BDBM50571872 CHEMBL4864508

SMILES OC(=O)C1(CCCCC1)NC(=O)c1cccc2cc(oc12)-c1ccc(Cl)cc1

InChI Key InChIKey=CAZIGEHCBGMUHD-UHFFFAOYSA-N

Data  3 IC50

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 3 hits for monomerid = 50571872   

TargetEndoplasmic reticulum aminopeptidase 1(Homo sapiens (Human))
Sanofi

Curated by ChEMBL
LigandPNGBDBM50571872(CHEMBL4864508)
Affinity DataIC50:  120nMAssay Description:Inhibition of wild type ERAP1 (unknown origin) using L-Rho-Succ-FKARKF as substrate preincubated for 15 mins followed by substrate addition and measu...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetAminopeptidase N(Homo sapiens (Human))
Sanofi

Curated by ChEMBL
LigandPNGBDBM50571872(CHEMBL4864508)
Affinity DataIC50: >3.00E+4nMAssay Description:Inhibition of APN (unknown origin) using Ala-AMC as substrateMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetEndoplasmic reticulum aminopeptidase 2(Homo sapiens (Human))
Sanofi

Curated by ChEMBL
LigandPNGBDBM50571872(CHEMBL4864508)
Affinity DataIC50: >3.00E+4nMAssay Description:Inhibition of ERAP2 (unknown origin) using Arg-AMC as substrateMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed