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Assay Detail

CHEMBL4775525

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Binding
Inhibition of human ACMSD using ACMS substrate by spectrometry
16
Total Activities
16
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

Publication

Diflunisal Derivatives as Modulators of ACMS Decarboxylase Targeting the Tryptophan-Kynurenine Pathway.
Yang Y,Borel T,de Azambuja F,Johnson D,Sorrentino JP,Udokwu C,Davis I,Liu A,Altman RA
J Med Chem (2021) 64 : 797 -811
PubMed 33369426 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 16 5.06 7.11

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL4796997 1 7.11
CHEMBL3126314 1 5.88
CHEMBL4798885 1 5.51
CHEMBL419420 1 5.48
CHEMBL121772 1 5.37
CHEMBL4777218 1 5.34
CHEMBL102336 1 5.05
CHEMBL4786884 1 4.96
CHEMBL898 DIFLUNISAL 4.0 1 4.87
CHEMBL4790894 1 4.87
CHEMBL4245097 1 4.70
CHEMBL4777331 1 4.57
CHEMBL4797549 1 4.43
CHEMBL3244578 1 4.36
CHEMBL4777119 1 4.32
CHEMBL475848 1 4.06

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL4796997 IC50 = 78.0 nM 7.11
CHEMBL3126314 IC50 = 1320.0 nM 5.88
CHEMBL4798885 IC50 = 3100.0 nM 5.51
CHEMBL419420 IC50 = 3290.0 nM 5.48
CHEMBL121772 IC50 = 4290.0 nM 5.37
CHEMBL4777218 IC50 = 4610.0 nM 5.34
CHEMBL102336 IC50 = 8830.0 nM 5.05
CHEMBL4786884 IC50 = 11100.0 nM 4.96
CHEMBL898 DIFLUNISAL IC50 = 13500.0 nM 4.87
CHEMBL4790894 IC50 = 13600.0 nM 4.87
CHEMBL4245097 IC50 = 20100.0 nM 4.70
CHEMBL4777331 IC50 = 27100.0 nM 4.57
CHEMBL4797549 IC50 = 37300.0 nM 4.43
CHEMBL3244578 IC50 = 44100.0 nM 4.36
CHEMBL4777119 IC50 = 47900.0 nM 4.32
CHEMBL475848 IC50 = 88000.0 nM 4.06