Misplaced Pages

EDMA

Article snapshot taken from Wikipedia with creative commons attribution-sharealike license. Give it a read and then ask your questions in the chat. We can research this topic together.

This is an old revision of this page, as edited by Cburnett (talk | contribs) at 16:52, 7 August 2011 (Bump box to top). The present address (URL) is a permanent link to this revision, which may differ significantly from the current revision.

Revision as of 16:52, 7 August 2011 by Cburnett (talk | contribs) (Bump box to top)(diff) ← Previous revision | Latest revision (diff) | Newer revision → (diff) Pharmaceutical compound
EDMA
Clinical data
Routes of
administration
Oral
ATC code
  • none
Legal status
Legal status
Identifiers
IUPAC name
  • 1-(2,3-dihydro-1,4-benzodioxin-6-yl)-N-methylpropan-2-amine
PubChem CID
ChemSpider
CompTox Dashboard (EPA)
Chemical and physical data
FormulaC12H17NO2
Molar mass207.269
3D model (JSmol)
SMILES
  • CC(Cc1ccc2c(c1)OCCO2)NC
InChI
  • InChI=1S/C12H17NO2/c1-9(13-2)7-10-3-4-11-12(8-10)15-6-5-14-11/h3-4,8-9,13H,5-7H2,1-2H3
  • Key:UJKWLAZYSLJTKA-UHFFFAOYSA-N
  (verify)
This article is about the amphetamine. For other uses, see EDMA (disambiguation). "MDMC" redirects here. For the airport with that ICAO code, see Osvaldo Virgil Airport.

3,4-Ethylenedioxy-N-methylamphetamine (EDMA; MDMC) is an entactogen drug of the amphetamine class. It is an analogue of MDMA where the methylenedioxy ring has been replaced by an ethylenedioxy ring. EDMA was first synthesized by Alexander Shulgin. In his book PiHKAL, the dosage is listed as 150–250 mg, and the duration listed as 3–5 hours. According to Shulgin, EDMA produces a bare threshold consisting of paresthesia, nystagmus, and hypnogogic imagery, with few to no other effects. Scientific research has demonstrated that EDMA acts as a non-neurotoxic serotonin releasing agent with moderately diminished potency relative to MDMA, and with negligible effects on dopamine release. Based on Shulgin's reports of essential inactivity at 150–250 mg, it may be more active at higher doses.

See also

References

  1. ^ Ann Shulgin; Alexander Shulgin (1991). Pihkal: A Chemical Love Story. Transform Press. ISBN 0-9630096-0-5.{{cite book}}: CS1 maint: multiple names: authors list (link)
  2. ^ McKenna DJ, Guan XM, Shulgin AT (1991). "3,4-Methylenedioxyamphetamine (MDA) analogues exhibit differential effects on synaptosomal release of 3H-dopamine and 3H-5-hydroxytryptamine". Pharmacology, Biochemistry, and Behavior. 38 (3): 505–12. doi:10.1016/0091-3057(91)90005-M. PMID 1829838. {{cite journal}}: Unknown parameter |month= ignored (help)CS1 maint: multiple names: authors list (link)

External links

Empathogens/entactogens
Phenylalkyl-
amines

(other than
cathinones)
Cyclized phenyl-
alkylamines
Cathinones
Tryptamines
Chemical classes
Serotonin receptor modulators
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
Phenethylamines
Amphetamines
Phentermines
Cathinones
Phenylisobutylamines
Phenylalkylpyrrolidines
Catecholamines
(and close relatives)
Miscellaneous

Template:PiHKAL

Categories: