BDBM50538252 CHEMBL4642167
SMILES [H][C@@]12CCCN1C(=O)[C@H](CCCNC(N)=N)NC(=O)[C@H](CC(N)=O)NC(=O)[C@@H](NC(=O)[C@]1([H])CCCN1C(=O)[C@]1([H])CSCc3cc(CSC[C@H](NC(=O)CNC2=O)C(=O)N[C@@H](C)C(N)=O)cc(CSC[C@H](NC(=O)C2CCCN2C(=O)[C@@H](NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](Cc2c[nH]cn2)NC(=O)[C@H](C)N)C(C)C)C(=O)N2CCC[C@@]2([H])C(=O)N[C@@H](Cc2c[nH]c4ccccc24)C(=O)NCC(=O)N2CCC[C@@]2([H])C(=O)N[C@@H](Cc2ccccc2)C(=O)N[C@@H](Cc2c[nH]c4ccccc24)C(=O)N1)c3)C(C)C
InChI Key InChIKey=SFQZXAOPWWKVLL-BJEKBVEWSA-N
Data 1 KI
Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB
Found 1 hit for monomerid = 50538252
Affinity DataKi: 0.540nMAssay 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