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Assay Detail

CHEMBL5331014

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

Functional
Cytotoxicity against human SNU-398 cells assessed as cell growth inhibition incubated for 72 hrs by SRB assay
13
Total Activities
13
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Functional
Organism Homo sapiens
Cell Type SNU-398
Confidence 1 — Organism
Curated By Autocuration

Target

SNU-398 (CHEMBL614454)
Type CELL-LINE
Organism Homo sapiens

Publication

Newly synthesized 6-substituted piperazine/phenyl-9-cyclopentyl containing purine nucleobase analogs act as potent anticancer agents and induce apoptosis <i>via</i> inhibiting Src in hepatocellular carcinoma cells.
Bilget Guven E, Durmaz Sahin I, Altiparmak D, Servili B, Essiz S, Cetin-Atalay R, Tuncbilek M.
RSC Med Chem (2023) 14 : 2658 -2676
PubMed 38107180 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 13 5.95 6.70

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL5399372 1 6.70
CHEMBL5417466 1 6.70
CHEMBL1568 FLUDARABINE 3.0 1 6.70
CHEMBL5419328 1 6.52
CHEMBL5396168 1 6.00
CHEMBL5414116 1 5.92
CHEMBL5395601 1 5.75
CHEMBL5401822 1 5.75
CHEMBL5425754 1 5.72
CHEMBL5399841 1 5.40
CHEMBL5405427 1 5.16
CHEMBL5413601 1 5.10
CHEMBL1619 CLADRIBINE 4.0 1 -

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL5399372 IC50 = 200.0 nM 6.70
CHEMBL5417466 IC50 = 200.0 nM 6.70
CHEMBL1568 FLUDARABINE IC50 = 200.0 nM 6.70
CHEMBL5419328 IC50 = 300.0 nM 6.52
CHEMBL5396168 IC50 = 1000.0 nM 6.00
CHEMBL5414116 IC50 = 1200.0 nM 5.92
CHEMBL5395601 IC50 = 1800.0 nM 5.75
CHEMBL5401822 IC50 = 1800.0 nM 5.75
CHEMBL5425754 IC50 = 1900.0 nM 5.72
CHEMBL5399841 IC50 = 4000.0 nM 5.40
CHEMBL5405427 IC50 = 6900.0 nM 5.16
CHEMBL5413601 IC50 = 8000.0 nM 5.10
CHEMBL1619 CLADRIBINE IC50 < 100.0 nM -