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Α-Methylserotonin

chemical compound

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Record originEnglish Wikipedia
Text licenseCC BY-SA 4.0
Source revisionJan 22, 2026
Entity authorityQ4734914
Source-derived summary

α-Methylserotonin (αMS), also known as α-methyl-5-hydroxytryptamine (α-methyl-5-HT) or as 5-hydroxy-α-methyltryptamine (5-HO-αMT), is a tryptamine derivative closely related to the neurotransmitter serotonin (5-HT). It acts as a non-selective serotonin receptor agonist and has been used extensively in scientific research to study the function of the serotonin system.

Use and effects

According to Alexander Shulgin in his book TiHKAL (Tryptamines I Have Known and Loved), αMS is well-studied in preclinical research but has not been tested in humans.

Pharmacology

Pharmacodynamics

αMS is a non-selective and near-full agonist of the serotonin 5-HT2 receptors. It has similar affinity for the 5-HT2A, 5-HT2B, and 5-HT2C receptors. The drug is also a ligand of the serotonin 5-HT1 receptors with high affinity, including of the serotonin 5-HT1A, 5-HT1B, and 5-HT1D receptors (Ki = 40–150 nM), but not of the serotonin 5-HT1E receptor (Ki > 10,000 nM). In addition to its actions at the serotonin receptors, αMS has been found to act as a norepinephrine releasing agent similarly to α-methylphenylalanine and to other α-alkylated tryptamines.

In contrast to DOI, and in spite of its potent serotonin 5-HT2A receptor agonism, αMS did not produce the head-twitch response, a behavioral proxy of psychedelic effects, in rats. However, it was only assessed at a dose of up to 1 mg/kg, which is around the maximally effective dose of DOI.

Pharmacokinetics

Unlike serotonin, αMS is not metabolized by monoamine oxidase on account of the α-methyl substituent blocking the enzyme's access to the amine. Similarly to serotonin however, αMS poorly crosses the blood–brain barrier due to its free hydroxyl group and poor lipophilicity, and thus may have weak or no central effects when administered peripherally.

Editorial summary

This brief starts where responsible research should: with the source description of “Α-Methylserotonin” as chemical compound. Everything that follows is an evidence route, not borrowed authority.

Editorial reviewA practical orientation to terminology and classification, particularly when read beside dated observations, specimens or technical literature. The current 272-word lead offers orientation but no explicit four-digit date, so chronology should not be assumed. The selected authority fields contribute no independent date. The account is most persuasive where Α-Methylserotonin, chemical and compound can be independently traced.
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The subject matters to the science & nature register because the source frames it as chemical compound. Its deeper value depends on whether names, dates, institutions and citations support that framing.

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The date and method of observation matter as much as the stated conclusion, especially where classification or consensus has changed. The source revision retrieved here is dated Jan 22, 2026. The linked authority identifier is Q4734914. None of the 0 selected statements returned an explicit reference.

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Source & attribution

This entry incorporates text from Α-Methylserotonin” on English Wikipedia. Contributors are listed in the page history. Text is available under the Creative Commons Attribution-ShareAlike 4.0 License. Selected authority identifiers and statements are retrieved from Wikidata under CC0; their references and qualifiers remain part of the verification path.