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Authordc.contributor.authorAraya Maturana, Ramiro 
Authordc.contributor.authorDelgado Castro, Tomás es_CL
Authordc.contributor.authorGárate, Mario es_CL
Authordc.contributor.authorFerreira Parker, Jorge es_CL
Authordc.contributor.authorPavani, Mario es_CL
Authordc.contributor.authorPessoa Mahana, Hernán es_CL
Authordc.contributor.authorCassels Niven, Brucees_CL
Admission datedc.date.accessioned2012-05-18T19:22:19Z
Available datedc.date.available2012-05-18T19:22:19Z
Publication datedc.date.issued2002-01-29
Cita de ítemdc.identifier.citationBioorganic & Medicinal Chemistry, 10: 3057–3060, 2002.es_CL
Identifierdc.identifier.issn3057–3060
Identifierdc.identifier.urihttps://repositorio.uchile.cl/handle/2250/119405
Abstractdc.description.abstractAbstract—A set of structurally related compounds incorporating a carbonyl group in the ortho position withregard to a phenol function were tested against the TA3 mouse carcinoma cell line and its multidrug-resistant variant TA3-MTX-R. The series consists of 20-hydroxyacetophenone, 40-hydroxyacetophenone 20,50-dihydroxyacetophenone, 4-acetyl-3,3-dimethyl-5-hydroxy-2-morpholino- 2,3-dihydrobenzobfuran, five 4,4-dimethyl-5,8-dioxygenated naphtalene-1-ones and three 4,4-dimethyl-5,8-dioxygenated tetralones. A tentative structure–activity relationship was found for this family of substances, suggesting that a coplanar ortho-carbonyl- 1,4-hydroquinone motif is able to cause inhibition of cellular respiration.es_CL
Patrocinadordc.description.sponsorshipThis work was supported by FONDECYT Grants No. 1950301, 1981066 and 1000859. We also acknowledge financial support by the Faculty of Chemical and Pharmaceutical Sciences, University of Chile, Grant P99–1. T.D.-C. thanks CONICYT for a fellowship.es_CL
Lenguagedc.language.isoenes_CL
Publisherdc.publisherElsevier Science Ltd.es_CL
Títulodc.titleEffects of 4,4-Dimethyl-5,8-dihydroxynaphtalene-1-one and 4,4-Dimethyl-5,8-dihydroxytetralone Derivatives onTumor Cell Respirationes_CL
Document typedc.typeArtículo de revista


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