BDBM50271549 1-(4-(3-bromophenoxy)butyl)-1H-imidazole::CHEMBL482686

SMILES Brc1cccc(OCCCCn2ccnc2)c1

InChI Key InChIKey=QWYZAVYFCGPMDM-UHFFFAOYSA-N

Data  1 KI  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 6 hits for monomerid = 50271549   

TargetHeme oxygenase 2(Rat)
University of Catania

Curated by ChEMBL
LigandPNGBDBM50271549(1-(4-(3-bromophenoxy)butyl)-1H-imidazole | CHEMBL4...)
Affinity DataIC50: 2.20E+3nMAssay Description:Inhibition of Sprague-Dawley rat brain HO-2 assessed as bilirubin formation after 60 mins by spectrophotometric analysisMore data for this Ligand-Target Pair
In Depth
Date in BDB:
4/13/2014
Entry Details Article
PubMed
TargetHeme oxygenase 1(Rat)
University of Catania

Curated by ChEMBL
LigandPNGBDBM50271549(1-(4-(3-bromophenoxy)butyl)-1H-imidazole | CHEMBL4...)
Affinity DataIC50: 2.10E+3nMAssay Description:Inhibition of Sprague-Dawley rat spleen microsomal HO-1 assessed as bilirubin formation after 60 mins by spectrophotometric analysisMore data for this Ligand-Target Pair
In Depth
Date in BDB:
4/13/2014
Entry Details Article
PubMed
TargetHeme oxygenase 1(Rat)
University of Catania

Curated by ChEMBL
LigandPNGBDBM50271549(1-(4-(3-bromophenoxy)butyl)-1H-imidazole | CHEMBL4...)
Affinity DataIC50: 2.10E+3nMAssay Description:Inhibition of heme oxygenase 1 in Sprague-Dawley rat spleen microsomal fraction assessed as decrease in bilirubin formation using biliverdin reductas...More data for this Ligand-Target Pair
In Depth
Date in BDB:
8/18/2020
Entry Details Article
PubMed
TargetHeme oxygenase 2(Human)
University of Catania

Curated by ChEMBL
LigandPNGBDBM50271549(1-(4-(3-bromophenoxy)butyl)-1H-imidazole | CHEMBL4...)
Affinity DataIC50: 2.20E+3nMAssay Description:Inhibition of HO-2 (unknown origin)More data for this Ligand-Target Pair
In Depth
Date in BDB:
2/28/2021
Entry Details Article
PubMed
TargetHeme oxygenase 1(Rat)
University of Catania

Curated by ChEMBL
LigandPNGBDBM50271549(1-(4-(3-bromophenoxy)butyl)-1H-imidazole | CHEMBL4...)
Affinity DataIC50: 2.10E+3nMAssay Description:Inhibition of HO-1 in Sprague-Dawley rat spleen microsomes using NADPH as substrate incubated for 60 mins by spectrometry based assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
2/28/2021
Entry Details Article
PubMed
TargetNitric oxide synthase, brain(Human)
Instituto De QuíMica MéDica

Curated by ChEMBL
LigandPNGBDBM50271549(1-(4-(3-bromophenoxy)butyl)-1H-imidazole | CHEMBL4...)
Affinity DataKi:  6.00E+4nMAssay Description:Inhibition of nNOS assessed as conversion of L-[3H]arginine to L-[3H]citrullineMore data for this Ligand-Target Pair
In Depth
Date in BDB:
1/11/2010
Entry Details Article
PubMed