BDBM50458155 CHEMBL4210593

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@@]([#8]-[#6@@H]-1-[#8]-[#6@H](-[#6]-[#8]S([#8-])(=O)=O)-[#6@H](-[#8]S([#8-])(=O)=O)-[#6@H](-[#8][C@]2([H])[#8]-[#6@H](-[#6](-[#8-])=O)[C@@]([H])([#8]-[#6@@H]-3-[#8]-[#6@H](-[#6]-[#8]S([#8-])(=O)=O)-[#6@H](-[#8]S([#8-])(=O)=O)-[#6@H](-[#8][C@]4([H])[#8]-[#6](=[#6]-[#6@H](-[#8][C@]5([H])[#8]-[#6@@H](-[#6])-[#6@@H](-[#8]S([#8-])(=O)=O)-[#6@@H](-[#8])-[#6@@H]5-[#8]S([#8-])(=O)=O)-[#6@H]4-[#8])-[#6](-[#8-])=O)-[#6@H]-3-[#7]-[#6](-[#6])=O)[#6@H](-[#8][C@]3([H])[#8]-[#6@@H](-[#6])-[#6@@H](-[#8]S([#8-])(=O)=O)-[#6@@H](-[#8])-[#6@@H]3-[#8]S([#8-])(=O)=O)-[#6@H]2-[#8])-[#6@H]-1-[#7]-[#6](-[#6])=O)([#6@H](-[#8])-[#6](-[#8-])=O)[#6@H](-[#8][C@]1([H])[#8]-[#6@@H](-[#6])-[#6@@H](-[#8]S([#8-])(=O)=O)-[#6@@H](-[#8])-[#6@@H]1-[#8]S([#8-])(=O)=O)-[#6@@H](-[#8])-[#6]-[#8]

InChI Key InChIKey=ZYWFTWDFMCXFPN-LYLAQKFRSA-A

Data  1 IC50

  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 = 50458155   

TargetCoagulation factor IX/VIII(Homo sapiens (Human))
Chinese Academy of Sciences

Curated by ChEMBL
LigandPNGBDBM50458155(CHEMBL4210593)
Affinity DataIC50:  98.7nMAssay Description:Inhibition of human intrinsic factor tenase using factor-10 as substrate preincubated for 2 mins followed by substrate addition for 1 min measured ev...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed