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

Podobne zapisy

• Merging the Structural Motifs of Functionalized Amino Acids and α-Aminoamides: Compounds with Significant Anticonvulsant Activities
  od: Salomé, Christophe, i wsp.
  Wydane: (2010)
• 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
  od: Park, Ki Duk, i wsp.
  Wydane: (2014)
• Development and Characterization of Novel Derivatives of the Antiepileptic Drug Lacosamide That Exhibit Far Greater Enhancement in Slow Inactivation of Voltage-Gated Sodium Channels
  od: Wang, Yuying, i wsp.
  Wydane: (2010)
• 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
  od: Torregrosa, Robert, i wsp.
  Wydane: (2015)
• CRMP2 and voltage-gated ion channels: potential roles in neuropathic pain
  od: Chew, Lindsey A., i wsp.
  Wydane: (2018)