Design, Synthesis, and Pharmacological Evaluation of Biaryl-Containing PD-1/PD-L1 Interaction Inhibitors Bearing a Unique Difluoromethyleneoxy Linkage

  • J Med Chem. 2021 Nov 25;64(22):16687-16702. doi: 10.1021/acs.jmedchem.1c01422.
Zilan Song  1  2  3  4 Bo Liu  2 Xia Peng  3 Wangting Gu  1 Yiming Sun  2 Li Xing  1 Yi Xu  5 Meiyu Geng  2  3  4 Jing Ai  2  4 Ao Zhang  1  2  3  4  6
Affiliations
  • 1. Pharm-X Center, School of Pharmacy, Shanghai Jiao Tong University, Shanghai 200240, China.
  • 2. State Key Laboratory of Drug Research, Shanghai Institute of Materia Medica (SIMM), Chinese Academy of Sciences, Shanghai 201203, China.
  • 3. School of Chinese Materia Medica, Nanjing University of Chinese Medicine, Nanjing 210023, China.
  • 4. University of Chinese Academy of Sciences, Beijing 100049, China.
  • 5. Shanghai Pinghe School, 261 Huangyang Road, Shanghai 201206, China.
  • 6. School of Life Science and Technology, Shanghai Tech University, Shanghai 201210, China.
Abstract

Blockade of immune checkpoint PD-1/PD-L1 has been a promising Anticancer strategy; however, clinically available PD-1/PD-L1 small-molecule inhibitors are lacking. In view of the high potency of compound 2 (BMS-1002), structural fine tuning of the methoxy linkage together with diverse modification in the solvent interaction region was conducted. A series of novel derivatives featuring a difluoromethyleneoxy linkage were designed. Compound 43 was identified as the most promising PD-1/PD-L1 inhibitor with an IC50 value of 10.2 nM in the HTRF assay. This compound is capable of promoting CD8+ T cell activation through inhibiting PD-1/PD-L1 cellular signaling. Moreover, in the Hepa1-6 syngeneic mouse model, administration of compound 43 at 1 mg/kg dosage promoted CD8+ T cell activation and delayed the tumor growth with good tolerance. Notably, the tumor in one mouse of the compound 43-treated group was completely regressed. These results indicate that compound 43 is a promising candidate worthy of further investigation.

Products