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Assay Detail

CHEMBL4029486

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

Binding
Inhibition of CDK8 in human A549 cells by mass spectrometric method
1
Total Activities
1
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Binding
Organism Homo sapiens
Cell Type A549
Confidence 9 — Direct single protein target
Curated By Autocuration

Target

Cyclin-dependent kinase 8 (CHEMBL5719)
Type SINGLE PROTEIN
Organism Homo sapiens

Publication

Design and synthesis of selective CDK8/19 dual inhibitors: Discovery of 4,5-dihydrothieno[3',4':3,4]benzo[1,2-d]isothiazole derivatives.
Ono K, Banno H, Okaniwa M, Hirayama T, Iwamura N, Hikichi Y, Murai S, Hasegawa M, Hasegawa Y, Yonemori K, Hata A, Aoyama K, Cary DR.
Bioorg Med Chem (2017) 25 : 2336 -2350
PubMed 28302507 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 1 7.66 7.66

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL3361254 1 7.66

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL3361254 IC50 = 22.0 nM 7.66