5 results match your criteria: "King's College London 150 Stamford Street[Affiliation]"
RSC Adv
September 2024
Department of Chemistry, University College London 20 Gordon Street London WC1H 0AJ UK
Biocatalysis offers a sustainable approach to drug synthesis, leveraging the high selectivity and efficiency of enzymes. This review explores the application of biocatalysis in the early-stage synthesis of antimicrobial compounds, emphasizing its advantages over traditional chemical methods. We discuss various biocatalysts, including enzymes and whole-cell systems, and their role in the selective functionalization and preparation of antimicrobials and antibacterial building blocks.
View Article and Find Full Text PDFRSC Chem Biol
May 2024
Sussex Drug Discovery Centre, School of Life Sciences, University of Sussex Falmer BN1 9QJ UK
Gemma Nixon, Khondaker Miraz Rahman and John Spencer introduce the themed collection on 'Medicinal Chemistry Small Molecule Probes'.
View Article and Find Full Text PDFOxazolidinone is a five-member heterocyclic ring with several biological applications in medicinal chemistry. Among the three possible isomers, 2-oxazolidinone is the most investigated in drug discovery. Linezolid was pioneered as the first approved drug containing an oxazolidinone ring as the pharmacophore group.
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December 2019
Institute of Pharmaceutical Science, School of Cancer and Pharmaceutical Science, King's College London 150 Stamford Street London SE1 9NH UK
Nanomedicine has shown potential in enabling oral administration of poorly absorbable drugs, such as biologics. As part of the process related to optimisation of the safety and efficacy of nanomedicines, it is imperative that the interaction of nanoparticles with the biological systems - including the gut - is fully characterised. In this article, we provide an overview of the major mechanisms by which nanoparticles may transform upon introduction in biological media.
View Article and Find Full Text PDFInt J Biochem Cell Biol
October 2001
Molecular and Cellular Protein Biochemistry Laboratory, Department of Nutrition and Dietetics, King's College London 150 Stamford Street, SE1 9NN, London, UK.
Reports in the literature indicate that the trifunctional amino acid D-penicillamine (D-P) induces a variety of muscle abnormalities, although the mechanisms are unknown. We hypothesised that defects may also arise due to the effects of D-P on rates of protein synthesis, possibly via changes in muscle metal composition. Male Wistar rats were injected with D-P at doses of 50 and 500 mg/kg body weight, i.
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