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Assay Detail

CHEMBL5045446

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

Binding
Inhibition of Candida albicans Fructose-1,6-Bisphosphate Aldolase C157S mutant transfected in Escherichia coli BL21 (DE3) incubated for 3 mins in presence of NADH by spectrophotometric analysis
3
Total Activities
3
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Binding
Organism Candida albicans
Confidence 0 — Uncurated / Unknown
Curated By Autocuration

Target

Unchecked (CHEMBL612545)
Type UNCHECKED

Publication

Structure-Guided Discovery of the Novel Covalent Allosteric Site and Covalent Inhibitors of Fructose-1,6-Bisphosphate Aldolase to Overcome the Azole Resistance of <i>Candidiasis</i>.
Wen W, Cao H, Huang Y, Tu J, Wan C, Wan J, Han X, Chen H, Liu J, Rao L, Su C, Peng C, Sheng C, Ren Y.
J Med Chem (2022) 65 : 2656 -2674
PubMed 35099959 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 3 6.35 7.51

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL51085 EBSELEN 3.0 1 7.51
CHEMBL5090832 1 6.64
CHEMBL5075467 1 4.90

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL51085 EBSELEN IC50 = 31.0 nM 7.51
CHEMBL5090832 IC50 = 227.0 nM 6.64
CHEMBL5075467 IC50 = 12500.0 nM 4.90