Research Article

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

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.

Article information

Journal

Journal of Chemistry Studies

Volume (Issue)

1 (1)

Pages

01-06

Published

2022-03-05

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

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Keywords:

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