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Assay Detail

CHEMBL2045973

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

Binding
Inhibition of COX2 expressed in baculovirus infected SF-21 cells assessed as formation of PGH2 from PGG2 using arachidonic acid as substrate preincubated for 5 mins
10
Total Activities
10
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Binding
Cell Type SF-21
Confidence 8 — Homologous single protein target
Curated By Autocuration

Target

Prostaglandin G/H synthase 2 (CHEMBL230)
Type SINGLE PROTEIN
Organism Homo sapiens

Publication

Development of potent and selective inhibitors of aldo-keto reductase 1C3 (type 5 17β-hydroxysteroid dehydrogenase) based on N-phenyl-aminobenzoates and their structure-activity relationships.
Adeniji AO, Twenter BM, Byrns MC, Jin Y, Chen M, Winkler JD, Penning TM.
J Med Chem (2012) 55 : 2311 -2323
PubMed 22263837 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 10 6.97 7.80

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL23588 FLUFENAMIC ACID 2.0 1 7.80
CHEMBL1682200 1 6.13
CHEMBL1682201 1 -
CHEMBL1682202 1 -
CHEMBL1682203 1 -
CHEMBL1682204 1 -
CHEMBL1682205 1 -
CHEMBL2041554 1 -
CHEMBL2041555 1 -
CHEMBL2041556 1 -

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL23588 FLUFENAMIC ACID IC50 = 16.0 nM 7.80
CHEMBL1682200 IC50 = 740.0 nM 6.13
CHEMBL1682201 IC50 > 100000.0 nM -
CHEMBL1682202 IC50 > 100000.0 nM -
CHEMBL1682203 IC50 - -
CHEMBL1682204 IC50 > 100000.0 nM -
CHEMBL1682205 IC50 > 100000.0 nM -
CHEMBL2041554 IC50 > 100000.0 nM -
CHEMBL2041555 IC50 > 100000.0 nM -
CHEMBL2041556 IC50 > 100000.0 nM -