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Assay Detail

CHEMBL5118630

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

Binding
Inhibition of glycoprotein in luciferase expressing pseudotyped VSV infected in human Huh-7 cells assessed as inhibition of viral entry by measuring inhibition of virus-expressed reporter bioluminescence pretreated with cells for 30 mins followed by incubation with pseudotyped virus for 2 days by luciferase reporter assay
4
Total Activities
4
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Binding
Organism Vesicular stomatitis virus
Cell Type Huh-7
Confidence 0 — Uncurated / Unknown
Curated By Autocuration

Target

Unchecked (CHEMBL612545)
Type UNCHECKED

Publication

Discovery of potent ebola entry inhibitors with (3S,4aS,8aS)-2-(3-amino-2-hydroxypropyl) decahydroisoquinoline-3-carboxamide scaffold.
Han S, Li H, Chen W, Yang L, Tong X, Zuo J, Hu Y.
Eur J Med Chem (2022) 240 : 114608 -114608
PubMed 35872393 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 4 4.96 5.52

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL5190865 1 5.52
CHEMBL5200629 1 4.85
CHEMBL1655 TOREMIFENE 4.0 1 4.75
CHEMBL114 SAQUINAVIR 4.0 1 4.71

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL5190865 IC50 = 3020.0 nM 5.52
CHEMBL5200629 IC50 = 14090.0 nM 4.85
CHEMBL1655 TOREMIFENE IC50 = 17790.0 nM 4.75
CHEMBL114 SAQUINAVIR IC50 = 19340.0 nM 4.71