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Assay Detail

CHEMBL5328400

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

Toxicity
Cytotoxicity against anti-humanCD3/anti-humanCD28 stimulated human CD3-positive T cells assessed as reduction in cell viability incubated for 48 hrs
7
Total Activities
7
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Toxicity
Organism Homo sapiens
Cell Type CD3-positive T cell
Confidence 0 — Uncurated / Unknown
Curated By Autocuration

Target

Unchecked (CHEMBL612545)
Type UNCHECKED

Publication

Discovery of quinazoline HPK1 inhibitors with high cellular potency.
Toure M, Johnson T, Li B, Schmidt R, Ma H, Neagu C, Lopez AU, Wang Y, Guler S, Xiao Y, Henkes R, Ho K, Zhang S, Chu CL, Gundra UM, Porichis F, Li L, Maurer CK, Fang Z, Musil D, DiPoto M, Friis E, Jones R, Jones C, Cummings J, Chekler E, Tanzer EM, Huck B, Sherer B.
Bioorg Med Chem (2023) 92 : 117423 -117423
PubMed 37531921 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 7 5.93 6.33

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL5430021 1 6.33
CHEMBL5441105 1 6.28
CHEMBL5425004 1 6.28
CHEMBL5412652 1 5.90
CHEMBL5396693 1 5.72
CHEMBL5439204 1 5.63
CHEMBL5440958 1 5.39

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL5430021 IC50 = 470.0 nM 6.33
CHEMBL5441105 IC50 = 525.0 nM 6.28
CHEMBL5425004 IC50 = 530.0 nM 6.28
CHEMBL5412652 IC50 = 1250.0 nM 5.90
CHEMBL5396693 IC50 = 1900.0 nM 5.72
CHEMBL5439204 IC50 = 2350.0 nM 5.63
CHEMBL5440958 IC50 = 4100.0 nM 5.39