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Assay Detail

CHEMBL869172

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

Binding
Inhibition of Saccharomyces cerevisiae ODCase at 25 degreeC by competitive binding assay
1
Total Activities
1
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Binding
Organism Saccharomyces cerevisiae
Confidence 8 — Homologous single protein target
Curated By Expert

Target

Orotidine 5'-phosphate decarboxylase (CHEMBL4858)
Type SINGLE PROTEIN
Organism Saccharomyces cerevisiae S288c

Publication

Design of inhibitors of orotidine monophosphate decarboxylase using bioisosteric replacement and determination of inhibition kinetics.
Poduch E, Bello AM, Tang S, Fujihashi M, Pai EF, Kotra LP.
J Med Chem (2006) 49 : 4937 -4945
PubMed 16884305 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
Ki 1 7.19 7.19

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL463480 6-AZA-URIDINE MONOPHOSPHATE 1 7.19

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL463480 6-AZA-URIDINE MONOPHOSPHATE Ki = 64.0 nM 7.19