BDBM50657599 CHEMBL6120493
SMILES N#CC1=C2N=C(N)c3ccccc3N2C2=C(C(=O)CCC2)C1c1ccc(-c2ccccc2)cc1
InChI Key InChIKey=HRXRHHQSLLMHJL-UHFFFAOYSA-N
Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB
Found 3 hits for monomerid = 50657599
TargetPhosphatidylinositol 3,4,5-trisphosphate 5-phosphatase 1(Human)
Purdue University
Curated by ChEMBL
Purdue University
Curated by ChEMBL
Affinity DataKi: 3.20E+3nMAssay Description:Competitive inhibition of human SHIP-1 (397 to 715 residues) catalytic domain expressed in Rosetta DE3 BL21 cells assessed as inhibition constant by ...More data for this Ligand-Target Pair
TargetPhosphatidylinositol 3,4,5-trisphosphate 5-phosphatase 1(Human)
Purdue University
Curated by ChEMBL
Purdue University
Curated by ChEMBL
Affinity DataIC50: 6.10E+3nMAssay Description:Inhibition of human SHIP-1 (397 to 715 residues) catalytic domain expressed in Rosetta DE3 BL21 cells using 1-(1,2-dioctanoylphosphatidyl) inositol-3...More data for this Ligand-Target Pair
TargetPhosphatidylinositol 3,4,5-trisphosphate 5-phosphatase 2(Human)
Purdue University
Curated by ChEMBL
Purdue University
Curated by ChEMBL
Affinity DataIC50: 4.32E+4nMAssay Description:Inhibition of human SHIP-2 (420 to 732 residues) catalytic domain expressed in Rosetta DE3 BL21 cells using -(1,2-dioctanoylphosphatidyflinosito1-3,4...More data for this Ligand-Target Pair
