The Theoretical Synthesis and in silico Modelling of Lysergic Acid Biscinnamylidene Amide from the Adduct Formation of d-Lysergic Acid Amide and Cinnamaldehyde

Authors

  • Victor Chiruta School of Health Sciences, University of South Australia, 101 Currie St, Adelaide, SA 5001, AU; Independent Food & Therapeutic Authority, M/134 Great Western Hwy, Blaxland, NSW 2774, AU; Mind Medicine Australia, 1/10 Dorcas St, South Melbourne, VIC 3205, AU

DOI:

https://doi.org/10.32996/jcs.2022.1.1.1

Keywords:

cinnamylidene-bislysergamide, cinnamylidene-bislysergic acid amide, CBLSA, LSC, LSBC, adduct, LSA, LSH, d-lysergic acid amide

Abstract

Here is a theoretical synthesis for a cinnamaldehyde adduct formation of a hypothetically proposed lysergamide derivative named cinnamylidene-bislysergamide or lysergic acid biscinnamylidene amide (LSBC). This lysergamide name and abbreviation is in keeping with names of other lysergamide derivatives, such as d-lysergic acid amine (LSA), lysergic acid 2-butyl amide (LSB), lysergic acid diethylamide (LSD), d-lysergic acid α-hydroxyethylamide (LSH), lysergic acid methylisopropylamide (LSMIP), and lysergic acid 3-pentyl amide (LSP). Lysergamides are generally psychedelic in nature. The evidence for LSBC adduct formation is plausible, but the evidence supporting its psychedelic effects is weak.

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Published

2022-03-05

Issue

Section

Research Article

How to Cite

Chiruta, V. (2022). The Theoretical Synthesis and in silico Modelling of Lysergic Acid Biscinnamylidene Amide from the Adduct Formation of d-Lysergic Acid Amide and Cinnamaldehyde. Journal of Chemistry Studies, 1(1), 01-06. https://doi.org/10.32996/jcs.2022.1.1.1