BDBM5279 3-carbamimidamido-4-[2-(hydroxymethyl)-5-oxopyrrolidin-1-yl]benzoic acid::Benzoic Acid Analog 8::CHEMBL57426

SMILES NC(=N)Nc1cc(ccc1N1C(CO)CCC1=O)C(O)=O

InChI Key InChIKey=JKEFEWCCNRASGF-UHFFFAOYSA-N

Data  4 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 4 hits for monomerid = 5279   

TargetNeuraminidase(Influenza A virus (N9))
University Of Alabama At Birmingham

LigandPNGBDBM5279(3-carbamimidamido-4-[2-(hydroxymethyl)-5-oxopyrrol...)
Affinity DataIC50:  2.00E+4nMpH: 6.5 T: 2°CAssay Description:A standard fluorimetric assay was used to measure influenza virus neuraminidase activity. The substrate 2 -(4-methylumbelliferyl)-alpha-D-acetylneura...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetNeuraminidase(Influenza A virus (A/Puerto Rico/8/34/Mount Sinai(...)
University Of Alabama At Birmingham

Curated by ChEMBL
LigandPNGBDBM5279(3-carbamimidamido-4-[2-(hydroxymethyl)-5-oxopyrrol...)
Affinity DataIC50:  2.00E+4nMAssay Description:In vitro inhibitory activity of the compound against H1N9 Influenza A Neuraminidase.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetNeuraminidase(Influenza B virus (B/Lee/40))
University Of Alabama At Birmingham

Curated by ChEMBL
LigandPNGBDBM5279(3-carbamimidamido-4-[2-(hydroxymethyl)-5-oxopyrrol...)
Affinity DataIC50:  1.00E+4nMAssay Description:In vitro inhibitory activity of the compound against B/Lee/40 Influenza B Neuraminidase.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetNeuraminidase(Influenza B virus (B/Lee/40))
University Of Alabama At Birmingham

Curated by ChEMBL
LigandPNGBDBM5279(3-carbamimidamido-4-[2-(hydroxymethyl)-5-oxopyrrol...)
Affinity DataIC50:  1.00E+4nMpH: 6.5 T: 2°CAssay Description:A standard fluorimetric assay was used to measure influenza virus neuraminidase activity. The substrate 2 -(4-methylumbelliferyl)-alpha-D-acetylneura...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed