Compile Data Set for Download or QSAR
Report error Found 9 Enz. Inhib. hit(s) with all data for entry = 7942
TargetCytochrome P450 3A4(Human)
Gilead Sciences

US Patent
LigandChemical structure of BindingDB Monomer ID 50134248BDBM50134248(Alpha-Hydroxy-Midazolam | [8-Chloro-6-(2-fluoro-ph...)
Affinity DataIC50: 2.70E+3nMAssay Description:Six test compound concentrations (0.1, 0.25, 1, 2.5, 10, 25 μM in DMSO; final DMSO concentration=0.26%) are incubated with human liver microsome...More data for this Ligand-Target Pair
In Depth
Date in BDB:
5/8/2017
Entry Details
US Patent

TargetCytochrome P450 3A4(Human)
Gilead Sciences

US Patent
LigandChemical structure of BindingDB Monomer ID 224815BDBM224815(US9333197, 6beta Hydroxytestosterone)
Affinity DataIC50: 1.05E+4nMAssay Description:Six test compound concentrations (0.1, 0.25, 1, 2.5, 10, 25 μM in DMSO; final DMSO concentration=0.275%) are incubated with human liver microsom...More data for this Ligand-Target Pair
In Depth
Date in BDB:
5/8/2017
Entry Details
US Patent

TargetCytochrome P450 2D6(Human)
Gilead Sciences

US Patent
LigandChemical structure of BindingDB Monomer ID 224023BDBM224023(Dextrorphan)
Affinity DataIC50: 1.77E+4nMAssay Description:Six test compound concentrations (0.1, 0.25, 1, 2.5, 10, 25 μM in DMSO; final DMSO concentration=0.25%) are incubated with human liver microsome...More data for this Ligand-Target Pair
In Depth
Date in BDB:
5/8/2017
Entry Details
US Patent

TargetCytochrome P450 2B6(Human)
Gilead Sciences

US Patent
LigandChemical structure of BindingDB Monomer ID 224811BDBM224811(US9333197, Hydroxybupropion)
Affinity DataIC50: 1.92E+4nMAssay Description:Six test compound concentrations (0.1, 0.25, 1, 2.5, 10, 25 μM in DMSO; final DMSO concentration=0.3%) are incubated with human liver microsomes...More data for this Ligand-Target Pair
In Depth
Date in BDB:
5/8/2017
Entry Details
US Patent

TargetCytochrome P450 2C8(Human)
Gilead Sciences

US Patent
LigandChemical structure of BindingDB Monomer ID 224812BDBM224812(US9333197, 6alpha-Hydroxypaclitaxel)
Affinity DataIC50: 2.16E+4nMAssay Description:Six test compound concentrations (0.1, 0.25, 1, 2.5, 10, 25 μM in DMSO; final DMSO concentration=0.3%) are incubated with human liver microsomes...More data for this Ligand-Target Pair
In Depth
Date in BDB:
5/8/2017
Entry Details
US Patent

TargetCytochrome P450 2C9(Human)
Gilead Sciences

US Patent
LigandChemical structure of BindingDB Monomer ID 224813BDBM224813(US9333197, 4-Hydroxytolbutamide)
Affinity DataIC50: 2.50E+4nMAssay Description:Six test compound concentrations (0.1, 0.25, 1, 2.5, 10, 25 μM in DMSO; final DMSO concentration=0.25%) are incubated with human liver microsome...More data for this Ligand-Target Pair
In Depth
Date in BDB:
5/8/2017
Entry Details
US Patent

TargetCytochrome P450 2C19(Human)
Gilead Sciences

US Patent
LigandChemical structure of BindingDB Monomer ID 224814BDBM224814(US9333197, 4-Hydroxymephenytoin)
Affinity DataIC50: 2.50E+4nMAssay Description:Six test compound concentrations (0.1, 0.25, 1, 2.5, 10, 25 μM in DMSO; final DMSO concentration=0.25%) are incubated with human liver microsome...More data for this Ligand-Target Pair
In Depth
Date in BDB:
5/8/2017
Entry Details
US Patent

TargetCytochrome P450 1A1(Human)
Gilead Sciences

US Patent
LigandChemical structure of BindingDB Monomer ID 195591BDBM195591(US9216974,Resorufin | US9333197, Resorufin)
Affinity DataIC50: 2.50E+4nMAssay Description:Six test compound concentrations (0.1, 0.25, 1, 2.5, 10, 25 μM in DMSO; final DMSO concentration=0.3%) are incubated with human liver microsomes...More data for this Ligand-Target Pair
In Depth
Date in BDB:
5/8/2017
Entry Details
US Patent

TargetCytochrome P450 1A2(Human)
Gilead Sciences

US Patent
LigandChemical structure of BindingDB Monomer ID 26197BDBM26197(Paracetamol | acetaminophen | CHEMBL112 | N-(4-hyd...)
Affinity DataIC50: 2.50E+4nMAssay Description:Six test compound concentrations (0.1, 0.25, 1, 2.5, 10, 25 μM in DMSO; final DMSO concentration=0.3%) are incubated with human liver microsomes...More data for this Ligand-Target Pair
In Depth
Date in BDB:
5/8/2017
Entry Details
US Patent