The aberrantly changed level of homocysteine (Hcy) triggers
a variety
of pathological symptoms and subsequently Hcy-related diseases. Direct
and selective visualization of Hcy in biological systems is pivotal
to understanding the pathological functions of Hcy at the molecular
level. Herein, a general strategy was developed for the specific fluorescence
imaging of Hcy through the combination of dual-binding sites and the
introduction of a nitro group at the 6-position of the 7-diethylaminocoumarin
fluorophore. Also, a series of novel fluorescent probes were exploited
for monitoring Hcy with excellent selectivity, high sensitivity, and
far-red/near-infrared fluorescence emission. Furthermore, fluorescence
imaging of endogenous Hcy dynamics in living cells and <i>in
vivo</i> was achieved, providing direct and solid evidence for
the increasement of endogenous Hcy in type 2 diabetes mellitus and
Alzheimer’s disease. This research will greatly advance the
development and understanding of the molecular nexus between the Hcy
metabolism cascade and the root causes of diseases related to Hcy.