MME (drug)

Pharmacology

Alexander Shulgin describes in PiHKAL an experiment with MME, in which he administered varying amounts of the drug to mice via injections. Shulgin reports that 7 of the 9 mice injected with MME died as a result. After describing his experiment, Shulgin speculates that MME may have an LD50 value of around 60–80 mg/Kg in mice when injected. Shulgin describes that one of the mice began convulsing after being administered MME: "[...] the mouse went into a twitching series of convulsions (known as clonic in the trade) and in five minutes he was dead." The convulsions Shulgin noted may have been a symptom of serotonin syndrome in the mouse due to MME's affinity towards serotonin transporter in Mus musculus.

Computational modeling predicts that MME has an LD50 of 330 mg/Kg. MME is also predicted to be neurotoxic (p=0.63), respiratorically toxic (p=0.69), carcinogenic (p=0.50), and ecotoxic (p=0.57). MME is predicted to cross the blood–brain barrier (p=0.79).

:[[File:Mmetoxicology.png|350px|thumb|left|upright=1.2|class=skin-invert-image|ProTox-3.0's predictions about MME's toxicological properties.]]

Chemistry

MME has several isomers. MEM is one of them along with EMM. According to Alexander Shulgin, EEM is not biologically active. MEM is biologically active in humans and also possesses an affinity for the 5-HT2A receptor.

Synthesis

Shulgin describes the synthesis of MME in his book PiHKAL. He starts with 4-ethoxy-3-methoxybenzaldehyde. Shulgin labels the 4-ethoxy-3-methoxybenzaldehyde as ethylvanillin, although ethylvanillin is in fact 3-ethoxy-4-hydroxybenzaldehyde. Ethylvanillin can be methylate to 4-ethoxy-3-methoxybenzladehyde. The 4-ethoxy-3-methoxybenzaldehyde is then subjected to a Bayer-Villiger oxidation with peracetic acid and acetic acid to yield 4-ethoxy-3-methoxyphenol. The 4-ethoxy-3-methoxyphenol is methylated to yield 2,4-dimethoxy-1-ethoxybenzene. The 2,4-dimethoxy-1-ethoxybenzene is subjected to Reimer-Tiemann formylated to 2,4-dimethoxy-5-ethoxybenzaldehyde. The 2,4-dimethoxy-5-ethoxybenzaldehyde by subjecting it to a Knoevenagel condensation with acetic acid, ammonium acetate and nitroethane, and reducing the resulting 1-(2,4-dimethoxy-5-ethoxyphenyl)-2-nitropropene to MME with lithium aluminium hydride under an inert atmosphere.

References

References

1. {{CitePiHKAL [http://www.erowid.org/library/books_online/pihkal/pihkal136.shtml MME entry]
2. (November 2013). "Animal models of the serotonin syndrome: a systematic review". Behavioural Brain Research.
3. (July 2024). "ProTox 3.0: a webserver for the prediction of toxicity of chemicals". Nucleic Acids Research.
4. (February 2010). "Psychedelics and the human receptorome". PLOS ONE.