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Assay Detail

CHEMBL3069591

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

Functional
Cytotoxicity against Homo sapiens (human) HuCCa1 cells assessed as inhibition of cell growth after 3 days by crystal violet staining
16
Total Activities
16
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Functional
Organism Homo sapiens
Cell Type HuCC-A1
Confidence 1 — Organism
Curated By Autocuration

Publication

Cytotoxicity and QSAR study of (thio)ureas derived from phenylalkylamines and pyridylalkylamines
Pingaew R, Tongraung P, Worachartcheewan A, Nantasenamat C, Prachayasittikul S, Ruchirawat S, Prachayasittikul V
Med Chem Res (2013) 22 : 4016 -4029
· DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 16 4.74 6.19

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL53463 DOXORUBICIN 4.0 1 6.19
CHEMBL1321159 1 4.72
CHEMBL2299368 1 4.46
CHEMBL2299369 1 4.28
CHEMBL1548970 1 4.07
CHEMBL44657 ETOPOSIDE 4.0 1 -
CHEMBL1719884 1 -
CHEMBL1492594 1 -
CHEMBL2299367 1 -
CHEMBL2299366 1 -
CHEMBL1595295 1 -
CHEMBL2299365 1 -
CHEMBL2299364 1 -
CHEMBL2299363 1 -
CHEMBL2299362 1 -
CHEMBL1360165 1 -

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL53463 DOXORUBICIN IC50 = 640.0 nM 6.19
CHEMBL1321159 IC50 = 19080.0 nM 4.72
CHEMBL2299368 IC50 = 34240.0 nM 4.46
CHEMBL2299369 IC50 = 52580.0 nM 4.28
CHEMBL1548970 IC50 = 84250.0 nM 4.07
CHEMBL44657 ETOPOSIDE IC50 - -
CHEMBL1719884 IC50 > 191050.0 nM -
CHEMBL1492594 IC50 > 180000.0 nM -
CHEMBL2299367 IC50 > 173420.0 nM -
CHEMBL2299366 IC50 > 181340.0 nM -
CHEMBL1595295 IC50 > 171350.0 nM -
CHEMBL2299365 IC50 > 165370.0 nM -
CHEMBL2299364 IC50 > 149340.0 nM -
CHEMBL2299363 IC50 = 139230.0 nM -
CHEMBL2299362 IC50 > 138340.0 nM -
CHEMBL1360165 IC50 > 181980.0 nM -