Compile Data Set for Download or QSAR

Found 3 hits Enz. Inhib. hit(s) with Target = 'Aminopeptidase N' and Ligand = 'BDBM50400529'   

Target/Host (Institution)	Ligand	Target/Host Links	Ligand Links	Trg + Lig Links	Ki nM	ΔG° kJ/mole	IC50 nM	Kd nM	EC50/IC50 nM	koff s-1	kon M-1s-1	pH	Temp °C
Aminopeptidase N (Sus scrofa (Pig))	BDBM50400529 (CHEMBL2204943) Show SMILES CC(C)C[C@H](NC(=O)Nc1cccc2ccccc12)C(=O)NO |r| Show InChI InChI=1S/C17H21N3O3/c1-11(2)10-15(16(21)20-23)19-17(22)18-14-9-5-7-12-6-3-4-8-13(12)14/h3-9,11,15,23H,10H2,1-2H3,(H,20,21)(H2,18,19,22)/t15-/m0/s1	PDB UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	99	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibition of APN in porcine kidney microsome assessed as inhibition of L-Leu-p-nitroanilide substrate hydrolysis incubated for 5 mins before substra...				ACS Med Chem Lett 3: 959-964 (2012) Article DOI: 10.1021/ml3000758 BindingDB Entry DOI: 10.7270/Q2QJ7JFR
					More data for this Ligand-Target Pair
Aminopeptidase N (Homo sapiens (Human))	BDBM50400529 (CHEMBL2204943) Show SMILES CC(C)C[C@H](NC(=O)Nc1cccc2ccccc12)C(=O)NO |r| Show InChI InChI=1S/C17H21N3O3/c1-11(2)10-15(16(21)20-23)19-17(22)18-14-9-5-7-12-6-3-4-8-13(12)14/h3-9,11,15,23H,10H2,1-2H3,(H,20,21)(H2,18,19,22)/t15-/m0/s1	PDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	480	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibition of APN in human ES2 cell surface assessed as inhibition of L-Leu-p-nitroanilide substrate hydrolysis incubated for 5 mins before substrate...				ACS Med Chem Lett 3: 959-964 (2012) Article DOI: 10.1021/ml3000758 BindingDB Entry DOI: 10.7270/Q2QJ7JFR
					More data for this Ligand-Target Pair
Aminopeptidase N (Mus musculus)	BDBM50400529 (CHEMBL2204943) Show SMILES CC(C)C[C@H](NC(=O)Nc1cccc2ccccc12)C(=O)NO |r| Show InChI InChI=1S/C17H21N3O3/c1-11(2)10-15(16(21)20-23)19-17(22)18-14-9-5-7-12-6-3-4-8-13(12)14/h3-9,11,15,23H,10H2,1-2H3,(H,20,21)(H2,18,19,22)/t15-/m0/s1	Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	2.26E+3	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibition of mouse APN				ACS Med Chem Lett 3: 959-964 (2012) Article DOI: 10.1021/ml3000758 BindingDB Entry DOI: 10.7270/Q2QJ7JFR
					More data for this Ligand-Target Pair