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Assay Detail

CHEMBL827987

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

Binding
Inhibition of rat intestinal maltase using disaccharide
11
Total Activities
11
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Binding
Organism Rattus norvegicus
Confidence 9 — Direct single protein target
Curated By Expert

Target

Sucrase-isomaltase, intestinal (CHEMBL3114)
Type SINGLE PROTEIN
Organism Rattus norvegicus

Publication

Alpha-1-C-alkyl-1-deoxynojirimycin derivatives as potent and selective inhibitors of intestinal isomaltase: remarkable effect of the alkyl chain length on glycosidase inhibitory profile.
Godin G, Compain P, Martin OR, Ikeda K, Yu L, Asano N.
Bioorg Med Chem Lett (2004) 14 : 5991 -5995
PubMed 15546715 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 11 5.39 5.89

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL187158 1 5.89
CHEMBL186068 1 5.82
CHEMBL186291 1 5.72
CHEMBL1029 MIGLUSTAT 4.0 1 5.68
CHEMBL364554 1 5.46
CHEMBL186150 1 5.43
CHEMBL184028 1 5.40
CHEMBL362754 1 5.16
CHEMBL3351101 1 4.92
CHEMBL187208 1 4.37
CHEMBL3349976 1 -

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL187158 IC50 = 1300.0 nM 5.89
CHEMBL186068 IC50 = 1500.0 nM 5.82
CHEMBL186291 IC50 = 1900.0 nM 5.72
CHEMBL1029 MIGLUSTAT IC50 = 2100.0 nM 5.68
CHEMBL364554 IC50 = 3500.0 nM 5.46
CHEMBL186150 IC50 = 3700.0 nM 5.43
CHEMBL184028 IC50 = 4000.0 nM 5.40
CHEMBL362754 IC50 = 7000.0 nM 5.16
CHEMBL3351101 IC50 = 12000.0 nM 4.92
CHEMBL187208 IC50 = 43000.0 nM 4.37
CHEMBL3349976 IC50 = 210000.0 nM -