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Assay Detail

CHEMBL4768325

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Binding
Inhibition of Influenza A virus (A/goose/Jiangsu/1306/2014 (H5N8)) group-1 Neuraminidase N8 preincubated for 10 mins followed by MUNANA substrate addition and measured after 40 to 60 mins by fluorescence method
12
Total Activities
12
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Binding
Organism Influenza A virus
Confidence 0 — Uncurated / Unknown
Curated By Autocuration

Target

Unchecked (CHEMBL612545)
Type UNCHECKED

Publication

Discovery of novel "Dual-site" binding oseltamivir derivatives as potent influenza virus neuraminidase inhibitors.
Ai W,Zhang J,Zalloum WA,Jia R,Cherukupalli S,Ding X,Sun Z,Sun L,Jiang X,Ma X,Li Z,Wang D,Huang B,Zhan P,Liu X
Eur J Med Chem (2020) 191 : 112147 -112147
PubMed 32092589 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 12 7.21 8.05

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL674 OSELTAMIVIR CARBOXYLATE -1.0 1 8.05
CHEMBL222813 ZANAMIVIR 4.0 1 8.00
CHEMBL4788464 1 7.48
CHEMBL4778066 1 7.26
CHEMBL4797291 1 7.21
CHEMBL4788913 1 7.11
CHEMBL4793273 1 7.08
CHEMBL4784077 1 7.04
CHEMBL4785103 1 7.03
CHEMBL4795384 1 6.96
CHEMBL4784537 1 6.76
CHEMBL4781455 1 6.51

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL674 OSELTAMIVIR CARBOXYLATE IC50 = 8.81 nM 8.05
CHEMBL222813 ZANAMIVIR IC50 = 9.99 nM 8.00
CHEMBL4788464 IC50 = 33.02 nM 7.48
CHEMBL4778066 IC50 = 55.25 nM 7.26
CHEMBL4797291 IC50 = 62.09 nM 7.21
CHEMBL4788913 IC50 = 78.06 nM 7.11
CHEMBL4793273 IC50 = 83.13 nM 7.08
CHEMBL4784077 IC50 = 90.06 nM 7.04
CHEMBL4785103 IC50 = 92.61 nM 7.03
CHEMBL4795384 IC50 = 108.57 nM 6.96
CHEMBL4784537 IC50 = 174.4 nM 6.76
CHEMBL4781455 IC50 = 309.0 nM 6.51