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Assay Detail

CHEMBL3072241

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

Functional
Antiviral activity against Influenza A virus H3N2 infected MDCK cells assessed as reduction of virus-induced cytopathic effect after 3 days by colorimetric formazan-based MTS assay
14
Total Activities
14
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Functional
Organism Influenza A virus H3N2
Cell Type MDCK
Confidence 1 — Organism
Curated By Autocuration

Target

Influenza A virus H3N2 (CHEMBL2366902)
Type ORGANISM
Organism Influenza A virus H3N2

Publication

Synthesis and biological evaluation of 2-(5-substituted-1-((diethylamino)methyl)-2-oxoindolin-3-ylidene)-<i>N</i>-substituted-hydrazinecarbothioamides.
Karki SS, Kulkarni AA, Kumar S, Veliyath SK, De Clercq E, Balzarini J.
Med Chem Res (2013) 22 : 2014 -2022
PubMed 32214762 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
EC50 14 5.83 7.10

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL959 RIMANTADINE 4.0 1 7.10
CHEMBL660 AMANTADINE 4.0 1 5.82
CHEMBL1229 OSELTAMIVIR 4.0 1 5.24
CHEMBL1643 RIBAVIRIN 4.0 1 5.17
CHEMBL2296652 1 -
CHEMBL2296651 1 -
CHEMBL2296650 1 -
CHEMBL2296649 1 -
CHEMBL2296648 1 -
CHEMBL2296647 1 -
CHEMBL2296646 1 -
CHEMBL2296654 1 -
CHEMBL2296653 1 -
CHEMBL2296655 1 -

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL959 RIMANTADINE EC50 = 80.0 nM 7.10
CHEMBL660 AMANTADINE EC50 = 1500.0 nM 5.82
CHEMBL1229 OSELTAMIVIR EC50 = 5700.0 nM 5.24
CHEMBL1643 RIBAVIRIN EC50 = 6800.0 nM 5.17
CHEMBL2296652 EC50 > 800.0 nM -
CHEMBL2296651 EC50 > 800.0 nM -
CHEMBL2296650 EC50 > 800.0 nM -
CHEMBL2296649 EC50 > 800.0 nM -
CHEMBL2296648 EC50 > 160.0 nM -
CHEMBL2296647 EC50 > 800.0 nM -
CHEMBL2296646 EC50 > 160.0 nM -
CHEMBL2296654 EC50 > 160.0 nM -
CHEMBL2296653 EC50 > 20000.0 nM -
CHEMBL2296655 EC50 > 20000.0 nM -