scholarly journals Dictyostelium discoideum as a pharmacological model system to study the mechanisms of medicinal drugs and natural products

2019 ◽  
Vol 63 (8-9-10) ◽  
pp. 541-550 ◽  
Author(s):  
Judith Schaf ◽  
Joseph Damstra-Oddy ◽  
Robin S.B. Williams

Developing novel compounds for the treatment of diseases remains one of the highest priorities in biomedical research, where it is critical to identify their targets and how they work at a cellular level. Most studies in this area employ mammalian models, since rodents or non-human primates are seen as a good approximation for humans. However, using mammalian models can be problematic for a range of reasons, including high genetic redundancy and the essential role for many proteins in development. More importantly, it is very difficult to identify how compounds function at a cellular or molecular level in these models without a previously suggested mechanism or target. So how can we identify targets of medicinal compounds? In this review we outline the use of an innovative and tractable model system, Dictyostelium discoideum, to provide useful insight to the cellular and molecular functions of both therapeutic drugs and pharmacologically active natural products. We outline the advantages of using this model, and then provide a range of exemplar studies using D. discoideum in pharmacological research to demonstrate breakthroughs in understanding the action and effects of compounds, and the subsequent translational of these advances to mammalian models leading to potential improvements in societal health.

Biomolecules ◽  
2021 ◽  
Vol 11 (5) ◽  
pp. 630
Author(s):  
José L. Medina-Franco

Natural products continue to be a significant source of active compounds [...]


2012 ◽  
Vol 66 (4) ◽  
pp. 229-232 ◽  
Author(s):  
Soura Challal ◽  
Nadine Bohni ◽  
Olivia E. Buenafe ◽  
Camila V. Esguerra ◽  
Peter A. M. de Witte ◽  
...  

Synthesis ◽  
2021 ◽  
Author(s):  
Francisco Javier Fuentes-Pantoja ◽  
Alejandro Cordero-Vargas

α,β-Unsaturated δ-lactones are structural motifs found in diverse pharmacologically active natural products. In fact, the unsaturated lactone is often responsible for the biological activity. Herein, we report a new approach for the syntheses of (R)-argentilactone and (R)-goniothalamin based on a photoredox intermolecular iodolactonization mediated by a photoredox process. This new approach, already employed in our research group, stands as a new methodology to achieve several natural products containing α,β-unsaturated δ-lactones.


2020 ◽  
Vol 25 (1) ◽  
pp. 27-37
Author(s):  
Axhell A. Cornejo-Báez ◽  
Luis M. Peña-Rodríguez ◽  
Radamés Álvarez-Zapata ◽  
Maribel Vázquez-Hernández ◽  
Alberto Sánchez-Medina

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