BDBM50350672 CHEMBL1813744

SMILES: CCCCc1nc(Cl)c(C2CC(=NN2C(C)=O)c2ccc(OC)cc2)n1C

InChI Key: InChIKey=UUTVVYJZNBHLRF-UHFFFAOYSA-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 = 50350672   

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)	BDBM50350672 (CHEMBL1813744) Show SMILES CCCCc1nc(Cl)c(C2CC(=NN2C(C)=O)c2ccc(OC)cc2)n1C |c:11| Show InChI InChI=1S/C20H25ClN4O2/c1-5-6-7-18-22-20(21)19(24(18)3)17-12-16(23-25(17)13(2)26)14-8-10-15(27-4)11-9-14/h8-11,17H,5-7,12H2,1-4H3	MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	2.33E+6	n/a	n/a	n/a	n/a	n/a	n/a
India Institute of Chemical Technology Curated by ChEMBL					Assay Description Inhibition of rabbit lung ACE assessed as reduction in hippuryl-histidyl-leucine substrate by colorimetric assay				Bioorg Med Chem 19: 4772-81 (2011) Article DOI: 10.1016/j.bmc.2011.06.085 BindingDB Entry DOI: 10.7270/Q27M089B
					More data for this Ligand-Target Pair