BDBM50002333 1-(4-Fluoro-phenyl)-3-[4-(5-fluoro-pyrimidin-2-yl)-piperazin-1-yl]-propan-1-one::CHEMBL139711

SMILES Fc1ccc(cc1)C(=O)CCN1CCN(CC1)c1ncc(F)cn1

InChI Key InChIKey=BGPJHKCGFSWCLH-UHFFFAOYSA-N

Data  3 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 = 50002333   

TargetD(2) dopamine receptor(Rattus norvegicus (rat))
Bristol-Myers Squibb

Curated by ChEMBL
LigandPNGBDBM50002333(1-(4-Fluoro-phenyl)-3-[4-(5-fluoro-pyrimidin-2-yl)...)
Affinity DataIC50: >1.00E+3nMAssay Description:In vitro inhibitory concentration against radioligand [3H]spiperone binding to rat striatal dopamine receptor D2More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAlpha-1A/Alpha-1B/Alpha-1D adrenergic receptor(Rattus norvegicus (rat))
Bristol-Myers Squibb

Curated by ChEMBL
LigandPNGBDBM50002333(1-(4-Fluoro-phenyl)-3-[4-(5-fluoro-pyrimidin-2-yl)...)
Affinity DataIC50:  523nMAssay Description:In vitro inhibitory concentration against radioligand [3H]WB-4101 binding to rat cortical alpha-1 adrenergic receptorMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSigma non-opioid intracellular receptor 1(RAT)
Bristol-Myers Squibb

Curated by ChEMBL
LigandPNGBDBM50002333(1-(4-Fluoro-phenyl)-3-[4-(5-fluoro-pyrimidin-2-yl)...)
Affinity DataIC50:  69nMAssay Description:Compound was tested in vitro for its ability to displace radioligand (+)-[3H]-3-PPP from rat cortical sigma receptorMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed