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Open Access Articles- Top Results for JM-1232

JM-1232

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JM-1232
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Systematic (IUPAC) name
(3R)-3-[2-(4-methylpiperazin-1-yl)-2-oxoethyl]-2-phenyl-3,5,6,7-tetrahydrocyclopenta[f]isoindol-1-one
Clinical data
Identifiers
PubChem CID 17755150
ChemSpider 26231036 7pxN
Chemical data
Formula C24H27N3O2
389.489 g/mol
 14pxN (what is this?)  (verify)

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

  1. ^ Kanamitsu N, Osaki T, Itsuji Y, Yoshimura M, Tsujimoto H, Soga M (December 2007). "Novel water-soluble sedative-hypnotic agents: isoindolin-1-one derivatives". Chemical & Pharmaceutical Bulletin 55 (12): 1682–8. PMID 18057740. doi:10.1248/cpb.55.1682. 
  2. ^ Nishiyama T, Chiba S, Yamada Y (October 2008). "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. PMID 18708047. doi:10.1016/j.ejphar.2008.07.054. 
  3. ^ Chiba S, Nishiyama T, Yamada Y (March 2009). "The antinociceptive effects and pharmacological properties of JM-1232(-): a novel isoindoline derivative". Anesthesia and Analgesia 108 (3): 1008–14. PMID 19224817. doi:10.1213/ane.0b013e318193678f. 
  4. ^ Masamune T, Sato H, Okuyama K, Imai Y, Iwashita H, Ishiyama T, Oguchi T, Sessler DI, Matsukawa T (July 2009). "The shivering threshold in rabbits with JM-1232(-), a new benzodiazepine receptor agonist". Anesthesia and Analgesia 109 (1): 96–100. PMID 19439682. doi:10.1213/ane.0b013e3181a1a5ed. 
  5. ^ Kuribayashi J, Kuwana S, Hosokawa Y, Hatori E, Takeda J (2010). "Effect of JM-1232(-), a new sedative on central respiratory activity in newborn rats". Advances in Experimental Medicine and Biology 669: 115–8. PMID 20217332. doi:10.1007/978-1-4419-5692-7_23. 
  6. ^ Sneyd JR, Rigby-Jones AE (September 2010). "New drugs and technologies, intravenous anaesthesia is on the move (again)". British Journal of Anaesthesia 105 (3): 246–54. PMID 20650920. doi:10.1093/bja/aeq190. 
  7. ^ EP Patent 1566378 Isoindoline Derivative
  8. ^ "First human administration of MR04A3: a novel water-soluble nonbenzodiazepine sedative.". Anesthesiology. 116: 385–95. Feb 2012. PMID 22222479. doi:10.1097/ALN.0b013e318242b2af. 


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