BDBM50342002 (2S,3aR,6S,6aR)-N-(cyclohexylmethyl)-6-(5-((R)-3-(pyrrolidin-1-ylmethyl)phenyl)-1H-tetrazol-1-yl)hexahydrofuro[3,2-b]furan-2-amine::(2S,3aR,6S,6aR)-N-(cyclohexylmethyl)-6-(5-(3-(pyrrolidin-1-ylmethyl)phenyl)-1H-tetrazol-1-yl)hexahydrofuro[3,2-b]furan-2-amine::CHEMBL472003
SMILES C(N[C@@H]1C[C@H]2OC[C@@H]([C@H]2O1)n1nnnc1-c1cccc(CN2CCCC2)c1)C1CCCCC1
InChI Key InChIKey=LFRRGQXSMKOSOQ-UHFFFAOYSA-N
Data 3 IC50
Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB
Found 3 hits for monomerid = 50342002
TargetTyrosine-protein phosphatase non-receptor type 11(Human)
Max Planck Institute of Molecular Physiology
Curated by ChEMBL
Max Planck Institute of Molecular Physiology
Curated by ChEMBL
Affinity DataIC50: 2.50E+3nMAssay Description:Inhibition of SHP-2More data for this Ligand-Target Pair
TargetTyrosine-protein phosphatase non-receptor type 11(Human)
Max Planck Institute of Molecular Physiology
Curated by ChEMBL
Max Planck Institute of Molecular Physiology
Curated by ChEMBL
Affinity DataIC50: 2.47E+3nMAssay Description:Inhibition of SHP2 catalytic domain (unknown origin) using p-nitrophenyl phosphate as substrate incubated for 10 to 15 minsMore data for this Ligand-Target Pair
TargetTyrosine-protein phosphatase non-receptor type 11(Human)
Max Planck Institute of Molecular Physiology
Curated by ChEMBL
Max Planck Institute of Molecular Physiology
Curated by ChEMBL
Affinity DataIC50: 2.47E+3nMAssay Description:Inhibition of SHP2 (unknown origin)More data for this Ligand-Target Pair