null
SMILES OC[C@H]1O[C@H](NC(=O)CCCCCNC(=O)CCCC[C@@H]2SC[C@@H]3NC(=O)N[C@H]23)[C@@H](O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O[C@H]3O[C@H](CO)[C@@H](O)[C@H](O[C@H]4O[C@H](CO)[C@@H](O)[C@H](O[C@H]5O[C@H](CO)[C@@H](O)[C@H](O)[C@@H]5O)[C@@H]4O)[C@@H]3O)[C@@H]2O)[C@@H](O)[C@@H]1O
InChI Key InChIKey=MGVBEWOSAICSFV-ASIRHVQNSA-N
Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB
Found 4 hits for monomerid = 50179256
Affinity DataIC50: 1.85E+3nMAssay Description:Inhibitory activity against human platelet heparanase by Microcon ultrafiltration assayMore data for this Ligand-Target Pair
TargetVascular endothelial growth factor A(Homo sapiens (Human))
Progen Industries Limited
Curated by ChEMBL
Progen Industries Limited
Curated by ChEMBL
Affinity DataKd: 7.20nMAssay Description:Binding affinity for VEGF by BIAcore solution affinity assayMore data for this Ligand-Target Pair
Affinity DataKd: 0.390nMAssay Description:Binding affinity for FGF1 by BIAcore solution affinity assayMore data for this Ligand-Target Pair
Affinity DataKd: 84nMAssay Description:Binding affinity for FGF2 by BIAcore solution affinity assayMore data for this Ligand-Target Pair