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

CHEMBL5262865

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

Binding
Inhibition of human SYK using 5-Fluo-Ahx-GAPDYENLQELNKK-Amid as substrate in presence of ATP by microfluidic mobility shift assay
10
Total Activities
10
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 SYK (CHEMBL2599)
Type SINGLE PROTEIN
Organism Homo sapiens

Publication

An overview on the recent developments of 1,2,4-triazine derivatives as anticancer compounds.
Cascioferro S, Parrino B, Spanò V, Carbone A, Montalbano A, Barraja P, Diana P, Cirrincione G.
Eur J Med Chem (2017) 142 : 328 -375
PubMed 28851503 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 10 9.10 9.10

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL3416026 1 9.10
CHEMBL3965225 1 9.10
CHEMBL3932871 1 9.10
CHEMBL3416027 1 9.10
CHEMBL3962214 1 9.10
CHEMBL3967315 1 9.10
CHEMBL3893313 1 9.10
CHEMBL3930413 1 9.10
CHEMBL3962915 1 9.10
CHEMBL3899231 1 9.10

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL3416026 IC50 = 0.8 nM 9.10
CHEMBL3965225 IC50 = 0.8 nM 9.10
CHEMBL3932871 IC50 = 0.8 nM 9.10
CHEMBL3416027 IC50 = 0.8 nM 9.10
CHEMBL3962214 IC50 = 0.8 nM 9.10
CHEMBL3967315 IC50 = 0.8 nM 9.10
CHEMBL3893313 IC50 = 0.8 nM 9.10
CHEMBL3930413 IC50 = 0.8 nM 9.10
CHEMBL3962915 IC50 = 0.8 nM 9.10
CHEMBL3899231 IC50 = 0.8 nM 9.10