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Assay Detail

CHEMBL4150690

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

Functional
Antiviral activity against Influenza A virus (A/Puerto Rico/8/1934(H1N1)) infected in MDCK cells assessed as reduction in plaque formation after 2 days by toluidine blue staining-based assay
7
Total Activities
7
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Functional
Organism Influenza A virus
Cell Type MDCK
Confidence 1 — Organism
Curated By Intermediate

Target

Influenza A virus (CHEMBL613740)
Type ORGANISM
Organism Influenza A virus

Publication

Optimization of N-Substituted Oseltamivir Derivatives as Potent Inhibitors of Group-1 and -2 Influenza A Neuraminidases, Including a Drug-Resistant Variant.
Zhang J, Poongavanam V, Kang D, Bertagnin C, Lu H, Kong X, Ju H, Lu X, Gao P, Tian Y, Jia H, Desta S, Ding X, Sun L, Fang Z, Huang B, Liang X, Jia R, Ma X, Xu W, Murugan NA, Loregian A, Huang B, Zhan P, Liu X.
J Med Chem (2018) 61 : 6379 -6397
PubMed 29965752 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
EC50 7 6.54 7.40

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL674 OSELTAMIVIR CARBOXYLATE -1.0 1 7.40
CHEMBL222813 ZANAMIVIR 4.0 1 7.30
CHEMBL4161935 1 7.16
CHEMBL4175983 1 6.66
CHEMBL4173256 1 6.16
CHEMBL4163386 1 5.71
CHEMBL4160858 1 5.36

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL674 OSELTAMIVIR CARBOXYLATE EC50 = 40.0 nM 7.40
CHEMBL222813 ZANAMIVIR EC50 = 50.0 nM 7.30
CHEMBL4161935 EC50 = 70.0 nM 7.16
CHEMBL4175983 EC50 = 220.0 nM 6.66
CHEMBL4173256 EC50 = 690.0 nM 6.16
CHEMBL4163386 EC50 = 1950.0 nM 5.71
CHEMBL4160858 EC50 = 4400.0 nM 5.36