BDBM8620 (4-Pyridylmethylene)indane 10a::4-{[(1E)-5-bromo-2,3-dihydro-1H-inden-1-ylidene]methyl}pyridine

SMILES Brc1ccc2\C(CCc2c1)=C\c1ccncc1

InChI Key InChIKey=MNQUPNOEJZVKRD-FMIVXFBMSA-N

Data  5 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 5 hits for monomerid = 8620   

TargetCytochrome P450 11B1, mitochondrial(Homo sapiens (Human))
Saarland University

LigandPNGBDBM8620((4-Pyridylmethylene)indane 10a | 4-{[(1E)-5-bromo-...)
Affinity DataIC50:  948nMAssay Description:The enzyme activity was assayed by monitoring the conversion of deoxycorticosterone to corticosterone in the presence of inhibitor compounds. The pro...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCytochrome P450 11B2, mitochondrial(Homo sapiens (Human))
Saarland University

LigandPNGBDBM8620((4-Pyridylmethylene)indane 10a | 4-{[(1E)-5-bromo-...)
Affinity DataIC50:  2.64E+3nMAssay Description:The enzyme activity was assayed by monitoring the conversion of deoxycorticosterone to corticosterone in the presence of inhibitor compounds. The pro...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
University Of Calcutta

Curated by ChEMBL
LigandPNGBDBM8620((4-Pyridylmethylene)indane 10a | 4-{[(1E)-5-bromo-...)
Affinity DataIC50:  3.40E+3nMAssay Description:Inhibition of aromataseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
University Of Calcutta

Curated by ChEMBL
LigandPNGBDBM8620((4-Pyridylmethylene)indane 10a | 4-{[(1E)-5-bromo-...)
Affinity DataIC50:  3.40E+3nMAssay Description:Inhibition of aromataseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
University Of Calcutta

Curated by ChEMBL
LigandPNGBDBM8620((4-Pyridylmethylene)indane 10a | 4-{[(1E)-5-bromo-...)
Affinity DataIC50: >3.60E+4nMAssay Description:The enzyme activity was assayed by measuring the 3H-labeled H2O formed from [1beta-3H] Androstenedione during aromatization. After incubation, the re...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed