null

SMILES COc1ccc2c(c1)oc(-c1ccc(cc1)[N+]([O-])=O)c(Cn1ccnc1)c2=O

InChI Key InChIKey=DTEZOESXMOWJRN-UHFFFAOYSA-N

  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 = 50191603   

TargetAromatase(Homo sapiens (Human))
University of Bologna

Curated by ChEMBL
LigandPNGBDBM50191603(3-((1H-imidazol-1-yl)methyl)-7-methoxy-2-(4-nitrop...)copy SMILEScopy InChI
Affinity DataIC50: 468nMAssay Description:Inhibition of CYP19More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2668CTWPubMed
TargetAromatase(Homo sapiens (Human))
University of Bologna

Curated by ChEMBL
LigandPNGBDBM50191603(3-((1H-imidazol-1-yl)methyl)-7-methoxy-2-(4-nitrop...)copy SMILEScopy InChI
Affinity DataIC50: 470nMAssay Description:Inhibition of human aromatase-mediated conversion of [1beta3H]androstenedione to estrone by liquid scintillation counting in presence of NADPHMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2SQ9080PubMed
TargetAromatase(Homo sapiens (Human))
University of Bologna

Curated by ChEMBL
LigandPNGBDBM50191603(3-((1H-imidazol-1-yl)methyl)-7-methoxy-2-(4-nitrop...)copy SMILEScopy InChI
Affinity DataIC50: 468nMAssay Description:Inhibition of CYP19More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2668CTWPubMed