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2,5-Dimethoxy-4-nitroamphetamine

From Wikipedia, the free encyclopedia
Pharmaceutical compound
DON
Clinical data
Other namesDON; 2,5-Dimethoxy-4-nitroamphetamine; 4-Nitro-2,5-dimethoxyamphetamine
Routes of
administration
Oral
Drug classSerotonin5-HT2 receptoragonist;Serotonergic psychedelic;Hallucinogen
Identifiers
  • 1-(2,5-dimethoxy-4-nitrophenyl)propan-2-amine
CAS Number
PubChemCID
ChemSpider
UNII
ChEMBL
CompTox Dashboard(EPA)
Chemical and physical data
FormulaC11H16N2O4
Molar mass240.259 g·mol−1
3D model (JSmol)
Melting point206 to 207 °C (403 to 405 °F) (hydrochloride)
231-232 °C ((R)-isomer)[1]
  • COc1cc(c(cc1CC(C)N)OC)N(=O)=O
  • InChI=1S/C11H16N2O4/c1-7(12)4-8-5-11(17-3)9(13(14)15)6-10(8)16-2/h5-7H,4,12H2,1-3H3 checkY
  • Key:JQJRESSXOVAECC-UHFFFAOYSA-N checkY
  (verify)

2,5-Dimethoxy-4-nitroamphetamine (DON) is apsychedelic drug andamphetamine.[1] It is ananalogue ofDOM andDOB.[1] It is also closely related to2C-N.[1] The drug is aserotonin5-HT2 receptoragonist.[2]

Use and effects

[edit]

In his bookPiHKAL,Alexander Shulgin lists a dosage of DON as being 3 to 4.5 mg orally with amphetamine-like stimulation and mildpsychedelic effects lasting 8 to 15 hours.[1]

Pharmacology

[edit]

DON acts as aserotonin5-HT2A and5-HT2C receptorpartial agonist, albeit with far lowerpotency andefficacy than other DOx drugs.[2] It is also a serotonin5-HT2B receptorpartial agonist.[3] Earlier studies have also reported itsaffinities atserotonin receptors, including the serotonin5-HT2 and5-HT1 receptors.[4][5] The drug produces thehead-twitch response, a behavioral proxy ofpsychedelic-like effects, in rodents.[6]

Chemistry

[edit]

DON is in a class of compounds commonly known as α-methylphenethylamines, oramphetamines and the full chemical name is 1-(2,5-dimethoxy-4-nitrophenyl)propan-2-amine. It has astereocenter.

Society and culture

[edit]

Legal status

[edit]

DON is unscheduled in theUnited States, but because of its close similarity in structure and effects toDOM andDOB, possession and sale of DON may be subject to prosecution under theFederal Analog Act.[citation needed] DON is listed as a Class A drug in theDrugs controlled by the UK Misuse of Drugs Act after the table of contents ofPiHKAL andTiHKAL were added to the schedules.

See also

[edit]

References

[edit]
  1. ^abcdeDON Entry in PiHKAL
  2. ^abAcuña-Castillo C, Villalobos C, Moya PR, Sáez P, Cassels BK, Huidobro-Toro JP (June 2002)."Differences in potency and efficacy of a series of phenylisopropylamine/phenylethylamine pairs at 5-HT(2A) and 5-HT(2C) receptors".Br J Pharmacol.136 (4):510–519.doi:10.1038/sj.bjp.0704747.PMC 1573376.PMID 12055129.
  3. ^Hemanth P, Nistala P, Nguyen VT, Eltit JM, Glennon RA, Dukat M (2023)."Binding and functional structure-activity similarities of 4-substituted 2,5-dimethoxyphenyl isopropylamine analogues at 5-HT2A and 5-HT2B serotonin receptors".Frontiers in Pharmacology.14 1101290.doi:10.3389/fphar.2023.1101290.PMC 9902381.PMID 36762110.
  4. ^Glennon RA (January 1987). "Central serotonin receptors as targets for drug research".J Med Chem.30 (1):1–12.doi:10.1021/jm00384a001.PMID 3543362.Table II. Affinities of Selected Phenalkylamines for 5-HT1 and 5-HT2 Binding Sites
  5. ^Shannon M, Battaglia G, Glennon RA, Titeler M (June 1984). "5-HT1 and 5-HT2 binding properties of derivatives of the hallucinogen 1-(2,5-dimethoxyphenyl)-2-aminopropane (2,5-DMA)".Eur J Pharmacol.102 (1):23–29.doi:10.1016/0014-2999(84)90333-9.PMID 6479216.
  6. ^Halberstadt AL, Chatha M, Klein AK, Wallach J, Brandt SD (May 2020)."Correlation between the potency of hallucinogens in the mouse head-twitch response assay and their behavioral and subjective effects in other species"(PDF).Neuropharmacology.167 107933.doi:10.1016/j.neuropharm.2019.107933.PMC 9191653.PMID 31917152.

External links

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