BDBM50087119 C-{[3-Biphenyl-4-yl-2-(1-carboxy-2-hydroxy-ethylcarbamoyl)-propyl]-hydroxy-phosphinoyl}-C-phenyl-methyl-ammonium

SMILES: [NH3+][C@H](c1ccccc1)P(O)(=O)C[C@@H](Cc1ccc(cc1)-c1ccccc1)C(=O)N[C@@H](CO)C(O)=O

InChI Key: InChIKey=AMVYHACYWKNDDZ-SGNDLWITSA-O

Data: 3 KI

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 3 hits for monomerid = 50087119   

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
Aminopeptidase N (Sus scrofa (Pig))	BDBM50087119 (C-{[3-Biphenyl-4-yl-2-(1-carboxy-2-hydroxy-ethylca...) Show SMILES [NH3+][C@H](c1ccccc1)P(O)(=O)C[C@@H](Cc1ccc(cc1)-c1ccccc1)C(=O)N[C@@H](CO)C(O)=O Show InChI InChI=1S/C26H29N2O6P/c27-24(21-9-5-2-6-10-21)35(33,34)17-22(25(30)28-23(16-29)26(31)32)15-18-11-13-20(14-12-18)19-7-3-1-4-8-19/h1-14,22-24,29H,15-17,27H2,(H,28,30)(H,31,32)(H,33,34)/p+1/t22-,23+,24+/m1/s1	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem Similars	PubMed	4.90	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
INSERM Curated by ChEMBL					Assay Description Inhibitory activity on aminopeptidase N (APN) using Ala-pNA as substrate.				J Med Chem 43: 1398-408 (2001) BindingDB Entry DOI: 10.7270/Q2TQ627J
					More data for this Ligand-Target Pair
Neprilysin (Oryctolagus cuniculus (rabbit))	BDBM50087119 (C-{[3-Biphenyl-4-yl-2-(1-carboxy-2-hydroxy-ethylca...) Show SMILES [NH3+][C@H](c1ccccc1)P(O)(=O)C[C@@H](Cc1ccc(cc1)-c1ccccc1)C(=O)N[C@@H](CO)C(O)=O Show InChI InChI=1S/C26H29N2O6P/c27-24(21-9-5-2-6-10-21)35(33,34)17-22(25(30)28-23(16-29)26(31)32)15-18-11-13-20(14-12-18)19-7-3-1-4-8-19/h1-14,22-24,29H,15-17,27H2,(H,28,30)(H,31,32)(H,33,34)/p+1/t22-,23+,24+/m1/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	PC cid PC sid UniChem Similars	PubMed	11.8	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
INSERM Curated by ChEMBL					Assay Description Inhibitory activity on neutral endopeptidase (NEP) using DGNPA as substrate.				J Med Chem 43: 1398-408 (2001) BindingDB Entry DOI: 10.7270/Q2TQ627J
					More data for this Ligand-Target Pair
Angiotensin-converting enzyme (Rattus norvegicus)	BDBM50087119 (C-{[3-Biphenyl-4-yl-2-(1-carboxy-2-hydroxy-ethylca...) Show SMILES [NH3+][C@H](c1ccccc1)P(O)(=O)C[C@@H](Cc1ccc(cc1)-c1ccccc1)C(=O)N[C@@H](CO)C(O)=O Show InChI InChI=1S/C26H29N2O6P/c27-24(21-9-5-2-6-10-21)35(33,34)17-22(25(30)28-23(16-29)26(31)32)15-18-11-13-20(14-12-18)19-7-3-1-4-8-19/h1-14,22-24,29H,15-17,27H2,(H,28,30)(H,31,32)(H,33,34)/p+1/t22-,23+,24+/m1/s1	KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	PC cid PC sid UniChem Similars	PubMed	>5.00E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
INSERM Curated by ChEMBL					Assay Description inhibitory activity on angiotensin I converting enzyme (ACE) using cbz-Phe-His-Leu as substrate.				J Med Chem 43: 1398-408 (2001) BindingDB Entry DOI: 10.7270/Q2TQ627J
					More data for this Ligand-Target Pair