Publications by authors named "Hussien Ahmed Khamees"

Article Synopsis
  • A series of novel 1,2,3-triazole and 1,2,3-triazoline glycosides were synthesized from d-arabinose to create hybrid molecules featuring sugar azide, with key steps involving the protection of hydroxyl groups and introduction of ethylene glycol.
  • The synthesis of azido ethyl-O-β-d-arabinofuranoside was achieved using sodium azide to replace a tosylate group, followed by a 1,3-dipolar cycloaddition reaction with various alkenes and alkynes to create new glycosides.
  • Characterization through various analytical techniques confirmed moderate to high antimicrobial activity against test microorganisms, alongside promising pharmacokinetic properties, with molecular docking analysis
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A sequence of novel 2-(4-benzoyl-2-methyl-phenoxy)-N-(3-chloro-2-oxo-4-phenyl-azetidin-1-yl)-acetamide analogues 9(a−n) were synthesized by multistep synthesis. The newly synthesized compounds were well characterized, and their antimicrobial activities were carried out by disc diffusion and broth dilution methods. Further, all the novel series of compounds (9a−n), were tested against a variety of bacterial and fungal strains in comparison to Ketoconazole, Chloramphenicol, and Amoxicillin as standard drugs, respectively.

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Angiogenesis plays an important role in the development of cancer since it allows for the delivery of oxygen, nutrients, and growth factors as well as tumor dissemination to distant organs. Inhibition of angiogenesis is an important strategy for the prevention of multiple solid tumors that depend on cutting or at least reducing the blood supply to tumor micro-regions, resulting in pan-hypoxia and pan-necrosis within solid tumor tissues. These drugs are an important part of treatment for some types of cancer.

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It is of interest to document the design, synthesis, docking, Hirshfeld surface analysis and DFT calculations of 2-methylxanthen-9-with the FtsZ protein (PDB ID: 3VOB) from Staphylococcus aureus for antimicrobial applications. We report the quantitative structure function data in this context.

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The title imidazo[1,2-] pyridine derivative, CHBrN, was synthesized a single-step reaction method. The title mol-ecule is planar, showing a dihedral angle of 0.62 (17)° between the phenyl and the imidazo[1,2-] pyridine rings.

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