Evaluation of NAD(H) analogues as selective inhibitors for Trypanosoma cruzi S-Adenosylhomocysteine hydrolase

Gelijkaardige items

• The antiviral drug ribavirin is a selective inhibitor of S-adenosyl-L-homocysteine hydrolase from Trypanosoma cruzi
  door: Cai, Sumin, et al.
  Gepubliceerd in: (2007)
• Comparative kinetics of cofactor association and dissociation for the human and trypanosomal S-adenosylhomocysteine hydrolases. 3. The role of lysyl and tyrosyl residues of the C-terminal extension
  door: Cai, Sumin, et al.
  Gepubliceerd in: (2010)
• The Rationale for Targeting the NAD/NADH Cofactor Binding Site of Parasitic S-Adenosyl-L-homocysteine Hydrolase for the Design of Anti-parasitic Drugs
  door: Cai, Sumin, et al.
  Gepubliceerd in: (2009)
• Synthesis of 5′-Functionalized Nucleosides: S-Adenosylhomocysteine Analogues with the Carbon-5′ and Sulfur Atoms Replaced by a Vinyl or Halovinyl Unit
  door: Wnuk, Stanislaw F., et al.
  Gepubliceerd in: (2008)
• Carbocyclic Pyrimidine Nucleosides as Inhibitors of S-Adenosylhomocysteine Hydrolase
  door: Mosley, Sylvester L., et al.
  Gepubliceerd in: (2006)