Para-Methoxy-N-ethylamphetamine

Chemical compound
Identifiers
  • N-ethyl-1-(4-methoxyphenyl)propan-2-amine
CAS Number
  • 14367-46-5 checkY
    93963-24-7 (hydrochloride)
PubChem CID
  • 85725
ChemSpider
  • 77316
UNII
  • CA3JZQ6AZC
CompTox Dashboard (EPA)
  • DTXSID00931981 Edit this at Wikidata
ECHA InfoCard100.034.839 Edit this at WikidataChemical and physical dataFormulaC12H19NOMolar mass193.290 g·mol−13D model (JSmol)
  • Interactive image
  • O(c1ccc(cc1)CC(NCC)C)C
InChI
  • InChI=1S/C12H19NO/c1-4-13-10(2)9-11-5-7-12(14-3)8-6-11/h5-8,10,13H,4,9H2,1-3H3
  • Key:USBWBBAUWVUJLA-UHFFFAOYSA-N
  (verify)

para-Methoxyethylamphetamine (PMEA), is a stimulant drug related to PMA. PMEA reputedly produces similar effects to PMA, but is considerably less potent[1] and seems to have slightly less tendency to produce severe hyperthermia, at least at low doses. At higher doses however the side effects and danger of death approach those of PMA itself, and PMEA should still be considered a potentially dangerous drug. Investigation of a drug-related death in Japan in 2005 showed PMEA to be present in the body and was thought to be responsible for the death.[2]

See also

References

  1. ^ Bustamante D, Díaz-Véliz G, Paeile C, Zapata-Torres G, Cassels BK (October 2004). "Analgesic and behavioral effects of amphetamine enantiomers, p-methoxyamphetamine and n-alkyl-p-methoxyamphetamine derivatives". Pharmacology, Biochemistry, and Behavior. 79 (2): 199–212. doi:10.1016/j.pbb.2004.06.017. PMID 15501295. S2CID 594578.
  2. ^ Zaitsu K, Katagi M, Kamata T, Kamata H, Shima N, Tsuchihashi H, et al. (May 2008). "Determination of a newly encountered designer drug "p-methoxyethylamphetamine" and its metabolites in human urine and blood". Forensic Science International. 177 (1): 77–84. doi:10.1016/j.forsciint.2007.11.001. PMID 18155375.
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DRAsTooltip Dopamine releasing agents
NRAsTooltip Norepinephrine releasing agents
SRAsTooltip Serotonin releasing agents
Others
See also: Receptor/signaling modulators • Monoamine reuptake inhibitors • Adrenergics • Dopaminergics • Serotonergics • Monoamine metabolism modulators • Monoamine neurotoxins
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Non-specific
AAADTooltip Aromatic L-amino acid decarboxylase
MAOTooltip Monoamine oxidase
Phenethylamines
(dopamine, epinephrine,
norepinephrine)
PAHTooltip Phenylalanine hydroxylase
THTooltip Tyrosine hydroxylase
DBHTooltip Dopamine beta-monooxygenase
PNMTTooltip Phenylethanolamine N-methyltransferase
  • Inhibitors: CGS-19281A
  • SKF-64139
  • SKF-7698
COMTTooltip Catechol-O-methyl transferase
Tryptamines
(serotonin, melatonin)
TPHTooltip Tryptophan hydroxylase
AANATTooltip Serotonin N-acetyl transferase
ASMTTooltip Acetylserotonin O-methyltransferase
Histamine
HDCTooltip Histidine decarboxylase
  • Substrates→Products: L-Histidine→Histamine
HNMTTooltip Histamine N-methyltransferase
  • Substrates→Products: Histamine→N-Methylhistamine
DAOTooltip Diamine oxidase
  • Substrates→Products: Histamine→Imidazole acetic acid
See also: Receptor/signaling modulators • Adrenergics • Dopaminergics • Melatonergics • Serotonergics • Monoamine reuptake inhibitors • Monoamine releasing agents • Monoamine neurotoxins
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Phenethylamines


Stimulants: Phenylethanolamine

Amphetamines
Phentermines
Cathinones
Phenylisobutylamines
Phenylalkylpyrrolidines
Catecholamines
(and close relatives)
Miscellaneous