BDBM214781 OPRT inhibitor, 4

SMILES OC1C(O)[C@H](Cn2cc(Br)c(=O)[nH]c2=O)[NH2+][C@@H]1COP(O)(O)=O

InChI Key

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 = 214781   

TargetUridine 5'-monophosphate synthase(Homo sapiens (Human))
Albert Einstein College of Medicine

LigandPNGBDBM214781(OPRT inhibitor, 4)
Affinity DataKi:  200nM ΔG°:  -9.13kcal/molepH: 8.0 T: 2°CAssay Description:Inhibition constants (Ki, equivalent to Kd for competitive inhibitors) were measured at 25 °C by adding purified OPRT enzymes (25 nM for PfOPRT a...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetOrotate phosphoribosyltransferase(Plasmodium falciparum)
Albert Einstein College of Medicine

LigandPNGBDBM214781(OPRT inhibitor, 4)
Affinity DataKi:  370nM ΔG°:  -8.77kcal/molepH: 8.0 T: 2°CAssay Description:Inhibition constants (Ki, equivalent to Kd for competitive inhibitors) were measured at 25 °C by adding purified OPRT enzymes (25 nM for PfOPRT a...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed