Chemistry:Rilmazafone
Rilmazafone[1] (リスミー, brand name Rhythmy; developmental code 450191-S) is a water-soluble prodrug developed by Shionogi and approved in Japan for the treatment of insomnia and as a pre-anesthetic agent. It is not a benzodiazepine in the pharmacological or structural sense — the parent compound contains no diazepine ring and has no affinity for benzodiazepine receptors — but is converted inside the body into several active benzodiazepine metabolites, principally rilmazolam, which produce sedative and hypnotic effects.[2][3] Outside Japan, rilmazafone has appeared as a new psychoactive substance (NPS) and has been implicated in fatal overdoses in Europe and North America.[4]
Chemistry
Rilmazafone is a 1H-1,2,4-triazolyl benzophenone derivative. Its molecular formula is C21H20Cl2N6O3 and it is freely soluble in water, which distinguishes it from most clinically used benzodiazepines and contributed to its design rationale as a prodrug. The parent compound contains no diazepine ring; the benzodiazepine scaffold is only present in the active metabolites formed after intestinal biotransformation.[5]
Pharmacology
Rilmazafone itself has negligible affinity for GABAA receptors and produces no psychoactive effects prior to metabolism. Its pharmacological activity is mediated entirely through its metabolites, particularly rilmazolam, which acts as a positive allosteric modulator of the GABAA receptor, enhancing the inhibitory effects of gamma-aminobutyric acid (GABA) in the central nervous system.[2][6] This produces sedative, hypnotic, anxiolytic, and muscle-relaxant effects characteristic of the benzodiazepine class.[7]
Because rilmazafone's prodrug structure bypasses direct receptor interaction until after intestinal metabolism, it was developed partly with the intention of reducing the abuse potential and side-effect profile associated with direct-acting benzodiazepines, though its metabolites retain the full pharmacodynamic profile of the class.
Metabolism and pharmacokinetics
After oral administration, rilmazafone undergoes rapid biotransformation by aminopeptidase enzymes in the small intestine, with cleavage producing a desglycylated intermediate (191DG) that undergoes spontaneous, non-enzymatic cyclization to form rilmazolam.[5][8] This activation occurs during a single passage through the intestinal wall, so the parent compound, rilmazafone, is not detectable in human plasma after common therapeutic doses of 1–2 mg.
Oral administration in humans produces at least five pharmacologically active metabolites. Rilmazolam (M-1) is the principal benzodiazepine metabolite, but — unlike the pattern observed in animal studies — M-4 is the predominant species in human plasma for up to six hours after dosing. Additional metabolites include M-2, M-A, and M-3. Rilmazolam itself undergoes further hepatic metabolism to yield N-desmethylrilmazolam, di-desmethylrilmazolam, and carboxy rilmazolam, all of which retain some pharmacological activity.[4]
Active metabolite: Rilmazolam
Rilmazolam (CAS 50330-59-1) is a triazolobenzodiazepine with the molecular formula C19H15Cl2N5O (molecular weight 400.26 g/mol). Its IUPAC name is 8-chloro-6-(2-chlorophenyl)-N,N-dimethyl-4H-[1,2,4]triazolo[1,5-a][1,4]benzodiazepine-2-carboxamide. The compound is soluble in methanol and chloroform. Rilmazolam has never been independently developed or approved for medical use in any country; it is encountered clinically and forensically only as a consequence of rilmazafone administration or misuse.[5]
Medical uses
In Japan, rilmazafone is approved under the brand name Rhythmy (リスミー) by Shionogi for two indications: treatment of insomnia at an oral dose of 1–2 mg once daily at bedtime, and as a pre-anesthetic medication at a dose of 2 mg administered before surgery. It is classified as a prescription medication in Japan and is not approved for medical use in any other country.
Adverse effects
As with other agents that produce active benzodiazepine metabolites, rilmazafone can cause dose-dependent central nervous system depression. Reported adverse effects include sedation, impaired motor coordination, anterograde amnesia, and next-day residual effects sometimes described as a "hangover." Overdose, particularly in combination with other CNS depressants such as ethanol or opioids, may result in respiratory depression, coma, and death.[4]
Several fatal overdoses have been attributed to rilmazafone and its metabolites in forensic case series, most in the context of non-medical use outside Japan. Rilmazolam and its downstream metabolites have been identified as the causative agents in these intoxications.[4]
New psychoactive substance status
Outside Japan, rilmazafone has been identified and monitored as a new psychoactive substance (NPS) by drug early-warning systems in the United States and Europe.[9][10] Because the parent compound lacks a diazepine ring, it is not classified as a controlled substance in the United States or in several other jurisdictions that rely on structural definitions for scheduling. This structural loophole has contributed to its circulation in illicit drug markets as an unscheduled or insufficiently scheduled substance.[10]
Legal status
See also
- Avizafone (diazepam prodrug)
- Noravizafone desglycyl (nordazepam prodrug)
- Alprazolam triazolobenzophenone
- Clonazafone desglycyl
- Diclazafone desglycyl
References
- ↑ Hirai KJ, Sugimoto HJ, "1-PHENYL-1H-1,2,4-TRIAZOL-DERIVATE, IHRE Salze mit Saeuren, Verfahren zu Ihrer Herstellung und Diese Verbindungen Enthaltende Arzneimittel", DE patent 2725164, published 1977-12-15, issued 1986-02-06, assigned to Shionogi & Co
- ↑ 2.0 2.1 "[Pharmacological studies of a new sleep-inducer, 1H-1,2,4-triazolyl benzophenone derivatives (450191-S) (I). Behavioral analysis]" (in Japanese). Nihon Yakurigaku Zasshi. Folia Pharmacologica Japonica 84 (1): 109–154. July 1984. doi:10.1254/fpj.84.109. PMID 6149174.
- ↑ "[Pharmacology of a new sleep inducer, 1H-1,2,4-triazolyl benzophenone derivative, 450191-S (II). Sleep-inducing activity and effect on the motor system]" (in Japanese). Nihon Yakurigaku Zasshi. Folia Pharmacologica Japonica 84 (1): 25–89. July 1984. doi:10.1254/fpj.84.25. PMID 6149175.
- ↑ 4.0 4.1 4.2 4.3 "Rilmazafone: A designer benzodiazepine pro-drug involved in fatal intoxications". Journal of Analytical Toxicology 47 (7): 640–643. 15 September 2023. doi:10.1093/jat/bkad041. PMID 37348041.
- ↑ 5.0 5.1 5.2 "Intestinal activation of a new sleep inducer 450191-S, a 1H-1,2,4-triazolyl benzophenone derivative, in rats". Journal of Pharmacobio-Dynamics 9 (3): 315–320. March 1986. doi:10.1248/bpb1978.9.315. PMID 3454653.
- ↑ "[Pharmacology of a 1H-1,2,4-triazolyl benzophenone derivative (450191-S), a new sleep-inducer (III). Behavioral study on interactions of 450191-S and other drugs in mice]" (in Japanese). Nihon Yakurigaku Zasshi. Folia Pharmacologica Japonica 84 (2): 155–173. August 1984. doi:10.1254/fpj.84.155. PMID 6149177.
- ↑ "[Pharmacological profiles of benzodiazepinergic hypnotics and correlations with receptor subtypes]". Nihon Shinkei Seishin Yakurigaku Zasshi = Japanese Journal of Psychopharmacology 25 (3): 143–151. June 2005. PMID 16045197.
- ↑ "Comparative hepatic transport of desglycylated and cyclic metabolites of rilmazafone in rats: analysis by multiple indicator dilution method". Biopharmaceutics & Drug Disposition 14 (4): 279–290. May 1993. doi:10.1002/bdd.2510140402. PMID 8499579.
- ↑ "Rilmazafone New Drug Monograph". Center for Forensic Science Research and Education (CFSRE). https://www.cfsre.org/images/monographs/Rilmazafone-New-Drug-Monograph-NPS-Discovery-112923.pdf.
- ↑ 10.0 10.1 "Designer benzodiazepines: an update". Expert Review of Clinical Pharmacology 16 (2): 109–117. February 2023. doi:10.1080/17512433.2023.2170349. PMID 36649662.
External links
- "リスミー錠 Rhythmy (rilmazafone hydrochloride hydrate, tablets) Prescribing Information" (in ja). Shionogi & Co., Ltd.. https://database.japic.or.jp/pdf/newPINS/00001601.pdf.
- Drug Information Sheet
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