6,11,13,15,25H,7-10H2,1-2H3,(H,19,23)(H,21,22)/t13-,15-/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL KEGG PC cid PC sid UniChem Similars	Article	n/a	n/a	6.30	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibition of Angiotensin I converting enzyme				Bioorg Med Chem Lett 4: 1795-1800 (1994) Article DOI: 10.1016/S0960-894X(01)80373-5 BindingDB Entry DOI: 10.7270/Q2Z60Q76
					More data for this Ligand-Target Pair