Chemistry:AH-7921

From HandWiki
Revision as of 19:40, 5 February 2024 by HamTop (talk | contribs) (change)
(diff) ← Older revision | Latest revision (diff) | Newer revision → (diff)
Short description: Opioid analgesic
AH-7921
AH-7921 structure.svg
AH-7921 3D BS.png
Clinical data
Other namesAH-7921
Routes of
administration		Recreational: insufflation, sublingual, intravenous, oral, rectal[1]
ATC code
  • none
Legal status
Legal status
  • AU: S9 (Prohibited substance)
  • BR: F1
  • CA: Schedule I
  • DE: Anlage II

In General Unscheduled, Illegal in Sweden, Czech Republic, China, Brazil and Israel.

Identifiers
CAS Number
PubChem CID
ChemSpider
UNII
KEGG
Chemical and physical data
FormulaC16H22Cl2N2O
Molar mass329.27 g·mol−1
3D model (JSmol)
 ☒N☑Y (what is this?)  (verify)

AH-7921 is an opioid analgesic drug selective for the μ-opioid receptor, having around 90% the potency of morphine when administered orally.[2][3][4] It was discovered in the 1970s[5] by a team at Allen and Hanburys located in the United Kingdom.[6] The drug is considered a new psychoactive substance (NPS) in which it is synthetically created in laboratories to mimic that of controlled substances. The substance has also been sold on the internet since 2012 as a "research chemical".[1] When sold online it may be called the alternative name doxylam, not to be confused with doxylamine.[7] AH-7921 has never progressed to clinical trials.[8] The DEA is not aware of any medical usage in the United States, and has not insisted the Health and Human Services department (HHS) to conduct any medical research of the substance's uses.[6]

Side effects and withdrawal

With doses that usually range from 10 to 150 mg, users are likely to experience effects similar to heroin, morphine, and fentanyl such as euphoria and respiratory depression.[1][8] When an overdose occurs users often experience tachycardia, hypertension, and seizures.[7] Mice, dogs, and monkeys, have been used in tests which showed the drug was almost equivalently potent to morphine, and had a very steep dose response curve.[9] Rats given 20 mg doses three times a day for five days, experienced withdrawal symptoms similar to other opioids. Reports have shown users to experience depression and insomnia when withdrawing from this drug.[1]

Chemistry

AH-7921 is commonly found as an off-white solid with a melting point between 215–216º Celsius.[1] It is one single covalently bonded unit with 4 rotatable bonds. It also has two hydrogen bond acceptors, and one hydrogen bond donor.[10]

Use

Although AH-7921 was extensively studied in vitro and in animals, though not in humans, by the developing company, it was never sold commercially for medical use. In 2013, AH-7921 was discovered to have been used as an active ingredient in "synthetic cannabis" products in Japan.[11] In October 2015, two horses (Bossmon and Literata) trained by owner-trainer Roy Sedlacek tested positive for AH-7921 at Belmont Park racetrack.[12] Norway and Iceland use this substance as an analytical reference standard in which it can be ordered online from chemical suppliers; however, labels are required to state that it is not for human consumption thus conforming to the law.[1] Within ten months from 2013 to 2014, there had been serious fatalities reported from this drug from four different countries.[9] The first fatality was a 19-year-old male who had a 3.9 mg/L AH-7921 concentration of heart blood leading medical examiners to confirm the death was an opioid intoxication.[13] In another case, a 22-year-old woman was found dead with a femoral blood to AH-7921 concentration of 450 μg/L.[14]

A 2018 review of published case reports found a total of 14 cases, of which 13 resulted in death.[15] The oral route of administration was reported in two cases, and most cases reported use of concomitant pharmaceutical agents. Postmortem autopsies found that pulmonary edema was the most common finding, with nine of the cases having heavier lungs. Overall, fatalities occurred with low and high concentrations of AH-7921 in femoral blood.[15]

Legality

AH-7921 was made a Prohibited Substance (Schedule 9 of the Standard for the Uniform Scheduling of Medicines and Poisons) in Australia in May 2014.[16] Although this amendment was repealed in June 2014,[17] which simply means the amendment document ceases, but the actual scheduling is permanent as part of the main document (all SUSMP amendments cease after a few weeks). It may, however, still be a banned import.

AH-7921 has been illegal to distribute in Israel since December 2013.[18]

In the UK, AH-7921 was included as a Class A drug in January 2015 as part of The Misuse of Drugs Act 1971 (Amendment) (No. 2) Order 2014.[19]

In Brazil, AH-7921 has been an illegal drug since May 2015.[20]

As of October 2015 AH-7921 is a controlled substance in China.[21]

AH-7921 is banned in the Czech Republic.[22]

In the United States, AH-7921 was placed into Schedule I of the Controlled Substances Act on May 16, 2016, due to its lack of medical use.[6][23] Furthermore, any person who wishes to manufacture, distribute, import, export, research, and educate using the substance, must be registered by the Drug Enforcement Administration.[6]

The Canadian Controlled Drugs and Substances Act was amended in 2016 to include the substance as a Schedule I substance. Possession without legal authority can result in maximum 7 years imprisonment. Further, Health Canada amended the Food and Drug Regulations in May, 2016 to classify AH-7921 as a restricted drug.[24] Only those with a law enforcement agency, person with an exemption permit or institutions with Minister's authorization may possess the drug in Canada.

See also

References

  1. ↑ 1.0 1.1 1.2 1.3 1.4 1.5 "AH-7921: the list of new psychoactive opioids is expanded". Forensic Toxicology 33 (2): 195–201. 2015. doi:10.1007/s11419-015-0271-z. PMID 26257832. 
  2. ↑ "Proceedings: Anti-nociceptive effects in N-substituted cyclohexylmethylbenzamides". British Journal of Pharmacology 49 (1): 158P–159P. September 1973. doi:10.1111/j.1476-5381.1973.tb08279.x. PMID 4207044. 
  3. ↑ "Determination of receptors that mediate opiate side effects in the mouse". British Journal of Pharmacology 79 (3): 731–736. July 1983. doi:10.1111/j.1476-5381.1983.tb10011.x. PMID 6317119. 
  4. ↑ "1-(3,4-Dichlorobenzamidomethyl)cyclohexyldimethylamine and related compounds as potential analgesics". Journal of Medicinal Chemistry 17 (11): 1188–1193. November 1974. doi:10.1021/jm00257a012. PMID 4416926. 
  5. ↑ Harper N, Veitch G, "1-(3,4-Dichlorobenzamidomethyl)-cyclohexyldimethylamine", US patent 3975443, issued 1976-08-17, assigned to Allen & Hanburys
  6. ↑ 6.0 6.1 6.2 6.3 "2016 - Final Order: Placement of AH-7921 Into Schedule I" (in en-US). http://www.deadiversion.usdoj.gov/fed_regs/rules/2016/fr0414_4.htm. 
  7. ↑ 7.0 7.1 "An Expanding World of Novel Psychoactive Substances: Opioids". Frontiers in Psychiatry 8: 110. 2017-06-30. doi:10.3389/fpsyt.2017.00110. PMID 28713291. 
  8. ↑ 8.0 8.1 "The New Wave of Designer Drugs" (in en-US). Forensic Scholars Today (Concordia University, St. Paul Online). 10 January 2017. http://online.csp.edu/blog/forensic-scholars-today/designer-drugs. 
  9. ↑ 9.0 9.1 "Metabolic characterization of AH-7921, a synthetic opioid designer drug: in vitro metabolic stability assessment and metabolite identification, evaluation of in silico prediction, and in vivo confirmation". Drug Testing and Analysis 8 (8): 779–791. August 2016. doi:10.1002/dta.1856. PMID 26331297. 
  10. ↑ "AH-7921: 3,4-dichloro-N-[[1-(dimethylamino)cyclohexyl]methyl]benzamide" (in en). PubChem. U.S. National Library of Medicine. https://pubchem.ncbi.nlm.nih.gov/compound/187760#section=chemical-and-physical-properties. 
  11. ↑ "Two new-type cannabimimetic quinolinyl carboxylates, QUPIC and QUCHIC, two new cannabimimetic carboxamide derivatives, ADB-FUBINACA and ADBICA, and five synthetic cannabinoids detected with a thiophene derivative α-PVT and an opioid receptor agonist AH-7921 identified in illegal products". Forensic Toxicology 31 (2): 223–240. July 2013. doi:10.1007/s11419-013-0182-9. 
  12. ↑ "Two horses test positive for designer drug". Racing Post. 12 November 2015. http://www.racingpost.com/news/horse-racing/usa-two-horses-test-positive-for-designer-drug/1987810/. 
  13. ↑ "A fatality involving AH-7921". Journal of Analytical Toxicology 38 (4): 226–230. May 2014. doi:10.1093/jat/bku011. PMID 24523294. 
  14. ↑ "Two fatalities associated with synthetic opioids: AH-7921 and MT-45". Forensic Science International 277: e30–e35. August 2017. doi:10.1016/j.forsciint.2017.04.003. PMID 28506719. 
  15. ↑ 15.0 15.1 "AH-7921: A review of previously published reports". Proceedings 31 (3): 303–306. July 2018. doi:10.1080/08998280.2018.1465320. PMID 29904293. 
  16. ↑ "Final decisions and reasons for decisions by delegates of the Secretary to the Department of Health". Therapeutic Goods Administration (TGA). Commonwealth of Australia. May 2014. https://www.tga.gov.au/sites/default/files/scheduling-decisions-1405-final.pdf. 
  17. ↑ "Poisons Standard Amendment No. 2 of 2014". Federal Register of Legislation. Commonwealth of Australia. 19 May 2014. https://www.legislation.gov.au/Details/F2014L00566. 
  18. ↑ "פקודת הסמים המסוכנים נוסח חדש, תשל"ג -1973" (in Hebrew). http://www.nevo.co.il/Law_word/law01/P170_001.doc. 
  19. ↑ "The Misuse of Drugs Act 1971 (Amendment) (No. 2) Order 2014". Legislation.gov.uk. http://www.legislation.gov.uk/uksi/2014/3271/made. 
  20. ↑ "Resolução da Diretoria Colegiada - RDC nº 87 de 28/06/2016" (in Portuguese). http://portal.anvisa.gov.br/documents/10181/2879690/(1)RDC_87_2016.pdf/. 
  21. ↑ "关于印发《非药用类麻醉药品和精神药品列管办法》的通知" (in Chinese). China Food and Drug Administration. 27 September 2015. http://www.sfda.gov.cn/WS01/CL0056/130753.html. 
  22. ↑ "Látky, o které byl doplněn seznam č. 4 psychotropních látek (příloha č. 4 k nařízení vlády č. 463/2013 Sb.)" (in Czech). Ministerstvo zdravotnictví. http://www.mzcr.cz/Admin/_upload/files/3/Nov%C3%A9%20PL.pdf. 
  23. ↑ "Schedules of Controlled Substances: Placement of AH-7921 Into Schedule I". Drug Enforcement Administration. U.S. Department of Justic. 14 April 2016. http://www.deadiversion.usdoj.gov/fed_regs/rules/2016/fr0414_4.htm. 
  24. ↑ "Regulations Amending the Food and Drug Regulations (Parts G and J — Lefetamine, AH-7921, MT-45 and W-18)". The Government of Canada. June 2016. http://www.gazette.gc.ca/rp-pr/p2/2016/2016-06-01/html/sor-dors106-eng.php. 



Retrieved from "https://handwiki.org/wiki/index.php?title=Chemistry:AH-7921&oldid=3320778"