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Assay Detail

CHEMBL2172908

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

Binding
Inhibition of human MAPK p38alpha by Z'-LYTE 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

Mitogen-activated protein kinase 13 (CHEMBL2939)
Type SINGLE PROTEIN
Organism Homo sapiens

Publication

Identification, synthesis, and biological evaluation of 6-[(6R)-2-(4-fluorophenyl)-6-(hydroxymethyl)-4,5,6,7-tetrahydropyrazolo[1,5-a]pyrimidin-3-yl]-2-(2-methylphenyl)pyridazin-3(2H)-one (AS1940477), a potent p38 MAP kinase inhibitor.
Asano T, Yamazaki H, Kasahara C, Kubota H, Kontani T, Harayama Y, Ohno K, Mizuhara H, Yokomoto M, Misumi K, Kinoshita T, Ohta M, Takeuchi M.
J Med Chem (2012) 55 : 7772 -7785
PubMed 22905713 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 1 7.96 7.96

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL2170294 AS1940477 1 7.96

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL2170294 AS1940477 IC50 = 11.0 nM 7.96