Precursors of Carboximidates Deriving from Thioamide-Trimethyl-Lock System: A General Method for Designing Stable Cascade Acid-Sensitive Prodrugs

We report a cascade acid-sensitive prodrug design strategy utilizing a thioamide-trimethyl-lock system. This approach successfully balances prodrug stability and high acid sensitivity, enabling precise drug release in acidic microenvironments. The thioamide system further acts as a hydrogen sulfide (H<sub>2</sub>S) donor, providing organ-protective effects. <i>In vivo</i> studies in a mouse MCAO stroke model and a 4T1 breast tumor model confirmed significant therapeutic efficacy, including reduced toxicity, enhanced tumor inhibition, and improved safety. Histological analysis revealed minimized systemic toxicity, particularly cardiotoxicity, compared to conventional treatments. This robust and versatile cascade acid-sensitive design has broad applications in chemical biology and drug delivery.

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Publication Details

Journal
Journal of the American Chemical Society
Published
2025-06-25
DOI
https://doi.org/10.1021/jacs.5c03565
Citations
3
Primary Topic
Synthesis and Reactivity of Sulfur-Containing Compounds
Type
article
Field-Weighted Citation Impact
2.81

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article

Precursors of Carboximidates Deriving from Thioamide-Trimethyl-Lock System: A General Method for Designing Stable Cascade Acid-Sensitive Prodrugs

Zhongbo Wang, Qiwei Zhou, Yueqin Zheng, Weiwei Guo et al.
3 citations
Journal of the American Chemical Society
Synthesis and Reactivity of Sulfur-Containing Compounds
2.81
article

Precursors of Carboximidates Deriving from Thioamide-Trimethyl-Lock System: A General Method for Designing Stable Cascade Acid-Sensitive Prodrugs

Zhongbo Wang, Qiwei Zhou, Yueqin Zheng, Weiwei Guo, Yanzhao Chen, Y. Wang, Yanping Xue, Peng Wen, Chao Ban, Hao Hao, Peiyuan Li, Yan Liang, Jianru Liu
article en
3 citations

Abstract

We report a cascade acid-sensitive prodrug design strategy utilizing a thioamide-trimethyl-lock system. This approach successfully balances prodrug stability and high acid sensitivity, enabling precise drug release in acidic microenvironments. The thioamide system further acts as a hydrogen sulfide (H<sub>2</sub>S) donor, providing organ-protective effects. <i>In vivo</i> studies in a mouse MCAO stroke model and a 4T1 breast tumor model confirmed significant therapeutic efficacy, including reduced toxicity, enhanced tumor inhibition, and improved safety. Histological analysis revealed minimized systemic toxicity, particularly cardiotoxicity, compared to conventional treatments. This robust and versatile cascade acid-sensitive design has broad applications in chemical biology and drug delivery.

Journal of the American Chemical SocietyVol. 147(27)
China Pharmaceutical University (CN), Drug Discovery Laboratory (Norway) (NO), State Key Laboratory of Natural Medicine
National Natural Science Foundation of China, State Key Laboratory of Natural Medicines
Openalex Percentile: Top 10%
Synthesis and Reactivity of Sulfur-Containing Compounds
2.81
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