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Assay Detail

CHEMBL5550428

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

Binding
Inhibition of human recombinant CDK9/cyclin T expressed in baculovirus-infected Sf9 cells using YSPTSPSYSPTSPSYSPTSPSKKKK as substrate incubated for 30 mins in presence of ATP by ADP-Glo kinase assay
4
Total Activities
4
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Binding
Organism Homo sapiens
Cell Type Sf9
Confidence 7 — Homologous single protein target
Curated By Autocuration

Target

CDK9/cyclin T1 (CHEMBL2111389)
Type PROTEIN COMPLEX
Organism Homo sapiens

Publication

Synthesis and biological evaluation of 1H-pyrrolo[3,2-g]isoquinolines.
Defois M, Josselin B, Brindeau P, Krämer A, Knapp S, Anizon F, Giraud F, Ruchaud S, Moreau P.
Bioorg Med Chem (2024) 100 : 117619 -117619
PubMed 38320389 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 4 6.56 6.82

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL5571626 1 6.82
CHEMBL5569099 1 6.75
CHEMBL5562930 1 6.65
CHEMBL5592689 1 6.00

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL5571626 IC50 = 151.0 nM 6.82
CHEMBL5569099 IC50 = 178.0 nM 6.75
CHEMBL5562930 IC50 = 222.0 nM 6.65
CHEMBL5592689 IC50 = 999.0 nM 6.00