BDBM214778 OPRT inhibitor, 1

SMILES OC[C@H]1O[C@@H](Oc2ccc(cc2)[N+]([O-])=O)C(O)C1O

InChI Key InChIKey=DUYYBTBDYZXISX-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 = 214778   

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

LigandPNGBDBM214778(OPRT inhibitor, 1 )
Affinity DataKi:  120nM ΔG°:  -9.43kcal/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
In Depth
Date in BDB:
3/1/2017
Entry Details Article
PubMed
TargetOrotate phosphoribosyltransferase(Plasmodium falciparum (isolate 3D7))
Albert Einstein College of Medicine

LigandPNGBDBM214778(OPRT inhibitor, 1 )
Affinity DataKi:  190nM ΔG°:  -9.16kcal/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
In Depth
Date in BDB:
3/1/2017
Entry Details Article
PubMed