Analogs of Iso-Azepinomycin as Potential Transition-State Analog Inhibitors of Guanase: Synthesis, Biochemical Screening, and Structure-Activity Correlations of Various Selectively Substituted Imidazo[4,5-e][1,4]diazepines

Gelijkaardige items

• Investigations into specificity of azepinomycin for inhibition of guanase: Discrimination between the natural heterocyclic inhibitor and its synthetic nucleoside analogues
  door: Chakraborty, Saibal, et al.
  Gepubliceerd in: (2012)
• A Novel Transition State Analogue Inhibitor of Guanase Based on Azepinomycin Ring Structure: Synthesis and Biochemical Assessment of Enzyme Inhibition
  door: Chakraborty, Saibal, et al.
  Gepubliceerd in: (2011)
• A Novel, Broad Spectrum Anti-Cancer Compound Containing the Imidazo[4,5-e][1,3]diazepine Ring System
  door: Xie, Min, et al.
  Gepubliceerd in: (2010)
• Structure-activity relationship studies on anti-HCV activity of ring-expanded (‘fat’) nucleobase analogues containing the imidazo[4,5-e][1,3]diazepine-4,8-dione ring system
  door: Zhang, Peng, et al.
  Gepubliceerd in: (2007)
• Dual inhibition of HCV and HIV by ring-expanded nucleosides containing the 5:7-fused imidazo[4,5-e][1,3]diazepine ring System. In vitro results and implications
  door: Zhang, Ning, et al.
  Gepubliceerd in: (2014)