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Psychedelic drugs: steric factors that predict psychotropic activity.

S H Snyder, E Richelson

Proc Natl Acad Sci U S A May 1, 1968 DOI: 10.1073/pnas.60.1.206 via PubMed Central

Summary

The article examines how the three-dimensional shapes of psychedelic molecules—their steric factors—influence their ability to produce psychotropic effects. By analyzing molecular structures, the authors identify specific spatial arrangements that correlate with psychoactive potency. The findings suggest that steric hindrance and molecular geometry play crucial roles in determining whether a compound will induce altered states of consciousness. This structural understanding may guide the design of new psychedelic compounds with predictable effects.

Study at a glance

Characteristics Theoretical or philosophical paper Peer reviewed
Citations 51
Key finding Steric factors, including molecular geometry and steric hindrance, predict the psychotropic activity of psychedelic drugs.

Abstract

Proceedings of the National Academy of Sciences (PNAS), a peer reviewed journal of the National Academy of Sciences (NAS) - an authoritative source of high-impact, original research that broadly spans the biological, physical, and social sciences.

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