BDBM50588608 CHEMBL5192123

SMILES CC(C)C[C@H](NC(=O)[C@H](Cc1ccc(N)cc1)NC(=O)CN1CCNCC1)C(=O)N[C@@H](C)C(=O)N[C@@H](Cc1ccc(cc1)-c1ccccc1C(F)(F)F)C(=O)N1CCC[C@H]1C(=O)N[C@@H](CC(O)=O)C(=O)N[C@@H](C)C(=O)N[C@@H](C1CCCCC1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](Cc1ccccc1)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N1CCC[C@H]1C(N)=O

InChI Key InChIKey=UUKDZYHYHXLKTO-LMEGGTDHSA-N

Data  1 IC50  1 Kd  1 EC50

  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 = 50588608   

TargetEphrin type-A receptor 2(Homo sapiens (Human))
University Of California Riverside

Curated by ChEMBL
LigandPNGBDBM50588608(CHEMBL5192123)
Affinity DataKd:  22nMAssay Description:Inhibition of EPHA2 (unknown origin) by ITCMore data for this Ligand-Target Pair
In DepthDetails PubMed
TargetEphrin type-A receptor 2(Homo sapiens (Human))
University Of California Riverside

Curated by ChEMBL
LigandPNGBDBM50588608(CHEMBL5192123)
Affinity DataEC50:  1.60E+3nMAssay Description:Antagonist activity at EPHA2 in human BXPC-3 cells assessed as inhibition of ephrinA1-Fc induced degradation pretreated for 20 mins followed by ephri...More data for this Ligand-Target Pair
In DepthDetails PubMed
TargetEphrin type-A receptor 2(Homo sapiens (Human))
University Of California Riverside

Curated by ChEMBL
LigandPNGBDBM50588608(CHEMBL5192123)
Affinity DataIC50:  11nMAssay Description:Inhibition of EPHA2 (unknown origin) by DELFIA assayMore data for this Ligand-Target Pair
In DepthDetails PubMed