Skip to main content
Free research Free research Free assay review with research home and workspace preview
Quick search ChEMBL 36
Assay Detail

CHEMBL705960

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

Functional
Concentration required for 50% reduction in KB cell number after 3-day incubation
15
Total Activities
15
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Functional
Organism Homo sapiens
Cell Type KB
Confidence 0 — Uncurated / Unknown
Curated By Autocuration

Target

ADMET (CHEMBL612558)
Type ADMET

Publication

Antitumor agents. 123. Synthesis and human DNA topoisomerase II inhibitory activity of 2'-chloro derivatives of etoposide and 4 beta-(arylamino)-4'-O-demethylpodophyllotoxins.
Hu H, Wang ZQ, Liu SY, Cheng YC, Lee KH.
J Med Chem (1992) 35 : 866 -871
PubMed 1312600 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 15 6.23 6.70

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL44657 ETOPOSIDE 4.0 1 6.70
CHEMBL281692 1 6.62
CHEMBL286509 1 6.35
CHEMBL283631 1 6.31
CHEMBL32519 1 6.17
CHEMBL169066 1 5.24
CHEMBL3085153 1 -
CHEMBL168532 1 -
CHEMBL170852 1 -
CHEMBL352613 1 -
CHEMBL168588 1 -
CHEMBL420565 1 -
CHEMBL353229 1 -
CHEMBL354213 1 -
CHEMBL168995 1 -

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL44657 ETOPOSIDE IC50 = 200.0 nM 6.70
CHEMBL281692 IC50 = 240.0 nM 6.62
CHEMBL286509 IC50 = 450.0 nM 6.35
CHEMBL283631 IC50 = 490.0 nM 6.31
CHEMBL32519 IC50 = 680.0 nM 6.17
CHEMBL169066 IC50 = 5700.0 nM 5.24
CHEMBL3085153 IC50 > 6400.0 nM -
CHEMBL168532 IC50 > 6800.0 nM -
CHEMBL170852 IC50 > 7200.0 nM -
CHEMBL352613 IC50 > 7000.0 nM -
CHEMBL168588 IC50 > 7200.0 nM -
CHEMBL420565 IC50 > 22300.0 nM -
CHEMBL353229 IC50 > 7500.0 nM -
CHEMBL354213 IC50 > 7200.0 nM -
CHEMBL168995 IC50 > 7300.0 nM -