null

SMILES: NCCCC[C@H](OP(O)(=O)CCCCc1ccccc1)C(=O)N(CC(O)=O)c1ccc2OCOc2c1

InChI Key: InChIKey=JIRRQHFGEPCVJU-QFIPXVFZSA-N

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50406389   

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
Angiotensin-converting enzyme (Homo sapiens (Human))	BDBM50406389 (CHEMBL35561) Show SMILES NCCCC[C@H](OP(O)(=O)CCCCc1ccccc1)C(=O)N(CC(O)=O)c1ccc2OCOc2c1 Show InChI InChI=1S/C25H33N2O8P/c26-14-6-4-11-22(35-36(31,32)15-7-5-10-19-8-2-1-3-9-19)25(30)27(17-24(28)29)20-12-13-21-23(16-20)34-18-33-21/h1-3,8-9,12-13,16,22H,4-7,10-11,14-15,17-18,26H2,(H,28,29)(H,31,32)/t22-/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	0.115	n/a	n/a	n/a	n/a	n/a	n/a
Washington University Curated by ChEMBL					Assay Description Inhibitory activity against angiotensin converting enzyme (ACE)				J Med Chem 36: 2390-403 (1993) BindingDB Entry DOI: 10.7270/Q2Z320V9
					More data for this Ligand-Target Pair
Angiotensin-converting enzyme (Oryctolagus cuniculus)	BDBM50406389 (CHEMBL35561) Show SMILES NCCCC[C@H](OP(O)(=O)CCCCc1ccccc1)C(=O)N(CC(O)=O)c1ccc2OCOc2c1 Show InChI InChI=1S/C25H33N2O8P/c26-14-6-4-11-22(35-36(31,32)15-7-5-10-19-8-2-1-3-9-19)25(30)27(17-24(28)29)20-12-13-21-23(16-20)34-18-33-21/h1-3,8-9,12-13,16,22H,4-7,10-11,14-15,17-18,26H2,(H,28,29)(H,31,32)/t22-/m0/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	24	n/a	n/a	n/a	n/a	n/a	n/a
Squibb Institute for Medical Research Curated by ChEMBL					Assay Description Inhibition of rabbit lung angiotensin I converting enzyme (ACE) using hippuryl-histidyl-leucine as substrate				J Med Chem 33: 1459-69 (1990) BindingDB Entry DOI: 10.7270/Q29G5P0D
					More data for this Ligand-Target Pair