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The current study examines the anti-dengue and antibacterial potential and in silico drug development of the andrographolide against the pathogens Staphylococcus aureus (1JIJ) and Pseudomonas aeruginosa (6MVN) and the dengue viral protein NS5. The phytochemical analysis identified the presence of flavonoids, alkaloids, saponins, tannins, phenols, glycosides, and steroids in the Andrographis paniculata methanolic leaf extract. Based on the GC-MS analysis, andrographolide was identified as the primary chemical constituent of the medicinal plant A.

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Article Synopsis
  • Emerging antibiotic resistance poses risks to immune functions and may worsen bone and arthritis issues.
  • Our study utilized advanced computational methods to discover new drug candidates resembling ciprofloxacin, focusing on their effects against a bacterial protein and one linked to gout.
  • We identified six potential compounds, with L6 showing the strongest binding affinities and favorable properties for both treating UTIs and gout, indicating its dual functionality and promising therapeutic potential.
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Competitive Inhibition of Okanin against Tyrosyl-tRNA Synthetase.

Int J Mol Sci

April 2024

School of Public Health (Shenzhen), Shenzhen Campus of Sun Yat-sen University, Sun Yat-sen University, Shenzhen 518107, China.

Malaria is a severe disease that presents a significant threat to human health. As resistance to current drugs continues to increase, there is an urgent need for new antimalarial medications. Aminoacyl-tRNA synthetases (aaRSs) represent promising targets for drug development.

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Glycolipid-based biosurfactants (BSs), known for their intriguing and diverse properties, represent a largely uncharted territory in the realm of potential biomedical applications. This field holds great promise yet remains largely unexplored. This investigation provides new insights into the isolation, characterization, and comprehensive biomedical assessment of a novel glycolipid biosurfactant derived from Bacillus species, meeting the growing demand for understanding its multifaceted impact on various biomedical issues.

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A series of chrysin derivatives were designed, synthesized, and evaluated for their antibacterial activity against four different bacterial strains. We have synthesized new propyl-substituted and butyl-substituted chrysin-piperazine derivatives, which show marvellous inhibition against and . The free hydroxyl group at the C-5 position of chrysin improved therapeutic efficacy and was a beneficial formulation for chemotherapy.

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