Structural highlights
FunctionPublication Abstract from PubMedThe global incidence of melanoma has risen substantially over the past two decades, driving an urgent need for novel therapeutic strategies. The nonreceptor protein tyrosine phosphatases PTPN2/PTPN1 have emerged as promising therapeutic targets, yet developing effective inhibitors faces significant drug-like property challenges. Through rational drug design, we discovered WS35 horizontal line a potent dual PTPN2/1 inhibitor exhibiting exceptional enzymatic activity (PTPN2 IC(50) = 5.8 nM, PTPN1 IC(50) = 12.8 nM), favorable safety profiles, and enhanced oral bioavailability (F = 7.1%). Mechanistic studies demonstrate that WS35 modulates the IFNgamma-JAK-STAT signaling axis, significantly augmenting CD8(+) T-cell tumor infiltration. In B16-OVA syngeneic models, WS35 monotherapy and its combination with an anti-PD-1 antibody achieved robust tumor growth suppression, outperforming AC484, with no observable systemic toxicity. Collectively, WS35 represents a preclinical candidate with validated efficacy and safety for developing novel antimelanoma therapeutics. Development of Novel PTPN2/1 Inhibitors for the Treatment of Melanoma.,Wang D, Song M, Tong C, Wang W, Li Q, Liu J, Chen A, Chen Y, Wang L, Hao H, Wang X, Han K, Xiao Y, Kuang W, Yang P J Med Chem. 2025 Oct 23;68(20):21917-21938. doi: 10.1021/acs.jmedchem.5c02300. , Epub 2025 Oct 5. PMID:41047545[1] From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine. References
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