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Assay Detail

CHEMBL3375391

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

Functional
Cytotoxicity against human HeLa cells after 2 days by CCK-8 assay
13
Total Activities
13
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Functional
Organism Homo sapiens
Cell Type HeLa
Confidence 1 — Organism
Curated By Autocuration

Target

HeLa (CHEMBL399)
Type CELL-LINE
Organism Homo sapiens

Publication

Design and synthesis of novel 2,4-diaryl-5H-indeno[1,2-b]pyridine derivatives, and their evaluation of topoisomerase inhibitory activity and cytotoxicity.
Kadayat TM, Park C, Jun KY, Magar TB, Bist G, Yoo HY, Kwon Y, Lee ES.
Bioorg Med Chem (2015) 23 : 160 -173
PubMed 25481396 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 13 5.53 6.40

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL65 CAMPTOTHECIN -1.0 1 6.40
CHEMBL53463 DOXORUBICIN 4.0 1 6.00
CHEMBL44657 ETOPOSIDE 4.0 1 5.90
CHEMBL3353769 1 5.50
CHEMBL3353768 1 5.38
CHEMBL3353767 1 5.28
CHEMBL3353763 1 5.09
CHEMBL3353783 1 4.69
CHEMBL3353770 1 -
CHEMBL3353766 1 -
CHEMBL3353765 1 -
CHEMBL3353775 1 -
CHEMBL3353776 1 -

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL65 CAMPTOTHECIN IC50 = 400.0 nM 6.40
CHEMBL53463 DOXORUBICIN IC50 = 1000.0 nM 6.00
CHEMBL44657 ETOPOSIDE IC50 = 1260.0 nM 5.90
CHEMBL3353769 IC50 = 3200.0 nM 5.50
CHEMBL3353768 IC50 = 4130.0 nM 5.38
CHEMBL3353767 IC50 = 5220.0 nM 5.28
CHEMBL3353763 IC50 = 8140.0 nM 5.09
CHEMBL3353783 IC50 = 20500.0 nM 4.69
CHEMBL3353770 IC50 > 50000.0 nM -
CHEMBL3353766 IC50 > 50000.0 nM -
CHEMBL3353765 IC50 > 50000.0 nM -
CHEMBL3353775 IC50 > 50000.0 nM -
CHEMBL3353776 IC50 > 50000.0 nM -