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Assay Detail

CHEMBL4233459

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Functional
Antiproliferative activity against human U937 cells after 48 hrs by MTT assay
12
Total Activities
12
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Functional
Organism Homo sapiens
Cell Type U-937
Confidence 1 — Organism
Curated By Intermediate

Target

U-937 (CHEMBL612794)
Type CELL-LINE
Organism Homo sapiens

Publication

Design, synthesis and anticancer evaluation of acridine hydroxamic acid derivatives as dual Topo and HDAC inhibitors.
Chen J, Li D, Li W, Yin J, Zhang Y, Yuan Z, Gao C, Liu F, Jiang Y.
Bioorg Med Chem (2018) 26 : 3958 -3966
PubMed 29954683 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 12 5.74 6.21

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL43 AMSACRINE 4.0 1 6.21
CHEMBL98 VORINOSTAT 4.0 1 6.14
CHEMBL4248676 1 6.12
CHEMBL4241141 1 6.05
CHEMBL4248226 1 5.95
CHEMBL4240694 1 5.91
CHEMBL4237410 1 5.87
CHEMBL4251261 1 5.57
CHEMBL4244419 1 5.53
CHEMBL4244887 1 5.45
CHEMBL4248856 1 5.41
CHEMBL4249316 1 4.67

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL43 AMSACRINE IC50 = 610.0 nM 6.21
CHEMBL98 VORINOSTAT IC50 = 720.0 nM 6.14
CHEMBL4248676 IC50 = 750.0 nM 6.12
CHEMBL4241141 IC50 = 900.0 nM 6.05
CHEMBL4248226 IC50 = 1120.0 nM 5.95
CHEMBL4240694 IC50 = 1240.0 nM 5.91
CHEMBL4237410 IC50 = 1340.0 nM 5.87
CHEMBL4251261 IC50 = 2670.0 nM 5.57
CHEMBL4244419 IC50 = 2940.0 nM 5.53
CHEMBL4244887 IC50 = 3550.0 nM 5.45
CHEMBL4248856 IC50 = 3870.0 nM 5.41
CHEMBL4249316 IC50 = 21390.0 nM 4.67