Drug intelligence / Profile preview

nalbuphine hydrochloride + flurbiprofen axetil

Development stage
Unknown
Lead developer
The Second Affiliated Hospital of Soochow University
Modality
Small Molecules
Administration
Intravenous
01

Overview

Anricafen is a fixed-dose combination analgesic consisting of **nalbuphine hydrochloride** and **flurbiprofen axetil**. Nalbuphine is a synthetic opioid agonist-antagonist that acts as a potent agonist at the kappa-opioid receptor and an antagonist at the mu-opioid receptor, providing effective analgesia with a lower risk of mu-mediated side effects such as respiratory depression and pruritus. Flurbiprofen axetil is an injectable lipid emulsion prodrug of the non-steroidal anti-inflammatory drug (NSAID) flurbiprofen, which inhibits cyclooxygenase (COX) enzymes to reduce the synthesis of inflammatory prostaglandins. By combining these two agents, Anricafen utilizes a multimodal approach to pain management, targeting both central opioid pathways and peripheral inflammatory mediators. It is primarily developed for the treatment of moderate to severe postoperative pain, particularly following abdominal surgeries, where it is often evaluated for its ability to provide superior comfort and safety compared to traditional mu-opioid agonists like morphine.

Brand names
Anricafen
Other names
Anricafennalbuphine/flurbiprofen axetil安瑞卡芬
02

Targets

PTGS2 (Prostaglandin-Endoperoxide Synthase 2)PGHS-1 (Prostaglandin G/H Synthase 1)KOR (Kappa opioid receptor)MOR (Mu opioid receptor)M-channel (M-type voltage-gated potassium channel)

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