Discovery of Substituted 1H-Pyrazolo[3,4-b]pyridine Derivatives as Potent and Selective FGFR Kinase Inhibitors

समान संसाधन

• Design, synthesis and biological evaluation of pyrazolo[3,4-d]pyridazinone derivatives as covalent FGFR inhibitors
  द्वारा: Wu, Xiaowei, और अन्य
  प्रकाशित: (2021)
• Screening of Heteroaromatic Scaffolds against Cystathionine Beta-Synthase Enables Identification of Substituted Pyrazolo[3,4-c]Pyridines as Potent and Selective Orthosteric Inhibitors
  द्वारा: Fantel, Anna-Maria, और अन्य
  प्रकाशित: (2020)
• Discovery and Evaluation of Pyrazolo[3,4-d]pyridazinone as a Potent and Orally Active Irreversible BTK Inhibitor
  द्वारा: Zhang, Xuejun, और अन्य
  प्रकाशित: (2019)
• Identification of 1H-pyrazolo[3,4-b]pyridine derivatives as potent ALK-L1196M inhibitors
  द्वारा: Nam, Yunju, और अन्य
  प्रकाशित: (2019)
• 3-Iodo-1H-pyrazolo­[3,4-b]pyridine
  द्वारा: Huang, Ping-Hsin, और अन्य
  प्रकाशित: (2014)