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首页> 外文期刊>Journal of Medicinal Chemistry >Modulation of Reactive Oxygen Species Photogeneration of Bacteriopheophorbide a Derivatives by Exocyclic E?Ring Opening and Charge Modifications
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Modulation of Reactive Oxygen Species Photogeneration of Bacteriopheophorbide a Derivatives by Exocyclic E?Ring Opening and Charge Modifications

机译:通过环外E-环的开放和电荷修饰来调节噬菌体a衍生物的活性氧的光生化

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With the knowledge that the dominant photodynamic therapy (PDT) mechanism of 1a (WST09) switched from type 2 to type 1 for 1b (WST11) upon taurine-driven E-ring opening, we hypothesized that taurine-driven E-ring opening of bacteriochlorophyll derivatives and net-charge variations would modulate reactive oxygen species (ROS) photogeneration. Eight bacteriochlorophyll a derivatives were synthesized with varying charges that either contained the E ring (2a?5a) or were synthesized by taurine-driven E-ring opening (2b?5b). Timedependent density functional theory (TDDFT) modeling showed that all derivatives would be type 2 PDT-active, and ROS-activated fluorescent probes were used to investigate the photogeneration of a combination of type 1 and type 2 PDT ROS in organic- and aqueous-based solutions. These investigations validated our predictive modeling calculations and showed that taurine-driven Ering opening and increasing negative charge generally enhanced ROS photogeneration in aqueous solutions. We propose that these structure?activity relationships may provide simple strategies for designing bacteriochlorins that efficiently generate ROS upon photoirradiation.
机译:认识到牛磺酸驱动的E环打开后,1a(WST09)的主要光动力学治疗(PDT)机制从2型变为1b的1b(WST11),我们假设牛磺酸驱动的细菌叶绿素E环打开衍生物和净电荷的变化将调节活性氧(ROS)的光生。合成了八种带有不同电荷的细菌叶绿素a衍生物,它们要么包含E环(2a→5a),要么通过牛磺酸驱动的E环开口(2b→5b)合成。时变密度泛函理论(TDDFT)建模显示,所有衍生物均具有2型PDT活性,并且使用ROS激活的荧光探针来研究1型和2型PDT ROS组合在有机基和水基中的光生解决方案。这些研究验证了我们的预测模型计算结果,并表明牛磺酸驱动的Ering开口和增加的负电荷通常会增强水溶液中ROS的光生作用。我们建议这些结构活性关系可以为设计在光辐照下有效产生ROS的细菌绿素提供简单的策略。

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