BDBM50483312 CHEMBL1641856

SMILES [#6]-[#6]-[#6](-[#6])-[#6](=O)-c1c(-[#8])c(-[#6]\[#6]=[#6](\[#6])-[#6])c(-[#8])c2c(cc(=O)oc12)-[#6](-[#6]-[#6])-[#8]-[#6](-[#6])=O

InChI Key InChIKey=GJFFYBHPULADFV-UHFFFAOYSA-N

Data  4 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 4 hits for monomerid = 50483312   

LigandPNGBDBM50483312(CHEMBL1641856)
Affinity DataIC50: 890nMAssay Description:Inhibition of 1, 10-phenanthroline-induced HIF1 activation in human T47D cells by HRE3-TK-luciferase reporter gene assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/28/2020
Entry Details Article
PubMed
LigandPNGBDBM50483312(CHEMBL1641856)
Affinity DataIC50: 960nMAssay Description:Inhibition of hypoxia-induced HIF1 activation in human T47D cells by HRE3-TK-luciferase reporter gene assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/28/2020
Entry Details Article
PubMed
LigandPNGBDBM50483312(CHEMBL1641856)
Affinity DataIC50: 2.00E+3nMAssay Description:Inhibition of hypoxia-induced HIF1 activation in human PC3 cells by HRE3-TK-luciferase reporter gene assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/28/2020
Entry Details Article
PubMed
LigandPNGBDBM50483312(CHEMBL1641856)
Affinity DataIC50: 6.50E+3nMAssay Description:Inhibition of 1, 10-phenanthroline-induced HIF1 activation in human PC3 cells by HRE3-TK-luciferase reporter gene assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/28/2020
Entry Details Article
PubMed