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Assay Detail

CHEMBL3591331

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

Binding
Inhibition of DYRK1A in human HeLa cells assessed as reduction of SF3B1 phosphorylation by immunoblotting analysis
2
Total Activities
1
Compounds Tested
2
Activity Types
0
Assay Parameters

Assay Information

Assay Type Binding
Organism Homo sapiens
Cell Type HeLa
Confidence 9 — Direct single protein target
Curated By Autocuration

Publication

10-iodo-11H-indolo[3,2-c]quinoline-6-carboxylic acids are selective inhibitors of DYRK1A.
Falke H, Chaikuad A, Becker A, Loaëc N, Lozach O, Abu Jhaisha S, Becker W, Jones PG, Preu L, Baumann K, Knapp S, Meijer L, Kunick C.
J Med Chem (2015) 58 : 3131 -3143
PubMed 25730262 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
Inhibition 1 - -
IC50 1 5.68 5.68

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL3589662 2 5.68

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL3589662 IC50 = 2100.0 nM 5.68
CHEMBL3589662 Inhibition - % -