Integrated computational and experimental identification of as a potent and selective TIM-3 inhibitor for NSCLC immunotherapy.

Non-small cell lung cancer (NSCLC) remains a significant clinical challenge, necessitating exploration of novel therapeutic targets such as TIM-3. In this study, integrated computational and experimental methods were utilized to identify potent TIM-3 inhibitors. Survival analysis revealed a significant correlation between elevated TIM-3 expression and decreased patient survival. Structure-based virtual screening and molecular dynamics simulations identified HIT104310526 , a candidate exhibiting superior binding affinity and stable interactions within the TIM-3 binding pocket. MMGBSA binding free energy calculations and metadynamics further confirmed its potent binding. Physicochemical evaluations indicated favorable drug-likeness, although solubility improvement is needed. Experimental validation showed selective cytotoxicity of HIT104310526 toward NSCLC cells (A549; IC = 37.74 μM), with negligible toxicity to normal bronchial epithelial cells (BEAS-2). However, potential cardiotoxicity risks were identified. Collectively, HIT104310526 demonstrates substantial promise as a selective TIM-3 inhibitor, warranting further optimization for NSCLC treatment.