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Assay Detail

CHEMBL3707604

Review assay metadata, readout intent, target linkage, and publication context from the same page.

Binding
Inhibition Assay: Mixtures of isozyme inhibitors (sulfaphenazole, tranylcypromine, and ketoconazole as specific inhibitors of isozymes 2C9, 2C19, and 3A4, respectively) were prepared containing each inhibitor at concentrations of 6000, 2000, 600, 200, 60, 20, 6, and 2 uM by serial dilution with DMSO:ACN (50:50 v/v). The mixed inhibitor solutions were then diluted 20-fold with DMSO:MeCN:deionized water (5:5:180 v/v/v) to concentrations of 300, 100, 30, 10, 3, 1, 0.3, and 0.1 uM. The percent of organic solvent attributable to the test compound or inhibitor mixture in the final reaction mixture was 2% v/v. Pooled human liver microsome suspension (20 mg/mL) was diluted with phosphate buffer to obtain a 5 mg/mL suspension. A solution of NADPH was prepared in phosphate buffer at a concentration of 5 mM. Separate stock solutions of each substrate were prepared in DMSO:MeCN (50:50 v/v), mixed, and diluted in phosphate buffer to obtain a single solution.
5
Total Activities
5
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Binding
Organism Homo sapiens
Tissue Liver
Confidence 9 — Direct single protein target
Curated By Autocuration

Target

Cytochrome P450 3A4 (CHEMBL340)
Type SINGLE PROTEIN
Organism Homo sapiens

Publication

Metalloenzyme inhibitor compounds
(2014)

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 5 5.33 5.85

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL3680983 1 5.85
CHEMBL3680985 1 5.42
CHEMBL3680984 1 5.24
CHEMBL3311223 1 4.80
CHEMBL3311224 1 -

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL3680983 IC50 = 1400.0 nM 5.85
CHEMBL3680985 IC50 = 3800.0 nM 5.42
CHEMBL3680984 IC50 = 5800.0 nM 5.24
CHEMBL3311223 IC50 = 16000.0 nM 4.80
CHEMBL3311224 IC50 > 60000.0 nM -