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Authordc.contributor.authorGómez Jeria, Juan 
Authordc.contributor.authorCassels Niven, Brucees_CL
Authordc.contributor.authorSaavedra Aguilar, Juan Carlos es_CL
Admission datedc.date.accessioned2012-05-28T15:18:47Z
Available datedc.date.available2012-05-28T15:18:47Z
Publication datedc.date.issued1987-06-05
Cita de ítemdc.identifier.citationEur. J. Med. Chem. 22, 433-437, 1987.es_CL
Identifierdc.identifier.issn0223-5234.
Identifierdc.identifier.urihttps://repositorio.uchile.cl/handle/2250/119424
Abstractdc.description.abstractThe electronic structure of 1-(2,5-dimethoxy-4-nitrophenyl)-2-aminopropane (DON) was calculated at the CND0/2 level, and the racemic compound was synthesized and found to be hallucinogenic at doses of 4 mg. DON differs from its similarly active congeners in that a hydrophilic nitro group replaces lipophilic substituents at C-4 of the benzene ring. The implications for the mechanism of serotonin receptor binding of these drugs are discussed.es_CL
Patrocinadordc.description.sponsorship(DIB Project Q 2442) and from the Chilean National Research Fund (Project 1075). One of us (J.S.G.-J.) thanks Drs. J. Maruani and A. Toro-LabbC for stimulating discussions.es_CL
Lenguagedc.language.isoenes_CL
Publisherdc.publisherElsevier Sciencees_CL
Keywordsdc.subjectCNDOes_CL
Títulodc.titleA quantum-chemical and experimental study of the hallucinogen (k)- 1-(2,5-dimethoxy-4-nitrophenyl)-2-aminopropane (DON)es_CL
Document typedc.typeArtículo de revista


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