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

CHEMBL960139

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

Functional
Antiproliferative activity against human HCT116 cells after 3 days
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 of new camptothecin analogs with improved antitumor activities.
Niizuma S, Tsukazaki M, Suda H, Murata T, Ohwada J, Ozawa S, Fukuda H, Murasaki C, Kohchi M, Morikami K, Yoshinari K, Endo M, Ura M, Tanimura H, Miyazaki Y, Takasuka T, Kawashima A, Nanba E, Nakano K, Ogawa K, Kobayashi K, Okabe H, Umeda I, Shimma N.
Bioorg Med Chem Lett (2009) 19 : 2018 -2021
PubMed 19254843 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 14 9.45 10.70

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL492573 1 10.70
CHEMBL492975 1 10.30
CHEMBL493935 1 9.92
CHEMBL492381 1 9.60
CHEMBL493949 1 9.44
CHEMBL493342 1 9.44
CHEMBL493368 1 9.40
CHEMBL523188 1 9.36
CHEMBL523182 1 9.28
CHEMBL837 7-ETHYL-10-HYDROXYCAMPTOTHECIN 2.0 1 9.26
CHEMBL492974 1 9.07
CHEMBL493146 1 8.66
CHEMBL493367 1 8.44
CHEMBL524170 1 -

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL492573 IC50 = 0.02 nM 10.70
CHEMBL492975 IC50 = 0.05 nM 10.30
CHEMBL493935 IC50 = 0.12 nM 9.92
CHEMBL492381 IC50 = 0.25 nM 9.60
CHEMBL493949 IC50 = 0.36 nM 9.44
CHEMBL493342 IC50 = 0.36 nM 9.44
CHEMBL493368 IC50 = 0.4 nM 9.40
CHEMBL523188 IC50 = 0.44 nM 9.36
CHEMBL523182 IC50 = 0.52 nM 9.28
CHEMBL837 7-ETHYL-10-HYDROXYCAMPTOTHECIN IC50 = 0.55 nM 9.26
CHEMBL492974 IC50 = 0.85 nM 9.07
CHEMBL493146 IC50 = 2.2 nM 8.66
CHEMBL493367 IC50 = 3.6 nM 8.44
CHEMBL524170 IC50 < 0.04 nM -