BDBM50327485 (R)-8-(1-isopropylpiperidin-4-yloxy)-4-methyl-3,4-dihydropyrazino[1,2-a]indol-1(2H)-one::CHEMBL1257851

SMILES CC(C)N1CCC(CC1)Oc1ccc2n3[C@H](C)CNC(=O)c3cc2c1

InChI Key InChIKey=JGXUYJUQTMMZNX-CQSZACIVSA-N

Data  1 KI  3 IC50  1 EC50

  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 = 50327485   

TargetHistamine H3 receptor(Human)
F. Hoffmann-La Roche

Curated by ChEMBL
LigandPNGBDBM50327485((R)-8-(1-isopropylpiperidin-4-yloxy)-4-methyl-3,4-...)
Affinity DataKi:  26nMAssay Description:Displacement of [3H]-RAMH from human histamine H3 receptorMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed

TargetCytochrome P450 3A4(Human)
F. Hoffmann-La Roche

Curated by ChEMBL
LigandPNGBDBM50327485((R)-8-(1-isopropylpiperidin-4-yloxy)-4-methyl-3,4-...)
Affinity DataIC50: >5.00E+4nMAssay Description:Inhibition of CYP3A4More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed

TargetHistamine H3 receptor(Human)
F. Hoffmann-La Roche

Curated by ChEMBL
LigandPNGBDBM50327485((R)-8-(1-isopropylpiperidin-4-yloxy)-4-methyl-3,4-...)
Affinity DataEC50:  29nMAssay Description:Inverse agonist activity at human recombinant histamine H3 receptor assessed as effect on [35S]GTPgammaS bindingMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed

TargetCytochrome P450 2C9(Human)
F. Hoffmann-La Roche

Curated by ChEMBL
LigandPNGBDBM50327485((R)-8-(1-isopropylpiperidin-4-yloxy)-4-methyl-3,4-...)
Affinity DataIC50: >5.00E+4nMAssay Description:Inhibition of CYP2C9More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed

TargetCytochrome P450 2D6(Human)
F. Hoffmann-La Roche

Curated by ChEMBL
LigandPNGBDBM50327485((R)-8-(1-isopropylpiperidin-4-yloxy)-4-methyl-3,4-...)
Affinity DataIC50:  2.20E+4nMAssay Description:Inhibition of CYP2D6More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed