双吖丙啶
部分
烷基
化学
荧光
立体化学
有机化学
物理
量子力学
作者
T. Nakashima,Takumi Iwanabe,Hiroki Tanimoto,Takenori Tomohiro
标识
DOI:10.1002/asia.202400288
摘要
A novel fluorogenic alkyl diazirine photocrosslinker bearing an o-hydroxycinnamate moiety has been developed for identification of the targets of bioactive molecules. The o-hydroxycinnamate moiety can be converted to the corresponding 7-hydroxycoumarin derivative, which should be created on the interacting site within the photocaptured target protein. The label yield and fluorescence intensity have been immensely improved in comparison with our previous aromatic crosslinkers to facilitate target identification in small quantities.
科研通智能强力驱动
Strongly Powered by AbleSci AI