Skip to main content
Free research Free research Free assay review with research home and workspace preview
Quick search ChEMBL 36
Assay Detail

CHEMBL4399071

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

Binding
Inhibition of human recombinant IDE expressed in Escherichia coli BL21 (DE3) cells using ATTO 655- Cys-Lys-Leu-Val-Phe-Phe-Ala-Glu-Asp-Trp as substrate preincubated for 10 mins followed by substrate addition and measured after 30 mins by spectrophotometric analysis
5
Total Activities
5
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

Insulin-degrading enzyme (CHEMBL1293287)
Type SINGLE PROTEIN
Organism Homo sapiens

Publication

Identification of ebselen as a potent inhibitor of insulin degrading enzyme by a drug repurposing screening.
Leroux F, Bosc D, Beghyn T, Hermant P, Warenghem S, Landry V, Pottiez V, Guillaume V, Charton J, Herledan A, Urata S, Liang W, Sheng L, Tang WJ, Deprez B, Deprez-Poulain R.
Eur J Med Chem (2019) 179 : 557 -566
PubMed 31276900 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 5 5.10 7.38

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL51085 EBSELEN 3.0 1 7.38
CHEMBL1201195 CEFMETAZOLE 4.0 1 5.16
CHEMBL1219 RABEPRAZOLE 4.0 1 4.96
CHEMBL1237046 ROLITETRACYCLINE 2.0 1 4.00
CHEMBL164 MYRICETIN 1 4.00

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL51085 EBSELEN IC50 = 42.0 nM 7.38
CHEMBL1201195 CEFMETAZOLE IC50 = 7000.0 nM 5.16
CHEMBL1219 RABEPRAZOLE IC50 = 11000.0 nM 4.96
CHEMBL1237046 ROLITETRACYCLINE IC50 = 100000.0 nM 4.00
CHEMBL164 MYRICETIN IC50 = 100000.0 nM 4.00