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Authordc.contributor.authorPessoa Mahana, Hernán es_CL
Authordc.contributor.authorGonzález Lira, Christian Guillermo es_CL
Authordc.contributor.authorAraya Maturana, Ramiro es_CL
Authordc.contributor.authorSaitz Barría, Claudio 
Authordc.contributor.authorPessoa, D. es_CL
Admission datedc.date.accessioned2009-08-25T16:58:24Z
Available datedc.date.available2009-08-25T16:58:24Z
Publication datedc.date.issued2009-06
Cita de ítemdc.identifier.citationJOURNAL OF THE CHILEAN CHEMICAL SOCIETY 54(2): 147-150en
Identifierdc.identifier.issn0717-9324
Identifierdc.identifier.urihttps://repositorio.uchile.cl/handle/2250/120779
Abstractdc.description.abstractNew benzothiophene arylpiperazine derivatives 7 (a-1) were synthesized as potential serotoninergic agents with 5-HT1A receptor affinity. Preparation of the derivatives was performed by reaction of 1-(4-aminophenyl)-4-[(4,7-dimethoxy-1-benzothien-2-yl)carbonyl] piperazine (6) with a series of substituted aroyl chlorides.en
Lenguagedc.language.isoenen
Publisherdc.publisherSOC CHILENA QUIMICAen
Keywordsdc.subjectSecotonineen
Títulodc.titleSynthesis of conformationally restricted N-{4-[4-(4,7-Dimethoxy-Benzo[b]Thiophene-2-Carbonyl)-1-Piperazinyl]-Phenyl}-Arylcarboxamides potential ligands with 5-HT1A binding affinityen
Document typedc.typeArtículo de revista


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