5-MeO-DBT


5-MeO-DBT, also known as 5-methoxy-N,''N-dibutyltryptamine, is a serotonin receptor modulator, and a rare substituted tryptamine derivative, which is thought to be a psychoactive substance.
Unlike many other related compounds it exhibits very low efficacy for the 5-HT2A receptor.
5-MeO-DBT was first described in the literature by Alexander Shulgin in his 1997 book
TiHKAL''. It was encountered as a novel designer drug by 2019 and was assessed pharmacologically in 2023. The drug is controlled under drug analogue legislation in a number of jurisdictions.

Use and effects

In his book TiHKAL, Alexander Shulgin briefly mentioned 5-MeO-DBT and described it as a known compound with unknown activity. Relatedly, the properties and effects of 5-MeO-DBT are unknown. In any case, related drugs like dibutyltryptamine and 4-HO-DPT have been reported to yield disappointing effects.

Interactions

Pharmacology

Pharmacodynamics

Based on limited evidence, 5-MeO-DBT acts as a non-selective serotonin receptor agonist with the highest potency and efficacy at the 5-HT1A receptor. It has a similar potency to 5-MeO-MiPT for this target. The substance, unlike many other substituted tryptamines, acts as a very weak and low efficacy partial agonist for the 5-HT2A receptor. Among the group of related tryptamine analogues it also displayed the lowest efficacy for the 5-HT2C receptor.
5-MeO-DBT decreased locomotor activity and failed to substitute for the discriminative stimulus effects of DOM in rodent drug discrimination tests.

Chemistry

Analogues

s of 5-MeO-DBT include dibutyltryptamine, 4-HO-DBT, 5-MeO-DMT, 5-MeO-DET, 5-MeO-DPT, 5-MeO-DiPT, 5-MeO-DALT, and 5-MeO-DsBT, among others.

History

5-MeO-DBT was first described in the literature by Alexander Shulgin in his 1997 book TiHKAL. It was encountered as a novel designer drug by 2019.

Society and culture

Legal status

United States

Alabama
5-MeO-DBT was made schedule I at the state level in Alabama on September 13, 2024.