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Assay Detail

CHEMBL4827647

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

Binding
Inhibition of human ATX assessed as reduction in LPA formation using FS-3 as substrate preincubated for 30 mins followed by substrate addition and measured after 2 hrs by FRET assay
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

Autotaxin (CHEMBL3691)
Type SINGLE PROTEIN
Organism Homo sapiens

Publication

Discovery of Potent Selective Nonzinc Binding Autotaxin Inhibitor BIO-32546.
Ma B, Zhang L, Sun L, Xin Z, Kumaravel G, Marcotte D, Chodaparambil JV, Wang Q, Wehr A, Jing J, Hong VS, Wang T, Huang C, Shao Z, Mi S.
ACS Med Chem Lett (2021) 12 : 1124 -1129
PubMed 34267882 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 13 7.24 9.00

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL4871014 1 9.00
CHEMBL4850429 1 8.85
CHEMBL4872157 1 8.44
CHEMBL4871067 1 8.09
CHEMBL4858196 1 7.55
CHEMBL4868783 1 7.42
CHEMBL4859055 1 7.00
CHEMBL1615121 1 6.96
CHEMBL4847281 1 6.64
CHEMBL4858465 1 6.48
CHEMBL4846048 1 6.43
CHEMBL4872976 1 5.89
CHEMBL4875797 1 5.43

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL4871014 IC50 = 1.0 nM 9.00
CHEMBL4850429 IC50 = 1.4 nM 8.85
CHEMBL4872157 IC50 = 3.6 nM 8.44
CHEMBL4871067 IC50 = 8.2 nM 8.09
CHEMBL4858196 IC50 = 28.0 nM 7.55
CHEMBL4868783 IC50 = 38.0 nM 7.42
CHEMBL4859055 IC50 = 100.0 nM 7.00
CHEMBL1615121 IC50 = 110.0 nM 6.96
CHEMBL4847281 IC50 = 230.0 nM 6.64
CHEMBL4858465 IC50 = 330.0 nM 6.48
CHEMBL4846048 IC50 = 370.0 nM 6.43
CHEMBL4872976 IC50 = 1300.0 nM 5.89
CHEMBL4875797 IC50 = 3700.0 nM 5.43