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Assay Detail

CHEMBL762444

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

Binding
Inhibition of Prostaglandin G/H synthase in intact RBL-1 cell line
17
Total Activities
17
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Binding
Cell Type RBL-1
Confidence 4 — Cell-line / Tissue
Curated By Autocuration

Target

Cyclooxygenase (CHEMBL2095157)
Type PROTEIN FAMILY
Organism Rattus norvegicus

Publication

Nonsteroidal antiinflammatory drug hydroxamic acids. Dual inhibitors of both cyclooxygenase and 5-lipoxygenase.
Flynn DL, Capiris T, Cetenko WJ, Connor DT, Dyer RD, Kostlan CR, Nies DE, Schrier DJ, Sircar JC.
J Med Chem (1990) 33 : 2070 -2072
PubMed 2115586 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 17 5.65 7.00

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL1562610 MECLOFENAMATE SODIUM 4.0 1 7.00
CHEMBL6 INDOMETHACIN 4.0 1 6.30
CHEMBL433287 1 6.26
CHEMBL295829 OXAMETACIN 2.0 1 5.96
CHEMBL65050 1 5.96
CHEMBL521 IBUPROFEN 4.0 1 5.70
CHEMBL303199 1 5.57
CHEMBL65490 1 5.28
CHEMBL65431 1 5.24
CHEMBL292707 IBUPROXAM 2.0 1 5.00
CHEMBL65535 1 4.82
CHEMBL65430 1 4.70
CHEMBL303307 1 -
CHEMBL15770 SULINDAC 4.0 1 -
CHEMBL65130 1 -
CHEMBL65759 1 -
CHEMBL65299 1 -

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL1562610 MECLOFENAMATE SODIUM IC50 = 100.0 nM 7.00
CHEMBL6 INDOMETHACIN IC50 = 500.0 nM 6.30
CHEMBL433287 IC50 = 550.0 nM 6.26
CHEMBL295829 OXAMETACIN IC50 = 1100.0 nM 5.96
CHEMBL65050 IC50 = 1100.0 nM 5.96
CHEMBL521 IBUPROFEN IC50 = 2000.0 nM 5.70
CHEMBL303199 IC50 = 2700.0 nM 5.57
CHEMBL65490 IC50 = 5200.0 nM 5.28
CHEMBL65431 IC50 = 5800.0 nM 5.24
CHEMBL292707 IBUPROXAM IC50 = 10000.0 nM 5.00
CHEMBL65535 IC50 = 15000.0 nM 4.82
CHEMBL65430 IC50 = 20000.0 nM 4.70
CHEMBL303307 IC50 - nM -
CHEMBL15770 SULINDAC IC50 - nM -
CHEMBL65130 IC50 < 200.0 nM -
CHEMBL65759 IC50 - nM -
CHEMBL65299 IC50 - nM -