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Assay Detail

CHEMBL4363628

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

Binding
Inhibition of influenza A virus H3N2 clinical isolate neuraminidase using NA-Fluor MUNANA as substrate preincubated for 20 to 30 mins followed by substrate addition and measured for 60 mins by fluorescence assay
3
Total Activities
3
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Binding
Organism Influenza A virus H3N2
Confidence 8 — Homologous single protein target
Curated By Autocuration

Target

Neuraminidase (CHEMBL6015)
Type SINGLE PROTEIN
Organism Influenza A virus (A/Memphis/1/1971(H3N2))

Publication

Novel N-Substituted oseltamivir derivatives as potent influenza neuraminidase inhibitors: Design, synthesis, biological evaluation, ADME prediction and molecular docking studies.
Ye J, Yang X, Xu M, Chan PK, Ma C.
Eur J Med Chem (2019) 182 : 111635 -111635
PubMed 31493744 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 3 9.16 9.96

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL674 OSELTAMIVIR CARBOXYLATE -1.0 1 9.96
CHEMBL4545891 1 8.79
CHEMBL4472001 1 8.72

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL674 OSELTAMIVIR CARBOXYLATE IC50 = 0.11 nM 9.96
CHEMBL4545891 IC50 = 1.63 nM 8.79
CHEMBL4472001 IC50 = 1.92 nM 8.72