Ing. Lucie Wohlrábová
+420 220 183 494
Vybrané publikace
BODIPY phototether enables oligonucleotide cyclization and subsequent deprotection by tissue-transparent red light
Chemical Communications 60 (32): 4366–4369 (2024)
meso-methyl-BODIPY photocages release a leaving group upon \nvisible light irradiation but often lack thermal stability. In turn, our\n thermally-stable, red-shifted BODIPY phototether allows oligonucleotide\n cyclization, preventing complementary strand hybridization. \nHybridization resumes upon red-NIR irradiation, disconnecting the \nphototether by oxidative cleavage, which is easily monitored by a blue \nshift in fluorescence.
Sulfonothioated meso-Methyl BODIPY Shows Enhanced Uncaging Efficiency and Releases H2Sn
Organic Letters 25 (36): 6705–6709 (2023)
Chalcogen-based ratiometric reversible BODIPY redox sensors for the determination of enantioselective methionine sulfoxide reductase activity
Chemical Communications 58 (44): 6389–6392 (2022)
Nejnovější publikace
Reversing protonation of weakly basic drugs greatly enhances intracellular diffusion and decreases lysosomal sequestration
eLife 13: RP97255 (2024)
BODIPY phototether enables oligonucleotide cyclization and subsequent deprotection by tissue-transparent red light
Chemical Communications 60 (32): 4366–4369 (2024)
Sulfonothioated meso-Methyl BODIPY Shows Enhanced Uncaging Efficiency and Releases H2Sn
Organic Letters 25 (36): 6705–6709 (2023)
Chalcogen-based ratiometric reversible BODIPY redox sensors for the determination of enantioselective methionine sulfoxide reductase activity
Chemical Communications 58 (44): 6389–6392 (2022)