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Assay Detail

CHEMBL2175689

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Binding
Inhibition of human recombinant AKR1C1 assessed as 1-acenaphthenol oxidation at 400 uM by spectrophotometry
15
Total Activities
15
Compounds Tested
2
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 C1 (CHEMBL5905)
Type SINGLE PROTEIN
Organism Homo sapiens

Publication

Selective inhibitors of aldo-keto reductases AKR1C1 and AKR1C3 discovered by virtual screening of a fragment library.
Brožič P, Turk S, Adeniji AO, Konc J, Janežič D, Penning TM, Lanišnik Rižner T, Gobec S.
J Med Chem (2012) 55 : 7417 -7424
PubMed 22881866 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
Inhibition 14 - -
Ki 1 8.39 8.39

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL387536 1 8.39
CHEMBL366350 1 -
CHEMBL2172259 1 -
CHEMBL2172258 1 -
CHEMBL2172253 1 -
CHEMBL2172250 1 -
CHEMBL2172249 1 -
CHEMBL2172248 1 -
CHEMBL2172247 1 -
CHEMBL2172246 1 -
CHEMBL2172245 1 -
CHEMBL2172244 1 -
CHEMBL2172242 1 -
CHEMBL2172240 1 -
CHEMBL2172239 1 -

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL387536 Ki = 4.1 nM 8.39
CHEMBL366350 Inhibition = 43.5 % -
CHEMBL2172259 Inhibition < 10.0 % -
CHEMBL2172258 Inhibition < 10.0 % -
CHEMBL2172253 Inhibition < 10.0 % -
CHEMBL2172250 Inhibition = 43.1 % -
CHEMBL2172249 Inhibition = 44.8 % -
CHEMBL2172248 Inhibition = 39.5 % -
CHEMBL2172247 Inhibition < 10.0 % -
CHEMBL2172246 Inhibition = 47.4 % -
CHEMBL2172245 Inhibition < 10.0 % -
CHEMBL2172244 Inhibition = 22.5 % -
CHEMBL2172242 Inhibition < 10.0 % -
CHEMBL2172240 Inhibition < 10.0 % -
CHEMBL2172239 Inhibition = 30.1 % -