Show simple item record

Authordc.contributor.authorGómez Jeria, Juan 
Authordc.contributor.authorMorales Lagos, D. es_CL
Authordc.contributor.authorRodríguez Gatica, J. I. es_CL
Admission datedc.date.accessioned2011-10-26T15:17:07Z
Available datedc.date.available2011-10-26T15:17:07Z
Publication datedc.date.issued1984-04-05
Cita de ítemdc.identifier.citationActa sud Americana de Química, Vol. 4, 1984.es_CL
Identifierdc.identifier.issn0716 - 0402
Identifierdc.identifier.urihttps://repositorio.uchile.cl/handle/2250/119339
Abstractdc.description.abstractThe molecular electrostatic potential maps of five protonated phenylethylamines have been calculated and compared with that of protonated serotonin. Protonation leads to a very similar potential área around the amine chain in all the molecules suggesting that this región may serve for the orientation and / or the interaction with the serotonergic receptor. It was not possible to obtain a qualitative relation between hallucinogenic potency and electrostatic potential valúes.es_CL
Patrocinadordc.description.sponsorshipThis work has received financial support from the Departamento de Desarrollo de la Investigación, Universidad de Chile, Project Q2001-8412.es_CL
Lenguagedc.language.isoenes_CL
Publisherdc.publisherEditorial Codelia, Publicaciones Científicases_CL
Títulodc.titleAPPROXEMATE MOLECULAR ELECTROSTATIC POTENTIALS OF PROTONATED MESCALINE ANALOGUESes_CL
Document typedc.typeArtículo de revista


Files in this item

Icon

This item appears in the following Collection(s)

Show simple item record