SYNTHESIS OF GERANYLHYDROQUINONE DERIVATIVES WITH POTENCIAL CYTOTOXIC ACTIVITY
dc.contributor.author | Baeza, Evelyn | |
dc.contributor.author | Catalan, karen | |
dc.contributor.author | Peña-Cortes, Hugo | |
dc.contributor.author | Espinoza, Luis | |
dc.date.accessioned | 2014-01-29T13:58:09Z | |
dc.date.accessioned | 2016-05-24T20:28:34Z | |
dc.date.available | 2014-01-29T13:58:09Z | |
dc.date.available | 2016-05-24T20:28:34Z | |
dc.date.issued | 2012 | |
dc.description | Indexación: Web of Science; Scielo | es |
dc.description.abstract | Natural geranylhydroquinone 1 and geranyl-p-methoxyphenol 2 were prepared by Electrophilic Aromatic Substitution (EAS) reactions between geraniol and 1,4-hydroquinone or p-methoxyphenol respectively, using BF3∙Et2O as a catalyst. Furthermore, natural geranylquinone 3, geranyl-1,4-dimethoxyquinone 4 and the new geranyl-4-methoxyphenyl acetate 5 were obtained by chemical transformations of 1 and 2. The compounds were evaluated for their in vitro cytotoxicity activities against cultured human cancer cells of PC-3 human prostate cancer, MCF-7 and MDA-MB-231 breast carcinoma, and Dermal Human Fibroblasts DHF. IC50 values were in the µM range. | es |
dc.description.uri | http://ref.scielo.org/zfnxqf | |
dc.identifier.citation | Quím. Nova vol.35 no.3 São Paulo 2012 | es |
dc.identifier.issn | 0100-4042 | |
dc.identifier.other | DOI: http://dx.doi.org/10.1590/S0100-40422012000300015 | |
dc.identifier.uri | http://repositorio.unab.cl/xmlui/handle/ria/2348 | |
dc.language.iso | english | es |
dc.publisher | Sociedade Brasileira de Química | es |
dc.subject | Natural geranylhydroquinone | es |
dc.subject | Electrophilic Aromatic Substitution | es |
dc.subject | hydroquinone or p-methoxypheno | es |
dc.subject | SYNTHESIS | es |
dc.subject | Cytotoxic activity | es |
dc.title | SYNTHESIS OF GERANYLHYDROQUINONE DERIVATIVES WITH POTENCIAL CYTOTOXIC ACTIVITY | es |
dc.type | Artículo | es |
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