化学
一氧化氮
天线(收音机)
光化学
氧化物
硝酸
纳米技术
生物物理学
生物活性
激进的
作者
Daisuke Saitoh,Sae Kitamura,Naoya Ieda,K. Oyama,Yuhei Ohta,Yuji Hotta,Masato Kobayashi,Mei Harada,Mikako Ogawa,Mitsuyasu Kawaguchi,Kazunori Kimura,Tetsuya Taketsugu,Hidehiko Nakagawa
标识
DOI:10.1021/acs.jmedchem.6c00784
摘要
To realize spatiotemporal control of nitric oxide (NO), a key signaling molecule for vasodilation in biological systems, we previously developed photocontrollable NO releasers such as NORD-1, whose NO release is triggered by photoinduced electron transfer (PeT) to a light-harvesting moiety. Here, we aimed to improve the PeT-driven NO release by investigating the structure–activity relationship of the rhodamine antenna, focusing on modifications of amino groups at the 3-/6-positions and the element at the 10-position. NO release from selenium- or tellurium-containing NO releasers (NO-SeR and NO-TeR) was significantly enhanced, whereas a phospharhodamine-type NO releaser (NO-POR) exhibited no detectable photodecomposition. Quantum-chemical calculations suggested that the charge-transfer state for NO-POR is stabilized compared to other NO releasers. We confirmed that NO-TeR showed more efficient vasodilation than NORD-1 in ex vivo studies. These findings are expected to facilitate the design of new PeT-driven compounds for biological and therapeutic applications.
科研通智能强力驱动
Strongly Powered by AbleSci AI