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Assay Detail

CHEMBL981177

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

Binding
Inhibition of human ZAP70
13
Total Activities
13
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

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

Target

Tyrosine-protein kinase ZAP-70 (CHEMBL2803)
Type SINGLE PROTEIN
Organism Homo sapiens

Publication

A novel Syk family kinase inhibitor: design, synthesis, and structure-activity relationship of 1,2,4-triazolo[4,3-c]pyrimidine and 1,2,4-triazolo[1,5-c]pyrimidine derivatives.
Hirabayashi A, Mukaiyama H, Kobayashi H, Shiohara H, Nakayama S, Ozawa M, Miyazawa K, Misawa K, Ohnota H, Isaji M.
Bioorg Med Chem (2008) 16 : 7347 -7357
PubMed 18585046 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 13 5.90 7.28

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL388978 STAUROSPORINE 1 7.28
CHEMBL472840 1 7.01
CHEMBL478642 1 6.96
CHEMBL475882 1 6.92
CHEMBL475609 1 6.92
CHEMBL475575 1 6.48
CHEMBL476741 1 5.96
CHEMBL476537 1 5.19
CHEMBL474582 1 5.08
CHEMBL514365 1 5.05
CHEMBL471901 1 4.95
CHEMBL513915 1 4.58
CHEMBL477165 1 4.30

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL388978 STAUROSPORINE IC50 = 53.0 nM 7.28
CHEMBL472840 IC50 = 97.0 nM 7.01
CHEMBL478642 IC50 = 110.0 nM 6.96
CHEMBL475882 IC50 = 120.0 nM 6.92
CHEMBL475609 IC50 = 120.0 nM 6.92
CHEMBL475575 IC50 = 330.0 nM 6.48
CHEMBL476741 IC50 = 1100.0 nM 5.96
CHEMBL476537 IC50 = 6400.0 nM 5.19
CHEMBL474582 IC50 = 8300.0 nM 5.08
CHEMBL514365 IC50 = 9000.0 nM 5.05
CHEMBL471901 IC50 = 11200.0 nM 4.95
CHEMBL513915 IC50 = 26000.0 nM 4.58
CHEMBL477165 IC50 = 50000.0 nM 4.30