Cargando…
A Paal–Knorr agent for chemoproteomic profiling of targets of isoketals in cells
Natural systems produce various γ-dicarbonyl-bearing compounds that can covalently modify lysine in protein targets via the classic Paal–Knorr reaction. Among them is a unique class of lipid-derived electrophiles – isoketals that exhibit high chemical reactivity and critical biological functions. Ho...
Autores principales: | Wang, Min-Ran, He, Jing-Yang, He, Ji-Xiang, Liu, Ke-Ke, Yang, Jing |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8580055/ https://www.ncbi.nlm.nih.gov/pubmed/34881007 http://dx.doi.org/10.1039/d1sc02230j |
Ejemplares similares
-
A fluorescent target-guided Paal–Knorr reaction
por: Wagh, Sachin B., et al.
Publicado: (2020) -
Polystyrenesulfonate-catalyzed synthesis of novel pyrroles through Paal-Knorr reaction
por: Banik, Mandira, et al.
Publicado: (2012) -
Chemoproteomic profiling of itaconations in Salmonella
por: Zhang, Yanling, et al.
Publicado: (2021) -
Iodonium salts as efficient iodine(iii)-based noncovalent organocatalysts for Knorr-type reactions
por: Yunusova, Sevilya N., et al.
Publicado: (2021) -
Total synthesis of diazaquinomycins H and J using double Knorr cyclization in the presence of triisopropylsilane
por: Prior, Allan M., et al.
Publicado: (2019)