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3,4-Ethylidenedioxyamphetamine

From Wikipedia, the free encyclopedia
(Redirected fromEthylidenedioxyamphetamine)
Chemical compound
Not to be confused with3,4-Ethylenedioxyamphetamine.
Pharmaceutical compound
EIDA
Clinical data
Other namesEIDA
ATC code
  • None
Legal status
Legal status
Identifiers
  • 1-(2-Methyl-1,3-benzodioxol-5-yl)propan-2-amine
CAS Number
PubChemCID
ChemSpider
UNII
CompTox Dashboard(EPA)
Chemical and physical data
FormulaC11H15NO2
Molar mass193.246 g·mol−1
3D model (JSmol)
  • CC(N)Cc2ccc1OC(C)Oc1c2
  • InChI=1S/C11H15NO2/c1-7(12)5-9-3-4-10-11(6-9)14-8(2)13-10/h3-4,6-8H,5,12H2,1-2H3
  • Key:SLXACJFRFCJPAH-UHFFFAOYSA-N
  (verify)

3,4-Ethylidenedioxyamphetamine (EIDA) is a substituted derivative of3,4-methylenedioxyamphetamine (MDA), which was developed byDavid E. Nichols and coworkers, in the course of research to determine the bulk tolerance around thebenzodioxole portion of the MDA molecule. EIDA was found to produce similar effects to MDA in animals but with less than half the potency, while the isopropylidenedioxy derivative (IPIDA, IDA) did not substitute for MDA and instead had sedative and convulsant effects. This shows limited bulk tolerance at this position and (as with2C-G-5) makes it likely the activity of EIDA will reside primarily in oneenantiomer, although only the racemic mix has been studied as yet.[1][2][3]

See also

[edit]

References

[edit]
  1. ^Nichols DE, Kostuba LJ (October 1979). "Steric effects of substituents on phenethylamine hallucinogens. 3,4-(Methylenedioxy)amphetamine analogues alkylated on the dioxole ring".Journal of Medicinal Chemistry.22 (10):1264–7.doi:10.1021/jm00196a022.PMID 513074.
  2. ^Nichols DE, Oberlender R, Burris K, Hoffman AJ, Johnson MP (November 1989). "Studies of dioxole ring substituted 3,4-methylenedioxyamphetamine (MDA) analogues".Pharmacology, Biochemistry, and Behavior.34 (3):571–6.doi:10.1016/0091-3057(89)90560-1.PMID 2623014.S2CID 7560526.
  3. ^Trachsel D, Hadorn M, Baumberger F (March 2006). "Synthesis of fluoro analogues of 3,4-(methylenedioxy)amphetamine (MDA) and its derivatives".Chemistry & Biodiversity.3 (3):326–36.CiteSeerX 10.1.1.688.5803.doi:10.1002/cbdv.200690035.PMID 17193269.S2CID 23036634.
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