In vitro metabolic fate of 1-[3-(trimethylsilyl)propanoyl] lysergic acid diethylamide (1S-LSD), a silicon-containing LSD analog.
Forensic Toxicology July 29, 2025 Yuki Azuma, Misa Tanaka, Akiko Asada et al. 1 citation
A new LSD analog, 1S-LSD, which contains a silicon atom, was metabolized in human liver microsomes at a moderately rapid rate, forming LSD early in the process. Sixty-two metabolites were observed, and a metabolic pathway was proposed. The major metabolites had hydroxyl groups on the silicon-containing acyl moiety. Five metabolites that retained this moiety were relatively abundant: N-deethylated 1S-LSD (Si04), N-deethylated and silanolized 1S-LSD (Si06), N-deethylated and monohydroxylated 1S-LSD (Si09 and Si11), and silanolized 1S-LSD (Si21). These five are recommended as target markers for proving 1S-LSD consumption.