Cargando…
Studies on Synthesis and Structure-Activity Relationship (SAR) of Derivatives of a New Natural Product from Marine Fungi as Inhibitors of Influenza Virus Neuraminidase
Based on the natural isoprenyl phenyl ether from a mangrove-derived fungus, 32 analogues were synthesized and evaluated for inhibitory activity against influenza H1N1 neuraminidase. Compound 15 (3-(allyloxy)-4-hydroxybenzaldehyde) exhibited the most potent inhibitory activity, with IC(50) values of...
Autores principales: | Li, Jing, Zhang, Dingmei, Zhu, Xun, He, Zhenjian, Liu, Shu, Li, Mengfeng, Pang, Jiyan, Lin, Yongcheng |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Molecular Diversity Preservation International
2011
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3210610/ https://www.ncbi.nlm.nih.gov/pubmed/22073001 http://dx.doi.org/10.3390/md9101887 |
Ejemplares similares
-
Studies on the Synthesis of Derivatives of Marine-Derived Bostrycin and Their Structure-Activity Relationship against Tumor Cells
por: Chen, Hong, et al.
Publicado: (2012) -
Consecutive influenza surveillance of neuraminidase mutations and neuraminidase inhibitor resistance in Japan
por: Chong, Yong, et al.
Publicado: (2019) -
Design and synthesis of constrained bicyclic molecules as candidate inhibitors of influenza A neuraminidase
por: Colombo, Cinzia, et al.
Publicado: (2018) -
Influenza neuraminidase
por: Air, Gillian M.
Publicado: (2011) -
Systematic review of influenza resistance to the neuraminidase inhibitors
por: Thorlund, Kristian, et al.
Publicado: (2011)