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Assay Detail

CHEMBL1767945

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

Binding
Inhibition of rat small intestinal isomaltase after 30 mins
9
Total Activities
9
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

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

Target

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

Publication

Role of the side chain stereochemistry in the α-glucosidase inhibitory activity of kotalanol, a potent natural α-glucosidase inhibitor.
Xie W, Tanabe G, Matsuoka K, Amer MF, Minematsu T, Wu X, Yoshikawa M, Muraoka O.
Bioorg Med Chem (2011) 19 : 2252 -2262
PubMed 21420866 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 9 5.24 5.89

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL1208974 SALACINOL 1 5.89
CHEMBL476960 VOGLIBOSE 4.0 1 5.68
CHEMBL1209027 SALAPRINOL 1 5.58
CHEMBL1093264 KOTALANOL 1 5.24
CHEMBL1765290 1 5.07
CHEMBL1765344 1 5.05
CHEMBL1765289 1 4.80
CHEMBL1765343 1 4.60
CHEMBL404271 ACARBOSE 4.0 1 -

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL1208974 SALACINOL IC50 = 1300.0 nM 5.89
CHEMBL476960 VOGLIBOSE IC50 = 2100.0 nM 5.68
CHEMBL1209027 SALAPRINOL IC50 = 2600.0 nM 5.58
CHEMBL1093264 KOTALANOL IC50 = 5700.0 nM 5.24
CHEMBL1765290 IC50 = 8500.0 nM 5.07
CHEMBL1765344 IC50 = 9000.0 nM 5.05
CHEMBL1765289 IC50 = 16000.0 nM 4.80
CHEMBL1765343 IC50 = 25000.0 nM 4.60
CHEMBL404271 ACARBOSE IC50 = 155000.0 nM -