BDBM50003192 2-(1-Aza-bicyclo[2.2.2]oct-3-ylamino)-N-(6-cyclohexylmethyl-7-hydroxy-10-morpholin-4-ylmethyl-4,8,14-trioxo-1,9-dioxa-5-aza-cyclotetradec-3-yl)-3-phenyl-propionamide::CHEMBL122437

SMILES: O[C@@H]1[C@H](CC2CCCCC2)NC(=O)[C@H](COC(=O)CCC[C@H](CN2CCOCC2)OC1=O)NC(=O)[C@H](Cc1ccccc1)NC1CN2CCC1CC2

InChI Key: InChIKey=KUQRLGWOANPHCW-PWCIQWMJSA-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 = 50003192   

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
Renin (Homo sapiens (Human))	BDBM50003192 (2-(1-Aza-bicyclo[2.2.2]oct-3-ylamino)-N-(6-cyclohe...) Show SMILES O[C@@H]1[C@H](CC2CCCCC2)NC(=O)[C@H](COC(=O)CCC[C@H](CN2CCOCC2)OC1=O)NC(=O)[C@H](Cc1ccccc1)NC1CN2CCC1CC2 |wU:13.34,wD:35.46,2.2,21.22,1.0,(15.07,-8.78,;13.73,-8.02,;12.4,-8.78,;12.4,-10.34,;13.51,-11.43,;14.96,-11.01,;16.02,-12.12,;15.65,-13.56,;14.17,-13.96,;13.1,-12.89,;11.06,-8.06,;9.73,-8.83,;9.75,-10.38,;8.39,-8.08,;8.36,-6.53,;7.02,-5.78,;6.99,-4.23,;5.65,-3.47,;8.34,-3.44,;9.69,-4.2,;11.03,-3.4,;12.38,-4.16,;13.72,-3.4,;15.26,-3.4,;16.05,-4.74,;17.58,-4.74,;18.34,-3.4,;17.57,-2.05,;16.02,-2.07,;12.37,-5.71,;13.72,-6.48,;15.05,-5.69,;7.04,-8.87,;5.69,-8.11,;5.67,-6.55,;4.36,-8.9,;4.37,-10.43,;3.61,-11.77,;4.35,-13.1,;3.58,-14.42,;2.03,-14.41,;1.28,-13.07,;2.05,-11.75,;3.03,-8.13,;1.68,-8.9,;1.67,-10.43,;.33,-11.2,;-.99,-10.41,;-.97,-8.87,;.36,-8.12,;-.35,-9.41,;.88,-10.05,)| Show InChI InChI=1S/C39H59N5O8/c45-35-13-7-12-30(24-44-18-20-50-21-19-44)52-39(49)36(46)31(22-27-8-3-1-4-9-27)41-38(48)34(26-51-35)42-37(47)32(23-28-10-5-2-6-11-28)40-33-25-43-16-14-29(33)15-17-43/h2,5-6,10-11,27,29-34,36,40,46H,1,3-4,7-9,12-26H2,(H,41,48)(H,42,47)/t30-,31+,32+,33?,34+,36-/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	1.30	n/a	n/a	n/a	n/a	7.4	n/a
Merck Research Laboratories Curated by ChEMBL					Assay Description Inhibitory activity against human renin inhibition (at pH 7.4)				J Med Chem 35: 3755-73 (1992) BindingDB Entry DOI: 10.7270/Q26W9BPZ
					More data for this Ligand-Target Pair