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Assay Detail

CHEMBL888940

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

Functional
Antiviral activity against influenza A virus (H3N2)-induced cytopathogenicity in MDCK cells by MTS method
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 (CHEMBL613740)
Type ORGANISM
Organism Influenza A virus

Publication

Influence of an additional 2-amino substituent of the 1-aminoethyl pharmacophore group on the potency of rimantadine against influenza virus A.
Tataridis D, Fytas G, Kolocouris A, Fytas C, Kolocouris N, Foscolos GB, Padalko E, Neyts J, De Clercq E.
Bioorg Med Chem Lett (2007) 17 : 692 -696
PubMed 17113287 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
EC50 14 4.36 4.74

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL1161992 1 4.74
CHEMBL535396 RIMANTADINE HYDROCHLORIDE 4.0 1 4.72
CHEMBL1161994 1 4.62
CHEMBL1569 AMANTADINE HYDROCHLORIDE 4.0 1 4.31
CHEMBL538581 1 4.29
CHEMBL1161993 1 4.25
CHEMBL535397 1 4.15
CHEMBL233117 1 4.14
CHEMBL232673 1 4.04
CHEMBL1161996 1 -
CHEMBL1161995 1 -
CHEMBL234973 1 -
CHEMBL398055 1 -
CHEMBL232481 1 -

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL1161992 EC50 = 18300.0 nM 4.74
CHEMBL535396 RIMANTADINE HYDROCHLORIDE EC50 = 19100.0 nM 4.72
CHEMBL1161994 EC50 = 24100.0 nM 4.62
CHEMBL1569 AMANTADINE HYDROCHLORIDE EC50 = 49100.0 nM 4.31
CHEMBL538581 EC50 = 51300.0 nM 4.29
CHEMBL1161993 EC50 = 56800.0 nM 4.25
CHEMBL535397 EC50 = 70500.0 nM 4.15
CHEMBL233117 EC50 = 72600.0 nM 4.14
CHEMBL232673 EC50 = 91800.0 nM 4.04
CHEMBL1161996 EC50 = 351000.0 nM -
CHEMBL1161995 EC50 = 197000.0 nM -
CHEMBL234973 EC50 = 604000.0 nM -
CHEMBL398055 EC50 = 107000.0 nM -
CHEMBL232481 EC50 = 269000.0 nM -