Chemical Reactivity Parameters to Analyze Psychedelics: How Do We Explain the Potency of the Drugs?

ACS Omega

Departamento de Materiales de Baja Dimensionalidad, Instituto de Investigaciones en Materiales, Universidad Nacional Autónoma de México, Circuito Exterior S. N. Ciudad Universitaria, CDMX, Mexico CP 04510, Mexico.

Published: September 2024

AI Article Synopsis

  • Psychedelics are substances that alter thoughts, feelings, and perceptions, with lysergic acid diethylamide (LSD) being the most powerful and the first semi-synthetic hallucinogen.
  • They are being researched for their potential therapeutic benefits in treating neuropsychiatric disorders and helping with addictions.
  • The analysis of 27 serotonergic psychedelic molecules reveals that their potency is linked to their ability to accept electrons and their global softness, enhancing our understanding of how these drugs work.

Article Abstract

Psychedelics are psychoactive substances that produce changes in thoughts and feelings and modifications in perceptions of reality. The most potent psychedelic is also the first semisynthetic hallucinogen (lysergic acid diethylamide). Psychedelics have been investigated for decades because of their potential therapeutic effects in the treatment of neuropsychiatric diseases and also because these drugs are useful in controlling addictions to other substances. In this investigation, we analyze 27 psychedelic molecules. These compounds are serotonergic psychedelics; that is, they are serotonin agonists. We analyze the electron transfer properties to better understand the mechanism of action of these substances. We found that the electron acceptance capacity is related to the potency of the drugs: the best electron acceptor is also the most potent drug. We also used global softness as a parameter of reactivity. Molecules with greater global softness are more polarizable and also have greater potency. These results are useful to continue our understanding of the mechanism of action of psychotropic drugs.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11425621PMC
http://dx.doi.org/10.1021/acsomega.4c05726DOI Listing

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