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Assay Detail

CHEMBL810667

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

Binding
Compound was tested for its inhibitory activity against B/Victoria/102/85 (N2) sialidases.
6
Total Activities
6
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

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

Target

Neuraminidase (CHEMBL3377)
Type SINGLE PROTEIN
Organism Influenza B virus (strain B/Lee/1940)

Publication

Dihydropyrancarboxamides related to zanamivir: a new series of inhibitors of influenza virus sialidases. 1. Discovery, synthesis, biological activity, and structure-activity relationships of 4-guanidino- and 4-amino-4H-pyran-6-carboxamides.
Smith PW, Sollis SL, Howes PD, Cherry PC, Starkey ID, Cobley KN, Weston H, Scicinski J, Merritt A, Whittington A, Wyatt P, Taylor N, Green D, Bethell R, Madar S, Fenton RJ, Morley PJ, Pateman T, Beresford A.
J Med Chem (1998) 41 : 787 -797
PubMed 9526555 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 6 6.48 8.70

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL222813 ZANAMIVIR 4.0 1 8.70
CHEMBL317645 1 6.14
CHEMBL295490 1 5.70
CHEMBL300461 1 5.36
CHEMBL419710 1 -
CHEMBL73669 1 -

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL222813 ZANAMIVIR IC50 = 2.0 nM 8.70
CHEMBL317645 IC50 = 730.0 nM 6.14
CHEMBL295490 IC50 = 2000.0 nM 5.70
CHEMBL300461 IC50 = 4400.0 nM 5.36
CHEMBL419710 IC50 > 560000.0 nM -
CHEMBL73669 IC50 - -