Structure via PubChem · Public domain (PubChem)
rilmazafone
Sign in to saveRilmazafone (リスミー, Rhythmy, previously known as 450191-S) is a water-soluble prodrug developed by Shionogi. Inside the human body, rilmazafone is converted into several benzodiazepine metabolites that have sedative and hypnotic effects.
Chemical data
- Formula
- C21H20Cl2N6O3
- Molecular weight
- 475.3 g/mol
- IUPAC name
- 5-[[(2-aminoacetyl)amino]methyl]-1-[4-chloro-2-(2-chlorobenzoyl)phenyl]-N,N-dimethyl-1,2,4-triazole-3-carboxamide
via PubChem
Drug data · ChEMBL
- Max clinical phase
- Phase 2
- Molecule type
- Small molecule
via ChEMBL · EBI
Research
44 papers- Rilmazafone: A designer benzodiazepine pro-drug involved in fatal intoxications.Journal of analytical toxicology · 2023
- Itraconazole Contaminated with Rilmazafone in Japan: A Retrospective Analysis Using the Japanese Adverse Drug Event Report Database.Drugs - real world outcomes · 2022
- Effects of melatonin and rilmazafone on nocturia in the elderly.The Journal of international medical research · 2007
- Residual effects of zolpidem, triazolam, rilmazafone and placebo in healthy elderly subjects: a randomized double-blind study.Sleep medicine · 2015
- Generic Drug Shortage in Japan: GMP Noncompliance and Associated Quality Issues.Journal of pharmaceutical sciences · 2023
via PubMed
~2 min read
Encyclopedic overview
3 sectionsContents
- See also
- References
- External links
Rilmazafone (リスミー, Rhythmy, previously known as 450191-S) is a water-soluble prodrug developed by Shionogi. Inside the human body, rilmazafone is converted into several benzodiazepine metabolites that have sedative and hypnotic effects.
Rilmazafone is not a benzodiazepine, since there is no benzene ring fused with a diazepine ring in the compound; in fact, the parent drug has no diazepine ring. It is therefore not classified as a benzodiazepine in several countries, including the United States, where it is not designated a controlled substance. Rilmazafone has no effects on benzodiazepine receptors itself, nor does it produce any psychoactive effects prior to metabolism. However, once inside the body it is metabolized by aminopeptidase enzymes in the small intestine to form the principal active benzodiazepine rilmazolam. As can be seen in the molecular diagram below, the principal metabolite contains a benzodiazepine ring structure (i.e., a benzene ring fused with a diazepine ring), unlike the parent compound (rilmazafone), which has no diazepine ring. Rilmazafone has been identified as a NPS (new psychoactive substance) in the U.S. and Europe.
Excerpted from Wikipedia’s “rilmazafone” article, available under the CC BY-SA 4.0 licence.