Compile Data Set for Download or QSAR

Found 2 hits Enz. Inhib. hit(s) with Target = 'Leucyl-cystinyl aminopeptidase' and Ligand = 'BDBM401367'   

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
Leucyl-cystinyl aminopeptidase (Rattus norvegicus)	BDBM401367 (US10005762, Example 47) Show SMILES CC(C)CC[C@H](N)[C@](O)(Cc1cc(CCCC2CC2)c(C)cn1)C(O)=O |r| Show InChI InChI=1S/C21H34N2O3/c1-14(2)7-10-19(22)21(26,20(24)25)12-18-11-17(15(3)13-23-18)6-4-5-16-8-9-16/h11,13-14,16,19,26H,4-10,12,22H2,1-3H3,(H,24,25)/t19-,21+/m0/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	0.650	n/a	n/a	n/a	n/a	n/a	n/a
Wyeth Research					Assay Description The inventors have assumed that inhibition of nocturnal activity of placental leucine aminopeptidase (P-LAP), i.e. aminopeptidase that cleaves AVP, w...				Bioorg Med Chem 17: 7933-48 (2009) BindingDB Entry DOI: 10.7270/Q2PG1V3Q
					More data for this Ligand-Target Pair
Leucyl-cystinyl aminopeptidase (Homo sapiens (Human))	BDBM401367 (US10005762, Example 47) Show SMILES CC(C)CC[C@H](N)[C@](O)(Cc1cc(CCCC2CC2)c(C)cn1)C(O)=O |r| Show InChI InChI=1S/C21H34N2O3/c1-14(2)7-10-19(22)21(26,20(24)25)12-18-11-17(15(3)13-23-18)6-4-5-16-8-9-16/h11,13-14,16,19,26H,4-10,12,22H2,1-3H3,(H,24,25)/t19-,21+/m0/s1	PDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	3.5	n/a	n/a	n/a	n/a	n/a	n/a
Wyeth Research					Assay Description The inventors have assumed that inhibition of nocturnal activity of placental leucine aminopeptidase (P-LAP), i.e. aminopeptidase that cleaves AVP, w...				Bioorg Med Chem 17: 7933-48 (2009) BindingDB Entry DOI: 10.7270/Q2PG1V3Q
					More data for this Ligand-Target Pair