Synthesis, biological evaluation and molecular docking analysis of vaniline–benzylidenehydrazine hybrids as potent tyrosinase inhibitors

Ítems similars

• Synthesis, biological evaluation and molecular docking analysis of vaniline–benzylidenehydrazine hybrids as potent tyrosinase inhibitors
  per: Aida Iraji, et al.
  Publicat: (2020-04-01)
• Design, synthesis, cytotoxicity evaluation and docking studies of 1,2,4-triazine derivatives bearing different arylidene-hydrazinyl moieties as potential mTOR inhibitors
  per: Ranjbar, Sara, et al.
  Publicat: (2018)
• Tetrahydroquinolinone derivatives as potent P-glycoprotein inhibitors: design, synthesis, biological evaluation and molecular docking analysis
  per: Ranjbar, S., et al.
  Publicat: (2017)
• Design and Synthesis of Novel 1-hydroxy-2,4,5-triaryl Imidazole Derivatives as Anti-cytokine Agents
  per: Haghighijoo, Zahra, et al.
  Publicat: (2020)
• Phenolic Content, Antioxidant Effects and Tyrosinase Inhibitory Activity of Extract of Some Stachys Species from Iran
  per: Najmeh Edraki, et al.
  Publicat: (2019-10-01)