BDBM50568078 CHEMBL4865518
SMILES [H][C@]12[C@H](C[C@@]3(C)C4=CCC5C(C)(C)[C@]([H])(CC[C@]5(C)[C@]4([H])CC[C@]13C(=O)O[C@@]2(C)CCCC(C)=C)O[C@@H]1OC[C@@H](OS([O-])(=O)=O)[C@H](O)[C@@]1([H])O[C@@H]1O[C@H](C)[C@@H](O[C@]2([H])OC[C@@H](O)[C@H](O[C@]3([H])O[C@H](CO)[C@@H](O)[C@H](OC)[C@H]3O)[C@H]2O)[C@H](O)[C@H]1O)OC(C)=O
InChI Key InChIKey=RCKPXCOTGSEBPP-UHFFFAOYSA-M
Data 2 IC50
Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB
Found 2 hits for monomerid = 50568078
Affinity DataIC50: 2.20E+3nMAssay Description:Inhibition of VEGFR2 in mouse NIH/3T3 cells assessed as reduction of VEGF-stimulated phosphorylationMore data for this Ligand-Target Pair
Affinity DataIC50: 4.80E+3nMAssay Description:Inhibition of PDGFRbeta in mouse NIH/3T3 cells assessed as reduction of PDGF-BB-stimulated phosphorylationMore data for this Ligand-Target Pair