Synthesis, Urease Inhibition, Antioxidant, Antibacterial, and Molecular Docking Studies of 1,3,4-Oxadiazole Derivatives

Ítems similars

• A multi-target therapeutic potential of Prunus domestica gum stabilized nanoparticles exhibited prospective anticancer, antibacterial, urease-inhibition, anti-inflammatory and analgesic properties.
  per: Islam, Nazar Ul, et al.
  Publicat: (2017)
• Molecular Docking and In Vitro Studies of Synthesized Oxadiazole Derivatives as Urease Inhibitors
  per: Kamran Mehdi, et al.
  Publicat: (2025-08-01)
• Molecular Docking, Computational, and Antithrombotic Studies of Novel 1,3,4-Oxadiazole Derivatives
  per: Batool, Majda, et al.
  Publicat: (2018)
• Identification of novel oxadiazole-based benzothiazole derivatives as potent inhibitors of α-glucosidase and urease: Synthesis, in vitro bio-evaluation and their in silico molecular docking study
  per: Yousaf Khan, et al.
  Publicat: (2023-07-01)
• Synthesis of a series of novel 2,5-disubstituted-1,3,4-oxadiazole derivatives as potential antioxidant and antibacterial agents
  per: Sindhe, M. Aruna, et al.
  Publicat: (2016)