BDBM50271548 1-(4-(2-bromophenoxy)butyl)-1H-imidazole::CHEMBL504297

SMILES Brc1ccccc1OCCCCn1ccnc1

InChI Key InChIKey=ITQSGIJZBMXRMD-UHFFFAOYSA-N

Data  1 KI  2 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 3 hits for monomerid = 50271548   

TargetNitric oxide synthase, brain(Homo sapiens (Human))
Instituto De QuíMica MéDica

Curated by ChEMBL
LigandPNGBDBM50271548(1-(4-(2-bromophenoxy)butyl)-1H-imidazole | CHEMBL5...)
Affinity DataKi:  1.80E+5nMAssay Description:Inhibition of nNOS (unknown origin) assessed as conversion of L-[3H]arginine to L-[3H]citrullineMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHeme oxygenase 2(Rattus norvegicus (rat))
University Of Catania

Curated by ChEMBL
LigandPNGBDBM50271548(1-(4-(2-bromophenoxy)butyl)-1H-imidazole | CHEMBL5...)
Affinity DataIC50:  2.40E+4nMAssay 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 DepthDetails ArticlePubMed
TargetHeme oxygenase 1(Rattus norvegicus (rat))
University Of Catania

Curated by ChEMBL
LigandPNGBDBM50271548(1-(4-(2-bromophenoxy)butyl)-1H-imidazole | CHEMBL5...)
Affinity DataIC50:  5.30E+4nMAssay 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 DepthDetails ArticlePubMed