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Assay Detail

CHEMBL4726245

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

Binding
Inhibition of human NEU3 expressed in HEK293A cells as substrate incubated for 1 hr by spectrofluorometric analysis
12
Total Activities
12
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Binding
Organism Homo sapiens
Cell Type HEK293
Confidence 9 — Direct single protein target
Curated By Autocuration

Target

Sialidase-3 (CHEMBL3046)
Type SINGLE PROTEIN
Organism Homo sapiens

Publication

2β-3,4-Unsaturated sialic acid derivatives: Synthesis optimization, and biological evaluation as Newcastle disease virus hemagglutinin-neuraminidase inhibitors.
La Rocca P,Rota P,Piccoli M,Cirillo F,Ghiroldi A,Franco V,Allevi P,Anastasia L
Bioorg Med Chem (2020) 28 : 115563 -115563
PubMed 32616179 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 12 5.52 5.62

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL96712 NEU5AC2EN 1 5.62
CHEMBL4745230 1 5.41
CHEMBL4792054 1 -
CHEMBL4779317 1 -
CHEMBL4761516 1 -
CHEMBL4746115 1 -
CHEMBL4764169 1 -
CHEMBL4753409 1 -
CHEMBL4743493 1 -
CHEMBL4744597 1 -
CHEMBL4751929 1 -
CHEMBL4750824 1 -

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL96712 NEU5AC2EN IC50 = 2400.0 nM 5.62
CHEMBL4745230 IC50 = 3900.0 nM 5.41
CHEMBL4792054 IC50 > 1000000.0 nM -
CHEMBL4779317 IC50 > 1000000.0 nM -
CHEMBL4761516 IC50 > 1000000.0 nM -
CHEMBL4746115 IC50 > 1000000.0 nM -
CHEMBL4764169 IC50 > 1000000.0 nM -
CHEMBL4753409 IC50 > 1000000.0 nM -
CHEMBL4743493 IC50 > 1000000.0 nM -
CHEMBL4744597 IC50 > 1000000.0 nM -
CHEMBL4751929 IC50 > 1000000.0 nM -
CHEMBL4750824 IC50 > 1000000.0 nM -