Skip to main content
Free research Free research Free assay review with research home and workspace preview
Quick search ChEMBL 36
Assay Detail

CHEMBL5041875

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

Binding
Inhibition of human recombinant soluble CD73 assessed as inhibition constant by radiometric assay
2
Total Activities
2
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

5'-nucleotidase (CHEMBL5957)
Type SINGLE PROTEIN
Organism Homo sapiens

Publication

Structure-Activity Relationship of 3-Methylcytidine-5'-α,β-methylenediphosphates as CD73 Inhibitors.
Scortichini M, Idris RM, Moschütz S, Keim A, Salmaso V, Dobelmann C, Oliva P, Losenkova K, Irjala H, Vaittinen S, Sandholm J, Yegutkin GG, Sträter N, Junker A, Müller CE, Jacobson KA.
J Med Chem (2022) 65 : 2409 -2433
PubMed 35080883 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
Ki 2 7.86 8.66

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL4755577 1 8.66
CHEMBL583969 PHOSPHOMETHYLPHOSPHONIC ACID ADENOSYL ESTER 1 7.05

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL4755577 Ki = 2.21 nM 8.66
CHEMBL583969 PHOSPHOMETHYLPHOSPHONIC ACID ADENOSYL ESTER Ki = 88.4 nM 7.05