Development of potent pyrazolopyrimidinone-based WEE1 inhibitors with limited single-agent cytotoxicity for cancer therapy

Eitemau Tebyg

• Substituted oxindol-3-ylidenes as AMP-activated protein kinase (AMPK) inhibitors
  gan: Matheson, Christopher J., et al.
  Cyhoeddwyd: (2020)
• Molecular docking of substituted pteridinones and pyrimidines to the ATP-binding site of the N-terminal domain of RSK2 and associated MM/GBSA and molecular field datasets
  gan: Casalvieri, Kimberly A., et al.
  Cyhoeddwyd: (2020)
• Evaluation of quantitative assays for the identification of direct signal transducer and activator of transcription 3 (STAT3) inhibitors
  gan: Furtek, Steffanie L., et al.
  Cyhoeddwyd: (2016)
• Pyrimidine-Based Tricyclic Molecules as Potent and Orally Efficacious Inhibitors of Wee1 Kinase
  gan: Tong, Yunsong, et al.
  Cyhoeddwyd: (2014)
• The Tumor-Selective Cytotoxic Agent ß-Lapachone is a Potent Inhibitor of IDO1
  gan: Hollie E. Flick, et al.
  Cyhoeddwyd: (2013-08-01)