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Assay Detail

CHEMBL4775166

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

Binding
Inhibition of 6His-tagged human RD52 assessed as reduction in RD52 binding to Cy3-dT30-Cy5 ssDNA incubated for 30 mins by FRET assay
3
Total Activities
3
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

DNA repair protein RAD52 homolog (CHEMBL2362978)
Type SINGLE PROTEIN
Organism Homo sapiens

Publication

Synthetic Lethality through the Lens of Medicinal Chemistry.
Myers SH,Ortega JA,Cavalli A
J Med Chem (2020) 63 : 14151 -14183
PubMed 33135887 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 3 6.04 6.56

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL297453 EPIGALOCATECHIN GALLATE 3.0 1 6.56
CHEMBL504212 STRICTININ 1 5.82
CHEMBL47386 EPIGALLOCATECHIN 1 5.75

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL297453 EPIGALOCATECHIN GALLATE IC50 = 277.0 nM 6.56
CHEMBL504212 STRICTININ IC50 = 1500.0 nM 5.82
CHEMBL47386 EPIGALLOCATECHIN IC50 = 1800.0 nM 5.75