BDBM50538253 CHEMBL4638393

SMILES [H][C@@]12CCCN1C(=O)CNC(=O)[C@H](Cc1c[nH]c3ccccc13)NC(=O)[C@]1([H])CCCN1C(=O)[C@H](CSCc1cc3CSC[C@H](NC(=O)[C@@]([H])(NC(=O)[C@H](CCCCN)NC(=O)CNC(=O)[C@H](Cc4cnc[nH]4)NC(=O)[C@@H](NC(=O)[C@]4([H])CCCN4C(=O)[C@]([H])(CSCc(c3)c1)NC(=O)[C@H](Cc1c[nH]c3ccccc13)NC(=O)[C@H](C)NC2=O)C(C)C)[C@H](C)O)C(=O)N[C@@H](C)C(N)=O)NC(=O)[C@H](C)N

InChI Key InChIKey=KZDTYJIPTBVDDV-OKJYKQJZSA-N

Data  1 KI

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
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Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 1 hit for monomerid = 50538253   

TargetEphrin type-A receptor 2(Homo sapiens (Human))
Bicycletx

Curated by ChEMBL
LigandPNGBDBM50538253(CHEMBL4638393)
Affinity DataKi:  263nMAssay Description:Binding affinity to 6x-His-tagged human EphA2 ecto-domain residues (Lys27 to Asn529 residues) expressed in HEK293 cells incubated for 60 mins by fluo...More data for this Ligand-Target Pair
Ligand InfoKEGGPC cidPC sid
In DepthDetails ArticlePubMed