BDBM50131498 CHEMBL3633453

SMILES CC(=O)N[C@@H]1[C@@H](O)[C@H](O)[C@@H](CO)O[C@@H]1OC[C@H](NC(=O)[C@H](Cc1ccccc1)NC(=O)[C@H](CCCNC(N)=N)NC(=O)[C@@H](N)CCC(N)=O)C(=O)N[C@@H](CCCNC(N)=N)C(O)=O

InChI Key InChIKey=JDHTWBCWXCCGJS-RRWJDLRRSA-N

Data  2 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 2 hits for monomerid = 50131498   

TargetNeprilysin(Homo sapiens (Human))
Institute Of Advanced Chemistry Of Catalonia (Iqac-Csic)

Curated by ChEMBL
LigandPNGBDBM50131498(CHEMBL3633453)
Affinity DataIC50: >1.00E+5nMAssay Description:Inhibition of human recombinant neutral endopeptidase using Ala-AMC as substrate after 20 to 40 mins by fluorometryMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAminopeptidase N(Homo sapiens (Human))
Institute Of Advanced Chemistry Of Catalonia (Iqac-Csic)

Curated by ChEMBL
LigandPNGBDBM50131498(CHEMBL3633453)
Affinity DataIC50:  3.20E+4nMAssay Description:Inhibition of human recombinant aminopeptidase N using AbzdR-G-L-EDDnp as substrate after 20 to 40 mins by fluorometryMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed