Affinity chromatography of murein precursors on vancomycin-sepharose [PDF]
MA Pedro, Ulrich T. Schwarz
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Abstract Affinity photolabeling is a smart method to study noncovalent and transient interactions and provide a submolecular picture of the contacts between interacting partners. In this review, we will focus on the identification of peptide partners using photoaffinity labeling coupled to mass spectrometry in different contexts such as in vitro with a
Astrid Walrant, Emmanuelle Sachon
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Development of a novel quantitative lateral flow assay for vancomycin for therapeutic drug monitoring. [PDF]
Riezk A+5 more
europepmc +1 more source
Abstract Cyclodepsipeptides (CDPs) represent a huge family of chemically and structurally diverse molecules with a wide ability for molecular interactions. CDPs are cyclic peptide‐related natural products made up of both proteinogenic and nonproteinogenic amino acids linked by amide and ester bonds.
Sophie Liuu+10 more
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Enhancing outcomes in medically inoperable early-stage NSCLC with gut-targeted antibiotics and stereotactic body radiotherapy: results from a randomized pilot study. [PDF]
Feigenberg SJ+24 more
europepmc +1 more source
In vitro activity of teichomycin and vancomycin alone and in combination with rifampin
Pietro E. Varaldo+2 more
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Anti‐Inflammatory and Antibacterial Properties of Curcuma longa Extract Against Helicobacter pylori
This study explored the effects of Curcuma longa extract (CLE) against H. pylori infection. CLE contained 18 chemical compounds and completely inhibited growth of H. pylori Sydney strain 1 (SS1) in vitro. In infected mice with H. pylori SS1, oral administration of CLE successfully eradicated H.
Jeongsook Kim+7 more
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Concentrations of vancomycin in bone and serum of normal rabbits and those with osteomyelitis
Katharine J. Wilson, Jon T. Mader
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Comparative activity of CGP 31608, nafcillin, cefamandole, imipenem, and vancomycin against methicillin-susceptible and methicillin-resistant staphylococci [PDF]
Meena Sachdeva+3 more
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Liposomes functionalized with tetraether lipids and cell‐penetrating peptides are explored as a platform technology for oral peptide delivery. Therefore, peptide drugs (GLP‐1 analogs) with different sizes and physicochemical properties are used as model drugs.
Lorenz Herbster+8 more
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