BDBM10027 5-[2-(1H-imidazol-1-yl)ethyl]-7,8-dihydroquinoline::5-[2-(Imidazol-1-yl)ethyl]-7,8-dihydroquinoline::CHEMBL293122::dihydroquinoline 31

SMILES C(Cn1ccnc1)C1=CCCc2ncccc12

InChI Key InChIKey=DJMSMHXCSIBVSA-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 = 10027   

TargetAromatase(Homo sapiens (Human))
Universitat Des Saarlandes

LigandPNGBDBM10027(5-[2-(1H-imidazol-1-yl)ethyl]-7,8-dihydroquinoline...)
Affinity DataIC50:  500nMpH: 7.4 T: 2°CAssay Description:The enzyme activity was assayed by measuring the 3H-labeled H2O formed from [1beta,2beta-3H]testosterone during aromatization. After incubation, the ...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
Universitat Des Saarlandes

LigandPNGBDBM10027(5-[2-(1H-imidazol-1-yl)ethyl]-7,8-dihydroquinoline...)
Affinity DataIC50:  500nMAssay 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 ArticlePubMed
TargetAromatase(Homo sapiens (Human))
Universitat Des Saarlandes

LigandPNGBDBM10027(5-[2-(1H-imidazol-1-yl)ethyl]-7,8-dihydroquinoline...)
Affinity DataIC50:  500nMAssay Description:Inhibition of aromatase (unknown origin)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetThromboxane-A synthase(Homo sapiens (Human))
Universitat Des Saarlandes

LigandPNGBDBM10027(5-[2-(1H-imidazol-1-yl)ethyl]-7,8-dihydroquinoline...)
Affinity DataIC50:  290nMAssay Description:Thromboxane A2 synthase activity was assayed by measuring the fragmentation of prostaglandin H2 to form 12-hydroxy-5, 8,10-heptadecatrienoic acid and...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed