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Assay Detail

CHEMBL807033

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

Binding
Inhibition of sialidase (Flu A, 5 nM)
14
Total Activities
14
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

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

Target

Neuraminidase (CHEMBL2051)
Type SINGLE PROTEIN
Organism Influenza A virus (A/Puerto Rico/8/1934(H1N1))

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 14 6.43 8.40

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL300461 1 8.40
CHEMBL163966 1 8.22
CHEMBL100991 1 7.60
CHEMBL167390 1 7.40
CHEMBL50254 1 6.75
CHEMBL419710 1 6.35
CHEMBL54149 1 6.30
CHEMBL100677 1 5.62
CHEMBL51451 1 4.72
CHEMBL164112 1 4.72
CHEMBL348821 1 4.70
CHEMBL350948 1 -
CHEMBL163885 1 -
CHEMBL167747 1 -

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL300461 IC50 = 4.0 nM 8.40
CHEMBL163966 IC50 = 6.0 nM 8.22
CHEMBL100991 IC50 = 25.0 nM 7.60
CHEMBL167390 IC50 = 40.0 nM 7.40
CHEMBL50254 IC50 = 180.0 nM 6.75
CHEMBL419710 IC50 = 450.0 nM 6.35
CHEMBL54149 IC50 = 500.0 nM 6.30
CHEMBL100677 IC50 = 2400.0 nM 5.62
CHEMBL51451 IC50 = 19000.0 nM 4.72
CHEMBL164112 IC50 = 19000.0 nM 4.72
CHEMBL348821 IC50 = 20000.0 nM 4.70
CHEMBL350948 IC50 > 390000.0 nM -
CHEMBL163885 IC50 = 420000.0 nM -
CHEMBL167747 IC50 > 480000.0 nM -