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Assay Detail

CHEMBL1912889

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

Functional
Cytotoxicity against human HCT116 cells after 48 hrs by Hoechst-33342 staining-based imaging analysis
14
Total Activities
14
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Functional
Organism Homo sapiens
Cell Type HCT-116
Confidence 1 — Organism
Curated By Autocuration

Target

HCT-116 (CHEMBL394)
Type CELL-LINE
Organism Homo sapiens

Publication

Synthesis and biological evaluation of new 3-(6-hydroxyindol-2-yl)-5-(Phenyl) pyridine or pyrazine V-Shaped molecules as kinase inhibitors and cytotoxic agents.
Kassis P, Brzeszcz J, Bénéteau V, Lozach O, Meijer L, Le Guével R, Guillouzo C, Lewiński K, Bourg S, Colliandre L, Routier S, Mérour JY.
Eur J Med Chem (2011) 46 : 5416 -5434
PubMed 21944287 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 14 5.31 5.82

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL1910201 1 5.82
CHEMBL1910197 1 5.70
CHEMBL1910194 1 5.60
CHEMBL1910193 1 5.52
CHEMBL1910195 1 5.52
CHEMBL1910198 1 5.52
CHEMBL1910192 1 5.22
CHEMBL1910196 1 5.22
CHEMBL1910191 1 5.10
CHEMBL1910377 1 5.10
CHEMBL14762 SELICICLIB 2.0 1 5.10
CHEMBL1910190 1 5.05
CHEMBL1910200 1 4.92
CHEMBL1910199 1 4.89

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL1910201 IC50 = 1500.0 nM 5.82
CHEMBL1910197 IC50 = 2000.0 nM 5.70
CHEMBL1910194 IC50 = 2500.0 nM 5.60
CHEMBL1910193 IC50 = 3000.0 nM 5.52
CHEMBL1910195 IC50 = 3000.0 nM 5.52
CHEMBL1910198 IC50 = 3000.0 nM 5.52
CHEMBL1910192 IC50 = 6000.0 nM 5.22
CHEMBL1910196 IC50 = 6000.0 nM 5.22
CHEMBL1910191 IC50 = 8000.0 nM 5.10
CHEMBL1910377 IC50 = 8000.0 nM 5.10
CHEMBL14762 SELICICLIB IC50 = 8000.0 nM 5.10
CHEMBL1910190 IC50 = 9000.0 nM 5.05
CHEMBL1910200 IC50 = 12000.0 nM 4.92
CHEMBL1910199 IC50 = 13000.0 nM 4.89