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Article 2018-09

Autor: Said, B. Montenegro, I. Valenzuela, M. Olguín, Y. Caro, N. Werner, E. Godoy, P. Villena, J. Madrid, A.

Six new cyclodiprenyl phenols were synthesized by direct coupling of perillyl alcohol and the appropriate phenol. Their structures were established by IR, HRMS and mainly NMR. Three human cancer cell lines-breast (MCF-7), prostate (PC-3) and colon (HT-29)-were used in antiproliferative assays, wi...

Enlace original: http://repositorio.unab.cl/xmlui/handle/ria/11249

Repositorio Universidad Andrés Bello
Enlace permanente

Said, B. ,  Montenegro, I. ,  Valenzuela, M. ,  Olguín, Y. ,  Caro, N. ,  Werner, E. ,  Godoy, P. ,  Villena, J. ,  Madrid, A. ,  [Synthesis and antiproliferative activity of new cyclodiprenyl phenols against select cancer cell lines] ,  Synthesis and antiproliferative activity of new cyclodiprenyl phenols against select cancer cell lines
Article 2017-06

Autor: Escobar, B. Montenegro, I. Villena, J. Werner, E. Godoy, P. Olguín, Y. Madrid, A.

An efficient synthesis of a series of 4-oxyalkyl-isocordoin analogues (2–8) is reported for the first time. Their structures were confirmed by1H-NMR,13C-NMR, and HRMS. Their anti-oomycete activity was evaluated by mycelium and spores inhibition assay against two selected pathogenic oomycetes stra...

Enlace original: http://repositorio.unab.cl/xmlui/handle/ria/4747

Repositorio Universidad Andrés Bello
Enlace permanente

Escobar, B. ,  Montenegro, I. ,  Villena, J. ,  Werner, E. ,  Godoy, P. ,  Olguín, Y. ,  Madrid, A. ,  [Hemi-Synthesis and Anti-Oomycete Activity of Analogues of Isocordoin] ,  Hemi-Synthesis and Anti-Oomycete Activity of Analogues of Isocordoin

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