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Assay Detail

CHEMBL772920

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

Binding
Inhibition of Prostaglandin G/H synthase 1 in U-937 cells from human histiocytic lymphoma
10
Total Activities
10
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Binding
Cell Type U-937
Confidence 8 — Homologous single protein target
Curated By Autocuration

Target

Prostaglandin G/H synthase 1 (CHEMBL221)
Type SINGLE PROTEIN
Organism Homo sapiens

Publication

Synthesis and SAR of a new series of COX-2-selective inhibitors: pyrazolo[1,5-a]pyrimidines.
Almansa C, de Arriba AF, Cavalcanti FL, Gómez LA, Miralles A, Merlos M, García-Rafanell J, Forn J.
J Med Chem (2001) 44 : 350 -361
PubMed 11462976 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 10 6.91 8.52

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL6 INDOMETHACIN 4.0 1 8.52
CHEMBL118 CELECOXIB 4.0 1 5.29
CHEMBL330976 1 -
CHEMBL331921 1 -
CHEMBL421259 1 -
CHEMBL120467 1 -
CHEMBL122357 1 -
CHEMBL123700 1 -
CHEMBL332169 1 -
CHEMBL120608 1 -

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL6 INDOMETHACIN IC50 = 3.0 nM 8.52
CHEMBL118 CELECOXIB IC50 = 5100.0 nM 5.29
CHEMBL330976 IC50 > 10000.0 nM -
CHEMBL331921 IC50 > 10000.0 nM -
CHEMBL421259 IC50 > 10000.0 nM -
CHEMBL120467 IC50 > 10000.0 nM -
CHEMBL122357 IC50 > 10000.0 nM -
CHEMBL123700 IC50 > 10000.0 nM -
CHEMBL332169 IC50 > 10000.0 nM -
CHEMBL120608 IC50 > 10000.0 nM -