Ciprofol: A Narrative Review of Clinical Research Progress

preprint OA: closed
View at publisher

Abstract

Ciprofol (HSK3486), a novel short-acting intravenous anesthetic, is a positive allosteric regulator and direct agonist of γ-aminobutyric acid type A (GABAA) receptor. It is synthetized by introducing a cyclopropyl group in the isopropyl side chain of propofol. The incorporation of cyclopropyl not only increases the steric effect, but also the new chiral molecules formed introduce stereoselective effects, thereby increasing the affinity for GABA receptors. Ciprofol activates GABAARs, producing sedative or anesthetic effects. Ciprofol is expected to become the new choice for intravenous anesthetics due to its characteristics of high potency, rapid onset, rapid recovery, and fewer adverse reactions. It is suitable for sedation and general anesthesia in the endoscopy center, operating room, and intensive care unit. This review summarizes the pharmacological characteristics and clinical research progress of ciprofol.

My notes (saved in your browser only)

Citation neighborhood (no data yet)

We don't have any in-corpus citations linked to this paper yet. This is a recent paper (2024) — citers typically take a year or two to land, and the OpenAlex reference graph may still be filling in.

Source provenance

europepmc
last seen: 2026-05-20T01:45:00.602351+00:00