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Assay Detail

CHEMBL4825196

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Binding
Inhibition of human ALDH1A1 assessed as NADH formation using propionaldehyde as substrate by spectrophotometry
8
Total Activities
8
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

Aldehyde dehydrogenase 1A1 (CHEMBL3577)
Type SINGLE PROTEIN
Organism Homo sapiens

Publication

Discovery of benzimidazole derivatives as potent and selective aldehyde dehydrogenase 1A1 (ALDH1A1) inhibitors with glucose consumption improving activity.
Ma Z, Jiang L, Li B, Liang D, Feng Y, Liu L, Jiang C.
Bioorg Med Chem (2021) 46 : 116352 -116352
PubMed 34403955 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 8 6.00 6.61

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL4871242 1 6.61
CHEMBL4847630 1 6.34
CHEMBL4854627 1 6.20
CHEMBL4862473 1 6.04
CHEMBL4855040 1 5.99
CHEMBL4845791 1 5.82
CHEMBL4871374 1 5.68
CHEMBL3416562 1 5.34

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL4871242 IC50 = 243.0 nM 6.61
CHEMBL4847630 IC50 = 458.0 nM 6.34
CHEMBL4854627 IC50 = 626.0 nM 6.20
CHEMBL4862473 IC50 = 921.0 nM 6.04
CHEMBL4855040 IC50 = 1023.0 nM 5.99
CHEMBL4845791 IC50 = 1498.0 nM 5.82
CHEMBL4871374 IC50 = 2110.0 nM 5.68
CHEMBL3416562 IC50 = 4600.0 nM 5.34