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Assay Detail

CHEMBL3624975

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

Functional
Cytotoxicity against human DU145 cells after 72 hrs by MTT assay
41
Total Activities
40
Compounds Tested
2
Activity Types
0
Assay Parameters

Assay Information

Assay Type Functional
Organism Homo sapiens
Cell Type DU-145
Confidence 1 — Organism
Curated By Autocuration

Target

DU-145 (CHEMBL613508)
Type CELL-LINE
Organism Homo sapiens

Publication

Ring fusion strategy for synthesis and lead optimization of sulfur-substituted anthra[1,2-c][1,2,5]thiadiazole-6,11-dione derivatives as promising scaffold of antitumor agents.
Lee YR, Chen TC, Lee CC, Chen CL, Ahmed Ali AA, Tikhomirov A, Guh JH, Yu DS, Huang HS.
Eur J Med Chem (2015) 102 : 661 -676
PubMed 26344783 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 40 5.11 5.76
Activity 1 - -

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL3621815 1 5.76
CHEMBL3621825 1 5.60
CHEMBL3622212 1 5.59
CHEMBL3622217 1 5.44
CHEMBL3622213 2 5.34
CHEMBL3622215 1 5.20
CHEMBL3622214 1 5.20
CHEMBL3621762 1 5.17
CHEMBL594366 1 5.13
CHEMBL3621764 1 5.12
CHEMBL3622216 1 5.12
CHEMBL3621830 1 5.10
CHEMBL3621826 1 5.08
CHEMBL3621837 1 5.08
CHEMBL3621832 1 5.04
CHEMBL3621766 1 5.02
CHEMBL3622218 1 5.01
CHEMBL3621816 1 4.97
CHEMBL3621817 1 4.95
CHEMBL3621827 1 4.92
CHEMBL3621767 1 4.90
CHEMBL3621835 1 4.89
CHEMBL3621819 1 4.88
CHEMBL3621824 1 4.86
CHEMBL3621831 1 4.85
CHEMBL3621823 1 4.84
CHEMBL3621828 1 4.80
CHEMBL3621763 1 -
CHEMBL3621765 1 -
CHEMBL3621833 1 -

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL3621815 IC50 = 1750.0 nM 5.76
CHEMBL3621825 IC50 = 2520.0 nM 5.60
CHEMBL3622212 IC50 = 2550.0 nM 5.59
CHEMBL3622217 IC50 = 3660.0 nM 5.44
CHEMBL3622213 IC50 = 4530.0 nM 5.34
CHEMBL3622215 IC50 = 6380.0 nM 5.20
CHEMBL3622214 IC50 = 6350.0 nM 5.20
CHEMBL3621762 IC50 = 6680.0 nM 5.17
CHEMBL594366 IC50 = 7410.0 nM 5.13
CHEMBL3621764 IC50 = 7640.0 nM 5.12
CHEMBL3622216 IC50 = 7510.0 nM 5.12
CHEMBL3621830 IC50 = 7880.0 nM 5.10
CHEMBL3621826 IC50 = 8380.0 nM 5.08
CHEMBL3621837 IC50 = 8260.0 nM 5.08
CHEMBL3621832 IC50 = 9120.0 nM 5.04
CHEMBL3621766 IC50 = 9580.0 nM 5.02
CHEMBL3622218 IC50 = 9650.0 nM 5.01
CHEMBL3621816 IC50 = 10680.0 nM 4.97
CHEMBL3621817 IC50 = 11120.0 nM 4.95
CHEMBL3621827 IC50 = 11970.0 nM 4.92
CHEMBL3621767 IC50 = 12680.0 nM 4.90
CHEMBL3621835 IC50 = 12910.0 nM 4.89
CHEMBL3621819 IC50 = 13280.0 nM 4.88
CHEMBL3621824 IC50 = 13850.0 nM 4.86
CHEMBL3621831 IC50 = 14090.0 nM 4.85
CHEMBL3621823 IC50 = 14600.0 nM 4.84
CHEMBL3621828 IC50 = 15890.0 nM 4.80
CHEMBL3621822 IC50 > 15000.0 nM -
CHEMBL3621212 IC50 > 15000.0 nM -
CHEMBL3621820 IC50 > 15000.0 nM -
CHEMBL3622213 Activity - -
CHEMBL3621829 IC50 > 15000.0 nM -
CHEMBL3621821 IC50 > 15000.0 nM -
CHEMBL3621834 IC50 > 15000.0 nM -
CHEMBL3621836 IC50 > 15000.0 nM -
CHEMBL3621818 IC50 > 15000.0 nM -
CHEMBL3621838 IC50 > 15000.0 nM -
CHEMBL3622211 IC50 > 15000.0 nM -
CHEMBL3621763 IC50 > 15000.0 nM -
CHEMBL3621833 IC50 > 15000.0 nM -
CHEMBL3621765 IC50 > 15000.0 nM -