Department of Chemistry, Stony Brook University, 100 Nicolls Road, Stony Brook, NY 11790, United States.
Departamento de Química Orgánica, Universitat de València, Avda. Vicente Andrés Estellés s/n, Burjassot, 46100, Valencia, Spain.
Chemistry. 2024 Feb 1;30(7):e202303465. doi: 10.1002/chem.202303465. Epub 2023 Dec 11.
Hydrogen sulfide (H S), one of the most important gasotransmitters, plays a critical role in endogenous signaling pathways of many diseases. However, developing H S donors with both tunable release kinetics and high release efficiency for subcellular delivery has been challenging. Here, we describe a click and release reaction between pyrone/pyranthiones and bicyclononyne (BCN). This reaction features a release of CO /COS with second-order rate constants comparable to Strain-Promoted Azide-Alkyne Cycloaddition reactions (SPAACs). Interestingly, pyranthiones showed enhanced reaction rates compared to their pyrone counterparts. We investigated pyrone biorthogonality and demonstrated their utility in protein labeling applications. Moreover, we synthesized substituted pyranthiones with H S release kinetics that can address the range of physiologically relevant H S dynamics in cells and achieved quantitative H S release efficiency in vitro. Finally, we explored the potential of pyranthiones as H S/COS donors for mitochondrial-targeted H S delivery in living cells.
硫化氢 (H₂S) 作为最重要的气体信号分子之一,在许多疾病的内源性信号通路中发挥着关键作用。然而,开发具有可调节释放动力学和高释放效率的用于亚细胞递送的 H₂S 供体一直具有挑战性。在这里,我们描述了吡喃酮/吡喃硫酮与二环壬炔 (BCN) 之间的点击和释放反应。该反应具有与应变促进叠氮-炔环加成反应 (SPAACs) 相当的释放 CO/COS 的二级速率常数。有趣的是,吡喃硫酮的反应速率比其吡喃酮对应物有所提高。我们研究了吡喃酮的生物正交性,并证明了它们在蛋白质标记应用中的实用性。此外,我们合成了具有 H₂S 释放动力学的取代吡喃硫酮,可满足细胞内生理相关 H₂S 动力学的范围,并实现了体外的定量 H₂S 释放效率。最后,我们探索了吡喃硫酮作为 H₂S/COS 供体用于活细胞中线粒体靶向 H₂S 递送的潜力。