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◆ Angewandte Chemie International Edition2025-11-20· Prodrug

CO/H <sub>2</sub> S Dual Prodrugs Activated by Proximity‐Enhanced Chemiexcitation for Suppression of Tumor Growth and Metastasis

Qingqiang Min, Zihui Ni, Dongguang Fan, Yicheng Wang, Jinjin Li, J. Zhang, Miao Liu, Huabing Chen, Hengte Ke, Xingyue Ji

原始摘要(英文原文)· Original abstract
Abstract Carbon monoxide (CO) and hydrogen sulfide (H 2 S) both exhibit significant therapeutic potential in antitumor therapy, highlighting the importance of developing dual prodrugs for combinatorial gas therapy. However, such dual prodrug systems remain largely unexplored. This study designed a series of CO/H 2 S dual prodrugs based on a proximity‐enhanced chemiexcitation mechanism. By directly conjugating a chemiexcitation‐triggering module with a photosensitive CO‐releasing moiety (3‐hydroxythioflavone), we constructed unimolecular prodrugs capable of light‐independent CO release specifically in response to H 2 O 2 . Leveraging the proximity effect between these modules, exceptional CO release efficiency exceeding 90% was achieved. Surprisingly, H 2 O 2 ‐induced chemiexcitation also facilitated H 2 S release from the 3‐hydroxythioflavone scaffold. Two representative prodrugs demonstrated simultaneous CO and H 2 S release in 4T1 cancer cells. Notably, in a 4T1 murine tumor model, these prodrugs effectively suppressed tumor growth and lung metastasis without inducing observable adverse effects. This work presents the first report of chemiexcitation‐triggered CO/H 2 S dual prodrugs, providing a promising strategy for combinatorial gas therapy in cancer treatment.
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CO/H <sub>2</sub> S Dual Prodrugs Activated by Proximity‐Enhanced Chemiexcitation for Suppression of Tumor Growth and Metastasis — 科研速览 Science Skim