Tryptamine psychoactive substances, such as α-methyltryptamine (AMT), are monoamine alkaloids characterized by an indole ring structure. Rapid, highly sensitive, and specific identification of trace amounts of AMT is crucial for maintaining social stability and ensuring public safety. However, accurately detecting AMT using specific fluorescent methods is challenging due to the presence of similar amine groups and benzene rings in various other amines.
To address this challenge, a research team led by Prof. Dou Xincun from the Xinjiang Technical Institute of Physics and Chemistry of the Chinese Academy of Sciences (CAS) has developed a novel molecular probe strategy to enhance detection sensitivity and selectivity for AMT.
Their findings, published in Analytical Chemistry, emphasize tuning the electron-withdrawing strength of the π-conjugate bridge to improve the reactivity of Schiff base-based fluorescence probes with amines.