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Assay Detail

CHEMBL643110

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

Binding
Tested for in vitro inhibition activity against human Aldose reductase (human AR)
2
Total Activities
2
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Binding
Confidence 8 — Homologous single protein target
Curated By Autocuration

Target

Aldo-keto reductase family 1 member B1 (CHEMBL1900)
Type SINGLE PROTEIN
Organism Homo sapiens

Publication

A potent aldose reductase inhibitor, (2S,4S)-6-fluoro-2', 5'-dioxospiro[chroman-4,4'-imidazolidine]-2-carboxamide (Fidarestat): its absolute configuration and interactions with the aldose reductase by X-ray crystallography.
Oka M, Matsumoto Y, Sugiyama S, Tsuruta N, Matsushima M.
J Med Chem (2000) 43 : 2479 -2483
PubMed 10882376 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 2 6.88 8.05

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL84446 FIDARESTAT 2.0 1 8.05
CHEMBL266497 SORBINIL 3.0 1 5.70

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL84446 FIDARESTAT IC50 = 9.0 nM 8.05
CHEMBL266497 SORBINIL IC50 = 2000.0 nM 5.70