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Assay Detail

CHEMBL1798628

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

Functional
Antiinflammatory activity in human U937 cells assessed as inhibition of LPS-induced TNFalpha production
2
Total Activities
2
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Functional
Organism Homo sapiens
Cell Type U-937
Confidence 1 — Organism
Curated By Autocuration

Target

U-937 (CHEMBL612794)
Type CELL-LINE
Organism Homo sapiens

Publication

Substituted N-aryl-6-pyrimidinones: a new class of potent, selective, and orally active p38 MAP kinase inhibitors.
Devadas B, Selness SR, Xing L, Madsen HM, Marrufo LD, Shieh H, Messing DM, Yang JZ, Morgan HM, Anderson GD, Webb EG, Zhang J, Devraj RV, Monahan JB.
Bioorg Med Chem Lett (2011) 21 : 3856 -3860
PubMed 21620699 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 2 7.84 8.23

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL1088751 PH-797804 2.0 1 8.23
CHEMBL1738710 1 7.45

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL1088751 PH-797804 IC50 = 5.9 nM 8.23
CHEMBL1738710 IC50 = 35.5 nM 7.45