null

SMILES Nc1ncc(OCc2ccccc2)c(N)n1

InChI Key InChIKey=QTGZSAGXWPWQQX-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 4 hits for monomerid = 50391240   

TargetRas-related C3 botulinum toxin substrate 1(Homo sapiens (Human))TBA
LigandPNGBDBM50391240(CHEBI:76228 | CHEMBL496240)copy SMILEScopy InChI
Affinity DataEC50:  574nMAssay Description:In vitro inhibition of angiotensin I converting enzyme in rabbit lung with hippuryl-histidyl-leucine as substrateMore data for this Ligand-Target Pair
In DepthDetails Article
TargetProstaglandin G/H synthase 1(Homo sapiens (Human))TBA
LigandPNGBDBM50391240(CHEBI:76228 | CHEMBL496240)copy SMILEScopy InChI
Affinity DataIC50: 460nMMore data for this Ligand-Target Pair
In DepthDetails
TargetProstaglandin G/H synthase 2(Homo sapiens (Human))TBA
LigandPNGBDBM50391240(CHEBI:76228 | CHEMBL496240)copy SMILEScopy InChI
Affinity DataIC50: 1.46E+3nMMore data for this Ligand-Target Pair
In DepthDetails
TargetCell division control protein 42 homolog(Homo sapiens (Human))TBA
LigandPNGBDBM50391240(CHEBI:76228 | CHEMBL496240)copy SMILEScopy InChI
Affinity DataEC50:  1.07E+3nMAssay Description:In vitro inhibition of angiotensin I converting enzyme in rabbit lung with hippuryl-histidyl-leucine as substrateMore data for this Ligand-Target Pair
In DepthDetails Article