Biography and Research Information
OverviewAI-generated summary
Maha Hanafi's research centers on the development of novel therapeutic agents, with a particular focus on pancreatic cancer. Her work involves the design and synthesis of compounds targeting specific molecular pathways implicated in cancer progression. Recent publications highlight efforts to discover agents that degrade key oncogenic proteins, such as PROTACs targeting ZFP91, and orally active compounds designed as sigma 2 receptor ligands. Further investigations explore the therapeutic vulnerabilities within the copper-KRAS-COX2 axis in pancreatic cancer. Hanafi also contributes to the review of emerging therapeutic strategies, such as rearranged during transfection (RET) kinase inhibitors. Her scholarship metrics include an h-index of 3 and 5 total publications with 87 citations.
Metrics
- h-index: 3
- Publications: 6
- Citations: 90
Selected Publications
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Discovery of Novel 1h-Pyrazolo[3,4-D]Pyrimidine Derivatives as Brk/Ptk6 Inhibitors (2025)
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An updated patent review of rearranged during transfection (RET) kinase inhibitors (2022-present) (2025)
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Discovery of the DNA-PKcs inhibitor DA-143 which exhibits enhanced solubility relative to NU7441 (2024)
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Discovery of 9H-pyrimido[4,5-b]indole derivatives as dual RET/TRKA inhibitors (2024)
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Kinase inhibitor macrocycles: a perspective on limiting conformational flexibility when targeting the kinome with small molecules (2023)
Collaboration Network
Top Collaborators
- Discovery of a Napabucasin PROTAC as an Effective Degrader of the E3 Ligase ZFP91
- Design and Synthesis of Orally Active Quinolyl Pyrazinamides as Sigma 2 Receptor Ligands for the Treatment of Pancreatic Cancer
- Copper-KRAS-COX2 Axis: A Therapeutic Vulnerability in Pancreatic Cancer
- Design and Synthesis of Orally Active Quinolyl Pyrazinamides as Sigma 2 Receptor Ligands for the Treatment of Pancreatic Cancer
- Copper-KRAS-COX2 Axis: A Therapeutic Vulnerability in Pancreatic Cancer
- Design and Synthesis of Orally Active Quinolyl Pyrazinamides as Sigma 2 Receptor Ligands for the Treatment of Pancreatic Cancer
- Copper-KRAS-COX2 Axis: A Therapeutic Vulnerability in Pancreatic Cancer
- Design and Synthesis of Orally Active Quinolyl Pyrazinamides as Sigma 2 Receptor Ligands for the Treatment of Pancreatic Cancer
- Copper-KRAS-COX2 Axis: A Therapeutic Vulnerability in Pancreatic Cancer
- Design and Synthesis of Orally Active Quinolyl Pyrazinamides as Sigma 2 Receptor Ligands for the Treatment of Pancreatic Cancer
- Copper-KRAS-COX2 Axis: A Therapeutic Vulnerability in Pancreatic Cancer
- Discovery of a Napabucasin PROTAC as an Effective Degrader of the E3 Ligase ZFP91
- Design and Synthesis of Orally Active Quinolyl Pyrazinamides as Sigma 2 Receptor Ligands for the Treatment of Pancreatic Cancer
- Design and Synthesis of Orally Active Quinolyl Pyrazinamides as Sigma 2 Receptor Ligands for the Treatment of Pancreatic Cancer
- Copper-KRAS-COX2 Axis: A Therapeutic Vulnerability in Pancreatic Cancer
- Copper-KRAS-COX2 Axis: A Therapeutic Vulnerability in Pancreatic Cancer
- An updated patent review of rearranged during transfection (RET) kinase inhibitors (2022-present)
- An updated patent review of rearranged during transfection (RET) kinase inhibitors (2022-present)
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