null
SMILES CCCCCCCCCC(O)(P(O)(O)=O)P(O)(O)=O
InChI Key InChIKey=NSCPCMXKWUFFNL-UHFFFAOYSA-N
PDB links: 1 PDB ID contains this monomer as substructures. 1 PDB ID contains inhibitors having a similarity of 90% to this monomer.
Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB
Found 10 hits for monomerid = 25269
TargetFarnesyl pyrophosphate synthase(Homo sapiens (Human))
University of Illinois at Urbana-Champaign
Curated by ChEMBL
University of Illinois at Urbana-Champaign
Curated by ChEMBL
Affinity DataKi: 230nMAssay Description:Binding affinity towards farnesyl Pyrophosphate Synthase using [14C]- isopentenyl pyrophosphate as radioligandMore data for this Ligand-Target Pair
TargetFarnesyl pyrophosphate synthase(Homo sapiens (Human))
University of Illinois at Urbana-Champaign
Curated by ChEMBL
University of Illinois at Urbana-Champaign
Curated by ChEMBL
Affinity DataIC50: 2.40E+3nMAssay Description:Inhibitory activity against farnesyl Pyrophosphate Synthase was determinedMore data for this Ligand-Target Pair
TargetGeranylgeranyl pyrophosphate synthase(Homo sapiens (Human))
University of Illinois at Urbana-Champaign
Curated by ChEMBL
University of Illinois at Urbana-Champaign
Curated by ChEMBL
Affinity DataIC50: 720nMAssay Description:Inhibitory activity against the human recombinant geranylgeranyl diphosphate synthase (GGPPSase).More data for this Ligand-Target Pair
TargetPhosphotransferase(Trypanosoma cruzi)
Instituto Venezolano de Investigaciones Cient£ficas
Curated by ChEMBL
Instituto Venezolano de Investigaciones Cient£ficas
Curated by ChEMBL
Affinity DataIC50: 810nMAssay Description:Inhibition of Trypanosoma cruzi hexokinaseMore data for this Ligand-Target Pair
TargetPhosphotransferase(Trypanosoma cruzi)
Instituto Venezolano de Investigaciones Cient£ficas
Curated by ChEMBL
Instituto Venezolano de Investigaciones Cient£ficas
Curated by ChEMBL
Affinity DataIC50: 2.75E+3nMAssay Description:Inhibitory activity against Trypanosoma cruzi hexokinaseMore data for this Ligand-Target Pair
TargetPolyprenyl synthetase family protein(Plasmodium falciparum (isolate 3D7))
University of Illinois at Urbana-Champaign
Curated by ChEMBL
University of Illinois at Urbana-Champaign
Curated by ChEMBL
Affinity DataIC50: 2.37E+3nMAssay Description:Inhibitory activity against FPPS in Leishmania majorMore data for this Ligand-Target Pair
TargetH(+)-exporting diphosphatase(Trypanosoma brucei)
University of Illinois at Urbana-Champaign
Curated by ChEMBL
University of Illinois at Urbana-Champaign
Curated by ChEMBL
Affinity DataIC50: 3.57E+5nMAssay Description:Inhibition of recombinant Trypanosoma brucei soluble vacuolar pyrophosphatase expressed in Escherichia coliMore data for this Ligand-Target Pair
TargetFarnesyl pyrophosphate synthase(Homo sapiens (Human))
University of Illinois at Urbana-Champaign
Curated by ChEMBL
University of Illinois at Urbana-Champaign
Curated by ChEMBL
Affinity DataIC50: 2.34E+3nMAssay Description:Inhibitory activity against farnesyl Pyrophosphate Synthase expressed as #NAME? (M)More data for this Ligand-Target Pair
TargetGeranylgeranyl pyrophosphate synthase(Homo sapiens (Human))
University of Illinois at Urbana-Champaign
Curated by ChEMBL
University of Illinois at Urbana-Champaign
Curated by ChEMBL
Affinity DataIC50: 890nMpH: 7.0 T: 2°CAssay Description:The inhibitory activity of each test compound was evaluated by monitoring the formation of [14C]GGPP from FPP, using [14C]IPP as the substrate. To co...More data for this Ligand-Target Pair
TargetPolyprenyl synthetase family protein(Plasmodium falciparum (isolate 3D7))
University of Illinois at Urbana-Champaign
Curated by ChEMBL
University of Illinois at Urbana-Champaign
Curated by ChEMBL
Affinity DataIC50: 2.37E+3nMAssay Description:Inhibitory activity against Leishmania major Farnesyl diphosphate synthaseMore data for this Ligand-Target Pair