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Assay Detail

CHEMBL645284

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

Binding
Compound was evaluated In vitro for inhibition of aldose reductase activity by 50% in dog RBC
3
Total Activities
3
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Binding
Organism Canis lupus familiaris
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

Novel spirosuccinimide aldose reductase inhibitors derived from isoquinoline-1,3-diones: 2-[(4-bromo-2-fluorophenyl)methyl]-6- fluorospiro[isoquinoline-4(1H),3'-pyrrolidine]-1,2',3,5'(2H)-tetrone and congeners. 1.
Malamas MS, Hohman TC, Millen J.
J Med Chem (1994) 37 : 2043 -2058
PubMed 8027986 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 3 7.75 7.91

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL273910 MINALRESTAT 2.0 1 7.91
CHEMBL62685 1 7.71
CHEMBL436 TOLRESTAT 4.0 1 7.62

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL273910 MINALRESTAT IC50 = 12.2 nM 7.91
CHEMBL62685 IC50 = 19.4 nM 7.71
CHEMBL436 TOLRESTAT IC50 = 23.9 nM 7.62