TIM-3 Inhibitor Development: Overcoming Immune Evasion in Cancer Therapy
Although immune checkpoint blockade therapies targeting PD-1/PD-L1 and CTLA-4 have achieved remarkable clinical success, limitations such as low response rates and acquired resistance remain significant challenges. TIM-3 has recently emerged as a key immunosuppressive receptor and a promising therapeutic target for augmenting antitumor immunity. However, the development of TIM-3 inhibitors is highly imbalanced: multiple antibody-based candidates have entered Phase III trials, whereas small-molecule inhibitors are still in the preclinical stage, with current research remaining fragmented and lacking systematic structure-activity relationship studies. This Account systematically summarizes the structural and functional mechanisms of TIM-3, with a focus on recent advances in the discovery and development of small-molecule TIM-3 inhibitors. We highlight representative lead compounds identified through virtual screening and rational design and discuss future directions to facilitate the development of novel TIM-3-targeted agents.
Authors
- Peng Yang (ORCID: https://orcid.org/0000-0002-2613-941X)
- Xiao Wang (ORCID: https://orcid.org/0000-0001-6117-6745)
- Binjian Jiang
- Hao Shen (ORCID: https://orcid.org/0000-0002-0344-5860)
- Chengliang Sun (ORCID: https://orcid.org/0000-0002-8428-0091)
- Lili Wang (ORCID: https://orcid.org/0009-0009-1660-3678)
Institutions
- China Pharmaceutical University (CN)
- National Medical Products Administration (CN)
- Medicina (PL)
- Innovative Research (United States) (US)
Publication Details
- Journal
- Journal of Medicinal Chemistry
- Published
- 2025-12-09
- DOI
- https://doi.org/10.1021/acs.jmedchem.5c02693
- Primary Topic
- Cancer Immunotherapy and Biomarkers
- Type
- article
- Field-Weighted Citation Impact
- 0.00