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Assay Detail

CHEMBL5146661

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

Toxicity
Cytotoxicity against HEK293T cells assessed as cell growth inhibition incubated for 72 hrs by cell titre glo luminescence assay
2
Total Activities
2
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Toxicity
Organism Homo sapiens
Cell Type HEK-293T
Confidence 1 — Organism
Curated By Autocuration

Target

HEK-293T (CHEMBL3706568)
Type CELL-LINE
Organism Homo sapiens

Publication

Synthesis and biological evaluation of 7H-pyrrolo [2,3-d] pyrimidine derivatives as potential p21-activated kinase 4 (PAK4) inhibitors.
Wang C, Xia J, Lei Y, Lu R, Zhang M, Lv H, Hong Q, Lu T, Chen Y, Li H.
Bioorg Med Chem (2022) 60 : 116700 -116700
PubMed 35272236 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 2 5.13 5.13

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL5183512 1 5.13
CHEMBL5180027 1 -

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL5183512 IC50 = 7393.0 nM 5.13
CHEMBL5180027 IC50 > 10000.0 nM -