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Assay Detail

CHEMBL4189995

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

Binding
Inhibition of human ALDH2 using NAD+/propionaldehyde as substrate/cofactor preincubated for 15 mins followed by substrate/cofactor addition measured for 30 mins by fluorescence assay
2
Total Activities
2
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, mitochondrial (CHEMBL1935)
Type SINGLE PROTEIN
Organism Homo sapiens

Publication

Discovery of Orally Bioavailable, Quinoline-Based Aldehyde Dehydrogenase 1A1 (ALDH1A1) Inhibitors with Potent Cellular Activity.
Yang SM, Martinez NJ, Yasgar A, Danchik C, Johansson C, Wang Y, Baljinnyam B, Wang AQ, Xu X, Shah P, Cheff D, Wang XS, Roth J, Lal-Nag M, Dunford JE, Oppermann U, Vasiliou V, Simeonov A, Jadhav A, Maloney DJ.
J Med Chem (2018) 61 : 4883 -4903
PubMed 29767973 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 2 5.30 5.30

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL4213848 1 5.30
CHEMBL4202537 1 5.30

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL4213848 IC50 = 5000.0 nM 5.30
CHEMBL4202537 IC50 = 5000.0 nM 5.30