BDBM50405604 CHEMBL68472

SMILES: NC(=N)NCCC[C@H](OP(O)(=O)CCCCc1ccccc1)C(=O)N1CCC[C@H]1C(O)=O

InChI Key: InChIKey=GPLWOAKVDXAIFY-ROUUACIJSA-N

Data: 1 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 1 hit for monomerid = 50405604   

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 (Oryctolagus cuniculus)	BDBM50405604 (CHEMBL68472) Show SMILES NC(=N)NCCC[C@H](OP(O)(=O)CCCCc1ccccc1)C(=O)N1CCC[C@H]1C(O)=O Show InChI InChI=1S/C21H33N4O6P/c22-21(23)24-13-6-12-18(19(26)25-14-7-11-17(25)20(27)28)31-32(29,30)15-5-4-10-16-8-2-1-3-9-16/h1-3,8-9,17-18H,4-7,10-15H2,(H,27,28)(H,29,30)(H4,22,23,24)/t17-,18-/m0/s1	MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	19	n/a	n/a	n/a	n/a	n/a	n/a
Squibb Institute for Medical Research Curated by ChEMBL					Assay Description In vitro inhibition of angiotensin I converting enzyme in rabbit lung with hippuryl-histidyl-leucine as substrate				J Med Chem 31: 204-12 (1988) BindingDB Entry DOI: 10.7270/Q2SN0B5P
					More data for this Ligand-Target Pair