ON THE CONFORMATIONS OF HALLUCINOGENIC MOLECULES AND THEIR CORRELATION
AUTOR(ES)
Chothia, Cyrus
RESUMO
There are only a few possible conformations of D-lysergic acid diethylamide and hallucinogenic derivatives of tryptamine and phenylethylamine. Of these possible conformations there is a high structural correlation among the probable conformations of active hallucinogenic molecules and between these conformations and the known conformations of several central nervous system transmitter molecules.
ACESSO AO ARTIGO
http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=223427Documentos Relacionados
- A relationship between the hallucinogenic activity of drugs and their electronic configuration.
- A comparison of the conformations adopted by some 5-bromovinyl-2'-deoxyuridines and a correlation with their antiviral properties: an X-ray study.
- Tracking the motion of chemisorbed molecules on their adsorption sites
- Intramolecular energy transfer in molecules with a large number of conformations
- Mg2+-dependent conformational change of RNA studied by fluorescence correlation and FRET on immobilized single molecules