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

CHEMBL4605528

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

Binding
Inhibition of oligomycin-treated GLUT in human HT1080 cells assessed as reduction in ATP level measured after 90 mins by Celltiter-glo luminescent assay
14
Total Activities
14
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Binding
Organism Homo sapiens
Cell Type HT-1080
Confidence 0 — Uncurated / Unknown
Curated By Autocuration

Target

Unchecked (CHEMBL612545)
Type UNCHECKED

Publication

Discovery and Optimization of Glucose Uptake Inhibitors.
Liu KG, Kim JI, Olszewski K, Barsotti AM, Morris K, Lamarque C, Yu X, Gaffney J, Feng XJ, Patel JP, Poyurovsky MV.
J Med Chem (2020) 63 : 5201 -5211
PubMed 32282207 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 14 6.65 7.44

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL4643788 1 7.44
CHEMBL4639095 1 7.42
CHEMBL4648466 1 7.13
CHEMBL4645191 1 6.96
CHEMBL4641937 1 6.84
CHEMBL4648818 1 6.82
CHEMBL4642673 1 6.70
CHEMBL4634911 1 6.59
CHEMBL4634395 1 6.55
CHEMBL4637469 1 6.53
CHEMBL4642368 1 6.48
CHEMBL4634177 1 6.46
CHEMBL4642715 1 5.70
CHEMBL4637224 1 5.46

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL4643788 IC50 = 36.0 nM 7.44
CHEMBL4639095 IC50 = 38.0 nM 7.42
CHEMBL4648466 IC50 = 74.0 nM 7.13
CHEMBL4645191 IC50 = 110.0 nM 6.96
CHEMBL4641937 IC50 = 146.0 nM 6.84
CHEMBL4648818 IC50 = 150.0 nM 6.82
CHEMBL4642673 IC50 = 200.0 nM 6.70
CHEMBL4634911 IC50 = 259.0 nM 6.59
CHEMBL4634395 IC50 = 282.0 nM 6.55
CHEMBL4637469 IC50 = 298.0 nM 6.53
CHEMBL4642368 IC50 = 328.0 nM 6.48
CHEMBL4634177 IC50 = 350.0 nM 6.46
CHEMBL4642715 IC50 = 1980.0 nM 5.70
CHEMBL4637224 IC50 = 3474.0 nM 5.46