Chimeric Derivatives of Functionalized Amino Acids and α-Aminoamides: Compounds with Anticonvulsant Activity in Seizure Models and Inhibitory Actions on Central, Peripheral, and Cardiac Isoforms of Voltage-gated Sodium Channels

Samankaltaisia teoksia

• Chimeric Agents Derived from the Functionalized Amino Acid, Lacosamide, and the α-Aminoamide, Safinamide: Evaluation of Their Inhibitory Actions on Voltage-Gated Sodium Channels, and Antiseizure and Antinociception Activities and Comparison with Lacosamide and Safinamide
  Tekijä: Park, Ki Duk, et al.
  Julkaistu: (2014)
• Merging Structural Motifs of Functionalized Amino Acids and α-Aminoamides Results in Novel Anticonvulsant Compounds with Significant Effects on Slow and Fast Inactivation of Voltage-Gated Sodium Channels and in the Treatment of Neuropathic Pain
  Tekijä: Wang, Yuying, et al.
  Julkaistu: (2011)
• Discovery of Lacosamide Affinity Bait Agents That Exhibit Potent Voltage-Gated Sodium Channel Blocking Properties
  Tekijä: Park, Ki Duk, et al.
  Julkaistu: (2012)
• Inhibitory effects of lappaconitine on the neuronal isoforms of voltage-gated sodium channels
  Tekijä: Li, Yan-fen, et al.
  Julkaistu: (2018)
• Substituted N-(Biphenyl-4′-yl)methyl (R)-2-Acetamido-3-methoxypropionamides: Potent Anticonvulsants That Affect Frequency (Use) Dependence and Slow Inactivation of Sodium Channels
  Tekijä: Lee, Hyosung, et al.
  Julkaistu: (2014)