BDBM50601266 CHEMBL5173479

SMILES [H][C@@]12[#6]-[#6]-[#6@@H](-[#6])[C@@]1([H])[#6@H](-[#8]-[#6](=O)\[#6]=[#6]\c1ccccc1)[C@@]1([#6]-[#6@@H](-[#8]-[#6](=O)-[#6]-[#8]-[#6](=O)\[#6]=[#6](\[#6])-[#6])[C@@]2([#6])[#8]1)[#6](-[#6])-[#6]

InChI Key InChIKey=AVGYEYLWRMVZCM-XBHLXOTJSA-N

Data  1 EC50

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
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   Substructure
Similarity at least:  must be >=0.5
Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 1 hit for monomerid = 50601266   

TargetShort transient receptor potential channel 5(Homo sapiens (Human))
National Cancer Institute

Curated by ChEMBL
LigandPNGBDBM50601266(CHEMBL5173479)
Affinity DataEC50:  1.25E+3nMAssay Description:Agonist activity at human TRPC5 stably expressed in T-REx-293 cells assessed as increase in calcium flux by Fura-2AM dye based fluorescence plate rea...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails PubMed