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Assay Detail

CHEMBL5235852

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

Binding
Inhibition of human wild type DYRK1A (M1 to S629) expressed in bacterial system by Ambit Kinomescan binding 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

Publication

DYRK1A Inhibitors as Potential Therapeutics for β-Cell Regeneration for Diabetes.
Kumar K, Suebsuwong C, Wang P, Garcia-Ocana A, Stewart AF, DeVita RJ.
J Med Chem (2021) 64 : 2901 -2922
PubMed 33682417 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 2 7.61 8.22

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL5186778 1 8.22
CHEMBL4638292 1 7.00

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL5186778 IC50 = 6.0 nM 8.22
CHEMBL4638292 IC50 = 100.0 nM 7.00