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Assay Detail

CHEMBL653209

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Functional
Inhibitory concentration against breast MCF-7 cell line
13
Total Activities
13
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Functional
Organism Homo sapiens
Cell Type MCF7
Confidence 1 — Organism
Curated By Intermediate

Target

MCF7 (CHEMBL387)
Type CELL-LINE
Organism Homo sapiens

Publication

Development of potential antitumor agents. Synthesis and biological evaluation of a new set of sulfonamide derivatives as histone deacetylase inhibitors.
Bouchain G, Leit S, Frechette S, Khalil EA, Lavoie R, Moradei O, Woo SH, Fournel M, Yan PT, Kalita A, Trachy-Bourget MC, Beaulieu C, Li Z, Robert MF, MacLeod AR, Besterman JM, Delorme D.
J Med Chem (2003) 46 : 820 -830
PubMed 12593661 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 13 5.25 6.16

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL147506 1 6.16
CHEMBL98669 1 5.82
CHEMBL317814 1 5.60
CHEMBL27759 ENTINOSTAT 3.0 1 5.30
CHEMBL148313 1 5.22
CHEMBL149444 1 5.22
CHEMBL353629 1 5.16
CHEMBL353658 1 5.10
CHEMBL99 TRICHOSTATIN 1.0 1 5.00
CHEMBL148968 1 4.96
CHEMBL346414 1 4.94
CHEMBL149172 1 4.54
CHEMBL168668 1 -

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL147506 IC50 = 700.0 nM 6.16
CHEMBL98669 IC50 = 1500.0 nM 5.82
CHEMBL317814 IC50 = 2500.0 nM 5.60
CHEMBL27759 ENTINOSTAT IC50 = 5000.0 nM 5.30
CHEMBL148313 IC50 = 6000.0 nM 5.22
CHEMBL149444 IC50 = 6000.0 nM 5.22
CHEMBL353629 IC50 = 7000.0 nM 5.16
CHEMBL353658 IC50 = 8000.0 nM 5.10
CHEMBL99 TRICHOSTATIN IC50 = 10000.0 nM 5.00
CHEMBL148968 IC50 = 11000.0 nM 4.96
CHEMBL346414 IC50 = 11500.0 nM 4.94
CHEMBL149172 IC50 = 29000.0 nM 4.54
CHEMBL168668 IC50 > 37000.0 nM -