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Authordc.contributor.authorGómez Jeria, Juan 
Authordc.contributor.authorCassels Niven, Bruce 
Authordc.contributor.authorSaavedra Aguilar, Juan Carlos 
Admission datedc.date.accessioned2019-01-29T14:47:56Z
Available datedc.date.available2019-01-29T14:47:56Z
Publication datedc.date.issued1987
Cita de ítemdc.identifier.citationEuropean Journal of Medicinal Chemistry, Volumen 22, Issue 5, 2018, Pages 433-437
Identifierdc.identifier.issn17683254
Identifierdc.identifier.issn02235234
Identifierdc.identifier.other10.1016/0223-5234(87)90032-8
Identifierdc.identifier.urihttps://repositorio.uchile.cl/handle/2250/160667
Abstractdc.description.abstractThe electronic structure of 1-(2,5-dimethoxy-4-nitrophenyl)-2-aminopropane (DON) was calculated at the CNDO/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. © 1987.
Lenguagedc.language.isoen
Type of licensedc.rightsAttribution-NonCommercial-NoDerivs 3.0 Chile
Link to Licensedc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/3.0/cl/
Sourcedc.sourceEuropean Journal of Medicinal Chemistry
Keywordsdc.subjectatomic charge
Keywordsdc.subjectCNDO/2
Keywordsdc.subjectDON
Keywordsdc.subjectelectrophilic superdelocalizability
Keywordsdc.subjectfrontier molecular orbitals
Keywordsdc.subjecthallucinogenic potency
Keywordsdc.subjectlipophilicity
Keywordsdc.subjectserotonin receptor affinity
Títulodc.titleA quantum-chemical and experimental study of the hallucinogen (±)-1-(2,5-dimethoxy-4-nitrophenyl)-2-aminopropane (DON)
Document typedc.typeArtículo de revista
Catalogueruchile.catalogadorSCOPUS
Indexationuchile.indexArtículo de publicación SCOPUS
uchile.cosechauchile.cosechaSI


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Except where otherwise noted, this item's license is described as Attribution-NonCommercial-NoDerivs 3.0 Chile