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Assay Detail

CHEMBL1293140

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

Binding
Inhibition of Plasmodium falciparum 3D7 HDAC1 in infected-human erythrocytes assessed as histone H4 hyperacetylation after 1.5 hrs by SDS-PAGE analysis
4
Total Activities
2
Compounds Tested
2
Activity Types
0
Assay Parameters

Assay Information

Assay Type Binding
Organism Plasmodium falciparum 3D7
Confidence 9 — Direct single protein target
Curated By Intermediate

Target

Histone deacetylase (CHEMBL1293190)
Type SINGLE PROTEIN
Organism Plasmodium falciparum 3D7

Publication

Antimalarial histone deacetylase inhibitors containing cinnamate or NSAID components.
Wheatley NC, Andrews KT, Tran TL, Lucke AJ, Reid RC, Fairlie DP.
Bioorg Med Chem Lett (2010) 20 : 7080 -7084
PubMed 20951583 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 2 7.09 7.11
Inhibition 2 - -

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL221655 2 7.11
CHEMBL220692 2 7.06

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL221655 IC50 = 78.0 nM 7.11
CHEMBL220692 IC50 = 87.0 nM 7.06
CHEMBL221655 Inhibition - % -
CHEMBL220692 Inhibition - % -