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Assay Detail

CHEMBL4003368

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

Binding
Inhibition of CHK1 (unknown origin) using polypeptide substrate after 40 mins in presence of [gamma-33P]ATP by scintillation counting method
1
Total Activities
1
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

Serine/threonine-protein kinase Chk1 (CHEMBL4630)
Type SINGLE PROTEIN
Organism Homo sapiens

Publication

Novel CLK1 inhibitors based on N-aryloxazol-2-amine skeleton - A possible way to dual VEGFR2 TK/CLK ligands.
Murár M, Dobiaš J, Šramel P, Addová G, Hanquet G, Boháč A.
Eur J Med Chem (2017) 126 : 754 -761
PubMed 27940419 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 1 6.14 6.14

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL255465 DEBROMOHYMENIALDISINE 1 6.14

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL255465 DEBROMOHYMENIALDISINE IC50 = 725.0 nM 6.14