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

CHEMBL3811432

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

Binding
Inhibition of N-terminal His-tagged Mer kinase (588 to 855 residues) (unknown origin) expressed in Escherichia coli BL21(DE3) cells measured every min by ADP Quest Assay
1
Total Activities
1
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 Mer (CHEMBL5331)
Type SINGLE PROTEIN
Organism Homo sapiens

Publication

Synthesis, biological evaluation, and physicochemical property assessment of 4-substituted 2-phenylaminoquinazolines as Mer tyrosine kinase inhibitors.
Wang SB, Cui MT, Wang XF, Ohkoshi E, Goto M, Yang DX, Li L, Yuan S, Morris-Natschke SL, Lee KH, Xie L.
Bioorg Med Chem (2016) 24 : 3083 -3092
PubMed 27238842 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 1 4.95 4.95

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL311228 1 4.95

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL311228 IC50 = 11300.0 nM 4.95