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Assay Detail

CHEMBL993579

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

Binding
Inhibition of maltase in human Caco-2 cell model system after 2 hrs
5
Total Activities
5
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Binding
Organism Homo sapiens
Cell Type Caco-2
Confidence 9 — Direct single protein target
Curated By Autocuration

Target

Lysosomal alpha-glucosidase (CHEMBL2608)
Type SINGLE PROTEIN
Organism Homo sapiens

Publication

In vitro inhibition of glycogen-degrading enzymes and glycosidases by six-membered sugar mimics and their evaluation in cell cultures.
Kuriyama C, Kamiyama O, Ikeda K, Sanae F, Kato A, Adachi I, Imahori T, Takahata H, Okamoto T, Asano N.
Bioorg Med Chem (2008) 16 : 7330 -7336
PubMed 18595718 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 5 6.54 7.22

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL307429 DUVOGLUSTAT 2.0 1 7.22
CHEMBL476960 VOGLIBOSE 4.0 1 7.16
CHEMBL501355 1 7.00
CHEMBL1561 MIGLITOL 4.0 1 6.00
CHEMBL404271 ACARBOSE 4.0 1 5.30

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL307429 DUVOGLUSTAT IC50 = 60.0 nM 7.22
CHEMBL476960 VOGLIBOSE IC50 = 70.0 nM 7.16
CHEMBL501355 IC50 = 100.0 nM 7.00
CHEMBL1561 MIGLITOL IC50 = 1000.0 nM 6.00
CHEMBL404271 ACARBOSE IC50 = 5000.0 nM 5.30