Skip to main content
Free research Free research Free assay review with research home and workspace preview
Quick search ChEMBL 36
Assay Detail

CHEMBL5216216

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

Binding
Inhibition of mTORC2 in human A-431 cells assessed as phosphorylated AKT level incubated for 3 hrs by HTRF assay
12
Total Activities
12
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Binding
Organism Homo sapiens
Cell Type A-431
Confidence 7 — Homologous single protein target
Curated By Autocuration

Target

mTORC2 (CHEMBL4523999)
Type PROTEIN COMPLEX
Organism Homo sapiens

Publication

Contemporary mTOR inhibitor scaffolds to diseases breakdown: A patent review (2015-2021).
Oleksak P, Nepovimova E, Chrienova Z, Musilek K, Patocka J, Kuca K.
Eur J Med Chem (2022) 238 : 114498 -114498
PubMed 35688004 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 12 8.52 9.00

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL5219718 1 9.00
CHEMBL5218727 1 8.96
CHEMBL5218916 1 8.92
CHEMBL5219710 1 8.82
CHEMBL5218988 1 8.66
CHEMBL5220152 1 8.62
CHEMBL5220536 1 8.57
CHEMBL5220948 1 8.55
CHEMBL5218590 1 8.23
CHEMBL5220383 1 8.20
CHEMBL5220500 1 7.94
CHEMBL5221072 1 7.79

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL5219718 IC50 = 1.0 nM 9.00
CHEMBL5218727 IC50 = 1.1 nM 8.96
CHEMBL5218916 IC50 = 1.2 nM 8.92
CHEMBL5219710 IC50 = 1.5 nM 8.82
CHEMBL5218988 IC50 = 2.2 nM 8.66
CHEMBL5220152 IC50 = 2.4 nM 8.62
CHEMBL5220536 IC50 = 2.7 nM 8.57
CHEMBL5220948 IC50 = 2.8 nM 8.55
CHEMBL5218590 IC50 = 5.9 nM 8.23
CHEMBL5220383 IC50 = 6.3 nM 8.20
CHEMBL5220500 IC50 = 11.4 nM 7.94
CHEMBL5221072 IC50 = 16.3 nM 7.79