Compile Data Set for Download or QSAR

Found 2 hits of ic50 for monomerid = 50148531   

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
Dipeptidase 1 (Homo sapiens (Human))	BDBM50148531 (2-[(1-Amino-2-cyclohexyl-ethyl)-hydroxy-phosphinoy...) Show SMILES OC(=O)C(Cc1ccc(I)cc1)CP(O)(=O)C(=N)CC1CCCCC1 Show InChI InChI=1S/C18H25INO4P/c19-16-8-6-14(7-9-16)10-15(18(21)22)12-25(23,24)17(20)11-13-4-2-1-3-5-13/h6-9,13,15,20H,1-5,10-12H2,(H,21,22)(H,23,24)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	8	n/a	n/a	n/a	n/a	n/a	n/a
The Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins Curated by ChEMBL					Assay Description Concentration required to inhibit renal dipeptidase (RDP) by 50% in crude lysates prepared from human colon cancer				Bioorg Med Chem Lett 14: 3531-3 (2004) Article DOI: 10.1016/j.bmcl.2004.04.057 BindingDB Entry DOI: 10.7270/Q2GX4B1C
					More data for this Ligand-Target Pair
Dipeptidase 1 (Homo sapiens (Human))	BDBM50148531 (2-[(1-Amino-2-cyclohexyl-ethyl)-hydroxy-phosphinoy...) Show SMILES OC(=O)C(Cc1ccc(I)cc1)CP(O)(=O)C(=N)CC1CCCCC1 Show InChI InChI=1S/C18H25INO4P/c19-16-8-6-14(7-9-16)10-15(18(21)22)12-25(23,24)17(20)11-13-4-2-1-3-5-13/h6-9,13,15,20H,1-5,10-12H2,(H,21,22)(H,23,24)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	25	n/a	n/a	n/a	n/a	n/a	n/a
The Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins Curated by ChEMBL					Assay Description Concentration required to inhibit renal dipeptidase (RDP) by 50% in crude lysates prepared from human colon cancer				Bioorg Med Chem Lett 14: 3531-3 (2004) Article DOI: 10.1016/j.bmcl.2004.04.057 BindingDB Entry DOI: 10.7270/Q2GX4B1C
					More data for this Ligand-Target Pair