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SMILES [Na;v0+].[Na;v0+].[Na;v0+].[Na;v0+].[Na;v0+].[Na;v0+].[Na;v0+].[Na;v0+].[Na;v0+].[Na;v0+].[Na;v0+].[Na;v0+].[Na;v0+].[H][C@@]1([#6]-[#6][C@@]2([H])[C@]3([H])[#6]-[#6][C@@]4([H])[#6][C@]([H])([#6]-[#6][C@]4([#6])[C@@]3([H])[#6]-[#6][C@]12[#6])[#8]-[#6@@H]-1-[#8]-[#6@H](-[#6]-[#8]S([#8-])(=O)=O)-[#6@@H](-[#8][C@]2([H])[#8]-[#6@H](-[#6]-[#8]S([#8-])(=O)=O)-[#6@@H](-[#8][C@]3([H])[#8]-[#6@H](-[#6]-[#8]S([#8-])(=O)=O)-[#6@@H](-[#8][C@]4([H])[#8]-[#6@H](-[#6]-[#8]S([#8-])(=O)=O)-[#6@@H](-[#8]S([#8-])(=O)=O)-[#6@H](-[#8]S([#8-])(=O)=O)-[#6@H]4-[#8]S([#8-])(=O)=O)-[#6@H](-[#8]S([#8-])(=O)=O)-[#6@H]3-[#8]S([#8-])(=O)=O)-[#6@H](-[#8]S([#8-])(=O)=O)-[#6@H]2-[#8]S([#8-])(=O)=O)-[#6@H](-[#8]S([#8-])(=O)=O)-[#6@H]-1-[#8]S([#8-])(=O)=O)[#6@H](-[#6])-[#6]-[#6]-[#6]-[#6](-[#6])-[#6]

InChI Key

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
Find this compound or compounds like it in BindingDB:
   Substructure
Similarity at least:  must be >=0.5
Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 1 hit for monomerid = 50612819   

TargetHeparanase(Homo sapiens (Human))TBA
LigandPNGBDBM50612819(CHEMBL5291042)copy SMILES
Affinity DataIC50: 12nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails