Structural modeling of GSK3β implicates the inactive (DFG-out) conformation as the target bound by TDZD analogs

Benzer Materyaller

• Design and Synthesis of Novel Hybrid 8-Hydroxy Quinoline-Indole Derivatives as Inhibitors of Aβ Self-Aggregation and Metal Chelation-Induced Aβ Aggregation
  Yazar:: Bowroju, Suresh K., ve diğerleri
  Baskı/Yayın Bilgisi: (2020)
• Heteroaromatic analogs of the resveratrol analog DMU-212 as potent anti-cancer agents
  Yazar:: Penthala, Narsimha Reddy, ve diğerleri
  Baskı/Yayın Bilgisi: (2015)
• Aggregate Interactome Based on Protein Cross-linking Interfaces Predicts Drug Targets to Limit Aggregation in Neurodegenerative Diseases
  Yazar:: Meenakshisundaram Balasubramaniam, ve diğerleri
  Baskı/Yayın Bilgisi: (2019-10-01)
• Aggregate Interactome Based on Protein Cross-linking Interfaces Predicts Drug Targets to Limit Aggregation in Neurodegenerative Diseases
  Yazar:: Balasubramaniam, Meenakshisundaram, ve diğerleri
  Baskı/Yayın Bilgisi: (2019)
• Synthesis and in vitro screening of novel N-benzyl aplysinopsin analogs as potential anticancer agents
  Yazar:: Penthala, Narsimha Reddy, ve diğerleri
  Baskı/Yayın Bilgisi: (2011)