Chemistry:JM-1232
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Short description: Chemical compound
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Formula | C24H27N3O2 |
Molar mass | 389.499 g·mol−1 |
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JM-1232 is a sedative and hypnotic drug being researched as a potential anesthetic. It has similar effects to sedative-hypnotic benzodiazepine drugs, but is structurally distinct and so is classed as a nonbenzodiazepine hypnotic.[1][2][3][4][5][6] It was developed by a team at Maruishi Pharmaceutica.[7]
A human study explored the sedation caused by infusions at a range of doses, finding a fair hemodynamic safety profile.[8]
References
- ↑ "Novel water-soluble sedative-hypnotic agents: isoindolin-1-one derivatives". Chemical & Pharmaceutical Bulletin 55 (12): 1682–1688. December 2007. doi:10.1248/cpb.55.1682. PMID 18057740.
- ↑ "Antinociceptive property of intrathecal and intraperitoneal administration of a novel water-soluble isoindolin-1-one derivative, JM 1232 (-) in rats". European Journal of Pharmacology 596 (1–3): 56–61. October 2008. doi:10.1016/j.ejphar.2008.07.054. PMID 18708047.
- ↑ "The antinociceptive effects and pharmacological properties of JM-1232(-): a novel isoindoline derivative". Anesthesia and Analgesia 108 (3): 1008–1014. March 2009. doi:10.1213/ane.0b013e318193678f. PMID 19224817.
- ↑ "The shivering threshold in rabbits with JM-1232(-), a new benzodiazepine receptor agonist". Anesthesia and Analgesia 109 (1): 96–100. July 2009. doi:10.1213/ane.0b013e3181a1a5ed. PMID 19439682.
- ↑ "Effect of JM-1232(-), a New Sedative on Central Respiratory Activity in Newborn Rats". New Frontiers in Respiratory Control. Advances in Experimental Medicine and Biology. 669. 2010. pp. 115–118. doi:10.1007/978-1-4419-5692-7_23. ISBN 978-1-4419-5691-0.
- ↑ "New drugs and technologies, intravenous anaesthesia is on the move (again)". British Journal of Anaesthesia 105 (3): 246–254. September 2010. doi:10.1093/bja/aeq190. PMID 20650920.
- ↑ Toyooka K, Kanamitsu N, Yoshimura M, Kuriyama H, Tamura T, "Isoindoline Derivative", EP patent 1566378, issued 15 August 2012, assigned to Maruishi Pharmaceutical Co Ltd.
- ↑ "First human administration of MR04A3: a novel water-soluble nonbenzodiazepine sedative". Anesthesiology 116 (2): 385–395. February 2012. doi:10.1097/ALN.0b013e318242b2af. PMID 22222479.
Original source: https://en.wikipedia.org/wiki/JM-1232.
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