BDBM50648763 CHEMBL5613338
SMILES CC(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](C)C(=O)N[C@@H](Cc1c[nH]c2ccccc12)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](C)C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](C)C(=O)N[C@@H](Cc1c[nH]c2ccccc12)C(N)=O
InChI Key
Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB
Found 2 hits for monomerid = 50648763
TargetPhosphatidylinositol 3,4,5-trisphosphate 5-phosphatase 2(Human)
Institute of Biostructures and Bioimaging
Curated by ChEMBL
Institute of Biostructures and Bioimaging
Curated by ChEMBL
Affinity DataKd: 2.90E+4nMAssay Description:Binding affinity to recombinant human 15N-labeled SHIP2 Sam domain (1194 to 1258 residues) extracted from Escherichia coli BL21 (DE3) cells assessed ...More data for this Ligand-Target Pair
TargetPhosphatidylinositol 3,4,5-trisphosphate 5-phosphatase 2(Human)
Institute of Biostructures and Bioimaging
Curated by ChEMBL
Institute of Biostructures and Bioimaging
Curated by ChEMBL
Affinity DataKd: 3.80E+4nMAssay Description:Binding affinity to recombinant human 15N-labeled SHIP2 Sam domain (1194 to 1258 residues) extracted from Escherichia coli BL21 (DE3) cells assessed ...More data for this Ligand-Target Pair
