FSL0616
- Structure
- InChI=1S/C13H18O2/c1-9(2)8-11-4-6-12(7-5-11)10(3)13(14)15/h4-7,9-10H,8H2,1-3H3,(H,14,15)
- InChIKey=HEFNNWSXXWATRW-UHFFFAOYSA-N
- Synonyms
-
- Origin
- Chemically synthesized
- Biological activities
- Inhibition of the COX-dependent formation of PGH2
- Therapeutic
-
Nonsteroidal antiinflammatory
- Target
-
COX-1
COX-2
- Assay information
-
Inhibitor of prostanoid formation determined in the COX-1 (IC50 = 7.6 μM) and COX-2 (IC50 = 7.2 μM)
S-ibuprofen: Inhibitor of PGHS-1 (IC50 = 2.1 μM) and PGHS-2 (IC50 1.6 μM)
R-ibuprofen: Inhibitor of PGHS-1 (IC50 = 34.9 μM)
R-ibuprofen: No inhibitor activity against PGHS-2
Binding to amyloid beta fibrils: Ki = 11.3 nM