Design, Synthesis, and Antitumor Evaluation of Novel Histone Deacetylase Inhibitors Equipped with a Phenylsulfonylfuroxan Module as a Nitric Oxide Donor

Схожие документы

• Discovery of the First N-Hydroxycinnamamide-Based Histone Deacetylase 1/3 Dual Inhibitors with Potent Oral Antitumor Activity
  по: Li, Xiaoyang, et al.
  Опубликовано: (2014)
• Novel Nitric Oxide Donors of Phenylsulfonylfuroxan and 3-Benzyl Coumarin Derivatives as Potent Antitumor Agents
  по: Guo, Yalan, et al.
  Опубликовано: (2018)
• Design, synthesis, and antitumor evaluation of histone deacetylase inhibitors with l-phenylglycine scaffold
  по: Zhang, Yingjie, et al.
  Опубликовано: (2015)
• Design and synthesis of a tetrahydroisoquinoline-based hydroxamate derivative (ZYJ-34v), an oral active histone deacetylase inhibitor with potent antitumor activity
  по: Zhang, Yingjie, et al.
  Опубликовано: (2013)
• Novel Histone Deacetylase Inhibitors with Enhanced Enzymatic Inhibition Effects and Potent in vitro and in vivo Anti-tumor Activities
  по: Zhang, Lei, et al.
  Опубликовано: (2013)