Skip to main content
Free research Free research Free assay review with research home and workspace preview
Quick search ChEMBL 36
Assay Detail

CHEMBL5717702

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

Binding
Inhibition of CDK9/Cyclin T1 (unknown origin) using ULight MBP peptide as substrate in presence of ATP incubated for 1 hr by FRET based LANCE Ultra KinaSelect screen assay
4
Total Activities
4
Compounds Tested
1
Activity Types
2
Assay Parameters

Assay Information

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

Target

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

Publication

Characterization of molecular and cellular functions of the cyclin-dependent kinase CDK9 using a novel specific inhibitor.
Albert TK, Rigault C, Eickhoff J, Baumgart K, Antrecht C, Klebl B, Mittler G, Meisterernst M.
Br J Pharmacol (2014) 171 : 55 -68
PubMed 24102143 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 4 7.59 9.00

Assay Parameters

Parameter Type Value Units Text
EFO_ID EFO_ID - EFO:0000095
EFO_TERM EFO_TERM - chronic lymphocytic leukemia

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL296468 BMS-387032 1.0 1 9.00
CHEMBL428690 ALVOCIDIB 3.0 1 8.30
CHEMBL5722954 1 7.36
CHEMBL375530 DICHLORORIBOBENZIMIDAZOLE 1 5.71

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL296468 BMS-387032 IC50 = 1.0 nM 9.00
CHEMBL428690 ALVOCIDIB IC50 = 5.0 nM 8.30
CHEMBL5722954 IC50 = 44.0 nM 7.36
CHEMBL375530 DICHLORORIBOBENZIMIDAZOLE IC50 = 1942.0 nM 5.71