Valproate uncompetitively inhibits arachidonic acid acylation by rat acyl-CoA synthetase 4: Relevance to valproate’s efficacy against bipolar disorder

Lignende værker

• Propylisopropylacetic acid (PIA), a constitutional isomer of valproic acid, uncompetitively inhibits arachidonic acid acylation by rat acyl-CoA synthetase 4: a potential drug for bipolar disorder
  af: Modi, Hiren R., et al.
  Udgivet: (2013)
• Valnoctamide, a non-teratogenic amide derivative of valproic acid, inhibits arachidonic acid activation in vitro by recombinant acyl-CoA synthetase-4
  af: Modi, Hiren R, et al.
  Udgivet: (2014)
• Valnoctamide, which reduces rat brain arachidonic acid turnover, is a potential non-teratogenic valproate substitute to treat bipolar disorder
  af: Modi, Hiren R., et al.
  Udgivet: (2017)
• Phosphorylation and Acetylation of Acyl-CoA Synthetase- I
  af: Frahm, Jennifer L., et al.
  Udgivet: (2011)
• Long-chain acyl-CoA synthetases and fatty acid channeling
  af: Mashek, Douglas G., et al.
  Udgivet: (2007)