Discovery and Development of ATP-Competitive mTOR Inhibitors Using Computational Approaches

作者：Luo, Yao; Wang, Ling^*

来源：Current Pharmaceutical Design, 2017, 23(29): 4321-4331.

DOI：10.2174/1381612823666170710150604

• Molecular docking
• drug discovery
• homology modeling
• molecular dynamics
• pharmacophore
• machine learning
• virtual screening

The mammalian target of rapamycin (mTOR) is a central controller of cell growth, proliferation, metabolism, and angiogenesis. This protein is an attractive target for new anticancer drug development. Significant progress has been made in hit discovery, lead optimization, drug candidate development and determination of the three-dimensional (3D) structure of mTOR. Computational methods have been applied to accelerate the discovery and development of mTOR inhibitors helping to model the structure of mTOR, screen compound databases, uncover structure-activity relationship (SAR) and optimize the hits, mine the privileged fragments and design focused libraries. Besides, computational approaches were also applied to study protein-ligand interactions mechanisms and in natural product-driven drug discovery. Herein, we survey the most recent progress on the application of computational approaches to advance the discovery and development of compounds targeting mTOR. Future directions in the discovery of new mTOR inhibitors using computational methods are also discussed.

• 出版日期2017
• 单位华南理工大学