From Wikipedia, the free encyclopedia
2-Methoxyamphetamine
Clinical data
Routes of
administration
Oral
ATC code
  • none
Identifiers
  • 1-(2-methoxyphenyl)propan-2-amine
CAS Number
PubChem CID
ChemSpider
ChEMBL
CompTox Dashboard ( EPA)
Chemical and physical data
FormulaC10H15NO
Molar mass165.236 g·mol−1
3D model ( JSmol)
  • O(c1ccccc1CC(N)C)C
  • InChI=1S/C10H15NO/c1-8(11)7-9-5-3-4-6-10(9)12-2/h3-6,8H,7,11H2,1-2H3 checkY
  • Key:VBAHFEPKESUPDE-UHFFFAOYSA-N checkY
 ☒NcheckY  (what is this?)   (verify)

2-Methoxyamphetamine (2-MA), also known as ortho- methoxy amphetamine (OMA), is a drug of the amphetamine class. It is substantially weaker in inhibiting the reuptake of and inducing the release of the monoamine neurotransmitters compared to related agents such as amphetamine, MMA, and PMA, [1] and may instead act as a β-adrenergic receptor agonist similarly to its N- methylated analogue methoxyphenamine. [2]

See also

References

  1. ^ Tseng LF, Menon MK, Loh HH (May 1976). "Comparative actions of monomethoxyamphetamines on the release and uptake of biogenic amines in brain tissue". The Journal of Pharmacology and Experimental Therapeutics. 197 (2): 263–271. PMID  1271280.
  2. ^ Shulgin A, Shulgin A (1991). Pihkal: A Chemical Love Story. Transform Press. ISBN  0-9630096-0-5.

External links

From Wikipedia, the free encyclopedia
2-Methoxyamphetamine
Clinical data
Routes of
administration
Oral
ATC code
  • none
Identifiers
  • 1-(2-methoxyphenyl)propan-2-amine
CAS Number
PubChem CID
ChemSpider
ChEMBL
CompTox Dashboard ( EPA)
Chemical and physical data
FormulaC10H15NO
Molar mass165.236 g·mol−1
3D model ( JSmol)
  • O(c1ccccc1CC(N)C)C
  • InChI=1S/C10H15NO/c1-8(11)7-9-5-3-4-6-10(9)12-2/h3-6,8H,7,11H2,1-2H3 checkY
  • Key:VBAHFEPKESUPDE-UHFFFAOYSA-N checkY
 ☒NcheckY  (what is this?)   (verify)

2-Methoxyamphetamine (2-MA), also known as ortho- methoxy amphetamine (OMA), is a drug of the amphetamine class. It is substantially weaker in inhibiting the reuptake of and inducing the release of the monoamine neurotransmitters compared to related agents such as amphetamine, MMA, and PMA, [1] and may instead act as a β-adrenergic receptor agonist similarly to its N- methylated analogue methoxyphenamine. [2]

See also

References

  1. ^ Tseng LF, Menon MK, Loh HH (May 1976). "Comparative actions of monomethoxyamphetamines on the release and uptake of biogenic amines in brain tissue". The Journal of Pharmacology and Experimental Therapeutics. 197 (2): 263–271. PMID  1271280.
  2. ^ Shulgin A, Shulgin A (1991). Pihkal: A Chemical Love Story. Transform Press. ISBN  0-9630096-0-5.

External links


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