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Assay Detail

CHEMBL5115593

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

Binding
Inhibition of PAK4 (unknown origin) using S2 as substrate incubated for 60 mins in the presence of ATP by time-resolved HTRF assay
1
Total Activities
1
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

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

Target

Serine/threonine-protein kinase PAK 4 (CHEMBL4482)
Type SINGLE PROTEIN
Organism Homo sapiens

Publication

Design, synthesis, and biological evaluation of novel pyrazolo [3,4-d]pyrimidine derivatives as potent PLK4 inhibitors for the treatment of TRIM37-amplified breast cancer.
Sun Y, Sun Y, Wang L, Wu T, Yin W, Wang J, Xue Y, Qin Q, Sun Y, Yang H, Zhao D, Cheng M.
Eur J Med Chem (2022) 238 : 114424 -114424
PubMed 35576702 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 1 8.23 8.23

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL5175418 1 8.23

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL5175418 IC50 = 5.9 nM 8.23