Drug intelligence / Profile preview

lornoxicam

Development stage
Phase 4
Lead developer
Roche
Modality
Small Molecules
Administration
Oral, Intravenous, Intramuscular
01

Overview

Lornoxicam (also known as chlortenoxicam) is a nonsteroidal anti-inflammatory drug (NSAID) of the oxicam class. It exhibits analgesic (pain-relieving), anti-inflammatory, and antipyretic (fever-reducing) properties. Lornoxicam acts primarily by inhibiting cyclooxygenase enzymes COX-1 and COX-2 with high potency (IC50 values of 5 nM for COX-1 and 8 nM for COX-2), thereby reducing prostaglandin synthesis involved in pain and inflammation. It does not inhibit 5-lipoxygenase activity or leukotriene synthesis. Lornoxicam may also activate the opioid neuropeptide system to exert central analgesic effects. The drug is used to treat various types of pain—especially those associated with inflammatory joint diseases such as osteoarthritis—as well as postoperative pain and sciatica[1][2][3][4][5][6]. It is available in both oral and parenteral formulations.

Brand names
XefoXefocamXafonLorcamAcabel
Other names
chlortenoxicam氯诺昔康
02

Targets

PGHS-1 (Prostaglandin G/H Synthase 1)PTGS2 (Prostaglandin-Endoperoxide Synthase 2)

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