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Assay Detail

CHEMBL5588486

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

Functional
Antiproliferative activity against human PC-9 cells incubated for 72 hrs by celltiter-glo luminescent assay
12
Total Activities
12
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Functional
Organism Homo sapiens
Cell Type PC-9
Confidence 1 — Organism
Curated By Autocuration

Target

PC-9 (CHEMBL614102)
Type CELL-LINE
Organism Homo sapiens

Publication

Discovery of Novel 2-Aminopyridine-Based and 2-Aminopyrimidine-Based Derivatives as Potent CDK/HDAC Dual Inhibitors for the Treatment of Refractory Solid Tumors and Hematological Malignancies.
Saidahmatov A, Li J, Xu S, Hu X, Gao X, Kan W, Gao L, Li C, Shi Y, Sheng L, Wang P, Zhou Y, Liang X, Li J, Liu H.
J Med Chem (2024) 67 : 15220 -15245
PubMed 39178382 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 12 5.82 7.52

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL3656841 1 7.52
CHEMBL5598116 1 6.72
CHEMBL5596602 1 6.16
CHEMBL5598168 1 6.00
CHEMBL98 VORINOSTAT 4.0 1 5.96
CHEMBL5597266 1 5.91
CHEMBL5597605 1 5.71
CHEMBL5598317 1 5.42
CHEMBL5598054 1 5.36
CHEMBL5598550 1 5.18
CHEMBL5597396 1 5.04
CHEMBL5598531 1 4.86

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL3656841 IC50 = 30.0 nM 7.52
CHEMBL5598116 IC50 = 190.0 nM 6.72
CHEMBL5596602 IC50 = 690.0 nM 6.16
CHEMBL5598168 IC50 = 1010.0 nM 6.00
CHEMBL98 VORINOSTAT IC50 = 1100.0 nM 5.96
CHEMBL5597266 IC50 = 1220.0 nM 5.91
CHEMBL5597605 IC50 = 1960.0 nM 5.71
CHEMBL5598317 IC50 = 3770.0 nM 5.42
CHEMBL5598054 IC50 = 4400.0 nM 5.36
CHEMBL5598550 IC50 = 6550.0 nM 5.18
CHEMBL5597396 IC50 = 9120.0 nM 5.04
CHEMBL5598531 IC50 = 13800.0 nM 4.86