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Authordc.contributor.authorPessoa Mahana, Hernán es_CL
Authordc.contributor.authorRecabarren Gajardo, Gonzalo Iván es_CL
Authordc.contributor.authorAraya Maturana, Ramiro es_CL
Authordc.contributor.authorKosche Cárcamo, Johann Albert 
Authordc.contributor.authorPessoa, D. es_CL
Admission datedc.date.accessioned2010-06-01T19:51:37Z
Available datedc.date.available2010-06-01T19:51:37Z
Publication datedc.date.issued2004-07
Cita de ítemdc.identifier.citationSYNTHETIC COMMUNICATIONS 34(14): 2513-2521en_US
Identifierdc.identifier.issn0039-7911
Identifierdc.identifier.urihttps://repositorio.uchile.cl/handle/2250/120948
Abstractdc.description.abstractWe report here the synthesis of substituted 4-chloro-N-[3-oxo-3-(4-aryl-1-piperazinyl)-propyl] benzamides (5-9), as potential new antidepressants, incorporating in a single molecule structural moieties related to a dual pharmacological profile: MAO-A inhibitor and 5-HT1A receptor affinity.en_US
Lenguagedc.language.isoenen_US
Publisherdc.publisherMARCEL DEKKER INCen_US
Keywordsdc.subjectArylpiperazineen_US
Títulodc.titleSynthesis of 4-arylpiperazine derivatives of moclobemide: Potential antidepressants with a dual mode of actionen_US
Document typedc.typeArtículo de revista


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