Development of Inhibitors of the Programmed Cell Death-1/Programmed Cell Death-Ligand 1 Signaling Pathway

  • J Med Chem. 2019 Feb 28;62(4):1715-1730. doi: 10.1021/acs.jmedchem.8b00990.
Tianyu Wang  1 Xiaoxing Wu  1 Changying Guo  1 Kuojun Zhang  1 Jinyi Xu  1 Zheng Li  2 Sheng Jiang  1
Affiliations
  • 1. State Key Laboratory of Natural Medicines and Department of Medicinal Chemistry, School of Pharmacy , China Pharmaceutical University , Nanjing 210009 , China.
  • 2. Department of Nanomedicine, Center for Bioenergetics , Houston Methodist Research Institute , 6670 Bertner Avenue , Houston , Texas 77030 , United States.
Abstract

The clinical success of inhibitors targeting the PD-1/PD-L1 pathway has made this an active field in Cancer Immunotherapy. Currently, most drugs targeting this pathway are monoclonal antibodies. Small-molecule inhibitors as the alternative to monoclonal antibodies are expected to overcome the disadvantages of mAbs which include production difficulties and their long half-life. Recently, progress has been reported on anti-PD-1/PD-L1 small-molecule inhibitors. In this paper, we review the development of inhibitors targeting the PD-1/PD-L1 pathway, focusing mainly on peptide-based and nonpeptidic small-molecule inhibitors. The structures and the preclinical and clinical studies of several peptide-based small-molecule candidate compounds in clinical trials are discussed. We also illustrate the design strategies underlying reported nonpeptidic small-molecule inhibitors and provide insight into possible future exploration. Development of small-molecule drugs for anti-PD-1/PD-L1 activity with specific Cancer applications is a promising and challenging prospect.

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