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Assay Detail

CHEMBL2329964

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

Binding
Inhibition of human recombinant IDE-mediated fluorescein-Abeta-(1-40)-Lys-biotin degradation
8
Total Activities
8
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

Optimization of peptide hydroxamate inhibitors of insulin-degrading enzyme reveals marked substrate-selectivity.
Abdul-Hay SO, Lane AL, Caulfield TR, Claussin C, Bertrand J, Masson A, Choudhry S, Fauq AH, Maharvi GM, Leissring MA.
J Med Chem (2013) 56 : 2246 -2255
PubMed 23437776 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
Ki 8 7.04 8.85

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL2324206 1 8.85
CHEMBL2324220 1 7.66
CHEMBL2324201 1 7.15
CHEMBL2324203 1 6.97
CHEMBL2324204 1 6.64
CHEMBL2324207 1 6.61
CHEMBL2324205 1 6.44
CHEMBL2324202 1 6.03

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL2324206 Ki = 1.4 nM 8.85
CHEMBL2324220 Ki = 21.7 nM 7.66
CHEMBL2324201 Ki = 70.3 nM 7.15
CHEMBL2324203 Ki = 107.0 nM 6.97
CHEMBL2324204 Ki = 228.0 nM 6.64
CHEMBL2324207 Ki = 246.0 nM 6.61
CHEMBL2324205 Ki = 365.0 nM 6.44
CHEMBL2324202 Ki = 927.0 nM 6.03