BDBM50133006 (6-Bromo-1H-indol-2-yl)-(4-methyl-piperazin-1-yl)-methanone::(6-bromo-1H-indol-2-yl)(4-methylpiperazin-1-yl)methanone::CHEMBL338001

SMILES CN1CCN(CC1)C(=O)c1cc2ccc(Br)cc2[nH]1

InChI Key InChIKey=YLJOIPRHXDRNJT-UHFFFAOYSA-N

Data  2 KI

  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 2 hits for monomerid = 50133006   

TargetHistamine H4 receptor(Homo sapiens (Human))
Johnson & Johnson Pharmaceutical Research And Development

Curated by ChEMBL
LigandPNGBDBM50133006((6-Bromo-1H-indol-2-yl)-(4-methyl-piperazin-1-yl)-...)
Affinity DataKi:  147nMAssay Description:Displacement of [3H]- histamine from the recombinant human histamine H4 receptorMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistamine H4 receptor(Homo sapiens (Human))
Johnson & Johnson Pharmaceutical Research And Development

Curated by ChEMBL
LigandPNGBDBM50133006((6-Bromo-1H-indol-2-yl)-(4-methyl-piperazin-1-yl)-...)
Affinity DataKi:  147nMAssay Description:Displacement of [3H]histamine from recombinant human histamine H4 receptor in SK-N-MC cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed