BDBM50520628 CHEMBL4526960

SMILES C[C@@H](O)[C@@H]1NC(=O)[C@H](C)NC(=O)[C@H](CCCNC(N)=N)NC(=O)[C@H](Cc2c[nH]c3ccccc23)NC(=O)[C@@H]2CCCN2C(=O)[C@H](N)CSCc2cccc(CSC[C@H](NC(=O)[C@H](Cc3ccccc3)NC(=O)[C@@H]3CCCN3C(=O)[C@H](CC(N)=O)NC1=O)C(O)=O)c2

InChI Key InChIKey=ZSTTYORYUJEOBU-YHVPXBQKSA-N

Data  1 Kd

  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 1 hit for monomerid = 50520628   

TargetEpidermal growth factor receptor substrate 15(Homo sapiens)
Astrazeneca

Curated by ChEMBL
LigandPNGBDBM50520628(CHEMBL4526960)
Affinity DataKd:  370nMAssay Description:Inhibition of stonin-2 binding to Eps15 (unknown origin)More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed