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Assay Detail

CHEMBL898688

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

Binding
Inhibition of human 15-hLO1
7
Total Activities
6
Compounds Tested
2
Activity Types
0
Assay Parameters

Assay Information

Assay Type Binding
Organism Homo sapiens
Confidence 9 — Direct single protein target
Curated By Intermediate

Target

Polyunsaturated fatty acid lipoxygenase ALOX15 (CHEMBL2903)
Type SINGLE PROTEIN
Organism Homo sapiens

Publication

Discovery of platelet-type 12-human lipoxygenase selective inhibitors by high-throughput screening of structurally diverse libraries.
Deschamps JD, Gautschi JT, Whitman S, Johnson TA, Gassner NC, Crews P, Holman TR.
Bioorg Med Chem (2007) 15 : 6900 -6908
PubMed 17826100 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 5 5.22 5.51
Ki 2 5.10 5.10

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL323197 MANGOSTIN 1 5.51
CHEMBL397803 MISCHELLAMINE B 1 5.12
CHEMBL391079 DYSIDENIN 1 5.10
CHEMBL238624 1 5.03
CHEMBL392270 NEODYSIDENIN 2 -
CHEMBL222808 1 -

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL323197 MANGOSTIN IC50 = 3100.0 nM 5.51
CHEMBL397803 MISCHELLAMINE B IC50 = 7600.0 nM 5.12
CHEMBL391079 DYSIDENIN Ki = 8000.0 nM 5.10
CHEMBL238624 IC50 = 9400.0 nM 5.03
CHEMBL392270 NEODYSIDENIN IC50 > 500000.0 nM -
CHEMBL222808 IC50 > 25000.0 nM -
CHEMBL392270 NEODYSIDENIN Ki > 500000.0 nM -