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

CHEMBL5326953

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

Toxicity
Cytotoxicity against human GES1 cells harboring low LSD1 expression assessed as inhibition of cell growth incubated for 72 hrs by celltiter glo assay
7
Total Activities
7
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Toxicity
Organism Homo sapiens
Cell Type GES1
Confidence 1 — Organism
Curated By Autocuration

Target

GES1 (CHEMBL4296415)
Type CELL-LINE
Organism Homo sapiens

Publication

Discovery of novel, potent, and orally bioavailable HDACs inhibitors with LSD1 inhibitory activity for the treatment of solid tumors.
Duan Y, Yu T, Jin L, Zhang S, Shi X, Zhang Y, Zhou N, Xu Y, Lu W, Zhou H, Zhu H, Bai S, Hu K, Guan Y.
Eur J Med Chem (2023) 254 : 115367 -115367
PubMed 37086699 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 7 5.05 5.06

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL5435925 1 5.06
CHEMBL5434546 1 5.05
CHEMBL98 VORINOSTAT 4.0 1 5.04
CHEMBL5433364 1 -
CHEMBL5440196 1 -
CHEMBL5406191 1 -
CHEMBL5440032 1 -

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL5435925 IC50 = 8660.0 nM 5.06
CHEMBL5434546 IC50 = 8890.0 nM 5.05
CHEMBL98 VORINOSTAT IC50 = 9180.0 nM 5.04
CHEMBL5433364 IC50 - -
CHEMBL5440196 IC50 - -
CHEMBL5406191 IC50 - -
CHEMBL5440032 IC50 - -