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Assay Detail

CHEMBL3767463

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

Binding
Inhibition of CDK9/Cyclin T1 (unknown origin) using (YSPTSPS)2KK peptide as substrate in presence of [gamma-33P]ATP
5
Total Activities
5
Compounds Tested
1
Activity Types
0
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

Synthesis, biological evaluation and molecular modeling of a novel series of 7-azaindole based tri-heterocyclic compounds as potent CDK2/Cyclin E inhibitors.
Baltus CB, Jorda R, Marot C, Berka K, Bazgier V, Kryštof V, Prié G, Viaud-Massuard MC.
Eur J Med Chem (2016) 108 : 701 -719
PubMed 26741853 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 5 6.24 7.00

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL3301610 ABEMACICLIB 4.0 1 7.00
CHEMBL2103840 DINACICLIB 3.0 1 6.75
CHEMBL3263773 1 6.64
CHEMBL1801932 1 5.75
CHEMBL3763161 1 5.05

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL3301610 ABEMACICLIB IC50 = 101.0 nM 7.00
CHEMBL2103840 DINACICLIB IC50 = 178.0 nM 6.75
CHEMBL3263773 IC50 = 230.0 nM 6.64
CHEMBL1801932 IC50 = 1790.0 nM 5.75
CHEMBL3763161 IC50 = 9000.0 nM 5.05