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Assay Detail

CHEMBL762445

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

Binding
Inhibition of Prostaglandin G/H synthase mediated PGF2-alpha formation in rat basophilic leukemia (RBL-1) cells
15
Total Activities
15
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Binding
Organism Rattus norvegicus
Cell Type RBL-1
Confidence 5 — Multiple protein complex / RNA
Curated By Autocuration

Target

Cyclooxygenase (CHEMBL2095157)
Type PROTEIN FAMILY
Organism Rattus norvegicus

Publication

1,3,4-Oxadiazole, 1,3,4-thiadiazole, and 1,2,4-triazole analogs of the fenamates: in vitro inhibition of cyclooxygenase and 5-lipoxygenase activities.
Boschelli DH, Connor DT, Bornemeier DA, Dyer RD, Kennedy JA, Kuipers PJ, Okonkwo GC, Schrier DJ, Wright CD.
J Med Chem (1993) 36 : 1802 -1810
PubMed 8515419 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 15 5.85 7.00

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL509 MECLOFENAMIC ACID 4.0 1 7.00
CHEMBL53610 1 6.60
CHEMBL298672 1 6.57
CHEMBL301586 1 6.29
CHEMBL50833 1 6.21
CHEMBL54156 1 6.16
CHEMBL299794 1 6.07
CHEMBL301990 1 6.00
CHEMBL417022 1 5.77
CHEMBL53532 1 5.72
CHEMBL53805 1 5.58
CHEMBL297733 1 5.21
CHEMBL300637 1 5.15
CHEMBL301136 1 4.96
CHEMBL298776 1 4.52

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL509 MECLOFENAMIC ACID IC50 = 100.0 nM 7.00
CHEMBL53610 IC50 = 250.0 nM 6.60
CHEMBL298672 IC50 = 270.0 nM 6.57
CHEMBL301586 IC50 = 510.0 nM 6.29
CHEMBL50833 IC50 = 610.0 nM 6.21
CHEMBL54156 IC50 = 700.0 nM 6.16
CHEMBL299794 IC50 = 850.0 nM 6.07
CHEMBL301990 IC50 = 1000.0 nM 6.00
CHEMBL417022 IC50 = 1700.0 nM 5.77
CHEMBL53532 IC50 = 1900.0 nM 5.72
CHEMBL53805 IC50 = 2600.0 nM 5.58
CHEMBL297733 IC50 = 6100.0 nM 5.21
CHEMBL300637 IC50 = 7100.0 nM 5.15
CHEMBL301136 IC50 = 11000.0 nM 4.96
CHEMBL298776 IC50 = 30000.0 nM 4.52