BDBM50047222 2-[2-(2-Benzyl-3-hydroxycarbamoyl-propionylamino)-3-methyl-pentanoylamino]-3-methyl-butyric acid::CHEMBL286500

SMILES CCC(C)C(NC(=O)[C@@H](CC(=O)NO)Cc1ccccc1)C(=O)NC(C(C)C)C(O)=O

InChI Key InChIKey=IEVZTPJUFMSHHO-UOBIKFCOSA-N

Data  5 KI

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
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   Substructure
Similarity at least:  must be >=0.5
Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 5 hits for monomerid = 50047222   

TargetNeprilysin(Rattus norvegicus (Rat))
Ccipe-Faculté

Curated by ChEMBL
LigandPNGBDBM50047222(2-[2-(2-Benzyl-3-hydroxycarbamoyl-propionylamino)-...)
Affinity DataKi:  31nMAssay Description:Inhibitory activity against endopeptidase 24.15More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetNeprilysin(Rattus norvegicus (Rat))
Ccipe-Faculté

Curated by ChEMBL
LigandPNGBDBM50047222(2-[2-(2-Benzyl-3-hydroxycarbamoyl-propionylamino)-...)
Affinity DataKi:  40nMAssay Description:Inhibitory activity against endopeptidase 24.11More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetLeucyl-cystinyl aminopeptidase(Homo sapiens (Human))
Ccipe-Faculté

Curated by ChEMBL
LigandPNGBDBM50047222(2-[2-(2-Benzyl-3-hydroxycarbamoyl-propionylamino)-...)
Affinity DataKi:  52nMAssay Description:Inhibitory activity against Leucine aminopeptidaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetNeprilysin(Rattus norvegicus (Rat))
Ccipe-Faculté

Curated by ChEMBL
LigandPNGBDBM50047222(2-[2-(2-Benzyl-3-hydroxycarbamoyl-propionylamino)-...)
Affinity DataKi:  58nMAssay Description:Inhibitory activity against endopeptidase 24.16More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAngiotensin-converting enzyme(Oryctolagus cuniculus)
Ccipe-Faculté

Curated by ChEMBL
LigandPNGBDBM50047222(2-[2-(2-Benzyl-3-hydroxycarbamoyl-propionylamino)-...)
Affinity DataKi:  7.00E+4nMAssay Description:Inhibitory activity against angiotensin converting enzymeMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed