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Assay Detail

CHEMBL3772620

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

ADMET
Cytotoxicity against HAF assessed as reduction in cell viability after 96 hrs by sulforhodamine B assay
15
Total Activities
15
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type ADMET
Organism Homo sapiens
Cell Type HAF
Confidence 0 — Uncurated / Unknown
Curated By Autocuration

Target

ADMET (CHEMBL612558)
Type ADMET

Publication

Synthesis and biological evaluation of D-ring fused 1,2,3-thiadiazole dehydroepiandrosterone derivatives as antitumor agents.
Cui HW, Peng S, Gu XZ, Chen H, He Y, Gao W, Lv F, Wang JH, Wang Y, Xie J, Liu MY, Yi Z, Qiu WW.
Eur J Med Chem (2016) 111 : 126 -137
PubMed 26866967 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 15 5.16 7.17

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL359744 DOXORUBICIN HYDROCHLORIDE 4.0 1 7.17
CHEMBL3770805 1 5.74
CHEMBL3770137 1 5.53
CHEMBL3769630 1 4.75
CHEMBL3769913 1 4.68
CHEMBL3770246 1 4.58
CHEMBL3771045 1 4.44
CHEMBL3770683 1 4.41
CHEMBL90593 PRASTERONE 4.0 1 -
CHEMBL3770372 1 -
CHEMBL3770168 1 -
CHEMBL3771344 1 -
CHEMBL3769515 1 -
CHEMBL3771030 1 -
CHEMBL3770344 1 -

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL359744 DOXORUBICIN HYDROCHLORIDE IC50 = 68.0 nM 7.17
CHEMBL3770805 IC50 = 1820.0 nM 5.74
CHEMBL3770137 IC50 = 2950.0 nM 5.53
CHEMBL3769630 IC50 = 18000.0 nM 4.75
CHEMBL3769913 IC50 = 21100.0 nM 4.68
CHEMBL3770246 IC50 = 26100.0 nM 4.58
CHEMBL3771045 IC50 = 36000.0 nM 4.44
CHEMBL3770683 IC50 = 39050.0 nM 4.41
CHEMBL90593 PRASTERONE IC50 > 50000.0 nM -
CHEMBL3770372 IC50 > 50000.0 nM -
CHEMBL3770168 IC50 > 50000.0 nM -
CHEMBL3771344 IC50 > 50000.0 nM -
CHEMBL3769515 IC50 > 50000.0 nM -
CHEMBL3771030 IC50 > 50000.0 nM -
CHEMBL3770344 IC50 > 50000.0 nM -