Cargando…
Synthesis and in-vitro Evaluation of S-allyl Cysteine Ester - Caffeic Acid Amide Hybrids as Potential Anticancer Agents
We have synthesized a series of S-allyl cysteine ester-caffeic acid amide hybrids and evaluated them in order to determine their possible anticancer activity and selectivity in colorectal cancer, which is still one of the leading causes of morbidity and mortality worldwide. All compounds were tested...
Autores principales: | Castrillón, Wilson, Herrera-R, Angie, Prieto, Laura Juliana, Conesa-Milián, Laura, Carda, Miguel, Naranjo, Tonny, Maldonado, Maria Elena, Cardona-G, Wilson |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Shaheed Beheshti University of Medical Sciences
2019
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7059070/ https://www.ncbi.nlm.nih.gov/pubmed/32184845 http://dx.doi.org/10.22037/ijpr.2019.15184.12921 |
Ejemplares similares
-
Clicked Cinnamic/Caffeic Esters and Amides as Radical Scavengers and 5-Lipoxygenase Inhibitors
por: Doiron, Jérémie A., et al.
Publicado: (2014) -
Resveratrol/Hydrazone Hybrids: Synthesis and Chemopreventive Activity against Colorectal Cancer Cells
por: Castrillón-López, Wilson, et al.
Publicado: (2022) -
Synthesis, Evaluation of Anticancer Activity and QSAR Study of Heterocyclic Esters of Caffeic Acid
por: Hajmohamad Ebrahim Ketabforoosh, Shima, et al.
Publicado: (2013) -
Molecular Characterization and Enhancement of Anticancer Activity of Caffeic Acid Phenethyl Ester by γ Cyclodextrin
por: Wadhwa, Renu, et al.
Publicado: (2016) -
Caffeic Acid Phenethyl Ester and Its Amide Analogue Are Potent Inhibitors of Leukotriene Biosynthesis in Human Polymorphonuclear Leukocytes
por: Boudreau, Luc H., et al.
Publicado: (2012)