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Assay Detail

CHEMBL5243072

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

Binding
Inhibition of human COX-2 using arachidonic acid as substrate preincubated for 10 mins followed by substrate addition and measured after 2 mins by ELISA
100
Total Activities
100
Compounds Tested
2
Activity Types
0
Assay Parameters

Assay Information

Assay Type Binding
Organism Homo sapiens
Confidence 9 — Direct single protein target
Curated By Autocuration

Target

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

Publication

Non-steroidal anti-inflammatory drugs: recent advances in the use of synthetic COX-2 inhibitors.
Ahmadi M, Bekeschus S, Weltmann KD, von Woedtke T, Wende K.
RSC Med Chem (2022) 13 : 471 -496
PubMed 35685617 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 99 6.81 7.41
INH 1 - -

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL5278569 1 7.41
CHEMBL5282152 1 7.41
CHEMBL5290194 1 7.41
CHEMBL5283848 1 7.41
CHEMBL5266071 1 7.41
CHEMBL5265750 1 7.41
CHEMBL5269531 1 7.39
CHEMBL5286186 1 7.39
CHEMBL5266705 1 7.39
CHEMBL5281678 1 7.36
CHEMBL5277494 1 7.36
CHEMBL5281053 1 7.36
CHEMBL5270815 1 7.36
CHEMBL5269100 1 7.36
CHEMBL5276590 1 7.36
CHEMBL6 INDOMETHACIN 4.0 1 7.35
CHEMBL416146 ETORICOXIB 4.0 1 7.16
CHEMBL5275204 1 7.05
CHEMBL5271871 1 7.05
CHEMBL5272361 1 7.05
CHEMBL5276822 1 7.05
CHEMBL5287114 1 7.05
CHEMBL5282180 1 7.05
CHEMBL5272671 1 7.05
CHEMBL5267656 1 7.05
CHEMBL5282918 1 7.05
CHEMBL5282397 1 7.05
CHEMBL5283995 1 7.05
CHEMBL5281704 1 7.05
CHEMBL5270094 1 7.05

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL5278569 IC50 = 39.0 nM 7.41
CHEMBL5282152 IC50 = 39.0 nM 7.41
CHEMBL5290194 IC50 = 39.0 nM 7.41
CHEMBL5283848 IC50 = 39.0 nM 7.41
CHEMBL5266071 IC50 = 39.0 nM 7.41
CHEMBL5265750 IC50 = 39.0 nM 7.41
CHEMBL5269531 IC50 = 41.0 nM 7.39
CHEMBL5286186 IC50 = 41.0 nM 7.39
CHEMBL5266705 IC50 = 41.0 nM 7.39
CHEMBL5269100 IC50 = 43.8 nM 7.36
CHEMBL5276590 IC50 = 43.8 nM 7.36
CHEMBL5270815 IC50 = 43.8 nM 7.36
CHEMBL5281053 IC50 = 43.8 nM 7.36
CHEMBL5277494 IC50 = 43.8 nM 7.36
CHEMBL5281678 IC50 = 43.8 nM 7.36
CHEMBL6 INDOMETHACIN IC50 = 45.0 nM 7.35
CHEMBL416146 ETORICOXIB IC50 = 70.0 nM 7.16
CHEMBL5282918 IC50 = 90.0 nM 7.05
CHEMBL5279175 IC50 = 90.0 nM 7.05
CHEMBL5271136 IC50 = 90.0 nM 7.05
CHEMBL5272126 IC50 = 90.0 nM 7.05
CHEMBL5268121 IC50 = 90.0 nM 7.05
CHEMBL5285788 IC50 = 90.0 nM 7.05
CHEMBL5279078 IC50 = 90.0 nM 7.05
CHEMBL5270094 IC50 = 90.0 nM 7.05
CHEMBL5281704 IC50 = 90.0 nM 7.05
CHEMBL5283995 IC50 = 90.0 nM 7.05
CHEMBL5267656 IC50 = 90.0 nM 7.05
CHEMBL5272671 IC50 = 90.0 nM 7.05
CHEMBL5282180 IC50 = 90.0 nM 7.05
CHEMBL5287114 IC50 = 90.0 nM 7.05
CHEMBL5276822 IC50 = 90.0 nM 7.05
CHEMBL5272361 IC50 = 90.0 nM 7.05
CHEMBL5271871 IC50 = 90.0 nM 7.05
CHEMBL5275204 IC50 = 90.0 nM 7.05
CHEMBL5282397 IC50 = 90.0 nM 7.05
CHEMBL5283644 IC50 = 100.0 nM 7.00
CHEMBL5266699 IC50 = 100.0 nM 7.00
CHEMBL5283788 IC50 = 100.0 nM 7.00
CHEMBL5275786 IC50 = 100.0 nM 7.00
CHEMBL5275772 IC50 = 100.0 nM 7.00
CHEMBL5281666 IC50 = 100.0 nM 7.00
CHEMBL5274992 IC50 = 220.0 nM 6.66
CHEMBL5271327 IC50 = 220.0 nM 6.66
CHEMBL5276722 IC50 = 220.0 nM 6.66
CHEMBL5273958 IC50 = 220.0 nM 6.66
CHEMBL5286663 IC50 = 220.0 nM 6.66
CHEMBL5273397 IC50 = 220.0 nM 6.66
CHEMBL5287406 IC50 = 220.0 nM 6.66
CHEMBL5279601 IC50 = 220.0 nM 6.66