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Assay Detail

CHEMBL5680486

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

Binding
Binding affinity to recombinant N-terminal truncated MK2 (45 to 371 residues) (unknown origin) expressed in Escherichia coli assessed as dissociation constant measured after 15 mins by surface plasmon resonance spectroscopy analysis
1
Total Activities
1
Compounds Tested
1
Activity Types
2
Assay Parameters

Assay Information

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

Target

MAP kinase-activated protein kinase 2 (CHEMBL2208)
Type SINGLE PROTEIN
Organism Homo sapiens

Publication

A benzothiophene inhibitor of mitogen-activated protein kinase-activated protein kinase 2 inhibits tumor necrosis factor alpha production and has oral anti-inflammatory efficacy in acute and chronic models of inflammation.
Mourey RJ, Burnette BL, Brustkern SJ, Daniels JS, Hirsch JL, Hood WF, Meyers MJ, Mnich SJ, Pierce BS, Saabye MJ, Schindler JF, South SA, Webb EG, Zhang J, Anderson DR.
J Pharmacol Exp Ther (2010) 333 : 797 -807
PubMed 20237073 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
Kd 1 8.23 8.23

Assay Parameters

Parameter Type Value Units Text
EFO_ID EFO_ID - HP:0001370
EFO_TERM EFO_TERM - rheumatoid arthritis

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL1231206 1 8.23

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL1231206 Kd = 5.9 nM 8.23