Capillary electrochromatography (CEC) plays a significant role in chiral separation via the double separation principle, partition coefficient difference between the two phases, and electroosmotic flow-driven separation. Given the distinct properties of the inner wall stationary phase (SP), the separation ability of each SP differs from one another. Particularly, it provides large room for promising applications of open tubular capillary electrochromatography (OT-CEC). We divided the OT-CEC SPs developed over the past four years into six types: ionic liquids, nanoparticle materials, microporous materials, biomaterials, non-nanopolymers, and others, to mainly introduce their characteristics in chiral drug separation. There also added a few classic SPs that occurred within ten years as supplements to enrich the features of each SP. Additionally, we discuss their applications in metabolomics, food, cosmetics, environment, and biology as analytes in addition to chiral drugs. OT-CEC plays an increasingly significant role in chiral separation and may promote the development of capillary electrophoresis (CE) combined with other instruments in recent years, such as CE with mass spectrometry (CE/MS) and CE with ultraviolet light detector (CE/UV).
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http://dx.doi.org/10.1016/j.jpha.2023.01.003 | DOI Listing |
QRB Discov
December 2024
Key Laboratory of RNA Innovation, Science and Engineering, Shanghai Institute of Biochemistry and Cell Biology, Center for Excellence in Molecular Cell Science, Chinese Academy of Sciences, China.
The TRiC/CCT complex assists in the folding of approximately 10% of cytosolic proteins through an ATP-driven conformational cycle, playing a crucial role in maintaining protein homeostasis. Despite our understanding of ATP-driven TRiC ring closing and substrate folding, the process and mechanisms underlying TRiC ring-opening and substrate release remain largely unexplored. In this study, by determining an ensemble of cryo-EM structures of yeast TRiC in the presence of ADP, including three intermediate transition states, we present a comprehensive picture of the TRiC ring-opening process.
View Article and Find Full Text PDFFood Chem
March 2025
College of Bioscience and Biotechnology, Hunan Agricultural University, Changsha 410128, PR China. Electronic address:
Strigolactones (SLs) are novel plant hormones that play crucial roles in regulating plant growth and development. The stereoisomers of SLs often exhibit distinct biological activities, making their chiral separation and analysis essential for understanding their regulatory roles in plant branching. This study focused on the chiral separation and characterization of SL stereoisomers, including GR24 (synthetic) and strigol (natural).
View Article and Find Full Text PDFAnal Chem
March 2025
State Key Laboratory of Green Pesticide, College of Chemistry, Central China Normal University, Wuhan 430079, China.
Fungicides have been widely used in agricultural production; however, their extensive use has caused serious environmental pollution. Because of its high efficiency, low toxicity, and high selectivity, chiral fungicides can effectively reduce the amount of fungicides and increase the efficiency. Hence, how to efficiently separate the enantiomers of chiral drugs with different structures is of significant research value.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
March 2025
University of Bristol, School of Chemistry, Cantock's Close, BS8 1TS, Bristol, UNITED KINGDOM OF GREAT BRITAIN AND NORTHERN IRELAND.
Colour vision relies on selective, reversible isomerisation by visible light of a mixture of retinyl chromophores in photoreceptor cells. Synthetic molecular mimics of this wavelength-dependent induction of function are rare, despite the attractiveness of controlling chemical processes solely by the wavelength of incident light. Here, we report a colour-responsive chemical system composed of a cationic receptor complex, two competing chiral anionic ligands and two metastable photoacids with contrasting absorption properties.
View Article and Find Full Text PDFJ Nat Prod
March 2025
School of Medicine, Henan Polytechnic University, Jiaozuo 454000, People's Republic of China.
The first total synthesis of (±)-talaroenamine B was achieved through a concise four-step procedure. The key feature of this synthetic strategy lies in a one-pot reaction involving I (III)-mediated oxidative dearomatization to construct a racemic cyclohexanedione unit, followed by imination using a chiral auxiliary to afford a separable mixture of diastereoisomers. A further acid-catalyzed substitution reaction of aniline with the diastereoisomers led to the natural product (-)-talaroenamine B and its enantiomer (+)-talaroenamine B.
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