Skip to main content
Free research Free research Free assay review with research home and workspace preview
Quick search ChEMBL 36
Assay Detail

CHEMBL2072029

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

Functional
Inhibition of human LAD2 cells degranulation preincubated for 30 mins before streptavidin stimulation measured after 30 mins by measuring beta-hexosaminidase activity
11
Total Activities
11
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Functional
Organism Homo sapiens
Cell Type LAD2
Confidence 1 — Organism
Curated By Autocuration

Target

LAD2 (CHEMBL4483253)
Type CELL-LINE
Organism Homo sapiens

Publication

Highly potent aminopyridines as Syk kinase inhibitors.
Castillo M, Forns P, Erra M, Mir M, López M, Maldonado M, Orellana A, Carreño C, Ramis I, Miralpeix M, Vidal B.
Bioorg Med Chem Lett (2012) 22 : 5419 -5423
PubMed 22877633 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 11 6.59 6.93

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL2069349 1 6.93
CHEMBL2069355 1 6.91
CHEMBL2069359 1 6.85
CHEMBL2069357 1 6.77
CHEMBL2069350 1 6.73
CHEMBL2069360 1 6.69
CHEMBL2069356 1 6.48
CHEMBL2069358 1 6.45
CHEMBL2069354 1 6.44
CHEMBL2069351 1 6.23
CHEMBL2069353 1 6.00

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL2069349 IC50 = 118.0 nM 6.93
CHEMBL2069355 IC50 = 122.0 nM 6.91
CHEMBL2069359 IC50 = 140.0 nM 6.85
CHEMBL2069357 IC50 = 169.0 nM 6.77
CHEMBL2069350 IC50 = 188.0 nM 6.73
CHEMBL2069360 IC50 = 204.0 nM 6.69
CHEMBL2069356 IC50 = 331.0 nM 6.48
CHEMBL2069358 IC50 = 352.0 nM 6.45
CHEMBL2069354 IC50 = 362.0 nM 6.44
CHEMBL2069351 IC50 = 585.0 nM 6.23
CHEMBL2069353 IC50 = 1000.0 nM 6.00