BDBM50349975 CHEMBL1812593

SMILES [#6]\[#6](-[#6])=[#6]\[#6]-c1cc(ccc1-[#8])-c1coc2cc(-[#8])cc(-[#8])c2c1=O

InChI Key InChIKey=SWDSVBNAMCDHTF-UHFFFAOYSA-N

Data  3 IC50

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 3 hits for monomerid = 50349975   

TargetEnoyl-ACP reductase(Plasmodium falciparum)
University Of Yaounde

Curated by ChEMBL
LigandPNGBDBM50349975(CHEMBL1812593)
Affinity DataIC50:  2.48E+5nMAssay Description:Inhibition of Plasmodium falciparum Enoyl-ACP reductase using crotonyl-CoA as substrate peincubated for 5 mins measured after 10 mins of substrate ad...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetNeuraminidase(Influenza A virus)
Chosun University

Curated by ChEMBL
LigandPNGBDBM50349975(CHEMBL1812593)
Affinity DataIC50: >1.47E+5nMAssay Description:Inhibition of influenza A virus H9N2 Neuraminidase using 4-methylumbelliferyl-alpha-D-N-acetylneuraminic acid sodium salt hydrate substrateMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetNeuraminidase(Influenza A virus)
Chosun University

Curated by ChEMBL
LigandPNGBDBM50349975(CHEMBL1812593)
Affinity DataIC50: >1.47E+5nMAssay Description:Inhibition of influenza A virus H1N1 Neuraminidase using 4-methylumbelliferyl-alpha-D-N-acetylneuraminic acid sodium salt hydrate substrateMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed