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Assay Detail

CHEMBL1022248

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

Binding
Reversible inhibition of human ODCase
7
Total Activities
7
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

Uridine 5'-monophosphate synthase (CHEMBL5216)
Type SINGLE PROTEIN
Organism Homo sapiens

Publication

Structure-activity relationships of orotidine-5'-monophosphate decarboxylase inhibitors as anticancer agents.
Bello AM, Konforte D, Poduch E, Furlonger C, Wei L, Liu Y, Lewis M, Pai EF, Paige CJ, Kotra LP.
J Med Chem (2009) 52 : 1648 -1658
PubMed 19260677 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
Ki 7 5.08 6.46

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL473587 1 6.46
CHEMBL474165 1 4.78
CHEMBL474163 1 4.01
CHEMBL512577 1 -
CHEMBL472783 1 -
CHEMBL514137 1 -
CHEMBL463623 1 -

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL473587 Ki = 350.0 nM 6.46
CHEMBL474165 Ki = 16600.0 nM 4.78
CHEMBL474163 Ki = 98000.0 nM 4.01
CHEMBL512577 Ki - -
CHEMBL472783 Ki - -
CHEMBL514137 Ki - -
CHEMBL463623 Ki - -