Drug intelligence / Profile preview

feprazone

Development stage
Unknown
Modality
Small Molecules
Administration
Oral
01

Overview

Feprazone is a nonsteroidal anti-inflammatory drug (NSAID) of the pyrazolone class, structurally related to phenylbutazone but with a prenyl group instead of an n-butyl group. It is primarily indicated for the relief of pain and inflammation associated with arthritis, gout, rheumatic fever, and other musculoskeletal disorders. Feprazone acts mainly by inhibiting cyclooxygenase (COX)-2 activity, thereby reducing prostaglandin synthesis involved in inflammation and pain signaling. Additional mechanisms include inhibition of matrix metalloproteinases (MMP-2 and MMP-9), reduction in cell adhesion molecules such as VCAM-1 and ICAM-1, and suppression of the TLR4/MyD88/NF-kB signaling pathway implicated in inflammatory responses[1][4][5][6]. The drug has been tested in phase III clinical trials for conditions like osteoarthritis and rheumatoid arthritis; however, its current approval status is unclear[5].

Brand names
FeprazonePrenazone
Other names
prenazone
02

Targets

RELA (Nuclear Factor Kappa B Subunit p65)ABCB11 (Bile salt export pump)PTGS2 (Prostaglandin-Endoperoxide Synthase 2)TLR4 (Toll-like receptor 4)ABCC2 (ATP-binding cassette sub-family C member 2)ABCC4 (Multidrug resistance-associated protein 4)ABCC3 (ATP-binding cassette sub-family C member 3)MYD88 (Myeloid differentiation primary response protein MyD88)PGHS-1 (Prostaglandin G/H Synthase 1)

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