Cargando…
Synthesis of montbretin A analogues yields potent competitive inhibitors of human pancreatic α-amylase
Simplified analogues of the potent human amylase inhibitor montbretin A were synthesised and shown to bind tightly, K(I) = 60 and 70 nM, with improved specificity over medically relevant glycosidases, making them promising candidates for controlling blood glucose. Crystallographic analysis confirmed...
Autores principales: | Tysoe, Christina R., Caner, Sami, Calvert, Matthew B., Win-Mason, Anna, Brayer, Gary D., Withers, Stephen G. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Royal Society of Chemistry
2019
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7069248/ https://www.ncbi.nlm.nih.gov/pubmed/32206255 http://dx.doi.org/10.1039/c9sc02610j |
Ejemplares similares
-
Potent Human α-Amylase Inhibition by
the β-Defensin-like Protein Helianthamide
por: Tysoe, Christina, et al.
Publicado: (2016) -
Folding Then Binding vs Folding Through Binding in
Macrocyclic Peptide Inhibitors of Human Pancreatic α-Amylase
por: Goldbach, Leander, et al.
Publicado: (2019) -
4-Coumaroyl-CoA ligases in the biosynthesis of the anti-diabetic metabolite montbretin A
por: Sunstrum, Frederick G., et al.
Publicado: (2021) -
Biosynthesis of the anti‐diabetic metabolite montbretin A: glucosylation of the central intermediate mini‐MbA
por: Irmisch, Sandra, et al.
Publicado: (2019) -
Substituted Benzimidazole Analogues as Potential α-Amylase
Inhibitors and Radical Scavengers
por: Akande, Akinsola Adegboye, et al.
Publicado: (2021)