1T-LSD
1T-LSD
1T-LSD is a psychedelic compound that is structurally related to lysergic acid diethylamide (LSD). It is part of a class of substances known as lysergamides, which are derivatives of lysergic acid. 1T-LSD is known for its psychoactive effects, which are similar to those of LSD, but it is distinguished by the presence of a thiophene ring in its chemical structure.
Chemical Structure
1T-LSD is chemically known as 1-thiophene-N,N-diethyllysergamide. The presence of the thiophene ring is a key differentiator from LSD, which contains an indole ring. This modification is believed to alter the compound's interaction with serotonin receptors in the brain, potentially leading to differences in its psychoactive effects.
Pharmacology
1T-LSD acts primarily as a partial agonist at the 5-HT2A receptor, which is the main target for classical psychedelics. The interaction with this receptor is responsible for the hallucinogenic effects experienced by users. Like other lysergamides, 1T-LSD may also interact with other serotonin receptor subtypes, contributing to its complex effects on perception, mood, and cognition.
Effects
The effects of 1T-LSD are similar to those of LSD, including altered sensory perception, changes in mood, and cognitive shifts. Users may experience visual hallucinations, a sense of euphoria, and altered time perception. The onset of effects typically occurs within 30 to 60 minutes after ingestion, with a duration of action lasting 6 to 12 hours.
Legal Status
The legal status of 1T-LSD varies by country. In some jurisdictions, it may be classified as a controlled substance due to its structural similarity to LSD and its psychoactive properties. In others, it may not be specifically scheduled, although it could still be subject to analogue laws that regulate substances similar to controlled drugs.
Related Compounds
1T-LSD is part of a broader class of lysergamides, which includes other compounds such as 1P-LSD, ALD-52, and ETH-LAD. These compounds share a common lysergic acid backbone but differ in their substituents, leading to variations in their pharmacological profiles and effects.
See Also
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Contributors: Prab R. Tumpati, MD