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Assay Detail

CHEMBL1010812

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

Binding
Irreversible inhibition of human ODCase
4
Total Activities
2
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

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 2 5.35 5.96
Kinact 2 - -

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL474164 2 5.96
CHEMBL514166 2 4.74

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL474164 Ki = 1100.0 nM 5.96
CHEMBL514166 Ki = 18200.0 nM 4.74
CHEMBL474164 Kinact = 158.0 /hr -
CHEMBL514166 Kinact = 41.0 /hr -