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Assay Detail

CHEMBL4628107

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

Functional
Antiproliferative activity in human A549 cells assessed as inhibition of cell viability after 72 hrs by MTS assay
8
Total Activities
8
Compounds Tested
2
Activity Types
0
Assay Parameters

Assay Information

Assay Type Functional
Organism Homo sapiens
Cell Type A549
Confidence 1 — Organism
Curated By Autocuration

Target

A549 (CHEMBL392)
Type CELL-LINE
Organism Homo sapiens

Publication

Pyrimethamine conjugated histone deacetylase inhibitors: Design, synthesis and evidence for triple negative breast cancer selective cytotoxicity.
Wu B, Fathi S, Mortley S, Mohiuddin M, Jang YC, Oyelere AK.
Bioorg Med Chem (2020) 28 : 115345 -115345
PubMed 32061484 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 5 4.51 5.00
Inhibition 3 - -

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL4634096 1 5.00
CHEMBL98 VORINOSTAT 4.0 1 4.80
CHEMBL4635479 1 4.18
CHEMBL4636452 1 4.05
CHEMBL4649487 1 -
CHEMBL4648403 1 -
CHEMBL4633409 1 -
CHEMBL36 PYRIMETHAMINE 4.0 1 -

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL4634096 IC50 = 10000.0 nM 5.00
CHEMBL98 VORINOSTAT IC50 = 15730.0 nM 4.80
CHEMBL4635479 IC50 = 65490.0 nM 4.18
CHEMBL4636452 IC50 = 88460.0 nM 4.05
CHEMBL4649487 Inhibition - % -
CHEMBL4648403 IC50 = 113750.0 nM -
CHEMBL4633409 Inhibition - % -
CHEMBL36 PYRIMETHAMINE Inhibition - % -