Sebastián Andrés Fuentes Retamal
Investigador Postdoctoral
Universidad de Chile
Santiago, Chile
metabolismo del cáncer, terapias dirigidas hacia la mitocondria, plasticidad mitocondrial
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Farmacología, UNIVERSIDAD DE CHILE. Chile, 2020
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Químico farmacéutico, UNIVERSIDAD DE CHILE. Chile, 2015
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Docente Part Time
UNIVERSIDAD DIEGO PORTALES
Facultad de Salud y odontología
Santiago, Chile
2017 - 2017
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Docente Part Time
UNIVERSIDAD ANDRES BELLO
Facultad de Medicina
Santiago, Chile
2018 - At present
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Docente Part Time
UNIVERSIDAD DE CHILE
Facultad de Medicina
Santiago, Chile
2018 - 2019
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Docente Part Time
UNIVERSIDAD DE CHILE
Facultad de Ciencias veterinarias y pecuarias
Santiago, Chile
2020 - At present
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Docente Part Time
UNIVERSIDAD DE CHILE
Facultad de Medicina
Chile
2021 - At present
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Docente Part Time
Universidad Andrés Bello
Chile
2018 - At present
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Docente Part Time
Universidad de Chile
Chile
2018 - At present
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Docente Part Time
Universidad Diego Portales
Chile
2017 - 2017
Dirección de tesis y seminarios de tílulo
Chapter 1 - Recent advances in molecular mechanisms of anticancer natural products that target mitochondrial bioenergetics |
α-KGDH inhibition prevents triple-negative breast cancer cell migration by mitophagy induction: a potential anti-cancer target. |
Lipophilic cations of esters of alkyltriphenylphosphonium polyhydroxybenzoates as mitochondriotropic antineoplastic agents. Antitumoral activity spectra on human tumour cells from different tissues |
Estudio de mecanismos de acción de cationes lipofílicos deslocalizados derivados de alquil-polihidroxibenzoatos unidos al grupo trifenilfosfonio como antineoplásicos de acción mitocondrial. |
Lipophilic cations of esters of alkyltriphenylphosphonium polyhydroxybenzoates as mitochondriotropic antineoplastic agents. Antitumoral activity spectra on human tumour cells from different tissues. |
Regio- and stereo-selective Diels-Alder reactions in the synthesis of CDC25B fosfatase inhibitors. |
A rational synthetic approach to 3-indolealkyl(aryl)piperazine derivatives as new hetero and homobivalent ligands with potential serotonergic activity. |