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Assay Detail

CHEMBL5588007

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

Binding
Inhibition of PI3Kgamma in mouse RAW264.7 cells assessed as reduction in AKT phosphorylation at S473 residue incubated for 2 hrs by Western blot analysis
2
Total Activities
2
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Binding
Organism Mus musculus
Cell Type RAW264.7
Confidence 9 — Direct single protein target
Curated By Autocuration

Publication

Discovery of Pyrazolo[1,5-<i>a</i>]pyridine Derivatives as Potent and Selective PI3Kγ/δ Inhibitors.
Wang C, Zou F, Qi Z, Liu Q, Shen L, Yuan X, Deng M, Wang A, Wang B, Wang L, Liang X, Liu Q, Liu J.
J Med Chem (2024) 67 : 15199 -15219
PubMed 39163191 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
EC50 2 7.35 7.55

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL5597218 1 7.55
CHEMBL3039502 DUVELISIB 4.0 1 7.14

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL5597218 EC50 = 28.0 nM 7.55
CHEMBL3039502 DUVELISIB EC50 = 72.0 nM 7.14