Skip to main content
Free research Free research Free assay review with research home and workspace preview
Quick search ChEMBL 36
Assay Detail

CHEMBL5634589

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

Binding
Inhibition of PRDX1 (unknown origin) in presence of cofactor A/cofactor B/NADPH incubated for 25 mins
13
Total Activities
13
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Binding
Organism Homo sapiens
Confidence 9 — Direct single protein target
Curated By Autocuration

Target

Peroxiredoxin-1 (CHEMBL5315)
Type SINGLE PROTEIN
Organism Homo sapiens

Publication

Development of novel celastrol-ligustrazine hybrids as potent peroxiredoxin 1 inhibitors against lung cancer.
Bai Y, Liang C, Zhou J, Liu Y, Wang F, Gao J, Wu J, Hu D.
Eur J Med Chem (2023) 259 : 115656 -115656
PubMed 37499289 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 13 6.10 6.79

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL5647448 1 6.79
CHEMBL5647239 1 6.78
CHEMBL5639299 1 6.62
CHEMBL5647369 1 6.54
CHEMBL5646554 1 6.32
CHEMBL5639325 1 6.28
CHEMBL5647003 1 6.01
CHEMBL5647534 1 5.83
CHEMBL5646385 1 5.81
CHEMBL301982 CELASTROL 1 5.79
CHEMBL5647082 1 5.60
CHEMBL4860684 1 4.83
CHEMBL303697 LIGUSTRAZINE 1 -

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL5647448 IC50 = 164.0 nM 6.79
CHEMBL5647239 IC50 = 165.0 nM 6.78
CHEMBL5639299 IC50 = 239.0 nM 6.62
CHEMBL5647369 IC50 = 285.0 nM 6.54
CHEMBL5646554 IC50 = 481.0 nM 6.32
CHEMBL5639325 IC50 = 525.0 nM 6.28
CHEMBL5647003 IC50 = 979.0 nM 6.01
CHEMBL5647534 IC50 = 1472.0 nM 5.83
CHEMBL5646385 IC50 = 1534.0 nM 5.81
CHEMBL301982 CELASTROL IC50 = 1622.0 nM 5.79
CHEMBL5647082 IC50 = 2488.0 nM 5.60
CHEMBL4860684 IC50 = 14800.0 nM 4.83
CHEMBL303697 LIGUSTRAZINE IC50 - -