Compile Data Set for Download or QSAR
Report error Found 11 Enz. Inhib. hit(s) with all data for entry = 50022187
TargetFarnesyl pyrophosphate synthase(Human)
National Research Centre

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 12578BDBM12578(CHEMBL924 | [1-hydroxy-2-(1H-imidazol-1-yl)-1-phos...)
Affinity DataIC50: 550nMAssay Description:Inhibition of human recombinant FPPS using IPP as substrate preincubated with enzyme for 15 mins followed by substrate addition and measured after 1 ...More data for this Ligand-Target Pair
In Depth
Date in BDB:
10/12/2025
Entry Details
PubMedPDB3D3D Structure (crystal)
TargetFarnesyl pyrophosphate synthase(Human)
National Research Centre

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50649163BDBM50649163(CHEMBL5619915)
Affinity DataIC50: 1.11E+3nMAssay Description:Inhibition of human recombinant FPPS using IPP as substrate preincubated with enzyme for 15 mins followed by substrate addition and measured after 1 ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In Depth
Date in BDB:
10/12/2025
Entry Details
PubMed
TargetFarnesyl pyrophosphate synthase(Human)
National Research Centre

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50649164BDBM50649164(CHEMBL5618314)
Affinity DataIC50: 1.24E+3nMAssay Description:Inhibition of human recombinant FPPS using IPP as substrate preincubated with enzyme for 15 mins followed by substrate addition and measured after 1 ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In Depth
Date in BDB:
10/12/2025
Entry Details
PubMed
TargetFarnesyl pyrophosphate synthase(Human)
National Research Centre

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50649169BDBM50649169(CHEMBL5618430)
Affinity DataIC50: 2.47E+3nMAssay Description:Inhibition of human recombinant FPPS using IPP as substrate preincubated with enzyme for 15 mins followed by substrate addition and measured after 1 ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In Depth
Date in BDB:
10/12/2025
Entry Details
PubMed
TargetFarnesyl pyrophosphate synthase(Human)
National Research Centre

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50649166BDBM50649166(CHEMBL5618141)
Affinity DataIC50: 3.22E+3nMAssay Description:Inhibition of human recombinant FPPS using IPP as substrate preincubated with enzyme for 15 mins followed by substrate addition and measured after 1 ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In Depth
Date in BDB:
10/12/2025
Entry Details
PubMed
TargetFarnesyl pyrophosphate synthase(Human)
National Research Centre

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50649171BDBM50649171(CHEMBL5619264)
Affinity DataIC50: 3.37E+3nMAssay Description:Inhibition of human recombinant FPPS using IPP as substrate preincubated with enzyme for 15 mins followed by substrate addition and measured after 1 ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In Depth
Date in BDB:
10/12/2025
Entry Details
PubMed
TargetFarnesyl pyrophosphate synthase(Human)
National Research Centre

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50649168BDBM50649168(CHEMBL5618666)
Affinity DataIC50: 5.54E+3nMAssay Description:Inhibition of human recombinant FPPS using IPP as substrate preincubated with enzyme for 15 mins followed by substrate addition and measured after 1 ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In Depth
Date in BDB:
10/12/2025
Entry Details
PubMed
TargetFarnesyl pyrophosphate synthase(Human)
National Research Centre

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50649165BDBM50649165(CHEMBL5619062)
Affinity DataIC50: 5.98E+3nMAssay Description:Inhibition of human recombinant FPPS using IPP as substrate preincubated with enzyme for 15 mins followed by substrate addition and measured after 1 ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In Depth
Date in BDB:
10/12/2025
Entry Details
PubMed
TargetFarnesyl pyrophosphate synthase(Human)
National Research Centre

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50649162BDBM50649162(CHEMBL5619109)
Affinity DataIC50: 1.26E+4nMAssay Description:Inhibition of human recombinant FPPS using IPP as substrate preincubated with enzyme for 15 mins followed by substrate addition and measured after 1 ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In Depth
Date in BDB:
10/12/2025
Entry Details
PubMed
TargetFarnesyl pyrophosphate synthase(Human)
National Research Centre

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50649167BDBM50649167(CHEMBL5619920)
Affinity DataIC50: 2.14E+4nMAssay Description:Inhibition of human recombinant FPPS using IPP as substrate preincubated with enzyme for 15 mins followed by substrate addition and measured after 1 ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In Depth
Date in BDB:
10/12/2025
Entry Details
PubMed
TargetFarnesyl pyrophosphate synthase(Human)
National Research Centre

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50649170BDBM50649170(CHEMBL5619599)
Affinity DataIC50: 2.27E+4nMAssay Description:Inhibition of human recombinant FPPS using IPP as substrate preincubated with enzyme for 15 mins followed by substrate addition and measured after 1 ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In Depth
Date in BDB:
10/12/2025
Entry Details
PubMed