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Assay Detail

CHEMBL649574

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

Binding
Inhibition of bovine kidney alpha-L-fucosidase
13
Total Activities
13
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Binding
Organism Bos taurus
Confidence 8 — Homologous single protein target
Curated By Expert

Target

Tissue alpha-L-fucosidase (CHEMBL4176)
Type SINGLE PROTEIN
Organism Homo sapiens

Publication

Convenient synthesis and evaluation of enzyme inhibitory activity of several N-alkyl-, N-phenylalkyl, and cyclic isourea derivatives of 5a-carba-alpha-DL-fucopyranosylamine.
Ogawa S, Mori M, Takeuchi G, Doi F, Watanabe M, Sakata Y.
Bioorg Med Chem Lett (2002) 12 : 2811 -2814
PubMed 12270152 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 13 5.73 6.96

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL314757 1 6.96
CHEMBL95106 1 6.62
CHEMBL316609 1 6.62
CHEMBL95110 1 6.57
CHEMBL314772 DEOXYFUCONOJIRIMYCIN 1 6.39
CHEMBL319008 1 6.04
CHEMBL96392 1 6.00
CHEMBL94486 1 5.12
CHEMBL2114287 1 5.03
CHEMBL316082 1 4.68
CHEMBL2115269 1 4.60
CHEMBL317565 1 4.14
CHEMBL97066 1 -

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL314757 IC50 = 110.0 nM 6.96
CHEMBL95106 IC50 = 240.0 nM 6.62
CHEMBL316609 IC50 = 240.0 nM 6.62
CHEMBL95110 IC50 = 270.0 nM 6.57
CHEMBL314772 DEOXYFUCONOJIRIMYCIN IC50 = 410.0 nM 6.39
CHEMBL319008 IC50 = 920.0 nM 6.04
CHEMBL96392 IC50 = 1000.0 nM 6.00
CHEMBL94486 IC50 = 7600.0 nM 5.12
CHEMBL2114287 IC50 = 9300.0 nM 5.03
CHEMBL316082 IC50 = 21000.0 nM 4.68
CHEMBL2115269 IC50 = 25000.0 nM 4.60
CHEMBL317565 IC50 = 72000.0 nM 4.14
CHEMBL97066 IC50 = 140000.0 nM -