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	<id>https://wikimd.org/index.php?action=history&amp;feed=atom&amp;title=5-MeS-DMT</id>
	<title>5-MeS-DMT - Revision history</title>
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	<updated>2026-04-27T05:41:10Z</updated>
	<subtitle>Revision history for this page on the wiki</subtitle>
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	<entry>
		<id>https://wikimd.org/index.php?title=5-MeS-DMT&amp;diff=5625516&amp;oldid=prev</id>
		<title>Prab: CSV import</title>
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		<updated>2024-04-18T18:27:09Z</updated>

		<summary type="html">&lt;p&gt;CSV import&lt;/p&gt;
&lt;p&gt;&lt;b&gt;New page&lt;/b&gt;&lt;/p&gt;&lt;div&gt;[[File:5-MeS-DMT.svg|5-MeS-DMT|thumb]]  &amp;#039;&amp;#039;&amp;#039;5-MeS-DMT&amp;#039;&amp;#039;&amp;#039; (&amp;#039;&amp;#039;&amp;#039;5-Methoxy-N,N-dimethyltryptamine&amp;#039;&amp;#039;&amp;#039;) is a [[psychedelic]] compound of the [[tryptamine]] class. It is a structural analog of [[DMT]] (N,N-Dimethyltryptamine) and [[5-MeO-DMT]] (5-Methoxy-N,N-Dimethyltryptamine), differing by the addition of a [[methyl]] group at the 5-position on the indole ring. This modification leads to a distinct pharmacological profile, affecting its potency, duration, and subjective effects when compared to its more widely studied relatives.&lt;br /&gt;
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==Chemistry==&lt;br /&gt;
5-MeS-DMT belongs to the tryptamine family, which is a group of [[alkaloid]]s commonly found in plants, fungi, and animals. These compounds share a core structure derived from the amino acid [[tryptophan]]. The chemical name for 5-MeS-DMT is 5-Methoxy-N,N-dimethyltryptamine, indicating the presence of a methoxy group (-OCH3) attached to the fifth carbon of the indole ring, in addition to two methyl groups attached to the nitrogen atom of the tryptamine backbone.&lt;br /&gt;
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==Pharmacology==&lt;br /&gt;
The pharmacological action of 5-MeS-DMT, like other psychedelics in its class, is primarily through agonism of the [[serotonin]] 5-HT2A receptor. This interaction is believed to be responsible for its psychedelic effects. However, the presence of the methoxy group at the 5-position can significantly influence its affinity and efficacy at this and other serotonin receptors, potentially leading to differences in psychoactive effects compared to DMT and 5-MeO-DMT.&lt;br /&gt;
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==Effects==&lt;br /&gt;
The subjective effects of 5-MeS-DMT are less documented than those of DMT or 5-MeO-DMT, due in part to its relative obscurity and limited availability. Anecdotal reports suggest that it produces a range of psychedelic experiences, including alterations in visual perception, sense of time, and emotional states. The intensity and duration of these effects can vary based on the dose, method of administration, and individual sensitivity.&lt;br /&gt;
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==Legal Status==&lt;br /&gt;
The legal status of 5-MeS-DMT varies by country, reflecting broader regulatory trends concerning psychedelic substances. In many jurisdictions, it may fall under analog acts or controlled substance laws that cover DMT and similar compounds. Potential users and researchers should consult their local regulations to understand the legal implications of possessing, using, or distributing 5-MeS-DMT.&lt;br /&gt;
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==Research==&lt;br /&gt;
Research on 5-MeS-DMT is limited, with most studies focusing on more common tryptamines like DMT and 5-MeO-DMT. The unique properties of 5-MeS-DMT, however, offer a valuable area for future investigation, particularly in understanding the role of methoxy substitution on the psychedelic experience and therapeutic potential.&lt;br /&gt;
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[[Category:Psychedelic drugs]]&lt;br /&gt;
[[Category:Tryptamines]]&lt;br /&gt;
{{Chemistry-stub}}&lt;/div&gt;</summary>
		<author><name>Prab</name></author>
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