null

SMILES CC(=O)N1CCC(CC1)Oc1ccc(F)c2CN(Cc12)c1cn[nH]c(=O)c1C(F)(F)F

InChI Key InChIKey=IUVYVCGUKJBIII-UHFFFAOYSA-N

  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 = 431013   

TargetProtein mono-ADP-ribosyltransferase TIPARP(Human)
Ribon Therapeutics Inc.

US Patent
LigandPNGBDBM431013(5-[4-[(1-acetylpiperidin-4-yl)oxy]-7-fluoro-2,3-di...)copy SMILEScopy InChI
Affinity DataIC50: 100nMAssay Description:Displacement of Probe A, a biotinylated probe binding to the TIPARP active site, was measured using a time-resolved fluorescence energy transfer (TR-...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2JM2D1ZUS Patent
TargetProtein mono-ADP-ribosyltransferase TIPARP(Human)
Ribon Therapeutics Inc.

US Patent
LigandPNGBDBM431013(5-[4-[(1-acetylpiperidin-4-yl)oxy]-7-fluoro-2,3-di...)copy SMILEScopy InChI
Affinity DataIC50: 100nMAssay Description:Displacement of Probe A, a biotinylated probe binding to the TIPARP active site, was measured using a time-resolved fluorescence energy transfer (TR-...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2V69NPPUS Patent
TargetProtein mono-ADP-ribosyltransferase TIPARP(Human)
Ribon Therapeutics Inc.

US Patent
LigandPNGBDBM431013(5-[4-[(1-acetylpiperidin-4-yl)oxy]-7-fluoro-2,3-di...)copy SMILEScopy InChI
Affinity DataIC50: 100nMAssay Description:Displacement of Probe A, a biotinylated probe binding to the TIPARP active site, was measured using a time-resolved fluorescence energy transfer (TR-...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2VQ35S4US Patent