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Assay Detail

CHEMBL5168692

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

ADMET
Inhibition of CYP1A2 in human liver microsomes at 0.01 to 30 uM using phenacetin as substrate in presence of NADPH by UPLC-MS/MS analysis
6
Total Activities
6
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

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

Target

Cytochrome P450 1A2 (CHEMBL3356)
Type SINGLE PROTEIN
Organism Homo sapiens

Publication

Discovery of Clinical Candidate NTQ1062 as a Potent and Bioavailable Akt Inhibitor for the Treatment of Human Tumors.
Ma C, Wu J, Wang L, Ji X, Wu Y, Miao L, Chen D, Zhang L, Wu Y, Feng H, Tang Y, Zhou Q, Pei J, Yang X, Xu D, You Q, Xie Y.
J Med Chem (2022) 65 : 8144 -8168
PubMed 35679512 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 6 4.77 5.19

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL5187508 1 5.19
CHEMBL5206905 1 4.60
CHEMBL5193325 1 4.52
CHEMBL5169427 1 -
CHEMBL5182446 1 -
CHEMBL5199199 1 -

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL5187508 IC50 = 6480.0 nM 5.19
CHEMBL5206905 IC50 = 25200.0 nM 4.60
CHEMBL5193325 IC50 = 30000.0 nM 4.52
CHEMBL5169427 IC50 > 50000.0 nM -
CHEMBL5182446 IC50 > 30000.0 nM -
CHEMBL5199199 IC50 > 30000.0 nM -