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

CHEMBL2444352

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

Binding
Competitive inhibition of human recombinant AKR1B10 W220Y mutant expressed in Escherichia coli using geraniol as substrate by double-reciprocal plot analysis in presence of NADP+
1
Total Activities
1
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

Aldo-keto reductase family 1 member B10 (CHEMBL5983)
Type SINGLE PROTEIN
Organism Homo sapiens

Publication

Synthesis and structure-activity relationship of 2-phenyliminochromene derivatives as inhibitors for aldo-keto reductase (AKR) 1B10.
Endo S, Hu D, Suyama M, Matsunaga T, Sugimoto K, Matsuya Y, El-Kabbani O, Kuwata K, Hara A, Kitade Y, Toyooka N.
Bioorg Med Chem (2013) 21 : 6378 -6384
PubMed 24071447 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
Ki 1 7.29 7.29

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL2440417 1 7.29

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL2440417 Ki = 51.0 nM 7.29