Cargando…
Structure-Based Design, Synthesis and Bioactivity of a New Anti-TNFα Cyclopeptide
As opposed to small molecules, macrocyclic peptides possess a large surface area and are recognised as promising candidates to selectively treat diseases by disrupting specific protein–protein interactions (PPIs). Due to the difficulty in predicting cyclopeptide conformations in solution, the de nov...
Autores principales: | Idress, Mohannad, Milne, Bruce F., Thompson, Gary S., Trembleau, Laurent, Jaspars, Marcel, Houssen, Wael E. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7071015/ https://www.ncbi.nlm.nih.gov/pubmed/32093030 http://dx.doi.org/10.3390/molecules25040922 |
Ejemplares similares
-
Synthesis of Hybrid Cyclopeptides through Enzymatic Macrocyclization
por: Oueis, Emilia, et al.
Publicado: (2016) -
Recent Developments on the Synthesis and Bioactivity of Ilamycins/Rufomycins and Cyclomarins, Marine Cyclopeptides That Demonstrate Anti-Malaria and Anti-Tuberculosis Activity
por: Kazmaier, Uli, et al.
Publicado: (2021) -
Structural and bioactive studies of terpenes and cyclopeptides from the Genus Rubia
por: Xu, Kuo, et al.
Publicado: (2013) -
Synthesis of novel cyclopeptides containing heterocyclic skeletons
por: Hamdan, Fatima, et al.
Publicado: (2018) -
A Blind Test of Computational Technique for Predicting
the Likelihood of Peptide Sequences to Cyclize
por: Booth, Jonathan, et al.
Publicado: (2017)