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Assay Detail

CHEMBL5332686

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

Functional
Antiproliferative activity against ATM-proficient human HT-29 cells assessed as reduction in cell proliferation incubated for 3 days by MTT assay
15
Total Activities
15
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Functional
Organism Homo sapiens
Cell Type HT-29
Confidence 1 — Organism
Curated By Autocuration

Target

HT-29 (CHEMBL384)
Type CELL-LINE
Organism Homo sapiens

Publication

Discovery of novel 7,7-dimethyl-6,7-dihydro-5H-pyrrolo[3,4-d]pyrimidines as ATR inhibitors based on structure-based drug design.
Qi Y, Wang K, Long B, Yue H, Wu Y, Yang D, Tong M, Shi X, Hou Y, Zhao Y.
Eur J Med Chem (2023) 246 : 114945 -114945
PubMed 36462444 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 15 6.10 6.71

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL5423608 1 6.71
CHEMBL5412393 1 6.51
CHEMBL5427147 1 6.45
CHEMBL5422058 1 6.41
CHEMBL5425498 1 6.38
CHEMBL5412749 1 6.37
CHEMBL5408725 1 6.35
CHEMBL5415921 1 6.31
CHEMBL2325697 1 6.19
CHEMBL5419225 1 5.79
CHEMBL5425941 1 5.61
CHEMBL5393965 1 5.59
CHEMBL5439160 1 5.37
CHEMBL5440718 1 5.34
CHEMBL4594429 AZD-1390 1.0 1 -

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL5423608 IC50 = 197.0 nM 6.71
CHEMBL5412393 IC50 = 307.0 nM 6.51
CHEMBL5427147 IC50 = 357.0 nM 6.45
CHEMBL5422058 IC50 = 387.0 nM 6.41
CHEMBL5425498 IC50 = 421.0 nM 6.38
CHEMBL5412749 IC50 = 431.0 nM 6.37
CHEMBL5408725 IC50 = 449.0 nM 6.35
CHEMBL5415921 IC50 = 487.0 nM 6.31
CHEMBL2325697 IC50 = 644.0 nM 6.19
CHEMBL5419225 IC50 = 1641.0 nM 5.79
CHEMBL5425941 IC50 = 2470.0 nM 5.61
CHEMBL5393965 IC50 = 2582.0 nM 5.59
CHEMBL5439160 IC50 = 4310.0 nM 5.37
CHEMBL5440718 IC50 = 4610.0 nM 5.34
CHEMBL4594429 AZD-1390 IC50 > 30000.0 nM -