2021
DOI: 10.1016/j.inoche.2021.109026
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A 1,8-naphthalimide-based turn-on fluorescent probe for imaging Cu2+ in lysosomes

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Cited by 8 publications
(1 citation statement)
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“…Moreover, the low toxicity of the probe found its application in the bioimaging of the HeLa cells for monitoring Cu 2 + in lysosomes. [127] Nur et al (2022) designed and synthesized a 1,8-napthalimide-based fluorescent chemoprobe 85 for the detection of Cu 2 + ions in environmental samples. In the first step, 6-bromo-1,8-naphthalic anhydride (1) was reacted with n-butylamine under acidic conditions forming compound 41 which on further reaction with hydrazine at high temperature yielded compound 51 via nucleophilic substitution reaction.…”
Section: Detection Of Cu 2 + Ionsmentioning
confidence: 99%
“…Moreover, the low toxicity of the probe found its application in the bioimaging of the HeLa cells for monitoring Cu 2 + in lysosomes. [127] Nur et al (2022) designed and synthesized a 1,8-napthalimide-based fluorescent chemoprobe 85 for the detection of Cu 2 + ions in environmental samples. In the first step, 6-bromo-1,8-naphthalic anhydride (1) was reacted with n-butylamine under acidic conditions forming compound 41 which on further reaction with hydrazine at high temperature yielded compound 51 via nucleophilic substitution reaction.…”
Section: Detection Of Cu 2 + Ionsmentioning
confidence: 99%