Russian Journal of General Chemistry, Год журнала: 2024, Номер 94(11), С. 2833 - 2840
Опубликована: Ноя. 1, 2024
Язык: Английский
Russian Journal of General Chemistry, Год журнала: 2024, Номер 94(11), С. 2833 - 2840
Опубликована: Ноя. 1, 2024
Язык: Английский
Sensors & Diagnostics, Год журнала: 2024, Номер 3(9), С. 1428 - 1441
Опубликована: Янв. 1, 2024
The constant need for cancer diagnosis in the early stages drives development of contrast agents and imaging methods.
Язык: Английский
Процитировано
5Chemical Science, Год журнала: 2024, Номер 15(36), С. 14913 - 14923
Опубликована: Янв. 1, 2024
The reactive partnership between azides and strained alkynes is at the forefront of bioorthogonal reactions, with their
Язык: Английский
Процитировано
4Chemical Science, Год журнала: 2025, Номер unknown
Опубликована: Янв. 1, 2025
Tetrazine-based fluorogenic labels are widely utilized in medical and biological studies, exhibiting substantial fluorescence enhancement (FE) following tetrazine degradation through bio-orthogonal reactions. However, the underlying mechanisms driving this response remain only partially resolved, particularly regarding diminished FE efficiency deep-red near-infrared (NIR) regions. This knowledge gap has impeded efforts to optimize these for extended emission wavelengths improved ratios. review offers a photophysical perspective, discussing quenching pathways (i.e., energy flows charge separation) that regulate properties exhibited various types of labels. Moreover, work examines emerging role intramolecular rotations certain tetrazine-based structures integration additional quencher units. The proposed alternative channel potential surpass traditional wavelength constraints while achieving FE. By examining mechanisms, aims advance understanding tetrazine-functionalized provide guiding principles their future design practical applications.
Язык: Английский
Процитировано
0Bioconjugate Chemistry, Год журнала: 2024, Номер 35(7), С. 1024 - 1032
Опубликована: Июль 4, 2024
Tetrazine-derived fluorogenic labels are extensively studied for their potential in biological and medical imaging. Nonetheless, the fluorescence quenching mechanism numerous precursors continues to be debated, particularly as wavelengths extend into red near-infrared (NIR) regions. This challenge poses obstacles systematically optimizing fluorogenicity, i.e., achieving red-shifted improved turn-on signals through click reactions. paper highlights significance of photoinduced charge centralization (PCC), a observed tetrazine-fused with integrated π-conjugations. PCC is primarily responsible effects such emitting red-to-NIR spectrum. Drawing from structure-property relationships, this study proposes two molecular design strategies that incorporate constitutional isomerization develop high-performance tetrazine-based labels. These facilitate multiplex imaging following reactions, promising significant advancements bio-orthogonal techniques.
Язык: Английский
Процитировано
2European Journal of Organic Chemistry, Год журнала: 2024, Номер unknown
Опубликована: Авг. 19, 2024
Abstract Proof‐of‐concept studies for the bioorthogonally controlled generation of pro‐fluorescent quinone‐methides are presented here. The novel concept relies on a click‐to‐release tetrazine unit that chemically cages quinone methide precursor. On synthetically readily accessible model compound we demonstrate IEDDA reaction with TCO leads to liberation methide, which is captured by nearby nucleophiles form fluorescent scaffold. Unlike in previous approaches access activatable fluorogenic probes, where acted as quencher fluorescence, role redefined Such repurposed tetrazines foreseen address limitations tetrazine‐quenched red/NIR excitable probes.
Язык: Английский
Процитировано
1Organic & Biomolecular Chemistry, Год журнала: 2024, Номер 22(37), С. 7637 - 7642
Опубликована: Янв. 1, 2024
Conjugates of benzothiophene-fused azacyclononyne BT9N-NH2 with fluorescent dyes were developed to visualise azidoglycans intracellularly. The significance the cycloalkyne core was demonstrated by comparing new reagents DBCO- and BCN-dye conjugates. To reduce non-specificity during intracellular bioconjugation using SPAAC, less reactive BT9N-dye are preferred over highly
Язык: Английский
Процитировано
0Russian Journal of General Chemistry, Год журнала: 2024, Номер 94(11), С. 2833 - 2840
Опубликована: Ноя. 1, 2024
Язык: Английский
Процитировано
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