BDBM50571874 CHEMBL4855038

SMILES OC(=O)C1(CCCCC1)NC(=O)c1cccc2c(Br)c(oc12)-c1ccc(Cl)cc1

InChI Key InChIKey=JXOQWYLAVQAJFL-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 = 50571874   

TargetEndoplasmic reticulum aminopeptidase 1(Human)
Sanofi

Curated by ChEMBL
LigandPNGBDBM50571874(CHEMBL4855038)
Affinity DataIC50: 151nMAssay 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
In Depth
Date in BDB:
8/21/2022
Entry Details Article
PubMed
TargetEndoplasmic reticulum aminopeptidase 2(Human)
Sanofi

Curated by ChEMBL
LigandPNGBDBM50571874(CHEMBL4855038)
Affinity DataIC50: 3.00E+4nMAssay Description:Inhibition of ERAP2 (unknown origin) using Arg-AMC as substrateMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/21/2022
Entry Details Article
PubMed
TargetAminopeptidase N(Human)
Sanofi

Curated by ChEMBL
LigandPNGBDBM50571874(CHEMBL4855038)
Affinity DataIC50: 3.00E+4nMAssay Description:Inhibition of APN (unknown origin) using Ala-AMC as substrateMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/21/2022
Entry Details Article
PubMed