Cargando…
Ring Expansion Leads to a More Potent Analogue of Ipomoeassin F
[Image: see text] Two new ring-size-varying analogues (2 and 3) of ipomoeassin F were synthesized and evaluated. Improved cytotoxicity (IC(50): from 1.8 nM) and in vitro protein translocation inhibition (IC(50): 35 nM) derived from ring expansion imply that the binding pocket of Sec61α (isoform 1) c...
Autores principales: | Zong, Guanghui, Hu, Zhijian, Duah, Kwabena Baffour, Andrews, Lauren E., Zhou, Jianhong, O’Keefe, Sarah, Whisenhunt, Lucas, Shim, Joong Sup, Du, Yuchun, High, Stephen, Shi, Wei Q. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical
Society
2020
|
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7808706/ https://www.ncbi.nlm.nih.gov/pubmed/33264019 http://dx.doi.org/10.1021/acs.joc.0c01659 |
Ejemplares similares
-
Synthesis, Biological Evaluation and Docking Studies of Ring-Opened Analogues of Ipomoeassin F
por: O’Keefe, Sarah, et al.
Publicado: (2022) -
Ipomoeassin-F disrupts multiple aspects of secretory protein biogenesis
por: Roboti, Peristera, et al.
Publicado: (2021) -
Ipomoeassin-F inhibits the in vitro biogenesis of the SARS-CoV-2 spike protein and its host cell membrane receptor
por: O’Keefe, Sarah, et al.
Publicado: (2021) -
Ipomoeassin-F inhibits the in vitro biogenesis of the SARS-CoV-2 spike protein and its host cell membrane receptor
por: O'Keefe, Sarah, et al.
Publicado: (2021) -
Ipomoeassin
F Binds Sec61α to Inhibit Protein
Translocation
por: Zong, Guanghui, et al.
Publicado: (2019)