Movatterモバイル変換


[0]ホーム

URL:


Jump to content
WikipediaThe Free Encyclopedia
Search

MPM (drug)

From Wikipedia, the free encyclopedia
(Redirected from4-Propoxy-2,5-dimethoxyamphetamine)
Pharmaceutical compound
MPM
Clinical data
Other names4-Propoxy-2,5-dimethoxyamphetamine; 2,5-Dimethoxy-4-propoxyamphetamine
Drug classSerotonin5-HT2 receptoragonist
ATC code
  • None
Identifiers
  • 1-(2,5-dimethoxy-4-propoxyphenyl)propan-2-amine
CAS Number
PubChemCID
ChemSpider
UNII
CompTox Dashboard(EPA)
Chemical and physical data
FormulaC14H23NO3
Molar mass253.342 g·mol−1
3D model (JSmol)
  • COc1cc(OC)c(cc1OCCC)CC(C)N
  • InChI=1S/C14H23NO3/c1-5-6-18-14-8-11(7-10(2)15)12(16-3)9-13(14)17-4/h8-10H,5-7,15H2,1-4H3 checkY
  • Key:FTJOFRCENIVFLC-UHFFFAOYSA-N checkY
  (verify)

MPM, also known as2,5-dimethoxy-4-propoxyamphetamine, is a lesser-known putativepsychedelic drug of thephenethylamine,amphetamine, andDOx families.[1][2] It is aderivative of the DOxpsychedelicsTMA-2 andMEM in which the 4-positionsubstituent has been extended.[1] The drug is also the α-methyl or amphetamineanalogue of2C-O-7.[1]

Use and effects

[edit]

In his bookPiHKAL (Phenethylamines I Have Known and Loved),Alexander Shulgin gives the dose range as "30 mg or more" and theduration as "probably short".[1] The drug produced weak or threshold effects at doses of 15 to 30 mg.[1][3] In another publication, Shulgin estimated an effective dose of MPM to be around 50 mg and the drug as being around half as potent as TMA-2 or MEM.[4]

Pharmacology

[edit]

MPM produces thehead-twitch response, a behavioral proxy of psychedelic effects, in rodents.[5] It shows about the samepotency as TMA-2 and MEM in this test.[5]

History

[edit]

MPM was first described in thescientific literature by Shulgin in 1978.[3] Subsequently, Shulgin described the drug in more detail in his bookPiHKAL.[1] The compound's name is said to derive from itsbenzenering substituents, "methoxypropoxymethoxy".[2]

See also

[edit]

References

[edit]
  1. ^abcdefMPM entry inPiHKAL on Erowid
  2. ^abKolaczynska KE, Luethi D, Trachsel D, Hoener MC, Liechti ME (2019)."Receptor Interaction Profiles of 4-Alkoxy-Substituted 2,5-Dimethoxyphenethylamines and Related Amphetamines".Frontiers in Pharmacology.10: 1423.doi:10.3389/fphar.2019.01423.PMC 6893898.PMID 31849671.
  3. ^abShulgin AT (1978)."Psychotomimetic Drugs: Structure-Activity Relationships". In Iversen LL, Iversen SD, Snyder SH (eds.).Stimulants. Boston, MA: Springer US. pp. 243–333.doi:10.1007/978-1-4757-0510-2_6.ISBN 978-1-4757-0512-6.
  4. ^Braun U, Braun G, Jacob P, Nichols DE, Shulgin AT (1978)."Mescaline Analogs: Substitutions at the 4-Position"(PDF). In Barnett G, Trsic M, Willette RE (eds.).QuaSAR: Quantitative Structure Activity Relationships Of Analgesics, Narcotic Antagonists, And Hallucinogens(PDF). National Institute on Drug Abuse Research Monograph Series. Vol. 22. National Institute on Drug Abuse. pp. 27–37.PMID 101882.
  5. ^abHalberstadt AL, Chatha M, Chapman SJ, Brandt SD (March 2019)."Comparison of the behavioral effects of mescaline analogs using the head twitch response in mice".J Psychopharmacol.33 (3):406–414.doi:10.1177/0269881119826610.PMC 6848748.PMID 30789291.

External links

[edit]


Tryptamines
No ring subs.
4-Hydroxytryptamines
5-Hydroxytryptamines
5-Methoxytryptamines
Other ring subs.
α-Alkyltryptamines
Others
Cyclized
Bioisosteres
Phenethylamines
Scalines
2C-x
3C-x
DOx
4C-x
Ψ-PEA
MDxx
FLY
25x-NB (NBOMes)
Others
Cyclized
Lysergamides
  • Bioisosteres:JRT
Others
Natural sources
5-HT1
5-HT1A
5-HT1B
5-HT1D
5-HT1E
5-HT1F
5-HT2
5-HT2A
5-HT2B
5-HT2C
5-HT37
5-HT3
5-HT4
5-HT5A
5-HT6
5-HT7
Phenethylamines
Amphetamines
Phentermines
Cathinones
Phenylisobutylamines
(and further-extended)
Catecholamines
(and close relatives)
Cyclized
phenethylamines
Phenylalkylpyrrolidines
2-Benzylpiperidines
(phenidates)
Phenylmorpholines
(phenmetrazines)
Phenyloxazolamines
(aminorexes)
Isoquinolines and
tetrahydroisoquinolines
2-Aminoindanes
2-Aminotetralins
Others / unsorted
Related compounds
Retrieved from "https://en.wikipedia.org/w/index.php?title=MPM_(drug)&oldid=1300555549"
Categories:
Hidden categories:

[8]ページ先頭

©2009-2025 Movatter.jp