BDBM50271513 1-(4-(4-bromophenoxy)butyl)-1H-imidazole::CHEMBL452156

SMILES Brc1ccc(OCCCCn2ccnc2)cc1

InChI Key InChIKey=NXYDWSHWKLXSEW-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 = 50271513   

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

Curated by ChEMBL
LigandPNGBDBM50271513(1-(4-(4-bromophenoxy)butyl)-1H-imidazole | CHEMBL4...)
Affinity DataKi:  3.20E+4nMAssay 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
LigandPNGBDBM50271513(1-(4-(4-bromophenoxy)butyl)-1H-imidazole | CHEMBL4...)
Affinity DataIC50:  7.50E+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
LigandPNGBDBM50271513(1-(4-(4-bromophenoxy)butyl)-1H-imidazole | CHEMBL4...)
Affinity DataIC50:  3.10E+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